Screening assessment for the challenge octamethylcyclotetrasiloxane (D4)

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Chemical Abstracts Service Registry Number
556-67-2

Environment Canada
Health Canada

November 2008

(PDF Version - 541 KB)

Synopsis

Pursuant to section 74 of the Canadian Environmental Protection Act, 1999 (CEPA 1999), the Ministers of the Environment and of Health have conducted a screening assessment on octamethylcyclotetrasiloxane (D4), Chemical Abstracts Service Registry Number 556-67-2. During the categorization process, this substance was identified as a high priority for screening assessment and included in the Ministerial Challenge because it had been considered to pose an intermediate potential for exposure to individuals in Canada and has been classified by another agency on the basis of reproductive toxicity. Further, it had initially been found to meet the ecological categorization criteria for persistence, bioaccumulation potential and inherent toxicity (PBiT) to non-human organisms and it is known to be in commerce in Canada.

Octamethylcyclotetrasiloxane, or D4, is an industrial chemical which was not manufactured by any company in Canada in 2006 in a quantity above the reporting threshold of 100 kg, but which was imported into the country in 2006 at a total quantity between 1 000 000 and 10 000 000 kg as an essentially pure substance, in mixtures with other cyclic siloxanes, as a residual in silicone polymers, and in finished consumer products.

The principal sources of release of D4 to the environment are industrial processes in which it is reacted to form silicone polymers, from blending, formulation and packaging operations. It is also released from the use and disposal of personal care products. Air, wastewater and agricultural soil are the principal receiving environmental media for D4 based on its physical-chemical properties and its use patterns.   

In air, D4 is persistent with calculated atmospheric half-lives of more than 5 days. D4 has the potential to be transported over long-distances in the atmosphere. However, it has a low potential to be deposited in water or soil in remote regions. The hydrolysis half-lives for D4 under Canadian water conditions (pH 6-9, temperature 5-25 °C) are estimated to range from hours to 45 days, indicating the substance is not persistent in water. The final hydrolysis product dimethylsilanediol is expected to biodegrade quite slowly.  D4 degradation in sediment appears to be much slower with half-lives of 49 to 588 days estimated under realistic Canadian sediment conditions (temperature of 5-25 °C), indicating the substance may be persistent in sediment. D4 is not considered persistent in soil, based on evidence of clay-catalysed degradation, with dimethylsilanediol being the stable hydrolysis product. Therefore, D4 has been determined to meet the persistence criterion as set out in the Persistence and Bioaccumulation Regulations.

The empirical bioconcentration factor and modelled bioaccumulation factor are both above 5000, indicating D4 may have a high potential to accumulate in aquatic organisms. However, data from a biomagnification study in fish and a biota-sediment accumulation study in invertebrates suggest that the bioaccumulation potential of D4 may be lower, possibly due to reduced bioavailability. Therefore, while D4 has the potential to accumulate in biota, it is not possible to conclude at this time that D4 meets the criterion for bioaccumulation as set out in thePersistence and Bioaccumulation Regulations based on consideration of the conflicting evidence from laboratory studies and predictive models.

Adverse effects from exposure to D4 in sediment-dwelling organisms were observed at concentrations above 44 mg/kg. The experimental toxicity data show that the substance can also cause long-term toxicity to sensitive pelagic aquatic organisms at relatively low concentrations (below its water solubility limit of 0.056 mg/L ). Risk quotients derived from exposure scenarios involving discharges of D4 from both consumer use and industrial operations, show a total of 249 sites (~23.4%) evaluated across Canada have predicted environmental concentrations in water higher than predicted no-effect concentrations for aquatic organisms. Considering D4's potential to bioaccumulate in biota and its high toxicity to sensitive aquatic organisms, long-term environmental exposure to D4 may cause adverse effects to aquatic organisms in certain Canadian environments. Based on this evidence, it is concluded that D4 has the potential to cause ecological harm.

Based principally on the weight of evidence-based assessments of the European Commission and the Danish EPA, an important effect of D4 exposure is impaired fertility. However, the Danish EPA also identified the liver as a target organ for D4 exposures. The critical effect level for repeated-dose toxicity via inhalation was based not only on increased liver weights, but also on effects observed in other organs (adrenals, thymus, lungs) in a three-month rat inhalation study. Comparison of the critical effect level for repeated dose effects via inhalation and the conservative upper-bounding exposure estimate via inhalation for D4 results in an adequate margin of exposure.  The critical effect level for repeated-dose toxicity via the oral route was based on decreased serum estradiol in 7-day mouse studies and decreased body-weights and relative liver weights in fetuses in 8-day rat studies (D4 administered to pregnant females). Comparison of the critical effect level for repeated dose effects via the oral route and the upper-bounding estimate of daily intake of D4 by the general population in Canada, results in an adequate margin of exposure.

Based on an independent review of a refined exposure assessment for personal care products, an adequate margin of exposure was derived by comparison of the critical effect level for repeated dose effects via the oral route and a conservative upper-bounding estimate of daily intake of D4 via use of personal care products.

Based on the available information on its potential to cause ecological harm, it is concluded that D4 is entering the environment in a quantity or concentration or under conditions that have or may have an immediate or long-term harmful effect on the environment or its biological diversity.

Based on the available information on its potential to cause harm to human health, it is concluded that D4 is not entering the environment in a quantity or concentration or under conditions that constitute or may constitute a danger in Canada to human life or health.

This substance will be included in the upcoming Domestic Substances List inventory update initiative. In addition and where relevant, research and monitoring will support verification of assumptions used during the screening assessment and, where appropriate, the performance of potential control measures identified during the risk management phase.

Based on the information available, it is concluded that D4 meets one or more of the criteria set out in section 64 of the Canadian Environmental Protection Act, 1999.

Introduction

The Canadian Environmental Protection Act, 1999 (CEPA 1999) (Canada 1999) requires the Minister of the Environment and the Minister of Health to conduct screening assessments of substances that have met the categorization criteria set out in the Act to determine whether these substances present or may present a risk to the environment or human health. Based on the results of a screening assessment, the Ministers can propose to take no further action with respect to the substance, to add the substance to the Priority Substances List (PSL) for further assessment, or to recommend that the substance be added to the List of Toxic Substances in Schedule 1 of the Act and, where applicable, the implementation of virtual elimination.

Based on the information obtained through the categorization process, the Ministers identified a number of substances as high priorities for action. These include substances that

The Ministers therefore published a notice of intent in theCanada Gazette, Part I, on December 9, 2006 (Canada 2006), that challenged industry and other interested stakeholders to submit, within specified timelines, specific information that may be used to inform risk assessment, and to develop and benchmark best practices for the risk management and product stewardship of those substances identified as high priorities.

The substance Cyclotetrasiloxane, octamethyl-, also known as D4, was identified as a high priority for assessment of human health risk because it was considered to present an IPE and had been classified by other agencies on the basis of reproductive toxicity. It was also identified as a high priority for assessment of ecological risk as it was found to be persistent (P), bioaccumulative (B) and inherently toxic (iT) to aquatic organisms and is known to be in commerce in Canada. The Challenge for this substance was published in the Canada Gazette on May 12, 2007 (Canada 2007). A substance profile was released at the same time. The substance profile presented the technical information available prior to December 2005 that formed the basis for categorization of this substance. As a result of the Challenge, more than 100 submissions of information were received for this substance pertaining to its physical and chemical properties, bioaccumulation potential, persistence, ecotoxicology, quantity in commerce, and so on.

Under CEPA 1999, screening assessments focus on information critical to determining whether a substance meets the criteria for defining a chemical as toxic as set out in section 64 of the Act, where

"64. [...] a substance is toxic if it is entering or may enter the environment in a quantity or concentration or under conditions that

(a) have or may have an immediate or long-term harmful effect on the environment or its biological diversity;
(b) constitute or may constitute a danger to the environment on which life depends; or
(c) constitute or may constitute a danger in Canada to human life or health."

Screening assessments examine scientific information and develop conclusions by incorporating a weight-of-evidence approach and precaution. 

This screening assessment includes consideration of information on chemical properties, hazards, uses and exposure, including the additional information submitted under the Challenge. Data relevant to the screening assessment of this substance were identified in original literature, review and assessment documents, stakeholder research reports and from recent literature searches, up to August 2008 for both human health and ecological sections of the document. Key studies were critically evaluated; modelling results may have been used to reach conclusions. When available and relevant, information presented in hazard assessments from other jurisdictions was considered. The screening assessment does not represent an exhaustive or critical review of all available data. Rather, it presents the most critical studies and lines of evidence pertinent to the conclusion.

Evaluation of risk to human health involves consideration of data relevant to estimation of exposure (non-occupational) of the general population, as well as information on health hazards (based principally on the weight-of-evidence assessments of other agencies that were used for prioritization of the substance). Decisions for human health are based on the nature of the critical effect and/or margins between conservative effect levels and estimates of exposure, taking into account confidence in the completeness of the identified databases on both exposure and effects, within a screening context. The screening assessment does not represent an exhaustive or critical review of all available data. Rather, it presents a summary of the critical information upon which the conclusion is based.

This screening assessment was prepared by staff in the Existing Substances Programs at Health Canada and Environment Canada and incorporates input from other programs within these departments. This assessment has undergone external written peer review/consultation. Comments on the technical portions relevant to human health were received from Toxicology Excellence for Risk Assessment (TERA). While external comments were taken into consideration, the final content and outcome of the screening risk assessment remain the responsibility of Health Canada and Environment Canada. Additionally, the draft of this screening assessment was subject to a 60-day public comment period. The critical information and considerations upon which the assessment is based are summarized below.

Substance identity

For the purposes of this document, Cyclotetrasiloxane, octamethyl- will be referred to as D4, an abbreviated name derived from the siloxane notation developed by General Electric (Hurd 1946).

D4 belongs to a group of cyclic volatile methyl-siloxanes (cVMS) with relatively low molecular weight (< 600) and high vapour pressure. These cVMS are volatile, low-viscosity silicone fluids consisting of [-Si(CH3)2O-]xstructure units in a cyclic configuration. D4 consists of four of these [-Si(CH3)2O-] structure units (x = 4) as shown in the chemical structure below (Table 1).

Table 1. Substance identity
Chemical Abstracts Service Registry Number (CAS RN) 556-67-2
Name on Domestic Substances List (DSL) Cyclotetrasiloxane, octamethyl-
National Chemical Inventories(NCI) names[1] Cyclotetrasiloxane, 2,2,4,4,6,6,8,8-octamethyl- (TSCA);
Cyclotetrasiloxane, octamethyl- (ENCS, AICS, PICCS, ASIA-PAC, NZIoC); Octamethylcyclotetrasiloxane (EINECS, ECL, PICCS); Cyclotetrasiloxane,octamethyl (PICCS)
Other names Cyclic dimethylsiloxane tetramer; D4; Tetracyclomethicone; Siloxane, octamethylcyclotetra-; Siloxanes and Silicones, octamethylcyclotetra-; Siloxanes, octamethylcyclotetra-; 1,1,3,3,5,5,7,7-Octamethylcyclotetrasiloxane; 2,4,6,8-Octamethylcyclotetrasiloxane; OMCTS; Cyclo(octamethyl)tetrasiloxane
Major chemical class or use Organosilicon compounds
Major chemical sub-class Cyclic volatile methyl siloxanes (cVMS)
Molecular formula C8H24O4Si4
Chemical structure  Chemical structure 540-97-6
Simplified Molecular Input Line Entry System (SMILES) C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1
Molecular mass 296.62 g/mol

[1] National Chemical Inventories (NCI). 2007: AICS (Australian Inventory of Chemical Substances); ASIA-PAC (Asia-Pacific Substances Lists); ECL (Korean Existing Chemicals List); EINECS (European Inventory of Existing Commercial Chemical Substances); NZIoC (New Zealand Inventory of Chemicals); PICCS (Philippine Inventory of Chemicals and Chemical Substances); and TSCA (Toxic Substances Control Act Chemical Substance Inventory).

It should be noted that D4 is also contained under another Chemical Abstracts Service Registry Number. This registry number, CAS RN 69430-24-6, refers to a mixture of dimethyl substituted cyclosiloxanes of the general structure [-Si(CH3)2O-]x in a cyclic configuration, where × is generally less than 8, and more commonly × is 3-7 (SEHSC 2007b). This CAS number is associated with the following names: cyclopolydimethylsiloxane, cyclopolydimethylsiloxane (DX), cyclosiloxanes di-Me, dimethylcyclopolysiloxane, polydimethyl siloxy cyclics, polydimethylcyclosiloxane, cyclomethicone and mixed cyclosiloxane. In this report it will be referred to as cyclomethicone, a term commonly used for the mixture in the cosmetics industry.

Physical and chemical properties

Table 2 contains experimental and modelled physical and chemical properties of D4 that are relevant to its environmental fate.

Table 2. Physical and chemical properties of D4
Property Type Value[1] Temperature (°C) Reference
Melting point
(°C)
Experimental 17.5[*]   PhysProp 2006
Modelled 1.78   MPBPWIN 2000
Boiling point
(°C)
Experimental 175.8[*]   PhysProp 2006
Modelled 159.41   MPBPWIN 2000
Density
(kg/m3)
Experimental 950 25 Hobson and Silberhorn 1995
Vapour pressure
(Pa)
Experimental 140[*]
(1.05 mm Hg)
25 Flaningam 1986
132
(0.99 mm Hg)
25 SEHSC 2007c
Modelled 157.3
(1.18 mm Hg)
25 MPBPWIN 2000
Henry's Law constant
(Pa·m3/mol)
Experimental 1 220 000[*]
(12.0 atm·m3/mol)
  Calculated from Kaw value of Xu and Kropscott 2007
11898
(0.117 atm·m3/mol)
25 Hamelink et al. 1996
60060
(0.593 atm·m3/mol)
28 Kochetkov et al.2001
57558
(0.568 atm·m3/mol)
28 Kochetkov et al.2001
Modelled 9119.3
(0.09 atm·m3/mol)
25 HENRIWIN 2000
Log Kaw
(Air-water partition coefficient)
(dimensionless)
Experimental 2.69[*] 21.7 Xu and Kropscott 2007
Log Kow
(Octanol-water partition coefficient)
(dimensionless)
Experimental 6.49[*] 25.1 Kozerski and Shawl 2007
5.1   TSCATS 2006
4.45   Bruggeman et al. 1984
Modelled 5.09   KOWWIN 2000
Log Koc
(Organic carbon-water partition coefficient) (dimensionless)
Experimental 4.22[*] 24 Miller 2007
Modelled 4.25   PCKOCWIN 2000
Water solubility
(mg/L)
Experimental 0.0562[*] 23 Varaprath et al.1996
0.074 (freshwater)   Hobson and Silberhorn 1995
0.033 (saltwater)   Hobson and Silberhorn 1995
Modelled 0.05 25 WSKOWWIN 2000
Log Koa
(Octanol-air partition coefficient)
(dimensionless)
Experimental 4.34[*] 25 Xu 2006
Modelled 4.42   Calculated from modelled Log Kow-Log Kaw

[1] If different, values and units in parentheses represent the original values as reported by the authors or as estimated by the models.
[*] Values used in modelling for this screening assessment.

A recent experimental log Kow for D4 (99.77% purity) at 25.1°C was determined by using the slow stir method following OECD Draft Guideline 123 (Kozerski and Shawl 2007). The measurement of Kow was carried out in triplicate with one blank control. Two-litre borosilicate glass vessels were used in performing the equilibrium and were charged with 1.6 L high-purity water followed by adding 0.11 L of 1-octanol carefully to minimize droplet formation. The test was initiated by adding 0.9 mL of D4 spiking solution (56.53 mg D4/g) in 1-octanol to the test vessel. The temperature was maintained at between 24.8 and 26.0°C (averaged 25.1°C) during the study, except when temperature temporarily reached 26.3°C eight hours after test initiation. It was concluded that equilibrium was achieved 24 hours after test initiation. The weighted average Kow was calculated to be 6.49. A headspace of 0.3 L (15% total volume) was present in the test vessels, indicating that D4 may have volatized into the headspace from the water phase (high vapour pressure, low water solubility). However, a flask mass balance check suggested that the total vaporized D4 was less than 2%. Therefore, the study is considered acceptable and the log Kow of 6.49 will be used for this screening assessment report.

Other log Kow values of 4.45 and 5.1 were reported by TSCATS (TSCATS 2006) and Bruggeman et al. (1984). The log Kow value of 5.1 was obtained from a direct experimental study of the octanol-water partition coefficient of D4 using the shake flask method. The study was unpublished and the detailed test design was not available. It is apparent that precautions were taken in the study to ensure that the D4 concentration in the aqueous phase was below its water solubility. The testing system was vigorously mixed followed by equilibration to separate the two phases. It was speculated (Kozerski and Shawl 2007) that microdroplets of octanol might be present in the aqueous phase due to the mixing method used. This could lead to the underestimation of the Kow value. The log Kow value of 4.45 was determined by Bruggeman et al. (1984) using a high-performance liquid chromatography (HPLC)-retention time method. The measurement was performed on an octadecylsilyl-bonded silica column with 90:10 methanol:water as the mobile phase. Homologous series of n-alkylbenzenes with known log Kowvalues were used as reference compounds to calibrate the method. The experimental details of this study are currently unavailable.

Recent experiments on the air-water partition coefficient for D4 and D5 were conducted by Xu Kropscott (2007). The partitioning equilibrium among air, water and an organic phase (octanol) was simultaneously achieved during the experiment; the log Koa was calculated to be 4.37 and the log Kow was calculated to be 6.98 for D4. Both values are reasonably consistent with the measured experimental values reported by Xu (2006, Table 2) and Kozerski and Shawl (2007),. The study is therefore considered acceptable and the log Kaw of 2.69 for D4 from the study will be used for this screening assessment report. A custom-made double syringe system was designed for measuring the partitioning equilibrium among the three phases. The system consisted of two air-tight syringes with the left syringe containing 5 mL octanol-saturated water, 14C-labelled D4 in octanol on top of the water phase, and a gas phase of 70-80 cm3. The right syringe contained a 60-80 mL octanol-saturated water phase and a 20-40 cm3 air phase. The air phases of the two syringes were connected during the test. The equilibrium between the air and water phase was accelerated by the slow stirring of water and was reached after 20 hours. The average log Kaw of 2.69 for D4 at 21.7°C was thus determined based on the total D4 radioactivity in air and water. This value is in good agreement with the equilibrium of log Kow = log Koa + log Kaw. The experimental Kaw gives a Henry's Law constant of 1 220 000 Pa·m3/mol at 21.7°C. 

For D4, other modelled physical and chemical properties are in good agreement with its measured experimental data. Except for the data discussed above, the most conservative experimental data, when applicable, are used in various model predictions in this screening assessment report.

Sources

There are no known natural sources of D4.

D4 is an industrial chemical which was not manufactured by any company in Canada in 2006 in a quantity above the reporting threshold of 100 kg, but which is imported into the country as an essentially pure substance (greater than 99% purity), in mixtures with other cyclic siloxanes, as a residual in silicone polymers, and in finished consumer products. From responses to a notice published under section 71 of CEPA 1999, it was determined that between 1 000 000 and 10 000 000 kg of D4 were imported into Canada in 2006, as raw materials or in finished products (Environment Canada 2007).

D4 is a constituent of CAS RN 69430-24-6, termed cyclomethicone in the cosmetics industry. Although cyclomethicone was not directly surveyed under CEPA section 71 by Environment Canada and Health Canada in 2007, it is evident that in some cases, responses to the notice published under section 71 of CEPA 1999 for the 2006 calendar year contained data on the quantity of D4 used or imported as CAS RN 69430-24-6 (Environment Canada 2007).

The quantity of CAS RN 69430-24-6 reported in commerce in Canada during the 1986 calendar year was 2 220 000 kg (Environment Canada 1988). In 2005, Canada was a net importer of 11 500 000 kg of all types of silicone polymers and siloxanes (Will et al.2007).

Polydimethylsiloxane (PDMS) silicone polymers are produced from D4, and all PDMS contains residual amounts of volatile cyclosiloxanes, including D4. The lower molecular weight (and consequently lower viscosity) polymers may contain from < 0.1% to 0.5% volatile cyclosiloxanes, and higher molecular weight (and consequently higher viscosity) polymers may contain 1-3% volatile cyclosiloxanes. The proportion of the volatile cyclosiloxanes that consists of D4 is highly product-specific. Release of D4 from some applications of PDMS is expected to occur once the PDMS product is in use (SEHSC 2007a).

D4 has been identified as a high production volume (HPV) chemical by the Organisation for Economic Co-operation and Development (OECD 2007), the European Chemicals Bureau (ECB 2007), and the US Environmental Protection Agency (US EPA 2007).

In the United States, there is a trend toward the increased use of volatile methyl-siloxanes, including D4, because of their exemption from volatile organic compound (VOC) legislation in 1994 (US EPA 1994). Volatile methyl-siloxanes were used as an alternative to chlorofluorocarbons (CFCs) as a means of reducing the regulated VOC content in products (specifically, precision and electronic cleaning applications). According to information from the US EPA, the import/production of D4 in the United States was in the range of 22 500-45 000 tonnes in all reporting years from 1986 to 2002. 

In Europe, D4 has been classified as R53, "may cause long-term adverse effects in the aquatic environment," and R62, "possible risk of impaired fertility" (ECB 2007). Four companies have been identified as producers/importers of D4 by the European Chemicals Bureau: Bayer AG and Wacker-Chemie GmBH of Germany, Rhone-Poulenc Chimie of France and Dow Corning Europe of Belgium (ECB 2007). The quantity of D4 used in the European Union as a site-limited intermediate and in household products during 2003-2004 is confidential information.

Uses

The most important use, worldwide and in Canada, of high-purity D4 is as a raw material in the manufacture of silicone polymers and copolymers. All silicone polymers contain trace residual amounts of volatile cyclosiloxanes, including D4. D4 is also used in personal care products. As indicated above, D4 is also a constituent of CAS RN 69430-24-6, cyclomethicone.

Cyclomethicone is a mixture of low molecular weight volatile cyclic siloxanes, the principal ingredients of which are octamethylcyclotetrasiloxane (D4), decamethylcyclopentasiloxane (D5) and dodecamethylcyclohexasiloxane (D6), in varying proportions. In Canada, the most important uses of the mixtures of low molecular weight volatile cyclic siloxanes, which may contain a high percentage of D4 or of D5, are in the preparation of personal care products, including hair and skin care products and antiperspirants (Environment Canada 2007).

Silicone polymers that contain trace amounts of D4 can be grouped as fluids, gums and resins. Uses of such polymers are described below.

Important uses of silicone fluids include as a formulation component of personal care products for hair and skin care, antiperspirants and deodorants; pharmaceuticals; processing aids such as defoamers; surfactants and mould release agents; lubricants; polishes and coatings on a range of substrates including textiles, carpeting and paper; sealants; architectural coatings; mechanical, heat transfer and dielectric fluids; and reprography (Will et al. 2007).

While it is anticipated that higher molecular weight polymers are used in most of these applications, D4 was reported for use as a defoamer (Environment Canada 2007). Defoamers are employed often at parts per million levels in a range of processing industries including pulp and paper, food, petrochemical, petroleum, and chemical manufacture as well as water treatment. Silicones are also used as defoamers in household products such as cleaners and detergents (Will et al. 2007).

The use of silicone formulants containing D4 in certain pesticide products is regulated in Canada under the Pest Control Products Act (PMRA 2007).

Biomedical uses of silicone gels and fluids in Canada include medical devices, blood-handling equipment, as a blood defoaming agent, as protective barriers and lubricants and as surface treatment of wound dressings. Silicone fluids have been approved as active and non-active ingredients in pharmaceuticals in Canada (DPD 2007), the most common use being in anti-flatulence drugs.

Silicone gums are used in the production of elastomers that are used as sealants and adhesives, and in moulded silicone rubber, film and fabric coatings and encapsulation. Silicone elastomers are used in the manufacture of consumer products such as pacifiers. Silicone elastomers are also used in a large number of biomedical applications including short- and long-term implants and prostheses, catheters, contact lenses and dentures (Will et al. 2007).

Silicone resins are primarily used in specialty coatings applications, and in the production of silicone-modified polymers (Will et al. 2007). Consumers may be exposed to D4 through the use of these products and by occupying enclosed spaces where coatings, caulking, sealants and silicone rubber are used as building materials or are present in consumer products.

Releases to the environment

D4 is not reported as part of Environment Canada's National Pollutant Release Inventory. This substance belongs to a chemical group used in various industry and consumer applications that are associated with widespread releases.

D4 may be emitted to the environment from industrial processes in which it is reacted to form silicone polymers and co-polymers and from blending, formulation and packaging operations. All of these operations take place in Canada (Environment Canada 2007). Industrial releases of D4 may also occur when silicone polymers are used in process industries as foam control agents, as mould release agents, as lubricants, and in other applications. The releases from industrial processes are expected to be to the atmosphere and wastewater. D4 will be released during the use of personal care products such as hair and skin care products, antiperspirants and others, and these releases will be to air and wastewater. It is estimated that 92% of D4 used in personal care products enters the atmosphere (Allen et al. 1997).

Detection of D4 at sewage treatment plants, landfills and near industrial plants as well as in indoor and ambient air away from industrial activity is evidence that both point sources and disperse sources contribute to the concentration of D4 in the environment (Norden 2005; Kaj et al. 2005; personal communication, Environment Canada, Canadian Centre for Inland Waters, 2007 [unreferenced]). The application of D4-containing pesticides on crops and the disposal of sewage sludge on agricultural lands and in landfills will result in the release of D4 to environmental media. There is some evidence that D4 is a transient degradation product of PDMS in contact with soil, while the principal degradation products are silanols prior to complete mineralization (Herner et al. 2002). Thus, in addition to release of residual D4 from PDMS manufacture, there may be de novo synthesis of D4 occurring in landfills and agricultural lands where sewage sludge containing PDMS is spread, although the overall contribution of PDMS degradation is not considered significant under environmental conditions.

Mass Flow Tool

To estimate the potential release of D4 to the environment at different stages of its life cycle, a Mass Flow Tool was used. Empirical data concerning releases of specific substances to the environment are seldom available. Therefore, for each identified type of use of the substance, the proportion and quantity of release to the different environmental media are estimated, as are the proportions of the substance chemically transformed or sent for waste disposal. Assumptions and input parameters used in making these estimates are based on information obtained from a variety of sources including responses to regulatory surveys, Statistics Canada, manufacturers' websites and technical databases. Of particular relevance are emission factors, which are generally expressed as the fraction of a substance released to the environment, particularly during its manufacture, transformation, and use associated with industrial processes. Sources of such information include emission scenario documents, often developed under the auspices of the Organisation for Economic Co-operation and Development (OECD), and default assumptions used by different international chemical regulatory agencies. It is noted that the level of uncertainty in the mass of substance and quantity released to the environment generally increases further down the life cycle.

Table 3. Estimated releases and losses of D4 to environmental media, transformation and distribution to management processes, based on the Mass Flow Tool
Fate Proportion of the mass (%)[1] Major life-cycle stage involved[2] 
Releases to environment:
 To soil 0.0 -
To air 11.9 Industrial use and consumer use
To sewer[*] 4.9 Production, formulation, industrial use and consumer use
Chemically transformed 82.5 Industrial use
Transferred to waste disposal sites (e.g., landfill, incineration) 0.8 Waste disposal

[*] Wastewater before any form of treatment
[1] For D4, information from the following OECD emission scenario documents was used to estimate releases to the environment and distribution of the substance as summarized in this table: OECD 2004; OECD 2006. Values presented for release to environmental media do not account for possible mitigation measures that may be in place in some locations (e.g., partial removal by sewage treatment plants). Specific assumptions used in the derivation of these estimates are summarized in Environment Canada 2008a.
[2] Applicable stage(s): production, formulation, industrial use, consumer use, service life of article/product, waste disposal.

Based on the information available, about 82.5% of the quantity of D4 imported into Canada is used as a chemical intermediate by the silicone industry and is thereby considered to be chemically transformed during the manufacturing process (Table 3). For the remaining D4, the main compartments of release are to air (11.9%) and wastewater (4.9%). Air receives the highest proportion of releases, a result of the use of consumer products such as skin creams, sun creams or polishes and also volatilization of residues in silicone polymers, especially during the first year of use. Releases to wastewater are estimated to be approximately 4.9% from point sources during on-site formulation of personal care products and from diffuse sources associated with the use of personal care products (e.g., hair care products).

Environmental fate

Based on its physical and chemical properties (Table 2) and the results of Level III fugacity modelling (Table 4; model input parameters are listed in Appendix 5 of this screening assessment), D4 may partition in significant quantities to any environmental medium, depending on the compartment of release.

Table 4. Results of the Level III fugacity modelling for D4 (EQC 2003)
Substance released to Percentage of substance partitioning into each compartment
Air Water Soil Sediment
Air (100%) 100.0 0.0 0.0 0.0
Water (100%) 13.6 72.2 0.0 14.2
Soil (100%) 88.5 0.0 11.5 0.0

Based on the available information (Table 3), the environmental release of D4 is estimated to be mainly to air (12% of the total mass). A vapour pressure of 132-157.3 Pa and a Henry's Law constant of 1 220 000 Pa·m3/mol, as well as a long half-life in air, indicate that 100% of the mass fraction released to air will remain there until it is degraded by hydroxyl radicals in air (Table 4).

When D4 is released to water it is expected to adsorb to suspended solids, such as sewage sludge and sediments, based on its log Koc value of 4.22. Results of the Level III fugacity simulation for release to water show that approximately 14.2% will reside in the solid phase (suspended sediment and bed sediments) and 72.2% will reside in the aqueous phase (water column). Although the log Koc for the compound is in the moderate to high sorption range, the rapid hydrolysis of D4 in water at ambient temperature reduces the fraction that is expected to be adsorbed to sediments. Volatilization from water surfaces is also expected based upon the air-water partition coefficient (Kaw); the mass fraction expected to partition to air from volatilization at 25oC is 13.6% (Table 4).

When D4 is released to soil through, for example, the application of sewage sludge on moist agricultural soils, approximately 88.5% of the mass fraction is estimated to partition to air. This estimate is consistent with the observation of Xu (1999) that volatilization is the major loss process of cyclic siloxanes from moist soils. Only a small percentage (11.5%) will remain in soil associated with solids, for the same reasons as described for sediment. In dry soil, D4 will be quickly degraded by clay minerals in soil to form dimethylsilanediol as the final breakdown product (Xu 1999, Xu and Chandra 1999).

Persistence and bioaccumulation potential

Environmental persistence

Atmospheric degradation

The Level III fugacity model results (Table 4) indicate that D4, when released to air, will remain in air, where it is expected to be slowly oxidized by the gas-phase reaction with photochemically produced hydroxyl radicals. The empirically derived half-life for D4 in the gas-phase hydroxyl (OH) radical reaction is 10.6 days (Atkinson 1989, 1991; see Table 5a). This is based on an experimental reaction rate of 1.01 × 10-12 cm3/mol.sec (Atkinson 1989), which may be converted to an estimated half-life of 10.6 days, assuming first-order kinetics, a 12-hour day, and 1.5 × 106 OH/cm3. D4 is not expected to react, or react appreciably, with other photo-oxidative species in the atmosphere, such as O3; nor is it likely to degrade via direct photolysis (Atkinson 1991). Therefore, it is expected that reactions with hydroxyl radicals will be the most important fate process in the atmosphere for this substance.

Recent measurements of hydroxyl radical concentrations in an urban environment (Ren et al. 2003, Kramp and Volz-Thomas 1997, Rivett et al. 2003) suggested that there is a higher OH concentration in the urban atmosphere than that observed in the rural and marine atmosphere due to higher OH radical precursors in polluted urban areas (SEHSC 2008b). Ren et al. (2003) have measured the concentration of hydroxyl radicals in the summer atmosphere in New York City, NY, USA. The measurement was conducted over a 34-day period. The average maximum hydroxyl radical concentration was reported to be 7 × 106 OH/cm3 and was comparable to those measured (1-10 × 106 OH/cm3) in similar urban environments of the United States (Los Angeles, CA, and Nashville, TN; SEHSC 2008b) and in European countries (Kramp and Volz-Thomas 1997, Rivettet al. 2003). However, most of these measurements were carried out during the summer, when the sunlight was strong and the atmospheric photochemistry was active. The OH radical concentration measured by Ren et al. (2006) in the winter in New York City was 5 times lower than in the summer at the same site. The measurement was conducted over a 28-day period and the maximum concentration was 1.4 × 106OH/cm3. Therefore, half-lives of 5.5 to 22.8 days can be calculated assuming first-order kinetics, a 12-hour day, and a daily average hydroxyl concentration of 3.5 × 106 OH/cm3and 0.7 × 106 OH/cm3 (daily average concentration = maximum concentration/2), in summer and winter, respectively. It is therefore concluded that D4 could be degraded more rapidly in urban centers in summer seasons when the atmospheric hydroxyl radicals are most abundant. However, when a yearly average removal half-life is considered, it is consistent with the half-life of 10.6 days estimated with a hydroxyl radical concentration of 1.5 × 106 OH/cm3. The degradation half-life of 10.6 days is considered critical and will be used for D4 in environmental fate modelling.

Navea et al. (2007) have investigated the effects of ozone, aerosols and solar radiation on the fate of D4 and D5 in a simulated environment chamber. They concluded that mineral aerosols such as kaolinite and hematite can significantly accelerate the removal of D4 and D5 from the gas phase of the atmosphere, especially under daytime conditions. The finding also indicated that ozone can further accelerate these removal processes for D4 and D5. Although obtained data suggested that mineral aerosols, combined with ozone, may have significant effects on the environmental fate of cVMS in the air, it is difficult to quantitatively extrapolate the results of the simulations to realistic environmental conditions. First, it should be noted that the study was conducted under unrealistically high concentrations of cVMS, mineral aerosols and ozone. Second, mineral and carbon black samples used in the study were high-purity (> 99%) analytical samples that provided maximum surface area and thus the maximally available sorption sites, i.e., ideal conditions for D4/D5 absorption. The degree to which these pure minerals are representative of the particulate matter in air is questionable. Third, it is reasonable to believe that minerals such as kaolinite and hematite can be found in atmospheric particular matter (PM); however, they are unlikely to be the most common and abundant components in atmospheric dust. In addition, it should be mentioned that the study was conducted in a simulated environment chamber and involved reacting the mineral aerosols with only one cVMS (D4 or D5) at a time. Under actual environmental conditions, thousands of chemicals compete for aerosols' adsorption sites. Therefore, in such conditions, the "effectiveness" of D4/D5 removal from ambient air could be significantly lower than that observed in the chamber's mono-component atmosphere. 

Thus, it may be concluded that the degree to which aerosols and ozone accelerate degradation of cVMS in air under realistic environmental conditions is uncertain.

The AOPWIN (2000) model (Table 5b) also provides evidence indicating the potential for persistence of this substance, with a predicted atmospheric oxidation half-life of 4-19 days. Thus, the empirical and model data both demonstrate that this substance is persistent in air (half-life > 2 days) in accordance with thePersistence and Bioaccumulation Regulations (Canada 2000).

Table 5a. Empirical data for persistence of D4
Medium Fate process Degradation value Degradation endpoint/units Reference
Air OH reaction 10.6 Half-life (days) Atkinson 1989, 1991
Air OH reaction 5.5-22.8 Half-life (days) Ren et al. 2003, 2006
Water Biodegradation 3.7 % 28 d degradation Springborn Smithers Laboratories 2005
Water Hydrolysis 0.04-45 Half-life (days)
pH 6-9
5-25°C
Durham 2005
Kozerski 2008
Bidleman 2008
Water/sediments Biodegradation No biodegradation 28d degradation Springborn Laboratories 1991
Water/sediments Abiotic degradation 49-588 Half-life (days)
neutral pH
5-25°C
Xu and Miller 2008
Soil (Wahiawa soils from Hawaii) Clay-catalyzed hydrolysis 1 hour
(32% relative humidity)
Half-life (hours) Xu 1999
Xu and Chandra 1999
Soil (Londo soils from Michigan) Clay-catalyzed hydrolysis 3.54 days (32% relative humidity);
5.25 days (93% relative humidity)
Half-life (days) Xu and Chandra 1999
Table 5b. Modelled data for persistence of D4
Medium Fate process Degradation value Degradation endpoint/units Model
Air Atmospheric oxidation 8.94 Half-life (days) AOPWIN 2000
Air Atmospheric oxidation 3.8-19.2 [2] Half-life (days) AOPWIN 2000
Air Ozone reaction Non-reactive Half-life AOPWIN 2000
Water Biodegradation 37.5 Half-life (days) BIOWIN 2000, Ultimate survey
Water Biodegradation 0.0 (does not biodegrade fast) Probability BIOWIN 2000, MITI Linear Probability
Water Biodegradation 0.0028 (does not biodegrade fast) Probability BIOWIN 2000, MITI Non-linear Probability
Water Biodegradation 2.9% BOD BOD (MITI 301C)[1] CATABOL c2004-2008
Water Biodegradation
(anaerobic)
0.2 (does not biodegrade fast) Probability BIOWIN 2000

[1] Results from CATABOL biodegradation simulation show that D4 is in the global parameter domain and metabolic domain, but out of the structural domain. The most important of these domains is the metabolic domain, and CATABOL suggests that the substance will not be degraded, as the probability of stable methyl group and aromatic ring oxidation products is low.
[2] Atmospheric oxidation half-lives re-calculated with measured OH radical concentrations from New York City in summer and winter, respectively.

Degradation in water and sediment

The empirical hydrolysis data for D4 (Durham 2005) were critically reviewed by internal experts (Bidleman 2008); the results of these reviews are summarized below. The hydrolysis kinetics of D4 were determined by measuring the disappearance of radio-labelled 14C-octamethylcyclotetrasiloxane (D4) as a function of time based on OECD Guideline 111. Reactions were investigated in flame-sealed borosilicate glass tubes at pH values of 4, 7 and 9 and temperatures of 10°C, 25°C and 35°C. The initial test concentration was targeted at 20 µg/L upon spiking, corresponding to ½ - 1/3 of the water solubility of D4. Tetrahydrofuran (THF) was used as a solubilizer at a concentration of 0.8% v/v. A similar hydrolysis kinetics study was also conducted for radio-labelled 14C-decamethylcyclopentasiloxane (D5) at the same laboratory (Durham 2006). The hydrolysis rates of D4 and D5 were reported to be pH-dependent and followed pseudo first-order kinetics. Both D4 and D5 were found to undergo rapid hydrolysis under acidic (pH 4) and basic (pH 9) conditions, with average half-lives (t½) ranging from minutes to less than 6.5 hours for D4 and from hours to less than 6 days for D5 at 10-35°C. Two additional hydrolysis tests were performed for D5 at near-neutral (pH 5.5 and 8) conditions at 25°C and their t½ were approximately 15 and 9 days, respectively. The half-lives at neutral pH 7 conditions increased significantly for D4 and D5. The hydrolysis products were intermediates dimethylsiloxane-alpha, and omega-diol oligomers HO(Me2SiO)nH (n=2-4 or 5), while dimethylsilanediol (DMSD) was the final hydrolysis product. Although the loss of parent compounds and poor reproducibility were reported at neutral pH, loss rates at neutral pH may be estimated using the second-order rate constants for the acid- and base-catalyzed reactions. The hydrolysis studies for D4 and D5 are thus considered reliable for this screening assessment. An error in the calculation of the hydroxide catalytic constant, kOH at temperatures other than 25°C has, however, been identified by Bidleman (2008). Table 6 lists revised second-order rate constants for hydronium and hydroxide-catalyzed hydrolysis of D4 (Kozerski 2008).

Table 6. Revised second-order hydrolysis rate constants (i.e., catalytic constants) for D4 (Kozerski 2008)
Rate constant (M-1h-1) Temperature (°C)
5 10 25 35
kH 1110 1560 3910 8020
kOH 28400 40200 73300 168000

The pseudo first-order rate constants, kobs, for the hydrolysis of D4 can be calculated using the following kinetic equation (assuming negligible contribution of uncatalyzed hydrolysis as, confirmed by the experiments at a pH of 7):

kobs = kH+[H+] + kOH-[OH-]

The calculated half-lives for D4 (Table 7) under realistic Canadian environmental conditions (pH 6-9, temperature 5-25°C) (GEMStat 2008, NOAA 2008) are in the range of 0.04-45 days.

Table 7. Calculated D4 half-lives under realistic Canadian environmental conditions
Temperature (°C) Water dissociation constant pKw pH Rate constant
k (h-1)
Half-life (days)
25 14 6 4.64E-03 6.2
7 7.72E-03 3.7
8 7.33E-02 0.4
9 7.33E-01 0.04
10 14.52 6 1.68E-03 17
7 1.37E-03 21
8 1.21E-02 2.4
9 0.121 0.24
5 14.73 6 1.16E-03 25
7 6.4E-04 45
8 5.30E-03 5.5
9 5.29E-02 0.55

New information received on microbial degradation indicates that D4 is not likely to be biodegraded in water. The 28-day ready-biodegradability test was performed in sealed vessels in accordance with OECD Draft Guideline 310 and data showed limited biodegradation (3.7%) of D4 over 28 days in a ready-biodegradation test (Springborn Smithers Laboratories 2005). These data are further supported by two of the models in Table 5b. These models indicate that the probability of biodegradation of D4 in water is effectively zero. Also, BIOWIN reported an overall weighted conclusion of "not readily biodegradable" based on the combined results of the BIOWIN3 and BIOWIN5 models.

Experimental and modelled biodegradation data indicate that D4 has little potential to biodegrade in aqueous environments. Therefore, hydrolysis is the major degradation process for D4 in water. The weight of evidence suggests that D4 will undergo hydrolysis with half-lives of less than 45 days in Canadian water (pH 6-9, temperature 5-25°C). It is therefore concluded that D4 does not meet the criterion of persistence in water (t½ > 182 days) under the Persistence and Bioaccumulation Regulations (Canada 2000).

A preliminary degradation study for D4 in a water/sediment system has been received recently (Xu and Miller 2008). A modified OECD 308 guideline was followed. The study was conducted at ambient temperature (22-25°C) with natural sediment (sandy silt, high OC content, 70% water content and 11% organic matter, pH 7) and water collected from deep under an uncontaminated lake. Radio-labelled D4 in diethylene glycol methyl ether was added via syringe at 10-15 spots on the surface sediment in each flask after the overlying water was carefully removed. Overlying water was again added onto the spiked sediment with minimum disturbance of sediment. Spiking of sediment instead of water ensured the substance's distribution in sediment. This properly addressed the substance's specific physical and chemical properties (high volatility and potential hydrolysis) and improved the reproducibility of the study. The concentrations of D4 measured from day 6 to day 22 (test termination) indicated that a steady state had been reached between water and sediment, with more than 95% D4 and radioactivity being detected in sediment. As demonstrated in the hydrolysis study of D4, the degradation products in sediment/water were intermediates dimethylsiloxane-alpha, and omega-diol oligomers HO(Me2SiO)nH (n=2-4), while dimethylsilanediol (DMSD) was the final degradation product. The calculated half-life for D4 degradation in sediment was 49 days at 22-25°C. The same degradation products observed in the study and in the hydrolysis study of D4 suggested that hydrolysis was the major degradation process in the sediment/water system. The major uncertainty in the study is the lack of test replicates.

An earlier study demonstrated no biodegradation of D4 in an enclosed water/sediment system (Springborn Laboratories 1991). A modified eco-core technique was used in the study of D4 biodegradation in sediment. Natural sediment (3.2% organic carbon, pH 5.5) and water were collected from an uncontaminated pond. Radio-labelled D4 was added directly to the aqueous phase of the test systems. The rate of mineralization and disappearance of the parent compound were determined by passing CO2-free air through the core chambers and trapping exhaust gases on a volatile organic trap and an alkaline CO2 trap. It was concluded that no biodegradation of D4 occurred in the water/sediment test system. It was also reported that the majority of the parent compound had been volatilized and collected in the organic trap. Furthermore, by day 28 of the study, only a small amount of D4 (< 5%) remained in water or had partitioned into sediment. A series of supplemental experiments were conducted to show that the small amount (< 10%) of degradation products recovered from the alkaline CO2 trap in the test systems and the sterile controls were caused by alkaline-catalyzed hydrolysis of D4. It is therefore concluded that D4 is not likely to biodegrade or biodegrade to a significant degree in sediment. In addition, the low D4 partitioning to sediment raises the question of whether the experimental design adequately addresses sediment degradation.

The study by Xu and Miller (2008) suggests that D4, indeed, breaks down to oligomer diols as intermediates, with the final product being dimethylsilanediol, under ambient conditions in sediment with a half-life of 49 days. Since no data were available for degradation half-lives at lower temperatures, a read-across approach using the D4 hydrolysis data was applied. The hydrolysis half-lives of D4 in water were 6-12 times longer when water temperatures were decreased to 5-10 °C from 25°C. Assuming a similar trend of decreases in sediment, the estimated half-lives for D4 in sediment are 294 and 588 days, at 10°C and 5°C, respectively. It is therefore concluded that D4 meets the criterion of persistence in sediment of t½ > 365 days in accordance with the Persistence and Bioaccumulation Regulations (Canada 2000). The extrapolation of D4 sediment degradation at lower temperatures based on hydrolysis, however, is not without uncertainty. The assumption that the loss of D4 in sediments is solely a function of hydrolysis in the pore water does not take into account the fraction that may be sorbed to the solid phase-degradation processes and rate of which are unknown.

Degradation in soil

Although no empirical data on biodegradation in soils are available, as noted above, microbial degradation of D4 in water and a water/sediment system is negligible based on the ready-biodegradation test (Springborn Smithers Laboratories 2005), sediment biodegradation test (Kent et al. 1994) and predictions of five of the six biodegradation models (Table 5b).

Xu (Xu 1999, Xu and Chandra 1999) has extensively investigated potential degradation pathways of cyclosiloxanes, including D4, D5 and D6, in Wahiawa soil from Hawaii at room temperature and 32% relative humidity. He concluded that the ring-opening polymerization reaction to form polydimethylsiloxane (PDMS), the demethylation of cyclosiloxanes and the hydrolysis were insignificant in soils at concentrations of < 200 mg/kg dry weight. Clay-catalyzed hydrolysis of D4 was observed in highly weathered Wahiawa soils. Tetramer, trimer, dimer and monomer diols were reported as the intermediates, and dimethylsilanediol (DMSD) was reported as the final hydrolysis product. Upon re-wetting of the soil after seven days, only D4, D3 and DMSD were present, and a small amount of D5 and D6, indicating that higher oligomer diols may undergo backward reaction of ring-opening process. The hydrolysis degradation half-life of D4 on Wahiawa soil (55% clay content, 2.1% water content) was 1 hour at 22°C under dry soil conditions. It was suggested that the dryness of soil severely limits the biological activity but promotes abiotic reactions such as surface-acid-catalyzed hydrolysis of PDMS, a polymer with the same dimethylsiloxane backbone as cyclosiloxanes (Xu 1999). The degradation rates of cyclosiloxanes were highly dependent on soil moisture, clay type and clay content, as well as the size of the siloxane molecules that determine the rate of diffusion to the surface catalytic sites. The hydrolysis rate of D4 decreased in temperate Londo soils from Michigan (22% clay content) to 3.54 days half-life at 32% relative humidity and 5.25 days half-life at 93% relative humidity. However, most of the D4 remained in Londo soil during the 21-day incubation in an enclosed system at 100% relative humidity, while the degradation half-life of D4 was less than 1 day in highly weathered Wahiawa soil under the same humidity. Volatilization becomes the major loss mechanism for D4 under such soil conditions in an open system.

Based on the available empirical studies that show the potential for rapid clay-catalyzed hydrolysis in surface soils, D4 is not considered persistent in soil according to the criterion of t½ >182 days as stated in the Persistence and Bioaccumulation Regulations (Canada 2000).

The available empirical and modelled data indicate that D4 meets the persistence criteria for air (half-life ≥ 2 days) and sediments (half-life ≥ 365 days) as set out in the Persistence and Bioaccumulation Regulations (Canada 2000), but that it does not meet the half-life criterion for soil and water (i.e., half-lives are 182 days).

Long-range transport potential

The Transport and Persistence Level III Model (TaPL3 2000), a regional model, was used to estimate the characteristic travel distance (CTD) of D4. CTD is defined as the maximum distance travelled in air by 63% of the substance. Beyer et al. (2000) have proposed that CTDs of > 2000 km represent high long-range atmospheric transport potential (LRATP), those of 700–2000 km represent moderate LRATP, and those of < 700 km represent low LRATP. Based on the CTD estimate of 5284 km, the long-range atmospheric transport potential of D4 is judged to be high. This means that D4 is subject to atmospheric transport to remote regions such as the Arctic.

Table 8. Model-predicted characteristic travel distance for D4
Characteristic travel distance Model (reference)
5284 km TaPL3 v. 2.10 (TaPL3 2000)
5254 km OECD LRTP POPs Tool v.2.0
(Scheringer et al. 2006)

The OECD POPs Screening Model can be used to help identify chemicals with high persistence and long-range transport potential (Scheringer et al. 2006). The OECD model is a global model which compartmentalizes the earth into air, water and soil. This model is "transport-oriented" rather than "target-oriented," as it simply identifies the CTD without indicating specifically where a substance may be transported (Fenner et al. 2005). Klasmeier et al. (2006) have suggested that a threshold of 5098 km, based on the model's CTD estimate for 2,2',3',4,4',5,5'-Heptachlorobiphenyl (PCB-180), can be used to identify substances with high long-range transport potential. PCB-180 has been found in remote regions. The CTD calculated for D4 using the OECD model is 5254 km, indicating that D4 has a high potential for long-range transport in air.

The OECD POPs Screening Model also calculates the transfer efficiency (TE), which is the percentage of emission flux to air that is deposited to the surface (water and soil) in a remote region (TE = D/E × 100, where E is the emission flux to air and D is the deposition flux to surface media in a target region). The TE for D4 was calculated to be 4.4E-06%, which is well below the boundary of 4.65E-04% (2,4,4'-trichlorobiphenyl, or PCB-28) established for the model's reference substances that are empirically known to be deposited from air to soil or water. The low TE means that D4 has the potential for long-range travel in the atmosphere without being deposited to Earth's surface in any particular remote region. In addition, the log Koa and log Kaw of D4 suggest that it will also have a low Arctic contamination potential (ACP) when examined using chemical partitioning space plots as described by Wania (2003, 2006).

A preliminary monitoring study of a remote ecosystem was conducted in Lake Opeongo, the largest lake in Algonquin Provincial Park, Ontario, Canada. The lake is relatively remote from potential sources of cVMS from sewage and runoff. Therefore, it was assumed that the only significant source of cVMS to the lake would be from atmosphere deposition (Powell 2008). Preliminary analysis of sediments and zooplankton samples for cVMS found no D4, suggesting that atmospheric deposition is not a significant source of D4 to Lake Opeongo. Limits of detection were 23.9 ng (background corrected mass) for both sediments and zooplankton.

It is therefore concluded that D4 has the potential to be transported over long distances in the atmosphere. However, the modelled TE for D4 is low, which suggests that it lacks the potential to be deposited in water or soil in remote regions. The monitoring results of Lake Opeongo also supported the low atmospheric deposition potential for D4. It is expected that airborne D4 will be eventually degraded by hydroxyl radicals in air.

Potential for bioaccumulation

The empirical and modelled log Kow values for D4 (Table 2) suggest that this substance has the potential to bioaccumulate in biota.

In the aquatic compartment

Empirical data indicate that D4 has the ability to bioconcentrate in aquatic organisms. A bioconcentration study for D4 was conducted on fathead minnows (Pimephales promelas) in a flow-through system (Fackler et al. 1995). The uptake of radio-labelled [14C] D4 in fish tissue was investigated at a concentration of 0.00023 mg/L (measured) over a 28-day period and depuration over a 14-day period. The mean steady-state bioconcentration factor (BCFss) was calculated to be 12 400 L/kg based on concentrations measured from day 7 to day 28. The kinetic bioconcentration factor (BCFk) was calculated to be 13 400 L/kg based on the uptake and depuration rates (k1/k2 = 2450/0.183). Fish tissue analysis also indicated that the depuration half-life for radio-labelled D4 was 7-12 days and that an average of 45% of accumulated D4 still remained in fish after 14 days of depuration. The metabolic potential of D4 was also investigated during this BCF study. In each tissue type, the entire extracted radioactivity (> 95%) was identified as D4, indicating that metabolism of D4 is negligible.

Table 9a. Empirical bioaccumulation data for D4
Test organism Endpoint[1] Value Reference
Pimephales promelas
(fathead minnow)
BCFss 12 400 L/kg wet wt Fackler et al. 1995
Pimephales promelas
(fathead minnow)
BCFk 13 400 L/kg wet wt Fackler et al. 1995
Oncorhynchus mykiss
(rainbow trout)
BMF 0.62-0.75 (lipid normalized) Drottar 2007; Domoradzki 2008a, 2008b; SEHSC 2008b

[1] BCFss: steady-state bioconcentration factor; BCFk: kinetic bioconcentration factor; BMF: biomagnification factor

New experimental data have also been received on a bioaccumulation study of aquatic organisms. A dietary bioaccumulation study of 14C-octamethylcyclotetrasiloxane (radiochemical purity 99.1%) in rainbow trout (Oncorhynchus mykiss) was carried out in a flow-through system (Drottar 2007; see Table 9a of this assessment) for 35 days, followed by 42 days of depuration. Fish were fed trout chow dosed with an average measured parent concentration of 457 µg/g. Feeding was adjusted to provide a feeding rate of 3% wet body weight per day. The higher feeding rate was modified to provide better instrument detection and is considered justified. No adverse effects on the fish were observed throughout the study. The entire extracted radioactivity from fish was identified as parent D4 and the non-extractable radioactivity from fish tissue was 7%, indicating that metabolism of D4 is very limited. The calculated elimination constant indicated that a period of 57 days would be required to achieve 90% of steady state instead of the 35-day uptake in the test. Therefore, a fish residue at day 57 uptake was extrapolated and the corrected fish biomagnifications factor, BMF (lipid-normalized), was 0.62. The kinetic BMF was calculated by a one-compartment model accounting for fish growth rates during the uptake and the depuration phases of the study, the amount of D4 in the fish over time, the mass of the fish over time, as well as the food consumption rate. The metabolic rate constant, kM, was assumed to be zero. Fish growth rates were calculated using linear regression (Domoradzki 2008a, 2008b). The resultant kinetic BMF (lipid-normalized) was 0.75. The BMF values agreed reasonably well. It is therefore considered that D4 did not show biomagnification potential in the laboratory fish dietary study.

The Arnot-Gobas model (Arnot and Gobas 2003) can be used to predict the bioaccumulation factor (BAF) of this substance, while taking into account any potential metabolism using a metabolic rate constant (kM). The available BCF and BMF in vivo tests data were used to derive an in vivo-based metabolic rate constant according to the method of Arnot et al. (2008a). In this method, kM is derived according to the following equation:

kM = (k1φ / BCF) - (k2 + kE + kG) (1)

where

kM = the metabolic rate constant (1/days)
k1 = the uptake rate constant (Arnot and Gobas 2003)
φ = fraction of freely dissolved chemical in water (Arnot and Gobas 2003)
BCF = the available empirical bioconcentration factor
k2 = the elimination rate constant (Arnot and Gobas 2003)
kE = fecal egestion rate constant (Arnot and Gobas 2003)
kG = growth rate constant (Arnot and Gobas 2003)

The method of Arnot et al. (2008a) provides for the estimation of confidence factors (CF) for the kM to account for error associated with the in vivo data (i.e., measurement variability, parameter estimation uncertainty and model error). A CF of ± 2.1 was calculated for the available BCF data.

Because metabolic potential can be related to body weight and temperature (e.g., Hu and Layton 2001, Nichols et al. 2007), the kM was further normalized to 15°C and then corrected for the body weight of the middle trophic level fish in the Arnot-Gobas model (184 g) (Arnot et al. 2008b). The middle trophic level fish was used to represent overall model output as suggested by the model developer (Arnot, personal communication to Bonnell M. of Environment Canada, 2008, [unreferenced]) and is most representative of fish weight likely to be consumed by an avian or terrestrial piscivore. After normalization routines, the kM ranges from ~0.008 to 0.08 with a median value of 0.02.

kM (middle trophic level normalized) day-1 log Kow used Arnot-Gobas BCF Arnot-Gobas BAF
7.80E-03 (2.5%) 6.5 12 589 467 735
2.25E-02 (average) 6.5 4365 89 125
8.18E-02 (97.5%) 6.5 1 413 12 022

The calculated kM values based on in vivo experiments suggest that the rate of metabolism of D4 is quite low (≤ 0.08 d-1 at best). The experimental BCF study on fathead minnows (Fackler et al. 1995) and the dietary bioaccumulation study on rainbow trout (Drottar 2007) demonstrated almost full recovery of the parent compound (> 95%), which generally supports the idea of limited metabolism of D4. The calculated BCF of 12 589 using the lower percentile rate constant (0.008) compares closely with the experimental BCF values from Fackler et al. (1995). Therefore, the corresponding BAF, corrected using this metabolic rate constant (467 735), was used to represent the bioaccumulation potential of D4 for fish in Canadian waters.

In the sediment compartment

The biota-sediment accumulation factor (BSAF) for D4 can be calculated using data from a Chirononmus tentans (midge) sub-chronic toxicity study (Kent et al. 1994). Midge were exposed to D4 in sediment of low (LOC), medium (MOC), and high (HOC) organic carbon content ranging from 0.27% to 4.1%. The average BSAFs were calculated (BSAF = Corganism tissuemg/kg /Csediment mg/kg) to be 0.7, 1.3 and 2.2, respectively, for the HOC, MOC and LOC phases. The results indicate that D4 may have some potential to bioaccumulate through exposure to sediment. However, this study did not specify whether the gut contents of test organisms had been purged before calculation of BSAF values. The BSAF value may thus be over-estimated due to the presence of D4 on sediments within the gut of the invertebrates.

In the soil compartment

No bioaccumulation information for D4 was available for the soil compartment.

In the terrestrial compartment

The Gobas mass-balance bioaccumulation model for terrestrial organisms (Gobas et al. 2003) uses a chemical's octanol-air and octanol-water partition co-efficient (Koa and Kow) to estimate the chemical's biomagnification (BMF) potential in terrestrial food chains. It was estimated that chemicals with a log Koa < 5 can biomagnify in terrestrial food chains if log Kow is < 2 and the rate of chemical transformation or metabolism is low. A log Koa of 4.34 indicates that D4 does not have the potential to biomagnify in terrestrial food chains.

Summary of the bioaccumulation potential of D4

Overall, the empirical steady-state and kinetic fish BCF study, optimized for water-borne exposure, has shown that the bioconcentration potential for D4 from water is high (i.e., ≥ 5000). Although the log Kow for D4 would suggest that dietary uptake of D4 will be significant and may predominate, it is not outside the range of log Kow values where bioconcentration in laboratory studies has been observed to be significant for many chemicals (e.g., Arnot and Gobas 2006). Predicted BCF values, corrected for metabolism, are also > 5000 and generally agree with empirical BCF values. Empirical and predicted BCF values exceed 5000, which suggests that there may be potential for high bioconcentration in other organisms at different trophic levels as well as fish, especially those with lower growth or metabolic rates (e.g., autotrophs). 

Predicted BAF values are also high and exceed 5000. As with other models, some uncertainty exists with predicted BCF and BAF values (e.g., uncertainty increases at higher log Kowvalues, as few chemicals have been studied for bioaccumulation in this range). Higher confidence is attributed to the predicted BAF value with a corresponding predicted BCF that most closely compares with the empirical BCF data (i.e., BAF = 4.7E05). The mass-balance kinetic model used is based on "first principles," meaning that the most important domain of the model is that a chemical obeys the principal mechanism of the model, in this case passive diffusion. D4 meets this domain and is within the model's log Kow and molecular weight boundaries as well. Therefore, the predictions for bioaccumulation are also considered to be applicable to D4.

BSAF values for D4 would suggest a relatively low level of accumulation in sediment macroinvertebrates. As this is the only sediment bioaccumulation test available for cVMS and there are no predictive models for sediment organisms, testing or field evidence at more realistic environmental loadings would help verify these values. The BMF values generated for D4 are less than 1, which suggests that there may be low biomagnification potential in fish for D4, but there is currently no evidence to suggest that this may be the case for other trophic levels. Field mesocosm studies are currently under way to examine trophic transfer of cVMSs in aquatic food webs, but these data are not yet available for full evaluation and were not considered for this assessment. 

Finally, there is conflicting evidence on the bioaccumulation potential of D4 tested under laboratory conditions. BMF studies in fish and BSAF studies in invertebrates suggest that the bioaccumulation potential of D4 is low, possibly due to reduced bioavailability. Available optimized BCF test data as well as predictive modelling suggest that there may be potential for significant bioconcentration of D4 in fish and potentially at lower levels of an aquatic food web. Therefore, it is reasonable to conclude that D4 has bioaccumulation potential in biota. However, considering the conflicting evidence, it is not possible to conclude that D4 meets the criterion for bioaccumulation (BCF or BAF ≥ 5000) as set out in the Persistence and Bioaccumulation Regulations (Canada 2000).

Potential to cause ecological harm

Ecological effects assessment

A - In the aquatic compartment

There is experimental evidence that D4 causes harm to aquatic organisms at very low concentrations (e.g., LC50 < 1 mg/L) (Table 10a). The empirical ecotoxicity values indicate that D4 is very toxic to sensitive aquatic organisms, with extremely high short- and long-term toxicity below its solubility limit (0.056 mg/L, Table 2). For small-sized (≤ 1g) rainbow trout, the lowest concentration causing 50% mortality (LC50) in an acute test is 0.01 mg/L, with a no-observed-effect concentration (NOEC) of 0.0044 mg/L and a lowest-observed-effect concentration (LOEC) of 0.0069 mg/L. Affected fish exhibited darkened pigmentation, loss of equilibrium, and lethargic behaviour before they died, consistent with a narcosis mechanism of toxicity (Sousaet al. 1995). A fish early life-stage study was also reported by Sousa et al. (1995). Rainbow trout embryos were exposed to D4 at concentration levels of 0.00025-0.0044 mg/L for 93 days. No adverse effects were observed to embryo viability, hatching success, larval survival, and growth at all treatment levels. Therefore, the chronic NOEC for 93-day fish early life-stage is 0.0044 mg/L, the highest concentration tested.

D4 caused significant mortality at 0.015 mg/L during a 21-day chronic toxicity study for the water flea, Daphnia magna, an important species of zooplankton in ecosystems. The chronic NOEC for Daphnia magna is 0.008 mg/L for survival and reproduction, and the LOEC for survival is 0.015 mg/L (Sousaet al. 1995).

Table 10a. Empirical aquatic toxicity data for D4
Test organism Type of test Duration Endpoint[1] Value (mg/L) Reference
Rainbow trout
Oncorhynchus mykiss
Acute 14 d LC50 0.010 Sousa et al. 1995
Rainbow trout
Oncorhynchus mykiss
Acute 14 d NOEC 0.0044 Sousa et al. 1995
Rainbow trout embryos
Oncorhynchus mykiss
Chronic 93 d NOEC 0.0044 Sousa et al. 1995
Shrimp Acute 96 hr LC50 > 0.0091 Sousa et al. 1995
Sheepshead minnow
Cyprinodon variegatus
Acute 14 d NOEC 0.063 Sousa et al. 1995
Sheepshead minnow
Cyprinodon variegatus
Acute 14 d LC50 > 0.063 Sousa et al. 1995
Water flea
Daphnia magna
Acute 48 hr NOEC 0.015 Sousa et al. 1995
Water flea
Daphnia magna
Chronic 21 d NOEC 0.008 Sousa et al. 1995
Water flea
Daphnia magna
Chronic 21 d LOEC 0.015 Sousa et al. 1995
Midge Chronic 14 d NOEC ≥ 0.015 Kent et al. 1994
Freshwater algae
Selenastrum capricornutum
Acute 96 hr EC50 invalid Springborn Laboratories 1990

[1] LC50: the lowest concentration causing 50% mortality; EC50: the lowest concentration causing sublethal effects in 50% of the population; NOEC: no-observed-effect concentration; LOEC: lowest-observed-effect concentration

New experimental data were received, specifically an acute toxicity study on freshwater algae, Selenastrum capricornutum, in a closed system under a 96-hour static exposure condition (Springborn Laboratories 1990). The toxicity test was performed following the Toxic Substances Control Act (TSCA) standard test method for algae. Algae were exposed to a saturated solution of D4 (> 99% active ingredient). However, the concentrations of the test solution decreased steadily from 0.022 mg/L at test initiation to under detection limit (< 0.001 mg/L) at the end of the 96-hour test. The pH was 7.5 at test initiation and increased to 10.0 during the 96-hour test, which reflected photosynthesis and respiration of the algae. The temperature during the study ranged from 23°C to 24°C. A decrease in mean cell densities was observed in D4-exposed algae. However, a significant reduction in cell density was observed in the closed-system control compared to that of the open system due to limited oxygen and carbon dioxide. Considering the rapid decrease of D4 concentrations during the test and the uncertainty surrounding the reduced growth rate in the control, the study is considered invalid.

The acute and chronic toxicity of D4 was predicted using ECOSAR (2004). Predicted results are given in Table 10b.

Table 10b. Modelled aquatic toxicity values for D4
Organism Type of test Endpoint[1] Duration Concentration (mg/L) Model
Fish Acute LC50 14 d 0.049 ECOSAR 2004 
Fish Chronic ChV 30 d 0.003 ECOSAR 2004
Daphnia Chronic EC50 16 d 0.007 ECOSAR 2004
Green Algae Acute EC50 96 h 0.015 ECOSAR 2004

[1] LC50: the lowest concentration causing 50% mortality; EC50: the lowest concentration causing 50% effects; ChV is the geometric mean of the NOEC (no-observed-effect concentration) and LOEC (lowest-observed-effect concentration).

The modelled 30-day fish result (ChV = 0.004 mg/L) for D4 using ECOSAR is in reasonably good agreement with the empirical fish data (14d ChV = 0.0055 mg/L, the geometric mean of the fish 14-day NOEC and LOEC); the predicted LC50 for fish 14-day exposure is 5 times lower than the empirical fish 14-day LC50(0.010 mg/L). The predicted EC50 for 16-day exposure toDaphnia is in agreement with the empirical NOEC in a 21-day exposure to Daphnia, indicating that the model overestimated the effect concentration for Daphnia. The modelled result suggests that there is also a possibility of adverse effects (i.e., acute EC50 < 1 mg/L) in algae at D4 concentration of 0.016 mg/L, however, some uncertainty exists with the predicted algae value since the log Kow for D4 (6.49) is slightly higher than the log Kow cut off (6.4) for reliable prediction of algae toxicity. Lack of siloxanes in the model's training set also adds uncertainty into the predicted values. Therefore, the predicted aquatic toxicity values were not considered further in this screening assessment.

The experimental data indicate that D4 has the potential to be highly hazardous to aquatic organisms (i.e., acute LC/EC50 <1.0 mg/L and chronic NOEC < 0.1 mg/L). However, it is interesting to note that the toxicity to both trout and Daphnia were not observed until these organisms were exposed to D4 for 7-14 days. The observation is consistent with the fish bioconcentration study which noted that the concentrations in fish tissue reached steady state after 7-14 days of exposure to D4, indicating that the observed toxicity may relate to D4 uptake kinetics and sufficient accumulation of the substance is required to cause toxicity (Sousa et al. 1995). It should also be mentioned that mortality was not observed in other aquatic organisms, such as shrimp or sheephead minnow and/or larger trout, as shown in the fish dietary and metabolism studies, indicating that D4 could be more toxic to sensitive aquatic organisms and/or aquatic organisms of sensitive early-life stages.

B - In other environmental compartments

In the sediment compartment

The sub-chronic toxicity of D4 in sediments was evaluated using Chironomus tentans (midges) in a series of 14-day exposures in three different sediments and in water only (Kentet al. 1994). Tests were conducted with sediments of low (LOC), medium (MOC), and high (HOC) organic carbon contents ranging from 0.27% to 4.1%. Mortality was observed at 250 and 170 mg/kg dw for the MOC and HOC sediments, respectively, and growth effects were observed at 130 mg/kg dwfor the LOC sediments. The NOECs for mortality were 130, 120, and 54 mg/kg for the HOC, MOC, and LOC sediments, respectively.

A prolonged sediment toxicity study to midges, Chironomus riparius, was conducted using spiked sediment (Krueger et al. 2008). The midges were exposed to mean measured concentrations of D4 ranging from 6.5 mg/kg dw to 355 mg/kg dw for 28 days at 20°C. The organic carbon content of the formulated sediment was 4.1%. The overlaying water was renewed every week due to the high ammonia measured in the test chamber. The observed NOEC for both percent survival and emergence was determined to be 44 mg/kg (measured). The calculated LC50 value for survival was 114 mg/kg and the observed LOEC for the emergence ratio was 131 mg/kg. Midges exposed to 355mg/kg of D4 showed a statistically significant reduction in development and the NOEC and LOEC for midge development was determined to be 131 mg/kg and 355mg/kg, respectively.

It should be mentioned that the sediment toxicity test was performed with sediment of high organic carbon content. The sediment toxicity data from Kent (1994) demonstrated an increased D4 toxicity, with decreased organic matter content of sediment due to increased bioavailability. Therefore, it is concluded that D4 is more likely to cause adverse effects to sediment-dwelling organisms in sediments with low organic matter content (i.e., mineral-rich sediments).

In the soil compartment

No effects studies for soil organisms were found for D4 or its analogues.

In the terrestrial compartment

No ecological studies were identified for terrestrial wildlife. Laboratory studies on mammals are discussed under the "Potential to Cause Harm to Human Health" section in this screening assessment.

Ecological exposure assessment

In air

In Canada, preliminary environmental measurements of volatile methyl-siloxanes, including D4, were conducted in the Great Lakes region during February and March of 2006 (personal communication, Environment Canada, Canadian Centre for Inland Waters, 2007 [unreferenced]). Eighteen outdoor air samples were collected from rural and urban areas in Ontario and D4 was present in almost all the samples collected, at concentration levels of < 1 µg/m3. This result is in agreement with what has been reported in other jurisdictions (Table 11a).

It is, however, possible that the detection of D4 in ambient air is in part a result of sample contamination. Volatile cyclosiloxanes are present in a wide variety of commercial products, and both Canadian and Nordic monitoring programs have reported problems of high levels of cyclosiloxanes in sample blanks. Very few duplicate measurements are available for outdoor air monitoring and the few that are available exhibit poor reproducibility (personal communication, Environment Canada, Canadian Centre for Inland Waters, 2007 [unreferenced]).

Table 11a. Concentrations of D4 in air
Medium Location; year Concentration Reference
Air Great Lakes region, Canada; February and March 2006 < 1 µg/m3 see footnote 2
Air Nordic countries[1]; 2004-2005 0.08-4 µg/m3 Norden 2005

[1] Outdoor samples (n=24) were collected in Nordic countries. The detection limit for D4 was 0.006 µg/m3.
[2] personal communication, Environment Canada, Canadian Centre for Inland Waters, 2007 [unreferenced]

 

In water

In Canada, water from a total of nine sewage treatment plants (STPs), including conventional secondary and tertiary water treatment plants and lagoons, in large urban centres in southwestern Ontario was sampled during October 2005 and winter 2005 (personal communication, Environment Canada, Canadian Centre for Inland Waters, 2007 [unreferenced]). D4 was detected in both influents and effluents with concentration levels of D4 at < 2-24 µg/L and < 2-2.92 µg/L, respectively, in the influents and effluents being measured. Seasonal differences of D4 in influents to STPs were also noted; most influent concentrations increased from < 2 µg/L in the fall to 2.78-21.42 µg/L in winter. Seasonal differences in D4 concentrations in effluents from STPs were insignificant. Similar monitoring results have been reported in other jurisdictions (Table 11b).

Table 11b. Concentrations of D4 in water
Medium Location; year Concentration Reference
STP
influents
Southwestern Ontario, Canada; October 2005 < 2-24 µg/L see footnote 4
STP
effluents
Southwestern Ontario, Canada; October 2005 < 2-2.92 µg/L see footnote 4
STP
influents
United States 0.64-7.09 µg/L HydroQual Inc. 1993
STP
effluents
United States 0.06-0.41 µg/L HydroQual Inc. 1993
Water Lake Pontchartrain, Louisiana, U.S. 0.03 µg/L McFall et al. 1985
Drinking water United States Qualitatively detected Wallace et al. 1984
Water Background and urban sites[1], Nordic countries < 0.1 (d.l.) Norden 2005, NILU 2007
STP
influents
Nordic countries[2] < 0.3-3.7 µg/L Norden 2005, NILU 2007
STP
effluents
Nordic countries[3] < 0.08 (d.l.) - 0.11µg/L Norden 2005, NILU 2007

[1] A total of 28 sampling sites excluding STP influents and effluents
[2] 7 STP influent sampling sites
[3] 12 STP effluent sampling sites
[4] personal communication, Environment Canada, Canadian Centre for Inland Waters, 2007 [unreferenced]
d.l. = detection limit

In sediments

In Canada, surface sediments and sediment cores were collected from Lake Ontario in July 2006 and analyzed for D4, D5, and D6 (Powell and Kozerski 2007). Surface sediments consisting of the upper 5 cm of sediment were collected from Toronto Harbour and the Kingston Basin. Sediment cores, which were sectioned into strata 5 mm thick, were collected from the Rochester, Mississauga, and Niagara basins. The surface sediments from Toronto Harbour and Kingston Basin contain moderate total organic carbon (TOC = 2.1-2.4% dw), while sediment cores contain high TOC (4-5% dw). Loss-on-ignition analysis of sediments also demonstrated lower water contents in surface sediments (55-70% ww) than in sediment cores (80-89%). Sediments in Toronto Harbour and the four sedimentary basins are known to be contaminated with a variety of organic compounds that enter the lake through direct discharges of treated wastewater, flow from the upper Great Lakes (Erie, Huron and Michigan) and the Niagara River, and atmospheric deposition. Surface sediments from Toronto Harbour contained the highest concentration of D4, at 0.29 µg/g dry weight. In contrast, concentrations of the cyclic siloxane materials in the surface sediments and sediment cores from the four sedimentary basins were all less than the analytical method detection limit, which was 0.006 µg/g for D4. Similar monitoring results have been reported in other jurisdictions, where D4 was detected in surface sediments from urban areas and point sources (Table 11c).

A preliminary monitoring study of a remote ecosystem was conducted in Lake Opeongo, the largest lake in Algonquin Provincial Park, Ontario, Canada. The lake is relatively remote from potential sources of cVMS from sewage and runoff (Powell 2008). Preliminary analysis of surface sediment and sediment core samples found no D4, with a limit of detection of 23.9 ng (background corrected mass).

The sediment monitoring results from Lake Opeongo and the Lake Ontario area suggest that D4 contamination is more likely to be found near urban centres and point sources.

Table 11c. Concentrations of D4 in sediments
Medium Location; year Concentration Reference
Surface sediments Toronto Harbour, Canada; July 2006 0.29 µg/g dw Powell and Kozerski 2007
Surface sediments Kingston Basin, Canada; July 2006 < 0.006 µg/g dw (d.l.) Powell and Kozerski 2007
Sediment cores Rochester, Mississauga, and Niagara basins, Canada; July 2006 < 0.006 µg/g dw (d.l.) Powell and Kozerski 2007
Surface sediments Lake Opeongo, Algonquin Provincial Park, Ontario, Canada; October 2007 < 23.9 ng (d.l.)[2] Powell 2008
Sediment cores Lake Opeongo, Algonquin Provincial Park, Ontario, Canada; October 2007 < 23.9 ng (d.l.)[2] Powell 2008
Sediments Nordic countries[1] < d.l. (varied from sample to sample)
- 0.084 µg/g dw
Norden 2005, NILU 2007

[1] A total of 30 sediment sampling sites;
[2] Background corrected mass as reported in the preliminary study;
dw = dry weight; d.l. = detection limit

 

In soil

D4 may enter soil from land application of sewage sludge. No monitoring data for D4 in sewage sludge are available for Canada. In Europe, D4 is present in sewage sludge at levels ranging from the µg/kg level up to 2.7 mg/kg dry weight (Norden 2005, Kajet al. 2005, NILU 2007).

No monitoring data are available for D4 in Canadian soil. D4 concentrations in two soil samples from the Faroe Islands were below detection limit (< 10 ng g dw) (Norden 2005).

In biota

A preliminary monitoring study of a remote ecosystem was conducted in Lake Opeongo, the largest lake in Algonquin Provincial Park, Ontario, Canada. The lake is relatively remote from potential sources of cVMS from sewage and runoff (Powell 2008). Preliminary analysis of zooplankton samples found no D4. Bulk zooplankton samples were pooled into a single sample for each of the two locations from the lake without being sorted into species. The limit of detection was 23.9 ng (background corrected mass).

In Europe, D4 was detected in the livers of fish and marine mammals in Nordic countries. The concentrations varied with species, gender and age. Among marine mammals monitored in Nordic countries, D4 was only detected in seal blubber in Denmark, at the level of 12 ng/g wet weight (ww) (Norden 2005). The concentrations in both freshwater and marine fish, from sampling sites in urban areas and near STPs, were generally in the range of < 5-13 ng/g ww, except for one sample of cod liver (9 livers pooled) collected at a location near a city centre in Norway that had a higher concentration of D4 (70 ng/g ww). The follow-up environmental monitoring program conducted by the Norwegian government confirmed that the same level of D4 was present in cod livers (NILU 2007). D4 was also found in common mussels, flounder livers and fillets, and in cod stomach contents from Norway in the same monitoring program. D4 was also detected in fish samples in Germany at concentrations ranging from 100 to 1 000 ng/g ww (SEHSC 2005). D4 was not detected in fish muscle samples in Sweden (Kaj et al. 2005).

The presence of D4 in European biota indicates that despite the low detected concentrations or even non-detection of the substance in or near fish habitats, D4 is available in the environment for biota to take up and accumulate.

Table 11d. Concentrations of D4 in biota
Organism Location; year Concentration Reference
Zooplankton Lake Opeongo, Algonquin Provincial Park, Ontario, Canada; October 2007 < 23.9 ng/g (d.l.) Powell 2008
Marine fish livers Nordic countries[1];
2002-2004
< 5 (d.l.)-70 ng/g ww Norden 2005
Freshwater fish livers Nordic countries[2]; 2002 < 5 (d.l.)-8.9 ng/g ww Norden 2005
Marine mammals Nordic countries[3]; 2002 < 5 (d.l.)-12 ng/g ww Norden 2005
Seabird eggs Nordic countries[4];
2000-2005
< 5 ng/g ww (d.l.) Norden 2005
Common mussels Norway[5]; 2006 1.3-2.3 ng/g ww NILU 2007
Flounder livers Norway[6]; 2006 2.6 ng/g ww NILU 2007
Flounder fillets Norway[6]; 2006 1.9 ng/g ww NILU 2007
Cod stomach contents Norway[7]; 2006 5.0-9.3 ng/g ww NILU 2007
Cod livers Norway[7]; 2006 81.2-134.4 ng/g ww NILU 2007
Fish Rhine River[8], Germany 100 (q.l.)-1000 ng/g ww SEHSC 2005

[1] A total of 11 sampling matrices for marine fish
[2] A total of 10 sampling matrices for freshwater fish
[3] A total of 7 sampling matrices for marine mammals
[4] A total of 17 sampling matrices for seabird eggs
[5] A total of 3 sampling matrices for mussel
[6] A total of 2 sampling matrices for flounder
[7] A total of 3 sampling matrices for cod
[8] A total of 5 fish matrices were sampled from Rhine River; a Danish salmon obtained from an unspecified location showed no detectable D4
ww = wet weight; d.l. = detection limit; q.l. = quantification limit

 

Characterization of ecological risk

The approach taken in this ecological screening assessment was to examine various supporting information and develop conclusions based on a weight-of-evidence approach and using the precaution as required under subsection 76.1 of CEPA 1999. Particular consideration was given to risk quotient analysis, persistence, bioaccumulation potential, toxicity, sources and fate in the environment.

Based on the information available for D4, this substance has been determined to be not persistent in water, but presents some bioaccumulative potential in aquatic organisms. A quantitative risk quotient evaluation of exposure and of ecological effects was therefore conducted as part of the weight-of-evidence evaluation of D4's potential to cause harm.

In the aquatic compartment, experimental acute and chronic toxicity studies for D4 were critically reviewed and accepted. D4 exhibited 50% mortality to fish in a 14-day study at a concentration of 0.01 mg/L, but showed no effect at a concentration of 0.0044 mg/L in the fish 14-day study and a fish early-life stage test. An application factor of 50 was applied to the sub-chronic LC50 of 0.01mg/L to account for extrapolations needed to arrive at a field based long-term multi-species no effect level. The calculated predicted no effect concentration (PNEC) is therefore 0.0002 mg/L.

A risk quotient (RQ) analysis, integrating the level of exposure with a toxicity threshold, was performed for D4. In order to address the potential risk of D4 on a national scale in Canada, a distribution profiling risk quotients in water at multiple release sites where the substance can be released by industry or by consumers (i.e., sewage treatment plants) was determined. This type of analysis provides a line of evidence for the risk assessment of a substance when the full range of geographic locations of the industrial and consumer releases of the substance cannot be fully established.

Specifically, when a substance is used by a number of industry sectors but the actual facilities involved cannot be identified, the aquatic exposure can be estimated for all sites where facilities related to these sectors are located. In addition to this, information on potential releases from consumer use can be integrated into the calculations. A predicted environmental concentration (PEC) for the water compartment is determined based on the use quantities identified from the section 71 survey submissions and estimates of releases from individual industrial sites and from consumers. The receiving water is either a watercourse or a lake, and a dilution factor based on the size of the receiving water--up to a maximum of 10--is used to estimate the PEC. The risk quotient at each site is then determined for the water column. The distribution indicates not only the proportion or number of threshold-exceeding sites, but also the magnitude of the exceedence at each of these sites. Further details on the approach are provided in Environment Canada (2008b).

The consumer releases used a database of approximately 1000 municipal discharge sites accounting for about 2/3 of the Canadian population. The industrial release analysis was done for 61 sites relating to 87 industrial facilities identified by NAICS code as possible users of D4. Under these scenarios, a total of 249 (23.4%) of all evaluated municipal discharge sites across Canada showed a risk to aquatic organisms, with RQs exceeding 1 (Figure 1). The equation and inputs used to calculate the PEC in the receiving watercourses are described in Environment Canada (2008c).

Figure 1. Aquatic risk distribution for D4 - Site Number (from 0 to 1000) by the Aquatic Risk Quotient (from 0.0001 to 100). Upward trend
Figure 1. Aquatic risk distribution for D4 (CAS#556-67-2)

The log Kow for D4 (6.5) is in the range where bioavailability to pelagic and benthic biota is not significantly reduced and would not be considered "super-hydrophobic". Appreciable bioconcentration observed in optimized laboratory tests and measurable tissue residue values from available field monitoring data also suggest that the potential for body burdens reaching critical internal levels may not be mitigated by low bioavailability.  Although the majority of the acute and chronic data reviewed suggest no effects at water saturated levels of D4, limited data suggest that D4 could potentially be highly toxic to specific aquatic species at sensitive early-life stages.

D4 is imported into Canada in significant quantities. Its uses suggest that this chemical is released into the Canadian environment in a dispersive manner. D4 has also been determined to be persistent in air and sediment, and has the potential to bioaccumulate in biota. In light of these findings and the estimated risk of D4 being released from municipal wastewater, long-term environmental exposure to D4 is expected to potentially have adverse effects on aquatic organisms in certain Canadian environments.

Therefore, because the physical-chemical property, bioconcentration and ecotoxicity profiles for D4 provide a consensus basis for the weight of evidence, it can be reasonably concluded that D4 has the potential to cause ecological harm, particularly from long term exposures near discharge zones.

Uncertainties in evaluation of ecological risk

D4 is imported into Canada at significant quantities. It is also one of the major components in CAS RN 69430-24-6. It is also present in PDMS at up to 3%. The Challenge to industry and other stakeholders issued by the Government of Canada (Canada 2007) did not survey CAS RN 69430-24-6 (cyclomethicone, the mixture) or PDMS. Even though there is evidence that some companies did report individual cVMS in the mixture under the survey, the quantities of these substances imported into Canada and their uses in 2006 are not completely known, and their releases into the Canadian environment are not considered fully in this screen assessment report.

Since no release information from industrial operations was available for the risk distribution analysis, it is assumed that releases to wastewater were uniformly distributed among 64 industrial sites evaluated. In reality, certain industrial sites may use higher quantities of D4 than others, resulting in higher releases to the municipal discharging sites associated with these industrial sites and therefore a higher risk than predicted. The distribution concentrations in the analysis applied instantaneous dilution of the effluent from sewage treatment plants (STP) into the receiving water. However, under realistic environmental conditions, the dilution may be gradual over a certain distance from the discharge point and the area near the discharge point of an STP may present a higher risk than predicted.

Sediment is an important media of concern for D4. The sediment degradation studies are not without uncertainties. Extrapolation of half-lives at low temperature in sediment based on hydrolysis data may also contribute to the overall uncertainty in sediment persistence. Limited data for bioaccumulation potential in this compartment also contributes to the overall ecological assessment uncertainty.

The available bioconcentration data and biomagnification factor and sediment accumulation values for D4 are conflicting. There is a lack of field data on bioaccumulation potential via the food web and in non-aquatic organisms.

Environmental monitoring data in Canada and elsewhere are limited. Sampling and analytical methodologies are still developing. Sample contamination is a potential problem in environmental monitoring due to D4's widespread uses. Data on environmental concentrations of D4 in biota and surface water in Canada are lacking and few environmental concentrations have been reported outside of urban areas in Canada. Consequently, monitoring data from European countries have been presented in this report. However, monitoring has been identified as a key component in the Chemicals Management Plan in Canada and D4 is being considered for environmental monitoring under the Plan. Environmental monitoring will contribute to a better understanding of the environmental presence and "true" environmental accumulation potential of the substance in the environment.

Potential to cause harm to human health

Exposure assessment

The data on levels of D4 found in environmental media including ambient air near and away from point sources, surface waters, sediments, sewage sludge and biota are described in this report in the section entitled "Ecological Exposure Assessment." Unpublished data from Canada include measurements taken of biogas at landfills (Cianciarelli 2007, unpublished results); air near and away from point sources (personal communication, Environment Canada, Canadian Centre for Inland Waters, 2007 [unreferenced]); air, influent and effluent water at wastewater treatment plants (personal communication, Environment Canada, Canadian Centre for Inland Waters, 2007 [unreferenced]); and Great Lakes sediment (Powell and Kozerski 2007). Many analyses of volatile siloxanes have been confounded by sample contamination during collection and analysis, resulting in siloxanes being detected in blanks at levels comparable in some cases to those in samples taken near point sources. Results of extensive sampling and measurement of siloxanes in environmental media in Scandinavia have been published by the Nordic Council of Ministers and the Swedish Environmental Research Institute (Norden 2005, Kaj et al. 2005). A survey of volatile organic chemicals, including siloxanes, in residential air was conducted from 2002 to 2004 in homes in Syracuse, New York, U.S.A. (NYIEQ 2005). Data from these reports were considered reliable and were used to produce the upper-bounding estimates of exposure to siloxanes in air, water and soil by the general population in Canada.

The upper-bounding estimates of daily intake of D4 for six age groups in the Canadian population are shown in Appendix 1. The estimates of intake from environmental media and diet range from 43.6 µg/kg body weight/day (µg/kg-bw/day) for adults aged 60 years and older to 132.5 µg/kg-bw/day for children aged 6 months to 4 years. The most significant contribution to daily intake from environmental media is inhalation of indoor air, based on a study of approximately 130 homes in Syracuse, New York, in which D4 was detected in 15% of samples. The mean concentration of D4 in indoor air measured in homes in this study was 32.5 µg/m3 and the maximum concentration was 249 µg/m3 (NYIEQ 2005). To compare the estimated exposure by inhalation to the critical effect level for D4 via inhalation, a time-weighted average air concentration based on maximum concentrations of D4 in indoor and ambient air of 218 µg/m3 was calculated based on occupancy of indoor and outdoor environments (Health Canada 1998).

Confidence in the upper-bounding estimate of exposure to D4 through environmental media and diet is moderate. No Canadian data were used, but data from studies in Scandinavia and the United States were available for ambient and indoor air, water and soil. The use of a regulatory limit for dimethylpolysiloxane in one quarter of dairy products and half of processed food may overestimate the dietary contribution to total exposure, but the estimated contribution from all food to exposure is less than one percent of the contribution from air.

Using ConsExpo 4.1, software developed to estimate exposure to consumer products, the potential absorbed dose of D4 through the use of personal care products was estimated for men and women that use skin care products, hair care products and antiperspirants (RIVM 2006). Manufacturers of personal care products are required to notify Health Canada of the concentration, within broad ranges, of siloxanes, including D4 and polydimethylcyclosiloxanes, termed cyclomethicone in personal care productsFootnote 1. Health Canada has been notified of approximately 100 cosmetic products that contain D4 and approximately 6000 cosmetic products that contain cyclomethicone or cyclomethicone mixtures (CNS 2007). Where only cyclomethicone and not D4 was listed as part of a product formulation, it was assumed that the cyclomethicone was composed of 100% D4. The data on the concentration of D4 in personal care products were obtained principally from the information provided by Canadian industry (Environment Canada 2007) and were supplemented by information from other sources noted in Appendix 2. Based on experimental observations that 88-95% of D4 evaporated from skin in 24 hours (Jovanovic et al. 2008, Zareba et al.2002), it was assumed that 90% of a product left on the skin evaporated during use and was therefore not available for dermal absorption. A distinction was made between products that are washed off and those that are left on the body. Other assumptions are noted in Appendix 2.

The results of a sample calculation for the application of body lotion are shown in Appendix 2, and summaries of the estimated absorbed dose arising from the use of personal care products by women and men are shown in tables 1 and 2. For women, the estimated maximum plausible daily absorbed dose from the modelled personal care products, aggregated over inhalation, dermal and oral exposure, is 0.243 mg/kg-bw/day. For men, the estimated maximum plausible daily absorbed dose, aggregated over inhalation, dermal and oral exposure, is 0.041 mg/kg bw/day. These estimates show that for the range of personal care products considered, the absorbed dose for women is much higher than for men, since women tend to use more products that are left on the skin. The use of personal care products by children was not modelled because of a lack of comprehensive product use pattern data for children.

An exposure assessment for use of D4, including personal care product uses, was submitted to the Government of Canada under the Challenge Program (SEHSC 2007d). The methodology is different from that shown in Appendix 2, tables 1 and 2, as a Monte Carlo probabilistic analysis was conducted and aggregate general population exposures from all sources (including personal care products) and routes (inhalation, dermal, ingestion) were derived. The contribution of the use of personal care products to total exposure via separate exposure routes (inhalation, dermal, oral) was characterized and then summed to arrive at an aggregated exposure estimate. Due to the fact that D4 and D6 were used as analogues to determine oral toxicity of D5, D5 is used here as a surrogate for validation of the D4 probabilistic exposure assessment. Thus, a probabilistic exposure assessment for use of D5 was also submitted to the Government of Canada under the Challenge Program (SEHSC 2008a). Independent review of the submitted probabilistic assessment showed that this assessment evaluated exposure to both user and non-user groups (see Appendix 4). The data were re-analyzed based on just user groups to allow comparison with the deterministic exposure assessment in this screening assessment. Based on user groups only, the probabilistic exposure values for adult females (most highly exposed adult group) were 10-16 times lower than the deterministic values shown for D5. Therefore, based on D5 used as an analogue to determine probabilistic exposure values for D4, it is expected that probabilistic exposure values for adult females (most highly exposed adult group) will be 10-6 times lower than the deterministic values shown in Appendix 2, Table 1. Note that due to the requirement for detailed analysis and validation of probabilistic exposure assessments, such assessments are normally outside the scope for conducting the exposure component of a screening assessment.

Based on user groups only in the D5 probabilistic exposure assessment, the exposure values for children aged 0-6 months (most highly exposed children's group) were in the range of 0.016-0.032 mg/kg bw/day (see Appendix 4). A comparison with a deterministic exposure assessment for children was not possible due to the lack of sufficient product use data required for modelling children's exposure in a deterministic exposure assessment. When the children's probabilistic exposure values are compared with the adult female deterministic exposure values, they are 5-10 times lower for D5. Therefore, based on D5 used as an analogue to determine probabilistic exposure values for D4, it is expected that if the children's probabilistic exposure values for D4 were compared to the adult female deterministic exposure values, they would be 5-10 times lower for D4.

Other types of consumer products such as surface coatings, caulking and cleaners were deemed to contribute significantly less to daily exposure through daily use and were not further considered in the modelling of daily dose through consumer exposure scenarios. Both personal care products and other consumer products such as surface coatings, caulking and cleaners contribute to the concentration of D4 in indoor and ambient air and thus to exposure by inhalation. The contribution of all consumer products to total exposure of non-occupationally exposed individuals is estimated via indoor air in the multi-media environmental exposure model discussed in the preceding text of this section.

A comparison of the estimated absorbed dose arising from the use of personal care products and the upper-bounding estimate of exposure arising from environmental media and diet can be made by converting the exposure estimate to an absorbed dose estimate. This is done using a figure of 12% for the absorbed dose by inhalation (Utell et al. 1998, SCCP 2005) and 52% for ingestion (Dow Corning 1998b). The ratio of absorbed dose estimated for women from the use of personal care products to the dose estimated to arise from environmental media and diet (Appendix 1, Table 1) is 243 µg/kg-bw/day to 6.24 µg/kg-bw/day, or 39:1. The ratio is considerably lower for adult men using personal care products, about 7:1.

Confidence in the estimate of absorbed dose of D4 through the use of personal care products is moderate to low. All estimates were made by the use of models and the use pattern data were not from Canadian studies. Responses to a notice published under section 71 of CEPA 1999 indicate that D5 was used more frequently than D4 in personal care products in Canada in 2006 (Environment Canada 2007). This is consistent with qualitative information that in the personal care products industry, D5 has largely replaced D4 in personal care formulations (Environment Canada 2007, SEHSC 2007a). Absorbed-dose estimates of D4 through the use of personal care products were made with the assumption that each modelled product contained D4 at the stated concentration. This approach may overestimate the absorbed dose.

Health effects assessment

Appendix 3 contains a summary of the available health effects information for octamethylcyclotetrasiloxane.

The European Commission has classified D4 as Category 3 for reproductive toxicity (possible risk of impaired fertility) (European Commission 2001, ESIS 2007). This classification was based on reproductive effects observed in rats following inhalation exposure, specifically that "inhalation exposure of female rats to D4 around the time of mating causes a dose-related reduction of numbers of corpora lutea, implantation sites and litter sizes. These effects occur in the absence of marked maternal toxicity" (European Commission 2006). Also, the Danish EPA has identified impaired fertility as the critical effect for D4, based on the same rat inhalation studies (Lassen et al. 2005).

When female rats were exposed to D4 for 28 days prior to mating, throughout mating and until gestation day 19, at 3600 mg/m3 (300 ppm) and above, there was a significant decrease in the number of corpora lutea. At higher doses-6100 mg/m3 (500 ppm) and 8500 mg/m3 (700 ppm)-there were significant decreases in the numbers of implantation sites and viable fetuses, as well as non-significant increases in early resorptions and post-implantation losses. Similar effects occurred when female rats were exposed to 8500 mg/m3 (700 ppm) D4 during the "fertilization phase" from three days prior to mating, throughout mating, to gestation day 3. A reduced pregnancy rate occurred in rats exposed to 700 ppm D4 for 6 hours one day before mating (Meeks et al. 2007). The value of 3600 mg/m3 is considered to be a critical effect level for reproductive inhalation exposure in this assessment.

At exposure levels of 6100 mg/m3 (500 ppm) and above in a 2-generation reproductive toxicity study, there were decreases in the mean litter size and the number of pups born to the F0 and F1 rats, and in the number of litters born to the F1 generation. There were also several F0 females in the 6100 mg/m3 (500 ppm) and 8500 mg/m3 (700 ppm) treatment groups that had extended parturition and dystocia, in two cases resulting in death. At 8500 mg/m3 (700 ppm), there was a decrease in the number of implantation sites in the F0 rats. At this concentration there was also an increase in the mean estrous cycle length and gestation time, and decreases in the mating and fertility indices in F1 rats (Siddiqui et al. 2007).

No significant changes were observed in any reproductive parameters when female rats were exposed to 8500 mg/m3 (700 ppm) D4 only during the "ovarian phase," (daily exposure for 28 days, then 3 days untreated, prior to mating); the "implantation phase" (daily exposure on gestation days 2 to 5); "post-mating" (daily exposure on gestation days 0 to 2); or following single 6-hour exposures on days 1, 2, 3 or 4 before mating or on gestation day 0, 1 or 2 (Meeks et al.2007).

In an oral range-finding developmental toxicity study in rabbits, increased spontaneous abortions occurred at 500 mg/kg-bw/day and above, and increased post-implantation losses and decreased number of live fetuses were observed at 1000 mg/kg-bw/day. These effects were likely secondary to maternal toxicity, which was observed at 50 mg/kg-bw/day and above. No teratogenicity was observed in this study or in inhalation developmental toxicity studies in rats and rabbits (IRDC 1993a, 1993b, 1993c; GSPA 1991).

In a combined chronic/carcinogenicity inhalation study of D4 in male and female rats for up to 2 years, uterine (endometrial) adenomas and hyperplasia were observed at the highest dose level of 8500 mg/m3 (700 ppm) (Dow Corning 2004). Although the Silicones Environmental, Health and Safety Council (SEHSC 2007d) argued that the endometrial adenomas and hyperplasia are not relevant to humans, this position has not been supported to date by international reviews due to lack of a thorough mode-of-action analysis. An increased incidence of mononuclear cell leukemia (MCL) was also observed in control and treated male rats. However, this tumour type is unique to rats and is common only in F344 rats, and the relevance to humans is unknown (Caldwell 1999). There was no evidence of treatment-related genotoxicity in a wide range ofin vitro and in vivo assays (see Appendix 3).

Studies on D4 in rats identified the liver as the most sensitive target organ. The lowest-observed-effect level (LOEL) for oral exposure was 5 mg/kg-bw/day based on increased liver enzymes (PROD, CYP2B1/2, CYP3A1/2) in two short-term gavage studies (Zhang et al. 2000, Falany and Li 2005). At higher test doses (≥ 20 mg/kg-bw/day) in short-term oral studies, relative liver weights were significantly increased (Zhang et al. 2000, Falany and Li 2005, Dow Corning 1990, 1997c). Although increased relative liver weights were observed only in female rats at 20 mg/kg-bw/day and higher (Zhang et al. 2000), increased relative liver weights were observed at 25 mg/kg-bw/day and higher in both sexes of rats in a 14-day oral study (Dow Corning 1990). Liver effects (accentuated lobular pattern of liver) were also observed in a 14-day oral rabbit study at 1000 mg/kg-bw/day (Dow Corning 1992). In addition, decreased fetal body weights and decreased relative liver weights in rat fetuses were observed when pregnant rats were dosed at 100 mg/kg-bw/day in 8-day studies (Falany and Li 2005), and in adult rats, decreased body weights and reduced thymus size were observed at doses of 500 mg/kg-bw/day and higher (Dow Corning 1992, IRDC 1993a).

Both relative and/or absolute liver weights were increased in short-term and long term inhalation studies as shown in Appendix 3. In some studies, these increases were preceded by induction of liver cell enzymes and/or cell proliferation at lower doses. It appeared that the liver weight increases may be associated with centrilobular hypertrophy of hepatocytes in 700-ppm male rats in the 6-month study (Dow Corning 2004). In the inhalation reproduction study in rats, hepatocyte hypertrophy increased in F1 females at 6100 and 8500 mg/m3 and in F1 males at 8500 mg/m3 and pigment in the liver and bile duct hyperplasia increased in F1 males at 8500 mg/m3. The Scientific Committee on Consumer Products (SCCP 2005) concluded that the liver weight increase with centrilobular hepatocyte hypertrophy should be attributed to a phenobarbital-like effect, which induces rat hepatic cytochrome P450 enzymes, is reversible (upon cessation of exposure), and is not associated with overt hepatotoxicity. They also argued that the mild enzyme induction is considered to be an adaptive response to xenobiotics. Zhang et al. (2000) noted an increased induction of the liver enzyme, CYP3A1/2, by D4 that was greater than the induction caused by phenobarbital in a 4-day oral rat study. They concluded that although similar to a phenobarbital type of induction caused by the CYP2B enzyme series, the results suggest that there may be important mechanistic differences in the induction caused by D4. However, Falany and Li (2005) also noted an increased induction of the liver enzyme, CYP3A1/2, by D4 in 8-day rat studies but suggested that this was part of the phenobarbital-type induction due to related induction of the CYP2B and PROD enzymes. Consequently, it was not considered appropriate to determine adverse effect levels based on enzyme induction alone.

It is uncertain whether liver weight increases due to treatment with D4 are adaptive or adverse, and increases in liver weight following administration of D4 are therefore considered together with effects in other organ systems observed at similar doses/concentrations of D4.

Several studies have investigated the estrogenic and androgenic potential of D4. In an uterotrophic assay, octamethylcyclotetrasiloxane increased uterine weight and uterine epithelial cell height (up to 30 µm) at doses of 250 mg/kg-bw/day and above in rats (McKim et al. 2001a). McKim et al. (2001a) concluded that octamethylcyclotetrasiloxane showed weak estrogenic and antiestrogenic activity in this assay. Studies conducted by Quinnet al. (2007a) in rats exposed by inhalation to D4, in receptor-binding studies and a luciferase reporter gene assay also showed weak estrogenic activity that is dose-dependent. In mice, serum estradiol levels decreased at oral doses of 100 mg/kg-bw/day and above (7-day studies); in ovariectomized mice, uterine weight was increased at 250 mg/kg-bw/day and up, and uterine peroxidase activity was increased at 1000 mg/kg-bw/day (3-day studies) (Heet al. 2003). As stated above, decreased body weights and relative liver weights were observed at 100 mg/kg-bw/day in fetuses in 8-day oral studies of pregnant rats. D4 did not result in any increase in reproductive organ weights following inhalation exposure for 10 days in male rats at 8500 mg/m3, thus indicating negative androgenic potential (Quinn et al.2007a, 2007b). Based on the 7-day oral studies in mice and the 8-day oral studies in rats, the value of 100 mg/kg-bw/day is considered to be a critical effect level for repeated-dose oral exposure in this assessment.

The lowest-observed-effect concentration (LOEC) for inhalation exposure was 85 mg/m3 (7 ppm), based on statistically significant increases in hepatic CYP2B1/2 and liver cell proliferation in a 5-day study in the rat (Dow Corning 1999, 2002; McKim et al. 2001b). At higher doses- ≥ 240 mg/m3(≥ 20 ppm)-in short- and long-term studies, additional effects included increased liver weight; increased kidney weight; nephropathy; reversible changes in organ weights (uterus, pituitary, adrenal, thymus, lung and ovary); and histopathological changes in the lung (increased focal alveolar histiocytosis) and female reproductive tract. No histopathological changes in the liver, kidney or pituitary were observed (Dow Corning1999, 2002, 2004; McKim et al. 1998, 2001b; Klykken et al.1999; Burns-Naas et al. 2002). In a 3-month inhalation study in rats, a LOEC of 420 mg/m3 (35 ppm) was determined based on increased absolute (20%) and relative (22%) liver weights, increased absolute and relative (17% increase) adrenal weights and decreased absolute and relative (17% decrease) thymus weights in females and alveolar macrophage foci and chronic interstitial inflammation of lung in both sexes (Burns-Naas et al. 2002, Dow Corning 1995b). A LOEC of 360 mg/m3(30 ppm) was determined in a 6-month rat study and a LOEC of 1800 mg/m3 (150 ppm) was determined in 24-month rat study based on increased liver weight in both studies (Dow Corning 2004). The value of 420 mg/m3 is considered to be a critical effect level for repeated-dose inhalation exposure in this assessment.

There were few data on toxicity of D4 in humans. Human volunteers (8 males and 4 females) exposed to 10 ppm of D4 (120 mg/m3) vapour for one hour via the mouth in a double-blind, randomized study showed no changes in lung function. The blood clearance was non-linear, with an elimination half-life of 330 min. The deposition of D4 was also measured with nasal and mouth breathing at resting ventilations in another 8 subjects. The overall average D4 absorption was 12% (Utell et al. 1998). In another study, an additional 6 human volunteers were exposed to 10 ppm of D4 (120 mg/m3) vapour for one hour via the mouth during alternating periods of rest and exercise; 13% of the absorbed dose was eliminated by exhalation 30 minutes after exposure, and blood concentrations of D4 decreased rapidly due to exhalation and metabolism (16% of absorbed dose in plasma 1 day after exposure). Human volunteers (number and sex not stated) exposed orally to 12 mg/day of D4 for 14 days in a double-blind, placebo-controlled crossover study did not show any immunotoxic or pro-inflammatory adjuvant effect (Dow Corning 1998c).

Based on validated studies in human skin, the SCCP (2005) suggested that the upper limit of dermal absorption is 0.94% of the applied dose of D4.

The confidence in the toxicity database is moderate to high, as there was sufficient information to address effects that may be of concern and identify critical endpoints based on oral and inhalation exposures, as well as available relevant supporting information. However, there was a lack of dermal and sometimes oral studies for some endpoints (subchronic, chronic toxicity/carcinogenicity, reproductive and developmental studies).

Although a thorough analysis of the mode of action of octamethylcyclotetrasiloxane is beyond the scope of this screening level assessment, it is recognized that an estrogenic effect or an indirect effect may contribute to the reproductive toxicity of octamethylcyclotetrasiloxane (Lassen et al. 2005). The reproductive toxicity of D4 was associated with inhibition of luteinizing hormone release in rats, and the relevance to humans of this mechanism is an area of uncertainty, as differing opinions have been expressed by SCCP (2005), SEHSC (2007d) and the European Commission (2006, 2007).

Characterization of risk to human health

Based principally on the weight-of-evidence assessments of the European Commission and the Danish EPA, an important effect of D4 exposure is impaired fertility. However, the Danish EPA also identified the liver as a target organ for D4 exposures. Although lower effect levels were determined in other repeated-dose studies (85 mg/m3 in a 5-day rat study, 360 mg/m3 in a 6-month rat study), the effects observed (increased liver weight, liver enzyme induction) were not considered to be adverse due to evidence for reversibility of the liver weight changes in rats, which were not associated with other signs of hepatotoxicity. Based on several effects including increased liver weights, increased adrenal weights, decreased thymus weights and alveolar macrophage foci and chronic interstitial inflammation of the lung in a 3-month rat inhalation study, the critical effect level for repeated-dose toxicity is considered to be 420 mg/m3 via inhalation. This level is also protective of reproductive effects, as such effects occurred at much higher doses in rats (≥ 3600 mg/kg-bw/day). Thus, comparison of the critical effect level for repeated-dose effects via inhalation (420 mg/m3) and the conservative upper-bounding exposure estimate via inhalation for octamethylcyclotetrasiloxane, 249 µg/m3, results in a margin of exposure of approximately 1700. Thus, the margins of exposure for repeated-dose effects and exposure via environmental media to the general population are considered to be adequate to account for uncertainties in the databases on exposure and effects. Margins of exposure based on consumer products are discussed below in the context of combined inhalation, dermal and oral exposures.

Although the focus of the assessment by the European Commission was inhalation, the Danish EPA assessment did not distinguish between exposure routes. Thus, it is considered prudent to establish a critical effect level for oral exposure, as a limited amount of oral toxicity data was available. As stated above, the critical effect level for repeated-dose toxicity is considered to be 100 mg/kg-bw/day via the oral route. This is based on decreased serum estradiol in the 7-day mouse studies and decreased body weights and relative liver weights in fetuses in 8-day rat studies (D4 administered to pregnant females).

Comparison of the critical effect dose level for repeated dosing via the oral route (100 mg/kg-bw/day) and the upper-bounding estimate of daily intake of octamethylcyclotetrasiloxane by the general population in Canada results in a margin of exposure of approximately 5800. This is based on adjusting the inhalation contribution to daily intake by an inhalation absorption value of 12%, resulting in a systemic exposure of 17.3 µg/kg-bw/day.

The apparent intake dose of 0.25 mg/kg-bw/day from personal care products which incorporates absorption factors for dermal, inhalation and oral exposure (Table 1, Appendix 2) was corrected by applying the reciprocals of the oral factors to calculate the equivalent systemic dose of 0.30 mg/kg-bw/day. Using this calculated upper-bounding estimate of 0.30 mg/kg-bw/day, a comparison with the critical effect dose level for repeated dosing via the oral route (100 mg/kg-bw/day) resulted in a margin of exposure of approximately 330 for personal care product scenarios. However, it is considered that the exposure estimates presented above are overestimates of actual exposure based on a submitted probabilistic assessment and information indicating that the percentage of personal care products containing D4 on the Canadian market may be lower than assumed in deriving exposure estimates. Based on values derived from an independent review of the probabilistic exposure assessment for D5, which is considered to be a surrogate for the D4 probabilistic exposure assessment, it appears that the margin of exposure from use of personal care products would be at least 10 times higher for adults and at least 5 times higher for children from that shown above (i.e. > 1500). On the basis of the above considerations, including consideration for the extent of its database, D4 is considered not to meet the criteria under paragraph 64(c) of CEPA 1999.

Uncertainties in evaluation of risk to human health

The scope of this screening assessment does not take into consideration a full analysis of the mechanism of action of octamethylcyclotetrasiloxane (D4), and it does not take into account possible differences between humans and experimental species in sensitivity to effects induced by this substance. There is uncertainty surrounding the mechanism of reproductive toxicity as well as the mechanism of action resulting in liver effects following exposure via the inhalation or oral routes. Also, due to a lack of dermal studies for some endpoints, there is uncertainty regarding route-specific effects following dermal administration.

Although physiologically based pharmacokinetic modelling of inhalation absorption data (Reddy et al. 2003) and dermal absorption data (Reddy et al. 2007) have been published, the results of such modelling is considered beyond the scope of a screening assessment and thus, only experimental data on absorption were used in this assessment.

There is uncertainty regarding the estimation of exposure and systemic dose because of the use of modelling and a lack of Canadian data. There is uncertainty associated with the use of models and the choice of variables related to the use of consumer products including quantity and frequency of use, absorbed fraction, and environmental parameters.

The cumulative exposures of the cyclosiloxanes in polydimethylsiloxanes (PDMS) are not considered in this assessment. However, D5 and D6 are considered in separate assessments.

Conclusion

Based on the information presented in this screening assessment on the potential of D4 to cause ecological harm, it is concluded that octamethylcyclotetrasiloxane is entering or may be entering the environment in a quantity or concentration or under conditions that have or may have an immediate or long-term harmful effect on the environment or its biological diversity.

Based on the available information on its potential to cause harm to human health, it is concluded that octamethylcyclotetrasiloxane is not entering the environment in a quantity or concentration or under conditions that constitute or may constitute a danger in Canada to human life or health.

It is therefore concluded that octamethylcyclotetrasiloxane meets the definition of toxic as set out in paragraph 64a of CEPA 1999. It is also concluded that octamethylcyclotetrasiloxane meets the criteria for persistence as set out in the Persistence and Bioaccumulation Regulations. However, it is not possible to conclude that octamethylcyclotetrasiloxane meets the criterion for bioaccumulation, considering the conflicting evidence presented in this screening assessment report.

The conclusion in this screening assessment is based on the available information at this time and acknowledges that there are uncertainties associated with this assessment. Research on cVMS is currently being conducted to help address these uncertainties, but some of this research has not been completed at this time. In the context of the Challenge program, any new information provided after the final screening assessment may be considered during the risk management phase.

Monitoring has also been identified as a key component in the Chemicals Management Plan in Canada and D4 is being considered for environmental monitoring under the Plan. Field level data will contribute to a better understanding of the distribution of D4 in the environment and its bioaccumulation potential in relevant food webs.

References

Allen RB, Kochs P, Chandra G. 1997. Industrial Organic Materials, Their Environmental Entry and Predicted Fate. In: Organosilicon Materials, Hutzinger, O. editor, Handbook of Environmental Chemistry. Berlin: Springer-Verlag. p1-25.

[AOPWIN] Atmospheric Oxidation Program for Windows [Estimation Model]. 2000. Version 1.91. Washington (DC): U.S. Environmental Protection Agency, Office of Pollution Prevention and Toxics; Syracuse (NY): Syracuse Research Corporation. Exposure Assessment Tools and Models.

Arnot JA, Gobas FAPC. 2003. A generic QSAR for assessing the bioaccumulation potential of organic chemicals in aquatic food webs. QSAR Comb Sci 22(3): 337-345 [cited 2008 October].

Arnot JA, Gobas FAPC. 2006. A review of bioconcentration factor (BCF) and bioaccumulation factor (BAF) assessments for organic chemicals in aquatic organisms. Environ Rev. 14(4): 257-297.

Arnot JA, Mackay D, Bonnell M. 2008a. Estimating Metabolic Biotransformation Rates in Fish from Laboratory Data. Envirion. Toxicol. Chem. 27(2): 341-351.

Arnot JA, MacKay D, Parkerton T, Bonnell M. 2008b. A database of fish biotransformation rate constants. Environ Sci Technol (in press).

Atkinson R. 1989. Kinetics and mechanisms of the gas-phase reactions of the hydroxyl radical with organics compounds. Journal of Physical and Chemical Reference Data. Monograph No. 1.

Atkinson R. 1991. Kinetics of the gas-phase reactions of a series of organosilicon compounds with OH and NO3 radicals and O3 at 297 ± 2 K. Environmental Science and Technology 25(5): 863-866.

Bayer AG. 1988. Subakute toxikologische Untersuchungen an Kaninchen. Report No. 16886. [cited in SCCP 2005, ref. 7; cited in IUCLID 2000, ref. 50; cited in SEHSC 2007d].

Beyer A, Mackay D, Matthies M, Wania F, Webster E. 2000. Assessing Long-Range Transport Potential of Persistent Organic Pollutants. Environ Sci Technol 34(4): 699-703.

Bidleman TF. 2008.  Review of the Dow-Corning Health & Environmental Sciences Technical Reports: "Hydrolysis of Octamethylcyclopentasiloxane (D4)" and "Hydrolysis of Decamethylcyclopentasiloxane (D5)". Centre for Atmospheric Research Experiments (Egbert, ON.). Science and Technology Branch, Environment Canada.

[BIOWIN] Biodegradation Probability Program for Windows [Estimation Model]. 2000. Version 4.02. Washington (DC): US Environmental Protection Agency, Office of Pollution Prevention and Toxics; Syracuse (NY): Syracuse Research Corporation. [cited 2007 Sept 12]. Exposure Assessment Tools and Models.

Burns-Naas LA, Meeks RG, Kolesar GB, Mast RW, Elwell MR, Hardisty JF, Thevenaz P. 2002. Inhalation toxicology of octamethylcyclotetrasiloxane (D4) following a 3-month nose-only exposure in Fischer 344 rats. Int J Toxicol 21(1):39-53.

Bruggeman WA, Weber-Fung D, Opperhuizen A, Van Der Steen J, Wijbenga A, Hutzinger O. 1984. Absorption and retention of polydimethylsiloxanes (silicones) in fish: preliminary experiments. Toxicological and Environmental Chemistry. 7: 287-296.

Canada. 1999. Canadian Environmental Protection Act, 1999. S.C., 1999, c. 33, Canada Gazette, Part III, Vol. 22, No. 3.

Canada. 2000. Canadian Environmental Protection Act:Persistence and Bioaccumulation Regulations, P.C. 2000-348, 23 March, 2000, SOR/2000-107, Canada Gazette, Part II, Vol. 134, No. 7.

Canada. Dept. of the Environment; Dept. of Health. 2006.Canadian Environmental Protection Act, 1999: Notice of intent to develop and implement measures to assess and manage the risks posed by certain substances to the health of Canadians and their environment. Ottawa: Public Works and Government Services Canada. Canada Gazette, Part I, Vol. 140, No. 49.

Canada. Dept. of the Environment, Dept. of Health. 2007.Canadian Environmental Protection Act, 1999: Notice of second release of technical information relevant to substances identified in the Challenge. Canada Gazette, Part I, Vol. 141. No. 19.

Caldwell DJ. 1999. Review of mononuclear cell leukemia in F-344 rat bioassays and its significance to human cancer risk: A case study using alkyl phthalates. Regul Toxicol Pharmacol 30(1):45-53.

[CATABOL] Probabilistic assessment of biodegradability and metabolic pathways [Computer Model]. c2004-2008. Version 5.10.2. Bourgas (BG): Prof. Assen Zlatorov University, Laboratory of Mathematical Chemistry. [2008 February 4]. OASIS Software.

Cianciarelli D. 2007. Personal communication from Cianciarelli, Environment Canada ETC, unpublished biogas measurement results. 2007.

[CNS] Cosmetic Notification System [proprietary database]. 2007. Ottawa (ON): Health Canada. [cited 2008 Jan.]

Domoradzki J. 2008a. Refinement in the determination of the BMF value for D4 from a fish feeding study in rainbow trout. Midland (MI): Dow Corning Corporation, Health and Environmental Sciences. 

Domoradzki J. 2008b. Refinement in the determination of the BMF value for D5 from a fish feeding study in rainbow trout. Midland (MI):Dow Corning Corporation, Health and Environmental Sciences.

Dow Corning (Corporation). 1982. Evaluation of D4 in the Rodent dominant lethal test. Report no. 1982-I0005-1029. [cited in SCCP 2005, ref. 53].

Dow Corning (Corporation). 1986. Summary of toxicology on cyclic and linear dimethyl-siloxane oligomers and polymers. March 14, 1986 [cited in IUCLID 2000, ref. 53].

Dow Corning (Corporation). 1988a. A 14-day range-finding vapour inhalation toxicity study with DC 244 fluid in the rat. Report no. 1988-I0005-2441, October 21, 1988. [cited in SEHSC (Silicones Environmental, Health and Safety Council). 2007d. Additional toxicity and exposure information for a screening health assessment of octamethylcyclotetrasiloxane (D4), CAS No. 556-67-2. November 13, 2007].

Dow Corning (Corporation). 1988b. A 14-day repeated dose inhalation study of D4 in the rat, Report No. I988-I0005-1760, March 22, 1988. [cited in SEHSC (Silicones Environmental, Health and Safety Council). 2007d. Additional toxicity and exposure information for a screening health assessment of octamethylcyclotetrasiloxane (D4), CAS No. 556-67-2. November 13, 2007].

Dow Corning (Corporation). 1989a. A 28-day repeated dose inhalation study of D4 in multiple species. Report no. 1989-I0005-2512, March 1, 1989. [cited in SEHSC (Silicones Environmental, Health and Safety Council). 2007d. Additional toxicity and exposure information for a screening health assessment of octamethylcyclotetrasiloxane (D4), CAS No. 556-67-2. November 13, 2007].

Dow Corning (Corporation). 1989b. A 90-day sub-chronic inhalation toxicity study of D4 in the rat. Report no. 1989-I0005-2511, March1, 1989. [cited in SEHSC (Silicones Environmental, Health and Safety Council). 2007d. Additional toxicity and exposure information for a screening health assessment of octamethylcyclotetrasiloxane (D4), CAS No. 556-67-2. November 13, 2007].

Dow Corning (Corporation). 1990. A 14-day subchronic oral gavage study with D4 in rats. Report No. 1990-10000-35072. Fiche #:OTS0528331. Doc#: 86-910000037. [cited in IUCLID 2000, ref 74].

Dow Corning (Corporation). 1992. A 14-day oral gavage study of D4 in female rabbits. Report No. 1992-I0000-37117. [cited in SCCP 2005, ref. 6].

Dow Corning (Corporation). 1994. 4-Hour Inhalation Toxicity Study with Octamethylcyclotetrasiloxane in Rats. Report No. 1994-I0000-39679. RCC Group. [cited in SCCP 2005, ref. 3].

Dow Corning (Corporation, RCC Group). 1995a. One-month repeated dose inhalation toxicity study with D4 in rats. Report No. 1995-I0000-40168, March 14, 1995. [cited in SEHSC (Silicones Environmental, Health and Safety Council). 2007d. Additional toxicity and exposure information for a screening health assessment of octamethylcyclotetrasiloxane (D4), CAS No. 556-67-2. November 13, 2007].

Dow Corning (Corporation). 1995b. Three month repeated toxicity study with D4 in rats. Report No. I995-I0000-40152, March 6, 1995. [cited in SEHSC (Silicones Environmental, Health and Safety Council). 2007d. Additional toxicity and exposure information for a screening health assessment of octamethylcyclotetrasiloxane (D4), CAS No. 556-67-2. November 13, 2007].

Dow Corning (Corporation, WIL Research Laboratories, Inc.). 1996a. An inhalation range finding reproductive toxicity study of D4 in rats. Report No. 1995-I0000-40919, March 7, 1996. [cited in SEHSC (Silicones Environmental, Health and Safety Council). 2007d. Additional toxicity and exposure information for a screening health assessment of octamethylcyclotetrasiloxane (D4), CAS No. 556-67-2. November 13, 2007].

Dow Corning (Corporation, WIL Research Laboratories, Inc.). 1996b. An inhalation range finding reproductive toxicity study of D4 in rats. Report No. 1996-I0000-41337, August 27, 1996. [cited in SEHCS (Silicones Environmental, Health and Safety Council). 2007. Additional toxicity and exposure information for a screening health assessment of octamethylcyclotetrasiloxane (D4), CAS No. 556-67-2. November 13, 2007].

Dow Corning (Corporation, WIL Research Laboratories, Inc). 1997a. An inhalation range finding reproductive toxicity study in male rats. Report No. 1997-I0000-43726. [cited in SCCP 2005, ref. 29].

Dow Corning (Corporation, WIL Research Laboratories, Inc.). 1997b. An inhalation range finding reproductive toxicity study of D4 in male rats. Report No. 1997-I0000-43725. [cited in SCCP 2005, ref. 30].

Dow Corning (Corporation, WIL Research Laboratories, Inc.). 1997c. Female rat inhalation reproductive study of D4. Report No. 1997-I0000-42936, July 29, 1997. [cited in SEHCS (Silicones Environmental, Health and Safety Council). 2007. Additional toxicity and exposure information for a screening health assessment of octamethylcyclotetrasiloxane (D4), CAS No. 556-67-2. November 13, 2007].

Dow Corning (Corporation, Medical College of Virginia). 1997d. Immunological evaluation of D4 using 28 day exposure in male and female rats. Report No. 1997-I0000-41338, December 29, 1997. [cited in SEHCS (Silicones Environmental, Health and Safety Council). 2007. Additional toxicity and exposure information for a screening health assessment of octamethylcyclotetrasiloxane (D4), CAS No. 556-67-2. November 13, 2007].

Dow Corning (Corporation, WIL Research Laboratories, Inc.). 1998a. An inhalation reproductive toxicity study of D4 in female rats using multiple exposure regimens. Report No. 1998-I0000-44490, May 22, 1998. [cited in SEHSC (Silicones Environmental, Health and Safety Council). 2007d. Additional toxicity and exposure information for a screening health assessment of octamethylcyclotetrasiloxane (D4), CAS No. 556-67-2. November 13, 2007].

Dow Corning Corporation. 1998b. An oral gavage study to compare the absorption potential of 14C-D4 in Fischer rats when delivered in various carriers. Report No. 1998-10000-44815. [cited in SCCP 2005, ref. 35].

Dow Corning (Corporation, University of Rochester Medical Center). 1998c. Clinical studies on the immune effects of gastrointestinal exposure to D4. Internal Report No. 1998-I0000-45117, Nov. 10, 1998. [cited in SEHSC (Silicones Environmental, Health and Safety Council). 2007d. Additional toxicity and exposure information for a screening health assessment of octamethylcyclotetrasiloxane (D4), CAS No. 556-67-2. November 13, 2007].

Dow Corning (Corporation). 1999. Effects of repeated whole body inhalation exposure to D4 vapors on hepatic microsomal CYP2B1/2 induction in female Fischer 344 rats. Report No. 1998-I0000-44687. [cited in SCCP 2005, ref. 60].

Dow Corning (Corporation). 2002. Non-regulated study. Effects of octamethylcyclotetrasiloxane (D4) on cell proliferation in the liver of female Fischer 344 rats: a 28-day inhalation study. 2002- Report No. I0000-52111.

Dow Corning (Corporation). 2004. 24-month combined chronic toxicity and oncogenicity whole body vapor inhalation study of octamethylcyclotetrasiloxane (D4) in Fischer 344 rats. Report no. 2004-10000-54091. [cited in SCCP 2005, ref. II-37].

[DPD] Drug Product Database [database on the internet]. 2007. Ottawa (ON): Health Canada. [cited 2008 Jan.]

Drottar K. 2007. 14C-Octamethylcyclotetrasiloxane (14C-D4): dietary bioaccumulation in the rainbow trout (Oncorhynchus mykiss) under flow-through conditions. Dow Corning Report No. 2007-I0000-57314.

Durham J. 2005. Hydrolysis of octamethylcyclotetrasiloxane (D4). Silicones Environment, Health and Safety Council. Study Number 10000-102.

Durham J. 2006. Hydrolysis of octamethylcyclotetrasiloxane (D5). Silicones Environment, Health and Safety Council. Study Number 10040-102.

[ECB] European Chemicals Bureau. 2007. ESIS (European chemical Substances Information System), Version 4.60. [cited 2007 Dec.]

[ECOSAR] Ecological Structural Activity Relationships [Internet]. 2004. Version 0.99g. Washington (DC): U.S. Environmental Protection Agency, Office of Pollution Prevention and Toxics; Syracuse (NY): Syracuse Research Corporation. Exposure Assessment Tools and Models.

Environment Canada. 1988. Data relating to the Domestic Substance List
(DSL) 1984-1986, collected under CEPA, 1988, s. 25(1). Based on: Reporting for the Domestic Substance List [guide], Data prepared by: Environment Canada, New Substances Division.

Environment Canada. 2007. Data for Batch 2 substances collected under the Canadian Environmental Protection Act, 1999, Section 71: Notice with respect to certain Batch 2 Challenge substances. Data prepared by: Environment Canada, Existing Substances Program.

Environment Canada. 2008a. Assumptions, limitations and uncertainties of the Mass Flow Tool for octamethylcyclotetrasiloxane, CAS RN 556-67-2. Existing Substances Division, Environment Canada, Gatineau (QC). Internal draft document available on request.

Environment Canada. 2008b. Guidance for conducting ecological assessments under CEPA, 1999: science resource technical series, technical guidance module: Overview of Aquatic Risk Distribution Methodology. Working document. Gatineau (QC): Environment Canada, Existing Substances Division.

Environment Canada. 2008c. Aquatic risk distribution summary for octamethylcyclotetrasiloxane: CAS RN 556-67-2. 2008-09-08. Unpublished report.  Gatineau (QC): Environment Canada, Existing Substances Division.

[EQC] Equilibrium Criterion Model. 2003. Version 2.02. Peterborough (ON): Trent University, The Canadian Environmental Modelling Centre and Chemistry - EQC Model.

[ESIS] European Chemical Substances Information System [database on the Internet]. 2007. Version 5.  European Chemical Bureau (ECB).

European Commission. 2001. Adapting to technical progress for the 28th time Council Directive 67/548/EEC on the approximation of the laws, regulations and administrative provisions relating to the classification, packaging and labelling of dangerous substances. Commission Directive 2001/59/EC - Annex I.

European Commission. 2006. Conclusions from the Meeting of the Commission Working Group of Specialised Experts on Reproductive Toxicity. Ispra, 20 September 2006. ECBI/121/06.

European Commission. 2007. Summary Record: Commission Working Group of Specialised Experts in the Field of Reproductive Toxicity. Ispra, 19-20 September 2006. ECBI/51/07.

Fackler PH, Dionne E, Hartley DA, Hamelink JL. 1995. Bioconcentration by fish of a highly volatile silicone compound in a totally enclosed aquatic exposure system. Environmental Toxicology and Chemistry 14(10):1649-1656.

Falany CN, Li G. 2005. Effects of age and pregnancy on cytochrome P450 induction by octamethyltetracyclosiloxane in female Sprague-Dawley rats. J Biochem Mol Toxicol. 19(2):129-138.

Felix K, Lin S, Bornkamm GW, Janz S. 1989. Tetravinyl-tetramethylcyclo-tetrasiloxane (tetravinyl D4) is a mutagen in Rat2lambda lacI fibroblasts. Carcinogenesis 19: 315-320.

Fenner K, Scheringer M, MacLeod M, Matthies M, McKone TE, Stroebe M, Beyer A, Bonnell M, Le Gall A, Klasmeier J, et al. 2005. Comparing estimates of persistence and long-range transport potential among multimedia models. Environmental Science and Technology 39:1932-1942.

Flaningam OL. 1986. Vapor pressure of poly (dimethylsiloxane) oligomers. J Chem Eng Data 31:266-272.

[GEMStat] Global Water Quality Data and Statistics [database on the internet] Burlington (OM) United Nations. Global Environment Monitoring System (GEMS) Water Programme.. [cited 2008 September]. About GEMStat.org.

Gobas FAPC, Kelly BC, Arnot JA. 2003. Quantitative structure activity relationship for predicting the bioaccumulation of POPs in terrestrial food-webs. QSAR Comb Sci 22: 329-335.

[GSPA] Global Silicone Producers Association, International Research and Development Corporation. 1991. Thirteen week subchronic inhalation toxicity study on D4 in rats. Report no. 416-074, February 08, 1991. [cited in SEHSC (Silicones Environmental, Health and Safety Council). 2007d. Additional toxicity and exposure information for a screening health assessment of octamethylcyclotetrasiloxane (D4), CAS No. 556-67-2. November 13, 2007].

[GSPA] Global Silicone Producers Association, International Research and Development Corporation. 1993a. Range-finding inhalation developmental toxicity study in rats with D4. Study No. 665-003, December 17, 1993. [cited in SEHSC (Silicones Environmental, Health and Safety Council). 2007d. Additional toxicity and exposure information for a screening health assessment of octamethylcyclotetrasiloxane (D4), CAS No. 556-67-2. November 13, 2007].

[GSPA] Global Silicone Producers Association, International Research and Development Corporation. 1993b. Range-finding inhalation developmental toxicity study in New Zealand White Rabbits with Dr. Study No. 665-002, December 17, 1993. [cited in SEHCS (Silicones Environmental, Health and Safety Council). 2007. Additional toxicity and exposure information for a screening health assessment of octamethylcyclotetrasiloxane (D4), CAS No. 556-67-2. November 13, 2007].

Hamelink JL, Simon PB, Silberhorn EM. 1996. Henry's Law Constant, volatilization rate, and aquatic half-life of octamethylcyclotetrasiloxane. Environ. Sci. Technol. 30: 1946-1952.

He B, Rhodes-Brower S, Miller MR, Munson AE, Germolec DR, Walker VR, Korach KS, Meade BJ. 2003. Octamethylcyclotetrasiloxane exhibits estrogenic activity in mice via ERa. Toxic appl Pharmac 192: 254-261.

Health Canada. 1998. Exposure factors for assessing total daily intake of priority substances by the general population of Canada. Unpublished report. Ottawa (ON): Health Canada, Environmental Health Directorate. Available upon request.

[HENRYWIN] Henry's Law Constant Program for Microsoft Windows [Estimation Model]. 2000. Version 3.10. Washington (DC): U.S. Environmental Protection Agency, Office of Pollution Prevention and Toxics; Syracuse (NY): Syracuse Research Corporation. Exposure Assessment Tools and Models.

Herner AV, Flassbeck D, Gruemping R. 2002. Organosilicon Compounds in the Environment. In: Craig PJ. editor, Organometallic Compounds in the Environment. 2nd ed. New York. John Wiley & Sons, Ltd. p. 324.

Hobson JF, Silberhorn EM. 1995. Octamethylcyclotetrasiloxane (OMCTS), a case study: summary and aquatic risk assessment. Environmental Toxicology and Chemistry 14(10):1667-1673.

Hu T-M, Layton WL. 2001. Allometric scaling of xenobiotic clearance: uncertainty versus universality. AAPS PharmSci. 3(4) Article 29 [cited 2008 October].

Hurd CB. 1946. Studies on siloxanes 1. The specific volume and viscosity in relation to temperature and constitution. J Am Chem Soc 68(3): 364.

HydroQual, Inc. 1993. Sampling and analysis of aquatic D4 at selected wastewater treatment plants. TSCA Docket OPTS-42071B, Toxic Substances Control Act Public Docket Office, Washington, DC. [cited in Hobson JG, Atkinson R, Carter, WPL. 1997. Volatile methylsiloxanes. In: The Handbook of Environmental Chemistry, Volume 3 Part H: Organosilicon Materials. Chandra G (editor). Springer-Verlag, New York, NY. Pp. 137-179].

[IRDC] International Research and Development Corporation. 1993a. Range-finding developmental toxicity study in New Zealand White rabbits. Study No. 665-001. [cited in SCCP 2005, ref. 24].

[IRDC] International Research and Development Corporation. 1993b. Inhalation developmental toxicity study in rats with D4. Study No. 665-004. [cited in SCCP 2005, ref. 25].

[IRDC] International Research and Development Corporation. 1993c. Inhalation developmental toxicity study in New Zealand White rabbits with D4. Study No. 665-005. [cited in SCCP 2005, ref. 26].

Isquith A, Matheson D, Slesinski R. 1988. Genotoxicity studies on selected organosilicon compounds: in vitro assays. Fd Chem Toxic 26:255-61.

[IUCLID] International Uniform Chemical Information Database. 2000. Dataset for CAS No. 556-67-2, Octamethylcylclotetrasiloxane. European Commission - European Chemicals Bureau. 18 February 2000.

Jovanovic ML, McMahaon JM, McNett DA, Tobin JM, Plotzke KP. 2008. In vitro and in vivo percutaneous absorption of 14C-octmethylcyclotetrasiloxane (14C-D4) and 14C-decamethylcyclopentasiloxane (14C-D5). Regul Toxicol Pharmacol: 50: 239-248.

Kaj L, Andersson J, Palm Cousins A, Remberger M, Ekheden Y, Dusan B, Bror-ström-Lundén E. 2005. Results from the Swedish National Screening Programme 2004: Subreport 4: Siloxanes - IVL.

Kent DJ, McNamara PC, Putt AE, Hobson JF, Siberhorn EM. 1994. Octamethylcyclotetrasiloxane in aquatic sediments: toxicity and risk assessment. Ecotoxicology and Environmental Safety 29(3):372-389.

Klasmeier J, Matthies M, MacLeod M, Fenner K, Scheringer M, Stroebe M, Le Gall AC, McKone TE, van de Meent D, Wania F. 2006. Application of multimedia models for screening assessment of long-range transport potential and overall persistence. Environmental Science and Technology 40(1): 53-60.

Klykken PC, Galbraith TW, Kolesar GB, Jean PA, Woolhiser MR, Elwell MR, Burns-Naas LA, Mast RW, McCay JA, White KL Jr et al. 1999. Toxicology and humoral immunity assessment of octamethylcyclotetrasiloxane (D4) following a 28-day whole body vapor inhalation exposure in Fischer 344 rats. Drug Chem Toxicol 22(4):655-77.

Kochetkov A, Smith JS, Ravikrishna R, Valsaraj KT, Thibodeaux LJ. 2001. Air-water partition constants for volatile methyl siloxanes. Environmental Toxicology and Chemistry. 20(10):2184-2188.

[KOWWIN] Octanol-Water Partition Coefficient Program for Microsoft Windows [Estimation Model]. 2000. Version 1.67. Washington (DC): U.S. Environmental Protection Agency, Office of Pollution Prevention and Toxics; Syracuse (NY): Syracuse Research Corporation. Exposure Assessment Tools and Models.

Kozerski G, Shawl H. 2007. Determination of the 1-octanol/water partition coefficient of octamethylcyclotetrasiloxane (D4) by the slow-stirring method using gas chromatography and mass spectrometry. SEHSC. Dow Corning Study No. 10198-102.

Kozerski G. 2008. SEHSC response to Dr. Bidleman's review on hydrolysis studies of D4 and D5. Dow Corning Corporation. July 2008.

Kramp F, Volz-Thomas A. 1997. On the budget of OH radicals and ozone in an urban plume from the decay of C5-C8 hydrocarbons and NOx. Journal of Atmospheric Chemistry. 28:263-282.

Krueger HO, Thomas ST, Kendall TZ. 2008. D4: a prolonged sediment toxicity test with Chironomus riparius using spiked sediment. Final report. Project number 570A-107. Silicones Environmental, Health and Safety Council.

Lassen C, Hansen CL, Mikkelson SJ, Maag J. 2005. Siloxanes - consumption, toxicity and alternatives. Danish Ministry of the Environment, Environmental Protection Agency (Danish EPA). Environmental Project No. 1031.

Lee MK et al. (other authors not stated). 2005. 24-month combined chronic toxicity and oncogenicity whole body vapour inhalation study of octomethylcyclotetrasiloxane (D4) in Fischer 344 rats. Report No. 2005-I0000-54091. [cited in SEHSC (Silicones Environmental, Health and Safety Council). 2007d. Additional toxicity and exposure information for a screening health assessment of octamethylcyclotetrasiloxane (D4), CAS No. 556-67-2. November 13, 2007d].

Maxim LD. 1998. D4, D5, and D6 Exposure in the manufacture and use of personal care products: an interim assessment. Dow Corning Corporation.

McFall JA, Antoine SR, DeLeon IR. 1985. Organics in the water column of Lake Pontchartrain. Chemosphere 14(9): 1253-1265.

McKim JM Jr, Wilga PC, Kolesar GB, Choudhuri S, Madan A, Dochterman LW, Breen JG, Parkinson A, Mast RW, Meeks RG. 1998. Evaluation of octamethylcyclotetrasiloxane (D4) as an inducer of rat hepatic microsomal cytochrome P450, UDP-glucuronosyltransferase, and epoxide hydrolase: a 28-day inhalation study. Toxicol Sci 41(1):29-41.

McKim JM Jr, Wilga PC, Breslin WJ, Plotzke KP, Gallavan RH, Meeks RG. 2001a. Potential estrogenic and antiestrogenic activity of the cyclic siloxane octamethylcyclotetrasiloxane (D4) and the linear siloxane hexamethyldisiloxane (HMDS) in immature rats using the uterotrophic assay. Toxicol Sci 63(1):37-46.

McKim JM Jr, Kolesar GB, Jean PA, Meeker LS, Wilga PC, Schoonhoven R, Swenberg JA, Goodman JI, Gallavan RH, Meeks RG. 2001b. Repeated inhalation exposure to octamethylcyclotetrasiloxane produces hepatomegaly, transient hepatic hyperplasia, and sustained hypertrophy in female Fischer 344 rats in a manner similar to phenobarbital. Toxicol Appl Pharmacol 172(2):83-92.

Meeks RG, Stump DG, Siddiqui WH, Holson JF, Plotzke KP, Reynolds VL. 2007. An inhalation reproductive toxicity study of octamethylcyclotetrasiloxane (D4) in female rats using multiple and single day exposure regimens. Reprod Toxicol 23(2):192-201.

Miller J. 2007. Soil-water distribution of octamethylcyclotetrasiloxane (D4) using a Batch Equilibrium Method. Draft Report. Centre Europeen des Silicones (CES).

[MPBPWIN] Melting Point Boiling Point Program for Microsoft Windows [Estimation Model]. 2000. Version 1.41. Washington (DC): U.S. Environmental Protection Agency, Office of Pollution Prevention and Toxics; Syracuse (NY): Syracuse Research Corporation. Exposure Assessment Tools and Models.

Navea JG, Stanier CO, Young MA, Grassian VH. 2007. A laboratory and modeling study at the University of Iowa designed to better understand the atmospheric fate of D4 and D5. Technical annual report (August 2006-July 2007). The University of Iowa, Department of Chemistry, and Chemical and Biochemical Engineering, Iowa City (IA), 52242.

[NCI] National Chemical Inventories [database on a CD-ROM]. 2007. Columbus (OH): American Chemical Society, Chemical Abstracts Service. [cited 2007 Apr 30]. National Chemical Inventory (NCI) System Requirements.

[NHW] National Health and Welfare. 1990. Present patterns and trends in infant feeding in Canada. Department of National Health and Welfare, Ottawa. [cited in Health Canada 1998].

[NMI] Non-Medicinal Ingredients [proprietary database]. 2007. Ottawa (ON): Health Canada. [cited 2008 Jan.]

Nichols JW, Fitzsimmons PN, Burkhard LP. 2007. In vitro - in vivo extrapolation of quantitative hepatic biotransformation data for fish. II. Modeled effects on chemical bioaccumulation. Environ. Toxicol. Chem. 26(6): 1304-1319.

[NILU] Norsk institutt for luftforskning.  2007.  Siloxanes in the Environment of the Inner Oslofjord.  Repport No. 986/2007. Kjeller(NO) Norvegian Institute of Air Research.

[NOAA] National Oceanic and Atmospheric Administration. 2008. NOAA CoastWatch Great Lakes Program. NOAA Great Lakes Environmental Research Laboratory [cited 2008 Sep].

Norden. 2005. Siloxanes in the Nordic Environment. TemaNord 2005:593. Copenhagen (NO), Nordic Council of Ministers.

[NYIEQ] New York Indoor Environmental Quality Center. 2005. Indoor Environmental Quality: Assessing and Mitigating the Impact of Exposure to Multiple Indoor Contaminants. Project No. R828605-01.

[OECD] Organisation for Economic Co-operation and Development. 2004. Emission Scenario Document on Plastics Additives [Internet]. Paris (FR): OECD Environmental Directorate, Environmental Health and Safety Division. [cited 2004 Sep]. Chemical Safety.

[OECD] Organisation for Economic Co-operation and Development. 2006. Draft Emission Scenario Document on Transport and Storage of Chemicals. Prepared by the Environment Agency (UK). Available on request from: Environment Canada, Existing Substances Division, Ottawa, K1A 0H3.

[OECD] Organisation for Economic Co-operation and Development. 2007. Manual for investigation of HPV chemicals. OECD Secretariat, July 2007. [cited 2008 Jan.]. Manual for the Assessment of Chemicals.

[PCKOCWIN] Organic Carbon Partition Coefficient Program for Windows [Estimation Model]. 2000. Version 1.66. Washington (DC): U.S. Environmental Protection Agency, Office of Pollution Prevention and Toxics; Syracuse (NY): Syracuse Research Corporation. Exposure Assessment Tools and Models.

[PMRA] Pest Management Regulatory Agency. 2007. Regulatory Note REG 2007-04: PMRA list of formulants [Internet]. Ottawa (ON): Health Canada, Pest Management Regulatory Agency. [cited 2008 Sep].

Powell D, Kozerski G. 2007. Cyclic methylsiloxane (cVMS) materials in surface sediments and cores for Lake Ontario. Centre Europeen des Silicones (CES). Draft Report.

Powell DE. 2008. Interim update on cyclic methylsiloxane (cVMS) materials in surface sediment, cores, and zooplankton for Lake Opeongo, Ontario, Canada. Centre Europeen des Silicones (CES). July 14, 2008.

[PhysProp] Interactive PhysProp Database [database on the Internet]. 2006. Syracuse (NY): Syracuse Research Corporation. [cited 2006 Mar] Interactive PhysProp Database Demo.

Quinn AL, Regan JM, Tobin JM, Marinik BJ, McMahon JM, NcNett DM, Sushynski CM, Crofoot SD, Jean PA, Plotzke KP. 2007a. In vitro and in vivo evaluation of the estrogenic, androgenic, and pregestagenic potential of two cyclic siloxanes. Toxicol Sci 96: 145-153.

Quinn AL, Dalu A, Meeker LS, Jean PA, Meeks RG, Crissman JW, Gallavan RH, Plotzke KP. 2007b. Effects of octamethylcyclotetrasiloxane (D4) on the luteinizing hormone (LH) surge and levels of various reproductive hormones in female Sprague-Dawley rats. Reprod Tox 23: 532-540.

Reddy MB, Andersen ME, Morrow PE, Dobrev ID, Varaprath S, Plotzke KP, Utell MJ 2003. Physiological modeling of inhalation kinetics of octamethylcyclotetrasiloxane in humans during rest and exercise. Toxicol Sci 72: 3-18.

Reddy MB, Looney RJ, Utell MJ, Plotzke KP, Andersen ME. 2007. Modeling of human dermal absorption of octamethylcyclotetrasiloxane (D4) and decamethylcyclopentasiloxane (D5). Toxicol Sci 99(2):422-431.

Ren X, Harder H, Martinez M, Lesher RL, Oliger A, Shirley T, Adams J, Simpas JB, Brune WH. 2003. HOx concentrations and OH reactivity observations in New York City during PMTACS-NY2001. Atmospheric Environment 37(26):3627-3637.

Ren X, Brune WH, Mao J, Mitchell MJ, Lesher RL, Simpas JB, Metcalf AR, Schwab JJ, Cai C, Li Y, et al. 2006. Behaviour of OH and HO2 in the winter atmosphere in New York City. Atmospheric Environment 40:S252-S263.

Rivett AC, Martin D, Gray DJ, Price CS, Nickless G, Simmonds PG, O'Doherty SJ, Greally BR, Knights A, Shallcross DE. 2003. The role of volatile organic compounds in the polluted urban atmosphere of Bristol, UK. Atmos Chem Phys Discuss 3:769-796.

[RIVM] Rijksinstituut voor Volksgezondheid en Milieu. 2006. Consumer Exposure (ConsExpo) Model - Version 4.1 [Internet]. Version 4.1. The Netherlands: The National Institute for Public Health and the Environment (Rijksinstituut voor Volksgezondheid en Milieu).

[RTECS] Registry of Toxic Effects of Chemical Substances. 2007. Record for Cyclotetrasiloxane, octamethyl- (556-67-2). Record last updated August 2007. MDL Informations Systems, Inc.

[SCCP] Scientific Committee on Consumer Products. 2005. Opinion on octamethylcyclotetrasiloxane (D4) cyclomethicone (INCI name). (Adopted by the SCCP during the 6th plenary meeting of 13th December 2005). European Commission, Health & Consumer Protection Directorate-General (Directorate C - Public Health and Risk Assessment). SCCP/0893/05.

Scheringer M, MacLeod M, Wegmann F 2006. The OECD POV and LRTP Screening Tool, Version 2.0.  Distributed at OECD/UNEP Workshop on "Application of Multimedia Models for Identification of Persistent Organic Pollutants", Ottawa, Canada, May 31 to June 3, 2006. [Cited 2008].

[SEHSC] Silicones Environmental, Health and Safety Council. 2005. Degussa Corporation/Goldschmidt GmbH: TSCA 8(e): Notification of Substantial Risk; Detection of Decamethylcyclopentasiloxane and Octamethylcyclotetrasiloxane in the tissue of Fish from the Rhine River in Germany, October 10, 2005. Data submitted to Environment Canada by the

SEHSC, Herndon, VA, December 20, 2005. Environment Canada submission # s70-2006-007.

[SEHSC] Silicones Environmental, Health and Safety Council. 2007a. SEHSC presentations to EC/HC on October 2nd, 2007.

[SEHSC] Silicones Environmental, Health and Safety Council. 2007b. SEHSC communication to EC/HC on CAS No. 69430-24-6, 2007.

[SEHSC] Silicones Environmental, Health and Safety Council. 2007c. Octamethylcyclotetrasiloxane (D4) background information, CAS No. 556-67-2. November 12, 2007.

[SEHSC] Silicones Environmental, Health and Safety Council. 2007d. Additional toxicity and exposure information for a screening health assessment of octamethylcyclotetrasiloxane (D4), CAS No. 556-67-2. November 13, 2007.

[SEHSC] Silicones Environmental, Health and Safety Council. 2008a. Additional toxicity and exposure information for a screening health assessment of decamethylcyclopentasiloxane (D5), CAS No. 541-02-6. November 13, 2007 (Updated February 13, 2008).

[SEHSC] Silicones Environmental, Health and Safety Council. 2008b. Silicone industry comments on Health and Environment Canada's Draft Screening Assessment of D4: Special pattern of cVMS environmental release and its effects on their half-lives in the atmosphere. July 16, 2008.

Siddiqui WH, Stump DG, Plotzke KP, Holson JF, Meeks RG. 2007. A two-generation reproductive toxicity study of octamethylcyclotetrasiloxane (D4) in rats exposed by whole-body vapor inhalation. Reprod Toxicol 23(2):202-15.

Sousa JV, McNamara PC, Putt AE, Machado MW, Surprenant DC, Hamelink JL, Kent DJ, Silberhorn EM, Hobson JF. 1995. Effects of octamethylcyclotetrasiloxane (OMCTS) on freshwater and marine organisms. Environmental Toxicology and Chemistry 14(10):1639-1647.

Springborn Laboratories. 1990. (Octamethylcyclotetrasiloxane) - Toxicity to the freshwater green alga Selenastrum capricornutum. SLI Report 90-3-3271.

Springborn Laboratories. 1991. Supplemental Study: Bioconcentration and elimination of C-14 residues by fathead minnows (Pimephales promelas) exposed to octamethylcyclotetra-siloxane. SLI Report No. 91-6-3809. Silicones Environmental, Health and Safety Council (SEHSC).

Springborn Smithers Laboratories. 2005. Determining the biodegradability of octamethylcyclotetrasiloxane based on the draft OECD 310 sealed vessel CO2 evolution biodegradation test. Study No. 12023.6146.

[TaPL3] Long Range Transport and Persistence Level III model [Internet]. 2000. Version 2.10.

Peterborough (ON): Trent University, The Canadian Environmental Modelling Centre and Chemistry - TaPL3.

[TSCATS] Toxic Substance Control Act Test Submission [database on the Internet]. 2006. Syracuse (NY): Syracuse Research Corporation. [cited 2007 Feb]. TSCATS Database.

Union Carbide Co. 1993. TSCATS: Miscellaneous toxicity studies with cover letter dated 090393. U.S. EPA/OPTS Public Files. Fiche #: OTS0538262. Doc#: 86-930000438. [cited in RTECS 2006]. Submitted to U.S. EPA, Office of Toxic Substances.

[US EPA] United States Environmental Protection Agency. 1994.  Environmental Protection Agency. 1994a. Federal Register Environmental Documents - Air Quality: Revision to Definition of Volatile Organic Compounds - Exclusion of Volatile Methyl Siloxanes and Parachlorobenzotrifluoride [cited 2008 Feb].

[US EPA] United States Environmental Protection Agency. 2007. High Production Volume (HPV) - Sponsored Chemicals. Sponsored Chemicals, September 2007. [cited 2008 Feb].

Utell MJ, Gelein R, Yu CP, Kenaga C, Geigel E, Torres A, Chalupa D, Gibb FR, Speers DM, Mast RW, Morrow PE. 1998. Quantitative exposure of humans to an octamethycyclotetrasiloxane (D4) vapour. Toxicol Sci 44: 206-213.

Varaprath S, Frye CL, Hamelink J. 1996. Aqueous solubility of permethylsiloxanes (silicones), Short Communication. Environmental Toxicology and Chemistry. 15(8):1263-1265.

Vergnes JS, Jung R, Thakur AK, Barfknecht TR, Reynolds VL. 2000. Genetic toxicity evaluation of octamethylcyclotetrasiloxane. Environ Mol Mutagen 36(1):13-21.

Wallace LA, Pellizzari E, Hartwell T, Rosenzweig M, Erickson M, Sparacino C, Zelon H. 1984. Personal exposure to volatile organic compounds. I. Direct measurements in breathing-zone air, drinking water, food, and exhaled breath. Environmental Research 35: 293-319.

Wania F. 2003. Assessing the potential of persistent organic chemicals for long-range transport and accumulation in polar regions. Environ Sci Technol. 37(7): 1344-1351.

Wania F. 2006. Potential of degradable organic chemicals for absolute and relative enrichment in the Arctic. Environ Sci Technol. 40(2): 569-577.

Will R, Löchner U, Masahiro Y. 2007. CEH Marketing Research Report Siloxanes. Menlo Park (CA). SRI Consulting.

[WSKOWWIN] Water Solubility for Organic Compounds Program for Microsoft Windows [Estimation Model]. 2000. Version 1.41 Washington (DC): U.S. Environmental Protection Agency, Office of Pollution Prevention and Toxics; Syracuse (NY): Syracuse Research Corporation. Exposure Assessment Tools and Models.

Xu S. 1999. Fate of cyclic methylsiloxanes in soils. 1. The degradation pathway. Environmental Science and Technology 33(4): 603-608.

Xu S. 2006. 1-Octanol/air partitioning coefficients of octamethylcyclotetrasiloxane (D4), decamethylcyclopentasiloxane (D5), and dodecamethylcyclohexasiloxane (D6) at different temperatures. Centre Européen des Silicones (CES). CES Report December 27, 2006.

Xu S, Chandra G. 1999. Fate of cyclic methylsiloxanes in soils 2. Rates of degradation and volatilization. Environmental Science and Technology 33(22):4034-4039.

Xu S, Kropscott G. 2007. Simultaneous determination of partition coefficients for octamethylcyclotetrasiloxane and decamethylcyclopentasiloxane.  Draft Report. Dow Corning non-regulated technical report. DCC study # 10336-101.

Xu S, Lehmann RG, Miller JR, Chandra G. 1998. Degradation of polydimethylsiloxanes (silicones) as influenced by clay minerals Environ Sci Technol 32: 1199-1206.

Xu S, Miller JA. 2008. Aerobic transformation of octamethylcyclotetrasiloxane (D4) in water/sediment system. Centre Européen des Silicones (CES). Interim report.

Zareba G, Gelein R, Morrow PE, Utell MJ. 2002. Percutaneous absorption studies of octamethylcyclotetrasiloxane using the human skin /nude mouse model. Skin Pharmacol Appl Skin Physiol 15: 184-194.

Zhang J, Falany JL, Xie X, Falany CN. 2000. Induction of rat hepatic drug metabolizing enzymes by dimethylcyclosiloxanes. Chem Biol Interact 124(2):133-47.

Appendix

Appendix of the Screening Assessment

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