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EC number: 240-816-6 | CAS number: 16753-62-1
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data

Endpoint summary
Administrative data
Description of key information
Key value for chemical safety assessment
Skin sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
No skin senstisation data are available for the registered substance. Reliable data from related alkoxysilanes are therefore read across as weight of evidence.
A Guinea Pig Maximisation study that was conducted using the Magnusson and Kligmann (1970) protocol (Hill Top Biolab Inc., 1988) concluded triethoxy(vinyl)silane to be mildly sensitising. However, in OECD Test Guideline 406 a positive response rate of 30% must be met for a substance to be concluded to be a mild/moderate sensitiser. In this test the positive response rate was 20%, and therefore according to current criteria was considered negative. In addition the control animal mean scores were not significantly different to those of the test substance.
The guinea pig maximisation study for trimethoxy(vinyl)silane study for skin sensitisation found the test material not sensitising (WIL 2000). The reported sensitization incidence index for the test group was 0% (0/20) following challenge.
READ-ACROSS JUSTIFICATION
To reduce animal testing REACH recommends to make use of a read-across approach where appropriate based on the high accordance in properties relevant for the specific endpoint. In the case of sensitisation the relevant properties are structural similarity as well as physical-chemical properties in the same range. In the following paragraphs the proposed read-across from trimethoxy(vinyl)silane and triethoxy(vinyl)silane to dimethoxy(methyl)vinylsilane is evaluated point by point.
A report considering read across for all endpoints is attached in Section 13.
Read-across hypothesis
The hypothesis is that source and target substances have similar toxicological properties because they are structurally similar and hydrolyse to similar silicon-containing hydrolysis products. The non-silanol hydrolysis products, methanol and ethanol, do not contribute to any adverse effects for sensitisation at the relevant concentrations based on publicly available information (OECD SIDS, 2004). This is discussed further below.
Read-across justification
The predicted hydrolysis half-lives of the registered substance, dimethoxy(methyl)vinylsilane, are 18.3 minutes at pH 7, <2 minutes at pH 2, and 0.7 minutes at pH 9, all at 25oC. The products of hydrolysis are methylvinylsilanediol and methanol.
The read-across substance triethoxy(vinyl)silane has predicted hydrolysis half-lives at 20-25°C of 0.1 hours at pH 4, 0.2 hours at pH 5 and 0.02 hours at pH 9. As the hydrolysis reaction may be acid or base catalysed, the rate of reaction is expected to be slowest at pH 7 and increase as the pH is raised or lowered. The hydrolysis products are vinylsilanetriol and ethanol.
The read-across substance trimethoxy(vinyl)silane has predicted hydrolysis half-lives at 25°C of 0.1 hours at pH 7, 0.04 hours at pH 4, and 0.004 hours at pH 9. The hydrolysis products are vinylsilanetriol and methanol.
Therefore, the predicted half-lives for the registration and read-across substances at physiological pH are generally comparable so during dermal exposure similar levels of parent and hydrolysis products will be present and so read-across from triethoxy(vinyl)silane and trimethoxy(vinyl)silane to dimethoxy(methyl)vinylsilane for sensitisation is valid.
Analogue approach justification
(a) Structural similarity
The registration and read-across substances are structurally similar and are members of an analogue group of methylvinyl silane substances. All contain a silicon atom to which is attached to a vinyl group which is identical for all three. The registered substance has two alkoxy groups bound to silicon, the read-across substances have three. For the registered substance the two alkoxy groups are methoxy, the read-across substance trimethoxy(vinyl)silane has three such groups, while for the other read-across substance triethoxy(vinyl)silane, the three alkoxy groups are ethoxy. All hydrolyse rapidly to produce the similar silicon-containing hydrolysis products, methylvinylsilanediol or vinylsilanetriol and methanol or ethanol.
(b) Similar physicochemical characteristics
The key physicochemical parameters are summarised below.
Table: Key physicochemical parameters
Target (registration substance)
Source (read-across substance
Source (read-across substance
CAS number
016753-62-1
000078-08-0
002768-02-7
EC number
240-816-6
201-081-7
220-449-8
Chemical Name
dimethoxy(methyl)vinylsilane
triethoxy(vinyl)silane
trimethoxy(vinyl)silane
Molecular weight
(gmol-1)132.23
190.31
148.23
log Kow(parent)
2.3
3
Not applicable
log Kow(silicon-containing hydrolysis product)
-0.1
-2.0
-2.0
Water solubility (parent)
3000 mg/L
930 mg/L
3E+04 mg/L
Water solubility (silicon-containing hydrolysis product)
5E+05 mg/L
1E+06 mg/L
1E+06 mg/L
Vapour pressure (parent)
3000 Pa
304 Pa
1190 Pa
Vapour pressure (silicon-containing hydrolysis product)
2.1 Pa
0.02 Pa
0.02 Pa
(c) Discussion of irritation properties of the non-silanol hydrolysis products
The non-silanol hydrolysis products, methanol and ethanol, do not contribute to any sensitisation effects at the relevant concentrations based on publicly available information.
Methanol and ethanol are not classified for sensitisation in Annex VI of Regulation (EC) No 1272/2008
OECD (2004): SIDS Initial Assessment Report for SIAM 19, Berlin, Germany, 18-20 October 2004, Methanol, CAS 67-56-1.
OECD (2004): SIDS Initial Assessment Report for SIAM 19, Berlin, Germany, 19-22 October 2004, Ethanol, CAS 64-17-5.
Migrated from Short description of key information:
The guinea pig maximisation tests for skin sensitisation conducted with trimethoxy(vinyl)silane and triethoxy(vinyl)silane found them to be non-sensitising.
Justification for selection of skin sensitisation endpoint:
The studies were conducted according to, or to a design comparable with, an appropriate guideline, and in compliance with GLP.
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Justification for classification or non-classification
Based on the available read-across data from trimethoxy(vinyl)silane and triethoxy(vinyl)silane, dimethoxy(methyl)vinylsilane does not require classification for sensitisation according to Regulation (EC) 1272/2008.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.

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