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EC number: 202-640-8 | CAS number: 98-13-5
- 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
Key value for chemical safety assessment
Additional information
Information is available from reliable studies for all the required in vitro endpoints. The results for cytogenicity (in vitro and in vivo) come from two closely related substances. The in vitro cytogenicity study gave a positive result, the results of all other tests were negative.
Short description of key information:
In vitro:
Gene mutation (Bacterial reverse mutation assay / Ames test): negative with and without activation in all strains tested (similar to OECD TG 471)
Cytogenicity in mammalian cells: read-across from analogous substance trimethoxyphenylsilane CAS 2996-92-1: positive in Chinese hamster lung fibroblasts (V79) cells with activation, negative without activation (OECD TG 473)
Mutagenicity in mammalian cells: negative in L5178Y mouse lymphoma cells (OECD TG 476)
In vivo:
Micronucleus assay inhalation study in rat:: read-across from analogous substance dimethoxymethylphenylsilane CAS 3027-21-2: Negative (micronucleus data from OECD TG 413)
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
The available information for the substance indicates that, when tested, trichloro(phenyl)silane (CAS number 98 -13 -5) did not induce mutations in bacterial or mammalian cells. There is evidence that the substance would be clastogenic in vitro, as the related substance trimethoxyphenylsilane CAS 2996-92-1 induced chromosome aberrations in mammalian cells in the presence of activation. This result is not supported by evidence from another closely related substance, dimethoxymethylphenylsilane CAS 3027-21-2, which has been tested in a 14 day inhalation study in mice, with no increase in the incidence of micronuclei in bone marrow. It is concluded that classification for mutagenicity is not required.
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