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EC number: 236-828-6 | CAS number: 13501-76-3
- 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
Skin irritation (OCED TG 404): irritating
Eye irritation (OECD TG 405): not irritating
Key value for chemical safety assessment
Skin irritation / corrosion
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (irritating)
Eye irritation
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not irritating)
Respiratory irritation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Studies were chosen as key when the available study was of relevance and of sufficient quality for classification, labelling and for risk assessment.
A key skin irritation study which was conducted according to OECD TG 404 and GLP, showed that (3-chloropropyl)diethoxymethylsilane was irritating to the skin of small white Russian rabbits. 30-60 minutes after removal of the dressing’s two rabbits had grade 2 erythema and edema, and one had grade 1 erythema and edema. After 24 and 48 hours the irritation had worsened so that the erythma was grade 2 and 3 and the edema was grade 2 and 4. The irritation then gradually reversed until there were no signs of erythema and edema on day 10. Yellow skin discolouration in animal 1 after 24 and 48 hours was observed. Dry or flaky skin in all animals after about a week was also observed. It was therefore concluded that (3-chloropropyl)diethoxymethylsilane was irritating to rabbit skin (Hüls AG, 1997c).
A key eye irritation study which was conducted to OECD TG 405 and GLP, showed that (3-chloropropyl)diethoxymethylsilane was only very slightly irritating to the eyes of small white Russian rabbits and therefore was not classified as an eye irritant. Within one hour of instillation there was some redness and edema of the conjunctiva. By 24 and 48 hours after instillation there was some redness, but no edema. At 72 hours there were no signs of irritation remaining. It was therefore concluded that (3-chloropropyl)diethoxymethylsilane was not an eye irritant (Hüls AG, 1997d).
Justification for selection of skin irritation / corrosion endpoint:
The key study was selected for assessment.
Justification for selection of eye irritation endpoint:
The key study was selected for assessment.
Effects on skin irritation/corrosion: irritating
Justification for classification or non-classification
Based on the available study for skin irritation, (3-chloropropyl)diethoxymethylsilane needs to be classified as R38 ‘’irritating to skin’’ according to the criteria of EU Directive 67/548/EEC, and Skin Irritant Category 2 under Regulation 1272/2008.
The available data on eye irritation of the registered substance do not meet the criteria for classification according to Regulation (EC) 1272/2008 or Directive 67/548/EEC, and are therefore conclusive but not sufficient for classification.
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