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EC number: 242-056-0 | CAS number: 18171-19-2
- 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
There are no skin sensitisation data for 3-chloropropyl(dimethoxy)methylsilane (CAS 18171-19-2; EC No. 242-056-0). Therefore, data have been read across from the structurally related 3-chloropropyl(diethoxy)methylsilane (CAS 13501-76-3; EC No. 236-828-6). In a skin sensitisation study (Buehler test), conducted to OECD Test Guideline 406 and in compliance with GLP (Hüls AG, 1997e, Reliability Score 1), 3-chloropropyl(diethoxy)methylsilane was not sensitising to the skin of guinea pigs. No local or systemic effects were observed in this study.
A skin sensitisation study conducted according to OECD Test Guideline 429 will be conducted and added to the dossier when available.
Key value for chemical safety assessment
Skin sensitisation
Link to relevant study records
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 23.09.1996 to 12.12.1996
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of study:
- Buehler test
- Justification for non-LLNA method:
- An LLNA study was not performed because there is an existing reliable study for skin sensitisation using the Buehler test method. Furthermore, the LLNA test method is not considered to be suitable for substances that contain silicon. Please refer to the attached document for further details.
- Species:
- guinea pig
- Strain:
- Dunkin-Hartley
- Sex:
- female
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: Harlan Winkelmann GmbH
- Age at study initiation: 'adult'
- Weight at study initiation: 500 g
- Housing: Maximum of 5 animals in Makrolon Type IV cages
- Diet: Ad libitum
- Water: Ad libitum
- Acclimation period: At least five days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22 ±3
- Humidity (%): 30-70
- Air changes (per hr): 15
- Photoperiod (hrs dark / hrs light): 12/12
IN-LIFE DATES: From: 23.09.1996 to 12.12.1996 - Route:
- epicutaneous, occlusive
- Vehicle:
- other: maize oil / in pre-test only
- Concentration / amount:
- 100%
- No.:
- #1
- Route:
- epicutaneous, occlusive
- Vehicle:
- other: maize oil / in pre-test only
- Concentration / amount:
- 100%
- No. of animals per dose:
- Pretest: 3
Main test: 20
Main control: 10 - Details on study design:
- RANGE FINDING TESTS: The undiluted test substance was determined to be the highest non-irritating concentration. Therefore the test substance was applied undiluted in the induction and challenge phases.
MAIN STUDY
A. INDUCTION EXPOSURE
- No. of exposures: three
- Exposure period: six hours
- Site: Flank regions (left)
- Frequency of applications: Day 0, day 7 and day 14
- Concentrations: 100 %
B. CHALLENGE EXPOSURE
- No. of exposures: one
- Day(s) of challenge: day 28
- Exposure period: six hours
- Site: right flank
- Concentrations: 100 %
- Evaluation (hr after challenge): 24 and 48 hours after patch removal. - Challenge controls:
- Test substance applied to animals exposed to vehicle only in induction phases.
- Positive control substance(s):
- yes
- Remarks:
- Results with a standard allergen are presented, but the identity of the allergen does not appear to have been included.
- Positive control results:
- Positive results were presented for a standard allergen, the identity of which was not included in the report.
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 100 %
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Clinical observations:
- No clinical observations or effects on body weight gain.
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 0 %
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Clinical observations:
- None
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 100 %
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Clinical observations:
- None
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- 0 %
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Clinical observations:
- None
- Remarks on result:
- no indication of skin sensitisation
- Group:
- positive control
- Remarks on result:
- other: Positive results were presented for a standard allergen, the identity of which was not included in the report.
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- In a skin sensitisation study (Buehler test) conducted according to OECD 406 and in compliance with GLP (reliability score 1), (3-chloropropyl)diethoxymethylsilane was not sensitising to the skin of guinea pigs. No local or systemic effects were observed in this study.
Reference
No irritation was observed in any of the animals during the three induction phases or the challenge phase.
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
There are no skin sensitisation data for 3-chloropropyl(dimethoxy)methylsilane. Therefore, data have been read across from the structurally related 3-chloropropyl(diethoxy)methylsilane. The key study was conducted according to OECD Test Guideline 406 and in compliance with GLP and was the only skin sensitisation study available for the source substance. The test substance was not sensitising to guinea pig skin (Huls AG, 1997b).
At induction, 100% of the test substance in maize oil vehicle was applied to the left flank region of the animals (day 0). This application process was repeated in total three times (day 7 and 14). The undiluted test substance was applied epicutaneously to the same area for 6 h.
At challenge, on day 28 (two weeks after the last topical induction application), 100 % of the test substance in maize oil as the vehicle, was applied to the right flank region for 6 h. Evaluation of sensitisation occurred 24 and 48 h after patch removal. No local or systemic effects were observed and no irritation was observed in any of the animals during the three induction phases or the challenge phase.
Skin sensitisation data are provided for the analogue substances (3-chloropropyl)trimethoxysilane (CAS 2530-87-2, Hüls, 1993e) and (3-chloropropyl)triethoxysilane (CAS 5089-70-3, Dow Corning Corporation, 1995) have been included in support of the analogue group approach taken for this substance.
See Section 13 of IUCLID for the read-across justification reports.
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
Justification for classification or non-classification
Based on read across data from 3-chloropropyl(diethoxy)methylsilane, 3-chloropropyl(dimethoxy)methylsilane is not classified as a skin sensitiser according to Regulation (EC) No 1272/2008.
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