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EC number: 219-637-2 | CAS number: 2487-90-3
- 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
Skin sensitisation
Administrative data
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- No data
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 995
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- GLP compliance:
- yes
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- An LLNA study was not performed because there is an existing reliable study for skin sensitisation using the Guinea Pig Maximisation test method.
Test material
- Reference substance name:
- Trimethoxysilane
- EC Number:
- 219-637-2
- EC Name:
- Trimethoxysilane
- Cas Number:
- 2487-90-3
- Molecular formula:
- C3H10O3Si
- IUPAC Name:
- Trimethoxysilane
Constituent 1
In vivo test system
Test animals
- Species:
- guinea pig
- Strain:
- not specified
- Sex:
- male/female
- Details on test animals and environmental conditions:
- No data in IUCLID summary.
Study design: in vivo (non-LLNA)
Induction
- Route:
- intradermal
- Vehicle:
- cotton seed oil
- Concentration / amount:
- 1st application: Induction 0.1 ml intracutaneous of 5% test substance in cottonseed oil, 5% test substance in a 1:1 mixture of Freund's Complete Adjuvant (FCA): cottonseed oil and FCA
2nd application: Induction 25 % test substance in occlusive epicutaneous - Day(s)/duration:
- Day 0 for intradermal induction and Day 7 for topical induction/48 hours occluded dermal exposure
- Adequacy of induction:
- highest concentration used causing mild-to-moderate skin irritation and well-tolerated systemically
Challenge
- Route:
- epicutaneous, open
- Vehicle:
- cotton seed oil
- Concentration / amount:
- 3rd application: Challenge 2.5 % open epicutaneous
- Day(s)/duration:
- Day 21/24 hours of occlusion
- Adequacy of challenge:
- highest non-irritant concentration
- No. of animals per dose:
- 10/sex/group
- Details on study design:
- The concentration of test material used for challenge was selected based on the results of range-finding experiment in the Primary Irritation Phase.
A Test Group of ten male and ten female guinea pigs was dosed with multiple intradermal injections on study day 0 and topical application on study day 7 to attempt to induce a sensitized state for evaluation of delayed contact hypersensitivity.
1st application: Induction 0.1 ml intracutaneous
2nd application: Induction 25 % occlusive epicutaneous
3rd application: Challenge 2.5 % open epicutaneous
Intradermal induction consisted of injections of 5% trimethoxysilane in cottonseed oil, 5% trimethoxysilane in a 1:1 mixture of Freund's Complete Adjuvant (FCA): cottonseed oil and FCA. Topical induction consisted of a 48-hour occluded dermal exposure to 25% trimethoxysilane. Fourteen days after topical induction, challenge dosing for detection of sensitization was performed.
For challenge dosing, an essentially non-irritating concentration (2.5%) of the test material was applied topically under occlusion for 24 hours. Vehicle control sites were also dosed at challenge for detection of potential dermal reactions related to the vehicle. A positive control group of five male and five female guinea pigs was included to verify the reliability of the test system. The positive control group was induced and challenged on a similar regimen as the Test Group using dinitrochlorobenzene (DNCB) in 80% ethanol as the positive control material. Separate sites were dosed with 80% ethanol to detect any reactions related to the vehicle. Reactions to challenge exposures were evaluated at approximately 24 and 48 hours after dosing for all groups. Body weights were recorded prior to study initiation and at termination. - Challenge controls:
- A negative control group of five male and five female guinea pigs was dosed with the vehicle during induction and in the same manner as the Test Group at challenge and served as irritation controls.
- Positive control substance(s):
- yes
- Remarks:
- dinitrochlorobenzene (DNCB)
Results and discussion
- Positive control results:
- Based on the Sensitization Incidence Index of 100 %, the positive control material, DNCB, was found to be an extreme sensitizing agent in the albino guinea pig under the conditions of this study, thereby verifying the reliability of the test system. The positive control vehicle, 80% ethanol, was demonstrated to be non-sensitizing under the conditions of this study.
In vivo (non-LLNA)
Resultsopen allclose all
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 2.5% test substance
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Clinical observations:
- No clinical signs of toxicity
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- cotton seed oil
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Clinical observations:
- No clinical signs of toxicity
- Remarks on result:
- no indication of skin sensitisation
- Key result
- Reading:
- 1st reading
- Hours after challenge:
- 48
- Group:
- positive control
- Dose level:
- dinitrochlorobenzene
- No. with + reactions:
- 10
- Total no. in group:
- 10
- Remarks on result:
- positive indication of skin sensitisation
Any other information on results incl. tables
There were no deaths, clinical findings or remarkable body
weight changes.
There were no sensitization reactions in the test group
following challenge, and the Sensitization Incidence Index
was calculated to be 0%. Based on these results, the test
material, trimethoxysilane, was found to be a non-sensitizer
in albino guinea pigs under the conditions of this study. The negative
control and vehicle, cottonseed oil, was also found to
be non-sensitizing under the conditions of this study.
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- In a skin sensitisation study (reliability score 1) conducted according to OECD Test Guideline 406 and in compliance with GLP, trimethoxysilane was not sensitising to the skin of guinea-pigs.
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