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Diss Factsheets
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EC number: 222-217-1 | CAS number: 3388-04-3
- 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
Acute Toxicity: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 1972
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: The study was conducted according to a scientifically acceptable protocol, however no analytical verification of exposure concentration was carried out.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 962
- Report date:
- 1962
Materials and methods
- GLP compliance:
- no
Test material
- Reference substance name:
- 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane
- EC Number:
- 222-217-1
- EC Name:
- 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane
- Cas Number:
- 3388-04-3
- Molecular formula:
- C11H22O4Si
- IUPAC Name:
- trimethoxy[2-(7-oxabicyclo[4.1.0]hept-3-yl)ethyl]silane
- Details on test material:
- - Physical state: clear liquid
Constituent 1
Test animals
- Species:
- rat
- Strain:
- not specified
- Sex:
- not specified
Administration / exposure
- Route of administration:
- inhalation: vapour
- Type of inhalation exposure:
- not specified
- Vehicle:
- not specified
- Details on inhalation exposure:
- Concentrated vapour was generated at a temperature of approximately 22C, by passing dried air at the rate of 2.5 litres per minute through a fritted glass disc immersed to a depth of at least one inch in 50 ml of test material. The exposure chamber was 9 litres.
- Analytical verification of test atmosphere concentrations:
- no
- Duration of exposure:
- 8 h
- Concentrations:
- 'concentrated vapour'
- No. of animals per sex per dose:
- six females
- Control animals:
- no
- Details on study design:
- - Duration of observation period following administration: 14 days
Results and discussion
Effect levels
- Sex:
- female
- Dose descriptor:
- LC50
- Exp. duration:
- 8 h
- Remarks on result:
- other: NO LC50 established. No analytical verification of exposure concentration conducted.
- Mortality:
- There were no mortalities.
- Clinical signs:
- other: The animals appeared to be normal upon removal from the chamber.
- Body weight:
- 5/6 animals gained weight normally during the 14 day observation period.
- Gross pathology:
- 60% lung consolidation was observed in the rat lost weight. The study authors attributed this pathology to a presumed pre-existing extraneous infection, which was considered not related to inhalation of the test material.
Any other information on results incl. tables
Exposure to concentrated vapours at room temperature for eight hours killed none of six animals. The substance is described as having 'slight hazard' via inhalation exposure.
Applicant's summary and conclusion
- Interpretation of results:
- other: data not sufficient for classification purposes
- Remarks:
- Criteria used for interpretation of results: not specified
- Conclusions:
- No deaths are reported in a summary report in response to an 8 hour exposure to concentrated vapours of the test material.
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