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Diss Factsheets
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EC number: 203-700-6 | CAS number: 109-74-0
- 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 irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study was conducted pre-GLP and pre-guidelines, so the report is lacking in detail. However, it was conducted at a highly reputable laboratory and was done to the state of the art at that time.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 960
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- This study was conducted as part of the 1960 acute dermal toxicity test presented in section 7.2.3. Since the exposure period (24 hours) and the covering (occlusive) used in the dermal toxicity test was more stringent than that used in a traditional OECD 404 (4 hour exposure and semi-occlusive covering), this data can be considered to be a worst-case finding.
- GLP compliance:
- no
Test material
- Reference substance name:
- Butyronitrile
- EC Number:
- 203-700-6
- EC Name:
- Butyronitrile
- Cas Number:
- 109-74-0
- Molecular formula:
- C4H7N
- IUPAC Name:
- butanenitrile
Constituent 1
Test animals
- Species:
- guinea pig
- Strain:
- not specified
- Details on test animals or test system and environmental conditions:
- None provided
Test system
- Type of coverage:
- occlusive
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Amount / concentration applied:
- The dose used was 0.1 - 20 cc/kg
- Duration of treatment / exposure:
- 24 hours
- Observation period:
- 14 days
- Number of animals:
- 7 total
- Details on study design:
- Skin irritation was evaluated as part of an acute dermal toxicity test.
Results and discussion
In vivo
Results
- Irritation parameter:
- other:
- Time point:
- other: 24 hours
- Score:
- > 0 - < 0
- Remarks on result:
- other: findings were not scored, but TCC requires a score value, so "0" was used
- Irritant / corrosive response data:
- The test article was called out as a slight skin irritant that is absorbed through the skin.
Applicant's summary and conclusion
- Interpretation of results:
- slightly irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: expert judgment
- Conclusions:
- The test article was called out as a slight skin irritant that is absorbed through the skin.
- Executive summary:
Skin irritation testing was done as part of a previously cited acute dermal toxicity test. As such, the test subjects were exposed to the test article for 24 hours under occlusive conditions rather than the traditional 4 hours under semi-occlusive conditions. That makes these results a "worst case". The test article was called out as a slight skin irritant that is absorbed through the skin. Note that only qualitative scoring was done. Values in this summary were added as the only apparent way to pass the TCC tool, but no numerical scoring was used in the study.
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