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Diss Factsheets
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EC number: 208-488-9 | CAS number: 530-62-1
- 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 vitro / ex vivo
- Type of information:
- other: data from hydrolysed substance
- Adequacy of study:
- key study
- Study period:
- 1979
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study without detailed documentation
- Justification for type of information:
- Substance 530-62-1 hydrolyses
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 979
- Report date:
- 1979
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- however occlusive exposure instead of semi-occulsive
- GLP compliance:
- no
Test material
- Reference substance name:
- Imidazole
- EC Number:
- 206-019-2
- EC Name:
- Imidazole
- Cas Number:
- 288-32-4
- Molecular formula:
- C3H4N2
- IUPAC Name:
- 1H-imidazole
Constituent 1
- Specific details on test material used for the study:
- 80%
In vitro test system
- Vehicle:
- not specified
Test animals
- Species:
- rabbit
- Strain:
- not specified
Test system
- Type of coverage:
- occlusive
- Preparation of test site:
- not specified
- Vehicle:
- water
- Controls:
- no
- Duration of treatment / exposure:
- 1-4h
- Observation period:
- 4h
- Number of animals:
- 2 animals
Results and discussion
In vivo
Results
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- 7 d
- Score:
- 2
- Reversibility:
- no data
Any other information on results incl. tables
Skin reactions after 1-hr exposure time:
Mild erythema was seen in all (4/4) animals 1 hr after removal of the occlusive dressing. Erythema subsided in one animal overnight. Focal necrosis developed in the other 3 animals within 24 and 48 hr. Findings at the end of the observation period (8 d) were as follows:
2/4 animals showed no erythema but showed desquamation (1/4) and focal necrosis (1/4). Slight erythema, desquamation and extended focal necrosis was seen in the 3rd animal, and severe erythema with superficial necrosis was noted in the 4th animal.
Oedema were absent after patch removal but grade 2 oedema were noted in 2/4 and 3/4 animals after 24 and 48 hr, respectively. Oedema had resolved on day 8 of observation.
Skin reactions after 4-hr exposure time:
Well defined, moderate erythema and oedema were seen in both animals after removal of the occlusive dressing. Erythema became severe overnight and rested severe until the end of the observation period. Soft necroses developed overnight in both animals. Leather-like necrosis indicative of full thickness necrosis was noted in both animals and confirmed by pathology after sacrifice of the animals. Oedema started to resolve overnight but rested as grade 2 until day 8.
General toxicity:
No signs noted after 1-hr or 4-hr exposure.
Applicant's summary and conclusion
- Interpretation of results:
- corrosive
- Conclusions:
- After 4-hr occlusive exposure moderate erythema and oedema were noted within 1 hr. Severe erythema developed overnight and persisted until day 8, the end of the observation period.
Soft necroses developed overnight. They hardened and changed into persistent leather-like necroses in both animals as noted on day 8. Slight oedema were noted at the end of the observation period.
No signs of general toxicity were noted.
Imidazole was corrosive. - Executive summary:
When 80 % Imidazole was applied to the intact rabbit skin as an aqueous paste for 1 or 4 hours under occlusive dressing skin reactions were noted as early as one hour after removal of the dressing. Focal necrosis developed overnight in all animals and was described as leather-like at the end of the observation period when pathology confirmed full thickness necrosis after sacrifice of the animals .
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