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EC number: 203-629-0 | CAS number: 108-91-8
- 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: dermal
Administrative data
- Endpoint:
- acute toxicity: dermal
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: individual doses and animal data are not shown
Data source
Reference
- Reference Type:
- publication
- Title:
- Range-finding Toxicity data: List VII
- Author:
- Smyth jr HF, Carpenter ChP, Weil CS, Pozzani UC, Striegel JA, Nycum JS
- Year:
- 1 969
- Bibliographic source:
- Am. Ind. Hyg. Assoc. J. 30, 470-476
Materials and methods
- Principles of method if other than guideline:
- Different doses of test substance was applied to the shaved skin of male rabbits for 24 hours and observed for mortality for 14 days.
- GLP compliance:
- no
- Test type:
- standard acute method
Test material
- Reference substance name:
- Cyclohexylamine
- EC Number:
- 203-629-0
- EC Name:
- Cyclohexylamine
- Cas Number:
- 108-91-8
- Molecular formula:
- C6H13N
- IUPAC Name:
- cyclohexanamine
- Details on test material:
- no further data
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- initial bod weight : 2.5 to 3.5 kg
Administration / exposure
- Type of coverage:
- occlusive
- Vehicle:
- unchanged (no vehicle)
- Details on dermal exposure:
- Different doses of test substance were applied to the shaved skin of male rabbits for 24 hours. The testsubstance is retained beneath an impervious plasma film.
- Duration of exposure:
- 24 hours
- Doses:
- individual doses are not given
- No. of animals per sex per dose:
- 4
- Control animals:
- no
- Details on study design:
- Different doses of test substance were applied to the shaved skin of male rabbits for 24 hours. The testsubstance is retained beneath an impervious plasma film. The animals are immobilized during the24 hour period, after which the film is removed. the rabbits are caged for the subsequent 14 day observation period. Based upon mortality during a 14-day observation period the most probable LD50 value and its fiducial range are estimated by the method of Thompson using the tables of Weil
- Statistics:
- the most probable LD50 value and its fiducial range are estimated by the method of Thompson using the tables of Weil
Results and discussion
Effect levels
- Sex:
- male
- Dose descriptor:
- LD50
- Effect level:
- ca. 275 mg/kg bw
- 95% CL:
- >= 208 - <= 372
- Mortality:
- Based upon mortality during a 14-day observation period the most probable LD50 value and its fiducial range are estimated by the method of Thompson using the tables of Weil (no further data)
- Clinical signs:
- other: no data
- Gross pathology:
- no data
- Other findings:
- no data
Any other information on results incl. tables
Different doses of cyclohexylamine were applied to the shaved skin of male rabbits for 24 hours under occlusive conditions. the LD50 is 275 mg/kg bw (Smyth 1969)
Applicant's summary and conclusion
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