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EC number: 211-779-3 | CAS number: 695-12-5
- 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: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- July - September 1965
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- documentation insufficient for assessment
Data source
Reference
- Reference Type:
- publication
- Title:
- The toxicology of vinylcyclohexane
- Author:
- Savchenkov M.F.
- Year:
- 1 965
- Bibliographic source:
- Gigiena i Sanitariya 30 Vol. 7, 32-37
Materials and methods
Test guideline
- Qualifier:
- no guideline available
- Principles of method if other than guideline:
- The test item was fed to mice and rats in doses of up to 2000 mg/kg bw and 4000 mg/kg bw pure substance.
- GLP compliance:
- not specified
- Test type:
- other: Acute experiment
- Limit test:
- no
Test material
- Reference substance name:
- Vinylcyclohexane
- EC Number:
- 211-779-3
- EC Name:
- Vinylcyclohexane
- Cas Number:
- 695-12-5
- Molecular formula:
- C8H14
- IUPAC Name:
- ethenylcyclohexane
Constituent 1
Test animals
- Species:
- other: white mice and albino rats
- Strain:
- not specified
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- Not specified
Administration / exposure
- Route of administration:
- oral: feed
- Vehicle:
- other: refined sunflower oil
- Details on oral exposure:
- VEHICLE: Refined Sunflower oil
DOSAGE PREPARATION (if unusual): The test item was fed to mice and rats in doses of up to 2 g / kg and another dose of 4 g / kg, pure substance mixed with sunflower oil. The dose of 4 g / kg was administered with and without sunflower oil. - Doses:
- 2000 mg/kg bw and 4000 mg/kg bw
- Control animals:
- not specified
- Details on study design:
- - Necropsy of survivors performed: yes
Results and discussion
Effect levels
- Key result
- Sex:
- male/female
- Dose descriptor:
- LD50
- Effect level:
- > 2 000 mg/kg bw
- Based on:
- test mat.
- Mortality:
- A dose of 4000 mg/kg bw killed some of the animals when administered in a mixture with refined flower oil and killed all of then when administered alone. At 2000 mg/kg bw pure substance mixed with sunflower oil had a slight toxic effect, causing the animals to loose weight.
- Gross pathology:
- Organs of the dead animals showed degenerative changes in the liver and kidneys and signs of stimulation in the spleen.
- Other findings:
- - Organ weights: there was a considerable increase in the weight coefficients of the liver and spleen (p >0.01).
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- Based on the results of this study, the oral LD50 can be considered to be greater than 2000 mg/kg bw in rat and mouse.
- Executive summary:
In an acute oral toxicity study, a dose of 4000 mg/kg bw of the test item killed some of the animals when administered in a mixture with refined flower oil and killed all of them when administered alone. At 2000 mg/kg bw the pure substance mixed with sunflower oil had only a slight toxic effect, causing the animals to loose weight. Moreover, organs of the dead animals showed degenerative changes in the liver and kidneys and signs of stimulation in the spleen and a considerable increase in the weight coefficients of the liver and spleen (p> 0.01) was recorded. Based on the results, the oral LD50 in rats and mice can be considered to be greater than 2000 mg/kg bw.
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