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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: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- 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 followed
- Principles of method if other than guideline:
- The experiments were performed on white mice and albino rats, some being healthy adult and young animals and some weakened by avitaminosis and insufficient feeding. The animals were kept in chambers that were exposed to vapours of the substance whose concentration was predetermined by a method developed by a worker at the Dushutin Institute.
- GLP compliance:
- not specified
- Test type:
- traditional method
- 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:
- inhalation: vapour
- Type of inhalation exposure:
- whole body
- Vehicle:
- air
- Details on study design:
- The experiments were performed on white mice and albino rats, some being healthy adult and young animals and some weakened by avitaminosis and insufficient feeding. The concentration of the substance in the chamber was determined by amethod developed by a worker at the Dushutin Institute which is based on the color resulting from the reaction of VCH with concentrated sulfuric acid.
Results and discussion
Effect levelsopen allclose all
- Sex:
- male/female
- Dose descriptor:
- LC50
- Effect level:
- 13.7 mg/L air
- Based on:
- test mat.
- Remarks on result:
- other: healthy mice
- Sex:
- male/female
- Dose descriptor:
- LC50
- Effect level:
- 20.5 mg/L air
- Based on:
- test mat.
- Remarks on result:
- other: healthy rats
- Mortality:
- Mortality occurred and some animals died during the spasmodic attacks.
- Clinical signs:
- other: - The animals exposed to high concentrations of these vapours immediately showed signs of excitation, increased breathing and staggering gait. They fell, rose again, were suddenly seized by tonic spasms of extreme intensity, fell on their sides and develo
- Body weight:
- Not specified
- Gross pathology:
- Not specified
- Other findings:
- - The substance possessed a narrow toxic range and was more highly toxic for the young and weakened animals
- There were no significant differences in the sensitivity of males and females
- the absolute lethal concentration was 15 mg/L and partially lethal concentration was 12.5 mg/L in healthy mice
- In case of weakened mice the LC50 was 10.6 mg/L
- The LC50 for young rats (60 - 80 g bw) was 17 mg/L
- Animals that had survived the acute poisoning (exposed to LD50) were again exposed to the test item vapour concentration of 15 mg/L for 2 hours the following day. Not a single experimental animal died and none even fell on its side
Applicant's summary and conclusion
- Interpretation of results:
- study cannot be used for classification
- Conclusions:
- Based on the results the LC50 for rats was estabilshed to be 20.5 mg/mL and 13.7 mg/L for mice.
- Executive summary:
Based on the results, the LC50 for rats was estabilshed to be 20.5 mg/mL and 13.7 mg/L for mice.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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