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EC number: 201-072-8 | CAS number: 77-95-2
- 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:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study is not done according to OECD guideline.
Data source
Referenceopen allclose all
- Reference Type:
- publication
- Title:
- Acute oral toxicity of selected flavor chemicals.
- Author:
- Moran, E. J. and Easterday, O. D.
- Year:
- 1 980
- Bibliographic source:
- Drug Chem Toxicol. 3(3):249-58
- Reference Type:
- secondary source
- Title:
- ChemIDplus Advanced
- Author:
- U.S. National Library of Medicine
- Year:
- 2 013
- Bibliographic source:
- http://chem.sis.nlm.nih.gov/chemidplus/
- Report date:
- 2013
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- The acute oral lethal doses was for determined for cyclohexanecarboxylic acid in rats. Tests were performed at Food and Drug Research Laboratories, Inc., Waverly, New York or Gulf South Research Institute, New Iberia, Louisiana. Groups of ten animals, five males and five females, weighing 40 to 60 g (FDRL Strain, Waverly, New York) were fasted overnight prior to treatment. The test substance was administered by oral gavage as a solution or suspension in corn oil. The concentration of the test substance in corn oil was adjusted so that each group of animals in a particular study received the same volume of solution with respect to body weight. Animals had free access to water at all times and to feed (Purina Laboratory Chow) following dosing. Animals were closely observed for mortality and pharmacologic effects on the day of dosing and daily thereafter for a total of 14 observation days. Rats were weighed prior to dosing.
- GLP compliance:
- not specified
- Test type:
- other: no details available
- Limit test:
- no
Test material
- Reference substance name:
- Cyclohexanecarboxylic acid
- EC Number:
- 202-711-3
- EC Name:
- Cyclohexanecarboxylic acid
- Cas Number:
- 98-89-5
- IUPAC Name:
- cyclohexanecarboxylic acid
- Test material form:
- not specified
- Details on test material:
- - Name of test material (as cited in study report): Cyclohexanecarboxylic acid
Constituent 1
Test animals
- Species:
- rat
- Strain:
- other: FDRL Strain
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Waverly, New York
- Weight at study initiation: 40 to 60 g
- Fasting period before study: fasted overnight prior to treatment
- Diet (e.g. ad libitum): free access to feed (Purina Laboratory Chow)
- Water (e.g. ad libitum): free access to water at all times
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- corn oil
- Doses:
- The concentration of the test substance in corn oil was adjusted so that each group of animals in a particular study received the same volume of solution with respect to body weight.
- No. of animals per sex per dose:
- Groups of ten animals: five males and five females
- Control animals:
- not specified
- Details on study design:
- - Duration of observation period following administration: 14 observation days
- Frequency of observations and weighing: Animals were closely observed for mortality and pharmacologic effects on the day of dosing and daily thereafter for a total of 14 observation days. Rats were weighed prior to dosing.
Results and discussion
Effect levels
- Sex:
- male/female
- Dose descriptor:
- LD50
- Effect level:
- ca. 3 265 mg/kg bw
- Based on:
- test mat.
- 95% CL:
- >= 2 791 - <= 3 820
Applicant's summary and conclusion
- Interpretation of results:
- not classified
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- The LD50 of the read across substance cyclohexanecarboxylic acid for rats is 3265 mg/kg bw. It is considered as harmful according to EU criteria and does not need to be classified.
- Executive summary:
The acute toxicity of the read across substance cyclohexanecarboxylic acid was tested on rats after oral application and was published by Moran, 1980. From this study it is shown, that the LD50 of cyclohexanecarboxylic acid is 3265 mg/kg bw. This indicates that cyclohexanecarboxylic acid is not harmful according to EU criteria. We consider that quinic acid has a similar LD50 value, so that quinic acid does not need to be considered as harmful according to EU criteria, too
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