Registration Dossier
Registration Dossier
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EC number: 202-711-3 | CAS number: 98-89-5
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2012
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- A reliable secondary source was used. However the primary sources were not revisited in order to verify their contents; for this reason reliability score 2 was used. The used secondary source has been updated on 2012; therefore it covers the most updated literature on the substance.
Data source
Referenceopen allclose all
- Reference Type:
- secondary source
- Title:
- Cyclohexanecarboxylic acid
- Year:
- 2 013
- Bibliographic source:
- CHEMIDplus
- Reference Type:
- secondary source
- Title:
- Cyclohexanecarboxylic acid
- Year:
- 2 013
- Bibliographic source:
- RTECS
- Reference Type:
- publication
- Title:
- No information
- Year:
- 1 980
- Bibliographic source:
- Drug and Chemical Toxicology. Vol. 3, Pg. 249, 1980.
Materials and methods
Test guideline
- Qualifier:
- no guideline available
- Principles of method if other than guideline:
- No data
- GLP compliance:
- no
- Test type:
- other: no data
Test material
- Reference substance name:
- Cyclohexanecarboxylic acid
- EC Number:
- 202-711-3
- EC Name:
- Cyclohexanecarboxylic acid
- Cas Number:
- 98-89-5
- Molecular formula:
- C7H12O2
- IUPAC Name:
- cyclohexanecarboxylic acid
- Test material form:
- other: liquid
Constituent 1
Test animals
- Species:
- rat
- Strain:
- not specified
- Sex:
- not specified
Administration / exposure
- Route of administration:
- oral: unspecified
- Vehicle:
- not specified
- Control animals:
- not specified
Results and discussion
Effect levels
- Sex:
- not specified
- Dose descriptor:
- LD50
- Effect level:
- 3 265 mg/kg bw
- Based on:
- test mat.
Applicant's summary and conclusion
- Interpretation of results:
- not classified
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- According to Directive 67/548/EEC and to Regulation (EC) n. 1272/2008, the substance should not be classified for oral acute toxicity.
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