Registration Dossier
Registration Dossier
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EC number: 213-192-8 | CAS number: 928-96-1
Acute Toxicity: dermal
Administrative data
- Endpoint:
- acute toxicity: dermal
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Secondary literature source.
Data source
Reference
- Reference Type:
- review article or handbook
- Title:
- 3-hexen-1-ol, (3Z)-; Exemption from the requirement of a tolerance
- Author:
- Anon
- Year:
- 2 005
- Bibliographic source:
- Federal Register. 70 (104): 31359-31365
- Report date:
- 2005
Materials and methods
Test guideline
- Qualifier:
- no guideline available
- GLP compliance:
- not specified
- Test type:
- other: No data
Test material
- Reference substance name:
- cis-hex-3-en-1-ol
- EC Number:
- 213-192-8
- EC Name:
- cis-hex-3-en-1-ol
- Cas Number:
- 928-96-1
- Molecular formula:
- C6H12O
- IUPAC Name:
- hex-3-en-1-ol
- Details on test material:
- - Name of test material (as cited in study report): cis-3-hexen-1-ol, leaf alcohol, 3-hexen-1-ol,(3Z)
- Physical state: liquid
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- not specified
- Sex:
- not specified
- Details on test animals or test system and environmental conditions:
- No data
Administration / exposure
- Type of coverage:
- not specified
- Vehicle:
- not specified
- Details on dermal exposure:
- No data
- Duration of exposure:
- No data
- Doses:
- No data
- No. of animals per sex per dose:
- No data
- Control animals:
- not specified
- Details on study design:
- No data
- Statistics:
- No data
Results and discussion
Effect levels
- Sex:
- not specified
- Dose descriptor:
- LD50
- Effect level:
- > 5 000 mg/kg bw
- Mortality:
- No data
- Clinical signs:
- other: No data
- Gross pathology:
- No data
- Other findings:
- No data
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- The test substance was assessed for acute toxicity via the dermal route and was found to have an LD50 of >5000 mg/kg. As such, the test substance is not considered to be acutely toxic by the dermal route.
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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