Registration Dossier
Registration Dossier
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 233-732-6 | CAS number: 10339-55-6
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- Not specified
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: pre-GLP study
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 967
- Report date:
- 1967
Materials and methods
Test guideline
- Qualifier:
- no guideline available
- Principles of method if other than guideline:
- No remarks
- GLP compliance:
- no
- Remarks:
- pre-GLP
- Test type:
- other: not specified
- Limit test:
- no
Test material
- Reference substance name:
- 3,7-dimethylnona-1,6-dien-3-ol
- EC Number:
- 233-732-6
- EC Name:
- 3,7-dimethylnona-1,6-dien-3-ol
- Cas Number:
- 10339-55-6
- Molecular formula:
- C11H20O
- IUPAC Name:
- 3,7-dimethylnona-1,6-dien-3-ol
- Details on test material:
- Ethyllinalool, no further information
Constituent 1
Test animals
- Species:
- mouse
- Strain:
- other: CFW
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- Weight: 17-22 g
Administration / exposure
- Route of administration:
- oral: unspecified
- Vehicle:
- unchanged (no vehicle)
- Details on oral exposure:
- 72 hours observation for mortality
- Doses:
- Not indicated
- No. of animals per sex per dose:
- 5
- Control animals:
- not specified
- Details on study design:
- No remarks
- Statistics:
- Not indicated
Results and discussion
- Preliminary study:
- Not indicated
Effect levels
- Key result
- Sex:
- male
- Dose descriptor:
- LD50
- Effect level:
- 5 283 mg/kg bw
- Mortality:
- The oral LD50 in mice was determined to be 5283 +/- 383 mg/kg bw.
LD50's were calculated by the method of Miller and Tainter (Proc. Soc. Exptl. Biol. Med. 57:261, 1944). - Clinical signs:
- other: Not indicated
- Gross pathology:
- Not indicated
- Other findings:
- Not indicated
Any other information on results incl. tables
Not relevant
Applicant's summary and conclusion
- Interpretation of results:
- not classified
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- The substance does not have to be classified according to the classification criteria outlined in 67/548/EEC and 1272/2008/EC.
- Executive summary:
The oral LD50 in mice was determined to be 5283 +/- 383 mg/kg bw.
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.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.
