Registration Dossier
Registration Dossier
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EC number: 221-602-1 | CAS number: 3158-91-6
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 2006
- Reliability:
- 2 (reliable with restrictions)
Data source
Materials and methods
- Principles of method if other than guideline:
- OECD-423
- GLP compliance:
- no
- Test type:
- acute toxic class method
Test animals
- Species:
- mouse
- Sex:
- male/female
- Details on test animals or test system and environmental conditions:
- Temperature: 22ºC (+3º)
Selective humidity: 30-70%
12 h of light and 12 h of darkness
Administration / exposure
- Route of administration:
- oral: feed
- Vehicle:
- unchanged (no vehicle)
- Doses:
- 2000 mg/1000 grs of animal weight
- No. of animals per sex per dose:
- 3 males
3 females - Control animals:
- no
Results and discussion
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- LD50 > 2000 mg/Kg (Non-toxic orally product)
The dose tested during the trial period (14 days) did not cause any death or any visual disturbance.
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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