Registration Dossier
Registration Dossier
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EC number: 675-511-0 | CAS number: 130336-16-2
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- other information
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Only short abstract available
Data source
Materials and methods
- Principles of method if other than guideline:
- not stated
- GLP compliance:
- not specified
- Test type:
- other: not stated
Test animals
- Species:
- mouse
- Strain:
- other: Crlj:CD1(ICR)
- Sex:
- male
Administration / exposure
- Vehicle:
- water
- Remarks:
- deionizied water
- Doses:
- 50 mg/kg bw
300 mg/kg bw - No. of animals per sex per dose:
- five animals per dose level
- Control animals:
- yes
Results and discussion
Effect levels
- Sex:
- male
- Dose descriptor:
- LD50
- Effect level:
- > 300 mg/kg bw
- Based on:
- other: ordinary substance
- Mortality:
- No animal died in any group.
- Clinical signs:
- other: General clinical Prone position was observed in each three animals of the 300 mg/kg at 60 minutes after administration, this symptom disappeared after that.
- Gross pathology:
- No macroscopic abnormalities were observed.
Applicant's summary and conclusion
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.
