Registration Dossier
Registration Dossier
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EC number: 269-246-6 | CAS number: 68201-95-6
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- documentation insufficient for assessment
- Remarks:
- Summary; test procedures are not documented and described, therefore information available do not permit an evaluation.
Data source
Reference
- Reference Type:
- other company data
- Title:
- Unnamed
- Year:
- 1 976
- Report date:
- 1976
Materials and methods
- Principles of method if other than guideline:
- No data available.
- GLP compliance:
- no
- Remarks:
- pre GLP
Test material
- Reference substance name:
- Direct Red 253
- IUPAC Name:
- Direct Red 253
Constituent 1
Test animals
- Species:
- rat
Administration / exposure
- Route of administration:
- oral: unspecified
Results and discussion
Effect levels
- Sex:
- not specified
- Dose descriptor:
- LD50
- Effect level:
- > 5 000 mg/kg bw
- Based on:
- not specified
Applicant's summary and conclusion
- Interpretation of results:
- not classified
- Remarks:
- according to CLP Regulation (Ec 1272/2008)
- Conclusions:
- LD50 > 5000 mg/kg
- Executive summary:
Only a summary is available, thus details on testing procedures and results are missing. The rat oral LD50 value has been stated higher than 5000 mg/kg.
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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