Registration Dossier
Registration Dossier
Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.
The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.
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EC number: 700-336-4 | CAS number: 1141-23-7
Acute Toxicity: oral
Administrative data
- Endpoint:
- acute toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- not stated
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: MSDS, original study not available
Data source
Reference
- Reference Type:
- secondary source
- Title:
- Unnamed
Materials and methods
- Principles of method if other than guideline:
- no data available
- GLP compliance:
- not specified
- Test type:
- other: no data
Test material
- Reference substance name:
- (3R)-4-carbamoyl-3-(4-chlorophenyl)butanoic acid; (3S)-4-carbamoyl-3-(4-chlorophenyl)butanoic acid
- EC Number:
- 700-336-4
- Cas Number:
- 1141-23-7
- Molecular formula:
- C11H12ClNO3
- IUPAC Name:
- (3R)-4-carbamoyl-3-(4-chlorophenyl)butanoic acid; (3S)-4-carbamoyl-3-(4-chlorophenyl)butanoic acid
- Reference substance name:
- 5-amino-3-(4-chlorophenyl)-5-oxopentanoic acid
- IUPAC Name:
- 5-amino-3-(4-chlorophenyl)-5-oxopentanoic acid
- Details on test material:
- no data available
Constituent 1
Constituent 2
Test animals
- Species:
- rat
- Strain:
- not specified
- Sex:
- not specified
Administration / exposure
- Route of administration:
- other: oral
- Vehicle:
- not specified
- Details on oral exposure:
- no data available
- Doses:
- no data available
- Control animals:
- not specified
- Details on study design:
- no data available
- Statistics:
- no data available
Results and discussion
Effect levels
- Sex:
- not specified
- Dose descriptor:
- LD50
- Effect level:
- 800 mg/kg bw
Applicant's summary and conclusion
- Interpretation of results:
- harmful
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Executive summary:
Oral rat LD50=800 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.
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.
