Registration Dossier
Registration Dossier
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EC number: 256-851-5 | CAS number: 50925-42-3
Endpoint summary
Administrative data
Link to relevant study record(s)
- Endpoint:
- basic toxicokinetics, other
- Remarks:
- Toxicokinetic assumption
- Type of information:
- other: Toxicokinetic assumption
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Toxicokinetic assumption
- Objective of study:
- other: Toxicokinetic assumption
- Principles of method if other than guideline:
- Toxicokinetic assumption
- GLP compliance:
- no
Reference
Description of key information
The data from the acute oral and repeated dose toxicity studies indicate no or a low absorption by the oral route based on the acute oral discriminating dose for male and female rats of 2000 mg/kg body weight and the NOAEL of 1000 mg/kg bw in the Combined Repeated Dose Toxicity Study with the Reproduction / Developmental Toxicity Screening Test.
Key value for chemical safety assessment
- Bioaccumulation potential:
- low bioaccumulation potential
Additional information
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.
