Registration Dossier
Registration Dossier
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EC number: 267-090-3 | CAS number: 67786-14-5
Endpoint summary
Administrative data
Description of key information
The test item has a LD50 >2000 mg/kg bw via oral exposure (gavage). The LD50 (oral) was determined in two OECD 401 studies with male and female rats. No other adverse effects were observed.
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
Acute toxicity: via inhalation route
Endpoint conclusion
- Endpoint conclusion:
- no study available
Acute toxicity: via dermal route
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Justification for classification or non-classification
Based on the LD50 (oral) in rats >2000 mg/kg bw, the substance is not classifiable according to the CLP Regulation.
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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