Registration Dossier
Registration Dossier
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EC number: 204-807-0 | CAS number: 126-83-0
Endpoint summary
Administrative data
Description of key information
Oral: rat LD50: >2000 mg/kg. OECD 420; Reliability = 1
Dermal: Data Waived (the substance does not meet the criteria for classification as acute toxicity by oral route)
Inhalation: Data Waived (exposure of humans via inhalation route is not likely)
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 an oral LD50s in rats of >2000 mg/kg, no classification is required for acute oral toxicity endpoint according to EU Classification, Labelling and Packaging of Substances and Mixtures (CLP) Regulation (EC) No. 1272/2008.
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.
