Registration Dossier
Registration Dossier
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EC number: 700-105-8 | CAS number: 16613-04-0
Endpoint summary
Administrative data
Description of key information
One acute oral study (limit test) according to OECD guideline 401 in compliance with GLP is available. Substance related effects were not observed.
Key value for chemical safety assessment
Additional information
The acute oral study (limit test) yielded an LD50 in excess of 2000 mg/kg bw. Mortality, clinical signs of toxicity or pathological abnormalities at necropsy were not observed in the study.
Justification for classification or non-classification
As no effects were observed in the oral study and no mortality was observed under the test conditions chosen, no classification of the test substance is required.
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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