Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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.

Diss Factsheets

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.