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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Acute oral toxicity, OECD401: LD50>2000 mg/kg body weight

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Dose descriptor:
2 000 mg/kg bw

Additional information

Acute oral toxicity (OECD401): The test substance caused transient central nervous effects and signs of reduced well-being and of pain at the dose of 2000 mg/kg body weight. No mortality occurred. The LD50,oral of the test substance was higher than 2000 mg/kg body weight in rats.

Justification for classification or non-classification

According to the results of an acute oral toxicity study in rats (OECD401) the test substance does not require classification for acute oral toxicity.