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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

oral (rat): >3000 mg/kg bw (m+f)
oral (guinea pig): >4700 mg/kg bw (m+f)
intraperitoneal (rat): >3000 mg/kg bw (m+f)

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Dose descriptor:
3 000 mg/kg bw

Additional information

The substance was tested for acute toxicity via oral and intraperitoneal application to different species.

Acute oral toxicity: Acute oral toxicity to rats is regarded as key study. An LD50 of > 3000 mg/kg bw was identified via oral application.

Justification for classification or non-classification

There are conclusive but not sufficient data for classification of the test substance with regard to acute toxicity.

The substance is not classified for acute toxicity via oral route in accordance to the CLP Regulation (EC) No 1272/2008.