Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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 (rat): LD50 > 2000 mg/kg bw

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
LD50
Value:
2 000 mg/kg bw

Additional information

The acute oral toxicity of the test substance was investigated in young adult Wistar rats according to OECD guideline 401. The test article was given orally by gavage in a dose of 2000 mg/kg body weight to 5 male and 5 female animals. The surviving rats were sacrified at the end of the observation period and a macroscopic postmortem examination was performed on all rats. The LD50 was >2000 mg/kg for male and female rats.

Justification for classification or non-classification

Based on results of the key studies the substance does not need to be classified according to GHS (Regulation (EU) 1272/2008) and also does not need to be classified according to DPD (67/548/EEC).