Registration Dossier

Diss Factsheets

Administrative data

Description of key information

LD50 > 2000 mg/kg bw was obtained in rats.

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
discriminating dose
2 000 mg/kg bw
Quality of whole database:
One guideline study

Additional information

Justification for classification or non-classification

The acute oral toxicity of the registration substance was investigated according to the Guideline OECD 423. Total six females were treated once per gavage at dose of 2000 mg/kg bw. No significant effect was found. The LD50 is higher than 2000 mg/kg bw. No classification is justified.