Registration Dossier

Administrative data

Description of key information

LD50 value > 2000 mg/kg bw for the pure substance (extrapolation based on results with mixture)

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

Acute toxicity: via inhalation route

Endpoint conclusion
Endpoint conclusion:
no study available

Acute toxicity: via dermal route

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

Justification for classification or non-classification

Based on the criteria defined by the EU and the CLP criteria, the test substance needs not to be labelled for acute oral toxicity because no death occurred in the highest dosing group of 2000 mg/kg bw that could be attributed to the test substance administration.