Registration Dossier

Diss Factsheets

Administrative data

Description of key information

In an OECD 401 study the registered substance did not induce mortality at the limit dose of 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
Quality of whole database:
Klimisch 1 study

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

The registered susbstance was tested in rats for acute oral toxicity in an OECD 401 study design under GLP conditions. No mortality occured. No macroscoplical pathological findings, clinical observations or body weight effects were noted. The LD50 is >2000 mg/kg bw..


Justification for selection of acute toxicity – oral endpoint
Klimisch 1 study

Justification for classification or non-classification