Registration Dossier

Administrative data

Description of key information

LD50 > 10000 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:
10 000 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

Acute toxicity means those adverse effects occurring following oral or dermal administration of a single dose of a substance or a mixture, or multiple doses given within 24 hours, or an inhalation exposure of 4 hours. Based on the CLP definition, the test substance cannot be allocated to one of four toxicity categories; based on acute toxicity by the oral route according to the numeric criteria shown in Table 3.1.1 of the CLP Regulation.

It can therefore be assumed that no classification for acute toxicity oral is warranted under the Regulation EC n. 1272/2008.