Registration Dossier

Administrative data

Description of key information

The tests of Acute oral toxicity and Acute dermal toxicity were performed according to the following methods: 
Method B.1 tris: Acute Oral Toxicity - Acute Toxic Class Method, Council Regulation (EC) No.440/2008, published in O.J. L 142, 2008.
Method B.3 Acute Toxicity (Dermal), Council Regulation (EC) No.440/2008, published in O.J. L 142, 2008.
Both: GLP study

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Dose descriptor:
LD50
2 000 mg/kg bw

Acute toxicity: via dermal route

Endpoint conclusion
Dose descriptor:
LD50
2 000 mg/kg bw

Additional information

Justification for classification or non-classification

From the results of both acute toxicity studies (oral and dermal) follows that the substance is not classified as hazard substance.

LD50 > 2000 mg/kg bw (oral)

LD50 > 2000 mg/kg bw (dermal)