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Description of key information

The oral and dermal LD50-values of the substance were found to be 2000 mg/kg bw.

Key value for chemical safety assessment

Additional information

In an acute oral toxicity GLP study according to OECD guideline 423 and EU Method B.1 tris, 2 groups of 3 female Wistar rats were dosed with 2000 mg kg/bw test substance. The clinical signs which were observed 1 hour after exposure had resolved 5 hours after exposure. A LD50 > 2000 mg/kg bw has been established.

In an acute dermal toxicity GLP study according to OECD guideline 402, 5 male and 5 female Wistar rats were dosed with 2000 mg kg/bw test substance. As no clinical signs were observed, a LD50 > 2000 mg/kg bw has been established.

Justification for classification or non-classification

Based on the results of an oral and a dermal acute toxicity study, classification is not warranted in the EU.