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Description of key information

The acute oral median lethal dose (LD50) of the test  material in the female rat was greater than 2000 mg/kg bodyweight. The acute dermal median lethal dose (LD50) of the test  material in rats was found to be  greater than 2000 mg/kg bodyweight.

Key value for chemical safety assessment

Additional information

Justification for classification or non-classification

No clinical effects and mortality were observed at 2000 mg/kg b.w. in acute dermal toxicity study (semiocclusive - fixed dose). No mortality but clinical signs ( piloerection, decreased motility, closed eyelids, hunched posture, narrowed palpebral fissure, poor reflexes, poor general condition, uncoordinated gait and abdominal and lateral position) were observed at 2000 mg/kg b.w. in a acute oral study. The results of the acute toxicity testing do not warrant classsification according to EU criteria.