Registration Dossier
Registration Dossier
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EC number: 854-058-4 | CAS number: 58625-89-1
Endpoint summary
Administrative data
Description of key information
Acute oral toxicity: similar to OECD TG 401: LD50 >5000 mg/kg bw.
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
- Dose descriptor:
- discriminating dose
- Value:
- 5 000 mg/kg bw
Additional information
Acute oral toxicity
The acute oral toxicity has been studied in a similar to OECD TG 401 test. The substance was administered at a dose of 5000 mg/kg bw to 5 male and 5 female SD rats and animals were observed for 14 days. No mortality and no clinical signs were observed. There were no treatment related necropsy findings. There were no adverse effects on bodyweight gain in animals of either sex except for one female losing 5 grams of weight between day 7 and 14. The acute oral toxicity (LD50) was determined to be >5000 mg/kg.
Justification for classification or non-classification
The substance does not have to be classified for Acute oral toxicity according to EU CLP (EC No. 1272/2008 and its amendments).
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