Registration Dossier
Registration Dossier
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EC number: 246-148-1 | CAS number: 24308-84-7
Endpoint summary
Administrative data
Description of key information
Acute oral toxicity: LD50 > 2000 mg/kg
Key value for chemical safety assessment
Acute toxicity: via oral route
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed
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
Acute oral toxicity was assessed following EU method B.1 tris. Female rats were dosed by gavage and observed for up to 14 days after dosing. No deaths were recorded up to 2000 mg/kg.
No pathologic changes and signs of intoxication were noted; increase in bodyweight was normal.
Justification for classification or non-classification
The CLP Regulation (EC 1272/2008), Annex I, Part 3, Table 3.1.1 gives the following criteria for acute oral toxicity: "Category 4: 300 < ATE ≤ 2 000," where ATE is acute toxicity estimates in mg/kg bodyweight.
No mortality was seen up to the highest tested dose of 2000 mg/kg bw, thus no LD50 value could be established. Test substance is considered as not acutely toxic by oral route.
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