Registration Dossier
Registration Dossier
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EC number: 601-495-1 | CAS number: 117829-74-0
Endpoint summary
Administrative data
Description of key information
oral: LD50 > 2000 mg/kg (male/female), OECD Guideline Study 423 (BASF 2001 (10A0616/001099)
Key value for chemical safety assessment
Additional information
Acute oral toxicity:
For oral toxicity, there is one study available done by BASF (2001) according to OECD Guideline 423. Three male and three female rats were treated orally by gavage with a single application of the test substance in aqua bidest at a dose level of 2000 mg/kg bw (application volume 10 ml/kg). The animals were observed for 14 days. All animals survived until the scheduled sacrifice. In the course of the study the animals did not show any clinical findings. Organs were without any findings at necropsy. Thus, under the present test conditions, the acute oral LD50 is > 2000 mg/kg bw in rats.
Justification for classification or non-classification
Dangerous Substance Directive (67/548/EEC)
The available study is considered reliable and suitable for classification purposes under 67/548/EEC. As a result the substance is not considered to be classified for acute oral toxicity under Directive 67/548/EEC, as amended for the 28th time in Directive 2001/59/EC.
Classification, Labelling, and Packaging Regulation (EC) No. 1272/2008
The available experimental test data is reliable and suitable for classification purposes under Regulation 1272/2008. As a result the substance is not considered to be classified for acute oral toxicity under Regulation (EC) No. 1272/2008.
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