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EC number: -
CAS number: -
Oral: OECD 425; rat LD50 was >5000 mg/kg. Reliability = 1Dermal: OECD 402; rat LD50 was >5000 mg/kg. Reliability = 1Inhalation: OECD 403; rat LC50 was >5.06 mg/L (>5060 mg/m3). Reliability = 1
The test substance has low oral, inhalation, and dermal toxicity in the
rat. The rat oral and dermal LD50s were >5000 mg/kg body weight. The
only clinical sign observed was reduced faecal volume in one rat on Day
1 of the oral study. No other effects in clinical signs, body weight, or
gross necropsy were observed in either study. The rat 4-hour inhalation
LC50 was >5.06 mg/L, the highest concentration tested. Following
exposure, all animals exhibited irregular respiration, but recovered by
Day 2. Some rats exhibited weight loss on day 1. No other effects were
observed during the study or at gross necropsy.
Based on oral and dermal LD50s in rats of >5000 mg/kg, and a 4-hour
inhalation LC50 in rats of >5.06 mg/L, no classification is required for
acute toxicity endpoints according to EU Classification, Labelling and
Packaging of Substances and Mixtures (CLP) regulation (EC) No. 1272/2008.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.
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