Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 276-057-2
CAS number: 71832-85-4
No clinical symptoms were recorded and no deaths occurred during the 14
day observation period. At autopsy no changes in organs or tissues
caused by the administration of the test compound were seen.
The test substance was tested for its acute toxicity potential in the standard acute test method, similar to OECD 401. Five male and female Sprague-Dawley rats were individually housed. The test substance was administered in a carboxymethyl cellulose vehicle as a limit dose of 5000 mg/kg bw. Animals were observed for clinical signs and an autopsy was performed at the end of the 14 day observation period. There were no clinical symptoms observed and no animal died during the study. At autopsy no changes in organs or tissues caused by the administration of the test compound were seen. The acute oral median lethal dose (LD50) was greater than 5000 mg/kg body weight and the test substance is not considered acute toxic in rats.
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.
Welcome to the ECHA website. This site is not fully supported in Internet Explorer 7 (and earlier versions). Please upgrade your Internet Explorer to a newer version.
Do not show this message again