Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Administrative data

Description of key information

Key value for chemical safety assessment

Additional information

Justification for classification or non-classification

Acute oral toxicity

The oral toxicity of the test substance to rats was assessed in two groups, each of three female WISTAR rats, treated with the test item by oral gavage administration at a dosage of 2000 mg/kg body weight. All animals survived until the end of the study without showing any test-item related signs of toxicity. At necropsy, no treatment-related macroscopic findings were observed in any animal of any step. The LD50 after a single oral administration to female rats is infinite (∞)

According to the EU Regulation No. 1272/2008 on the Classification, Labelling and Packaging of Substances and Mixtures (CLP) the substance is not considered to be classified as acute toxic because the LD50 is > 2000 mg/kg bw (Table 3.1.1).