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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

acute and sub-chronic neurotoxicity studies (rat, oral exposure): no indication for neurotoxicity

Key value for chemical safety assessment

Additional information

The acute and sub-chronic neurotoxicity of the substance has been evaluated in the rat. There was no indication that the substance was neurotoxic. In the acute study, single gavage doses of 0, 10, 30 and 80 mg/kg/day did not produce any functional or pathological indications of neurotoxicity, although signs of general toxicity were observed at 30 mg/kg and above. In the sub-chronic neurotoxicity study, 90 days dietary administration at 0, 100, 250 and 800 ppm (males)/500 ppm (females) did not result in any indications of functional or pathological neurotoxicity. The NOAEL for generalized systemic toxicity was 100 ppm for males and 250 ppm for females, corresponding to 6.31 and 19.17 mg/kg/day respectively.

Remark of the registrant: The endpoint study record of the acute neurotoxicity study is missing in this dossier. It will be added in a subsequent update.

Justification for classification or non-classification