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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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 Toxicity - Oral LD50 >2000 mg/kg for study substance in Wistar rat (OECD TG 420)


Dermal Toxicity - Dermal LD50 >2000 mg/kg for study substance in Wistar rat (OECD TG 402)

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed

Acute toxicity: via dermal route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed

Additional information

Acute exposure to the study substance has a low potential for toxicity via the oral and dermal routes.  The LD50 via the oral and dermal routes is greater than 2,000 mg/kg body weight.

Justification for classification or non-classification

"No Classification" according to the classification, labelling and packaging (CLP) regulation (EC) No 1272/2008.