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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

oral (rat): > 2000 mg/kg bw (m+f)
dermal (rat): > 2000 mg/kg bw (m+f)

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Dose descriptor:
LD50
Value:
2 000 mg/kg bw

Acute toxicity: via dermal route

Endpoint conclusion
Dose descriptor:
LD50
Value:
2 000 mg/kg bw

Additional information

Tests on acute oral and dermal toxicity were performed with the test substance, LD50 of > 2000 mg/kg bw were identified via oral or dermal application for rats.

Acute inhalation toxicity: Inhalative exposure is no human relevant route of exposure due to its low vapor pressure.

Justification for classification or non-classification

There are conclusive but not sufficient data for classification of the test substance with regard to acute toxicity.

The test substance is not classified for acute toxicity via oral or dermal route in accordance to the CLP Regulation (EC) No 1272/2008.