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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

LD50 (oral) > 2000 mg/kg bw

LD50 (dermal) > 2000 mg/kg bw

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed

Acute toxicity: via inhalation route

Endpoint conclusion
Endpoint conclusion:
no study available

Acute toxicity: via dermal route

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed

Additional information

The acute oral toxicity of the test substance was evaluated in rats in a limit test according to the EU method B.1 (92/69/EEC) and in compliance with GLP. Five animals per sex were dosed at 2000 mg/Kg bw. No mortality occured and no clinical signs as well as no treatment-related macroscopic findings were observed. All animals showed expected gains in bodyweight over the study period.

LD50 (oral) > 2000 mg/kg bw

The acute dermal toxicity of the test substance was evaluated in rats in a semiocclusive limit test according to the EU method B.3 (92/69/EEC) and in compliance with GLP. Five animals per sex were dosed at 2000 mg/Kg bw. No mortality occured and no clinical signs as well as no treatment-related macroscopic findings were observed.

LD50 (dermal) > 2000 mg/kg bw

Justification for classification or non-classification

In the acute oral toxicity test and in the acute dermal toxicity test LD50 was found to be > 2000 mg/kg bw. Therefore, the substance shall not be classified as harmful or toxic according to the CLP Regulation (EC) No. 1272/2008.