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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

No valid information on repeated oral, dermal or inhalation toxicity is available. The invalid studies have the following outcome:

- Repeated dose toxicity-oral: 30 male Wistar rats were exposed to increasing doses of the test substance on 5 consecutive days, observed parameter: Mortality; cumulative LD50 = 868 mg/kg bw.

- Repeated dose toxicity-inhalation: 10 male Wistar rats were exposed to 2.475 mg test substance/L air for 4h on 5 days per week for a total exposure time of 4 weeks; LC50 > 2.475 mg/L, no adverse effects observed up to highest concentration.

- Repeated dose-dermal: no study available

Key value for chemical safety assessment

Repeated dose toxicity: via oral route - systemic effects

Endpoint conclusion
Endpoint conclusion:
no study available

Repeated dose toxicity: inhalation - systemic effects

Endpoint conclusion
Endpoint conclusion:
no study available

Repeated dose toxicity: inhalation - local effects

Endpoint conclusion
Endpoint conclusion:
no study available

Repeated dose toxicity: dermal - systemic effects

Endpoint conclusion
Endpoint conclusion:
no study available

Repeated dose toxicity: dermal - local effects

Endpoint conclusion
Endpoint conclusion:
no study available

Additional information

Justification for classification or non-classification

No valid information on repeated oral, dermal or inhalation toxicity is available. Based on available data the test substance does not need to be classified according to regulation (EC) 1272/2008 (CLP).