Registration Dossier

Administrative data

Description of key information

In line with ECHA final decision number TPE-D-2114449802-46-01/F, there is an ongoing 90 -day repeated dose toxicity study in rat, conducted according to OECD Test Guideline 408 and in compliance with GLP. The study results will not be available in time for the final decision deadline of 30th Nov 2020. The study result will therefore be submitted at a later date.

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

In the absence of data, the substance is not classified for specific target organ toxicity following repeated exposures according to Regulation (EC) No 1272/2008.