Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Endpoint:
short-term repeated dose toxicity: inhalation
Data waiving:
study scientifically not necessary / other information available
Justification for data waiving:
other:
Justification for type of information:
In accordance with REACH sections 8.6.1 and 8.6.2 the repeat dose toxicity testing should be conducted in the most appropriate route of administration. In accordance with ECHA’s request a 90-day repeated dose oral toxicity study is being conducted to OECD Guideline TG 408 combined with OECD TG 424. The oral route is the most relevant and as such testing via the inhalation route does not need to be conducted.

Data source

Materials and methods

Results and discussion

Target system / organ toxicity

Critical effects observed:
not specified

Applicant's summary and conclusion