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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
acute toxicity: dermal
Data waiving:
study scientifically not necessary / other information available
Justification for data waiving:
other:
Justification for type of information:
In accordance with Annex XI No 1.2 it is scientifically not necessary to perform an acute dermal toxicity study, because existing data indicate that it can be plausibly assumed that a dermal LD50 of > 2000 mg/kg would result based
- on the findings of an acute oral toxicity study in rats with a LD50 > 2000 mg/kg,
- on the findings of an OECD 422 study with oral application which did not reveal adverse effects up to the limit dose of 1000 mg/kg/d,
- on the plausible assumption that dermal absorption would not exceed oral absorption.

Data source

Materials and methods

Results and discussion

Applicant's summary and conclusion