Registration Dossier

Diss Factsheets

Administrative data

Endpoint:
sub-chronic toxicity: inhalation
Type of information:
experimental study planned
Study period:
The test is part of an Integrated Testing Strategy (ITS), and will be planned and performed after approval by ECHA.

Data source

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 413 (Subchronic Inhalation Toxicity: 90-Day Study)

Results and discussion

Target system / organ toxicity

Critical effects observed:
not specified

Applicant's summary and conclusion