Registration Dossier

Administrative data

Endpoint:
sub-chronic toxicity: inhalation
Type of information:
experimental study planned
Study period:
after approval by ECHA
Rationale for reliability incl. deficiencies:
other: Test study will be conducted with the registered substance via the inhaled route.

Data source

Materials and methods

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

Test material

Reference
Name:
Unnamed
Type:
Constituent

Test animals

Species:
rat
Sex:
male/female

Administration / exposure

Route of administration:
inhalation

Results and discussion

Target system / organ toxicity

Critical effects observed:
not specified

Applicant's summary and conclusion