Registration Dossier

Administrative data

Endpoint:
repeated dose toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
study well documented, meets generally accepted scientific principles, acceptable for assessment

Data source

Referenceopen allclose all

Reference Type:
study report
Title:
Unnamed
Year:
1953
Report Date:
1953
Reference Type:
secondary source
Title:
Unnamed
Report Date:
1953

Materials and methods

Principles of method if other than guideline:
BASF-Test
GLP compliance:
no

Test material

Reference
Name:
Unnamed
Type:
Constituent

Test animals

Species:
other: mammal
Strain:
not specified
Sex:
not specified

Administration / exposure

Route of administration:
inhalation
Duration of treatment / exposure:
4 Tage
Frequency of treatment:
6 h/Tag
Doses / concentrations
Remarks:
gesaettigte Atmosphaere (Zimmertemperatur) entspr. 0,3-1 mg/l
Control animals:
other: no data specified
Details on study design:
Post-exposure period: keine Angabe

Results and discussion

Results of examinations

Details on results:
1 Maus unter Dyspnoe gestorben, sonst symptomlos vertragen.

Effect levels

Dose descriptor:
NOAEC
Remarks on result:
other: not determined

Target system / organ toxicity

Critical effects observed:
not specified

Applicant's summary and conclusion