Registration Dossier

Administrative data

Endpoint:
acute toxicity: oral
Remarks:
USE OF (ROBUST) STUDY SUMMARIES PROVIDED BY ECHA, the study data of the Robust Study Summaries are older than 12 years.
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
other: USE OF (ROBUST) STUDY SUMMARIES PROVIDED BY ECHA.
Title:
Unnamed
Year:
1991

Materials and methods

Test guideline
Qualifier:
according to
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
GLP compliance:
not specified
Test type:
other: not specified
Limit test:
yes

Test material

Reference
Name:
Unnamed
Type:
Constituent
Test material form:
liquid

Test animals

Species:
rat

Administration / exposure

Route of administration:
oral: unspecified
Doses:
2000 mg/kg bw
Control animals:
no

Results and discussion

Effect levels
Key result
Sex:
not specified
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Based on:
test mat.
Mortality:
no information provided
Clinical signs:
no information provided
Body weight:
no information provided
Gross pathology:
no information provided

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
the substance should not be classified for acute oral toxicity