Registration Dossier

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
weight of evidence
Study period:
1982
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
secondary literature

Data source

Reference
Reference Type:
publication
Title:
Unnamed
Year:
1982
Report Date:
1982

Materials and methods

Principles of method if other than guideline:
no guideline specified
GLP compliance:
not specified
Test type:
other: not specified

Test material

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

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified

Administration / exposure

Route of administration:
oral: unspecified

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
505 mg/kg bw
Based on:
test mat.

Applicant's summary and conclusion

Interpretation of results:
other: Category 4 based on EU GHS criteria
Conclusions:
The LD50 of the test item in the rat was determined to be 505 mg/kg bw.
Executive summary:

In an report published by Federation Proceedings, Federation of American Societies for Experimental Biology and cited in RTECS, the test item revealed an oral LD50 in the rat of 505 mg/kg bw.