Registration Dossier

Administrative data

Endpoint:
acute toxicity: other routes
Type of information:
experimental study
Adequacy of study:
disregarded due to major methodological deficiencies
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: The data were based on secondary source (MSDS, ChemID, RTECS. Primary source (Industrial Hygiene and Toxicology, 2nd ed., Patty, F.A., ed., New York, John Wiley & Sons, Inc., 1958-63Vol. 2, Pg. 1882, 1963) could not be retrieved.

Data source

Referenceopen allclose all

Reference Type:
secondary source
Title:
Unnamed
Reference Type:
secondary source
Title:
No information
Author:
ChemID

Materials and methods

Test guideline
Qualifier:
no guideline followed
GLP compliance:
not specified

Test material

Reference
Name:
Unnamed
Type:
Constituent

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified

Results and discussion

Effect levels
Dose descriptor:
LD50
Effect level:
600 mg/kg bw
Remarks on result:
other: intraperitoneal

Applicant's summary and conclusion

Conclusions:
LD50 after intraperitoneal administration in rats was 600 mg/kg bw.

Executive summary:

LD50 was reported to be 600 mg/kg bw after intraperitoneal administration in rats. This information was based on secondary source; no further information could be retrieved from primary sources.