Registration Dossier

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
4 (not assignable)

Data source

Referenceopen allclose all

Reference Type:
publication
Title:
Acta Neurologia et Psychiatrica Belgica. Vol. 61, Pg. 611, 1961
Year:
1961
Bibliographic source:
ChemIDplus Lite
Reference Type:
publication
Title:
Pharmacology: International Journal of Experimental and Clinical Pharmacology. Vol. 15, Pg. 485, 1977.
Year:
1977
Bibliographic source:
ChemIDplus Lite data base

Materials and methods

Principles of method if other than guideline:
Method not available
GLP compliance:
not specified

Test material

Reference
Name:
Unnamed
Type:
Constituent

Test animals

Species:
other: rat and mouse
Strain:
not specified
Sex:
not specified

Administration / exposure

Route of administration:
oral: unspecified

Results and discussion

Effect levelsopen allclose all
Sex:
not specified
Dose descriptor:
LD50
Effect level:
160 mg/kg bw
Based on:
not specified
Remarks on result:
other: on rat
Sex:
not specified
Dose descriptor:
LD50
Effect level:
490 mg/kg bw
Based on:
test mat.
Remarks on result:
other: on mouse

Applicant's summary and conclusion

Interpretation of results:
other: Toxic if swllowed
Conclusions:
Following CLP criteria the substance is classified into category 4, Toxic if swallowed.