Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Journal reports value without giving detailed information on method.

Data source

Reference
Reference Type:
secondary source
Title:
Recherche de veratre blanc et d'ortho-Nitrobenzaldehyde dans des poudres a eternuer
Author:
J.-P. Goiffon et. al.
Year:
1983
Bibliographic source:
Ann. Fals. Exp. Chim. - 76 - No 815 - pp. 65-71

Materials and methods

Principles of method if other than guideline:
Experimental measurement (data is taken from a secondary source, information about the methodology is not available).
GLP compliance:
not specified
Test type:
other: not published

Test material

Constituent 1
Reference substance name:
ortho-nitrobenzaldehyde
IUPAC Name:
ortho-nitrobenzaldehyde
Test material form:
solid - liquid: suspension

Test animals

Species:
mouse
Strain:
not specified
Sex:
female

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
not specified

Results and discussion

Effect levels
Sex:
female
Dose descriptor:
LD50
Effect level:
600 mg/kg bw
Based on:
not specified

Applicant's summary and conclusion

Interpretation of results:
harmful
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
LD50 oral mouse = 600 mg/kg bw