Registration Dossier

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1977
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Literature data (1977)
Cross-referenceopen allclose all
Reason / purpose:
reference to same study
Reason / purpose:
reference to other study

Data source

Reference
Reference Type:
publication
Title:
Report to RIFM
Author:
Moreno O. M.
Year:
1977
Bibliographic source:
cited in: Food and Chemical Toxicology, Vol. 30, pg 129S, 1992

Materials and methods

Test guideline
Qualifier:
no guideline available
Principles of method if other than guideline:
Not applicable
GLP compliance:
not specified
Test type:
acute toxic class method

Test material

Reference
Name:
Unnamed
Type:
Constituent
Details on test material:
Not available

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified

Administration / exposure

Route of administration:
other: no data
Vehicle:
not specified
Doses:
No data
No. of animals per sex per dose:
No data
Control animals:
not specified

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
> 5 000 mg/kg bw

Any other information on results incl. tables

Not relevant

Applicant's summary and conclusion

Interpretation of results:
practically nontoxic
Remarks:
Migrated information Criteria used for interpretation of results: OECD GHS
Conclusions:
The oral LD50 of Dihydro-C14-aldehyde in rats exeeded 5000 mg/kg bw.
Executive summary:

The oral LD50 of Dihydro-C14-aldehyde in rats exeeded 5000 mg/kg bw based on 2/10 deaths at that dose.