Registration Dossier

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
weight of evidence
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: US EPA publication.

Data source

Reference
Reference Type:
secondary source
Title:
Unnamed
Year:
1991

Materials and methods

Principles of method if other than guideline:
No data on test method.
GLP compliance:
not specified
Test type:
other: no data

Test material

Reference
Name:
Unnamed
Type:
Constituent
Details on test material:
- Name of test material (as cited in study report): Sodium diacetate

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified

Administration / exposure

Route of administration:
oral: unspecified
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:
5 600 mg/kg bw
Based on:
test mat.

Any other information on results incl. tables

The oral LD50 of Sodium diacetate for rats is 5600 mg/kg bw.

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
The oral LD50 of Sodium diacetate for rats is 5600 mg/kg bw.
Executive summary:

The oral LD50 of Sodium diacetate for rats was determined to be 5600 mg/kg bw.