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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Constituent 1
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.