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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Type of coverage:
not specified
Vehicle:
not specified
Details on dermal exposure:
No data
Duration of exposure:
No data
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:
> 2 000 mg/kg bw
Based on:
test mat.

Any other information on results incl. tables

The dermal LD50 of Sodium diacetate for rats is greater than 2000 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 dermal LD50 of Sodium diacetate for rats is greater than 2000 mg/kg bw.
Executive summary:

The dermal LD50 of Sodium diacetate for rats is greater than 2000 mg/kg bw.