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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: oral

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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: No specific test guideline was reported; however, a scientifically defensible approach was used to conduct the study.

Data source

Referenceopen allclose all

Reference Type:
publication
Title:
Unnamed
Year:
1969
Reference Type:
publication
Title:
Unnamed
Year:
1962

Materials and methods

Principles of method if other than guideline:
Single oral toxicity is estimated by the gastric intubation of groups of five non-fasted, Carworth-Wistar rats, four to five weeks of age and 90 to 120 grams in weight, which have been reared in the laboratory own colony and mantained from time of weaning on Rockland rat diet, complete. Dose: 3.25g/kg (2.48-4.26). The observation period was 14 days.
GLP compliance:
no
Test type:
other: metod described
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Potassium acetate
EC Number:
204-822-2
EC Name:
Potassium acetate
Cas Number:
127-08-2
Molecular formula:
C2H4O2.K
IUPAC Name:
potassium acetate
Details on test material:
- Name of test material (as cited in study report): Potassium acetate
- Molecular formula (if other than submission substance): KOOCCH3

Test animals

Species:
rat
Strain:
other: Carworth-Wistar
Sex:
male

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
not specified
Doses:
3.25 g/kg (2.48-4.26)
No. of animals per sex per dose:
Five male rats per group
Control animals:
not specified

Results and discussion

Effect levels
Sex:
male
Dose descriptor:
LD50
Effect level:
ca. 3.25 other: g/kg bw
Based on:
test mat.

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
Potassium acetate LD50 is 3.25 g/kg (2.48-4.26).
Executive summary:

Single oral toxicity is estimated by the gastric intubation of groups of five non-fasted, Carworth-Wistar rats, four to five weeks of age and 90 to 120 grams in weight, which have been reared in the laboratory own colony and mantained from time of weaning on Rockland rat diet, complete. Dose: 3.25g/kg (2.48-4.26). The observation period was 14 days.

Potassium acetate LD50is 3.25 g/kg (2.48-4.26).