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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
key study
Study period:
Not specified
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
study well documented, meets generally accepted scientific principles, acceptable for assessment

Data source

Reference
Reference Type:
publication
Title:
Toxicological Study of Potassium Bromate. I. Absorption, Metabolism and Excretion of Potassium Bromate after oral Administration in Rats
Author:
Kawana, K.; Nakaoka, T.; Horiguchi, Y.; Watanabe, S.; Watanabe, S.; Kawauchi, S.
Year:
1991
Bibliographic source:
Eisei Kaguku 1991, 37, (4), 258-265.

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Deviations:
not specified
GLP compliance:
not specified
Test type:
fixed dose procedure
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Potassium bromate
EC Number:
231-829-8
EC Name:
Potassium bromate
Cas Number:
7758-01-2
Molecular formula:
BrHO3.K
IUPAC Name:
potassium bromate
Test material form:
solid: crystalline

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female

Administration / exposure

Route of administration:
oral: unspecified
Doses:
85, 159, 177, 325, 337, 602 mg/kg body weight
No. of animals per sex per dose:
85 mg/kg: 5 m
159 mg/kg: 5 m
177 mg/kg: 5 f
325 mg/kg: 5 m
337 mg/kg: 5 f
602 mg/kg: 5 m
Control animals:
no

Results and discussion

Effect levels
Key result
Sex:
male/female
Dose descriptor:
LD50
Effect level:
157 mg/kg bw
Based on:
test mat.

Applicant's summary and conclusion

Interpretation of results:
Category 2 based on GHS criteria
Conclusions:
Under the experimental conditions, the substance had a LD50 by oral administration of 157 mg/kg bw in male and female rats.