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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
in vitro gene mutation study in bacteria
Type of information:
experimental study
Adequacy of study:
key study
Study period:
not specified
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
data from handbook or collection of data

Data source

Reference
Reference Type:
publication
Title:
Final Report on the Safety Assessment of Sodium Iodate
Author:
Cosmetic Ingredient Review (Expert Panel)
Year:
1995
Bibliographic source:
Journal of the American College of Toxicology 14(3):231-239, Raven Press, Ltd., New York

Materials and methods

Test guideline
Qualifier:
no guideline available
Principles of method if other than guideline:
An Ames test was conducted with the substance
GLP compliance:
not specified
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Chemical structure
Reference substance name:
Sodium iodate
EC Number:
231-672-5
EC Name:
Sodium iodate
Cas Number:
7681-55-2
Molecular formula:
HIO3.Na
IUPAC Name:
sodium iodate

Results and discussion

Test results
Key result
Species / strain:
not specified
Metabolic activation:
not specified
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not specified
Vehicle controls validity:
not specified
Untreated negative controls validity:
not specified
Positive controls validity:
not specified

Applicant's summary and conclusion

Conclusions:
The test material showed no mutagenic activity by the Ames test.
Executive summary:

The test material showed no mutagenic activity by the Ames test.