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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Genetic toxicity: in vitro

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Administrative data

Endpoint:
in vitro gene mutation study in bacteria
Remarks:
Type of genotoxicity: gene mutation
Type of information:
experimental study
Adequacy of study:
supporting study
Study period:
1996
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: with scientific toxicity testing methodology

Data source

Reference
Reference Type:
publication
Title:
Unnamed
Year:
1996
Report date:
1996

Materials and methods

Test guideline
Qualifier:
no guideline followed
GLP compliance:
no
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Reference substance name:
Salicylazosulfapyridine (SASP)
IUPAC Name:
Salicylazosulfapyridine (SASP)
Test material form:
not specified
Details on test material:
No data

Method

Target gene:
salmonella typhimurim histidine(his) reversion system; E. coli
Species / strain
Species / strain / cell type:
other: TA95, TA98, TA100, TA1535, WP2p, WP2 uvrA-p
Additional strain / cell type characteristics:
not specified
Metabolic activation:
with and without
Metabolic activation system:
s9 Mix
Test concentrations with justification for top dose:
0.4 to 6250 μg/plate
Vehicle / solvent:
corn oil
Details on test system and experimental conditions:
No data
Evaluation criteria:
No data
Statistics:
No data

Results and discussion

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information):
negative

The test article showed no mutagenic effect for Salmonella typhimurium and E. coli at all test concentrations.
Executive summary:

The study was performed with the Salmonella typhimurium(TA 95,TA 100, TA 1535, WP2p and WP2 uvrA-p ) at dose levels from 0.4 to 6250 μg/plate both in the presence and absence of metabolic activation to check the potential of mutagenicity. No mutagenic effect was found. Thus, we can conclude the substance dose not induce mutagenicity.