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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Remarks:
Type of genotoxicity: gene mutation
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1982
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
comparable to guideline study with acceptable restrictions

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1982
Report date:
1982

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 471 (Bacterial Reverse Mutation Assay)
Deviations:
yes
Remarks:
only 4 tester strains tested; no tester strain to detect cross-linking mutagens was included (TA 102 or E.coli WP2 uvra); maximum concentration tested 2000 mg/plate and not 5000 g/plate as recommended by the guideline as of today;
Principles of method if other than guideline:
None
GLP compliance:
no
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Chemical structure
Reference substance name:
Sodium [3-hydroxy-4-[(1-hydroxy-5-sulpho-2-naphthyl)azo]naphthalene-1-sulphonato(4-)]chromate(1-)
EC Number:
289-530-3
EC Name:
Sodium [3-hydroxy-4-[(1-hydroxy-5-sulpho-2-naphthyl)azo]naphthalene-1-sulphonato(4-)]chromate(1-)
Cas Number:
89899-25-2
Molecular formula:
C20H10CrN2O8S2.Na
IUPAC Name:
Sodium [3-(hydroxy-​κO)-4-{[1-(hydroxy-​κO)-5-sulfonaphthalen-2-yl]diazenyl-​κN1}naphthalene-1-sulfonato(4-)]chromate(1-)
Test material form:
other: solid
Details on test material:
None

Method

Target gene:
Histidine gene

Species / strain
Species / strain / cell type:
S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
Additional strain / cell type characteristics:
not specified
Metabolic activation:
with and without
Metabolic activation system:
S9 mix
Test concentrations with justification for top dose:
Mutagenicity tests: 0.2, 2, 20, 200 and 2000 µg (or nl) per Petri dish
Vehicle / solvent:
No data
Controls
Untreated negative controls:
yes
Negative solvent / vehicle controls:
yes
True negative controls:
no
Positive controls:
yes
Positive control substance:
9-aminoacridine
other: 2-anthramine; N-methyl-N'-nitro-N-nitrosoguanidine (MNNG), Daunomycine:
Details on test system and experimental conditions:
No data
Evaluation criteria:
The criteria of mutagenicity used in this test are a doubling of the spontaneous reversion rate and a dose-effect relationship.
Statistics:
No data.

Results and discussion

Test results
Species / strain:
S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
no cytotoxicity
Vehicle controls validity:
valid
Untreated negative controls validity:
not examined
Positive controls validity:
valid
Additional information on results:
The substance FAT 20290/A was tested with the Salmonella typhimurium strains TA 1535, TA 1537, TA 98 and TA 100 at concentrations from 0.2 to 2000 M9 (or nl) per Petri dish both in the presence and absence of metabolic activation.

No mutagenic effect was observed.

Applicant's summary and conclusion

Conclusions:
FAT 20290/A was considered to be non-mutagenic in the Salmonella typhimurium reverse mutation assay.
Executive summary:

An in vitro study was performed to investigate the potential of the test substance to induce gene mutations according to method equivalent to OECD Guideline 471.

The substance was tested for mutagenic effects with Salmonella typhimurium TA 1535, TA 1537, TA 98 and TA 100 without and with metabolic activation at doses from 0.2 to 2000 µg active ingredient/plate. The lack of evidence for mutagenicity existed both in the absence and presence of metabolic activation.

Under the experimental conditions followed in the protocol, and employing a doubling of the spontaneous reversion rate and dose-effect relationship as criteria of mutagenicity, the product FAT 20290/A was not mutagenic for S. typhimurium strains TA 1535, TA 1537, TA 98 and TA 100.

Therefore, FAT 20290/A was considered to be non-mutagenic in the Salmonella typhimurium reverse mutation assay.