Benzoic acid, 2-[[(4-hydroxyphenyl)sulfonyl]oxy]-, methyl ester

Genetic toxicity: in vitro

Administrative data

Endpoint:

in vitro gene mutation study in bacteria

Remarks:

Type of genotoxicity: genome mutation

Type of information:

experimental study

Adequacy of study:

key study

Study period:

7-16 December 2011

Reliability:

1 (reliable without restriction)

Rationale for reliability incl. deficiencies:

other: Data have been generated according to current internationally recognised study guidelines and in accordance with GLP

Data source

Reference

Reference Type:

study report

Title:

Unnamed

Year:

2012

Report date:

2012

Materials and methods

Test guideline

Qualifier:

according to guideline

Guideline:

OECD Guideline 471 (Bacterial Reverse Mutation Assay)

GLP compliance:

yes (incl. QA statement)

Type of assay:

bacterial reverse mutation assay

Test material

Test material information

Constituent 1

Reference substance name:

methyl 2-[(4-hydroxybenzenesulfonyl)oxy]benzoate

Cas Number:

1432505-97-9

Molecular formula:

C14H12O6S

IUPAC Name:

methyl 2-[(4-hydroxybenzenesulfonyl)oxy]benzoate

Test material form:

solid: particulate/powder

Remarks:

migrated information: powder

Method

Species / strain

Species / strain 1

Species / strain / cell type:

S. typhimurium TA 1535, TA 1537, TA 98 and TA 100

Species / strain 2

Species / strain / cell type:

E. coli WP2 uvr A

Metabolic activation:

with and without

Metabolic activation system:

S9

Test concentrations with justification for top dose:

Concentrations of 5000; 2500; 1000; 316; 100; 31.6 and 10 μg/plate were examined in the range Finding Test. Based on the results of the Range Finding Test, the test item concentrations in the Initial Mutation Test were 5000; 1581; 500; 158.1; 50; 15.81 and 5 μg/plate. In the Confirmatory Mutation Test, concentrations of 5000; 1581; 500; 158.1; 50; 15.81; 5 and 1.581 μg/plate were examined.

Vehicle / solvent:

The behaviour of the test item solutions with the solution of top agar and phosphate buffer was examined in a preliminary solubility test. Dimethyl sulfoxide was used as solvent to prepare the stock formulation of the test material. Test solutions were freshly prepared at the beginning of the experiments in the testing laboratory by diluting the stock formulation using the selected vehicle.

Controls

Untreated negative controls:

no

Negative solvent / vehicle controls:

yes

Remarks:

DMSO and distilled water

Positive controls:

yes

Positive control substance:

9-aminoacridine

sodium azide

other: 4-nitro-1,2-phenylene-diamine (NPD), Methyl-methanesulfonate (MMS), 2-aminoanthracene (2AA)

Results and discussion

Test results

Test results 1

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:

cytotoxicity

Remarks:

5000 μg/plate

Vehicle controls validity:

valid

Positive controls validity:

valid

Test results 2

Species / strain:

E. coli WP2 uvr A

Metabolic activation:

with and without

Genotoxicity:

negative

Cytotoxicity / choice of top concentrations:

cytotoxicity

Remarks:

5000 μg/plate

Vehicle controls validity:

valid

Positive controls validity:

valid

Remarks on result:

other: all strains/cell types tested

Remarks:

Migrated from field 'Test system'.

Any other information on results incl. tables

Precipitate was observed on the plates in the Confirmatory Mutation Test in all examined strains at 5000 μg/plate concentration with and without metabolic activation.

Untreated, negative (solvent) and positive controls were run concurrently. The mean values of revertant colony numbers of untreated, negative (solvent) and positive control plates were within the historical control range. At least five analyzable concentrations were presented in all strains of the main tests.

The reference mutagens showed a distinct increase of induced revertant colonies. The viability of the bacterial cells was checked by a plating experiment in each test. The tests were considered to be valid.

Applicant's summary and conclusion

Conclusions:

Interpretation of results (migrated information):
negative

The test item had no mutagenic activity in the applied bacterium tester strains under the test conditions used in this study.

Executive summary:

The mutagenic potential has been assessed by exposure to S. typhimurium TA 1535, TA 1537, TA 98 and TA 100 and E. coli WP2 uvr A in DMSO with and without S9 metabolic activations in accordance with the OECD 471 test guideline in compliance with GLP. Under the conditions of the test, the test substance was shown to have no mutagenic activity to bacterium tester strains.