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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
key study
Reliability:
1 (reliable without restriction)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1993

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
OECD Guideline 471 (Bacterial Reverse Mutation Assay)
Qualifier:
according to guideline
Guideline:
OECD Guideline 472 (Genetic Toxicology: Escherichia coli, Reverse Mutation Assay)
GLP compliance:
yes
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Chemical structure
Reference substance name:
2,2'-dithiodi(benzoic acid)
EC Number:
204-352-8
EC Name:
2,2'-dithiodi(benzoic acid)
Cas Number:
119-80-2
Molecular formula:
C14H10O4S2
IUPAC Name:
2-[(2-carboxyphenyl)disulfanyl]benzoic acid
Test material form:
other: Solid
Details on test material:
The test material had a purity of 75.7%

Method

Species / strainopen allclose all
Species / strain / cell type:
S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
Species / strain / cell type:
E. coli WP2
Species / strain / cell type:
E. coli WP2 uvr A
Metabolic activation:
with and without
Metabolic activation system:
Liver S9 from phenobarbital/beta-naphthaflavone induced male rats
Test concentrations with justification for top dose:
5000, 2500, 1000, 500, 200, 100 ug/plate
Vehicle / solvent:
DMSO
Controls
Untreated negative controls:
no
Negative solvent / vehicle controls:
yes
True negative controls:
no
Positive controls:
yes
Positive control substance:
sodium azide
N-ethyl-N-nitro-N-nitrosoguanidine
mitomycin C
other: Acridine mutagen, 2-aminoanthracene & Daunomycin HCl
Details on test system and experimental conditions:
Incubation period: 3 days
Incubation temperature: 37 degrees C
Revertant colonies were counted using an automated elctronic colony counter (AMS 40-10 Image Analyser fitted with appropriate software)
Evaluation criteria:
Test was considered valid when: (a) concurrent solvent control data are acceptable (b) positive control data show unequivocal positive response (c) at least the lowest test compound dose shows no evidence of toxicity and at least 3 test doses show no significant toxicity (i.e. significnat loss of background growth and/or reductions in colony numbers)
-Positive response achieved when: (a) statistically significant dose-related increase in mean number of revertant colonies is obtained and/or (b) twofold or greater increase in the mean number of revertant colonies (over that observed for the concurrent solvent control plastes) which is statistically significant in observed at at least one dose level. For a positive response in an individual experiment to be considered indicative of an unequivocal positive i.e. mutagenic results fot that strain S9 combination then the observed effect msut be consistently reproducible.
-Negative response acjieved when: (a) no statistically significant dose-related increase in the mean number of revertant colonies per plate observed for the test compound and (b) in the absence of any such dose response, no increase in colony numbers is observed (at any test dose) which exceeds 2x the concurrent solvent control
Statistics:
An assessment of statistical significance was carried out using a one-tailed Student's t-test. The corresponding probabiltiy for each dose level was derived by computer using the appropriate degrees of freedom. Values of p,0.01 are treated as significant, with values 0.01,p,0.05 being indicative of a possible effect.

Results and discussion

Test resultsopen allclose all
Species / strain:
S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
Metabolic activation:
with and without
Genotoxicity:
positive
Cytotoxicity / choice of top concentrations:
cytotoxicity
Vehicle controls validity:
valid
Positive controls validity:
valid
Species / strain:
E. coli WP2
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
cytotoxicity
Vehicle controls validity:
valid
Positive controls validity:
valid
Species / strain:
E. coli WP2 uvr A
Metabolic activation:
with and without
Genotoxicity:
other: Slight effects
Cytotoxicity / choice of top concentrations:
cytotoxicity
Vehicle controls validity:
valid
Positive controls validity:
valid
Additional information on results:
Slight effects were observed in E. coli WP2P uvrA +S9 however they did not exceed 1.8x background in either of 2 experiments.
Remarks on result:
other: all strains/cell types tested
Remarks:
Migrated from field 'Test system'. Remarks: Positive in TA98 with and without metabolic activation. Also in TA1537 with metabolic activation

Applicant's summary and conclusion

Conclusions:
Interpretation of results (migrated information):
positive

DTBA gave a positive response in S. typhimurium strain TA98 in both the presence and absence of S9 and in strain TA1537 in the presence of S9. Slight effects were also observed in E. coli strain W2P2 uvrA in the presence of S9.