Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Currently viewing:

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:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: The tests were conducted to generally acceptable scientific standards, with acceptable restrictions, i.e. no mention of cytotoxic concentrations and positive controls; no appropriate 5th strain

Data source

Reference
Reference Type:
publication
Title:
Primary Mutagenicity Screening of Food Additives Currently Used in Japan.
Author:
Ishidate M J R, Sofuni T, Yoshikawa M, Hayashi T, Noshmi T, Sawada M, Matsuoka A
Year:
1984
Bibliographic source:
Fd Chem Toxic 22(8): 623-636

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 471 (Bacterial Reverse Mutation Assay)
Deviations:
yes
Remarks:
specific positive controls not included; no appropriate 5th strain included
GLP compliance:
not specified
Type of assay:
bacterial reverse mutation assay

Test material

Constituent 1
Chemical structure
Reference substance name:
Citric acid
EC Number:
201-069-1
EC Name:
Citric acid
Cas Number:
77-92-9
Molecular formula:
C6H8O7
IUPAC Name:
2-hydroxypropane-1,2,3-tricarboxylic acid
Details on test material:
- Name of test material (as cited in study report): citric acid
- Substance type: single component substance
- Analytical purity: 99.9%

Method

Target gene:
histidine operon
Species / strain
Species / strain / cell type:
S. typhimurium, other: TA 1535, TA 100, TA 98, TA 1537, TA92 and TA 94
Metabolic activation:
with and without
Metabolic activation system:
polychlorinated biphenyl induced rat liver S9
Test concentrations with justification for top dose:
Up to 5000 µg/plate
Vehicle / solvent:
- Vehicle(s)/solvent(s) used: phosphate buffer
- Justification for choice of solvent/vehicle: sample soluble in water
Controls
Untreated negative controls:
no
Negative solvent / vehicle controls:
other: control was exposed to appropriate solvent or untreated
True negative controls:
no
Positive controls:
other: specific controls not tested, but positive results obtained with some test substances screened
Positive control substance:
other: include Fast Green FCF (with activation), L cysteine monohydrochloride (with and without activation)
Details on test system and experimental conditions:
METHOD OF APPLICATION: preincubation

DURATION
- Preincubation period: 20 min
- Exposure duration: 48 hours
- Fixation time (start of exposure up to fixation or harvest of cells): 48 hours

NUMBER OF REPLICATIONS: duplicate plates were used

DETERMINATION OF CYTOTOXICITY
- Method: other: not described
Evaluation criteria:
The result was considered positive if the number of colonies found was twice the number in the control (exposed to the appropriate solvent or untreated). If no reasonable dose-response was found, the experiment was repeated using different doses.
Statistics:
No statistical analysis is described.

Results and discussion

Test resultsopen allclose all
Key result
Species / strain:
S. typhimurium TA 1535
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not specified
Vehicle controls validity:
not specified
Untreated negative controls validity:
not specified
Positive controls validity:
other: positive results were obtained with some substances tested
Key result
Species / strain:
S. typhimurium TA 1537
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not specified
Vehicle controls validity:
not specified
Untreated negative controls validity:
not specified
Positive controls validity:
other: positive results were obtained with some substances tested
Key result
Species / strain:
S. typhimurium TA 100
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not specified
Vehicle controls validity:
not specified
Untreated negative controls validity:
not specified
Positive controls validity:
other: positive results were obtained with some substances tested
Key result
Species / strain:
S. typhimurium TA 98
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not specified
Vehicle controls validity:
not specified
Untreated negative controls validity:
not specified
Positive controls validity:
other: positive results were obtained with some substances tested
Key result
Species / strain:
S. typhimurium, other: TA 92
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not specified
Vehicle controls validity:
not specified
Untreated negative controls validity:
not specified
Positive controls validity:
other: positive results were obtained with some substances tested
Key result
Species / strain:
S. typhimurium, other: TA 94
Metabolic activation:
with and without
Genotoxicity:
negative
Cytotoxicity / choice of top concentrations:
not specified
Vehicle controls validity:
not specified
Untreated negative controls validity:
not specified
Positive controls validity:
other: positive results were obtained with some substances tested

Applicant's summary and conclusion

Conclusions:
Citric acid has been tested in a bacterial reverse mutation assay conducted according to a protocol similar to OECD Test Guideline 471. No significant increase in the number of revertant colonies was detected in any Salmonella typhimurium strains TA 1535, TA 1537, TA98, TA 100, TA 92 and TA 94 at the maximum dose, using the preincubation method with and without metabolic activation. It is concluded that citric acid is negative for mutagenicity to bacteria under the conditions of this test.