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EC number: 201-069-1 | CAS number: 77-92-9
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Genetic toxicity: in vitro
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:
- 1 984
- 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
- 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%
Constituent 1
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.
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