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EC number: 257-269-4 | CAS number: 51548-48-2
- 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:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Data is from peer reviewed publication
Data source
Reference
- Reference Type:
- publication
- Title:
- Mutagenicity testing of some commonly used dyes.
- Author:
- K T Chung, G E Fulk and A W Andrews
- Year:
- 1 981
- Bibliographic source:
- APPLIED AND ENVIRONMENTAL MICROBIOLOGY, Oct. 1981, p. 641-648
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other:
- Principles of method if other than guideline:
- Gene mutation toxicity study was performed to evaluate the mutagenic response for the test chemical sodium 4-aminonaphthalene-1-sulphonate.
- GLP compliance:
- not specified
- Type of assay:
- bacterial reverse mutation assay
Test material
- Reference substance name:
- Sodium 4-aminonaphthalene-1-sulphonate
- EC Number:
- 204-975-5
- EC Name:
- Sodium 4-aminonaphthalene-1-sulphonate
- Cas Number:
- 130-13-2
- IUPAC Name:
- sodium 4-aminonaphthalene-1-sulfonate
- Details on test material:
- CAS number: 130-13-2
Chemical Name: sodium 4-aminonaphthalene-1-sulphonate
Molecular formula: C10H9NO3S.Na
Molecular weight: 245.233 g/mol
Substance type: Organic
Smiles: c12c(c(ccc1S(=O)(=O)[O-])N)cccc2.[Na+]
Constituent 1
Method
- Target gene:
- No data
Species / strainopen allclose all
- Species / strain / cell type:
- S. typhimurium TA 1538
- Details on mammalian cell type (if applicable):
- Not applicable
- Additional strain / cell type characteristics:
- not specified
- Species / strain / cell type:
- S. typhimurium TA 98
- Details on mammalian cell type (if applicable):
- Not applicable
- Additional strain / cell type characteristics:
- not specified
- Species / strain / cell type:
- S. typhimurium TA 100
- Details on mammalian cell type (if applicable):
- Not applicable
- Additional strain / cell type characteristics:
- not specified
- Metabolic activation:
- with and without
- Metabolic activation system:
- rat Aroclor S9 mix
- Test concentrations with justification for top dose:
- 5, 10, 25, 50, 100, 250, 500, 1000, 2500, 5000 µg
- Vehicle / solvent:
- No data
Controls
- Untreated negative controls:
- not specified
- Negative solvent / vehicle controls:
- not specified
- True negative controls:
- not specified
- Positive controls:
- yes
- Positive control substance:
- 2-nitrofluorene
- sodium azide
- other: Dimethyl sulfoxide,2-Aminoanthracene
- Details on test system and experimental conditions:
- The Salmonella typhimurium tester strains TA1535, TA1537, TA1538, TA98,and TA100 were grown in nutrient broth shaken for 14 h at 370C. The plate incorporation assays were performed as described by Ames with the modifications of Andrews. The liquid preincubation assays (1, 21) were timed for 30 min at 37°C in a Dri-block. The revertant colonies were counted by using a hand-held tally. Dimethyl sulfoxide was the solvent, except sterile distilled water was the solvent when sulfanilic acid was used. Liver homogenates (S9) were prepared from male Sprague-Dawley rats stimulated with Aroclor 1254 (500 mg/kg intraperitoneally 5 days before sacrifice). The S9 mix, added in samples of 0.5 ml per plate, contained 3 mg of protein, determined by the method of Lowry et al. (16). The positive control chemicals sodium azide, 9-aminoacridine, 2-nitrofluorene, and 2-aminoanthracene were used with the tester strains. The dose-response curves for the mutagenic compounds used the tester strain which showed maximum mutagenicity and covered a range of 1 to 1,000 or 5 to 5,000 tig. Mutagenic compounds were assayed by using duplicate plates in at least two independent dose-response curves; the mean values of representative curves are used in the table. A compound was considered mutagenic when the number of revertants above background was at least twice the value of the historical control mean or twice the value of the current control mean, whichever was greater,and a dose-response curve could be demonstrated
- Evaluation criteria:
- An increase in the number of revertnats was counted
- Statistics:
- No data
Results and discussion
Test resultsopen allclose all
- Species / strain:
- S. typhimurium TA 1538
- 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:
- valid
- 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:
- valid
- 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:
- valid
- Additional information on results:
- No data
- Remarks on result:
- other: all strains/cell types tested
- Remarks:
- Migrated from field 'Test system'.
Applicant's summary and conclusion
- Conclusions:
- Interpretation of results (migrated information):
negative with and without
Maximum nontoxic dose of test substance sodium 4-aminonaphthalene-1-sulphonate was tested that was nonmutagenic in TA1535, TA1537, TA1538, TA98,or TA100 with and without male rat Aroclor S9 mix. - Executive summary:
Gene mutation toxicity study was performed to evaluate the mutagenic response for the test chemical sodium 4-aminonaphthalene-1-sulphonate. The study was performed using Salmonella typhimurium strains TA1537, TA1538, TA98,or TA100 with and without S9 metabolic activation system at dose levels of 5, 10, 25, 50, 100, 250, 500, 1000, 2500, 5000 µg.
Maximum nontoxic dose of test substance sodium 4-aminonaphthalene-1-sulphonate was tested that was nonmutagenic TA1537, TA1538, TA98,or TA100 with and without male rat Aroclor S9 mix. Thus, the test compound is not likely to be gene mutant in vitro.
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