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EC number: 229-029-9 | CAS number: 6406-56-0
- 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
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- data from handbook or collection of data
- Justification for type of information:
- Data is from peer reviewed publication
Data source
Reference
- Reference Type:
- publication
- Title:
- Mutagenic activity of some textile dyes in different test systems
- Author:
- Barbara Przybojewska, Boguslaw Barariski, Ewa Spiechowicz and Krystyna Sitarek
- Year:
- 1 988
- Bibliographic source:
- Toxicology letters, 40 (1988) 183-192
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 471 (Bacterial Reverse Mutation Assay)
- Principles of method if other than guideline:
- Salmonella/microsome mammalian assay was performed to determine the mutagenic nature of Direct Red 81
- GLP compliance:
- not specified
- Type of assay:
- bacterial reverse mutation assay
Test material
- Reference substance name:
- Direct Red 81
- Cas Number:
- 2610-11-9
- Molecular formula:
- C29H19N5O8S2.2Na
- IUPAC Name:
- Direct Red 81
- Details on test material:
- - Name of test material: Direct Red 81
- IUPAC name: Direct Red 81
- Molecular formula: C29H19N5O8S2.2Na
- Molecular weight: 675.6081 g/mol
- Substance type: Organic
- Physical state: No data
- Purity: No data
- Impurities (identity and concentrations): 8.14% Cl
Constituent 1
- Specific details on test material used for the study:
- - Name of test material: Direct Red 81
- IUPAC name: Direct Red 81
- Molecular formula: C29H19N5O8S2.2Na
- Molecular weight: 675.6081 g/mol
- Substance type: Organic
- Physical state: No data
- Purity: No data
- Impurities (identity and concentrations): 8.14% Cl
Method
- Target gene:
- Histidine
Species / strain
- Species / strain / cell type:
- S. typhimurium, other: TA 1535, TA 1537, TA 1538, TA 98 and TA 100
- Details on mammalian cell type (if applicable):
- No data
- Additional strain / cell type characteristics:
- not specified
- Cytokinesis block (if used):
- No data
- Metabolic activation:
- with and without
- Metabolic activation system:
- S-9 mix was prepared from liver homogenate of rats treated with Aroclor 1254
- Test concentrations with justification for top dose:
- 0, 10, 100, 500 or 1000 µg/plate
- Vehicle / solvent:
- - Vehicle(s)/solvent(s) used: Aqua distilled
- Justification for choice of solvent/vehicle: The test chemical was soluble in Aqua distilled
Controls
- Untreated negative controls:
- not specified
- Negative solvent / vehicle controls:
- yes
- Remarks:
- Aqua distilled
- True negative controls:
- not specified
- Positive controls:
- yes
- Positive control substance:
- 9-aminoacridine
- sodium azide
- other: TA1538, TA98, +S9 - 2-Aminofluorene -S9 - 4-Nitro-o-phcnylenediamine / TA100, +S9 - 2-Aminofluorene
- Details on test system and experimental conditions:
- METHOD OF APPLICATION: in agar (plate incorporation)
DURATION
- Preincubation period: No data
- Exposure duration: 48 hrs
- Expression time (cells in growth medium): 48 hrs
- Selection time (if incubation with a selection agent): No data
- Fixation time (start of exposure up to fixation or harvest of cells): No data
SELECTION AGENT (mutation assays): No data
SPINDLE INHIBITOR (cytogenetic assays): No data
STAIN (for cytogenetic assays): No data
NUMBER OF REPLICATIONS: Duplicate
NUMBER OF CELLS EVALUATED: No data
DETERMINATION OF CYTOTOXICITY
- Method: mitotic index; cloning efficiency; relative total growth; other: Yes, cell growth was noted
OTHER EXAMINATIONS:
- Determination of polyploidy: No data
- Determination of endoreplication: No data
- Other: No data
OTHER: No data - Rationale for test conditions:
- No data
- Evaluation criteria:
- An investigated compound was judged to have induced a positive response when a dose-related increase in the number of revertants was observed and the number of revertants exceeded the negative control values by at least 2-foId in at least two successive concentrations of the test chemical.
- Statistics:
- Mean ± SD
Results and discussion
Test results
- Species / strain:
- S. typhimurium, other: TA 1535, TA 1537, TA 1538, TA 98 and TA 100
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- cytotoxicity
- Remarks:
- Toxicity was noted at 1000 µg/plate
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not specified
- Positive controls validity:
- valid
- Additional information on results:
- TEST-SPECIFIC CONFOUNDING FACTORS
- Effects of pH: No data
- Effects of osmolality: No data
- Evaporation from medium: No data
- Water solubility: No data
- Precipitation: No data
- Other confounding effects: No data
RANGE-FINDING/SCREENING STUDIES: The highest doses of the dyes in the Salmonella/microsome test were chosen after preliminary solubility study.
COMPARISON WITH HISTORICAL CONTROL DATA: No data
ADDITIONAL INFORMATION ON CYTOTOXICITY: No data - Remarks on result:
- other: No mutagenic potential
Any other information on results incl. tables
Table: Mutagenic response of Salmonella typhimurium mutants to Direct Red 81
Dose (µg/plate) |
TA1537 |
TA100 |
TA1537 |
TA1538 |
TA98 |
|||||
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
|
0 |
16 ± 7 |
12 ± 4 |
133 ± 14 |
118 ± 6 |
9 ± 3 |
12 ± 4 |
18 ± 4 |
27± 2 |
28 ± 5 |
39 ± 5 |
10 |
16 ± 3 |
13 ± 3 |
134 ± 13 |
129 ± 7 |
8 ± 2 |
10 ± 3 |
18 ± 3 |
24 ± 4 |
26 ± 4 |
32 ± 6 |
100 |
19 ± 8 |
10 ± 2 |
127 ± 19 |
145 ± 33 |
12 ± 7 |
10 ± 2 |
17 ± 3 |
28 ± 1 |
26 ± 1 |
30 ± 3 |
500 |
20±3 |
16 ± 2 |
148 ± 30 |
136 ± 25 |
9 ± 2 |
7 ± 1 |
19 ± 7 |
28 ± 4 |
20 ± 2 |
35 ± 2 |
1000 |
13 ± 5 |
9 ± 5 |
123 ± 12 |
128 ± 9 |
8 ± 4 |
10 ± 1 |
15 ± 5 |
22 ± 4 |
29 ± 5 |
33 ± 5 |
Table: Positive mutagen data
Strain |
S9 mix |
Compounds |
Dose level (µg/plate) |
His+ colonies/plate |
No. of spontaneous revertants/plate |
TA1535 |
- |
Sodium azide |
1.5 |
1080±172 |
19±5 |
TA1537 |
- |
9-Aminoacridine |
10 |
144±9 |
8±1 |
TA1538 |
- |
4-Nitro-o-phenylenediamine |
10 |
1374±82 |
16±4 |
+ |
2-Aminofluorene |
10 |
> 2000 |
21±7 |
|
TA98 |
- |
4-Nitro-o-phenylenediamine |
10 |
1014±118 |
21±1 |
+ |
2-Aminofluorene |
10 |
> 2000 |
23±4 |
|
TA100 |
- |
Sodium azide |
1.5 |
1452±165 |
119±16 |
+ |
2-aminofluorene |
10 |
> 2000 |
131±17 |
Applicant's summary and conclusion
- Conclusions:
- Direct Red 81 did not induce gene mutation in Salmonella typhimurium strains TA 1535, TA 1537, TA 1538, TA 98 and TA 100 in the presence and absence of S9 metabolic activation system and hence it is not likely to classify as a gene mutant.
- Executive summary:
Salmonella/microsome mammalian assay was performed to determine the mutagenic nature of Direct Red 81. The study was performed using Salmonella typhimurium strains TA 1535, TA 1537, TA 1538, TA 98 and TA 100 in the presence and absence of S9 metabolic activation system. The test chemical was dissolved in Aqua distilled and used at dose levels of 0, 10, 100, 500 or 1000µg/plate. The doses for the main study were decided on the basis of preliminary dose range finding study. The plates were incubated for 48 hrs at 37˚C. An investigated compound was judged to have induced a positive response when a dose-related increase in the number of revertants was observed and the number of revertants exceeded the negative control values by at least 2-foId in at least two successive concentrations of the test chemical. Direct Red 81 did not induce gene mutation in Salmonella typhimurium strains TA 1535, TA 1537, TA 1538, TA 98 and TA 100 in the presence and absence of S9 metabolic activation system and hence it is not likely to classify as a gene mutant.
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