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EC number: 280-960-7 | CAS number: 83817-60-1
- 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:
- key study
- Study period:
- 15 - 24 Aug 2016
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 016
- Report date:
- 2016
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 471 (Bacterial Reverse Mutation Assay)
- Version / remarks:
- 21 July 1997
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.13/14 (Mutagenicity - Reverse Mutation Test Using Bacteria)
- Version / remarks:
- 30 May 2008
- Deviations:
- not specified
- Qualifier:
- according to guideline
- Guideline:
- EPA OPPTS 870.5100 - Bacterial Reverse Mutation Test (August 1998)
- Version / remarks:
- Aug 1998
- Deviations:
- not specified
- Qualifier:
- according to guideline
- Guideline:
- other: ICH Guidance S2(R1): Guidance on Genotoxicity Testing and Data Interpretation for Pharmaceuticals Intended for Human Use
- Version / remarks:
- June 2012
- Deviations:
- not specified
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- OGYÉI, Országos Gyógyszerészeti és Élelmezés-egészségügyi Intézet, Budapest, Hungary
- Type of assay:
- bacterial reverse mutation assay
Test material
- Reference substance name:
- Ethyl 9-oxo-9H-thioxanthene-2-carboxylate
- EC Number:
- 280-960-7
- EC Name:
- Ethyl 9-oxo-9H-thioxanthene-2-carboxylate
- Cas Number:
- 83817-60-1
- Molecular formula:
- C16H12O3S
- IUPAC Name:
- ethyl 9-oxo-9H-thioxanthene-2-carboxylate
Constituent 1
- Specific details on test material used for the study:
- STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material as recommended by supplier: < 25 °C in a tighly closed container, protected from direct sunlight and heat
- Storage condition at the testing facility: at room temperature
Method
- Target gene:
- his operon, tryp operon
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 uvr A
- Metabolic activation:
- with and without
- Metabolic activation system:
- cofactor-supplemented post-mitochondrial fraction (S9 mix), prepared from the livers of rats, treated with phenobarbital and β-naphthoflavone
- Test concentrations with justification for top dose:
- Prior to the main experiments, a range-finder study was performed using the TA 98 and TA 100 strains with following test concentrations: 5, 16, 50, 160, 500, 1600 and 5000 µg/plate; testing was done in presence and absence of S9 mix. Precipitation was noticed at both, 1600 and 5000 µg/plate, in absence and presence of S9 mix; however, precipitation did not disturb the scoring at 1600 µg/plate. Therefore, 1600 µg/plate was selected as top concentration to be tested within the main experiments.
- Vehicle / solvent:
- - Vehicle(s)/solvent(s) used: DMSO
- Justification for choice of solvent/vehicle: Due to the good solubility of the test substance in DMSO and its compatibility with the bacteria and the S9 mix activity, DMSO was selected as the vehicle.
Controls
- Untreated negative controls:
- yes
- Remarks:
- untreated
- Negative solvent / vehicle controls:
- yes
- Remarks:
- DMSO
- True negative controls:
- no
- Positive controls:
- yes
- Positive control substance:
- 9-aminoacridine
- sodium azide
- methylmethanesulfonate
- other: 4-Nitro-1,2-phenylenediamine (NPD); 2-aminoanthracene (2AA)
- Details on test system and experimental conditions:
- METHOD OF APPLICATION: in agar (plate incorporation) (Range Finding Test and first experiment); preincubation (second, confirmatory experiment)
DURATION
- Preincubation period: 20 min
- Exposure duration: 48 h
NUMBER OF REPLICATIONS: triplicates each in two independent experiments
DETERMINATION OF CYTOTOXICITY
- Method: revertant colony number and inspection of the bacterial background lawn - Evaluation criteria:
- Acceptance criteria
The study was considered valid if:
- the phenotypes of the tester strains could be confirmed
- the number of revertant colonies of the negative (solvent) and positive controls were in the historical control range in all strains
- the tester strain culture titers are in the 10^9 cells/mL order
- the batch of S9 used in this study shows the appropriate biological activity
- the reference mutagens show an increase of at least: 3-fold in induced revertant colonies over the mean value of the respective vehicle control
- at least five analyzable concentrations were presented in all strains of the main tests (a minimum of three non-toxic dose levels is required to evaluate assay data)
Evaluation criteria
When the test substance shows a biologically relevant and dose-related increase in the number of revertant colonies of more than two times (TA 100) or three times (TA 98, TA 1535, TA 1537 and WP2 uvrA) compared to that of the solvent control, the response is judged to be positive. Additionally, the positive response should be reproducible for at least one of the dose groups and should occur in at least one strain with or without metabolic activation. The biological relevance of the results is the criterion for the interpretation of results, a statistical evaluation of the results is therefore not regarded as necessary.
The test item is considered to have no mutagenic activity in bacteria if it produces neither a dose-related increase in the number of revertants nor a reproducible biologically relevant positive response at any of the dose groups, with or without metabolic activation. - Statistics:
- Mean values and standard deviations were calculated.
Results and discussion
Test resultsopen allclose all
- Key result
- Species / strain:
- S. typhimurium TA 98
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity, but tested up to precipitating concentrations
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Key result
- Species / strain:
- S. typhimurium TA 100
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity, but tested up to precipitating concentrations
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Key result
- Species / strain:
- S. typhimurium TA 1535
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity, but tested up to precipitating concentrations
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Key result
- Species / strain:
- S. typhimurium TA 1537
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity, but tested up to precipitating concentrations
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Key result
- Species / strain:
- E. coli WP2 uvr A
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity, but tested up to precipitating concentrations
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Remarks on result:
- other: Precipitation occurred at 500 and 1600 µg/plate without S9 mix and at 1600 µg/plate with S9 Mix in both, the first and the second confirmatory experiment.
Any other information on results incl. tables
Table 1:Summary of test results (experiment 1; Initial Mutation Test, Plate Incorporation Method)
With or without S9-Mix |
Test substance concentration (μg/plate) |
Mean number of revertant colonies per plate |
||||
Frameshift type |
Base-pair substitution type |
|||||
TA1537 |
TA98 |
TA100 |
TA1535 |
WP2 uvrA |
||
– |
Solvent control (ultrapure water) |
- |
- |
102.7 ± 2.31 |
7.3 ± 1.15 |
17.7 ± 3.79 |
Solvent control (DMSO) |
5.3 ± 0.58 |
19.0 ± 1.73 |
85.7 ± 6.03 |
11.3 ± 4.04 |
17.0 ± 3.00 |
|
Untreated control |
6.7 ± 2.08 |
18.0 ± 1.00 |
104.0 ± 9.17 |
8.7 ± 5.13 |
20.0 ± 0.00 |
|
5 |
5.0 ± 1.00 |
15.7 ± 2.31 |
87.0 ± 5.57 |
11.0 ± 1.00 |
23.0 ± 4.36 |
|
16 |
5.3 ± 4.04 |
16.0 ± 3.46 |
84.3 ± 12.06 |
8.7 ± 4.93 |
25.0 ± 5.57 |
|
50 |
4.7 ± 0.58 |
16.3 ± 9.24 |
84.0 ± 13.00 |
13.7 ± 2.31 |
22.3 ± 2.52 |
|
160 |
5.3 ± 2.31 |
15.7 ± 4.51 |
81.3 ± 8.50 |
11.7 ± 2.08 |
28.7 ± 3.51 |
|
500 |
13.3 ± 1.15 P |
12.3 ± 3.21 P |
71.0 ± 7.94 P |
13.7 ± 0.58 P |
22.7 ± 1.53 P |
|
1600 |
6.7 ± 3.06 P |
17.3 ± 3.06 P |
77.7 ± 4.62 P |
12.3 ± 1.15 P |
24.3 ± 7.09 P |
|
Positive controls (unit/plate) |
9AA |
NPD |
SA |
SA |
MMS |
|
Mean No. of colonies/plate (average of 3 plates) |
750.0 ± 84.59 |
342.7 ± 26.10 |
1245.3 ± 185.44 |
672.0 ± 66.81 |
818.7 ± 118.68 |
|
+ |
Solvent control (DMSO) |
7.3 ± 3.06 |
21.7 ± 3.61 |
128.0 ± 18.33 |
14.0 ± 2.56 |
28.0 ± 2.00 |
Untreated control |
6.3 ± 1.53 |
21.7 ± 6.11 |
132.0 ± 11.14 |
12.3 ± 4.93 |
29.3 ± 4.16 |
|
5 |
8.3 ± 3.51 |
23.3 ± 2.89 |
124.0 ± 2.00 |
12.3 ± 3.51 |
26.7 ± 3.21 |
|
16 |
7.7 ± 3.06 |
27.0 ± 7.94 |
113.3 ± 3.06 |
13.3 ± 5.51 |
33.0 ± 4.58 |
|
50 |
9.0 ± 2.00 |
29.3 ± 3.51 |
108.0 ± 5.29 |
13.0 ± 1.73 |
28.7 ± 0.58 |
|
160 |
10.0 ± 4.58 |
24.3 ± 2.52 |
104.7 ± 6.43 |
15.0 ± 5.29 |
29.7 ± 4.16 |
|
500 |
9.0 ± 3.61 |
28.0 ± 4.36 |
116.0 ± 5.29 |
14.3 ± 2.52 |
24.3 ± 3.51 |
|
1600 |
4.3 ± 2.31 P |
30.0 ± 5.29 P |
128.7 ± 6.43 P |
14.3 ± 2.52 P |
34.0 ± 2.65 P |
|
Positive controls (µg/plate) |
2AA |
2AA |
2AA |
2AA |
2AA |
|
Mean No. of colonies/plate (average of 3 plates) |
110.0 ± 17.06 |
1512.0 ± 246.45 |
2200.0 ± 381.58 |
199.3 ± 37.65 |
234.0 ± 15.62 |
SD = standard deviation
9AA = 9-aminoacridine
NPD = 4-nitro-1,2-phenylene-diamine
SA = sodium azide
MMS = methylmethanesulfonate
2AA = 2-aminoanthracene
P = precipitate
Table 2: Summary of test results (experiment 2; Confirmatory Mutation Test, Pre-Incubation Method)
With or without S9-Mix |
Test substance (μg/plate) |
Mean number of revertant colonies per plate (average of 3 plates) |
||||
Frameshift type |
Base-pair substitution type |
|||||
TA1537 |
TA98 |
TA100 |
TA1535 |
WP2 uvrA |
||
– |
Solvent control (ultrapure water) |
- |
- |
93.3 ± 6.66 |
11.7 ± 3.79 |
28.3 ± 1.15 |
Solvent control (DMSO) |
8.0 ± 4.00 |
16.7 ± 0.58 |
78.0 ± 9.64 |
11.0 ± 3.00 |
24.3 ± 6.43 |
|
Untreated control |
8.0 ± 2.65 |
17.7 ± 9.07 |
90.3 ± 13.20 |
9.3 ± 2.52 |
19.3 ± 2.52 |
|
5 |
6.7 ± 4.51 |
25.0 ± 10.44 |
78.7 ± 11.72 |
9.7 ± 1.15 |
14.0 ± 4.00 |
|
16 |
8.3 ± 4.93 |
17.0 ± 2.65 |
78.7 ± 6.11 |
8.7 ± 4.73 |
16.0 ± 3.61 |
|
50 |
8.0 ± 2.65 |
15.3 ± 3.51 |
75.3 ± 4.16 |
11.3 ± 6.43 |
22.3 ± 6.51 |
|
160 |
8.0 ± 4.58 |
16.3 ± 3.06 |
82.0 ± 10.00 |
15.0 ± 2.00 |
15.7 ± 3.21 |
|
500 |
7.0 ± 5.20 P |
17.3 ± 5.51 P |
84.3 ± 10.12 P |
10.7 ± 1.53 P |
20.0 ± 5.29 P |
|
1600 |
8.3 ± 4.04 P |
18.7 ± 1.53 P |
86.7 ± 5.03 P |
15.0 ± 1.00 P |
31.7 ± 5.51 P |
|
Positive controls (unit/plate) |
9AA |
NPD |
SA |
SA |
MMS |
|
Mean No. of colonies/plate (average of 3 plates) |
356.0 ± 107.63 |
254.0 ± 40.60 |
1210.7 ± 122.46 |
965.3 ± 53.27 |
962.7 ± 158.86 |
|
+ |
Solvent control (DMSO) |
6.3 ± 3.06 |
27.7 ± 2.89 |
108.7 ± 17.62 |
13.3 ± 3.21 |
27.7 ± 4.04 |
Untreated control |
7.7 ± 4.93 |
28.7 ± 3.51 |
129.7 ± 8.96 |
11.7 ± 0.58 |
32.3 ± 4.51 |
|
5 |
6.7 ± 2.31 |
20.7 ± 8.02 |
100.0 ± 8.72 |
9.3 ± 2.89 |
28.7 ± 3.21 |
|
16 |
6.0 ± 2.65 |
19.7 ± 6.66 |
100.3 ± 8.14 |
12.0 ± 3.46 |
31.3 ± 3.51 |
|
50 |
5.3 ± 3.21 |
20.3 ± 6.11 |
100.7 ± 8.33 |
12.0 ± 4.58 |
35.0 ± 9.85 |
|
160 |
11.7 ± 1.53 |
17.7 ± 7.23 |
94.7 ± 5.03 |
15.0 ± 1.00 |
35.7 ± 2.52 |
|
500 |
8.3 ± 3.21 |
19.7 ± 5.13 |
108.0 ± 17.09 |
9.3 ± 4.04 |
33.3 ± 5.03 |
|
1600 |
5.0 ± 0.00 P |
22.3 ± 4.16 P |
126.7 ± 11.02 P |
14.7 ± 1.15 P |
36.7 ± 11.68 P |
|
Positive controls (µg/plate) |
2AA |
2AA |
2AA |
2AA |
2AA |
|
Mean No. of colonies/plate (average of 3 plates) |
164.7 ± 9.02 |
1117.3 ± 120.09 |
1114.7 ± 360.65 |
138.0 ± 7.81 |
170.3 ± 15.57 |
SD = standard deviation
9AA = 9-aminoacridine
NPD = 4-nitro-1,2-phenylene-diamine
SA = sodium azide
MMS = methylmethanesulfonate
2AA = 2-aminoanthracene
P = precipitate
Applicant's summary and conclusion
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