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EC number: 947-264-1 | CAS number: -
- 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
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- 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:
- 31 July - 15 September 2017
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Remarks:
- GLP study conducted according to OECD Guideline 471 without any deviation
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 017
- Report date:
- 2017
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 471 (Bacterial Reverse Mutation Assay)
- Version / remarks:
- dated 21 July 1997
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.13/14 (Mutagenicity - Reverse Mutation Test Using Bacteria)
- Version / remarks:
- dated 30 May 2008
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EPA OPPTS 870.5100 - Bacterial Reverse Mutation Test (August 1998)
- Version / remarks:
- August 1998
- Deviations:
- no
- Principles of method if other than guideline:
- Not applicable
- GLP compliance:
- yes (incl. QA statement)
- Remarks:
- 28 October 2016
- Type of assay:
- bacterial reverse mutation assay
Test material
- Reference substance name:
- Benzoic acid
- EC Number:
- 200-618-2
- EC Name:
- Benzoic acid
- Cas Number:
- 65-85-0
- Molecular formula:
- C7H6O2
- IUPAC Name:
- benzoic acid
- Reference substance name:
- Benzyl benzoate
- EC Number:
- 204-402-9
- EC Name:
- Benzyl benzoate
- Cas Number:
- 120-51-4
- Molecular formula:
- C14H12O2
- IUPAC Name:
- benzyl benzoate
- Reference substance name:
- Benzyl cinnamate
- EC Number:
- 203-109-3
- EC Name:
- Benzyl cinnamate
- Cas Number:
- 103-41-3
- Molecular formula:
- C16H14O2
- IUPAC Name:
- benzyl-3-phenylprop-2-enoate
- Reference substance name:
- trans-cinnamic acid
- EC Number:
- 205-398-1
- EC Name:
- trans-cinnamic acid
- Cas Number:
- 140-10-3
- Molecular formula:
- C9H8O2
- IUPAC Name:
- (2E)-3-phenylprop-2-enoic acid
- Reference substance name:
- 3,7,11-trimethyldodeca-1,6,10-trien-3-ol,mixed isomers
- EC Number:
- 230-597-5
- EC Name:
- 3,7,11-trimethyldodeca-1,6,10-trien-3-ol,mixed isomers
- Cas Number:
- 7212-44-4
- Molecular formula:
- C15H26O
- IUPAC Name:
- 3,7,11-trimethyldodeca-1,6,10-trien-3-ol
- Reference substance name:
- Vanillin
- EC Number:
- 204-465-2
- EC Name:
- Vanillin
- Cas Number:
- 121-33-5
- Molecular formula:
- C8H8O3
- IUPAC Name:
- 4-hydroxy-3-methoxybenzaldehyde
- Test material form:
- liquid
- Details on test material:
- Appearance: Pale yellow to amber-orange viscous liquid
Manufacturing date: July 2017
Expiry date: July 2020
Constituent 1
Constituent 2
Constituent 3
Constituent 4
Constituent 5
Constituent 6
- Specific details on test material used for the study:
- STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material: Room temperature in the dark
TREATMENT OF TEST MATERIAL PRIOR TO TESTING
- The test item was briefly vortexed before being accurately weighed and, on the day of each experiment, approximate half-log dilutions prepared in dimethyl sulphoxide by mixing on a vortex mixer. No correction was required for purity allowance. Prior to use, the solvent was dried to remove water using molecular sieves i.e. 2 mm sodium alumino-silicate pellets with a nominal pore diameter of 4 x 10^-4 microns. All formulations were used within four hours of preparation and were assumed to be stable for this period.
Method
- Target gene:
- histidine locus for Salmonella strains and tryptophan for E. coli strain
Species / strain
- Species / strain / cell type:
- S. typhimurium TA 1535, TA 1537, TA 98, TA 100 and E. coli WP2
- Details on mammalian cell type (if applicable):
- Not applicable
- Additional strain / cell type characteristics:
- not applicable
- Cytokinesis block (if used):
- Not applicable
- Metabolic activation:
- with and without
- Metabolic activation system:
- rat liver homogenate metabolizing system (10% liver S9 in standard co-factors)
- Test concentrations with justification for top dose:
- Experiment 1 - Plate Incorporation Method: 1.5, 5, 15, 50, 150, 500, 1500 and 5000 µg/plate, with and without S9-mix
Experiment 2 - Pre-Incubation Method: 15, 50, 150, 500, 1500 and 5000 µg/plate, with and without S9-mix - Vehicle / solvent:
- - Vehicle(s)/solvent(s) used: Dimethyl sulphoxide
- Justification for choice of solvent/vehicle: The test item was immiscible in sterile distilled water at 50 mg/mL but was fully miscible in dimethyl sulphoxide at the same concentration in solubility checks performed in-house. Dimethyl sulphoxide was therefore selected as the vehicle.
Controlsopen allclose all
- Untreated negative controls:
- yes
- Remarks:
- untreated
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Positive control substance:
- 4-nitroquinoline-N-oxide
- 9-aminoacridine
- N-ethyl-N-nitro-N-nitrosoguanidine
- Remarks:
- without metabolic activation
- Untreated negative controls:
- yes
- Remarks:
- untreated
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Positive control substance:
- benzo(a)pyrene
- other: 2-Aminoanthracene
- Remarks:
- with metabolic activation
- Details on test system and experimental conditions:
- SOURCE OF TEST SYSTEM: The bacteria used in the test were obtained from:
- University of California, Berkeley, on culture discs, on 04 August 1995
- British Industrial Biological Research Association, on a nutrient agar plate, on 17 August 1987
METHOD OF APPLICATION: in agar (plate incorporation) and preincubation
DURATION
- Preincubation period: 20 minutes in Experiment 2.
- Exposure duration: ca. 48 hours
CONTROLS:
- Vehicle/solvent control: Dimethyl sulphoxide; performed in triplicate
- Negative (untreated) controls were performed to assess the spontaneous revertant colony rate; performed in triplicate
- Positive control items used demonstrated a direct and indirect acting mutagenic effect depending on the presence or absence of metabolic activation; performed in triplicate
- Sterility controls were performed in triplicate as follows:
Top agar and histidine/biotin or tryptophan in the absence of S9-mix;
Top agar and histidine/biotin or tryptophan in the presence of S9-mix; and
The maximum dosing solution of the test item in the absence of S9-mix only (test in singular only).
NUMBER OF REPLICATIONS: Triplicate
- OTHER: All of the plates were incubated at 37 ± 3 °C for approximately 48 hours and scored for the presence of revertant colonies using an automated colony counting system. The plates were viewed microscopically for evidence of thinning (toxicity). Several manual counts were required due to revertant colonies spreading slightly, thus distorting the actual plate count. - Rationale for test conditions:
- The dose range for Experiment 1 was predetermined and was 1.5 to 5000 µg/plate (i.e. maximum recommended dose level). The experiment was repeated on a separate day (pre-incubation method) using fresh cultures of the bacterial strains and fresh test item formulations. The dose range was amended, following the results of Experiment 1, and was 15 to 5000 µg/plate. Six test item dose levels per bacterial strain were selected in the second mutation test in order to achieve both a minimum of four non-toxic dose levels and the potential toxic limit of the test item following the change in test methodology from plate incorporation to pre-incubation.
- Evaluation criteria:
- Criteria for determining a positive result:
- A dose-related increase in mutant frequency over the dose range tested (De Serres and Shelby, 1979).
- A reproducible increase at one or more concentrations.
- Biological relevance against in-house historical control ranges.
- Fold increase greater than two times the concurrent solvent control for any tester strain (especially if accompanied by an out of historical range response (Cariello and Piegorsch, 1996)).
A test item will be considered non-mutagenic (negative) in the test system if the above criteria are not met.
Although most experiments will give clear positive or negative results, in some instances the data generated will prohibit making a definite judgment about test item activity. Results of this type will be reported as equivocal. - Statistics:
- None
Results and discussion
Test results
- Key result
- Species / strain:
- other: S. typhimurium TA 1535, TA 1537, TA 98, TA 100 and E. coli WP2
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- cytotoxicity
- Remarks:
- refer Tables 7.6.1/1 to 7.6.1/5
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Additional information on results:
- TEST-SPECIFIC CONFOUNDING FACTORS
- Precipitation: A test item precipitate (white and particulate in appearance) was noted at 5000 μg/plate, this observation did not prevent the scoring of revertant colonies.
MUTAGENICITY
- The vehicle (dimethyl sulphoxide) control plates gave counts of revertant colonies within the normal range. All of the positive control chemicals used in the test induced marked increases in the frequency of revertant colonies, both with or without metabolic activation. Thus, the sensitivity of the assay and the efficacy of the S9-mix were validated.
- In the first mutation test (plate incorporation method), there was no visible reduction in the growth of the bacterial background lawn at any dose level, either in the presence or absence of metabolic activation (S9-mix), and consequently the same maximum dose level was used in the second mutation test. In the second mutation test (pre-incubation method), the test item induced a toxic response with weakened bacterial background lawns and/or reductions in revertant colony frequency noted to all of the Salmonella strains noted at 5000 μg/plate in both the absence and presence of S9-mix. No toxicity was noted to Escherichia coli strain WP2uvrA at any test item dose level. The sensitivity of the bacterial tester strains to the toxicity of the test item varied slightly between strain type, exposures with or without S9-mix and experimental methodology.
- No increases in the frequency of revertant colonies were recorded for any of the bacterial strains, with any dose of the test item, either with or without metabolic activation (S9-mix) in Experiment 1 (plate incorporation method) and in Experiment 2 (pre incubation method).
- Refer Tables 7.6.1/1 to 7.6.1/5 for more details.
HISTORICAL CONTROL DATA (with ranges, means and standard deviation and confidence interval (e.g. 95%)
- Positive historical control data: Refer Table 7.6.1/6
- Negative (solvent/vehicle) historical control data: Refer Table 7.6.1/6
OTHERS:
- Prior to use, the master strains were checked for characteristics, viability and spontaneous reversion rate (all were found to be satisfactory). The amino acid supplemented top agar and the S9-mix used in both experiments was shown to be sterile. The test item formulation was also shown to be sterile.
- Results for the negative controls (spontaneous mutation rates) are presented in 7.6.1/1 and were considered to be acceptable. These data are for concurrent untreated control plates performed on the same day as the Mutation Test.
Any other information on results incl. tables
Table 7.6.1/1:Spontaneous Mutation Rates (Concurrent Negative Controls)
Number of revertants (mean number of colonies per plate) |
|||||||||
Base-pair substitution type |
Frameshift type |
||||||||
Experiment 1 |
|||||||||
TA100 |
TA1535 |
WP2uvrA |
TA98 |
TA1537 |
|||||
82 |
|
24 |
|
32 |
|
34 |
|
15 |
|
88 |
(90) |
31 |
(27) |
38 |
(37) |
29 |
(31) |
14 |
(16) |
99 |
|
27 |
|
40 |
|
29 |
|
18 |
|
Experiment 2 |
|||||||||
TA100 |
TA1535 |
WP2uvrA |
TA98 |
TA1537 |
|||||
106 |
|
21 |
|
14 |
|
28 |
|
9 |
|
110 |
(104) |
16 |
(18) |
23 |
(16) |
33 |
(28) |
16 |
(14) |
95 |
|
16 |
|
11 |
|
24 |
|
18 |
|
Table 7.6.1/2:Test Results: Experiment 1 – Without Metabolic Activation
Test Period |
From: 05 September 2017 |
To: 08 September 2017 |
||||||||||
S9-Mix (-) |
Dose Level Per Plate |
Number of revertants (mean) +/- SD |
||||||||||
Base-pair substitution strains |
Frameshift strains |
|||||||||||
TA100 |
TA1535 |
WP2uvrA |
TA98 |
TA1537 |
||||||||
Solvent Control (DMSO) |
71 80 87 |
(79) 8.0# |
23 21 22 |
(22) 1.0 |
31 25 27 |
(28) 3.1 |
30 39 34 |
(34) 4.5 |
22 17 17 |
(19) 2.9 |
||
1.5 µg |
72 95 74 |
(80) 12.7 |
26 31 25 |
(27) 3.2 |
18 34 30 |
(27) 8.3 |
32 22 32 |
(29) 5.8 |
13 26 12 |
(17) 7.8 |
||
5 µg |
91 96 73 |
(87) 12.1 |
22 23 20 |
(22) 1.5 |
24 22 31 |
(26) 4.7 |
26 27 24 |
(26) 1.5 |
23 25 20 |
(23) 2.5 |
||
15 µg |
69 81 78 |
(76) 6.2 |
28 22 33 |
(28) 5.5 |
37 23 19 |
(26) 9.5 |
39 26 31 |
(32) 6.6 |
22 15 20 |
(19) 3.6 |
||
50 µg |
93 85 96 |
(91) 5.7 |
21 21 25 |
(22) 2.3 |
27 31 29 |
(29) 2.0 |
29 31 28 |
(29) 1.5 |
13 19 18 |
(17) 3.2 |
||
150 µg |
101 79 88 |
(89) 11.1 |
23 28 22 |
(24) 3.2 |
35 18 33 |
(29) 9.3 |
31 32 18 |
(27) 7.8 |
14 15 15 |
(15) 0.6 |
||
500 µg |
80 69 84 |
(78) 7.8 |
28 26 22 |
(25) 3.1 |
27 20 37 |
(28) 8.5 |
22 28 25 |
(25) 3.0 |
15 19 20 |
(18) 2.6 |
||
1500 µg |
90 75 71 |
(79) 10.0 |
28 26 27 |
(27) 1.0 |
28 18 29 |
(25) 6.1 |
20 19 22 |
(20) 1.5 |
21 19 19 |
(20) 1.2 |
||
5000 µg |
67 P 72 P 99 P |
(79) 17.2 |
28 P 23 P 27 P |
(26) 2.6 |
20 P 20 P 24 P |
(21) 2.3 |
25 P 18 P 28 P |
(24) 5.1 |
10 P 5 P 10 P |
(8) 2.9 |
||
Positive controls S9-Mix (-) |
Name Dose Level No. of Revertants |
ENNG |
ENNG |
ENNG |
4NQO |
9AA |
||||||
3 µg |
5 µg |
2 µg |
0.2 µg |
80 µg |
||||||||
575 599 616 |
(597) 20.6 |
714 788 846 |
(783) 66.2 |
606 572 579 |
(586) 18.0 |
248 235 234 |
(239) 7.8 |
442 429 467 |
(446) 19.3 |
|||
ENNG:N-ethyl-N'-nitro-N-nitrosoguanidine
4NQO:4-Nitroquinoline-1-oxide
9AA: 9-Aminoacridine
P: Test ítem precipitate
#: Standard deviation
Table 7.6.1/3:Test Results: Experiment 1 – With Metabolic Activation
Test Period |
From: 05 September 2017 |
To: 08 September 2017 |
||||||||||
S9-Mix (+) |
Dose Level Per Plate |
Number of revertants (mean) +/- SD |
||||||||||
Base-pair substitution strains |
Frameshift strains |
|||||||||||
TA100 |
TA1535 |
WP2uvrA |
TA98 |
TA1537 |
||||||||
Solvent Control (DMSO) |
63 75 72 |
(70) 6.2# |
19 17 29 |
(22) 6.4 |
30 20 29 |
(26) 5.5 |
21 19 20 |
(20) 1.0 |
15 15 22 |
(17) 4.0 |
||
1.5 µg |
68 68 76 |
(71) 4.6 |
26 25 27 |
(26) 1.0 |
35 31 27 |
(31) 4.0 |
19 22 22 |
(21) 1.7 |
16 22 21 |
(20) 3.2 |
||
5 µg |
68 79 60 |
(69) 9.5 |
22 25 24 |
(24) 1.5 |
35 29 31 |
(32) 3.1 |
22 29 29 |
(27) 4.0 |
10 13 14 |
(12) 2.1 |
||
15 µg |
76 75 80 |
(77) 2.6 |
19 21 16 |
(19) 2.5 |
37 32 39 |
(36) 3.6 |
34 19 28 |
(27) 7.5 |
11 22 19 |
(17) 5.7 |
||
50 µg |
84 74 88 |
(82) 7.2 |
20 24 24 |
(23) 2.3 |
38 25 30 |
(31) 6.6 |
39 17 40 |
(32) 13.0 |
21 21 23 |
(22) 1.2 |
||
150 µg |
71 83 94 |
(83) 11.5 |
14 25 26 |
(22) 6.7 |
25 25 39 |
(30) 8.1 |
26 19 27 |
(24) 4.4 |
17 15 7 |
(13) 5.3 |
||
500 µg |
92 94 97 |
(94) 2.5 |
27 32 28 |
(29) 2.6 |
27 35 39 |
(34) 6.1 |
25 26 39 |
(30) 7.8 |
16 21 10 |
(16) 5.5 |
||
1500 µg |
80 80 81 |
(80) 0.6 |
19 20 21 |
(20) 1.0 |
35 25 28 |
(29) 5.1 |
25 18 30 |
(24) 6.0 |
10 17 26 |
(18) 8.0 |
||
5000 µg |
69 P 66 P 64 P |
(66) 2.5 |
22 P 19 P 23 P |
(21) 2.1 |
27 P 39 P 23 P |
(30) 8.3 |
32 P 27 P 25 P |
(28) 3.6 |
20 P 12 P 15 P |
(16) 4.0 |
||
Positive controls S9-Mix (+) |
Name Dose Level No. of Revertants |
2AA |
2AA |
2AA |
BP |
2AA |
||||||
1 µg |
2 µg |
10 µg |
5 µg |
2 µg |
||||||||
1882 1877 2019 |
(1926) 80.6 |
291 294 350 |
(312) 33.2 |
320 314 289 |
(308) 16.4 |
228 215 277 |
(240) 32.7 |
412 401 365 |
(393) 24.6 |
|||
2AA: 2-Aminoanthracene
BP: Benzo(a)pyrene
P: Test ítem precipitate
#: Standard deviation
Table 7.6.1/4:Test Results: Experiment 2 – Without Metabolic Activation
Test Period |
From: 12 September 2017 |
To: 15 September 2017 |
||||||||||
S9-Mix (-) |
Dose Level Per Plate |
Number of revertants (mean) +/- SD |
||||||||||
Base-pair substitution strains |
Frameshift strains |
|||||||||||
TA100 |
TA1535 |
WP2uvrA |
TA98 |
TA1537 |
||||||||
Solvent Control (DMSO) |
83 97 90 |
(90) 7.0# |
14 19 21 |
(18) 3.6 |
21 23 18 |
(21) 2.5 |
29 27 34 |
(30) 3.6 |
15 17 14 |
(15) 1.5 |
||
15 µg |
79 103 106 |
(96) 14.8 |
17 19 17 |
(18) 1.2 |
17 12 23 |
(17) 5.5 |
32 22 24 |
(26) 5.3 |
19 16 13 |
(16) 3.0 |
||
50 µg |
95 99 104 |
(99) 4.5 |
18 20 21 |
(20) 1.5 |
10 16 14 |
(13) 3.1 |
18 19 31 |
(23) 7.2 |
14 11 9 |
(11) 2.5 |
||
150 µg |
99 101 99 |
(100) 1.2 |
14 16 17 |
(16) 1.5 |
18 20 22 |
(20) 2.0 |
28 12 25 |
(22) 8.5 |
13 10 9 |
(11) 2.1 |
||
500 µg |
75 90 80 |
(82) 7.6 |
19 21 20 |
(20) 1.0 |
18 28 22 |
(23) 5.0 |
11 20 14 |
(15) 4.6 |
12 13 14 |
(13) 1.0 |
||
1500 µg |
73 110 71 |
(85) 22.0 |
19 22 14 |
(18) 4.0 |
22 13 16 |
(17) 4.6 |
12 13 15 |
(13) 1.5 |
17 4 8 |
(10) 6.7 |
||
5000 µg |
57 SP 54 SP 50 SP |
(54) 3.5 |
12 SP 14 SP 15 SP |
(14) 1.5 |
11 P 19 P 19 P |
(16) 4.6 |
6 P 20 P 12 P |
(13) 7.0 |
6 SP 4 SP 2 SP |
(4) 2.0 |
||
Positive controls S9-Mix (-) |
Name Dose Level No. of Revertants |
ENNG |
ENNG |
ENNG |
4NQO |
9AA |
||||||
3 µg |
5 µg |
2 µg |
0.2 µg |
80 µg |
||||||||
1561 1362 1253 |
(1392) 156.2 |
1423 1133 1506 |
(1354) 195.8 |
776 793 785 |
(785) 8.5 |
350 382 341 |
(358) 21.5 |
501 318 293 |
(371) 113.6 |
|||
ENNG:N-ethyl-N'-nitro-N-nitrosoguanidine
4 NQO:4-Nitroquinoline-1-oxide
9AA: 9-Aminoacridine
P: Precipitate
S: Sparse bacterial background lawn
#: Standard deviation
Table 7.6.1/5:Test Results: Experiment 2 – With Metabolic Activation
Test Period |
From: 12 September 2017 |
To: 15 September 2017 |
||||||||||
S9-Mix (+) |
Dose Level Per Plate |
Number of revertants (mean) +/- SD |
||||||||||
Base-pair substitution strains |
Frameshift strains |
|||||||||||
TA100 |
TA1535 |
WP2uvrA |
TA98 |
TA1537 |
||||||||
Solvent Control (DMSO) |
74 102 94 |
(90) 14.4# |
27 19 20 |
(22) 4.4 |
19 25 26 |
(23) 3.8 |
28 39 28 |
(32) 6.4 |
18 12 16 |
(15) 3.1 |
||
15 µg |
84 81 99 |
(88) 9.6 |
27 17 19 |
(21) 5.3 |
26 32 17 |
(25) 7.5 |
28 32 25 |
(28) 3.5 |
16 13 18 |
(16) 2.5 |
||
50 µg |
93 81 79 |
(84) 7.6 |
26 20 21 |
(22) 3.2 |
21 18 17 |
(19) 2.1 |
27 29 28 |
(28) 1.0 |
12 12 14 |
(13) 1.2 |
||
150 µg |
84 90 96 |
(90) 6.0 |
24 19 21 |
(21) 2.5 |
20 24 22 |
(22) 2.0 |
28 25 29 |
(27) 2.1 |
14 13 9 |
(12) 2.6 |
||
500 µg |
84 91 89 |
(88) 3.6 |
22 21 19 |
(21) 1.5 |
24 18 20 |
(21) 3.1 |
28 31 27 |
(29) 2.1 |
14 22 17 |
(18) 4.0 |
||
1500 µg |
79 72 82 |
(78) 5.1 |
20 22 17 |
(20) 2.5 |
22 27 22 |
(24) 2.9 |
27 23 29 |
(26) 3.1 |
14 18 18 |
(17) 2.3 |
||
5000 µg |
54 SP 55 SP 55 SP |
(55) 0.6 |
14 SP 17 SP 9 SP |
(13) 4.0 |
26 P 18 P 26 P |
(23) 4.6 |
7 SP 13 SP 13 SP |
(11) 3.5 |
7 SP 0 SP 4 SP |
(4) 3.5 |
||
Positive controls S9-Mix (+) |
Name Dose Level No. of Revertants |
2AA |
2AA |
2AA |
BP |
2AA |
||||||
1 µg |
2 µg |
10 µg |
5 µg |
2 µg |
||||||||
1540 1631 1545 |
(1572) 51.2 |
235 258 284 |
(259) 24.5 |
376 385 385 |
(382) 5.2 |
187 247 248 |
(227) 34.9 |
487 518 469 |
(491)24.8 |
|||
2AA: 2-Aminoanthracene
BP: Benzo(a)pyrene
P: Precipitate
S: Sparse bacterial background lawn
#: Standard deviation
Table 7.6.1/6:History Profile of Vehicle and Positive Control Values
COMBINED VEHICLE AND UNTREATED CONTROL VALUES 2015 |
|||||||||||||||||||||||||||||||||
Strain S9-Mix |
TA100 |
TA1535 |
TA102 |
WP2uvrA |
TA98 |
TA1537 |
WP2uvrA pKM101 |
WP2pKM101 |
|||||||||||||||||||||||||
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
||||||||||||||||||
Values† |
274 |
278 |
504 |
285 |
26 |
13 |
461 |
229 |
526 |
299 |
506 |
282 |
42 |
51 |
39 |
49 |
|||||||||||||||||
Min |
60 |
61 |
7 |
7 |
222 |
278 |
10 |
12 |
11 |
10 |
4 |
6 |
87 |
98 |
89 |
93 |
|||||||||||||||||
Max |
166 |
175 |
31 |
29 |
376 |
388 |
58 |
43 |
45 |
46 |
27 |
27 |
237 |
254 |
174 |
177 |
|||||||||||||||||
Mean |
91 |
95 |
16 |
14 |
286 |
333 |
24 |
27 |
21 |
24 |
12 |
13 |
156 |
164 |
123 |
137 |
|||||||||||||||||
SD |
19.3 |
19.1 |
4.5 |
4.0 |
48.7 |
37.6 |
5.6 |
5.9 |
6.2 |
6.1 |
3.8 |
3.4 |
42.2 |
35.6 |
23.1 |
21.2 |
|||||||||||||||||
POSITIVE CONTROL VALUES 2015 |
|
||||||||||||||||||||||||||||||||
Strain S9-Mix |
TA100 |
TA1535 |
TA102 |
WP2uvrA |
TA98 |
TA1537 |
WP2uvrA pKM101 |
WP2pKM101 |
|
||||||||||||||||||||||||
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
|
|||||||||||||||||
Values |
276 |
280 |
252 |
264 |
13 |
13 |
231 |
227 |
262 |
276 |
253 |
261 |
20 |
35 |
20 |
35 |
|
||||||||||||||||
Min |
222 |
250 |
79 |
118 |
953 |
673 |
116 |
103 |
100 |
78 |
164 |
97 |
430 |
494 |
745 |
325 |
|
||||||||||||||||
Max |
2266 |
2402 |
2779 |
457 |
3140 |
1655 |
2769 |
550 |
502 |
705 |
2318 |
823 |
1696 |
2264 |
3662 |
1174 |
|
||||||||||||||||
Mean |
614 |
927 |
472 |
246 |
2303 |
1093 |
792 |
266 |
222 |
218 |
911 |
336 |
761 |
1461 |
2257 |
569 |
|
||||||||||||||||
SD |
260.6 |
452.5 |
434.8 |
55.7 |
815.2 |
376.5 |
342.1 |
97.7 |
70.2 |
107.6 |
412.4 |
135.7 |
350.0 |
382.0 |
790.7 |
220.3 |
|
||||||||||||||||
COMBINED VEHICLE AND UNTREATED CONTROL VALUES 2016 |
|||||||||||||||||||||||||||||||||
Strain S9-Mix |
TA100 |
TA1535 |
TA102 |
WP2uvrA |
TA98 |
TA1537 |
WP2uvrA pKM101 |
WP2pKM101 |
|||||||||||||||||||||||||
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
||||||||||||||||||
Values |
399 |
401 |
758 |
393 |
60 |
30 |
690 |
345 |
788 |
415 |
762 |
398 |
32 |
32 |
16 |
24 |
|||||||||||||||||
Min |
63 |
66 |
8 |
8 |
216 |
221 |
10 |
13 |
8 |
12 |
3 |
4 |
97 |
104 |
78 |
52 |
|||||||||||||||||
Max |
154 |
156 |
34 |
39 |
340 |
375 |
53 |
53 |
49 |
51 |
24 |
23 |
268 |
243 |
148 |
166 |
|||||||||||||||||
Mean |
90 |
93 |
15 |
15 |
268 |
310 |
22 |
27 |
21 |
25 |
12 |
13 |
161 |
159 |
118 |
110 |
|||||||||||||||||
SD |
14.5 |
14.3 |
4.5 |
5.2 |
26.4 |
31.1 |
5.8 |
6.3 |
4.8 |
5.7 |
3.5 |
3.5 |
39.2 |
32.3 |
17.0 |
29.3 |
|||||||||||||||||
POSITIVE CONTROL VALUES 2016 |
|
||||||||||||||||||||||||||||||||
Strain S9-Mix |
TA100 |
TA1535 |
TA102 |
WP2uvrA |
TA98 |
TA1537 |
WP2uvrA pKM101 |
WP2pKM101 |
|
||||||||||||||||||||||||
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
-S9 |
+S9 |
|
|||||||||||||||||
Values |
409 |
406 |
381 |
386 |
30 |
28 |
341 |
335 |
388 |
385 |
379 |
381 |
14 |
24 |
8 |
16 |
|
||||||||||||||||
Min |
221 |
284 |
84 |
92 |
897 |
629 |
107 |
102 |
100 |
96 |
95 |
101 |
445 |
574 |
1674 |
372 |
|
||||||||||||||||
Max |
2222 |
2863 |
2994 |
879 |
2326 |
2140 |
1611 |
637 |
449 |
4357 |
1413 |
639 |
1117 |
1855 |
2823 |
945 |
|
||||||||||||||||
Mean |
724 |
1264 |
854 |
240 |
1633 |
950 |
718 |
240 |
186 |
188 |
406 |
290 |
743 |
1271 |
2379 |
535 |
|
||||||||||||||||
SD |
320.4 |
562.9 |
664.9 |
62.1 |
564.5 |
382.7 |
338.6 |
98.2 |
49.8 |
230.8 |
227.0 |
92.7 |
214.6 |
326.5 |
426.2 |
143.3 |
|
||||||||||||||||
SD: Standard deviation
Min: Minimum value
Max: Maximum value
†: Number of mean values used to create dataset
Applicant's summary and conclusion
- Conclusions:
- Under the test conditions, the test item is not considered as mutagenic in Salmonella typhimurium strains TA1535, TA1537, TA98 and TA100, and Escherichia coli strain WP2uvrA.
- Executive summary:
In a reverse gene mutation assay in bacteria, performed according to the OECD Guideline 471 and in compliance with GLP, Salmonella typhimurium strains TA1535, TA1537, TA98 and TA100, and Escherichia coli strain WP2uvrA were exposed to the test item at the following concentrations:
- Experiment 1 - Plate Incorporation Method: 1.5, 5, 15, 50, 150, 500, 1500 and 5000 µg/plate, with and without S9-mix
- Experiment 2 - Pre-Incubation Method: 15, 50, 150, 500, 1500 and 5000 µg/plate, with and without S9-mix
Rat liver homogenate (10% liver S9 in standard co-factors) was used as a metabolizing system. Vehicle control, negative (untreated) and positive control groups were also included in mutagenicity tests.
The vehicle (dimethyl sulphoxide) control plates gave counts of revertant colonies within the normal range. All of the positive control chemicals used in the test induced marked increases in the frequency of revertant colonies, both with or without metabolic activation. Thus, the sensitivity of the assay and the efficacy of the S9-mix were validated.
In the first mutation test (plate incorporation method), there was no visible reduction in the growth of the bacterial background lawn at any dose level, either in the presence or absence of metabolic activation (S9-mix), and consequently the same maximum dose level was used in the second mutation test. In the second mutation test (pre-incubation method), the test item induced a toxic response with weakened bacterial background lawns and/or reductions in revertant colony frequency noted to all of the Salmonella strains noted at 5000 μg/plate in both the absence and presence of S9-mix. No toxicity was noted to Escherichia coli strain WP2uvrA at any test item dose level. The sensitivity of the bacterial tester strains to the toxicity of the test item varied slightly between strain type, exposures with or without S9-mix and experimental methodology.
A test item precipitate (white and particulate in appearance) was noted at 5000 μg/plate, this observation did not prevent the scoring of revertant colonies.
No increases in the frequency of revertant colonies were recorded for any of the bacterial strains, with any dose of the test item, either with or without metabolic activation (S9-mix) in Experiment 1 (plate incorporation method) and in Experiment 2 (pre incubation method).
Under the test conditions, the test item is not considered as mutagenic in these bacterial systems.
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