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EC number: 264-719-3 | CAS number: 64173-96-2
- 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
Endpoint summary
Administrative data
Key value for chemical safety assessment
Genetic toxicity in vitro
Description of key information
OECD 471: positive
Link to relevant study records
- Endpoint:
- in vitro gene mutation study in bacteria
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 21 Aug - 01 Sep 2017
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 471 (Bacterial Reverse Mutation Assay)
- Version / remarks:
- 1997
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- JAPAN: Guidelines for Screening Mutagenicity Testing Of Chemicals
- Version / remarks:
- 1993
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.13/14 (Mutagenicity - Reverse Mutation Test Using Bacteria)
- Version / remarks:
- 2008
- Deviations:
- no
- GLP compliance:
- yes
- Type of assay:
- bacterial reverse mutation assay
- Target gene:
- his operon, trp operon
- Species / strain / cell type:
- S. typhimurium TA 1535, TA 1537, TA 98, TA 100 and E. coli WP2
- Metabolic activation:
- with and without
- Metabolic activation system:
- Rat liver S9 induced by ß-Naphthoflavone/phenobarbital
- Test concentrations with justification for top dose:
- 1st series: 5, 15.8, 50, 158, 500, 1580, 5000 µg/plate (with and without S9 mix)
2nd series: 158, 500, 1580, 2810, 5000 µg/plate (with and without S9 mix) - Vehicle / solvent:
- - Solvent used: ultra pure water, final concentration 100 µL per plate
- Justification for choice of solvent: solubitlity properties of the test item, non toxicity to bacteria - Untreated negative controls:
- no
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Positive control substance:
- 4-nitroquinoline-N-oxide
- 9-aminoacridine
- sodium azide
- other: 2-aminoanthracene 2-10 µg/plate, daunomycin 1 µg/plate
- Details on test system and experimental conditions:
- METHOD OF APPLICATION: in agar (plate incorporation)
DURATION
- Exposure duration: 2-3 days
NUMBER OF REPLICATIONS: 3 replicates for test item concentrations and positive controls, 6 replicates for solvent controls
DETERMINATION OF CYTOTOXICITY
- Method: counting numbers of revertants
OTHER:
-S9 concentration: 1st series 10%, 2nd series 20% - Evaluation criteria:
- A test material was to be defined as positive or mutagenic in this assay if
- the assay is considered valid AND
- a biologically relevant increase in the mean number of revertants above a threshold of 2-fold (TA98, TA100, WP2 uvrA) or 3-fold (TA1535, TA1537) as compared to the concurrent negative controls is observed.
- an increase exceeding the threshold at only one concentration is considered as biologically meaningful if reproduced in a 2nd independent experiment.
- a concentration-dependent increase is considered biologically meaningful if the threshold is exceeded at more than one concentration
A test material is considered negative or non-mutagenic in this assay if
- the assay is considered valid AND
- none of the above criteria are met - Statistics:
- Not performed as not mandatory for this test system.
- Key result
- Species / strain:
- S. typhimurium TA 1535
- Metabolic activation:
- without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not examined
- Positive controls validity:
- valid
- Key result
- Species / strain:
- S. typhimurium TA 1535
- Metabolic activation:
- with
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not examined
- Positive controls validity:
- valid
- Key result
- Species / strain:
- S. typhimurium TA 1537
- Metabolic activation:
- without
- Genotoxicity:
- positive
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not examined
- Positive controls validity:
- valid
- Key result
- Species / strain:
- S. typhimurium TA 1537
- Metabolic activation:
- with
- Genotoxicity:
- positive
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not examined
- Positive controls validity:
- valid
- Key result
- Species / strain:
- S. typhimurium TA 98
- Metabolic activation:
- without
- Genotoxicity:
- positive
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not examined
- Positive controls validity:
- valid
- Key result
- Species / strain:
- S. typhimurium TA 98
- Metabolic activation:
- with
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not examined
- Positive controls validity:
- valid
- Key result
- Species / strain:
- S. typhimurium TA 100
- Metabolic activation:
- without
- Genotoxicity:
- positive
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not examined
- Positive controls validity:
- valid
- Key result
- Species / strain:
- S. typhimurium TA 100
- Metabolic activation:
- with
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not examined
- Positive controls validity:
- valid
- Key result
- Species / strain:
- E. coli WP2 uvr A
- Metabolic activation:
- without
- Genotoxicity:
- positive
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not examined
- Positive controls validity:
- valid
- Key result
- Species / strain:
- E. coli WP2 uvr A
- Metabolic activation:
- with
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not examined
- Positive controls validity:
- valid
- Additional information on results:
- Following treatment with the test item, no precipitation on the agar plates occurred. No toxicity to the bacteria was observed.
Under the experimental conditions described, the test item induced relevant, concentration-dependent increases in revertant numbers exceeding a threshold of 2-fold (TA98, TA100, WP2 uvrA) or 3-fold (TA1535, TA1537) of the negative control value in all tester strains in the absence of S9-mix with the exception of TA1535. In the presence of S9-mix there was a relevant increase present in TA1537 only.
According to the criteria for negative and positive results as predetermined in the study plan, the test item was clearly mutagenic under the described experimental conditions. - Conclusions:
- The test item is considered mutagenic in bacteria under the test conditions described.
Reference
Table 1: Summary of Experiment 1
Metabolic Activation |
Test material |
Concentr. (µg/plate) |
Revertant Colony Counts (Mean ± SD) |
||||
TA 98 |
TA 100 |
TA 1535 |
TA 1537 |
WP2 uvrA |
|||
Without Activation |
H20 |
|
34 +/- 11 |
124 +/- 5 |
29 +/- 6 |
9 +/- 4 |
33 +/- 8 |
Test item |
5 |
30 +/- 10 |
129 +/- 9 |
21 +/- 2 |
8 +/- 3 |
39 +/- 6 |
|
15.8 |
38 +/- 12 |
139 +/- 23 |
25 +/- 6 |
10 +/- 6 |
37 +/- 6 |
||
50 |
37 +/- 8 |
140 +/- 19 |
26 +/- 5 |
14 +/- 1 |
37 +/- 2 |
||
158 |
40 +/- 7 |
168 +/- 16 |
18 +/- 1 |
27 +/- 4 |
44 +/- 7 |
||
500 |
42 +/- 1 |
223 +/- 18 |
20 +/- 4 |
71 +/- 5 |
75 +/- 9 |
||
1580 |
52 +/- 13 |
444 +/- 3 |
38 +/- 7 |
187 +/- 10 |
184 +/- 17 |
||
5000 |
112 +/- 16 |
1435 +/- 126 |
49 +/- 10 |
506 +/- 9 |
605 +/- 19 |
||
DAUN |
1 |
166 +/- 26 |
|
|
|
|
|
NaN3 |
2 |
|
1365 +/- 14 |
787 +/-/ 13 |
|
|
|
9-AA |
50 |
|
|
|
1153 +/- 266 |
|
|
NQO |
2 |
|
|
|
|
2101 +/- 163 |
|
With Activation |
H20 |
|
46 +/- 3 |
125 +/- 12 |
17 +/- 6 |
10 +/- 5 |
41 +/- 4 |
Test item |
5 |
35 +/- 6 |
119 +/- 15 |
22 +/- 1 |
10 +/- 6 |
43 +/- 11 |
|
15.8 |
37 +/- 8 |
119 +/- 14 |
19 +/- 3 |
10 +/- 4 |
37 +/- 6 |
||
50 |
43 +/- 5 |
133 +/- 18 |
22 +/- 3 |
15 +/- 3 |
41 +/- 2 |
||
158 |
42 +/- 15 |
141 +/- 7 |
22 +/- 2 |
19 +/- 4 |
32 +/- 6 |
||
500 |
37 +/- 12 |
150 +/- 9 |
16 +/- 6 |
25 +/- 3 |
41 +/- 6 |
||
1580 |
39 +/- 5 |
168 +/- 11 |
22 +/- 2 |
67 +/- 4 |
54 +/- 5 |
||
5000 |
41 +/- 2 |
218 +/- 33 |
22 +/- 9 |
173 +/- 5 |
58 +/- 6 |
||
2-AA |
2 |
614 +/- 17 |
1237 +/- 276 |
|
|
||
2-AA |
5 |
|
|
209 +/- 12 |
275 +/- 27 |
|
|
2-AA |
10 |
|
|
|
|
320 +/- 18 |
Table 1: Summary of Experiment 2
Metabolic Activation |
Test material |
Concentr. (µg/plate) |
Revertant Colony Counts (Mean ± SD) |
||||
TA 98 |
TA 100 |
TA 1535 |
TA 1537 |
WP2 uvrA |
|||
Without Activation |
H20 |
|
31 +/- 10 |
132 +/- 19 |
27 +/- 7 |
8 +/- 3 |
31 +/- 7 |
Test item |
5 |
-- |
-- |
-- |
-- |
-- |
|
15.8 |
-- |
-- |
-- |
-- |
-- |
||
158 |
32 +/- 10 |
161 +/- 4 |
23 +/- 3 |
34 +/- 5 |
50 +/- 6 |
||
500 |
32 +/- 4 |
240 +/- 10 |
24 +/- 7 |
74 +/- 3 |
105 +/- 18 |
||
1582 |
55 +/- 11 |
484 +/- 9 |
30 +/- 9 |
232 +/- 31 |
242 +/- 8 |
||
2810 |
81 +/- 5 |
845 +/- 38 |
30 +/- 4 |
360 +/- 16 |
401 +/- 24 |
||
5000 |
106 +/- 22 |
1576 +/- 31 |
51 +/- 3 |
576 +/- 31 |
688 +/- 12 |
||
DAUN |
1 |
192 +/- 45 |
|
|
|
|
|
NaN3 |
2 |
|
1754 +/- 45 |
887 +/- 62 |
|
|
|
9-AA |
50 |
|
|
|
580 +/- 44 |
|
|
NQO |
2 |
|
|
|
|
2170 +/- 127 |
|
With Activation |
H20 |
|
41 +/- 7 |
150 +/- 14 |
15 +/- 6 |
12 +/- 3 |
42 +/- 6 |
Test item |
5 |
-- |
-- |
-- |
-- |
-- |
|
15.8 |
-- |
-- |
-- |
-- |
-- |
||
158 |
42 +/- 1 |
145 +/- 7 |
18 +/- 6 |
13 +/- 3 |
34 +/- 6 |
||
500 |
33 +/- 4 |
135 +/- 10 |
14 +/- 2 |
19 +/- 9 |
41 +/- 1 |
||
1580 |
27 +/- 11 |
158 +/- 8 |
10 +/- 3 |
40 +/- 14 |
52 +/- 4 |
||
2810 |
32 +/- 9 |
176 +/- 23 |
11 +/- 3 |
56 +/- 9 |
53 +/- 8 |
||
5000 |
28 +/- 5 |
202 +/- 17 |
8 +/- 1 |
86 +/- 13 |
72 +/- 8 |
||
2-AA |
2 |
183 +/- 2 |
815 +/- 59 |
|
|
||
2-AA |
5 |
|
|
80 +/- 5 |
127 +/- 9 |
|
|
2-AA |
10 |
|
|
|
|
221 +/- 14 |
Key to Positive Controls
NaN3 Sodium azide
2-AA 2-Aminoanthracene
9-AA 9-Aminoacridine
DAUN Daunomycin
NQO 4-Nitroquinoline-N-oxide
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed (positive)
Genetic toxicity in vivo
Endpoint conclusion
- Endpoint conclusion:
- no study available
Additional information
Justification for classification or non-classification
Based on the provided information no conclusion for classification can be made according to the EU Regulation (EC) No 1272/2008 on Classification, Labelling and Packaging of Substances and Mixtures, as amended for the 10th time in Regulation (EU) No 2017/776.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.