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EC number: 248-470-8 | CAS number: 27458-93-1
- 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
- Remarks:
- Type of genotoxicity: gene mutation
- Type of information:
- migrated information: read-across based on grouping of substances (category approach)
- Adequacy of study:
- key study
- Study period:
- 1980
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study was conducted according to an appropriate OECD test guideline, with acceptable restrictions. The restrictions were that only duplicate plates were used, and positive controls all required activation.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 980
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 471 (Bacterial Reverse Mutation Assay)
- Deviations:
- yes
- Remarks:
- range of strains; duplicate not triplicate
- GLP compliance:
- not specified
- Type of assay:
- bacterial reverse mutation assay
Test material
- Reference substance name:
- Alcohols, C12-13
- EC Number:
- 278-306-0
- EC Name:
- Alcohols, C12-13
- Cas Number:
- 75782-86-4
- IUPAC Name:
- dodecan-1-ol
Constituent 1
Method
Species / strain
- Species / strain / cell type:
- bacteria, other: Salmonella typhimurium strains TA98, 100, 1535, 1537 and 1538; Escherichia coli strains WP2 and WP2 uvrA
- Metabolic activation:
- with and without
- Metabolic activation system:
- Aroclor induced rat liver S9
- Test concentrations with justification for top dose:
- 0, 0.2, 2, 20, 200 (or 500 E. coli) and 2000 µg/plate
Results and discussion
Test results
- Species / strain:
- bacteria, other: Salmonella typhimurium strains TA98, 100, 1535, 1537 and 1538; Escherichia coli strains WP2 and WP2 uvrA
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity nor precipitates, but tested up to recommended limit concentrations
- Remarks:
- >2000 µg/plate
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not applicable
- Positive controls validity:
- valid
- Additional information on results:
- PRECIPITATION CONCENTRATION: None reported
- Remarks on result:
- other: all strains/cell types tested
- Remarks:
- Migrated from field 'Test system'.
Any other information on results incl. tables
GENOTOXIC EFFECTS:
- With and without metabolic activation: There was no increase in reverse mutation rate in any of the test organisms.
Table 1a Experiment 1 and 3* Plate incorporation: revertants per plate (mean of 2 plates)
Concentration µg/plate |
E coli WP2 |
E coli WP2 uvrA |
TA 100 |
TA 1535 |
||||
-MA |
+MA |
-MA |
+MA |
-MA |
+MA |
-MA |
+MA |
|
0 |
9.8 |
10.3 |
9.55 |
17.5 |
38.8 |
47.0 |
7.0 |
4.0 |
0.2 |
13.3 |
9.3 |
7.8 |
19.0 |
46.3 |
55.8 |
10.3 |
4.8 |
2 |
12.3 |
11.0 |
7.5 |
18.5 |
46.0 |
52.0 |
5.5 |
5.0 |
20 |
9.5 |
9.8 |
7.3 |
15.8 |
48.0 |
55.0 |
6.5 |
3.8 |
200 |
11.8 |
7.5 |
13.5 |
13.5 |
44.3 |
56.8 |
12.5 |
.7.0 |
2000 |
11.5 |
18.0 |
6.8 |
3.5 |
49.8 |
60.0 |
8.5 |
10.0 |
Positive control |
143.8 |
24.8 |
109.2 |
454.0 |
50.3 |
158.3 |
1122.0 |
1077.3 |
* Salmonella strains were tested in experiment 3, E.coli in experiment 1
Table 1b Experiment 3 Plate incorporation: revertants per plate (mean of 2 plates)
Concentration µg/plate |
TA 1538 |
TA 98 |
TA 1537 |
|||
-MA |
+MA |
-MA |
+MA |
-MA |
+MA |
|
0 |
7.8 |
11.0 |
7.3 |
13.5 |
7.8 |
5.8 |
0.2 |
3.8 |
11.0 |
4.0 |
12.3 |
6.8 |
6.5 |
2 |
4.8 |
9.8 |
5.8 |
14.5 |
5.5 |
4.8 |
20 |
3.8 |
11.0 |
6.5 |
12.8 |
6.8 |
6.3 |
200 |
5.0 |
12.8 |
7.5 |
10.8 |
10.0 |
12.3 |
2000 |
5.3 |
16.0 |
7.0 |
11.0 |
6.0 |
5.8 |
Positive control |
4.3 |
47.8 |
6.0 |
144.8 |
8.3 |
12.8 |
Table 2a Experiment 2 and 4* Plate incorporation: revertants per plate (mean of 2 plates)
Concentration µg/plate |
E coli WP2 |
E coli WP2 uvrA |
TA 100 |
TA 1535 |
||||
-MA |
+MA |
-MA |
+MA |
-MA |
+MA |
-MA |
+MA |
|
0 |
9.5 |
6.3 |
7.5 |
8.3 |
107.5 |
105.7 |
2.5 |
2.8 |
0.2 |
7.8 |
8.3 |
7.5 |
10.8 |
106.8 |
93.0 |
1.3 |
2.0 |
2 |
5.5 |
8.0 |
6.5 |
9.8 |
111.0 |
85.8 |
3.0 |
1.8 |
20 |
6.3 |
6.3 |
11.0 |
14.5 |
105.3 |
98.0 |
2.0 |
2.0 |
200 |
4.8 |
7.8 |
8.3 |
9.8 |
107.0 |
93.8 |
1.8 |
2.5 |
2000 |
5.8 |
7.3 |
7.5 |
10.8 |
101.8 |
95.0 |
0.8 |
1.5 |
Positive control |
179 |
15.8 |
353.3 |
606 |
117.3 |
203.5 |
476.3 |
569.0 |
* Salmonella strains were tested in experiment 4 (TA 100 in experiment 5), E.coli in experiment 2
Table 2b Experiment 4 Plate incorporation: revertants per plate (mean of 2 plates)
Concentration µg/plate |
TA 1538 |
TA 98 |
TA 1537 |
|||
-MA |
+MA |
-MA |
+MA |
-MA |
+MA |
|
0 |
2.8 |
13.0 |
3.0 |
5.3 |
2.3 |
2.0 |
0.2 |
1.0 |
8.8 |
1.3 |
6.5 |
2.5 |
3.0 |
2 |
1.0 |
8.5 |
1.3 |
6.5 |
5.0 |
2.8 |
20 |
1.3 |
7.8 |
3.0 |
6.5 |
2.5 |
3.5 |
200 |
2.3 |
7.3 |
1.8 |
8.5 |
1.5 |
4.0 |
2000 |
1.5 |
3.8 |
0.3 |
7.8 |
2.5 |
2.3 |
Positive control |
2.0 |
34.8 |
2.5 |
28.5 |
2.8 |
8.0 |
Applicant's summary and conclusion
- Conclusions:
- Interpretation of results (migrated information):
negative with and without metabolic activation
The C12-13 alcohol Dobanol 23 has been tested according to a method that is similar to OECD 471. The test substance did not increase the reverse mutation rate in histidine dependent bacterial strains of Salmonella typhimurium TA98, 100, 1535, 1537 and 1538 or tryptophan-dependent Escherichia coli strains WP2 and WP2 uvrA in the presence or absence of metabolic activation at dose levels up to 2000 µg/plate. Vehicle and positive controls produced expected results. There was no evidence of cytotoxicity at any dose level. It is concluded that the test substance is negative for mutagenicity to bacteria under the conditions of the test.
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