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EC number: 307-301-9 | CAS number: 97593-01-6
- 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:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1995-09-22 to 1995-10-17
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: This study is classified as reliable without restriction because it was conducted in accordance with OECD 471 guideline for reversion assays and was GLP compliant.
- Justification for type of information:
- A discussion and report on the read across strategy is given as an attachment in Section 13.
Cross-reference
- Reason / purpose for cross-reference:
- read-across: supporting information
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 995
- Report date:
- 1995
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 471 (Bacterial Reverse Mutation Assay)
- GLP compliance:
- yes
- Type of assay:
- bacterial reverse mutation assay
Test material
- Reference substance name:
- Alkenes, C6-8
- IUPAC Name:
- Alkenes, C6-8
- Details on test material:
- - Name of test material (as cited in study report): SHOP Internal Olefins C6-8
- Substance type: Alkenes, C6-8
- Physical state: Clear colourless liquid
Constituent 1
Method
- Target gene:
- Not specified
Species / strain
- Species / strain / cell type:
- S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
- Metabolic activation:
- with and without
- Test concentrations with justification for top dose:
- 50, 158, 500, 1580, and 5000 ug/plate
- Vehicle / solvent:
- - Vehicle(s)/solvent(s) used: DMSO
- Justification for choice of solvent/vehicle: Not provided
Controls
- Untreated negative controls:
- yes
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Positive control substance:
- other: Benzo(a)pyrene and 2-nitrofluorene
- Details on test system and experimental conditions:
- METHOD OF APPLICATION: in agar (plate incorporation)
DURATION
- Preincubation period: 10 hours
- Exposure duration: 2 days
NUMBER OF REPLICATIONS: 3
- Evaluation criteria:
- The Salmonella strains are checked by testing for growth inhibition in spot tests by using 1) Crystal violet inhibition zone at greater than 14 mm in diameter when 10 µl of a 1 mg/mL crystal violet solution was spotted onto plate centre indicated a possession of deep-rough (rfa) character, or when 2) Mitomycin C solution was spotted onto plate centre indicated a defective DNA repair system (uvrB).
- Statistics:
- Statistical methods, if employed, are not reported in the study.
Results and discussion
Test results
- Species / strain:
- S. typhimurium TA 1535, TA 1537, TA 98 and TA 100
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- valid
- Positive controls validity:
- valid
- Remarks on result:
- other: all strains/cell types tested
- Remarks:
- Migrated from field 'Test system'.
Any other information on results incl. tables
The preliminary toxicity test did not cause any visible thinning of the background lawn of non-revertant cells as a result of exposure to Shop IO C6-8. Positive controls indicated that the test system was working appropriately. In the main mutagenicity test, no increase in revertant colony numbers over control were obtained with any of the four tester strains exposed to Shop IO C6-8 at concentrations ranging from 50 to 5000 µg/plate. Based on these results, SHOP Internal Olefins C6-8 was not mutagenic in the presence or absence of S9.
Applicant's summary and conclusion
- Conclusions:
negative
SHOP Internal Olefins C6-8 is not mutagenic in the presence or absence of S9.- Executive summary:
In a bacterial reverse mutation assay, Shop IO C6-8 was initially tested to determine its potential to cause cytotoxicity. Based on the outcome of this experiment, the main mutagenicity study was conducted on Salmonella typhimurium strains, TA1537, TA1535, TA100 and TA98 using 50, 158, 500, 1580, or 5000 µg/plate both in the presence and absence of S9. This test was conducted in triplicate. After a 2 day incubation period, number of revertant colonies was counted, either manually or with an automated colony counter. Growth of the background lawn of non-revertant cells on minimal plates was also verified. Results obtained with all strains were confirmed in a second, independent experiment.
The preliminary toxicity test did not cause any visible thinning of the background lawn of non-revertant cells as a result of exposure to Shop IO C6-8. Positive controls indicated that the test system was working appropriately. In the main mutagenicity test, no increase in revertant colony numbers over control were obtained with any of the four tester strains exposed to Shop IO C6-8 at concentrations ranging from 50 to 5000 µg/plate. Based on these results, SHOP Internal Olefins C6-8 was not mutagenic in the presence or absence of S9.
This study received a Klimisch score of 1 and is classified as “reliable without restrictions” because it was conducted in accordance with OECD 471 guideline for reversion assays and was GLP compliant.
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