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EC number: 206-337-1 | CAS number: 328-84-7
- 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
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Non-GLP, non-guideline study, available as unpublished report, limitations in design and/or reporting (for some strains inappropiate positive control reference substances were used), but otherwise adequate for assessment
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 987
- Report date:
- 1987
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- The substance was tested in a reverse mutation assay (Ames test) using five strains of Salmonella typhimurium (TA 1535, TA 1537, TA 1538, TA 98, TA 100) and one strain of Escherichia coli (WP2 uvrA pKM 101) in the presence and absence of metabolic activation.
- GLP compliance:
- no
- Type of assay:
- bacterial reverse mutation assay
Test material
- Reference substance name:
- 3,4-dichloro-α,α,α-trifluorotoluene
- EC Number:
- 206-337-1
- EC Name:
- 3,4-dichloro-α,α,α-trifluorotoluene
- Cas Number:
- 328-84-7
- Molecular formula:
- C7H3Cl2F3
- IUPAC Name:
- 1,2-dichloro-4-(trifluoromethyl)benzene
- Details on test material:
- - Name of test material (as cited in study report): 3,4-dichlorobenzotrifluoride
- Appearance: clear colourless liquid
Constituent 1
Method
- Target gene:
- - S.typhimurium: His-locus
- E.coli: Trp-locus
Species / strainopen allclose all
- Species / strain / cell type:
- S. typhimurium, other: TA 1535, TA 1537, TA 1538, TA 98, TA 100
- Additional strain / cell type characteristics:
- not applicable
- Species / strain / cell type:
- E. coli WP2 uvr A pKM 101
- Additional strain / cell type characteristics:
- not applicable
- Metabolic activation:
- with and without
- Metabolic activation system:
- Aroclor induced rat liver S9 mix
- Test concentrations with justification for top dose:
- 31.25, 62.5, 125, 250, 500, 1000, 2000, 4000 µg/plate
- Vehicle / solvent:
- DMSO
Controlsopen allclose all
- Untreated negative controls:
- no
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Remarks:
- 20 µg/plate
- Positive control substance:
- benzo(a)pyrene
- Remarks:
- TA 1538, TA 98, TA 100 (with and without metabolic activation)
- Untreated negative controls:
- no
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Remarks:
- 20 µg/plate
- Positive control substance:
- other: neutral red
- Remarks:
- TA 1537 (with and without metabolic activation)
- Untreated negative controls:
- no
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Remarks:
- 5 µg/plate
- Positive control substance:
- sodium azide
- Remarks:
- TA 1535 (with and without metabolic activation)
- Untreated negative controls:
- no
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Remarks:
- 20 µg/plate
- Positive control substance:
- other: potassium dichromate
- Remarks:
- E.coli (with and without metabolic activation)
- Details on test system and experimental conditions:
- - METHOD OF APPLICATION: in medium; in agar (plate incorporation)
- DURATION: Exposure duration: 48-72 h
- NUMBER OF REPLICATIONS: 3
- DETERMINATION OF CYTOTOXICITY: Reduction in background - Evaluation criteria:
- Reproducable values of 2.5 x control value or greater are considered to indicate a mutagenic response
Results and discussion
Test resultsopen allclose all
- Species / strain:
- S. typhimurium, other: TA 1537, TA1538, TA 98, TA 100
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- cytotoxicity
- Remarks:
- only without metabolic activation
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not applicable
- Positive controls validity:
- other: For TA 1538, TA 98, TA 100, and TA 1537 only a valid positive control for assays with metabolic activation was tested.
- Species / strain:
- S. typhimurium TA 1535
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not applicable
- Positive controls validity:
- other: For TA 1535 only a valid positive control for assays without metabolic activation was tested.
- Species / strain:
- E. coli WP2 uvr A pKM 101
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- cytotoxicity
- Remarks:
- only without metabolic activation
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not applicable
- Positive controls validity:
- other: Only valid without metabolic activation.
- Additional information on results:
- TEST-SPECIFIC CONFOUNDING FACTORS
- Effects of pH: The addition of 4000 µg/plate caused the pH of the medium to change from 7.31 to 7.32.
- Water solubility: The test compound formed small, oily pools in the top agar at amount of 1000 µg/plate and above, showing that is was not totally miscible in the aqueous test system.
ADDITIONAL INFORMATION ON CYTOTOXICITY:
Microscopal evaluation of the background showed evidence of cytotoxicity in all of the bacterial tester strains, except TA 1535, in the absence of rat liver S9 fraction only. In the E.coli this was observed at 250 µg/plate onward, and in the S.typhimurium strains it was observed at 500 µg/plate onward. - Remarks on result:
- other: all strains/cell types tested
- Remarks:
- Migrated from field 'Test system'.
Applicant's summary and conclusion
- Conclusions:
- Interpretation of results (migrated information):
negative
It is concluded that there is no evidence of induction of gene mutations by the test substance and its metabolites in the five S.typhimurium and one E.coli strains used in this study. - Executive summary:
The substance was tested for its mutagenic potential based on the ability to induce point mutations in several strains of Salmonella typhimurium (TA 1535, TA 1537, TA 1538, TA 98, TA 100) and one E.coli strain (WP2 uvrA pKM 101), with and without metabolic activation. Strains were exposed in a standard plate-incorporation test to 0, 31.25, 62.5, 125, 250, 500, 1000, 2000, and 4000 µg/plate. The test compound formed small, oily pools in the top agar at amount of 1000 µg/plate and above, showing that is was not totally miscible in the aqueous test system. The addition of 4000 µg/plate caused a small change in the pH of the medium. Microscopal evaluation of the background showed evidence of cytotoxicity in all of the bacterial tester strains, except TA 1535, in the absence of rat liver S9 fraction only. In the E.coli this was observed ate 250 µg/plate onward, and in the S.typhimurium strains it was observed at 500 µg/plate onward. An increase in the number of his+ or trp+ revertants was not observed with or without a metabolizing system. It was therefore concluded that the test substance is not mutagenic under these experimental conditions.
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