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EC number: 200-666-4 | CAS number: 67-72-1
- 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
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Study period:
- 1978
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: test performed prior to guideline availability but with procedures similar to standard methods and with acceptable restrictions
Data source
Referenceopen allclose all
- Reference Type:
- other: Published toxicological report
- Title:
- Unnamed
- Year:
- 2 011
- Reference Type:
- other: Published toxicological report
- Title:
- Toxicological Profile for Hexachloroethane
- Author:
- Agency for Toxic Substances and Disease Registry (ATSDR)
- Year:
- 1 997
- Bibliographic source:
- Not reported
- Reference Type:
- publication
- Title:
- The toxicity of hexachloroethane in laboratory animals.
- Author:
- Weeks MH, Angerhofer RA, Bishop R, Thomasino J, Pope CR.
- Year:
- 1 979
- Bibliographic source:
- Am Ind Hyg Assoc J. 1979 Mar;40(3):187-99. doi: 10.1080/15298667991429499. PMID: 495459.
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 978
Materials and methods
Test guideline
- Qualifier:
- no guideline available
- Principles of method if other than guideline:
- - Principle of test: determine the mutagenicity potential of the test material in bacteria exposed to hexachloroethane with or without metabolic activation, followed by a quantification of revertant colonies.
- Short description of test conditions: in plate assay, S. typhimurium and S. cerevisiae strains were exposed to the test material in DMSO at concentrations up to the induction of cytotoxic effects. Vehicle and positive controls were included.
- Parameters analysed / observed: revertant colonies - GLP compliance:
- not specified
- Type of assay:
- bacterial reverse mutation assay
Test material
- Reference substance name:
- Hexachloroethane
- EC Number:
- 200-666-4
- EC Name:
- Hexachloroethane
- Cas Number:
- 67-72-1
- Molecular formula:
- C2Cl6
- IUPAC Name:
- hexachloroethane
- Test material form:
- solid: crystalline
Constituent 1
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Source and lot/batch number of test material: Hummel Chemical Company, specifications MIL-H-235B, national stock number 6810-00-N00-001
- Purity: technical grade, 99.8%
Method
Species / strainopen allclose all
- Species / strain / cell type:
- S. typhimurium, other: TA-1535, TA-1537, TA-1538, TA-98, TA-100
- Species / strain / cell type:
- Saccharomyces cerevisiae
- Additional strain / cell type characteristics:
- other: D4 strain
- Metabolic activation:
- with and without
- Metabolic activation system:
- Liver microsomal enzyme preparation from Sprague Dawley rats pretreated 5 days prior to kill with Aroclor 1254
- Test concentrations with justification for top dose:
- 0.1, 1.0, 10, 100 and 500 µg/plate - The compound was tested over a series of concentrations such that there was either quantitative or qualitative evidence of some chemically induced physiological effects at the high dose level. The low dose in all cases was below a concentration that demonstrated any toxic effect.
- Vehicle / solvent:
- - Vehicle(s)/solvent(s) used: DMSO
- Justification for choice of solvent/vehicle and percentage of solvent in the final culture medium: not specified
Controls
- Untreated negative controls:
- no
- Negative solvent / vehicle controls:
- yes
- Remarks:
- but no details
- True negative controls:
- no
- Positive controls:
- yes
- Positive control substance:
- not specified
- Details on test system and experimental conditions:
- METHOD OF TREATMENT/ EXPOSURE:
- Plate assay
Results and discussion
Test resultsopen allclose all
- Key result
- Species / strain:
- S. typhimurium, other: TA-1535, TA-1537, TA-1538, TA-98, TA-100
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- not specified
- Species / strain:
- Saccharomyces cerevisiae
- Remarks:
- D4 strain
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- not specified
Applicant's summary and conclusion
- Conclusions:
- According to the authors, the test material did not induce any significant increase in revertant colonies with or without metabolic activation, neither in S. tiphymurium nor in S. cerevisiae strains.
- Executive summary:
The mutagenicity potential of hexachloroethane was assessed by performing a bacterial reverse mutation assay in S. typhimurium TA-1535, TA-1537, TA-1538, TA-98, TA-100 and S. cerevisiae D4 strains, with or without metabolic activation. There was no information regarding a standardised method or GLP.
The test material was prepared in DMSO solvent and doses of 0.1, 1.0, 10, 100 and 500 µg/plate were applied to bacteria with or without metabolic activation system, i.e. liver microsomal enzyme preparation from Sprague Dawley rats pre-treated 5 days prior to kill with Aroclor 1254. Solvent and positive controls were included in this plate assay.
No result details were available. According to the authors, the test material did not induce any significant increase in revertant colonies with or without metabolic activation, neither in S. typhimurium nor in S. cerevisiae strains.
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