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Diss Factsheets
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EC number: 202-636-6 | CAS number: 98-09-9
- 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 cytogenicity / micronucleus study
- Remarks:
- Type of genotoxicity: chromosome aberration
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Well documented study according OECD guideline 487
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 007
- Report date:
- 2007
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: OECD 487
- GLP compliance:
- yes
- Type of assay:
- in vitro mammalian cell micronucleus test
Test material
- Reference substance name:
- Benzenesulphonyl chloride
- EC Number:
- 202-636-6
- EC Name:
- Benzenesulphonyl chloride
- Cas Number:
- 98-09-9
- Molecular formula:
- C6H5ClO2S
- IUPAC Name:
- benzenesulfonyl chloride
- Details on test material:
- - Name of test material (as cited in study report): Benzène sulfochlorure
- Physical state: colourless liquid
- Analytical purity: 99.73%
- Lot/batch No.: S24711-466
- Storage condition of test material: room temperature
Constituent 1
Method
Species / strain
- Species / strain / cell type:
- mouse lymphoma L5178Y cells
- Details on mammalian cell type (if applicable):
- - Source: ATCC
- Properly maintained: stored at -180°C in liquid nitrogen
- Periodically checked for Mycoplasma contamination: yes
- Metabolic activation:
- with and without
- Metabolic activation system:
- S9 from liver and S9 from kidney
- Test concentrations with justification for top dose:
- Test 1: S9- (3h/+21h) : (0.078) - 0.156 - 0.312 - 0.625 - 1.25 - (2.5) - (5) - (10) µg/ml
Test 2: S9- (24h) : (0.078) - (0.156) - (0.312) - 0.625 - 1.25 - 2.5 - 5 - (10) µg/ml
Test 3: S9+/5% S9 liver (3h/+21h) : (0.312) - 0.625 - 1.25 - 2.5 - 5 - (10) - (20) - (40) µg/ml
Test 4: S9+/5% S9 kidney (3h/+21h) : (0.312) - 0.625 - 1.25 - 2.5 - 5 - (10) - (20) - (40) µg/ml
Values between brackets have not been retained for evaluation - Vehicle / solvent:
- -ethanol absolu (MERCK, lot K365 899 983 638)
Controls
- Untreated negative controls:
- no
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Positive control substance:
- other: Test 1: Mitomycine C 0.2 µg/ml and Taxol 25 µg/ml. Test 2: Mitomycine C 0.1 µg/ml and Griseéofulvine 12.5 µg/ml. Test 3: Cyclophosphamide 6 µg/ml. Test 4: Streptozotocine 500 µg/ml and Streptozotocine 250 µg/ml.
- Details on test system and experimental conditions:
- METHOD OF APPLICATION: added in medium
DURATION
- Exposure duration: 24h
NUMBER OF REPLICATIONS: 2
NUMBER OF CELLS EVALUATED: 1000 per test
DETERMINATION OF CYTOTOXICITY
- Method: % of relative survival/control
Results and discussion
Test results
- Species / strain:
- mouse lymphoma L5178Y cells
- Metabolic activation:
- with and without
- Genotoxicity:
- positive
- Remarks:
- Genotoxic with metablic activation from kidney at concentration of 2.5µg/ml. Not genotoxic without metabolic activation and with metabolic activation from liver.
- Cytotoxicity / choice of top concentrations:
- cytotoxicity
- Remarks:
- Moderate to strong cytotoxic at concentrations of 2.44 µg/ml to 625 µg/ml without metabolic activation and moderate to strong cytotoxic at concentrations of 4.88 or 9.77 µg/ml to 625 µg/ml with metabolic activation from kidney and liver respectively
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not examined
- Positive controls validity:
- valid
- Remarks on result:
- other: strain/cell type: mouse lymphoma L51784 cells/ATCC
- Remarks:
- Migrated from field 'Test system'.
Applicant's summary and conclusion
- Conclusions:
- Interpretation of results (migrated information):
positive with metabolic activation kidney
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