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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Toxicological information

Genetic toxicity: in vitro

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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:
2007
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

Constituent 1
Chemical structure
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

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