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EC number: 202-943-5 | CAS number: 101-43-9
- 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 / chromosome aberration study in mammalian cells
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 993
- Report date:
- 1993
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 473 (In Vitro Mammalian Chromosome Aberration Test)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of assay:
- other: In Vitro Mammalian Chromosome Aberration Test
Test material
- Reference substance name:
- Cyclohexyl methacrylate
- EC Number:
- 202-943-5
- EC Name:
- Cyclohexyl methacrylate
- Cas Number:
- 101-43-9
- Molecular formula:
- C10H16O2
- IUPAC Name:
- cyclohexyl 2-methylprop-2-enoate
Constituent 1
- Specific details on test material used for the study:
- - Lot/batch No.: 12-208-222
Method
Species / strain
- Species / strain / cell type:
- lymphocytes: human
- Additional strain / cell type characteristics:
- not applicable
- Metabolic activation:
- with and without
- Metabolic activation system:
- S9 mix
- Test concentrations with justification for top dose:
- Experiment I:
without S9 mix (exposure period 24 h and 48 h)
24h: 10, 30, 100 µg/mL
48h: 100 µg/mL
with S9 mix (exposure period 4 h)
24h: 300, 600, 1680 µg/mL
48h: 1680 µg/mL
Experiment II
without S9 mix (exposure period 24 h and 48 h)
24h: 30, 100, 150 µg/mL
48h: 200 µg/mL
with S9 mix (exposure period 4 h)
24h: 500, 1000, 1680 µg/mL
48h: 1680 µg/mL - Vehicle / solvent:
- - Vehicle(s)/solvent(s) used: DMSO
Controlsopen allclose all
- Untreated negative controls:
- yes
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Positive control substance:
- ethylmethanesulphonate
- Remarks:
- without S9 mix (0.30 mg/mL)
- Untreated negative controls:
- yes
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- no
- Positive controls:
- yes
- Positive control substance:
- cyclophosphamide
- Remarks:
- with S9 mix (30 µg/mL)
- Details on test system and experimental conditions:
- METHOD OF APPLICATION: in medium
DURATION
- Exposure duration: 4, 24, 48 hours
- Fixation time (start of exposure up to fixation or harvest of cells): 3 hours before harvesting
SPINDLE INHIBITOR (cytogenetic assays): Colcemid
STAIN (for cytogenetic assays): Giemsa
NUMBER OF REPLICATIONS: 2
NUMBER OF CELLS EVALUATED: 200 per dose
DETERMINATION OF CYTOTOXICITY
- Method: mitotic index - Statistics:
- Statistical significance at the five per cent level (p < 0.05) was evaluated by means of the chi-square test. Evaluation was performed only for cells carrying aberrations exclusive gaps.
Results and discussion
Test results
- Key result
- Species / strain:
- lymphocytes: human
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not examined
- Positive controls validity:
- valid
Any other information on results incl. tables
Experiment I (exposure period 24 h)
fixation interval 24 h after start of the treatment
Test groups |
S9 mix |
Analyses of chromosomes |
|
Incl. Gaps % |
Excl. gaps % |
||
Negative control |
- |
2.00 |
1.00 |
1% Solvent control DMSO |
- |
1.50 |
0.50 |
0.33 mg/ml Positive contol |
- |
16.00 |
13.0 |
10 µg/ml Test article |
- |
1.00 |
1.0 |
30 µg/ml Test article |
- |
0.00 |
0.00 |
100 µg/ml Test article |
- |
1.00 |
0.50 |
Experiment I (exposure period 48 h)
fixation interval 48 h after start of the treatment
Test groups |
S9 mix |
Analyses of chromosomes |
|
Incl. Gaps % |
Excl. gaps % |
||
1% Solvent control DMSO |
- |
1.50 |
1.00 |
100 µg/ml Test article |
- |
1.50 |
0.50 |
Experiment II (exposure period 24 h)
fixation interval 24 h after start of the treatment
Test groups |
S9 mix |
Analyses of chromosomes |
|
Incl. Gaps % |
Excl. gaps % |
||
Negative control |
- |
3.50 |
1.50 |
1.0% Solvent control DMSO |
- |
2.00 |
1.50 |
0.33 mg/ml Positive contol |
- |
14.50 |
10.00 |
30 µg/ml Test article |
- |
2.00 |
1.00 |
100 µg/ml Test article |
- |
1.50 |
0.50 |
150 µg/ml Test article |
- |
1.00 |
0.50 |
Experiment II (exposure period 48 h)
fixation interval 48 h after start of the treatment
Test groups |
S9 mix |
Analyses of chromosomes |
|
Incl. Gaps % |
Excl. gaps % |
||
1.0% Solvent control DMSO |
- |
0.00 |
0.00 |
150 µg/ml Test article |
- |
3.00 |
2.00 |
Experiment I (exposure period 4 h)
fixation interval 24 h after start of the treatment
Test groups |
S9 mix |
Analyses of chromosomes |
|
Incl. Gaps % |
Excl. gaps % |
||
Negative control |
+ |
0.50 |
0.00 |
1.0% Solvent control DMSO |
+ |
0.50 |
0.50 |
30.0 µg/ml Positive contol CPA |
+ |
17.00 |
14.00 |
300 µg/ml Test article |
+ |
0.50 |
0.00 |
600 µg/ml Test article |
+ |
2.00 |
1.00 |
1680 µg/ml Test article |
+ |
1.00 |
0.50 |
Experiment I (exposure period 4 h)
fixation interval 48 h after start of the treatment
Test groups |
S9 mix |
Analyses of chromosomes |
|
Incl. Gaps % |
Excl. gaps % |
||
1.0% Solvent control DMSO |
+ |
1.00 |
0.50 |
1680 µg/ml Test article |
+ |
0.00 |
0.00 |
Experiment II (exposure period 4 h)
fixation interval 24 h after start of the treatment
Test groups |
S9 mix |
Analyses of chromosomes |
|
Incl. Gaps % |
Excl. gaps % |
||
Negative control |
+ |
2.00 |
1.00 |
1.0% Solvent control DMSO |
+ |
1.50 |
0.00 |
30.0 µg/ml Positive contol CPA |
+ |
10.50 |
10.00 |
500 µg/ml Test article |
+ |
1.00 |
0.00 |
1000 µg/ml Test article |
+ |
1.00 |
0.50 |
1680 µg/ml Test article |
+ |
0.00 |
0.00 |
Experiment II (exposure period 4 h)
fixation interval 48 h after start of the treatment
Test groups |
S9 mix |
Analyses of chromosomes |
|
Incl. Gaps % |
Excl. gaps % |
||
1.0% Solvent control DMSO |
+ |
0.50 |
0.50 |
1680 µg/ml Test article |
+ |
2.50 |
1.50 |
Applicant's summary and conclusion
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