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EC number: 200-262-8 | CAS number: 56-23-5
- 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 vivo
Administrative data
- Endpoint:
- in vivo mammalian somatic cell study: cytogenicity / erythrocyte micronucleus
- Remarks:
- Type of genotoxicity: chromosome aberration
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 997
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 474 (Mammalian Erythrocyte Micronucleus Test)
- Deviations:
- no
- Principles of method if other than guideline:
- Adminstration of test material
1 or 2 times per gavage 24 hours apart
1 x by intraperitoneal route - Type of assay:
- micronucleus assay
Test material
- Reference substance name:
- Carbon tetrachloride
- EC Number:
- 200-262-8
- EC Name:
- Carbon tetrachloride
- Cas Number:
- 56-23-5
- Molecular formula:
- CCl4
- IUPAC Name:
- tetrachloromethane
- Details on test material:
- - Name of test material (as cited in study report): Carbon tetrachloride
- Physical state: liquid
- Lot/batch No.: purchased from Wako Pure Chemical Co, Osaka, Japan
Constituent 1
Test animals
- Species:
- mouse
- Strain:
- other: BDF1
- Sex:
- male
Administration / exposure
- Route of administration:
- other: 1 or 2 x per gavage, alternatively 1 x ip
- Duration of treatment / exposure:
- one or two gavage treatments 24 hours apart for bone marrow examination
single ip treatment for peripheral blood assay - Frequency of treatment:
- one or two gavage treatments 24 hours apart for bone marrow examination
single ip treatment for peripheral blood assay - Post exposure period:
- 24 hours after last treatment for bone marrow assessment
24, 48 and 72 hours after ip injection for peripheral blood assay
Doses / concentrationsopen allclose all
- Remarks:
- Doses / Concentrations:
1000, 2000 and 3000 mg/kg intraperitoneal
Basis:
nominal conc.
- Remarks:
- Doses / Concentrations:
500, 1000 and 2000 mg/kg by gavage
Basis:
nominal conc.
- No. of animals per sex per dose:
- 5 per dose and treatment schedule
- Control animals:
- yes, concurrent vehicle
Examinations
- Tissues and cell types examined:
- Bone marrow cell smears from femur, slides fixed with methanol and stained with 2.5 % Giemsa solution.
5 microL of blood placed on acridine orange-coated slide and covered.
Results and discussion
Test results
- Sex:
- male
- Genotoxicity:
- negative
- Toxicity:
- no effects
- Vehicle controls validity:
- valid
- Negative controls validity:
- not specified
- Positive controls validity:
- valid
Any other information on results incl. tables
Bone marrow test (Table 1):
There was no increase in the frequency of micronucleated polychromatic erythrocytes due to the treatment of carbon tetrachloride after either one or two treatments. Mitomycin C (single treatment) produced a statistically significant increase at all three time points .
Table 1: Bone marrow micronucleus test of carbon tetrachloride with oral gavage:
Dose (mg/kg) | No of mice | No of injections | mean Micronuc. PCEs | PCE ratios | |
0 (corn oil) | 5 | 1 | 0.20 +/- 0.16 | 38.1 +/- 5.3 | |
500 | 5 | 1 | 0.20 +/- 0.10 | 27.4 +/- 6.2 | |
1000 | 5 | 1 | 0.38 +/- 0.18 | 29.7 +/- 10.7 | |
2000 | 5 | 1 | 0.22 +/- 0.16 | 24.8 +/- 5.0 | |
Mitomycin C 0.5 mg/kg | 5 | 1 | 1.58 +/- 0.61 (p< 0.01) | 39.7 +/- 3.2 | |
0 (corn oil) | 5 | 2 | 0.12 +/- 0.04 | 36.0 +/- 3.5 | |
500 | 5 | 2 | 0.28 +/- 0.16 | 26.0 +/- 3.9 | |
1000 | 5 | 2 | 0.28 +/- 0.22 | 22.5 +/- 9.6 | |
2000 | 5 | 2 | 0.20 +/- 0.19 | 20.8 +/- 8.6 |
Peripheral blood test (Table 2):
There was no inclrease in the frequency of micronucleated reticulcytes due to the teatment of carbon tetrachloride at any observation time point. Mitomycin C produced a statistically significant increase
Table 2: Peripheral blood micronucleus test of carbon tetrachloride with intraperitoneal injection
Dose (mg/kg) | No of mice | Treatment time | % Micronucl. RET, means +/- SD |
1000 | 5 | 0 | 0.20 +/- 0.07 |
5 | 24 | 0.24 +/- 0.09 | |
5 | 48 | 0.20 +/- 0.12 | |
5 | 72 | 0.26 +/- 0.17 | |
2000 | 5 | 0 | 0.18 +/- 0.13 |
5 | 24 | 0.18 +/- 0.16 | |
5 | 48 | 0.26 +/- 0.11 | |
5 | 72 | 0.28 +/- 0.13 | |
3000 | 5 | 0 | 0.16 +/- 0.09 |
5 | 24 | 0.26 +/- 0.05 | |
5 | 48 | 0.20 +/- 0.10 | |
5 | 72 | 0.20 +/- 0.16 | |
Mitomycin C | 5 | 0 | 0.16 +/- 0.09 |
1 mg/kg | 5 | 24 | 0.56 +/- 0.34 (p<0.01) |
5 | 48 | 3.90 +/- 0.67 (p<0.01) | |
5 | 72 | 0.96 +/- 0.37 (p<0.01) |
Applicant's summary and conclusion
- Conclusions:
- Interpretation of results (migrated information): negative
Carbon tetrachloride does not induce micronuclei and thus devoid of a mutagenic potential in this test system. - Executive summary:
Carbon tetrachloride was investigated in a mouse micronucleus test. Administrations were once or twice (24 hours apart) by gavage and sampling 24 hours later for the bone marrow assay or once by the ip route with samplings after 0, 24, 48 and 72 hours for the peripheral blood assay.
In none of the investigations were the micronucleated polychromatic erythrocytes (bone marrow) or micronucleated reticulocytes (peripheral blood) increased at any time point, while Mitmycin C showed the expected increases.
Carbon tetrachloride is devoid of a mutagenic potential in this test system.
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