Registration Dossier
Registration Dossier
Diss Factsheets
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 213-235-0 | CAS number: 931-40-8
- 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
- Remarks:
- Type of genotoxicity: chromosome aberration
- Type of information:
- migrated information: read-across from supporting substance (structural analogue or surrogate)
- Adequacy of study:
- key study
- Study period:
- Not stated
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: The study was conducted according to guideline and/or standard method but was non-GLP.
Data source
Reference
- Reference Type:
- publication
- Title:
- The genotoxic activity of glycerol in an in vitro test battery
- Author:
- Doolittle, D
- Year:
- 1 988
- Bibliographic source:
- Fd Chem Toxic 26(7): 631-635
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 473 (In Vitro Mammalian Chromosome Aberration Test)
- Deviations:
- yes
- Remarks:
- highest dose tested was 1000 ug/ml with no evidence of cytotoxicity or precipitate formation
- GLP compliance:
- not specified
- Type of assay:
- in vitro mammalian chromosome aberration test
Test material
- Reference substance name:
- Glycerol
- EC Number:
- 200-289-5
- EC Name:
- Glycerol
- Cas Number:
- 56-81-5
- Molecular formula:
- C3H8O3
- IUPAC Name:
- propan-1,2,3-triol
- Details on test material:
- purity >99.5%
Constituent 1
Method
- Target gene:
- chromosomal aberrations
Species / strain
- Species / strain / cell type:
- Chinese hamster Ovary (CHO)
- Metabolic activation:
- with and without
- Metabolic activation system:
- rat S-9
- Test concentrations with justification for top dose:
- 100, 200, 400, 600, 800 and 1000 ug/mL
- Vehicle / solvent:
- water
Controls
- Untreated negative controls:
- no
- Negative solvent / vehicle controls:
- yes
- True negative controls:
- not specified
- Positive controls:
- yes
- Remarks:
- triethylenemelamine(-S9); cyclophosphamide (+S9)
- Details on test system and experimental conditions:
- SYSTEM OF TESTING
- Species/cell type: CHO-cells WBL
- Metabolic activation system: rat S-9
- No. of cells scored: 100/concentration (50 for positive controls)
ADMINISTRATION:
- Dosing: 100, 200, 400, 600, 800 and 1000 ug/mL
- Treatment: 10 and 14 hours (with S-9) without recovery; 2 hours (without S-9) with 10 and 14 hr recovery
- Negative control: water (solvent)
- Positive control groups: triethylenemelamine(-S9); cyclophosphamide (+S9) - Evaluation criteria:
- CRITERIA FOR EVALUATING RESULTS:
A statistically significant, reproducible and dose-dependent increase in frequency of cells with aberrations compared to solvent control. - Statistics:
- No additional information available.
Results and discussion
Test results
- Species / strain:
- Chinese hamster Ovary (CHO)
- Metabolic activation:
- with and without
- Genotoxicity:
- negative
- Cytotoxicity / choice of top concentrations:
- no cytotoxicity
- Vehicle controls validity:
- valid
- Untreated negative controls validity:
- not specified
- Positive controls validity:
- valid
- Additional information on results:
- GENOTOXIC EFFECTS:
- With metabolic activation: negative
- Without metabolic activation: negative
In the initial assay with metabolic activation a statistically significant increase in the number of aberrations compared to controls was seen only at 200 ug/mL (recovery period 10 hr)
PRECIPITATION CONCENTRATION: not indicated
MITOTIC INDEX:
without S-9 (10 hr): 84-97% of control
without S-9 (14 hr): 78-101% of control
with S-9 (10 hr rec.): 59-92% of control (no relationship with concentration)
with S-9 (14 hr rec): no decrease observed
CYTOTOXIC CONCENTRATION:
No cytotoxicity observed with concentrations tested.
Any other information on results incl. tables
Table 1 Chromosome aberration assay
Treatment and concentration (ug/ml) | Duration of treatment or recovery (h) | Mitotic index (%) | No. of cells scored | No. of aberrations/cell | Cells with aberrations (%) |
Non-activation assay | |||||
Solvent control (H2O) | 10 | 8.6 | 100 | 0.02 | 1.0 |
Positive control | 10 | 3.4 | 50 | 0.44 | 36.0* |
Glycerol | |||||
100 | 10 | 7.3 | 100 | 0.07 | 6.0 |
200 | 10 | 7.4 | 100 | 0.01 | 1.0 |
400 | 10 | 8.0 | 100 | 0.06 | 5.0 |
600 | 10 | 8.0 | 100 | 0.02 | 2.0 |
800 | 10 | 8.3 | 100 | 0.01 | 1.0 |
Solvent control (H2O) | 14 | 12.1 | 100 | 0.02 | 2.0 |
Positive control | 14 | 3.8 | 50 | 1.04 | 68.0* |
Glycerol | |||||
100 | 14 | 11.1 | 100 | 0.02 | 2.0 |
200 | 14 | 9.4 | 100 | 0.03 | 2.0 |
400 | 14 | 10.1 | 100 | 0.04 | 3.0 |
600 | 14 | 11.3 | 100 | 0.01 | 1.0 |
800 | 14 | 12.2 | 100 | 0.00 | 0.0 |
1000 | 14 | 11.7 | 100 | 0.00 | 0.0 |
Activation assay | |||||
Solvent control (H2O) | 10 | 5.1 | 100 | 0.03 | 3.0 |
Positive control | 10 | 6.3 | 50 | 1.98 | 78.0* |
Glycerol | |||||
100 | 10 | 4.7 | 100 | 0.01 | 1.0 |
200 | 10 | 3.0 | 100 | 0.18 | 9.0* |
400 | 10 | 3.7 | 100 | 0.02 | 2.0 |
600 | 10 | 3.7 | 100 | 0.04 | 3.0 |
800 | 10 | 3.3 | 100 | 0.04 | 4.0 |
1000 | 10 | 3.2 | 100 | 0.02 | 2.0 |
100 | 14 | 11.0 | 100 | 0.00 | 0.0 |
200 | 14 | 11.4 | 100 | 0.00 | 0.0 |
400 | 14 | 12.3 | 100 | 0.02 | 2.0 |
600 | 14 | 11.3 | 100 | 0.01 | 1.0 |
800 | 14 | 11.7 | 100 | 0.00 | 0.0 |
1000 | 14 | 12.3 | 100 | 0.02 | 2.0 |
Applicant's summary and conclusion
- Conclusions:
- Interpretation of results (migrated information):
negative
The test material did not induce a mutagenic response in the Chinese Hamster Ovary assay with and without metabolic activation. - Executive summary:
The test material was evaluated in the Chinese hamster ovary Chromosomal Aberration assay. The test material did not induce a mutagenic response in the Chinese hamster ovary CA assay with and without metabolic activation.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.

EU Privacy Disclaimer
This website uses cookies to ensure you get the best experience on our websites.