Registration Dossier
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EC number: 211-765-7 | CAS number: 693-98-1
- 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

Specific investigations: other studies
Administrative data
- Endpoint:
- cytotoxicity
- Adequacy of study:
- other information
Data source
Reference
- Reference Type:
- publication
- Title:
- Cytotoxicity testing of 114 compouds by the determination of the protein content in the HEP G2 cell culture
- Author:
- Dierickx, P.J.
- Year:
- 1 989
- Bibliographic source:
- Toxic. in Vitro Vol. 3, No. 3, pp. 189-193
Materials and methods
- Principles of method if other than guideline:
- The cellular protein content measured in cultured Hep G2 cells was used as the endpoint for determining die cytotoxicity of a range of 114 chemical campounds. The relative toxicity of the test compounds was quantified by the determination of the PI50, which is the concentration of xenobiotic required to produce a 50% reduction in protein content of the culture after 24 hr.
Test material
- Reference substance name:
- 2-methylimidazole
- EC Number:
- 211-765-7
- EC Name:
- 2-methylimidazole
- Cas Number:
- 693-98-1
- Molecular formula:
- C4H6N2
- IUPAC Name:
- 2-methyl-1H-imidazole
Constituent 1
Results and discussion
- Details on results:
- Surfactants and heavy metais consistently had low PI50 values. Hep G2 cells were very sensitive to compaunds with more than one carboxyl group. Triacetin and glutathione were identified as false positives. The results suggest that the PI50 assay could be a useful pre-screening method to test for the cytotoxicity of chemicals.
Alkylation of a compound consistently lowered the PI50. This can be seen in the table for imidazole (45 mM) and 2-methyl imidazole (18 mM).
Applicant's summary and conclusion
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