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EC number: 200-449-4 | CAS number: 60-00-4
- 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
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- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
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- 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
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- 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:
- genetic toxicity in vitro
- Remarks:
- Type of genotoxicity: other: DNA demage, Mouse lymphoma assay
- Type of information:
- other: literature review
- Adequacy of study:
- key study
- Study period:
- 2004
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Data prepared by European Chemical Bureau.
Data source
Reference
- Reference Type:
- review article or handbook
- Title:
- European Risk Assessment Report CAS 60-00-4 EC 200-449-4 edetic acid (EDTA)
- Author:
- European Chemical Bureau Institute of Health and Consumer Protection
- Year:
- 2 004
- Bibliographic source:
- European Chemical Bureau Institute of Health and Consumer Protection
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- other: DNA damage; alkaline elution; V79 cells
- Qualifier:
- according to guideline
- Guideline:
- other: Mouse lymphoma assay
- GLP compliance:
- not specified
- Type of assay:
- other: DNA damage; alkaline elution; V79 cells; Mouse lymphoma assay
Test material
- Reference substance name:
- Edetic acid
- EC Number:
- 200-449-4
- EC Name:
- Edetic acid
- Cas Number:
- 60-00-4
- Molecular formula:
- C10H16N2O8
- IUPAC Name:
- 2,2',2'',2'''-(ethane-1,2-diyldinitrilo)tetraacetic acid
- Reference substance name:
- EDTA
- IUPAC Name:
- EDTA
Constituent 1
Constituent 2
Results and discussion
Any other information on results incl. tables
Mammalian cell culture tests were performed with EDTA (free acid). In a mouse lymphoma assay which was done only without metabolic activation, 2-fold to 6-fold increases of mutant frequencies were induced by EDTA at very high concentrations of 25 and 30 mmol/l and a treatment time of 4 hours; relative total growths at these concentrations were 57% and 16% respectively. The pH, measured in a parallel experiment where EDTA was dissolved in culture medium (pH of 7.2), was reduced to 5.8 at 30 mmol/l and to 6.1 at 20 mmol/l, when measured directly after preparation of the solution. Whether the mutagenic activity was due to pH effects or due to the high tested concentrations seems to be unclear (Wangenheim and Bolcsfoldi, 1988). In an alkaline elution assay with mouse lymphoma cells EDTA induced DNA single strand breaks in very high concentrations from 40 mmol/l upwards. Data on toxicity were not given; the assay was conducted without a metabolic activation system only (Garberg et al., 1988). In concentrations up to 30 mmol/l EDTA induced no effects with and without S-9 mix in alkaline elution assays with V79 cells (Swenberg et al., 1976; Swenberg, 1981).
Applicant's summary and conclusion
- Conclusions:
- Interpretation of results (migrated information):
other: negative and positive but only at ery high concentrations
EDTA is not mutagenic for humans. - Executive summary:
Mutations and DNA damage were found in mouse lymphoma cells after exposure to very high concentrations. EDTA has a low mutagenic potential at extremely high doses. On the basis of the various negative findings and the assumption of a threshold mode-of action for aneugens, it can be concluded that EDTA is not mutagenic for humans.
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