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Diss Factsheets
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EC number: 679-526-3 | CAS number: 337906-36-2
- 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
Endpoint summary
Administrative data
Key value for chemical safety assessment
Additional information
Overall, the genotoxicity of 2-methoxy-methyl-p-phenylenediamine is sufficiently investigated in valid genotoxicity tests for the 3 endpoints of genotoxicity: gene utations, chromosome aberrations and aneuploidy.
2-Methoxy-methyl-p-phenylenediamine was mutagenic in all in vitro tests performed. It did induce gene mutations both in a gene mutation test in bacteria as well as in a mouse
lymphoma assay in mammalian cells and chromosome aberrations in an in vitro micronucleus test although these positive findings were considered of questionable biological importance. The finding in the mouse lymphoma assay that both the number of large and small colonies increased and the ratio large/small colonies decreased indicated to a clastogenic effect of 2-methoxy-methyl-p-phenylenediamine next to a mutagenic one.
The positive findings from the in vitro tests could not be confirmed in in vivo tests. In an UDS test exposure to 2-methoxy-methyl-p-phenylenediamine did not result in unscheduled DNA synthesis in liver of rats. In an in vivo micronucleus test, an increase in bone marrow cells with micronuclei was not seen indicating that 2-methoxy-methyl-p- phenylenediamine is not clastogenic nor aneugenic in this test. The results of a comet assay, an indicator test covering gene mutations and chromosome aberrations, confirmed that 2-methoxy-methylp-phenylenediamine is not genotoxic (mutagenic and clastogenic) in stomach cells and bladder epithelial cells of rats.
Although the results obtained in the comet assay for liver cells were equivocal, the negative UDS test covers for DNA damage in these cells.
Consequently, based on these tests, 2-methoxy-methyl-p-phenylenediamine can be considered to have no genotoxic potential and additional tests are unnecessary.
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
In in vitro studies some mutagenic effects were reported, but this was not confirmed in in vivo studies therefore, the substance was not considered as genotoxic.
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.
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