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EC number: 234-974-5 | CAS number: 12047-11-9
- 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
Two different in vitro studies were performed to evaluate the mutagenicity of barium hexaferrite. In Salmonella and E.coli the substance did not shown mutagenic activity, while some positive results were observed in vitro micronucleus test performed on V79 and CHO cell lines. During the preliminary citotoxicity test (performed in order to evaluate the most suitable concentrations of test substance for both CHO and V79 cells), an unexpected, marked citotoxicity was observed in CHO cells not exposed to the substance but treated with metabolic activator S9. For this reason, CHO cells were tested with the substance only in absence of S9 activation, while V79 cells were exposed to barium hexaferrite both with and without S9. Positive results were observed at the highest concentration levels tested for both CHO and V79 cells; in V79 cells the mutagen activity was observed only in presence of metabolic system. Overall, the results are unclear. The citotoxicity due to S9 in CHO cells and the different results observed in the two cell lines would make desirable a verification by means of an in vivo test, as it is foreseen by the Regulation EC 1907/2006. However, toxicokinetics evidences do not support the adsorption (after oral administration) and the subsequently reaching of the target tissue by the substance, making non reliable the validated in vivo mutagenicity tests. Indeed, B.11 (In Vivo Mammalian Bone Marrow Chromosome Aberration Test) and B.12 (In Vivo Mammalian Erythrocyte Micronucleus Test) sections of the Regulation CE 440/2008 reports that: "If there is evidence that the test substance, or a reactive metabolite, will not reach the target tissue, it is not appropriate to use this test".
In light of above issue, no further test was performed.
Short description of key information:
In vitro studies gave conflicting results. The Ames test was negative in all tested strains without and with metabolic activation, regardless the concentration tested. In vitro micronucleus test in V79 and CHO cells showed some mutagenic activity at the highest dose levels tested. In vivo testing was considered scientifically unjustified. Because the toxicokinetics evidences show that barium hexaferrite is not able to reach target organs.
Endpoint Conclusion:
Justification for classification or non-classification
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