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EC number: 222-429-4 | CAS number: 3468-63-1
- 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

Endpoint summary
Administrative data
Key value for chemical safety assessment
Additional information
Mutaginicity data for C.I Pigment Orange 5 are characterized by a certain inconsistency. Most bacterial gene mutation (OECD 471) assays were positive and one test revealed an equivocal result. However there was neither consistency with regard to the requirement of metabolic activation nor with regard to the strains affected. As an overall conclusion, a gene mutation potential of C.I Pigment Orange 5 in bacteria can not be excluded.
Clear and negative studies for mutaginicity have been seen in vitro in OECD 473 and OECD 476. In vivo there were no marked increases in the incidence of unscheduled DNA synthesis in animals dosed with the test item (OECD 486) and PO5 is not mutagenic in the in vivo chromosome aberration test in bone marrow cells of the Chenese hamster (OECD 475).
Overall conclusion: the test item is not considered to be mutagenic.
Justification for selection of genetic toxicity endpoint
No adverse effects have been seen in vitro in OECD 473, OECD 476 while ambiguous or possitive test results have been seen in Ames tests with and without metabolic activation (OECD 471). In vivo there were no marked increases in the incidence of unscheduled DNA synthesis in animals dosed with the test item (OECD 486) and PO5 is not mutagenic in the in vivo chromosome aberration test in bone marrow cells of the Chenese hamster (OECD 475).
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
C.I Pigment Orange 5 does not have to be classified for mutagenicity according to the criteria laid down in the EU Dangerous Substances Directive (67/548/EEC) and in the EU Classification Labelling and Packaging Regulation (1272/2008/EC) because no adverse effects due to the test item have been seen in vitro in OECD 473 and OECD 476 studies while ambiguous, possitive and negative test results have been seen in Ames tests with and without metabolic activation (OECD 471). In vivo there were no marked increases in the incidence of unscheduled DNA synthesis in animals dosed with the test item (OECD 486).
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