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EC number: 229-313-2 | CAS number: 6471-49-4
- 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
- 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
Link to relevant study record(s)
- Endpoint:
- basic toxicokinetics in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- data from handbook or collection of data
- Justification for type of information:
- Data is from NTP
- Qualifier:
- according to guideline
- Guideline:
- other: as below
- Principles of method if other than guideline:
- Metabolism and disposition of C.1. Pigment Red 23 in rats
- GLP compliance:
- not specified
- Specific details on test material used for the study:
- Name: 3-hydroxy-4-[(2-methoxy-5-nitrophenyl)azo]-N-(3-nitrophenyl)naphthalene-2-carboxamide
SMILES:COc1ccc(N(=O)=O)cc1N=Nc1c2ccccc2cc(C(=O)Nc2cccc(N(=O)=O)c2)c1O
InChI:1S/C24H17N5O7/c1-36-21-10-9-17(29(34)35)13-20(21)26-27-22-18-8-3-2-5-14(18)11-19(23(22)30)24(31)25-15-6-4-7-16(12-15)28(32)33/h2-13,30H,1H3,(H,25,31)/b27-26+
Molecular Formula: C24H17N5O7
Molecular Weight: 487.4263 g/mole - Radiolabelling:
- no
- Species:
- rat
- Strain:
- Fischer 344
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- - Age at study initiation: 7 to 8 weeks old)
- Route of administration:
- oral: unspecified
- Vehicle:
- not specified
- Details on exposure:
- not specified
- Duration and frequency of treatment / exposure:
- single dose
- Dose / conc.:
- 5.3 mg/kg bw/day
- No. of animals per sex per dose / concentration:
- not specified
- Control animals:
- not specified
- Positive control reference chemical:
- not specified
- Details on study design:
- not specified
- Details on dosing and sampling:
- not specified
- Statistics:
- not specified
- Preliminary studies:
- not specified
- Type:
- excretion
- Results:
- Nearly all of the pigment (93% ± 16%) was recovered in the feces 48 hours after administration. No pigment was found in plasma, whole blood, liver, kidney, or lungs of treated animals at any time period even after administering 10 times this dose
- Details on absorption:
- not specified
- Details on distribution in tissues:
- not specified
- Details on excretion:
- Nearly all of the pigment (93% ± 16%) was recovered in the feces 48 hours after administration. No pigment was found in plasma, whole blood, liver, kidney, or lungs of treated animals at any time period even after administering 10 times this dose
- Metabolites identified:
- no
- Details on metabolites:
- not specified
- Bioaccessibility (or Bioavailability) testing results:
- not specified
- Conclusions:
- C.1. Pigment Red 23 was considered to be have Low bio-accumulation potential in rats based on study results.
- Executive summary:
Upon oral administration, C.1. Pigment Red 23 were Nearly all of the pigment (93% ± 16%) was recovered in the feces 48 hours after administration. No pigment was found in plasma, whole blood, liver, kidney, or lungs of treated animals at any time period even after administering 10 times this dose. Therefore, C.1. Pigment Red 23 was considered to be have Low bio-accumulation potential in rats based on study results.
Reference
Description of key information
C.1. Pigment Red 23 was considered to be have Low bio-accumulation potential in rats based on study results.
Key value for chemical safety assessment
- Bioaccumulation potential:
- low bioaccumulation potential
Additional information
Upon oral administration, C.1. Pigment Red 23 were Nearly all of the pigment (93% ± 16%) was recovered in the feces 48 hours after administration. No pigment was found in plasma, whole blood, liver, kidney, or lungs of treated animals at any time period even after administering 10 times this dose. Therefore, C.1. Pigment Red 23 was considered to be have Low bio-accumulation potential in rats based on study results.
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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