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EC number: 219-372-2 | CAS number: 2425-85-6
- 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
Description of key information
Key value for chemical safety assessment
Skin sensitisation
Link to relevant study records
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 1992
- Reliability:
- 1 (reliable without restriction)
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- GLP compliance:
- yes
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- Old study available from the time where the non-LLNA study was not available
- Species:
- guinea pig
- Strain:
- other: Hoe: DHPK (SPFLac)
- Sex:
- female
- Route:
- intradermal and epicutaneous
- Vehicle:
- petrolatum
- Route:
- epicutaneous, semiocclusive
- Vehicle:
- petrolatum
- No. of animals per dose:
- 10 amimals in the treatment group and 5 animals in the control
- Reading:
- 1st reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 1% C.I. Pigment Red 3 in petrolatum
- No. with + reactions:
- 4
- Total no. in group:
- 10
- Clinical observations:
- Very slight up to well-defined erythema and very slight oedema were observed in four animals
- Remarks on result:
- other: see Remark
- Remarks:
- Reading: 1st reading. . Hours after challenge: 48.0. Group: test group. Dose level: 1% C.I. Pigment Red 3 in petrolatum. No with. + reactions: 4.0. Total no. in groups: 10.0. Clinical observations: Very slight up to well-defined erythema and very slight oedema were observed in four animals.
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 1% C.I. Pigment Red 3 in petrolatum
- No. with + reactions:
- 1
- Total no. in group:
- 10
- Clinical observations:
- One animal of the treated group showed very slight to well-defined erythema
- Remarks on result:
- other: see Remark
- Remarks:
- Reading: 2nd reading. . Hours after challenge: 48.0. Group: test group. Dose level: 1% C.I. Pigment Red 3 in petrolatum. No with. + reactions: 1.0. Total no. in groups: 10.0. Clinical observations: One animal of the treated group showed very slight to well-defined erythema.
- Interpretation of results:
- not sensitising
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Executive summary:
Testing for sensitizing properties of Pigment Red 3 was performed in female Guinea pigs according to the method of Magnusson & Kligman.
Intra dermal induction was performed using 0.2% Pigment Red 2 in semi-liquid paraffin. Dermal induction was carried out with 5%, challenge treatment with 1% Pigment Red 3 in petrolatum.
Four animals of the treatment group showed a positive skin response after the first challenge procedure and one animal reacted after the second challange. If the effects observed at the first challange are due to sensitization, then equal or even stronger reactions would be expected after the second challenge procedure. Therefore, the reactions noted in the three other animals at the first challange are considered to be rather unspecific irritation effects than allergic reactions.
Based on the results of this study Pigment Red 3 is not considered to be a skin sensitizer.
Reference
Endpoint conclusion
- Endpoint conclusion:
- no adverse effect observed (not sensitising)
- Additional information:
Skin sensitisation
Skin sensitising potential of Pigment Red 3 was tested in female Guinea pigs. Four animals of the treatment group showed a positive skin response after the first challenge procedure and one animal reacted after the second challenge. If the effects observed at the first challange are due to sensitization, then equal or even stronger reactions would be expected after the second challange procedure. Therefore, the reactions noted in the three other animals at the first challenge are considered to be rather unspecific irritation effects than allergic reactions.
Based on the results of this study Pigment Red 3 is not considered to be a skin sensitizer.
The following information is taken into account for any hazard / risk assessment:
Pigment Red 3 has been tested in female Guinea pigs to assess the sensitising potential of the test item. Based on the results of this study Pigment Red 3 is not considered to be a skin sensitizer.
Value used for CSA: not sensitising
Respiratory sensitisation
Endpoint conclusion
- Endpoint conclusion:
- no study available
- Additional information:
Respiratory sensitisation
The following information is taken into account for any hazard / risk assessment:
Respiratory tract sensitisation:
Substance is not classified for this endpoint. The substance is considered not to exert any sensitizing effects on the respiratory tract; when aerosolized in respirable form, the substance is considered likely to behave like an inert dust.
Non-human information: This information is not available.
Justification for classification or non-classification
Pigment Red 3 did not show skin sensitising properties in female Guinea pigs. No skin reactions were seen in 28 healthy young female volunteers in a 48 hour patch test with 1% C.I. Pigment Red 3 in petrolatum (Kgzuka et al.1980)
However allergic skin reactions or case reports of acute contact dermatitis to Pigment Red 3 have been described in the literature. Slight erythema or erythema with edema were observed in patients with pigmented cosmetic dermatitis in patch or photopatch tests with C.I. Pigment Red 3 after application for 48 or 72 hours. Positive reactivity was 34.2% (13/38) (Sugai et al.1977). The reddening and swelling of the skin were seen in five of 155 patients with cosmetic dermatitis in a 48-h path tests with 5% C.I. Pigment Red 3 in polyethylene glycol; slight reddening was seen in another 25 of the patients (MJCDRG 1978). In a patch test, negative reaction was observed with 1% Pigment Red 3 (in petrolatum) in the skin of patients who were suffered from dermatitis caused by Brilliant Lake Red R.
It can reasonably be deduced that Pigment Red 3 does not cause respiratory tract sensitization and thus does not have to be classified 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
- Pigment Red 3 did not cause skin sensitization, and
- it is unlikely that Pigment Red 3 can interact with the immune system due to its extremely low solubility in water and n-octanol.
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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