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EC number: 942-100-5 | CAS number: -
- 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
Skin sensitisation
Administrative data
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- From February 28 to April 13, 1989
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 989
- Report date:
- 1989
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.6 (Skin Sensitisation)
- Deviations:
- not specified
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- Deviations:
- not specified
- Qualifier:
- according to guideline
- Guideline:
- other: Mangusson, B., Kligman, A.M., 1970. " Allergenic Contact Dermatitis in the Guinea-Pig: Identification of Contact Allergens"
- Deviations:
- not specified
- GLP compliance:
- yes
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- A LLNA study has not been conducted because adequate data from guinea pig Maximisation test study are already available.
Test material
- Reference substance name:
- Reaction products of copper phthalocyanine, sulfuric acid, and sodium carbonate
- EC Number:
- 942-100-5
- Molecular formula:
- Not applicable: UVCB substance
- IUPAC Name:
- Reaction products of copper phthalocyanine, sulfuric acid, and sodium carbonate
- Test material form:
- solid: particulate/powder
- Remarks:
- migrated information: powder
Constituent 1
In vivo test system
Test animals
- Species:
- guinea pig
- Strain:
- Dunkin-Hartley
- Sex:
- male/female
- Details on test animals and environmental conditions:
- TEST ANIMALS
- Source: Kleintierfarm Madoerin AG
- Age at study initiation: 7 - 8 weeks
- Weight at study initiation: 230 - 343 g (♂); 263 - 317 g (♀)
- Housing: Individually in Makrolon type-3 cages with standard softwood bedding ("Lignocel", Schill AG, 4132 Muttenz, Switzerland).
- Diet (e.g. ad libitum): Pelleted standard Kliba 342, Batch 50/89 guinea pig breeding/ maintenance diet ("Kliba", Klingentalmuehle AG, 4303 Kaiseraugst, Switzerland) ad libitum.
- Water (e.g. ad libitum): Community tap water from Itingen, ad libitum
- Acclimation period: Six days under test conditions after veterinary examination
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 22 ±3 °C
- Humidity (%):40-70 %
- Air changes (per hr): 10-15 air changes per hour and hourly monitored environment
- Photoperiod (hrs dark / hrs light): 12 hours artificial fluorescent light/12 hours dark.
- Music/light period
Study design: in vivo (non-LLNA)
Inductionopen allclose all
- Route:
- other: Pretest intradermal injection
- Vehicle:
- water
- Concentration / amount:
- 5%, 3%, 1%
- Route:
- other: Pretest epidermal application
- Vehicle:
- petrolatum
- Concentration / amount:
- 25%, 10%, 5%, 3%
Challengeopen allclose all
- No.:
- #1
- Route:
- intradermal
- Vehicle:
- petrolatum
- Concentration / amount:
- 3%
- No.:
- #2
- Route:
- other: epidermal application
- Vehicle:
- petrolatum
- Concentration / amount:
- 5 %
- No. of animals per dose:
- Pretest
Intradermal injection: 1 animals per sex, 3 concentrations per animal
Epidermal application: 2 animals per sex, 4 concentrations per animal
Main study
10 animals per sex per concentration - Details on study design:
- RANGE FINDING TESTS:
MAIN STUDY
A. INDUCTION EXPOSURE
- No. of exposures: three pair of intradermal injection
- Exposure period:
injection: 1 week before epidermal treatment,
epidermal exposure: 48 hours
- Test groups: 10 males and 10 females guinea pig
- Control group: 5 males and 5 females guinea pig treated as the test group with the omission of the test article
- Site: area of dorsal skin from the scapular region (ca. 6*8 cm) clipped free of hair
- Concentrations of intradermal injection :
1) Freunds' complete adjuvant 50:50 with distilled water for injection;
2) the test article, diluited to 3% with distilled water;
3) the test article at concentration used in 2), emulsified in a 50:50 mixture of Freunds' complete adjuvant and the vehicle used in 2)
- Concentrations of epidermal application: 10% in petrolatum oil
B. CHALLENGE EXPOSURE
- No. of exposures: 1
- Day(s) of challenge: 2 weeks after the epidermal induction application
- Exposure period: 24 hours after the application, the patches were removed
- Test groups: 10 males and 10 females guinea pig
- Control group: 5 males and 5 females guinea pig treated as the test group (with 5% of the test substance)
- Site: clipped and shaved area of 5*5 cm in the left and right flank of each guinea pig
- Concentrations: 5% in petrolatum oil on the right flank of guinea pigs; only vehicle on the left flank of guinea pigs
- Evaluation (hr after challenge): immediately, 24 hours and 48 hours after removal of patches
OTHER:
RE-CHALLENGE EXPOSURE
- No. of exposures: 1
- Day(s) of challenge: 2 weeks after the first challenge
- Exposure period: 24 hours after the application, the patches were removed
- Test groups:10 males and 10 females guinea pig
- Control group:5 males and 5 females guinea pig treated as the test group with the vehicle only
- Site: clipped and shaved area of 5*5 cm in the left and right flank of each guinea pig
- Concentrations:
Test group: 5% in petrolatum oil on the right flank of guinea pigs; only vehicle on the left flank of guinea pigs
Control group: vehicle only on the left flank
- Evaluation (hr after challenge): immediately, 24hours and 48 hours after removal of patches
Test condtions
Pretest intradermal injection: Distilled water;
Pretest epidermal application: Petrolatum oil;
Main test: Petrolatum oil
Pretest (intradermal injection)
5%, 3%, 1%
Pretest (epidermal application)
25%, 10%, 5%, 3%
Main test (intradermal injection)
According to the Mangusson-Kligman, and to the findings observed, the concentration selected for the main study was 3%
Main test (epidermal application)
According to the Mangusson-Kligman, and to the findings observed, the concentration selected for the induction period was 10% and for the challenge procedure 5%. - Positive control substance(s):
- yes
- Remarks:
- A control group is tested with Dinitro-chloro-benzene twice a year as a sensitivity check of the guinea pig strain
Results and discussion
- Positive control results:
- positive control with DNCB
positive reaction/total animals: 67%
In vivo (non-LLNA)
Resultsopen allclose all
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- other: Control Group
- Dose level:
- 5% in petrolatum oil
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: other: Control Group. Dose level: 5% in petrolatum oil. No with. + reactions: 0.0. Total no. in groups: 10.0.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- other: Control Group
- Dose level:
- only vehicle
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: other: Control Group. Dose level: only vehicle. No with. + reactions: 0.0. Total no. in groups: 10.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- other: Control Group
- Dose level:
- 5% in petrolatum oil
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: other: Control Group. Dose level: 5% in petrolatum oil. No with. + reactions: 0.0. Total no. in groups: 10.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- other: Control Group
- Dose level:
- only vehicle
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: other: Control Group. Dose level: only vehicle. No with. + reactions: 0.0. Total no. in groups: 10.0.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 5% in petrolatum oil
- No. with + reactions:
- 3
- Total no. in group:
- 20
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: test group. Dose level: 5% in petrolatum oil. No with. + reactions: 3.0. Total no. in groups: 20.0.
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- only vehicle
- No. with + reactions:
- 0
- Total no. in group:
- 2
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 24.0. Group: test group. Dose level: only vehicle. No with. + reactions: 0.0. Total no. in groups: 2.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 5% in petrolatum oil
- No. with + reactions:
- 1
- Total no. in group:
- 20
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: test group. Dose level: 5% in petrolatum oil. No with. + reactions: 1.0. Total no. in groups: 20.0.
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- only vehicle
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 48.0. Group: test group. Dose level: only vehicle. No with. + reactions: 0.0. Total no. in groups: 20.0.
- Reading:
- rechallenge
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- only vehicle
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: rechallenge. . Hours after challenge: 24.0. Group: negative control. Dose level: only vehicle. No with. + reactions: 0.0. Total no. in groups: 10.0.
- Reading:
- rechallenge
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- only vehicle
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Remarks on result:
- other: Reading: rechallenge. . Hours after challenge: 48.0. Group: negative control. Dose level: only vehicle. No with. + reactions: 0.0. Total no. in groups: 10.0.
- Reading:
- rechallenge
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 5% in petrolatum oil
- No. with + reactions:
- 2
- Total no. in group:
- 20
- Remarks on result:
- other: Reading: rechallenge. . Hours after challenge: 24.0. Group: test group. Dose level: 5% in petrolatum oil. No with. + reactions: 2.0. Total no. in groups: 20.0.
- Reading:
- rechallenge
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 5% in petrolatum oil
- No. with + reactions:
- 1
- Total no. in group:
- 20
- Remarks on result:
- other: Reading: rechallenge. . Hours after challenge: 48.0. Group: test group. Dose level: 5% in petrolatum oil. No with. + reactions: 1.0. Total no. in groups: 20.0.
- Reading:
- rechallenge
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- only vehicle
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- other: Reading: rechallenge. . Hours after challenge: 24.0. Group: test group. Dose level: only vehicle. No with. + reactions: 0.0. Total no. in groups: 20.0.
- Reading:
- rechallenge
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- only vehicle
- No. with + reactions:
- 0
- Total no. in group:
- 20
- Remarks on result:
- other: Reading: rechallenge. . Hours after challenge: 48.0. Group: test group. Dose level: only vehicle. No with. + reactions: 0.0. Total no. in groups: 20.0.
Applicant's summary and conclusion
- Interpretation of results:
- other: CLP criteria not met
- Conclusions:
- Not sensitising
- Executive summary:
The substance was tested according to OECD 406, EU Method B.6 and according to Mangusson, B., Kligman, A.M., 1970. " Allergenic Contact Dermatitis in the Guinea-Pig: Identification of Contact Allergens". During the test 5 males and 5 females guinea pigs were used as control group, treated with vehicle only during the Induction test and 10 males and 10 females were used as test group, treated with test article during the all parts of the experiment.
The test shows low reactions to the test item, up to 15% of positive reaction.
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