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EC number: 612-722-9 | CAS number: 61931-07-5
- 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:
- 1984
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 985
- Report date:
- 1985
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- other: MAGNUSSON B. - KLIGMAN A.M. The identification of contact allergens by animal assay "The guinea pig maximization test". J. Invest. Derm. 1969,52,3,268-276
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 406 (Skin Sensitisation)
- GLP compliance:
- yes
- Type of study:
- guinea pig maximisation test
- Justification for non-LLNA method:
- An in vitro or in chemico skin sensitisation study does not need to be conducted because adequate data from an in vivo skin sensitisation study (different from LLNA test) is available.
Test material
- Reference substance name:
- Reaction products of diazotised 4'-aminoazobenzene-4-sulphonic acid, coupled with resorcinol and diazotised sodium 4-aminobenzenesulfonate, sodium salts
- EC Number:
- 612-722-9
- Cas Number:
- 61931-07-5
- Molecular formula:
- not applicable
- IUPAC Name:
- Reaction products of diazotised 4'-aminoazobenzene-4-sulphonic acid, coupled with resorcinol and diazotised sodium 4-aminobenzenesulfonate, sodium salts
- Test material form:
- solid: particulate/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: C.E.R.J. (53940 Saint Berthevin, France)
-Weight at study initiation:
test group: 374 g for the males and 360 g for the females
control group: 369 g for the males and 356 g for the females.
-Housing: the animals were housed individually in polypropylene cages (0,43 x 0,23 x 0,17 m). Each cage was equipped with a food container and a water bottle. Wooden saw dust chemical analysis was carried out periodically by the Laboratoire Municipal de Rouen (76000 Rouen, France).
-Diet: the animals were fed ad libitum during the study, with a certified pelleted diet Rabbit diet S.Q.C. (Special Diets Services Ltd., Nitham, Essex, England).
-Water: the animals had free access to bottles containing tap water filtered with Millipore filters (0,22 micron) and supplemented with vitamin C. Bacteriological and chemical water analysis and detection for major contaminants were performed regularly by the Laboratoire Municipal de Rouen (76000 Rouen, France).
-Acclimation period: 7 days.
ENVIRONMENTAL CONDITIONS
-Temperature (°C): 18 ± 3 °C
-Humidity (%): 50 ± 20 %
-Air changes (per hr): The animals were maintained in an air conditioned room. The incoming, non-recycled air, was filtered with an absolute filter.
-Photoperiod (hrs dark / hrs light): the light/dark cycle was 12 hours per day.
Study design: in vivo (non-LLNA)
Inductionopen allclose all
- Route:
- intradermal
- Vehicle:
- water
- Concentration / amount:
- 2.5 %
- Day(s)/duration:
- day 0
- Route:
- epicutaneous, semiocclusive
- Vehicle:
- unchanged (no vehicle)
- Concentration / amount:
- 0.5 g
- Day(s)/duration:
- day 8 for 48 hours
Challenge
- No.:
- #1
- Route:
- epicutaneous, semiocclusive
- Vehicle:
- water
- Concentration / amount:
- 0.5 g
- Day(s)/duration:
- day 25 for 24 hours
- No. of animals per dose:
- 10 per sex per dose
- Details on study design:
- RANGE FINDING TESTS: yes
MAIN STUDY
-INDUCTION EXPOSURE
- No. of exposures: 3 x 2 intradermal injections 0.1 ml each
-Exposure period: day 0
-Test groups: 20 animals (10 ♂ - 10 ♀)
-Control group: 10 animals (5 ♂ - 5 ♀)
-Site: on the scapula on a surface area of 4 x 2 cm (one injection of each solution per flank).
-Concentrations:
Test group: 2.5 %
Control group: vehicle only
-Solutions for each injection site
Test group
1. Freund's complete adjuvant at 50 % in saline (NaCl 9 x 0/00)
2. Test sample at the concentration of 2.5 % in distilled water.
3. A 50/50 (v/v) mixture of Freund's complete adjuvant diluted at 50 % in saline (NaCl 9 x 0/00) and test sample at the concentration previously determined in a preliminary study.
Control group
1. Freund's complete adjuvant at 50 % in saline (NaCl 9 x 0/00)
2. Distilled water.
3. A 50/50 (v/v) mixture of Freund's complete adjuvant diluted at 50 % in saline (NaCl 9 x 0/00) and distilled water.
-CHALLENGE EXPOSURE
-No. of exposures: one
-Day(s) of challenge: day 8
- Test groups: 20 animals (10 ♂ - 10 ♀)
- Control group: 10 animals (5 ♂ - 5 ♀)
-Site: scapular region
-Concentrations:
Test group: 0.5 g
Control group: 0.5 ml of the vehicle
-Evaluation (hr after challenge): 48 h
-Other: On Day 7; 0.5 ml of sodium lauryl sulfate 10 % in codex vaseline were applied on the scapular region to provoke a local irritation.
B. CHALLENGE EXPOSURE
- No. of exposures: 1
- Day(s) of challenge: 25
- Test groups: 20 animals (10 ♂ - 10 ♀)
- Control group: 10 animals (5 ♂ - 5 ♀)
- Site: flanks
- Concentrations:
Test group: 0.5 g undiluted test sample
Control group: 0.5 ml of the vehicle (distilled water)
- Evaluation (hr after challenge): 24 h
-Other: occlusive patch tests were applied on 4 cm². The patches were kept in place by an hypo-allergenic tape. The right flank was used as negative control. - Positive control substance(s):
- no
Results and discussion
In vivo (non-LLNA)
Resultsopen allclose all
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- test chemical
- Dose level:
- 2.5 % in distilled water (intradermal induction)
- No. with + reactions:
- 0
- Total no. in group:
- 19
- Clinical observations:
- no change in behaviour nor clinical signs due to treatment were observed during the study
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 2.5 % in distilled water (intradermal induction)
- No. with + reactions:
- 0
- Total no. in group:
- 19
- Clinical observations:
- no change in behaviour nor clinical signs due to treatment were observed during the study
- Remarks on result:
- no indication of skin sensitisation
- Reading:
- 1st reading
- Hours after challenge:
- 24
- Group:
- negative control
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Clinical observations:
- no change in behaviour nor clinical signs due to treatment were observed during the study
- Reading:
- 2nd reading
- Hours after challenge:
- 48
- Group:
- negative control
- Dose level:
- 0
- No. with + reactions:
- 0
- Total no. in group:
- 10
- Clinical observations:
- no change in behaviour nor clinical signs due to treatment were observed during the study
- Group:
- positive control
- Remarks on result:
- not measured/tested
Any other information on results incl. tables
-Mortality
One male of the treated group was found dead on Day 22.
-Macroscopic and microscopic observation:
Individual macroscopic and microscopic observations are given thereafter.
1. Macroscopic observations
No local reaction was observed on the right flank 24 and 48 h after patch removal. Due to the staining of the skin by the test sample, the scoring of the cutaneous reaction was not recorded of the left flank. No oedematous reaction was observed 24 h and 48 h after patch removal.
2. Microscopic observation:
The slight differences in cutaneous reactions noted between animals from groups I and II were considered to be of no toxicological importance. Occasionnal foci of inflammatory cells in the upper dermis were more frequently observed in animals from group II (more often in the right flank than the left one).
One animal showed an epidermic vesicle (n° 314, group II, left flank). Two others showed lninimal spongiosis (n° 326, group II, right flank n° 329, group II, left flank).
Treated areas were coloured by the test sample. In general, the microscopic observations showed that only ea few keratinized flakes were coloured by the test sample. In two cases (n° 305 and n° 317, group I), they appeared on the control flank due to a technical artefact. In two cases (n° 318, group I - n° 325 group II), they did not appear on any flank.
Applicant's summary and conclusion
- Interpretation of results:
- other: not classified according to the CLP Regulation (EC 1272/2008)
- Conclusions:
- Under the experimental conditions, the test item did not provoke any cutaneous sensitization in the guinea pig.
- Executive summary:
The sensitizing potential of substance was tested after intradermal injections and cutaneous applications in ten male and ten female Albino Guinea Pigs, to the method established by B. Magnusson and A. Kligman *. The intradermal induction was performed at the concentration of 2.5 % in distilled water. In the epicutaneous induction and in the challenge patch with undiluted test item were used. The behaviour of the animals was not influenced by the treatment. Due to the staining of the skin, no local reaction was noted 24 h and 48 h after removal of the challenge patch test.
Skin samples of both flanks were taken and fixed in formalin 10 %. Histological examination of the skin samples did not reveal evidence of a sensitization reaction.
In conclusion, under the experimental conditions, the test sample did not provoke any cutaneous sensitization in the guinea pig.
*MAGNUSSON B. - KLIGMAN A.M. The identification of contact allergens by animal assay "The guinea pig maximization test". J. Invest. Derm. 1969,52,3,268-276
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