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EC number: 267-758-4 | CAS number: 67923-43-7
- 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 irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- From April 27 to 30, 1993
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 993
- Report date:
- 1993
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- 3,3'-[[4-[(2-chloro-4-nitrophenyl)azo]phenyl]imino]bis[propiononitrile]
- EC Number:
- 223-765-4
- EC Name:
- 3,3'-[[4-[(2-chloro-4-nitrophenyl)azo]phenyl]imino]bis[propiononitrile]
- Cas Number:
- 4058-30-4
- Molecular formula:
- C18H15ClN6O2
- IUPAC Name:
- 3,3'-({4-[(2-chloro-4-nitrophenyl)diazenyl]phenyl}imino)dipropanenitrile
- Test material form:
- solid
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST SYSTEM
- Species: Albino Rabbit, New Zealand White, (SPF-Quality)
- Original Source: Broekman Institute, Someren, The Netherlands
- Selection of animals: Healthy animals, not previously used, were selected prior to treatment. Both flanks of each animal were free of interfering lesions, irritation or defects.
- Total number of animals: 3 male rabbits
- Allocation and age at start of treatment: Animals 1248, 1249 & 1254; approx. 12 weeks
- Identification: Ear tag.
- Acclimatisation: At least five days after veterinary examination.
HUSBANDRY
- Room No.: Animal 1254 was housed in room 11 during acclimatisation, but was moved to room 10 at day -1 (one day before treatment). Animals 1248 and 1249 were housed in room 10 during acclimatisation. All animals were housed in room 10 during the observation period of the study.
- Conditions: Standard Laboratory Conditions. Air-conditioned with 15 air changes per hour and controlled environment with optimal conditions considered as being a temperature of 21°C and a relative humidity of 55%. Fluctuations from these optimal conditions were noted, but were considered not to have affected study integrity. Lighting was 12 hours artificial fluorescent light and 12 hours dark per day. Music during the light period.
- Accommodation: Individually in labelled cages with perforated floors and equipped with an automatic drinking system (ITL, Bergen, The Netherlands).
- Diet: Standard laboratory rabbit diet (LKK-20, pellet diameter 4mm, Hope Farms, Woerden, The Netherlands) approx. 100 gram per day.
this report.
- Water: Free access to tap-water diluted with decalcified water.
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- shaved
- Vehicle:
- not specified
- Controls:
- not specified
- Amount / concentration applied:
- 0.5 g
- Duration of treatment / exposure:
- 4 hours
- Observation period:
- 72 hours
- Number of animals:
- 3
- Details on study design:
- TREATMENT
Approximately 24 hours before treatment, the dorsal fur was shaved with electric clippers, exposing an area of approximately 150 square centimeters (10x15 cm2). Prior to test substance administration, the animals were physically examined and the shaved area of skin to be treated was normal.
On test day 1, 0.5 gram of the test substance was applied to the intact skin of the shaved area on one flank, using a Scotchpak-non-woven patch (2x3 cm, 3M,
St.Paul, U.S.A.) mounted on Micropore tape (3M, St. Paul, U.S.A.). The contralateral flank was similarly prepared (but without test substance) to act as a procedural control. The dressing was wrapped around the abdomen and secured with an elastic bandage (Coban, 3M, St. Paul, U.S.A.).
Four hours after the application, the dressing was removed and the remaining test substance removed using a tissue moistened with tap-water and subsequently a dry tissue.
The skin areas concerned of the animals were re-shaved at least 3 hours before the observations, when considered necessary to facilitate scoring.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- no indication of irritation
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- no indication of irritation
- Other effects:
- COLOURATION
Red staining of the treated skin by the test substance was observed during the observation period. The staining did not interfere with the scoring of the erythema.
BODY WEIGHTS
The body weights and variability in body weight gain of the animals were considered to be normal.
TOXICITY SYMPTOMS / MORTALITY
No symptoms of systemic toxicity were observed in the animals during the test period and no mortality occurred.
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- The substance did not cause any signs of irritation on rabbit skin. The substance is not classifiable according to GHS criteria.
- Executive summary:
Method
The Skin irritation was determined in an irritation test on rabbits according to the OECD Guideline 404 and the EU Method B.4.
Observations
The test substance was applied onto shaved skin of three male albino rabbits using semi-occlusive dressings for 4 hours, followed by four observations at approximately 1, 24, 48 and 72 hours days after removal of the dressings and remaining test substance. Under the conditions of this study, no skin irritation was caused by the test substance and no corrosive effect occurred on the skin in any of the three rabbits. In the area of application, red staining of the treated skin was observed, which did not interfere with the scoring of erythema. No signs of systemic intoxication were observed during the study period. The test substance resulted in a primary irritation index of 0.0 (non-irritating) when applied to the intact rabbit skin.
Result
Not irritant.
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