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Diss Factsheets
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EC number: 947-662-5 | 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
Eye irritation
Administrative data
- Endpoint:
- eye irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Study performed comparable to OECD 405, but without rinsing, little information on test material, Non GLP. Animals were not specific-pathogen free (non SPF)
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 978
- Report date:
- 1978
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- After the first hour, no rinsing was performed although colouring by the substance interfered with scoring. Directly after applications, eyelids were moved up and down for several seconds.
- Principles of method if other than guideline:
- according to Fed. Reg. 38, No. 187, § 1500.42, 1973 (Draize test)
- GLP compliance:
- no
Test material
- Reference substance name:
- Reaction Products of Naphthalene-1,6-diol with 2-Benzofuran-1,3-dione, sodium salt
- EC Number:
- 947-662-5
- Molecular formula:
- C28H14Na2O5
- IUPAC Name:
- Reaction Products of Naphthalene-1,6-diol with 2-Benzofuran-1,3-dione, sodium salt
- Test material form:
- solid
- Details on test material:
- Name of the test substance used in the study report: Scheckfarbstoff AS
The purity is stated as 100% of the drawn chemical structure in the order sheet. (Chemical structure is identical to the main component of the UVCB, CAS 6359-10-9)
The substance is stated to be a sales product.
The water solubility is indicated to be 20g/L. No information on pH is provided.
Constituent 1
- Specific details on test material used for the study:
- solid
Scheckfarbstoff A.S.
Content: 100%
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- Mean body weight: 2.5 kg
The rabbits are kept in individual cages measuring 540 x 360 x 315 mm or in restraining devices. The animal house is ventilated (renewal of air = 12 times per hour; temperature 22°C; hygrometry 55 +/- 10%). The ear of each animal is pierced and a metal tag attached for individual identification.
200 g of food is provided per animal and day in the form of granules; water is given automatically and ad libitum.
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: untreated eye of the same animal
- Amount / concentration applied:
- 100 mg
- Duration of treatment / exposure:
- Single treatment
- Observation period (in vivo):
- 21 days
- Number of animals or in vitro replicates:
- 6
- Details on study design:
- Single instillation into the conjunctival sac of the right eyelid; the test substance was not washed out. The eye lids were held closed for several seconds and moved gently up and down to voiding loss of the substance .
Readings are made 1 hour, 24 hours, 2 days, 3 days, 4 days and 7 days after instillation. When irritation is persistent, readings are made each week over a maximum periodof 2 weeks. If the lesions are too important and prevent the ocular observations or if the intensity of the lesions increases after 7 days, the animals are sacrificed and the eye examined macrosopically.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- other: 24 - 72 h
- Score:
- 1.4
- Max. score:
- 3
- Reversibility:
- fully reversible within: 14 days
- Irritation parameter:
- iris score
- Basis:
- mean
- Time point:
- other: 24 - 72 h
- Score:
- 1
- Max. score:
- 1
- Reversibility:
- not fully reversible within: 21 days
- Remarks on result:
- other: Circumcorneal injection and congestion of the iris
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Time point:
- other: 24 - 72 h
- Score:
- 3.34
- Max. score:
- 4
- Reversibility:
- not fully reversible within: within 21 days
- Remarks:
- Fully reversible in four rabbits, almost reversed in one animal and strong chemosis in one animal.
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: Days 1, 2, and 3
- Score:
- 35
- Max. score:
- 110
- Reversibility:
- other: not applicable
- Remarks on result:
- other: Index of Ocular Irritation
Any other information on results incl. tables
1 Hour | 24 Hours | 48 Hours | |||||||||||||||||
Range | Animal 1 | Animal 2 | Animal 3 | Animal 4 | Animal 5 | Animal 6 | Animal 1 | Animal 2 | Animal 3 | Animal 4 | Animal 5 | Animal 6 | Animal 1 | Animal 2 | Animal 3 | Animal 4 | Animal 5 | Animal 6 | |
A) Chemosis | 0 - 4 | 2 | 3 | 2 | 2 | 3 | 2 | 3 | 3 | 3 | 3 | 4 | 4 | 3 | 4 | 4 | 2 | 4 | 4 |
B) Discharge | 0 - 3 | 2 | 1 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 2 |
C) Redness | 0 - 3 | 2 | 2 | blue color | 1 | blue color | 2 | 2 | 2 | 2 | 3 | 2 | 3 | 3 | 3 | 3 | 2 | 2 | 2 |
DIRECT PHOTOMOTOR REFLEX OF PUPIL |
Normal | Normal | Normal | Normal | Normal | Normal | Normal | Normal | Normal | Normal | Normal | Normal | Normal | Normal | Normal (Permanent-myosis with preservation of direct photomotor reflex) | Normal (Permanent-myosis with preservation of direct photomotor reflex) | Normal | Normal | |
Congestion of iris | 0-2 | 1 (Cìrcumcorneal injection) | 1 (Circumcorneal injection + congestion of the iris) | ||||||||||||||||
Opacity of cornea | 0-4 | 3 | 3 | 3 | 2 | 3 | 2 | 2 | 2 | 2 | 2 | 2 | 2 | 3 | 3 | 2 | 2 | 2 | 2 |
72 Hours | Day 4 | Day 7 | |||||||||||||||||
Range | Animal 1 | Animal 2 | Animal 3 | Animal 4 | Animal 5 | Animal 6 | Animal 1 | Animal 2 | Animal 3 | Animal 4 | Animal 5 | Animal 6 | Animal 1 | Animal 2 | Animal 3 | Animal 4 | Animal 5 | Animal 6 | |
A) Chemosis | 0 - 4 | 3 | 3 | 4 | 2 | 4 | 3 | 3 | 1 | 4 | 1 | 4 | 2 | 2 | 1 | 4 | 1 | 3 | 1 |
B) Discharge | 0 - 3 | 2 | 1 | 2 | 2 | 3 | 2 | 1 | 0 | 2 | 0 | 1 | 0 | 0 | 0 | 1 | 0 | 2 | 0 |
C) Redness | 0 - 3 | 3 | 2 | 3 | 2 | 2 | 2 | 1 | 1 | 3 | 1 | 3 | 1 | 1 | 1 | 2 | 1 | 2 | 1 |
DIRECT PHOTOMOTOR REFLEX OF PUPIL |
Normal | Normal (Permanent-myosis with preservation of direct photomotor reflex) | Normal | Normal | Normal | Normal (+myosis) | Normal | Normal (+myosis) | Normal | Normal | Normal | Normal (+myosis) | Normal | Normal (+myosis) | Normal | ||||
Congestion of iris | 0-2 | 1 (Circumcorneal injection + congestion of the iris) | 1 (C.i.) | 1 (C.i.) | 1 (C.i.) | 1 (C.i. + C.I.) | 1 (C.i.) | 1 (C.i. + C.I.) | 1 (C.i.) | 1 (C.i.) | 1 (C.i.) | 1 (C.i. + C.I.) | 0 | 1 (C.i. + C.I.) | 1 (C.i.) | ||||
Opacity of cornea | 0-4 | 2 | 2 | 2 | 2 | 2 | 0 | 2 | 0 | 2 | 0 | 2 | 0 | 0 | 0 | 2 | 0 | 3 | 0 |
14 Days | 21 Days | ||||||||||||
Range | Animal 1 | Animal 2 | Animal 3 | Animal 4 | Animal 5 | Animal 6 | Animal 1 | Animal 2 | Animal 3 | Animal 4 | Animal 5 | Animal 6 | |
A) Chemosis | 0 - 4 | 1 | 0 | 4 | 1 | 2 | 1 | 0 | 0 | 1 | 0 | 4 | 0 |
B) Discharge | 0 - 3 | 0 | 0 | 1 | 0 | 2 | 0 | 0 | 0 | 0 | 0 | 2 | 0 |
C) Redness | 0 - 3 | 0 | 0 | 1 | 0 | 1 | 1 | 0 | 0 | 0 | 0 | 2 | 0 |
DIRECT PHOTOMOTOR REFLEX OF PUPIL |
Normal | Normal | Normal | Normal | Normal | Normal | Normal | Normal | Normal | Normal | Normal | Normal | |
Congestion of iris | 0-2 | 1 (C.i. + C.I.) | 1 (C.i.) | 1 (C.i.) | 0 | 1 (C.i. + C.I.) | 1 (C.i.) | 1 (C.i.) | 0 | 1 (C.i.) | 0 | 1 (C.i. + C.I.) | 0 |
Opacity of cornea | 0-4 | 0 | 0 | 0 | 0 | 0* | 0 | 0 | 0 | 0 | 0 | 0* | 0 |
*Revascularization zone well defined on 1/4 of the corneal surface.
Applicant's summary and conclusion
- Interpretation of results:
- Category 1 (irreversible effects on the eye) based on GHS criteria
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