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Diss Factsheets
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EC number: - | 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, other
- Remarks:
- An in vitro eye irritation study does not need to be conducted because adequate data from an in vivo study are available.
- Type of information:
- other: read across from supporting substance
- Adequacy of study:
- key study
- Study period:
- September 11, 1975
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 975
- Report date:
- 1975
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: "Hazardous Substances Regulations" under the U.S.A. federal Hazardous Substances Labelling Act Sect. 191.12 (February 1965)
- Deviations:
- not specified
- GLP compliance:
- no
- Remarks:
- Study conducted before 1981
Test material
- Reference substance name:
- Acid Blue 158
- IUPAC Name:
- Acid Blue 158
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Strain: Porton strain
- Age at study initiation: 9-15 weeks old
- Weight at study initiation: 2.44 kgs. (♂) 30d 2.10 kgs. (♀)
- Housing: bred on the premises and maintained under a semi-barrier system
- Diet: A commercial irradiated diet (Styles-Oxoid) was fed ad libitum
- Water: Sterile filtered water was available at all times
- Acclimation period: one week prior to the start of the trial
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20 ± 1°C
- Humidity (%): 50-70 %
- Photoperiod (hrs dark / hrs light): Animals were exposed to artificial light for 10 hours daily from 08.00-18.00 hours
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- yes, concurrent no treatment
- Amount / concentration applied:
- TEST MATERIAL
- Amount applied: 100 mg - Duration of treatment / exposure:
- Single injection
- Observation period (in vivo):
- The rabbits were examined 1, 24, 48 and 72 hours, 6, 10 and 14days after application of the test compound and for any further period that was considered necessary.
- Number of animals or in vitro replicates:
- 5 male and 1 female
- Details on study design:
- REMOVAL OF TEST SUBSTANCE
- Washing: yes, after 30 seconds the compound was, as far as possible, flushed out of the eye of three of the rabbits with warm water for 1 minute
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- cornea opacity score
- Basis:
- animal: 14, 15, 16
- Time point:
- other: Mean score after 24, 48 and 72 hours
- Score:
- ca. 0
- Max. score:
- 4
- Reversibility:
- other: no eye effect observed
- Remarks on result:
- other: Rinsed
- Irritation parameter:
- conjunctivae score
- Basis:
- animal: 14, 15
- Time point:
- other: Mean score after 24, 48 and 72 hours
- Score:
- ca. 1
- Max. score:
- 3
- Reversibility:
- not fully reversible within: 72 hours
- Remarks on result:
- other: Rinsed
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- animal: 16
- Time point:
- other: Mean score after 24, 48 and 72 hours
- Score:
- ca. 1.33
- Max. score:
- 3
- Reversibility:
- fully reversible within: 6 days
- Remarks on result:
- other: Rinsed
- Irritation parameter:
- chemosis score
- Basis:
- animal: 14, 15
- Time point:
- other: Mean score after 24, 48 and 72 hours
- Score:
- ca. 0
- Max. score:
- 4
- Reversibility:
- other: no eye effect observed
- Remarks on result:
- other: Rinsed
- Irritation parameter:
- chemosis score
- Basis:
- animal: 16
- Time point:
- other: Mean score after 24, 48 and 72 hours
- Score:
- ca. 0.66
- Max. score:
- 4
- Reversibility:
- fully reversible within: 6 days
- Remarks on result:
- other: Rinsed
Any other information on results incl. tables
A slight to mild conjunctival reaction was seen in all treated eyes one hour after application of the compound. Generally there was very little change by 24 hours and thereafter the reactions subsided slowly with 3/3 washed and 2/3 unwashed eyes returning to normal as follows:- 72 hours (2/3 washed eyes), 6 days (1/3 washed eyes) and 10 days (2/3 unwashed eyes). The remaining unwashed eye still showed a very slight reaction at the termination of the study on day 14. Staining of the conjunctivae by the compound was seen in all eyes for up to 48 hours in the washed eyes, 10 days for 2/3 unwashed eyes and the duration for the remaining eye.
A slight corneal reaction consisting of slight opacity and damage to the surface epithelium was seen in 2/3 unwashed eyes at 24 and 48 hours. Staining of the cornea by the compound was also seen in the unwashed eyes for up to 10 days for 2/3 and the duration for the remaining one.
Applicant's summary and conclusion
- Interpretation of results:
- other: Not classified according to the CLP Regulation (EC n. 1272/2008)
- Conclusions:
- The substance is not irritating for rabbit eyes.
- Executive summary:
The substance has been tested for eye irritation according to The method "Hazardous Substances Regulations" under the U.S. federal Hazardous Substances Labelling Act Sect. 191.12 (February 1965). During the test 5 male and 1 female rabbits are treated with 100 mg of the test compound. After 14 days only one animal (n. 13) showed a redness score (1), nevertheless in order to evaluate the irritation potential of the test item this animal was not considerd because his eyes were not rinsed after application.
The substance is considered to be not irritant for rabbit eyes.
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