Registration Dossier
Registration Dossier
Use of this information is subject to copyright laws and may require the permission of the owner of the information, as described in the ECHA Legal Notice.
EC number: 304-762-8 | CAS number: 94279-16-0
Toxicological information
Eye irritation
Currently viewing:
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:
- study well documented, meets generally accepted scientific principles, acceptable for assessment
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 000
- Report date:
- 2000
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: Real Decree 363/1995 and Real Decree 1078/93
- Principles of method if other than guideline:
- Real Decree 363/1995 is the transposition of Directive 67/548/EEC in Spanish legislation
- GLP compliance:
- no
- Remarks:
- Centre Certificated ISO 9001 by National Accreditation Programme (certificate N. 98 - 1101)
Test material
- Reference substance name:
- Tetrasodium 4-[[3,5-bis[[4-[(4-nitro-2-sulphonatophenyl)amino]phenyl]azo]-2,4(or 2,6)-dihydroxyphenyl]azo]-5-hydroxynaphthalene-2,7-disulphonate
- EC Number:
- 304-762-8
- EC Name:
- Tetrasodium 4-[[3,5-bis[[4-[(4-nitro-2-sulphonatophenyl)amino]phenyl]azo]-2,4(or 2,6)-dihydroxyphenyl]azo]-5-hydroxynaphthalene-2,7-disulphonate
- Cas Number:
- 94279-16-0
- Molecular formula:
- C40H24N10Na4O19S4
- IUPAC Name:
- tetrasodium 4-[(1E)-2-{2,6-dihydroxy-3,5-bis[(1E)-2-{4-[(4-nitro-2-sulfonatophenyl)amino]phenyl}diazen-1-yl]phenyl}diazen-1-yl]-5-hydroxynaphthalene-2,7-disulfonate
- Test material form:
- solid: particulate/powder
- Remarks:
- migrated information: powder
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: certificated provider
- Sex: males
- Housing: individual inoxidable steel cages, Tecniplast
- Diet: daily 150 g of special fodder for experimental rabbits, supplied by an authorized provider
- Water: automatic ad libitum, treated and filtered
- Marking: tatoo on the upper side of ear
- Acclimation period: 7 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 21 ± 2
- Humidity (%): 55 ± 25
- Air changes (per hr): 15 changes of pre-filtered air per hour
- Photoperiod (hrs dark / hrs light): 12/12
Other materials used:
Balance: COBOS D 6000-SX
Gloves: vinyl and latex gloves
Syringes: 1 mL of volume
Manual lamp
Wash bottle with saline solution
Colircusi fluorescein or equivalent authorized
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- yes, concurrent no treatment
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied: in case of liquid substance were administrated 0.1 mL, in case of solid substance 0.1 g - Duration of treatment / exposure:
- 72 hours
- Observation period (in vivo):
- 7 days
- Number of animals or in vitro replicates:
- 3 males
- Details on study design:
- TOOL USED TO ASSESS SCORE: light of a manual lamp for examing the reactions and fluorescein for evaluating corneal lesions
SCORING SYSTEM:
Cornea
Opacity: degree of density (readings should be taken from most dense area)*
No ulceration or opacity: 0 Scattered or diffuse areas of opacity (other than slight dulling of normal lustre);
details of iris clearly visible: 1
Easily discernible translucent area; details of iris slightly obscured: 2
Nacrous area; no details of iris visible; size of pupil barely discernible: 3
Opaque cornea; iris not discernible through the opacity: 4
Maximum possible: 4
* The area of corneal opacity should be noted
Iris
Normal: 0
Markedly deepened rugae, congestion, swelling, moderate circumcorneal hyperaemia;
or injection; iris reactive to light (a sluggish reaction is considered to be an effect: 1
Hemorrhage, gross destruction, or no reaction to light: 2
Maximum possible: 2
Conjunctivae
Redness (refers to palpebral and bulbar conjunctivae; excluding cornea and iris)
Normal: 0
Some blood vessels hyperaemic (injected): 1
Diffuse, crimson colour; individual vessels not easily discernible: 2
Diffuse beefy red: 3
Maximum possible: 3
Chemosis
Swelling (refers to lids and/or nictating membranes)
Normal: 0
Some swelling above normal: 1
Obvious swelling, with partial eversion of lids: 2
Swelling, with lids about half closed: 3
Swelling, with lids more than half closed: 4
Maximum possible: 4
DEFINITIONS:
1. Eye irritation is the production of changes in the eye following the application of a test substance to the anterior surface of the eye, which are fully reversible within 21 days of application.
2.Eye corrosion is the production of tissue damage in the eye, or serious physical decay of vision, following application of a test substance to the anterior surface of the eye, which is not fully reversible within 21 days of application.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 1
- Max. score:
- 4
- Reversibility:
- fully reversible
- Remarks:
- within 7 days for all rabbits
- Irritation parameter:
- iris score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- ca. 0.67
- Max. score:
- 2
- Reversibility:
- fully reversible
- Remarks:
- Rabbit 1: 72 hours; Rabbit 2: 48 hours; Rabbit 3: 7 days
- Irritation parameter:
- conjunctivae score
- Remarks:
- Congiuntival erythema
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- ca. 1.89
- Max. score:
- 3
- Reversibility:
- fully reversible
- Remarks:
- within 14 days for rabbit 1 and 3; within 7 days for rabbit 2
- Irritation parameter:
- chemosis score
- Remarks:
- Congiuntival edema
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- ca. 1.44
- Max. score:
- 4
- Reversibility:
- fully reversible
- Remarks:
- wihtin 7 days for all rabbits
Any other information on results incl. tables
Results
| Rabbit 1 |
Rabbit 2 | Rabbit 3 | |||||||||||||||||
| 1h | 24h | 48h | 72h | 7d | 1h | 24h | 48h | 72h | 7d | 1h | 24h | 48h | 72h | 7d | |||||
| Corneal opacity | 0 | 1 | 1 | 1 | 0 | 0 | 1 | 1 | 1 | 0 | 0 | 1 | 1 | 1 | 0 | ||||
| Iris | 0 | 1 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 1 | 1 | 1 | 0 | ||||
| Conjunctival erythema | 0 | 2 | 2 | 2 | 1 | 0 | 2 | 2 | 1 | 0 | 0 | 2 | 2 | 2 | 1 | ||||
| Conjuntival oedema | 3 | 2 | 2 | 1 | 0 | 3 | 2 | 1 | 1 | 0 | 3 | 2 | 1 | 1 | 0 | ||||
Applicant's summary and conclusion
- Interpretation of results:
- GHS criteria not met
- Conclusions:
- Some irritating effects on all rabbits fully reversible within 14 days.
- Executive summary:
- The substance was tested for eye irritation according to the Real Decree 363/1995 is the transposition of Directive 67/548/EEC in Spanish legislation. Based on test results, the susbtance needs to be considered as eye irritant and required the hazard statement H319, Causes serious eye irritation.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
Reproduction or further distribution of this information may be subject to copyright protection. Use of the information without obtaining the permission from the owner(s) of the respective information might violate the rights of the owner.
