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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: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- From 1992-07-27 to 1992-07-31
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: see 'Remark'
- Remarks:
- GLP study in accordance with recognised test guideline but: Lot/batch No.: not stated Expiration date of the lot/batch: not stated NOTE: study deemed acceptable because spectral data for test item are available, covering approximately before and after the test period - see section 1.4 Analytical Information.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 992
- Report date:
- 1992
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- Version / remarks:
- 1987
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.5 (Acute Toxicity: Eye Irritation / Corrosion)
- Version / remarks:
- 1984
- Deviations:
- no
- GLP compliance:
- yes
Test material
Constituent 1
- Specific details on test material used for the study:
- Purity: Ca. 100%
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: Rosemead Rabbits, Rosemead, Waltham Abbey, Essex, England
- Age at study initiation: 4 - 4 1/2 months
- Weight at study initiation: 3.31 - 3.52 kg
- Housing: Individually in suspended stainless steel cages (Type RC10/L/TR6) monted in mobile batteries (Modular Sysytems and Development Company Limited, London, England). The cages measured 61 x 76 x 46 cm high and were fitted with perforayed countersunk floor panels. A tray beneath the floor was lined with absorbent paper which was changed regularly.
- Diet (e.g. ad libitum): Animals had free access to food hoppers containing standard pelleted rabbit diet, (S.Q.C. Rabbit Diet - Special Diets Services
Limited, Witham, Essex, England). The manufacturer supplied analytical data with each batch of diet supplied. This included the concentration of nutritional components, aflatoxins and selected heavy metals, pesticides and micro-organisms. The diet contains no added antibiotic or other chemotherapeutic or prophylactic treatment.
- Water (e.g. ad libitum): The rabbits had free access to tap water taken from the public supply
- Acclimation period: Three weeks.
ENVIRONMENTAL CONDITIONS
- Temperature (°C): Target value 18ºC, actual range 15ºC to 23ºC
- Humidity (%): Target value 55% RH, actual range 40% - 70% RH
- Air changes (per hr): 15
- Photoperiod (hrs dark / hrs light): 12 / 12
IN-LIFE DATES: From: 27 July 1992 To 31 July 1992
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- yes, concurrent no treatment
- Amount / concentration applied:
- 100 mg of unchanged substance was instilled into the right eye.
- Duration of treatment / exposure:
- Indeterminate
- Observation period (in vivo):
- 72 hours
- Number of animals or in vitro replicates:
- 3 animals were used in this study
- Details on study design:
- REMOVAL OF TEST SUBSTANCE
- Washing (if done): No
SCORING SYSTEM: Darize
Refer to Attached Background Information for details of the scoring system used.
TOOL USED TO ASSESS SCORE: Ophthalmoscope
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Remarks on result:
- other: for all three animal tested
- Irritation parameter:
- iris score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 0
- Remarks on result:
- other: for all three animal tested
- Irritation parameter:
- conjunctivae score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- >= 0.3 - <= 0.7
- Max. score:
- 2
- Reversibility:
- fully reversible within: 72h
- Remarks on result:
- other: for all three animal tested
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Time point:
- 24/48/72 h
- Score:
- 0
- Max. score:
- 1
- Reversibility:
- not fully reversible within: 24h
- Remarks on result:
- other: for all three animal tested
- Irritant / corrosive response data:
- A crimson-red conjunctival appearance, very slight chemosis and very slight discharge were observed in all animals one hour after instillation of test item. Injection of the conjunctival blood vessels persisted up to the 48 hour observation.
The eyes of all rabbits were overtly normal by the 72 hour examination. - Other effects:
- Instillation of the test material caused a very slight or slight initial pain response.
Any other information on results incl. tables
Individual scores:
Animal No. |
cornea opacity |
iris |
conjunctivae |
chemosis |
||||||||||||
1h |
24h |
48h |
72h |
1h |
24h |
48h |
72h |
1h |
24h |
48h |
72h |
1h |
24h |
48h |
72h |
|
27TK333M |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
2 |
1 |
1 |
0 |
1 |
0 |
0 |
0 |
27TK336M |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
2 |
1 |
0 |
0 |
1 |
0 |
0 |
0 |
27TK337M |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
2 |
1 |
1 |
0 |
1 |
0 |
0 |
0 |
Applicant's summary and conclusion
- Interpretation of results:
- other: not irritating
- Conclusions:
- Under the conditions of the test, the test item was classified as 'non-irritant' to the eye.
- Executive summary:
The potential of test item to cause damage to the conjunctiva, iris or cornea was assessed in three New Zealand White rabbits, each subject to single ocular instillation of 100 mg of the test material according to OECD 405. Ocular reactions were examined 1, 24, 48 and 72 hours after treatment. Crimson-red conjunctival appearance and very slight chemosis and discharge were observed in all animals one hour after instillation. Injection of the conjunctival blood vessels persisted up to the 48 hour observation. The eyes of all rabbits were overtly normal by the 72 hour examination. Instillation of the test material caused a very slight or slight initial pain response. Under the conditions of this test, the test item was classified as 'non-irritant' to the eye.
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.
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