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EC number: 221-346-0 | CAS number: 3072-84-2
- Life Cycle description
- Uses advised against
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![](https://echa.europa.eu./o/diss-blank-theme/images/factsheets/A-REACH/factsheet/print_toxicological-information.png)
Eye irritation
Administrative data
- Endpoint:
- eye irritation, other
- Remarks:
- In vivo study was available and therefore was used in this record
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 05/07/1999-08/07/1999
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 999
- Report date:
- 1999
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.5 (Acute Toxicity: Eye Irritation / Corrosion)
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- GLP compliance:
- yes
Test material
- Test material form:
- solid: particulate/powder
- Remarks:
- migrated information: powder
- Details on test material:
- - Name of test material (as cited in study report):F-2200HM
- Physical state:Off-white powder
- Analytical purity: >99%
- Lot/batch No.:290110772
- Expiration date of the lot/batch: 12/2014
- Storage condition of test material:
- Other: ambient storage conditions in darkness
Constituent 1
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: Charles River Nederland, The Netherlands
- Age at study initiation: at least 6 weeks old
- Weight at study initiation: less than 3.5 kg
- Housing: Individually housed in labelled cages with perforated floors (Scanbur, Denmark) and equipped with an automatic drinking system
- Diet (e.g. ad libitum): approx. 100g per day
- Water (e.g. ad libitum):ad libitum
- Acclimation period: 5 days
ENVIRONMENTAL CONDITIONS
- Temperature (°C):21°C
- Humidity (%): 50%
- Air changes (per hr): 15
- Photoperiod (hrs dark / hrs light): 12hours artificial fluorescent light and 12 hours dark
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 100mg (99.5-100.5mg) - Duration of treatment / exposure:
- 24 hours
- Observation period (in vivo):
- 72 hours
- Number of animals or in vitro replicates:
- 3
- Details on study design:
- REMOVAL OF TEST SUBSTANCE
- Washing (if done): 2% fluorescein in water (adjusted to pH7)
- Time after start of exposure: 24hours
SCORING SYSTEM:
Corneal irritation:
Opacity: degree of density (area most dense taken for reading)
No ulceration or opacity (may include slight dulling of normal lustre): 0
Scattered or diffuse areas of opacity, details of iris clearly visible: 1
Easily discernible translucent area, details or iris slightly obscured: 2
Necreous aera, no details of iris visible, size of pupil barely discernible: 3
Opaque cornea, iris not discernible throught the opacity: 4
Area of cornea involved:
No ulceration or opacity: 0
One quarter or less but not zer: 1
Greater than one quarter, but less than half: 2
Greater than half, but less than three quarters: 3
Greater than three quarters, up to whole area: 4
Iris:
Normal: 0
Markedly deopened rugae, congestion, swelling, moderate circumcorneal hyperaomia, or injection, any of these combination thereof, iris still reacting to light (slugggish reaction is possitive): 1
No reaction to light, hemmorrhage, gross destruction (any or all of these): 2
Conunctival irritation:
Redness (refers to palpebrae and sclera, excluding cornea and iris):
Blood vessels normal: 0
Some blood vessels definitely hyperaemic (injected): 1
Diffuse, crimson color, individual vessels not easily discernable: 2
Diffuse beefy red: 3
Chemosis (refers to lids and/or nictitating membranes):
No swelling: 0
Any swelling above normal (includes nictating membranes): 1
Obvious swelling with partial eversion of lids: 2
Swelling with lids about half closed: 3
Swelling with lids more than half closed: 4
Discharge: No discharge (may include small amounts observed in inner canthus of normal animals): 0
Any amount different from normal and/or lacrimation: 1
Discharge with moistening of the lids and hairs just adjecent to lids: 2
Discharge with moistening of the lids and hairs (considerable area around the eye): 3
TOOL USED TO ASSESS SCORE: fluorescein + an ophthalmic examination lamp
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- other: 1 hour
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- fully reversible within: 72 hours
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- other: 24 hours
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 72 hrs
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- other: 48 hours
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- other: 72 hours
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- iris score
- Basis:
- mean
- Time point:
- other: 1 hour
- Score:
- 0.67
- Max. score:
- 2
- Reversibility:
- fully reversible within: 1 hr
- Irritation parameter:
- iris score
- Basis:
- mean
- Time point:
- other: 24hours
- Score:
- 0
- Max. score:
- 2
- Reversibility:
- fully reversible within: 1hr
- Irritation parameter:
- iris score
- Basis:
- mean
- Time point:
- other: 48 hours
- Score:
- 0
- Max. score:
- 2
- Reversibility:
- fully reversible within: 1hr
- Irritation parameter:
- iris score
- Basis:
- mean
- Time point:
- other: 72
- Score:
- 0
- Max. score:
- 2
- Reversibility:
- fully reversible within: 1hr
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- mean
- Time point:
- other: 1hour
- Score:
- 2
- Max. score:
- 3
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- mean
- Time point:
- other: 24 hours
- Score:
- 1.67
- Max. score:
- 3
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- mean
- Time point:
- other: 48hours
- Score:
- 1
- Max. score:
- 3
- Reversibility:
- fully reversible within: 72 hrs
- Irritation parameter:
- conjunctivae score
- Remarks:
- redness
- Basis:
- mean
- Time point:
- other: 72hours
- Score:
- 0
- Max. score:
- 3
- Reversibility:
- fully reversible within: 72 hrs
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Time point:
- other: 1 hour
- Score:
- 1.67
- Max. score:
- 4
- Reversibility:
- fully reversible within: 72 hrs
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Time point:
- other: 24hours
- Score:
- 1.5
- Max. score:
- 4
- Reversibility:
- fully reversible within: 72 hrs
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Time point:
- other: 48hours
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- chemosis score
- Basis:
- mean
- Time point:
- other: 72hours
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- other: Discharge
- Basis:
- mean
- Time point:
- other: 1 hour
- Score:
- 1
- Max. score:
- 3
- Reversibility:
- fully reversible within: 72 hrs
- Irritation parameter:
- other: Discharge
- Basis:
- mean
- Time point:
- other: 24hours
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- fully reversible within: 72 hrs
- Irritation parameter:
- other: Discharge
- Basis:
- mean
- Time point:
- other: 48hours
- Score:
- 0
- Max. score:
- 4
- Irritation parameter:
- other: Discharge
- Basis:
- mean
- Time point:
- other: 72hours
- Score:
- 0
- Max. score:
- 4
- Irritant / corrosive response data:
- Corneal injury was seen in one animal as opacity (fmax. grade 1) and epithelial damage (max. 25% of the corneal area). The corneal injury had resolved within 72 hours?
Irridial irritation (grade 1) was observed in two animals after 1 hour only. Irritation of the conjunctivae was seen as redness, chemosis and discharge, which had completely resolved within 72 hours in all animals. - Other effects:
- Colouration: remnants of the test substance were present in the eyes of all animals on day 1.
Applicant's summary and conclusion
- Interpretation of results:
- not classified
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Based on these results and according to the EC criteria for classification and labelling requirements for dangerous substances and preparations (Guidelines in Commision Directive 93/21/EEC), F-2200HM does not have to be classified for eye irritation and has no obligatory labelling requirement for eye irritation.
- Executive summary:
Acute eye irritation/corrosion study with F-2200HM in the rabbit.
The study was carried out based on the guideline described in: EC Commission Directive 92/69/EEC, B., Acute Toxicity. Eye irritation and OECD No. 405, 'Acute Eye Irritation/Corrosion'.
Single samples of approximately 100mg of F-2200HM (a volume of approximately 0.1ml) were instilled into one eye of each of three rabbits. Observations were made 1, 24, 48 and 72 hours after instillation.
Instillation of the test substance resulted in effects on the cornea, iris and conjunctivae.
Corneal injury was seen in one animal as opacity (max grade 1) and epithelial damage (max. 25% of the corneal area). The corneal injury had resolved within 72 hours.
Irridial irritation (grade 1) was observed in two animals after 1 hour only. Irritation of the conjunctivae was seen as redness. Chemosis and discharge which had completely resolved within 72 hours in all animals.
Remnants of the test substance were present in the eyes of all animals on day 1.
Based on these results and according to the EC criteria for classification and labelling requirements for dangerous substances and preparations (Guidelines in Commission Directive 93/21/EEC). F-2200HM does not have to be classified and has no obligatory labelling requirement for 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.
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