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EC number: 221-111-2 | CAS number: 3006-86-8
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- Endpoint summary
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- Endpoint summary
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- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
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- Long-term toxicity to aquatic invertebrates
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- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
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- 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:
- 1978
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: No GLP, not a guideline study (although similar to present OECD guideline)
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:
- OECD Guideline 405 (Acute Eye Irritation / Corrosion)
- GLP compliance:
- no
Test material
Reference
- Name:
- Unnamed
- Type:
- Constituent
- Test material form:
- other: liquid
Test animals / tissue source
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or tissues and environmental conditions:
- TEST ANIMALS
- Source: H.A.R.E. Rabbits for Research, Hewitt, New Jersey
- Weight at study initiation: 2236 to 2903 grams
- Housing: The rabbits were individually housed in hanging wire-mesh cages in temperature and humidity controlled quarters.
- Diet: ad libitum
- Water: ad libitum
- acclimization period: 20 days
Test system
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: the left eye served as-the untreated control for each rabbit
- Amount / concentration applied:
- 0.1 mL of the test material
- Duration of treatment / exposure:
- Single treatment
- Observation period (in vivo):
- 1, 24, 48, 72 hours and 7 days after application
- Number of animals or in vitro replicates:
- 6 rabbits (3 males and 3 females)
- Details on study design:
- REMOVAL OF TEST SUBSTANCE
- Washing: not done
SCORING SYSTEM: Draize, J. H., Appraisal of the Safety of Chemicals in Foods, Drugs and Cosmetics, Assoc. Food and Drug Officials of the U.S., Austin, Texas, 1959, page 51, Modified according to revision of 1964. Edited"by A. J. Lehman. Further modified (inclusion of-0.5 scores) at International Research and Developmen.
Corporation.
TOOL USED TO ASSESS SCORE: fluorescein
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- cornea opacity score
- Basis:
- mean
- Time point:
- other: 24/48/72 hours
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- other: males and females
- Irritation parameter:
- iris score
- Basis:
- mean
- Time point:
- other: 24/48/72 h
- Score:
- 0
- Max. score:
- 2
- Remarks on result:
- other: males and females
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #1
- Time point:
- other: 24/48/72 h
- Score:
- 0
- Max. score:
- 3
- Remarks on result:
- other: male
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #2
- Time point:
- other: 24/48/72 h
- Score:
- 0.8
- Max. score:
- 3
- Reversibility:
- fully reversible within: 7 days
- Remarks on result:
- other: male
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #3
- Time point:
- other: 24/48/72 h
- Score:
- 0
- Max. score:
- 3
- Remarks on result:
- other: male
- Irritation parameter:
- chemosis score
- Basis:
- animal #1
- Time point:
- other: 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- other: male
- Irritation parameter:
- chemosis score
- Basis:
- animal #2
- Time point:
- other: 24/48/72 h
- Score:
- 0.17
- Max. score:
- 4
- Reversibility:
- fully reversible within: 7 days
- Remarks on result:
- other: male
- Irritation parameter:
- chemosis score
- Basis:
- animal #3
- Time point:
- other: 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- other: male
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #1
- Time point:
- other: 24/48/72 h
- Score:
- 0.8
- Max. score:
- 3
- Reversibility:
- fully reversible within: 7 days
- Remarks on result:
- other: female
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #2
- Time point:
- other: 24/48/72 h
- Score:
- 0.17
- Max. score:
- 3
- Reversibility:
- fully reversible within: 7 days
- Remarks on result:
- other: female
- Irritation parameter:
- conjunctivae score
- Basis:
- animal #3
- Time point:
- other: 24/48/72 h
- Score:
- 0.17
- Max. score:
- 3
- Reversibility:
- fully reversible within: 7 days
- Remarks on result:
- other: female
- Irritation parameter:
- chemosis score
- Basis:
- animal #1
- Time point:
- other: 24/48/72 h
- Score:
- 0.17
- Max. score:
- 4
- Reversibility:
- fully reversible within: 7 days
- Remarks on result:
- other: female
- Irritation parameter:
- chemosis score
- Basis:
- animal #2
- Time point:
- other: 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- other: female
- Irritation parameter:
- chemosis score
- Basis:
- animal #3
- Time point:
- other: 24/48/72 h
- Score:
- 0
- Max. score:
- 4
- Remarks on result:
- other: female
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- The test substance examined in this study, 65 % 1,1-Di (t-butyl peroxy) cyclohexane, was considered not to be irritating to the eyes.
- Executive summary:
The test substance, 65 % 1,1-Di (t-butyl peroxy) cyclohexane was examined for its eye irritation potential in 6 New Zealand White rabbits. The rabbits were administered with 0.1 mL of the test substance, placed into the cupped conjunctival sac of the right eye of each rabbit while the left eye served as-the untreated control for each rabbit. The eyes were not washed and observations/ scoring with sodium fluorescein solution were performed at 24, 48, 72 hours and 7 days after application. Results were scored by modified Draize scoring method (scoring with 0.5 intervals), showing according to the grading used in the study, regulations of the Federal Hazardous Substances Act., (and in accordance with present regulation, OECD GHS) that the test material is not be considered a primary eye-irritant.
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