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EC number: 281-199-3 | CAS number: 83897-91-0
- Life Cycle description
- Uses advised against
- Endpoint summary
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- Particle size distribution (Granulometry)
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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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- Terrestrial toxicity
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- 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

Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- June 14, 1993 - August 19, 1993
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: This study predates and contains a few minor deviations from the current guideline study. However, the study is similar to a OECD 404 study and it is performed according to EPA TSCA Good Laboratory Practice Standards (40 CFR 792).
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 993
- Report date:
- 1993
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- yes
- Remarks:
- The exposure period of test substance. Reversibility of skin ractions were not recorded. Age of animals and their weight at the end of study missing. Two other test substances were tested concurrently on separate test sites on these rabbits
- Principles of method if other than guideline:
- Exposure time of the test substance was 24 hours (OECD 404; 4 hours) and the test sites were evaluated for erythema, edema and other evidence of dermal effects at 24, 48 and 72 hours (OECD 404; 1, 24, 48, 72 hours after patch removal) after application of the test substance. Two other test substances were tested concurrently on separate test sites on these rabbits. Age of the animals were not mentioned at start of the study and weight of the animals were not measured at conclusion of the study. Furthermore, clinical signs were not reported and the reversibility of skin reactions were not observed up to 14 days after removal of the patches.
- GLP compliance:
- yes
Test material
- Reference substance name:
- Titanium tetra(octanolate), branched and linear
- EC Number:
- 281-199-3
- EC Name:
- Titanium tetra(octanolate), branched and linear
- Cas Number:
- 83897-91-0
- Molecular formula:
- C32H68O4Ti, molecular weight range not applicable (UVCB substance)
- IUPAC Name:
- titanium tetra(octanolate), branched and linear
- Details on test material:
- - Name of test material (as cited in study report): H20206
- Substance type: organometallic
- Physical state: liquid
- Analytical purity: 100%
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Hare Marland, Hewitt, New Jersey
- Weight at study initiation: 2638 - 3293g
- Housing: singly in suspended, stainless steel, wire-mesh cages
- Diet (e.g. ad libitum): conventional laboratory diet ad libitum. During exposure period of 24hours animals did not have access to food.
- Water (e.g. ad libitum): drinking water ad libitum. During exposure period of 24hours animals did not have access to food.
- Acclimation period: two weeks
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20°C +/- 2°C
- Humidity (%): 50% +/- 10%
- Photoperiod (hrs dark / hrs light): 12/12
Test system
- Preparation of test site:
- shaved
- Vehicle:
- unchanged (no vehicle)
- Controls:
- not required
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5ml
- Concentration (if solution): 100% - Duration of treatment / exposure:
- 24 hours
- Observation period:
- 72 hours
- Number of animals:
- 6
- Details on study design:
- TEST SITE
- Area of exposure: 2-inch gauze square
- % coverage
- Type of wrap if used: piece of rubber sheeting
REMOVAL OF TEST SUBSTANCE
- Washing (if done): with water and soap
- Time after start of exposure: 24 hours
SCORING SYSTEM:
The application site was examined for erythema and oedema according to the Draize technique.
Erythema and eschar formation:
No erythema 0
Very slight erythema (barely perceptible) 1 (slight)
Well-defined erythema 2 (mild)
Moderate to severe erythema 3 (moderate)
Severe erythema (beet redness) to slight eschar formation (injuries in depth) 4 (severe)
Edema formation:
No edema 0
Very slight edema (barely perceptible) 1 (slight)
Slight edema (edges of area well defined by definite raising) 2 (mild)
Moderate edema (raised approximately 1.0 mm) 3 (moderate)
Severe edema (raised more than 1.0 mm extending beyond the area of exposure) 4 (severe)
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 24 h
- Score:
- 1
- Max. score:
- 8
- Reversibility:
- no data
- Remarks on result:
- other: The scores are the sum of mean erythema and edema scores
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 48 h
- Score:
- 1.2
- Max. score:
- 8
- Reversibility:
- no data
- Remarks on result:
- other: The scores are the sum of mean erythema and edema scores
- Irritation parameter:
- overall irritation score
- Basis:
- mean
- Time point:
- other: 72 h
- Score:
- 1.5
- Max. score:
- 8
- Reversibility:
- no data
- Remarks on result:
- other: The scores are the sum of mean erythema and edema scores
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 24 h
- Score:
- 1
- Max. score:
- 4
- Reversibility:
- no data
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 48 h
- Score:
- 1.2
- Max. score:
- 4
- Reversibility:
- no data
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- other: 72 h
- Score:
- 1.5
- Max. score:
- 4
- Reversibility:
- no data
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 24 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- no data
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 48 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- no data
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- other: 72 h
- Score:
- 0
- Max. score:
- 4
- Reversibility:
- no data
- Irritant / corrosive response data:
- Table 1 Individual skin irritation scores
Skin responses observed in test rabbits following topical exposure to H-20206
Rabbit Erythema Edema
Number 24 hr 48 hr 72 hr 24 hr 48 hr 72 hr
28096 1 2 2 0 0 0
28223 1 1 2 0 0 0
28179 1 1 1 0 0 0
28100 1 1 1 0 0 0
28101 1 1 1 0 0 0
28184 1 1 2 0 0 0
Applicant's summary and conclusion
- Interpretation of results:
- not classified
- Remarks:
- Migrated information Criteria used for interpretation of results: expert judgment
- Conclusions:
- The primary dermal irritation/corrosion potential of Titanium tetra(octanolate), branched and linear was evaluated when applied to the skin of rabbits for 24 hours. By the study report, the test substance was a mild skin irritant under conditions of this study.
- Executive summary:
This study was regarded reliable with restrictions since there was a few minor deviations from current guideline study (two other test substances were tested concurrently on separate test sites on these rabbits, clinical signs were not reported, test substance exposure time was 24h, animals were not observed to determine reversibility of skin reactions and there was not available physicochemical properties of test material).
Slight erythema was observed in all six rabbits by 24 hours following application. By 48 hours, slight erythema was observed in 5 rabbits and mild erythema in 1. By 72 hours, 3 rabbits exhibited mild erythema. No edema was observed throughout this study. By the study report the test substance is evaluated a mild skin irritant. The result of this study is used as a key value in hazard assessment.
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