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EC number: 221-140-0 | CAS number: 3010-96-6
- 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
Skin irritation / corrosion
Administrative data
- Endpoint:
- skin irritation: in vivo
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- February 17 - 20, 2006
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- other: Study followed OECD protocol 404 and was conducted under various GLP assurances
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 006
- Report date:
- 2006
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- no
- GLP compliance:
- yes
Test material
- Reference substance name:
- 2,2,4,4-tetramethylcyclobutane-1,3-diol, mixed isomers
- EC Number:
- 221-140-0
- EC Name:
- 2,2,4,4-tetramethylcyclobutane-1,3-diol, mixed isomers
- Cas Number:
- 3010-96-6
- Molecular formula:
- C8H16O2
- IUPAC Name:
- 2,2,4,4-tetramethylcyclobutane-1,3-diol
- Details on test material:
- The test substance consisted of white crystals and was stored at room temperature. Prior to use, the
test substance was ground with a mortar and pestle. In order to insure adequate skin contact with the
skin, the sample was applied as a dry paste (75% w/w minture in mineral oil). Purity was noted to be 99.6%.
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- Number of Animals: 3
Sex: 2 Males and I Female. The female assigned to test was nulliparous and nonpregnant.
Species/Strain: Rabbit/New Zealand albino.
Age: Young adult.
Source: Received from Robinson Services, Inc. Clemmons, NC on January 25, 2006.
Housing: The animals were singly housed in suspended stainless steel caging with mesh floors Litter paper was placed beneath the cage and was
changed at least three times per week.
Animal Room Temperature Range: 19-24°C
Photoperiod: 12-hour light/dark cycle
Acclimation Period: 23 days
Food: Pelleted Purina Rabbit Chow #5326
Water: Filtered tap water was supplied ad-libitum by an automatic water dispensing system.
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- shaved
- Vehicle:
- other: mineral oil
- Controls:
- no
- Amount / concentration applied:
- Prior to application, the test substance was ground to a powder with a mortar and pestle then moistened with mineral oil to achieve a dry paste by
preparing a 75% w/w mixture. Five-tenths of a milliliter of the test substance (0.67 g of the test mixture) was placed on a l-inch x l-inch, 4-ply gauze
pad and applied to one 6-cm2 intact dose site on each animal. - Duration of treatment / exposure:
- 4 hours
- Observation period:
- Individual dose sites were scored at approximately 30-60 minutes, 24, 48, and 72 hours after patch removal.
- Number of animals:
- 3
- Details on study design:
- On the day before application, a group of animals was prepared by clipping the dorsal area and the trunk. On the day of dosing, but prior to
application, the animals were examined for health and the skin checked for any abnormalities. Three healthy animals without pre-existing skin
irritation were selected for test.
Prior to application, the test substance was ground to a powder with a mortar and pestle then moistened with mineral oil to achieve a dry paste by
preparing a 75% w/w mixture. Five-tenths of a milliliter of the test substance (0.67 g of the test mixture) was placed on a l-inch x l-inch, 4-ply gauze
pad and applied to one 6-cm2 intact dose site on each animal. The pad and entire trunk of each animal were then wrapped with semi-occlusive
3-inch Micropore tape to avoid dislocation of the pad. Elizabethan collars were placed on each rabbit and they were returned to their designated
cages. After 4 hours of exposure to the test substance, the pads and collars were removed and the test sites
were gently cleansed of any residual test substance.
The animals were observed for signs of gross toxicity and behavioral changes at least once daily during the test period. Observations included gross evaluation of skin and fur, eyes and mucous membranes, respiratory, circulatory, autonomic and central nervous systems, somatomotor activity and
behavior pattern. Particular attention was directed to observation of tremors, convulsions, salivation, diarrhea, and coma.
Individual dose sites were scored according to the Draize scoring system at approximately 30-60 minutes, 24, 48, and 72 hours after patch removal. The classification of irritancy was obtained by adding the average erythema and edema scores for the 30-60 minute, 24, 48, and 72-hour scoring
intervals and dividing by the number of evaluation intervals.
Results and discussion
In vivo
Results
- Irritation parameter:
- primary dermal irritation index (PDII)
- Basis:
- mean
- Time point:
- other: 72 hrs
- Score:
- 1.6
- Max. score:
- 3
- Reversibility:
- fully reversible within: 72 hrs
- Other effects:
- All animals appeared active and healthy during the study. Apart from the dermal irritation noted, there were no other signs of gross toxicity, adverse pharmacologic effects, or abnormal behavior.
Any other information on results incl. tables
|
Incidence of Irritation |
|
Time After Patch Removal |
Erythema |
Edema |
30-60 minutes |
3/3 |
3/3 |
24 hours |
3/3 |
3/3 |
48 hours |
2/3 |
0/3 |
72 hours |
0/3 |
0/3 |
TimeAfterPatch Removal |
Severity of Irritation-Mean Score |
30-60 minutes |
3.0 |
24 hours |
2.7 |
48 hours |
0.7 |
72 hours |
0 |
Applicant's summary and conclusion
- Interpretation of results:
- slightly irritating
- Remarks:
- Migrated information
- Conclusions:
- Under the conditions of this study, 2,2,4,4-Tetramethyl-1,3-cyclobutanediol is classified as slightly irritating to the skin.
- Executive summary:
All three animals appeared active and healthy during the study. Apart from the dermal irritation noted below, there were no other signs of gross toxicity, adverse pharmacologic effects, or abnormal behavior. Within one hour of patch removal, all three treated sites exhibited well-defined erythema and very slight edema. The overall incidence and severity of irritation decreased with time. All animals were free of dermal irritation by 72 hours. The Primary Dermal Irritation Index was 1.6 which correlates to a classification of slightly irritating.
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.
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