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EC number: 420-640-8 | CAS number: 138495-42-8
- 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
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 993
- Report date:
- 1993
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- no
- Remarks:
- The study was conducted according to the guideline in effect at the time of study conduct.
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.4 (Acute Toxicity: Dermal Irritation / Corrosion)
- Deviations:
- no
- Remarks:
- The study was conducted according to the guideline in effect at the time of study conduct.
- GLP compliance:
- yes
Test material
- Reference substance name:
- -
- EC Number:
- 420-640-8
- EC Name:
- -
- Cas Number:
- 138495-42-8
- Molecular formula:
- C5H2F10
- IUPAC Name:
- (3R,4R)-1,1,1,2,2,3,4,5,5,5-decafluoropentane; (3S,4S)-1,1,1,2,2,3,4,5,5,5-decafluoropentane
- Details on test material:
- -Purity: 97.6%
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Age at study initiation: Not reported
- Weight at study initiation: 2734-3108 g
- Housing: Singly in suspended, stainless steel, wire-mesh cages
- Diet (e.g. ad libitum): 125 g rabbit chow daily, except for approximately 24 hours when in stocks
- Water (e.g. ad libitum): ad libitum, except for approximately 24 hours when in stocks
- Acclimation period: Approximately 2 weeks
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 20±2°C
- Humidity (%): 50±10%
- Air changes (per hr): Not reported
- Photoperiod (hrs dark / hrs light): 12-hour light/12-hour dark
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- shaved
- Vehicle:
- unchanged (no vehicle)
- Controls:
- other: Adjacent areas of untreated skin were used for comparison.
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.5 mL
- Concentration (if solution): undiluted - Duration of treatment / exposure:
- 24 hours
- Observation period:
- 1, 24, 48, and 72 hours after test substance removal
- Number of animals:
- 2 female and 1 male
- Details on study design:
- TEST SITE
- Area of exposure: Scapular to lumbar region of the back
- % coverage: Not reported
- Type of wrap if used: A 2-inch gauze square was placed over the test site. The patch was held in place with non-irritating tape. Rubber sheeting was then wrapped around the animals and secured with clips.
REMOVAL OF TEST SUBSTANCE
- Washing (if done): The test sites were gently washed with Ivory® soap and warm water and gently wiped dry.
- Time after start of exposure: 4 hours
SCORING SYSTEM: Draize scale
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- other: range
- Time point:
- other: 1 hour to 72 hours
- Score:
- 0 - 1
- Max. score:
- 1
- Reversibility:
- fully reversible
- Irritation parameter:
- edema score
- Basis:
- other: range
- Time point:
- other: 1 hour to 72 hours
- Score:
- 0
- Max. score:
- 0
- Irritant / corrosive response data:
- No irritation was observed in any rabbit by 1 hour after patch removal. By 24 hours, 1 rabbit exhibited slight erythema, which cleared by 48 hours. No other dermal irritation was observed throughout the study.
Any other information on results incl. tables
Table 1: Individual Animal Dermal Effects |
||||
ERYTHEMA |
||||
Rabbit Number |
Evaluation after Removal of Test Substance |
|||
1 Hour |
24 Hours |
48 Hours |
72 Hours |
|
27900 |
0 |
0 |
0 |
0 |
27901 |
0 |
0 |
0 |
0 |
28034 |
0 |
1 |
0 |
0 |
|
||||
EDEMA |
||||
Rabbit Number |
Evaluation after Removal of Test Substance |
|||
1 Hour |
24 Hours |
48 Hours |
72 Hours |
|
27900 |
0 |
0 |
0 |
0 |
27901 |
0 |
0 |
0 |
0 |
28034 |
0 |
0 |
0 |
0 |
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: other: EEC Directive 91/325
- Conclusions:
- The study and the conclusions which are drawn from it fulfil the quality criteria (validity, reliability, repeatability). No dermal irritation was observed in any rabbit by 1 hour after patch removal. By 24 hours, 1 rabbit exhibited slight erythema which cleared by 48 hours.
- Executive summary:
The test substance was evaluated for acute skin irritation potential in 1 male and 2 female New Zealand White rabbits. Approximately 0.5 mL was administered to a localized test site on the back of each animal. The test sites were covered with a semi-occlusive dressing to ensure contact between the skin and test substance. The animals were exposed to the test substance for 4 hours. The test sites were evaluated and scored according to a numerical scale, 1, 24, 48, and 72 hours after the end of the 4-hour exposure period. No dermal irritation was observed in any rabbit by 1 hour after patch removal. By 24 hours, 1 rabbit exhibited slight erythema which cleared by 48 hours.
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