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EC number: 246-690-9 | CAS number: 25167-70-8
- 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:
- other: GLP compliant, guideline study, available as unpublished report, no restrictions, fully adequate for assessment
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 996
- Report date:
- 1996
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- EU Method B.4 (Acute Toxicity: Dermal Irritation / Corrosion)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
Test material
- Reference substance name:
- 2,4,4-trimethylpentene
- EC Number:
- 246-690-9
- EC Name:
- 2,4,4-trimethylpentene
- Cas Number:
- 25167-70-8
- Molecular formula:
- C8H16
- IUPAC Name:
- 2,4,4-trimethylpent-1-ene
- Details on test material:
- - Name of test material (as cited in study report): 2,4,4-trimethylpentene (also known as diisobutylene and diisobutene)
- Physical state: clear, colourless liquid
- Analytical purity: 95.19%
- Lot/batch No.: Batch No. 2 (a 50:50 mixture of two original batches of 2,4,4-trimethylpentene - Batch No. R11 supplied by Shell and Batch No. 155833 supplied by Erdolchemie).
- Expiration date of the lot/batch: 29 April 1997
- Storage condition of test material: Under nitrogen, protected from light, in a cool store.
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Froxfield SPF Rabbits, Broadway Farm, Froxfield, Hampshire, England
- Age at study initiation: Approximately 3 months
- Weight at study initiation: 2.23-2.52 kg
- Housing: Individually housed in suspended stainless steel cages
- Diet: Standard pelleted rabbit diet (STANRAB (P) SQC - Special Diets Services Ltd., Witham, Essex, England) ad libitum
- Water: Tap water ad libitum
- Acclimation period: Not reported
ENVIRONMENTAL CONDITIONS
- Temperature: 18-25°C
- Humidity: 40-68%
- Air changes: at least 10/hr
- Photoperiod: 12 hrs dark / 12 hrs light
IN-LIFE DATES: From: 28 May 1996 To: 12 June 1996
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- shaved
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Amount / concentration applied:
- TEST MATERIAL
Amount(s) applied: 0.5 mL - Duration of treatment / exposure:
- 4 hours
- Observation period:
- 16 days
- Number of animals:
- 3
- Details on study design:
- TEST SITE
- Day prior to application, the dorsum between the limb girdles was clipped
- Two areas 6 cm x 6 cm on either side of dorsum were marked
- Area of exposure: 3 cm x 2 cm on left dorsum
- Type of wrap: gauze patch (3 cm x 2 cm) held in place by strips of Blenderm. Pads of cotton wool and elasticated bandage used to protect patches and ensure good contact between skin and test substance
- Control site: 3 cm x 2 cm on right dorsum was covered by similar semi-occlusive dressing but otherwise remained untreated
REMOVAL OF TEST SUBSTANCE
- Washing: skin sites gently washed with warm water and dried with paper tissues
- Time after start of exposure: 4 hours
SCORING SYSTEM: Draize, 1959
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- 24 h
- Score:
- 2
- Max. score:
- 2
- Reversibility:
- fully reversible within: 13 days
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- 48 h
- Score:
- 1
- Irritation parameter:
- erythema score
- Basis:
- mean
- Time point:
- 72 h
- Score:
- 1
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- 24 h
- Score:
- 0
- Max. score:
- 0
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- 48 h
- Score:
- 0
- Irritation parameter:
- edema score
- Basis:
- mean
- Time point:
- 72 h
- Score:
- 0
- Irritant / corrosive response data:
- Very slight/ well defined erythema, spreading beyond test site, was present during first 7-10 days after application. Eschar formation was apparent in all animals 24 hours after dressing removal, resolving in one rabbit at 48 hours and in others by day 7. Exfoliation was evident at all test sites during the 2nd week and was still present in one animal at termination on day 16.
Any other information on results incl. tables
Skin irritation scores according to the Draize scheme
Time |
Erythema (Test/Control sites) |
Oedema (Test/Control sites) |
||||
Animal number |
837 |
847 |
766 |
837 |
847 |
766 |
after 1 hour |
0 / 0 |
0 / 0 |
0 / 0 |
0 / 0 |
0 / 0 |
0 / 0 |
after 24 hours |
2*s/ 0 |
2*s/ 0 |
2*s/ 0 |
0 / 0 |
0 / 0 |
0 / 0 |
after 48 hours |
1*/ 0 |
1*s/ 0 |
2*s/ 0 |
0 / 0 |
0 / 0 |
0 / 0 |
after 72 hours |
1*/ 0 |
1*s/ 0 |
2*s/ 0 |
0 / 0 |
0 / 0 |
0 / 0 |
mean scores 24-72h |
1.3 |
1.3 |
2 |
0 |
0 |
0 |
Overall mean score (24-72 h) |
1.6 |
0 |
* lesion spread beyond test site
s eschar formation
Applicant's summary and conclusion
- Interpretation of results:
- not irritating
- Remarks:
- Migrated information Criteria used for interpretation of results: EU
- Conclusions:
- Mean values for erythema and oedema (at 24, 48 and 72 hours after application) did not equal or exceed EU limit values. Therefore, 2,4,4-trimethylpentene does not require classification for skin irritation.
- Executive summary:
Skin irritation was assessed in a group of New Zealand white rabbits by applying 0.5 mL undiluted 2,4,4-trimethylpentene to the shaved skin under a semi-occlusive dressing for 4 hours. Very slight/ well defined erythema, spreading beyond test site, was present during first 7-10 days after application. Eschar formation was apparent in all animals 24 hours after dressing removal, resolving in one rabbit at 48 hours and in others by day 7. Exfoliation was evident at all test sites during the 2nd week and was still present in one animal at termination on day 16. Mean values for erythema and oedema (at 24, 48 and 72 hours after application) did not equal or exceed EU limit values. Therefore, 2,4,4-trimethylpentene does not require classification for skin irritation.
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