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EC number: 224-778-8 | CAS number: 4488-57-7
- 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, near guideline study, available as unpublished report, minor restrictions in design or reporting but otherwise adequate for assessment.
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 980
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Skin irritation assessed, using Draize scale, after 24 hour dermal exposure to 3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-indene on abraded skin.
- GLP compliance:
- yes
Test material
- Reference substance name:
- 3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-indene
- EC Number:
- 224-778-8
- EC Name:
- 3a,4,5,6,7,7a-hexahydro-4,7-methano-1H-indene
- Cas Number:
- 4488-57-7
- Molecular formula:
- C10H14
- IUPAC Name:
- tricyclo[5.2.1.0²,⁶]dec-3-ene
- Reference substance name:
- Dihydro dicyclopentadiene
- IUPAC Name:
- Dihydro dicyclopentadiene
- Details on test material:
- - Name of test material (as cited in study report): DHDCPD
- Physical state: Liquid
- Density: 1.04 g/ml
- Analytical purity: Not reported
- Stability under test conditions: Not reported
- Storage condition of test material: Not reported
Constituent 1
Constituent 2
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: A USDA approved supplier (further details not reported)
- Weight at study initiation: 2.65-3.2 kg (males), 2.42-3.3 kg (females).
- Housing: Individually in stainless steel or galvanised cages.
- Diet : Charles River Rabbit chow (ad libitum)
- Water : Tap water (ad libitum)
- Acclimation period: 2 weeks
ENVIRONMENTAL CONDITIONS - not reported
IN-LIFE DATES: From: 16th January 1980 To: 30th January 1980
Test system
- Type of coverage:
- semiocclusive
- Preparation of test site:
- abraded
- Vehicle:
- unchanged (no vehicle)
- Controls:
- no
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 2g/kg
- Concentration (if solution): administered as supplied - Duration of treatment / exposure:
- 24 h
- Observation period:
- 14 days
- Number of animals:
- 10 (5/sex)
- Details on study design:
- TEST SITE
- Area clipped 24 hours prior to dosing. Just prior to dosing the skin was abraded longitudinally every 2-3 cm over the dosing area, deep enough to penetrate the stratum corneum but not so deep as to disturb the derma or produce bleeding.
- Area of exposure: 4" x 12"
- % coverage: 10%
- Type of wrap if used: gauze
REMOVAL OF TEST SUBSTANCE
- Washing (if done): Area thoroughly wiped
- Time after start of exposure: 24 hours
SCORING SYSTEM: Erythema and oedema assessed using scoring system of Draize et al. 1944
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- mean
- Remarks:
- 10 rabbits
- Time point:
- other: 24.5 h
- Score:
- 3.7
- Max. score:
- 4
- Reversibility:
- no data
- Remarks on result:
- other: 24 h exposure to abraded skin
- Irritation parameter:
- edema score
- Basis:
- mean
- Remarks:
- 10 rabbits
- Time point:
- other: 24.5 h
- Score:
- 3.5
- Max. score:
- 4
- Reversibility:
- no data
- Remarks on result:
- other: 24 h exposure to abraded skin
Any other information on results incl. tables
Skin Irritation scores at 24.5 hours after application (Draize et al 1944).
Score |
Erythema |
Oedema |
3 (moderate to severe) |
3 males |
4 males and 1 female |
4 (Severe) |
2 males and 5 females |
1 male and 4 females |
Mean score |
3.7 |
3.5 |
Applicant's summary and conclusion
- Conclusions:
- DHDCPD was irritant to the abraded skin of rabbits following a 24 hour dermal application.
- Executive summary:
Groups of 5 male and 5 female New Zealand white rabbits rats were dosed with 2000 mg/kg of dihydro dicycolpentadiene (DHDCPD) as a 24- hour dermal application to abraded skin (under a semi-occlusive dressing) and were observed daily for 14 days after dosing. One male died on day 12 of the observation period. Redness of the back was seen clinically in 4 males and 5 females and the skin sites were assessed for erythema and oedema, using the Draize scoring system, at the end of the exposure period. The mean scores were 3.7 for erythema and 3.5 for oedema for the 10 rabbits. DHDCPD was irritant to the abraded skin of rabbits following a 24 hour dermal application.
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