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EC number: 220-246-4 | CAS number: 2687-12-9
- 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:
- 1985-10-01 to 1985-10-25
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study with acceptable restrictions
- Remarks:
- Comparable to OECD Guideline 404 study with acceptable restrictions.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 985
- Report date:
- 1985
Materials and methods
Test guideline
- Qualifier:
- equivalent or similar to guideline
- Guideline:
- OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
- Deviations:
- no
- Principles of method if other than guideline:
- This study follows the guidelines published in the Federal Register Vol. 43 No. 163 Part IV, EPA July 26, 1979.
- GLP compliance:
- not specified
Test material
- Reference substance name:
- (3-chloroprop-1-enyl)benzene
- EC Number:
- 220-246-4
- EC Name:
- (3-chloroprop-1-enyl)benzene
- Cas Number:
- 2687-12-9
- Molecular formula:
- C9H9Cl
- IUPAC Name:
- (3-chloroprop-1-enyl)benzene
- Test material form:
- liquid
- Details on test material:
- - Name of test material (as cited in study reports): JNJ-118872-AAA (T000749)
- Physical state: liquid
- Appearance: Light yellow, light brown liquid
Constituent 1
Test animals
- Species:
- rabbit
- Strain:
- New Zealand White
- Remarks:
- Albino
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: Laboratory in-house stock colony
- Age at study initiation: No data
- Weight at study initiation: 4.35 - 4.45 kg
- Housing: Housed in a wire cage in compliance with AALAC regulations.
- Diet: ad libitum
- Water: ad libitum
- Acclimation period: No data
ENVIRONMENTAL CONDITIONS: no data
IN-LIFE DATES: No data
Test system
- Type of coverage:
- open
- Preparation of test site:
- other: intact or abraded
- Vehicle:
- not specified
- Controls:
- other: the back of the rabbits with intact skin
- Amount / concentration applied:
- TEST MATERIAL
- Amount(s) applied (volume or weight with unit): 0.1 mL
- Concentration (if solution): undiluted
VEHICLE: no data - Duration of treatment / exposure:
- Single dose for 6 hour exposure
- Observation period:
- after 24 hours, 2, 3, 4, 5, 6, 7, 10 and 14 days, etc. until reactions proved to be reversible.
- Number of animals:
- Two males
- Details on study design:
- TEST SITE
- Area of exposure: The skin at the right side of the back was abraded, whereas the left side was left intact. A definite sample was applied for each side to an area of 1" x 1" skin square on the intact and on the abraded skin.
- % coverage: No data
- Type of wrap if used: Not applicable.
REMOVAL OF TEST SUBSTANCE
- Washing (if done): The materials were flushed and washed with handwarm water and gently dried.
- Time after start of exposure: after 6 hours
SCORING SYSTEM:
The reactions were evaluated in both the group with intact skin and the group with abraded skin after 24 hours, 2, 3, 4, 5, 6, 7, 10 and 14 days, etc. until reactions proved to be reversible. The Primary Irritation Index (PII) and Classification was according to Draize and evaluated after 24 and 72 hours of application.
Results and discussion
In vivo
Resultsopen allclose all
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 1.67
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 13 days
- Remarks on result:
- other: Intact skin
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 13 days (score 1 on days 7, 10 and 13)
- Remarks on result:
- other: Intact skin
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 13 days
- Remarks on result:
- other: Intact skin
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 1.33
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 13 days
- Remarks on result:
- other: Intact skin
- Irritation parameter:
- erythema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 1.67
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 13 days
- Remarks on result:
- other: abraded skin
- Irritation parameter:
- edema score
- Basis:
- animal #1
- Time point:
- 24/48/72 h
- Score:
- 0.33
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 13 days
- Remarks on result:
- other: abraded skiin
- Irritation parameter:
- erythema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 2
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 13 days
- Remarks on result:
- other: abraded skin
- Irritation parameter:
- edema score
- Basis:
- animal #2
- Time point:
- 24/48/72 h
- Score:
- 1.33
- Max. score:
- 4
- Reversibility:
- not fully reversible within: 13 days
- Remarks on result:
- other: abraded skin
- Irritant / corrosive response data:
- T 749 resulted in a slight irritation to the skin of the rabbits.
Applicant's summary and conclusion
- Interpretation of results:
- Category 2 (irritant) based on GHS criteria
- Conclusions:
- Under the conditions of this study, the test item resulted in a slight irritation to the skin of the rabbits. Based on the results of this study and the criteria of the CLP Regulation, the substance is classified as irritating to the skin based on persisting inflammation observed until day 14 which is reflected in the scoring of erythema and edema until day 14.
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