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Diss Factsheets
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EC number: 227-678-2 | CAS number: 5932-68-3
- 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
Exposure related observations in humans: other data
Administrative data
- Endpoint:
- exposure-related observations in humans: other data
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 1979
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- documentation insufficient for assessment
Cross-reference
- Reason / purpose for cross-reference:
- reference to same study
Data source
Reference
- Reference Type:
- publication
- Title:
- Unnamed
- Year:
- 1 979
Materials and methods
- Type of study / information:
- Skin irritation
- Endpoint addressed:
- skin irritation / corrosion
- Principles of method if other than guideline:
- A panel of 50 adult male volunteers were dermally exposed to the test material, under a patch, for 48 h and then scored for irritation reactions.
- GLP compliance:
- no
Test material
- Reference substance name:
- Isoeugenol
- EC Number:
- 202-590-7
- EC Name:
- Isoeugenol
- Cas Number:
- 97-54-1
- IUPAC Name:
- 2-methoxy-4-prop-1-en-1-ylphenol
- Test material form:
- not specified
- Details on test material:
- - Storage condition of test material: Kept in light-intercepting ampoule at 5 °C.
Constituent 1
Method
- Ethical approval:
- not applicable
- Details on study design:
- - A panel of 50 adult male volunteers was dermally exposed to 0.05 mL of Iso-eugenol (32 % in acetone) under a 15 mm lint patch.
- Individuals with known allergic reactions were excluded.
- Patches were placed in contact with the skin on the back of each subject and left for 48 h. The patches were then removed and the sites were swabbed with dry gauze to remove any residual test materials. 30 minutes later, the test sites were evaluated for dermal reactions. If necessary, 72, 96 and 120 h readings were performed.
- Scoring of patch test reactions:
-: negative reading
±: questionable erythema not covering the entire patch area
+: definite erythema of the entire patch area
++: erythema and edema
+++: erythema, edema, and vesicles (or papules)
++++: bullous reaction - Exposure assessment:
- measured
- Details on exposure:
- TYPE OF EXPOSURE: Under occlusive patches
EXPOSURE LEVELS: 0.05 mL of Iso-eugenol (32 % in acetone) under a 15 mm lint patch
EXPOSURE PERIOD: 48h
POSTEXPOSURE PERIOD: The patches were then removed and the sites were swabbed with dry gauze to remove any residual test materials
Results and discussion
- Results:
- Iso-eugenol induced moderate skin irritation in human and the irritation score was 2.
Any other information on results incl. tables
None
Applicant's summary and conclusion
- Conclusions:
- In humans, a solution of 32% Isoeugenol in acetone was found to be moderately irritating when applied to the skin of 50 adult males in occlusive patches over 48 hours
- Executive summary:
In a dermal irritation study, a panel of 50 adult male volunteers was dermally exposed to 0.05 mL of Iso-eugenol (32 % in acetone) under a 15 mm lint patch. Individuals with known allergic reactions were excluded. The patches were placed in contact with the skin on the back of each subject and left for 48 h. The patches were then removed and the sites were swabbed with dry gauze to remove any residual test materials. 30 minutes later, the test sites were evaluated for dermal reactions. If necessary, 72, 96 and 120 h readings were performed.
Iso-eugenol induced moderate skin irritation in human and the irritation score was 2.
In humans, the solution of 32% Isoeugenol in acetone was found to be moderately irritating when applied to the skin of 50 adult males in occlusive patches over 48 hours
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