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Diss Factsheets
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EC number: 204-587-6 | CAS number: 122-97-4
- 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:
- weight of evidence
- Study period:
- 1968
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- data from handbook or collection of data
- Remarks:
- publication including a sufficiently documented study description
Data source
Reference
- Reference Type:
- publication
- Title:
- Fundamental studies of safe compound perfumes for cosmetics, Part 1.
- Author:
- Takenaka, T., Hasegawa, E., Takenaka, U., Saito, F., Odaka, T.
- Bibliographic source:
- Preprint of Scientific Papers - The Fifth Congress of International Federation of Societies of Cosmetic Chemists, May 12-17, 1968, Tokyo, 313-329.
Materials and methods
- Type of study / information:
- in vivo
- Endpoint addressed:
- skin irritation / corrosion
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- Closed patches were applied to the skin of the subjects (forearmes and inside of upper arms) from 24 to 48 hours and the results were read 30 minutes after removal.
- GLP compliance:
- no
Test material
- Reference substance name:
- 3-phenylpropan-1-ol
- EC Number:
- 204-587-6
- EC Name:
- 3-phenylpropan-1-ol
- Cas Number:
- 122-97-4
- Molecular formula:
- C9H12O
- IUPAC Name:
- 3-phenylpropan-1-ol
Constituent 1
Method
- Ethical approval:
- not specified
- Details on study design:
- 82 volunteers were treated with the test substance for 24-48 hours under occlusion. The test material concentration was 0.05 % - 0.5 %.
The following substances were used as a vehicle: ethanol or cream base containing squalen, lanoline, stearic acid, cetyl alcohol, polyoxyethylene cetylalcohol, preservatives, polyethylene glycol, d-sorbitol, citric acid and distilled water. Skin reactions were read 30 min after removal of the patch. - Details on exposure:
- TYPE OF EXPOSURE MEASUREMENT: Exposure pads
EXPOSURE LEVELS: 0.05 % - 05 %
EXPOSURE PERIOD: 24 - 48 hours
POSTEXPOSURE PERIOD: 30 min
Results and discussion
- Results:
- No signs of skin irriation were found.
Applicant's summary and conclusion
- Conclusions:
- Tested on 82 volunteers, the test substance was not irritating to skin at concentrations of 0.05 - 0.5 %.
- Executive summary:
In this publication the testing of several chemicals on the skin of human volunteers is described. The test substance was exposed to the skin sites under occlusion for 24 - 48 hours at a concentration of 0.05 - 0.5 % to 82 humans. As a result, no skin reactions were seen.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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