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EC number: 231-246-9 | CAS number: 7460-74-4
- 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
Skin sensitisation
Administrative data
- Endpoint:
- skin sensitisation: in vivo (non-LLNA)
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- data from handbook or collection of data
- Justification for type of information:
- Data is from peer reviewed journal.
Data source
Referenceopen allclose all
- Reference Type:
- review article or handbook
- Title:
- Fragrance material review on phenethyl butyrate
- Author:
- D. McGinty, C.S. Letizia, A.M. Api
- Year:
- 2 012
- Bibliographic source:
- Food and Chemical Toxicology, 50 (2012) S398–S401
- Reference Type:
- review article or handbook
- Title:
- A toxicological and dermatological assessment of aryl alkyl alcohol simple acid ester derivatives when used as fragrance inl and dermatological assessment of aryl alkyl alcohol simple acid ester derivatives when used as fragrance ingredients
- Author:
- The RIFM Expert Panel,D. Belsito , D. Bickers , M. Bruze , P. Calow , M.L. Dagli , A.D. Fryer ,H. Greim , Y. Miyachi , J.H. Saurat , I.G. Sipes
- Year:
- 2 012
- Bibliographic source:
- Food and Chemical Toxicology 50 (2012) S269–S313
Materials and methods
Test guideline
- Qualifier:
- according to guideline
- Guideline:
- other: as mentioned below
- Principles of method if other than guideline:
- A human maximization assay was conducted to evaluate the sensitization potential of phenethyl butyrate .
- GLP compliance:
- not specified
- Type of study:
- other: Human Maximization test
- Justification for non-LLNA method:
- Not specified
Test material
- Reference substance name:
- Phenethyl butyrate
- EC Number:
- 203-119-8
- EC Name:
- Phenethyl butyrate
- Cas Number:
- 103-52-6
- Molecular formula:
- C12H16O2
- IUPAC Name:
- 2-phenylethyl butyrate
- Reference substance name:
- phenethyul butyrate
- IUPAC Name:
- phenethyul butyrate
- Test material form:
- other: liquid
- Details on test material:
- - Name of test material (as cited in study report): Phenethyl butyrate
- Molecular formula: C12H16O2
- Molecular weight: 192.106 g/mol
- Substance type: Organic
- Physical state: Liquid
Constituent 1
Constituent 2
- Specific details on test material used for the study:
- Name of test material (as cited in study report): Phenethyl butyrate
- Molecular formula: C12H16O2
- Molecular weight: 192.106 g/mol
- Substance type: Organic
- Physical state: Liquid
In vivo test system
Test animals
- Species:
- human
- Strain:
- not specified
- Sex:
- male/female
- Details on test animals and environmental conditions:
- no data
Study design: in vivo (non-LLNA)
Induction
- Route:
- epicutaneous, occlusive
- Vehicle:
- petrolatum
- Concentration / amount:
- 8% (5520µg/cm2)
- Adequacy of induction:
- not specified
Challenge
- No.:
- #1
- Route:
- epicutaneous, occlusive
- Vehicle:
- petrolatum
- Concentration / amount:
- 8% (5520µg/cm2)
- Adequacy of challenge:
- not specified
- No. of animals per dose:
- 25 male and female
- Details on study design:
- MAIN STUDY
A. INDUCTION EXPOSURE
- No. of exposures:5
- Exposure period: 48 h
- Test groups: 25 Male and Females
- Control group: no data
- Site: Application was under occlusion to the same site on the forearm or back of all subjects
- Frequency of applications: for five alternate day
- Duration: no data
- Concentrations: 8%(5520 µg/cm2) phenethyl butyrate in petrolatum
B. CHALLENGE EXPOSURE
- No. of exposures: single
- Day(s) of challenge:Following a 10 day rest period
- Exposure period: 48 hours
- Test groups: 25 male and female
- Control group: no data
- Site: challenge patches were applied to fresh sites on the back for 48 h under occlusion
- Concentrations: 8%(5520 µg/cm2) phenethyl butyrate in petrolatum
- Evaluation (hr after challenge): The challenge site was evaluated at 48 and 72 h. - Challenge controls:
- no data
- Positive control substance(s):
- not specified
Results and discussion
- Positive control results:
- no data
In vivo (non-LLNA)
Resultsopen allclose all
- Reading:
- 1st reading
- Hours after challenge:
- 48
- Group:
- test chemical
- Dose level:
- 8% in petrolatum
- No. with + reactions:
- 0
- Total no. in group:
- 25
- Clinical observations:
- Not sensitizing
- Remarks on result:
- other: Reading: 1st reading. . Hours after challenge: 48.0. Group: test group. Dose level: 8% in petrolatum. No with. + reactions: 0.0. Total no. in groups: 25.0. Clinical observations: Not sensitizing.
- Reading:
- 2nd reading
- Hours after challenge:
- 72
- Group:
- test chemical
- Dose level:
- 8%
- No. with + reactions:
- 0
- Total no. in group:
- 25
- Clinical observations:
- Not sensitizing
- Remarks on result:
- other: Reading: 2nd reading. . Hours after challenge: 72.0. Group: test group. Dose level: 8% . No with. + reactions: 0.0. Total no. in groups: 25.0. Clinical observations: Not sensitizing.
Any other information on results incl. tables
No skin reactions were observed on humans.
Applicant's summary and conclusion
- Interpretation of results:
- other: Not sensitizing
- Conclusions:
- No reaction was observed in any human volunteers during the assay.Hence Phenethyl butyrate phenethyl butyrate (CAS No: 103-52-6 ) was considered to be not sensitizing to human skin.
- Executive summary:
A human maximization assay was conducted to evaluate the sensitization potential of phenethyl butyrate phenethyl butyrate.
The assay was carried out with 8% (5520µg/cm2) phenethyl butyrate in petrolatum on 25 healthy male and female volunteers. Application was under occlusion to the same site on the forearm or back of all subjects for five alternate day 48 h periods. The patch sites were pretreated for 24 h with 2.5% or 5% aqueous sodium lauryl sulfate (SLS) under occlusion. Following a 10 day rest period, challenge patches were applied to fresh sites on the back for 48 h under occlusion. The challenge site was pretreated for 1 h with 5–10% SLS. The challenge patches were applied to fresh sites on the back for 48 h under occlusion. The challenge site was evaluated at 48 and 72 h.
No reaction was observed in any human volunteers during the assay. Therefore Phenethyl butyrate phenethyl butyrate was considered to be not sensitizing to human skin.
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