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General Material Information

Preferred name phenethyl alcohol
Trivial Name 2-Phenylethanol
Short Description 2-phenylethanol
Formula C8 H10 O
CAS Number 60-12-8
Deleted CAS Number 2043361-12-0
FEMA Number 2858
Flavis Number 2.019
ECHA Number 200-456-2
FDA UNII ML9LGA7468
Nikkaji Number J1.924K
Beilstein Number 1905732
MDL MFCD00002886
COE Number 68
Bio Activity Summary External link
NMR Predictor External link
JECFA Food Flavoring 987 phenethyl alcohol
FDA Patent No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm 60-12-8 ; PHENETHYL ALCOHOL
Synonyms
  • benzene ethanol
  • benzeneethanol
  • benzyl carbinol
  • benzyl methanol
  • 2-hydroxyethyl benzene
  • (2-hydroxyethyl)benzene
  • 2-hydroxyethylbenzene
  • b- hydroxyethylbenzene
  • mellol
  • beta- p.e.a.
  • b- phenethanol
  • 2-phenethyl alcohol
  • phenethyl alcohol nat.
  • phenethyl alcohol natural
  • phenethyl alcohol turkey, natural isolated constituent
  • phenethylalcohol
  • phenethylol
  • 2-phenyl ethan-1-ol
  • phenyl ethanol
  • 2-phenyl ethanol
  • beta- phenyl ethanol
  • phenyl ethyl alcohol
  • 2-phenyl ethyl alcohol
  • beta- phenyl ethyl alcohol
  • nat. phenyl ethyl alcohol
  • phenyl ethyl alcohol extra
  • phenyl ethyl alcohol FCC
  • phenyl ethyl alcohol natural
  • phenyl ethyl alcohol USP 24
  • 1-phenyl-2-ethanol
  • phenylethanol
  • 2-phenylethanol
  • b- phenylethanol
  • phenylethanol nat
  • phenylethyl alcohol
  • b- phenylethyl alcohol
  • phenylethyl alcohol (2-phenyl-1-ethanol)
  • phenylethyl alcohol FCC
  • phenylethyl alcohol USP/NF
  • viguard CPEA
  • Ethanol, 2-phenyl-
  • β-(Hydroxyethyl)benzene
  • PEA
  • β-PEA
  • Phenethanol
  • 2-Phenylethanol
  • β-Phenylethyl alcohol
  • β-Phenethyl alcohol
  • β-Phenylethanol
  • 2-Phenylethyl alcohol
  • 2-Phenethyl alcohol
  • β-Phenethanol
  • 2-Phenethanol
  • 2-Phenyl-1-ethanol
  • (2-Hydroxyethyl)benzene
  • NSC 406252
  • β-Phenethylol
  • Methyl 3-[(4-Chlorobenzyl)oxy]-4-iodobenzoate
  • Microcare PEA
  • AR 606
  • Dermosoft PEA
  • MeSH ID: D010626

US / EU / FDA / JECFA / FEMA / Scholar / Patents

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Literature & References

2-phenylethanol
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:60-12-8
Pubchem (cid):6054
Pubchem (sid):134972772
Flavornet:60-12-8
Pherobase:View
Publications by Info
Volatile Flavor Components in Bogyojosaeng and Suhong Cultivars of Strawberry (Fragaria ananassa Duch.)
Publications by PubMed
Identification of Potent Odorants in a Novel Nonalcoholic Beverage Produced by Fermentation of Wort with Shiitake (Lentinula edodes).
Transgenic hybrid poplar for sustainable and scalable production of the commodity/specialty chemical, 2-phenylethanol.
Characterization of aroma compounds of Chinese famous liquors by gas chromatography-mass spectrometry and flash GC electronic-nose.
Characterization of the key aroma compounds in two bavarian wheat beers by means of the sensomics approach.
Flavor of cold-hardy grapes: impact of berry maturity and environmental conditions.
Characterization of odor-active compounds in sweet-type Chinese rice wine by aroma extract dilution analysis with special emphasis on sotolon.
Characterization of the key aroma compounds in Bartlett pear brandies by means of the sensomics concept.
Xylosylation as an effective means for reducing yeast growth inhibition by 2-phenylethanol.
Influence of endogenous ferulic acid in whole wheat flour on bread crust aroma.
Enhancement of volatile aglycone recovery facilitated by acid hydrolysis of glucosides from Nicotiana flower species.
Characterization of aroma compounds in Chinese bayberry (Myrica rubra Sieb. et Zucc.) by gas chromatography mass spectrometry (GC-MS) and olfactometry (GC-O).
Impact of different distribution scenarios and recommended storage conditions on flavor related quality attributes in ripening fresh tomatoes.
Volatile organic compounds from a Tuber melanosporum fermentation system.
1-methylcyclopropene effects on temporal changes of aroma volatiles and phytochemicals of fresh-cut cantaloupe.
Production of aromatic compounds by metabolically engineered Escherichia coli with an expanded shikimate pathway.
Effect of maturity stage and storage on flavor compounds and sensory description of berrycactus (Myrtillocactus geometrizans).
Microbial ecology studies of spontaneous fermentation: starter culture selection for prickly pear wine production.
The compositions of volatiles and aroma-active compounds in dried omija fruits (Schisandra chinensis Baillon) according to the cultivation areas.
Classification of wines from five Spanish origin denominations by aromatic compound analysis.
Impact of fat reduction on flavor and flavor chemistry of Cheddar cheeses.
Ghanaian cocoa bean fermentation characterized by spectroscopic and chromatographic methods and chemometrics.
Effect of halotolerant starter microorganisms on chemical characteristics of fermented chum salmon (Oncorhynchus keta) sauce.
Bioproduction of 2-phenylethanol in a biphasic ionic liquid aqueous system.
Characterization of aroma compounds in Chinese rice wine Qu by solvent-assisted flavor evaporation and headspace solid-phase microextraction.
Chemical composition of French mimosa absolute oil.
Bioproduction of the aroma compound 2-phenylethanol in a solid-liquid two-phase partitioning bioreactor system by Kluyveromyces marxianus.
Headspace solid-phase microextraction-gas chromatography-mass spectrometry for profiling free volatile compounds in Cabernet Sauvignon grapes and wines.
Changes in key aroma compounds of Criollo cocoa beans during roasting.
[Rapid determination of volatile flavor compounds in soy sauce using head space solid-phase microextraction and gas chromatography-mass spectrometry].
Studies on the aroma of five fresh tomato cultivars and the precursors of cis- and trans-4,5-epoxy-(E)-2-decenals and methional.
Influence of aeration during propagation of pitching yeast on fermentation and beer flavor.
Short communication: Identification of the aroma compounds responsible for the floral/rose flavor in water-soluble fractions of Manchego cheese.
Tomato phenylacetaldehyde reductases catalyze the last step in the synthesis of the aroma volatile 2-phenylethanol.
Characterization of the key aroma compounds in soy sauce using approaches of molecular sensory science.
Changes in key odorants of raw coffee beans during storage under defined conditions.
Characterization of aroma compounds in apple cider using solvent-assisted flavor evaporation and headspace solid-phase microextraction.
The FEMA GRAS assessment of aromatic substituted secondary alcohols, ketones, and related esters used as flavor ingredients.
Tomato aromatic amino acid decarboxylases participate in synthesis of the flavor volatiles 2-phenylethanol and 2-phenylacetaldehyde.
Characterization of the key aroma compounds in the beverage prepared from Darjeeling black tea: quantitative differences between tea leaves and infusion.
Characterization of odor-active volatiles in champa (Campomanesia lineatifolia R. and P.).
The FEMA GRAS assessment of phenethyl alcohol, aldehyde, acid, and related acetals and esters used as flavor ingredients.
Characterization of aroma compounds responsible for the rosy/floral flavor in Cheddar cheese.
Aroma extract dilution analysis of cv. Meeker (Rubus idaeus L.) red raspberries from Oregon and Washington.
Comparison of volatile compounds produced in model cheese medium deacidified by Debaryomyces hansenii or Kluyveromyces marxianus.
Synthesis of flavor and fragrance esters using Candida antarctica lipase.
Flavor composition of cashew (Anacardium occidentale) and marmeleiro (Croton species) honeys.
Application of pulsed field gradient NMR techniques for investigating binding of flavor compounds to macromolecules.
Application of the porapak q column extraction method for tomato flavor volatile analysis.
Identification of malodorous, a wild species allele affecting tomato aroma that was aelected against during domestication.
Headspace solid phase microextraction (SPME) analysis of flavor compounds in wines. Effect of the matrix volatile composition in the relative response factors in a wine model.
Identification of impact odorants in Bordeaux red grape juice, in the commercial yeast used for its fermentation, and in the produced wine.
Production of 2-phenylethyl alcohol by Kluyveromyces marxianus.
Isolation and genetic study of p-fluoro-DL-phenylalanine-resistant mutants overproducing beta-phenethyl-alcohol in Saccharomyces cerevisiae.
Volatile Flavor Compounds Produced by Molds of Aspergillus, Penicillium, and Fungi imperfecti.
Identification of Potent Odorants in a Novel Nonalcoholic Beverage Produced by Fermentation of Wort with Shiitake (Lentinula edodes).
Metabolic engineering of Escherichia coli for production of 2-phenylethanol from renewable glucose.
Subjective olfactory desensitization and recovery in humans.
Characterization of the key aroma compounds in two bavarian wheat beers by means of the sensomics approach.
Characterization of the key aroma compounds in Bartlett pear brandies by means of the sensomics concept.
Metabolic engineering of Saccharomyces cerevisiae for the production of 2-phenylethanol via Ehrlich pathway.
Volatile composition of six horsetails: prospects and perspectives.
Characterization of volatile components in makgeolli, a traditional Korean rice wine, with or without pasteurization, during storage.
Relation between HLA genes, human skin volatiles and attractiveness of humans to malaria mosquitoes.
Yarrowia lipolytica: the novel and promising 2-phenylethanol producer.
Neuropeptide receptors provide a signalling pathway for trigeminal modulation of olfactory transduction.
Characterization of aroma compounds in Chinese bayberry (Myrica rubra Sieb. et Zucc.) by gas chromatography mass spectrometry (GC-MS) and olfactometry (GC-O).
Identification and quantification of aroma compounds of tartary buckwheat (Fagopyrum tataricum Gaertn.) and some of its milling fractions.
Solid phase microextraction as a reliable alternative to conventional extraction techniques to evaluate the pattern of hydrolytically released components in Vitis vinifera L. grapes.
Physical and chemical properties and stability of sodium cefazolin in buffered eye drops determined with HPLC method.
Fear-like behavioral responses in mice in different odorant environments: Trigeminal versus olfactory mediation under low doses.
Quality evaluation of olive oil by statistical analysis of multicomponent stable isotope dilution assay data of aroma active compounds.
Evaluation of differences in the aroma composition of free-run and pressed neutral grape juices obtained from Emir (Vitis vinifera L.).
Stability of cefuroxime in 1% and 5% buffered eye drops determined with HPLC method.
Predication of Japanese green tea (Sen-cha) ranking by volatile profiling using gas chromatography mass spectrometry and multivariate analysis.
Stability of ceftazidime in 1% and 5% buffered eye drops determined with HPLC method.
Time and intensity factors in identification of components of odor mixtures.
Olfactory dysfunction in narcolepsy with and without cataplexy.
Cross-modal integration between odors and abstract symbols.
Localisation of unilateral nasal stimuli across sensory systems.
Bioproduction of 2-phenylethanol in a biphasic ionic liquid aqueous system.
Functional MRI of regional brain responses to 'pleasant' and 'unpleasant' odors.
A gender difference related to the effect of a background odor: a magnetoencephalographic study.
Comparison between odor thresholds for phenyl ethyl alcohol and butanol.
Influence of simultaneous gustatory stimuli on orthonasal and retronasal olfaction.
Characterization of selected South African young cultivar wines using FTMIR spectroscopy, gas chromatography, and multivariate data analysis.
Advanced time-series analysis of MEG data as a method to explore olfactory function in healthy controls and Parkinson's disease patients.
Are there sex-related differences in responses to repetitive olfactory/trigeminal stimuli?
Changes in key aroma compounds of Criollo cocoa beans during roasting.
Differences in odor-active compounds of trincadeira wines obtained from five different clones.
Studies on the aroma of five fresh tomato cultivars and the precursors of cis- and trans-4,5-epoxy-(E)-2-decenals and methional.
A male-produced aggregation pheromone blend consisting of alkanediols, terpenoids, and an aromatic alcohol from the cerambycid beetle Megacyllene caryae.
Olfactory influences on mood and autonomic, endocrine, and immune function.
Characterization of the most odor-active volatiles of orange wine made from a Turkish cv. Kozan (Citrus sinensis L. Osbeck).
Characterization of the key aroma compounds in soy sauce using approaches of molecular sensory science.
Characterization of aroma compounds in apple cider using solvent-assisted flavor evaporation and headspace solid-phase microextraction.
Characteristic component odors emerge from mixtures after selective adaptation.
Comparison of three lychee cultivar odor profiles using gas chromatography-olfactometry and gas chromatography-sulfur detection.
Olfactory imprinting is correlated with changes in gene expression in the olfactory epithelia of the zebrafish.
Aroma extraction dilution analysis of Sauternes wines. Key role of polyfunctional thiols.
A comparison of methods for sniff measurement concurrent with olfactory tasks in humans.
[Subjective and objectifying olfactometry by means of flow-olfactometer].
The clinical significance of electrophysiological measures of olfactory function.
Characterization of odor-active volatiles in champa (Campomanesia lineatifolia R. and P.).
Sit up and smell the roses better: olfactory sensitivity to phenyl ethyl alcohol is dependent on body position.
Attraction of two lacewing species to volatiles produced by host plants and aphid prey.
Comparison of volatile compounds produced in model cheese medium deacidified by Debaryomyces hansenii or Kluyveromyces marxianus.
Off-vine grape drying effect on volatile compounds and aromatic series in must from Pedro Ximénez grape variety.
A simple and reliable method for clinical assessment of odor thresholds.
Gas chromatography-olfactometry and chemical quantitative study of the aroma of six premium quality spanish aged red wines.
Individual differences in sensitivity to the odor of 4,16-androstadien-3-one.
Influences of feedback and ascending and descending trial presentations on perithreshold odor detection performance.
Olfactory function in workers exposed to styrene in the reinforced-plastics industry.
Depth of olfactory sulcus and olfactory function.
Rapid olfactory processing implicates subcortical control of an olfactomotor system.
Flavor composition of cashew (Anacardium occidentale) and marmeleiro (Croton species) honeys.
Intranasal volume and olfactory function.
Acute sensory irritation from exposure to isopropanol (2-propanol) at TLV in workers and controls: objective versus subjective effects.
Controlled exposures to volatile organic compounds in sensitive groups.
Identification of odoriferous compounds from adults of a swallowtail butterfly, Papilio machaon (Lepidoptera: Papilionidae).
Quality of odor and olfactory lateralization processes in humans.
Odor threshold, recognition, discrimination and identification in centenarians.
Environment and medication use influence olfactory abilities of older adults.
[Olfactory event-related potentials to isoamyl acetate in congenital anosmia].
Effects of the sniffing port air makeup in gas chromatography-olfactometry.
Evaluation of odor and sensory irritation thresholds for methyl isobutyl ketone in humans.
Odor perception: multiple chemical sensitivities, chronic fatigue, and asthma.
Identification of impact odorants in Bordeaux red grape juice, in the commercial yeast used for its fermentation, and in the produced wine.
Similarities in the aroma chemistry of Gewürztraminer variety wines and lychee (Litchi chinesis sonn.) fruit.
Alterations of chemosensory function in end-stage liver disease.
Perceived odor, irritation, and health symptoms following short-term exposure to acetone.
Olfactory event-related potentials to amyl acetate in congenital anosmia.
The influence of cognitive bias on the perceived odor, irritation and health symptoms from chemical exposure.
Intranasal chemoreception in patients with multiple chemical sensitivities: a double-blind investigation.
Evaluating the 'Labeled Magnitude Scale' for measuring sensations of taste and smell.
Electrocortical and autonomic alteration by administration of a pleasant and an unpleasant odor.
Enhanced sensitivity to androstenone following regular exposure to pemenone.
[Posturographic registration of body sway after odor stimulation].
Twin analysis of odor identification and perception.
Discrimination of oilseed rape volatiles by honey bee: Novel combined gas chromatographic-electrophysiological behavioral assay.
Functional imaging of the human olfactory cortex by magnetic resonance imaging.
Olfaction and multiple chemical sensitivity.
Effects of odorants and irritants on respiratory behavior.
[Specific odor component produced by Mycobacterium lepraemurium on Ogawa yolk medium].
Identification of floral compounds fromAbelia grandiflora that stimulate upwind flight in cabbage looper moths.
A method for establishing a five odorant identification confusion matrix task in rats.
Olfactory sensitivity, nasal resistance, and autonomic function in patients with multiple chemical sensitivities.
Olfactory dysfunction in parkinsonism: a general deficit unrelated to neurologic signs, disease stage, or disease duration.
Relationship of CDC group EO-2 and psychrobacter immobilis.
Age-related changes in the phenyl ethyl alcohol odor detection threshold.
Optimum perception of odor intensity by humans.
Olfactory detection thresholds using pyridine, thiophene, and phenethyl alcohol.
Olfactory memory in patients with anterior temporal lobectomy.

Other Information

(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
FDA Substances Added to Food (formerly EAFUS):View
CHEBI:View
CHEMBL:View
Golm Metabolome Database:Search
Metabolomics Database:Search
KEGG (GenomeNet):C05853
HMDB (The Human Metabolome Database):HMDB33944
FooDB:FDB012152
YMDB (Yeast Metabolome Database):YMDB01072
Export Tariff Code:2901.29.5000
Typical G.C.
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View

Suppliers

Advanced Biotech Alfrebro
Ambles Nature et Chimie Aquila Organics
Aromiens International Artiste
Associate Allied Chemicals Augustus Oils
Aurochemicals Axxence Aromatic
Beijing Lys Chemicals Berjé
BeYonde BOC Sciences
Charkit Chemical Citrus and Allied Essences
CJ Latta & Associates Connect Chemicals
Creatingperfume.com Diffusions Aromatiques
ECSA Chemicals Ernesto Ventós
Eternis Fine Chemicals Excellentia International
ExtraSynthese Firmenich
Fleurchem Foreverest Resources
Fuzhou Farwell Glentham Life Sciences
Global Essence Grau Aromatics
H. Interdonati, Inc. Hermitage Oils
Indenta Group Indis NV
Indukern F&F John Kellys (London)
K.L. Koh Enterprise Keva
Kun Shan P&A Lluch Essence
M&U International Moellhausen
Myrazine Naturamole
Odowell Co.,ltd OQEMA
PCW France Pearlchem Corporation
Pell Wall Perfumes Penta International
PerfumersWorld Perfumery Laboratory
Phoenix Aromas & Essential Oils Primechem
Prinova Prodasynth
R C Treatt & Co Ltd Reincke & Fichtner
Riverside Aromatics Robertet
Sigma-Aldrich SRS Aromatics
Sunaux International Symrise
Taytonn ASCC TCI AMERICA
The John D. Walsh Company The Lermond Company
The Perfumers Apprentice Tianjin Danjun International
TRI-K Industries Ungerer & Company
Universal Preserv-A-Chem Inc. Vigon International
WEN International WholeChem
Zanos Advanced Biotech. Inc.
Alfrebro LLC/ Archer Daniels Midland Company Augustus Oils Ltd
Axxence Aromatic GmbH Beijing Lys Chemicals Co, LTD.
Berje Inc. Charkit Chemical Corporation
CJ Latta & Associates, LLC Firmenich Inc.
Fleurchem, Inc. Foreverest Resources Ltd.
Glentham Life Sciences Ltd Global Essence Inc.
Hermitage Oils / Neroli S.R.L. Indukern, S.A. F&F Ingredients Division
Lluch Essence S.L. M&U International LLC
Moellhausen S.P.A. Myrazine LLC
Penta International Corporation PerfumersWorld Ltd.
Anhui Primechem Co., Ltd. Riverside Aromatics Ltd.
Robertet, Inc. SRS Aromatics Ltd
Symrise AG Taytonn ASCC Pte Ltd
The John D. Walsh Company, Inc Tianjin Danjun International Trade Co., LTD.
R C Treatt and Co Ltd Ernesto Ventós S.A.
WholeChem, LLC Zanos Ltd.

PhysChem Properties

Material listed in food chemical codex Yes
Molecular weight 122.16690063477
Specific gravity @ 25 °C
Pounds per Gallon 8.446 to 8.512
Specific gravity @ 20 °C
Pounds per Gallon 8.464 to 8.531
Refractive Index 1.53 to 1.534 @ 20 °C
Melting Point -27 to -25.8°C @ 760 mm Hg
Boiling Point 219 to 221°C @ 760 mm Hg
Boiling Point 136 to 137°C @ 50 mm Hg
Vapor Pressure 0.0868 mmHg @ 25 °C
Vapor Density 4.21
Flash Point TCC Value 102 °C TCC
logP (o/w) 1.36
Shelf life 24 months (or longer if stored properly.)
Storage notes Store in cool, dry place in tightly sealed containers, protected from heat and light.
Solubility
alcohol Yes
dipropylene glycol Yes
fixed oils Yes
kerosene Yes
mineral oil, slightly Yes
propylene glycol Yes
water, 2.199e+004 mg/L @ 25 °C (est) Yes
water, 2.22E+04 mg/L @ 25 °C (exp) Yes
paraffin oil No
Stability
alcoholic lotion Unspecified
antiperspirant Unspecified
bleach Unspecified
deo stick Unspecified
detergent perborate Unspecified
fabric softener Unspecified
hair spray Unspecified
hard surface cleaner Unspecified
liquid detergent Unspecified
non-discoloring in most media Unspecified
shampoo Unspecified

Organoleptic Properties

Odor Type: Floral
floral, rose, rose dried rose, sweet, fresh, bready, honey
Odor strength medium
Substantivity 32 hour(s) at 100.00 %
Luebke, William tgsc, (1981) At 100.00 %. floral rose dried rose flower rose water
Mosciano, Gerard P&F 18, No. 4, 51, (1993) Sweet, floral, fresh and bready with a rosey honey nuance
Flavor Type: Floral
floral, sweet, rose, bready
Mosciano, Gerard P&F 18, No. 4, 51, (1993) At 20.00 ppm. Floral, sweet, rosey and bready
General comment Honey, fruity, sweet, floral

Occurrences

Safety Information

Safety information

Preferred SDS: View
European information :
Most important hazard(s):
Xn - Harmful.
R 21/22 - Harmful in contact with skin and if swallowed.
R 36/38 - Irritating to skin and eyes.
S 02 - Keep out of the reach of children.
S 20/21 - When using do not eat, drink or smoke.
S 24/25 - Avoid contact with skin and eyes.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 36 - Wear suitable protective clothing.
Hazards identification
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
Acute toxicity, Oral (Category 4), H302
Eye irritation (Category 2A), H319
GHS Label elements, including precautionary statements
Pictogramexclamation-mark.jpg
Signal word Warning
Hazard statement(s)
H302 - Harmful if swallowed
H319 - Causes serious eye irritation
Precautionary statement(s)
P264 - Wash skin thouroughly after handling.
P270 - Do not eat, drink or smoke when using this product.
P280 - Wear protective gloves/protective clothing/eye protection/face protection.
P301 + P312 - IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P305 + P351 + P338 - IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P330 - Rinse mouth.
P337 + P313 - IF eye irritation persists: Get medical advice/attention.
P501 - Dispose of contents/ container to an approved waste disposal plant.
Human Experience:
100 %: no skin irritation. 8 % solution: non-sensitising.
Oral/Parenteral Toxicity:
oral-mouse LD50 800 - 1500 mg/kg
(Fassett, 1963)

oral-guinea pig LD50 400 - 800 mg/kg
(Fassett, 1963)

oral-rat LD50 1800 mg/kg
(Rumyantsev et al., 1987)

oral-rat LD50 [sex: M] 1900 mg/kg
2 Test substance administered as 5% musk ambrette in phenethyl alcohol.
(Moreno, 1982e)

gavage-rat LD50 [sex: M,F] 1790 mg/kg
(Jenner et al., 1964)

oral-rat LD50 2234 mg/kg
1 Value based on specific gravity = 1.02.
(Zeller & Hoffmann, 1974)

oral-rat LD50 [sex: M] 2100 mg/kg
3 Test substance administered as 20% musk ambrette in phenethyl alcohol.
(Moreno, 1982f)

gavage-rat LD50 [sex: M,F] 2540 mg/kg
(Zaitsev & Rakhmanina, 1974)

gavage-mouse LD50 [sex: M,F] 2540 mg/kg
(Zaitsev & Rakhmanina, 1974)

gavage-guinea pig LD50 [sex: M,F] 2540 mg/kg
(Zaitsev & Rakhmanina, 1974)

gavage-rat LD50 [sex: M,F] 1609 mg/kg
(Mallory et al., 1982a)

oral-rat LD50 [sex: M,F] 2509 mg/kg
1 Value based on specific gravity = 1.02.
(Carpenter et al., 1974)

gavage-rat LD50 [sex: F] 3100 mg/kg
4 Test substance administered as beta-phenethyl alcohol.
(Grote & Woods, 1955)

intraperitoneal-guinea pig LD50 200 mg/kg
"Patty's Industrial Hygiene and Toxicology," 3rd rev. ed., Clayton, G.D., and F.E. Clayton, eds., New York, John Wiley & Sons, Inc., 1978-82. Vol. 3 originally pub. in 1979; pub. as 2n rev. ed. in 1985.Vol. 2C, Pg. 4642, 1982.

oral-guinea pig LD50 2540 mg/kg
Voprosy Pitaniya. Problems of Nutrition. Vol. 33(5), Pg. 48, 1974.

oral-mouse LD50 2540 mg/kg
Voprosy Pitaniya. Problems of Nutrition. Vol. 33(5), Pg. 48, 1974.

oral-rabbit LDLo 2000 mg/kg
Journal of Economic Entomology. Vol. 48, Pg. 139, 1955.

oral-rat LD50 1790 mg/kg
GASTROINTESTINAL: GASTRITIS BEHAVIORAL: COMA
Food and Cosmetics Toxicology. Vol. 2, Pg. 327, 1964.

Dermal Toxicity:
skin-guinea pig LD50 > 5 ml/kg
Food and Cosmetics Toxicology. Vol. 2, Pg. 327, 1964.

subcutaneous-mouse LDLo 1640 mg/kg
BEHAVIORAL: COMA BEHAVIORAL: ATAXIA BEHAVIORAL: GENERAL ANESTHETIC
Journal of Pharmacology and Experimental Therapeutics. Vol. 14, Pg. 211, 1920.

skin-rabbit LD50 790 uL/kg
Toxicology and Applied Pharmacology. Vol. 28, Pg. 313, 1974.

Inhalation Toxicity:
inhalation-rat LC50 > 500 mg/m3
BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BLOOD: NORMOCYTIC ANEMIA
Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 52(10), Pg. 83, 1987.

Safety in use information

Category:
flavor and fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for phenethyl alcohol usage levels up to:
40.0000 % in the fragrance concentrate.
Maximised Survey-derived Daily Intakes (MSDI-EU): 1200.00 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 330.00 (μg/capita/day)
Structure Class: I
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 3. Update in publication number(s): 29
Click here to view publication 3
average usual ppmaverage maximum ppm
baked goods: 27.0000033.00000
beverages(nonalcoholic): 13.0000018.00000
beverages(alcoholic): 250.00000250.00000
breakfast cereal: --
cheese: --
chewing gum: 25.0000080.00000
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: 0.050000.10000
fish products: --
frozen dairy: 19.0000023.00000
fruit ices: --
gelatins / puddings: 6.0000010.00000
granulated sugar: --
gravies: --
hard candy: 2.0000012.00000
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: --
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: 26.0000030.00000
soups: --
sugar substitutes: --
sweet sauces: --

Safety references

European Food Safety Athority(EFSA):Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...

European Food Safety Authority (EFSA) reference(s):

Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) related to: Flavouring Group Evaluation 14 (FGE.14): Phenethyl alcohol, aldehyde, esters, and related phenylacetic acid esters from chemical group 15 (Commission Regulation (EC) No 1565/2000 of 18 July 2000)
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Flavouring Group Evaluation 55 (FGE.55): Consideration of phenyl-substituted aliphatic alcohols and related aldehydes and esters evaluated by JECFA (63rd meeting) structurally related to phenethyl alcohol, aldehyde, esters and related phenylacetic acid esters evaluated by EFSA in FGE.14 (2005) and aryl-substituted saturated and unsaturated primary alcohol/aldehyde/acid/ester derivatives evaluated by EFSA in FGE.15 (2005) (Commission Regulation (EC) No 1565/2000 of 18 July 2000) - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC)
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Flavouring Group Evaluation 53 (FGE.53): Consideration of phenethyl alcohol, aldehyde, acid and related acetals and esters evaluated by JECFA (59th meeting) structurally related to phenethyl alcohol, aldehyde, esters and related phenylacetic acid esters evaluated by EFSA in FGE.14 (2005) and one phenoxyethyl ester evaluated in FGE.23 (2006) (Commission Regulation (EC) No 1565/2000 of 18 July 2000) - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC)
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Flavouring Group Evaluation 14, Revision 1 (FGE.14Rev1): Phenethyl alcohol, aldehyde, acetals, carboxylic acid and related esters from chemical group 15 and 22 [1] - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
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Flavouring Group Evaluation 53, Revision 1 (FGE.53Rev1): Consideration of phenethyl alcohol, aldehyde, acid and related acetals and esters evaluated by JECFA (59th meeting) FGE.23Rev1 (2008)
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Safety of 31 flavouring compounds belonging to different chemical groups when used as feed additives for all animal species
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2-phenylethanol
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