phenethyl benzoate
Notes:
Rounds off eugenols.
  • Berjé
    • Berjé Inc.
      The solution is clear
      Where the world comes to its senses - Berjé is a global distributor of Essential Oils and Aromatic Chemicals.
      Berjé is a family-owned business that has been in operation for six decades. The company's origins and strength lie in a profound understanding of the supply and the quality of the diverse raw materials consumed by the flavor and fragrance industries. This base was expanded upon more than two decades ago to include fragrance production. The company's unparalleled raw material expertise is focused on the supply of essential oils and aromatic chemicals. This is supported by our long-standing relationships with a worldwide fabric of producers ensuring the greatest prospects for uninterrupted supply in markets that are often volatile and unpredictable.
      Email: For Information
      Email: For Sales
      Voice: 973-748-8980
      Fax: 973-680-9618
      Product(s):
      Phenyl Ethyl Benzoate
       
  • Fleurchem
    • Fleurchem, Inc.
      Have A Flavorful Day
      A leading global manufacturer and supplier of ingredients for Flavors, Fragrances, AromaTherapy, Foods, Beverages, Personal Care Products, and other uses.
      Operating out of the 200,000 sq. ft., former Hercules/PFW facility in Middletown, NY; Fleurchem produces a full range of natural isolates, synthetic chemicals & specialities, essential oils and flavors. Additionally, the company performs toll manufacturing, as well as custom chemical synthesis for a wide range of clients.
      Email: Information
      US Voice: 845-341-2100
      US Fax: 845-341-2121
      Product(s):
      phenyl ethyl benzoate natural
       
  • Indukern F&F
  • Lluch Essence
    • Lluch Essence S.L.
      A family company dedicated to sales and distribution
      Flexibility, availability, price and quality.
      Flexibility, availability, price and quality make LLUCH ESSENCE S.L. one of Europe’s references when it comes to essential oils and aroma chemicals, and it is now well known all around the world.
      Email: Info
      Voice: 34 93 379 38 49
      Fax: 34 93 370 65 04
      Product(s):
      PHENYL ETHYL BENZOATE
       
  • Penta International
    • Penta International Corporation
      Chemistry innovation
      At Penta, our products and services help businesses do business better.
      For over 30 years, Penta Manufacturing Company has played a growing role in worldwide chemistry innovations and applications. As an industry leader, Penta continues to pioneer chemistry-based solutions for practically every area of commerce. Our products and expertise have helped fuel technical advances in dozens of commercial applications including flavoring, coloring, fragrances and chemical processes.
      US Email: Technical Services
      US Email: Sales
      US Voice: (973) 740-2300
      US Fax: (973) 740-1839
      Product(s):
      16-30400 PHENYLETHYL BENZOATE, Kosher
       
  • SAFC Global
    • SAFC
      Complete Supply Chain
      The perfect blend of products and services that bring your creativity to life.
      Sigma-Aldrich is a leading Life Science and High Technology company dedicated to providing high-quality, safe and certified flavor ingredients with transparent and easily accessible documentation to customers around the globe. Sigma-Aldrich also provides a suite of analytical tools that allow food analysts to simplify sample preparation, cleanup and analysis steps, while increasing sensitivity to trace ingredients and harmful substances to meet regulations and quality standards.
      Email: Information
      US Email: Sales
      US Voice: 800-244-1173
      US Fax: 800-368-4661
      Product(s):
      W286001 Phenethyl benzoate ≥99%
      MSDS
       
  • SRS Aromatics
    • SRS Aromatics Ltd
      For over 25 years
      Bringing flavour and fragrance into your world.
      As suppliers / distributors of ingredients to the fragrance and flavour industries, our goal is to provide high quality materials at competitive prices with an exceptional level of service. Established in 1984, SRS Aromatics Ltd is an independent family owned business which has become very well-respected within the fragrance and flavour industry as a reliable and trustworthy partner. Over the years this has allowed the company to develop strong relationships with many global manufacturers; several of whom we represent in the UK. A core aim of our business is to work extremely closely with both our suppliers and customers to maximise service levels with minimum disruption to supply.
      Email: Info
      Email: Sales
      Voice: +44 (0) 1284 704076
      Fax: +44 (0) 1284 760819
      Product(s):
      PHENYL ETHYL BENZOATE
       
  • The John D. Walsh Company
    • The John D. Walsh Company, Inc
      Suppliers Since 1942
      Supplying the fragrance and flavor industry with high quality products.
      The John D. Walsh Company, Inc. has evolved from its beginnings as an agent/broker into a distributor of essential oils, aroma chemicals, concretes and absolutes. We currently represent the following companies, as their North American distributor: Destilerias Munoz Galvez, S.A. International Flavors & Fragrances PFW Aroma Chemicals B.V. Innospec Widnes Limited Hydrodiffusion de Guatemala, S. A. DSM Nutritional Products The John D. Walsh Company, Inc. is proud to be a founding member of IFEAT, an active member of IFRA, North America, and a corporate sponsor of the WFFC.
      Email: Information
      Email: Sales
      Email: Firmenich Flavor inquiries
      Voice: 973-962-1400
      Fax: 973-962-1557
      Firmenich Flavor Phone:973-962-1888
      Firmenich Flavor Fax:973-962-1898
      Product(s):
      Phenyl Ethyl Benzoate
      MSDS
       
  • Treatt
    • Treatt PLC
      Full Range of Naturals
      World-leading, independent ingredients supplier to the flavour and fragrance industries.
      We are proud of our heritage in trading essential oils. Our founder Richard Court Treatt's charismatic and personable approach still embodies the spirit of Treatt today.
      Email: Enquiries
      US Email: Enquiries
      Voice: +44 (0) 1284 702500
      Fax: +44 (0) 1284 703809
      US Voice: +1 863 668 9500
      US Fax: +1 863 668 3388
      Product(s):
      Phenyl Ethyl Benzoate
       
  • Ernesto Ventós
 
Synonyms   Articles   Notes   Search
Fragrance Demo Formulas
2-phenylethyl benzoate (Click)
CAS Number: 94-47-3
ECHA EC Number: 202-336-5
FDA UNII: 0C143929GK
Beilstein Number: 2052132
MDL: MFCD00020681
FEMA Number: 2860
CoE Number: 667
XlogP3: 4.00 (est)
Molecular Weight: 226.27498000
Formula: C15 H14 O2
BioActivity Summary: listing
NMR Predictor: Predict
Category: cosmetic, flavor and fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Perfumer and Flavorist: Search
Google Patents: Search
US Patents: Search
EU Patents: Search
IBM Patents: Obtain
Pubchem Patents: Search
PubMed: Search
NCBI: Search
Flavis Number: 09.774 (Old)
EU SANCO Food Flavourings: 09.774  phenethyl benzoate

FEMA Number: 2860  phenethyl benzoate
FDA Mainterm: PHENETHYL BENZOATE
FDA Regulation:
FDA PART 172 -- FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION
Subpart F--Flavoring Agents and Related Substances
Sec. 172.515 Synthetic flavoring substances and adjuvants.
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance: colorless to pale yellow clear oily liquid (est)
Assay: 98.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 1.09300 @  25.00 °C.
Specific Gravity: 1.09100 to 1.09900 @  20.00 °C.
Pounds per Gallon - est.: 9.089 to 9.155
Boiling Point: 189.00 °C. @ 12.00 mm Hg
Boiling Point: 330.00 to  332.00 °C. @ 760.00 mm Hg
Acid Value: 1.00 max. KOH/g
Vapor Pressure: 0.000034 mm/Hg @ 25.00 °C. (est)
Flash Point: > 212.00 °F. TCC ( > 100.00 °C. )
logP (o/w): 4.010
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
Odor Type: floral
Odor Strength: low
Odor Description:
at 100.00 %. 
soft rose balsam honey floral
Luebke, William tgsc, (1984)
Odor sample from: PPF Norda, Inc
Substantivity: 400 Hour(s)
  
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: emollients
perfuming agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
Berjé
Phenyl Ethyl Benzoate
CG Herbals
Phenyl Ethyl Benzoate
Odor: Soft Rose Balsam Honey Floral
Ernesto Ventós
PHENYL ETHYL BENZOATE IFF
Odor: FLORAL, BALSAMIC
Fleurchem
phenyl ethyl benzoate natural
Grau Aromatics
PHENYLETHYL-BENZOATE
NI, Kosher
Indukern F&F
PHENYL ETHYL BENZOATE
Odor: SWEET, SMOOTH, FRUITY, ROSE
Inoue Perfumery
PHENETHYL BENZOATE
Lluch Essence
PHENYL ETHYL BENZOATE
Moellhausen
PHENETHYL BENZOATE
Nature-identical
Penta International
PHENYLETHYL BENZOATE, Kosher
Reincke & Fichtner
Phenethyl Benzoate
SAFC Global
Phenethyl benzoate
≥99%
Odor: honey; rose
SRS Aromatics
PHENYL ETHYL BENZOATE
Taytonn
Phenyl Ethyl Benzoate
The John D. Walsh Company
Phenyl Ethyl Benzoate
The Perfumers Apprentice
Phenethyl Benzoate ( Phenyl Ethyl Benzoate)
Odor: Balsamic, Floral, Rose
Treatt
Phenyl Ethyl Benzoate
Synonyms   Articles   Notes   Search   Top
Safety Information:
European information :
Most important hazard(s):
Xi - Irritant
  R 36/38 - Irritating to skin and eyes.
S 02 - Keep out of the reach of children.
S 24/25 - Avoid contact with skin and eyes.
S 36 - Wear suitable protective clothing.
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Human Experience:
 8 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
  gavage-rat LD50  5000 mg/kg
(Wohl, 1974i)

oral-rat LD50  5000 mg/kg
Food and Cosmetics Toxicology. Vol. 13, Pg. 905, 1975.

Dermal Toxicity:
  skin-rabbit LD50 > 5000 mg/kg
Food and Cosmetics Toxicology. Vol. 13, Pg. 905, 1975.

Inhalation Toxicity:
  Not determined
Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
Category: cosmetic, flavor and fragrance agents
Maximised Survey-derived Daily Intakes (MSDI-EU): 33.00 (μg/capita/day)
Modified Theoretical Added Maximum Daily Intake (mTAMDI): 5700 (μg/person/day)
Threshold of Concern:1800 (μg/person/day)
Structure Class: I
Recommendation for phenethyl benzoate usage levels up to:
  10.0000 % in the fragrance concentrate.
Recommendation for phenethyl benzoate flavor usage levels up to:
  5.0000 ppm in the finished product.
 
Food categories according to Commission Regulation EC No. 1565/2000 (EC, 2000) in FGE.06 (EFSA, 2002a). According to the Industry the "normal" use is defined as the average of reported usages and "maximum use" is defined as the 95th percentile of reported usages (EFSA, 2002i).
Note: mg/kg = 0.001/1000 = 0.000001 = 1/1000000 = ppm.
 average usage mg/kgmaximum usage mg/kg
Dairy products, excluding products of category 02.0 (01.0): 2.000008.00000
Fats and oils, and fat emulsions (type water-in-oil) (02.0): --
Edible ices, including sherbet and sorbet (03.0): 2.0000080.00000
Processed fruit (04.1): --
Processed vegetables (incl. mushrooms & fungi, roots & tubers, pulses and legumes), and nuts & seeds (04.2): --
Confectionery (05.0): 60.00000100.00000
Cereals and cereal products, incl. flours & starches from roots & tubers, pulses & legumes, excluding bakery (06.0): 1.200007.00000
Bakery wares (07.0): 2.400006.00000
Meat and meat products, including poultry and game (08.0): 1.000005.00000
Fish and fish products, including molluscs, crustaceans and echinoderms (MCE) (09.0): 1.0000010.00000
Eggs and egg products (10.0): --
Sweeteners, including honey (11.0): --
Salts, spices, soups, sauces, salads, protein products, etc. (12.0): 10.0000060.00000
Foodstuffs intended for particular nutritional uses (13.0): --
Non-alcoholic ("soft") beverages, excl. dairy products (14.1): 6.0000010.00000
Alcoholic beverages, incl. alcohol-free and low-alcoholic counterparts (14.2): 80.00000100.00000
Ready-to-eat savouries (15.0): 1.000007.00000
Composite foods (e.g. casseroles, meat pies, mincemeat) - foods that could not be placed in categories 01.0 - 15.0 (16.0): --
Synonyms   Articles   Notes   Search   Top
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):
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
page or pdf
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)
page or pdf
EPI System: View
Chemicalize.org: Calculate predicted properties
EPA Substance Registry Services (TSCA): 94-47-3
EPA ACToR: Toxicology Data
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 2
 2-phenylethyl benzoate
DTP/NCI: 24096
Chemidplus: 0000094473
RTECS: DH6288000 for cas# 94-47-3
Synonyms   Articles   Notes   Search   Top
References:
 2-phenylethyl benzoate
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 94-47-3
Pubchem (cid): 7194
Pubchem (sid): 134971288
Flavornet: 94-47-3
Pherobase Floral: View
Synonyms   Articles   Notes   Search   Top
Other Information:
(IUPAC): Atomic Weights of the Elements 2009
(IUPAC): Atomic Weights of the Elements 2009 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
FDA Everything Added to Food in the United States (EAFUS): View
Export Tariff Code: 2916.31.0000
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 acetophenoneFL/FR
1-acetyl cyclohexyl acetateFL
 ambrette seed oilFL/FR
 ambroxanFL/FR
alpha-amyl cinnamaldehydeFL/FR
isoamyl salicylateFL/FR
isoamyl undecylenateFL/FR
 amyris wood oilFL/FR
 animal carbolactoneFR
para-anisyl alcoholFL/FR
para-anisyl phenyl acetateFL/FR
 beeswax absoluteFL/FR
siam benzoin resinoidFL/FR
 benzophenoneFL/FR
 benzyl alcoholFL/FR
 benzyl cinnamateFL/FR
 benzyl salicylateFL/FR
isobornyl acetateFL/FR
 butyl benzyl etherFL/FR
 butyl phenyl acetateFL/FR
isobutyl salicylateFL/FR
 caramel furanoneFL
 cassia bark oil chinaFL/FR
 cinnamaldehydeFL/FR
 cinnamyl alcoholFL/FR
 cistus twig/leaf oilFL/FR
 citronellolFL/FR
 citronellyl acetoneFL/FR
 citronellyl isovalerateFL/FR
 citronellyl phenyl acetateFL/FR
 citronellyl propionateFL/FR
 clove bud oilFL/FR
 cocoa butenalFL/FR
 cocoa pentenalFL/FR
 costus valerolactoneFR
para-cresyl caprylateFL/FR
para-cresyl phenyl acetateFL/FR
(E)-alpha-damasconeFL/FR
(E)-beta-damasconeFL/FR
(Z)-alpha-damasconeFL/FR
(Z)-beta-damasconeFL/FR
beta-damasconeFL/FR
gamma-damasconeFR
isodecanalFL/FR
(Z)-4-decen-1-yl acetateFL/FR
 decyl formateFR
 dihydrocarvyl acetateFL/FR
 dihydrojasmoneFL/FR
 dimethyl benzyl carbinolFL/FR
 ethyl cinnamateFL/FR
 ethyl hydrocinnamateFL/FR
 ethyl laurateFL/FR
 ethyl phenyl acetateFL/FR
 ethyl vanillinFL/FR
isoeugenyl phenyl acetateFL/FR
 farnesyl acetateFL/FR
 fir balsam absoluteFR
 floral pyranFR
 floral pyranolFR
 floral undecenoneFR
 frankincense oilFL/FR
 galbanum oilFL/FR
 geraniolFL/FR
 geranyl acetateFL/FR
(E)-geranyl linaloolFL/FR
 geranyl phenyl acetateFL/FR
 globulol 
 guaiacwood oilFL/FR
 hawthorn ethanolFR
 heliotropinFL/FR
 heliotropyl acetoneFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 hyacinth acetalsFL/FR
 indoleFL/FR
 jasmin absolute egypt (from concrete)FL/FR
 juniper berry oilFL/FR
 labdanum resinoidFR
 leerallFR
 lilyallFR
laevo-linaloolFL/FR
 linalyl phenyl acetateFL/FR
 methyl benzoateFL/FR
 methyl cedryl ketoneFL/FR
2-methyl octanalFL/FR
 methyl phenyl acetateFL/FR
2-methyl undecanal (aldehyde C-12 mna)FL/FR
4-methyl-4-phenyl pentanoneFR
 musk acetateFR
beta-naphthyl ethyl etherFL/FR
 narcissus flower absoluteFR
 nerolidolFL/FR
 neryl acetateFL/FR
 neryl isovalerateFL/FR
 nonanal diethyl acetalFL/FR
 nonanolFL/FR
 ocean propanalFL/FR
 octyl isovalerateFL/FR
bitter orangeflower absolute moroccoFL/FR
 orris rhizome absolute (iris pallida)FL/FR
 patchouli ethanoneFR
 patchouli oilFL/FR
 phenethyl acetateFL/FR
 phenethyl alcoholFL/FR
 phenethyl anthranilateFL/FR
 phenethyl cinnamateFL/FR
 phenethyl furoateFL/FR
 phenethyl hexanoateFL/FR
 phenethyl isobutyrateFL/FR
 phenethyl phenyl acetateFL/FR
 phenethyl propionateFL/FR
 phenethyl salicylateFL/FR
 phenoxyethanolFL/FR
 phenyl acetaldehydeFL/FR
 phenyl acetaldehyde digeranyl acetalFR
 phenyl acetic acidFL/FR
 phenyl glycol diacetateFR
3-phenyl propyl alcoholFL/FR
3-phenyl propyl formateFL/FR
 propyl phenyl acetateFL/FR
isopropyl phenyl acetateFL/FR
 raspberry ketone methyl etherFL/FR
 rhodinyl phenyl acetateFL/FR
 rose absolute (rosa centifolia) moroccoFL/FR
 rose carboxylateFR
laevo-rose oxideFL/FR
 santalyl phenyl acetateFL/FR
 strawberry glycidate 1 (aldehyde C-16 (so-called))FL/FR
 strawberry glycidate 2FL/FR
 styralyl propionateFL/FR
para-tolualdehydeFL/FR
 tonka bean absoluteFR
 tuberose absolute (from pommade)FL/FR
(E)-2-undecen-1-olFL/FR
2-undecen-1-olFL/FR
 vanilla bean absolute (vanilla planifolia)FL/FR
 veramossFR
 waxy acetateFR
 woody acetateFR
 ylang ylang flower oilFL/FR
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 balsamFR
 carnation dianthus oeilletFR
 emollients 
 fixer 
 honey mielFR
 natural 
 orange blossomFR
 roseFR
 strawberryFR
Synonyms   Articles   Notes   Search   Top
Natural Occurrence in: note
 bilberry - 0.1 mg/kg
GRIN Trop Picture
 buckthorn sea buckthorn - 0.03 mg/kg
GRIN Trop Picture
 champaca concrete @ 0.50%
Data  GC  GRIN Trop Picture
 jasmin sambac absolute egypt @ 1.26%
Data  GC  GRIN Trop Picture
 orangeflower
GRIN Trop Picture
 rose flower
GRIN Trop Picture
 ylang ylang oil CO2 extract @ 0.02%
Data  GC  GRIN Trop Picture
Synonyms   Articles   Notes   Search   Top
Synonyms:
 benzoic acid 2-phenyl ethyl ester
 benzoic acid 2-phenylethyl ester
 benzoic acid phenethyl ester
 benzoic acid, 2-phenylethyl ester
 benzoic acid, phenethyl ester
 benzyl carbinyl benzoate
 benzylcarbinyl benzoate
 phenethyl alcohol benzoate
 phenethyl alcohol, benzoate
 phenyl ethyl benzoate
2-phenyl ethyl benzoate
2-phenylethyl benzoate
 phenylethyl-benzoate
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed: [Chemical constituents from Commelina communis].
PubMed: Synthesis and antiradical/antioxidant activities of caffeic acid phenethyl ester and its related propionic, acetic, and benzoic acid analogues.
PubMed: SIRT1 inactivation induces inflammation through the dysregulation of autophagy in human THP-1 cells.
PubMed: Protective effect of Heliotropium foertherianum (Boraginaceae) folk remedy and its active compound, rosmarinic acid, against a Pacific ciguatoxin.
PubMed: The estrogenic potential of salicylate esters and their possible risks in foods and cosmetics.
PubMed: 4-[Bis(4-fluorophenyl)methyl]piperazin-1-ium 2-(2-phenylethyl)benzoate.
PubMed: Exploiting mitochondrial dysfunction for effective elimination of imatinib-resistant leukemic cells.
PubMed: Structure activity relationship analysis of phenolic acid phenethyl esters on oral and human breast cancers: the grey GM(0, N) approach.
PubMed: Characterization of new PPARgamma agonists: benzimidazole derivatives - the importance of position 2.
PubMed: Distinct molecular requirements for activation or stabilization of soluble guanylyl cyclase upon haem oxidation-induced degradation.
PubMed: Acaricidal constituents isolated from Sinapis alba L. seeds and structure-activity relationships.
PubMed: Effective killing of Gleevec-resistant CML cells with T315I mutation by a natural compound PEITC through redox-mediated mechanism.
PubMed: Novel coumarin glycoside and phenethyl vanillate from Notopterygium forbesii and their binding affinities for opioid and dopamine receptors.
PubMed: Fragrance material review on phenethyl salicylate.
PubMed: Induction of p-coumaroyldopamine and feruloyldopamine, two novel metabolites, in tomato by the bacterial pathogen Pseudomonas syringae.
PubMed: In vitro and in vivo stability of caffeic acid phenethyl ester, a bioactive compound of propolis.
PubMed: Targeting the heme-oxidized nitric oxide receptor for selective vasodilatation of diseased blood vessels.
PubMed: Synthesis, characterization, antimicrobial and single crystal X-ray crystallographic studies of some new sulfonyl, 4-chloro phenoxy benzene and dibenzoazepine substituted benzamides.
PubMed: Characterization of the first potent and selective PDE9 inhibitor using a cGMP reporter cell line.
PubMed: Induction of glutathione S-transferase and glutathione by toxic compounds and elicitors in reed canary grass.
PubMed: Cytotoxicity of phenolic acid phenethyl esters on oral cancer cells.
PubMed: Very low doses of ethanol induce behavioral changes involving dopamine D2 receptors.
PubMed: Mechanisms of nitric oxide independent activation of soluble guanylyl cyclase.
PubMed: Endomorphins 1 and 2 induce amnesia via selective modulation of dopamine receptors in mice.
PubMed: Prior exposure to lipopolysaccharide potentiates expression of plant defenses in response to bacteria.
PubMed: Pharmacokinetics of salicylate ester prodrugs of cyclic HPMPC in dogs.
PubMed: Bromocriptine protects dopaminergic neurons from levodopa-induced toxicity by stimulating D(2)receptors.
PubMed: ESR study of MMA polymerization by a peroxide/amine system: bone cement formation.
PubMed: Stability and DNA alkylation rates of the simplest functional analogues of CC-1065, para-hydroxy and para-amino phenethyl bromides.
PubMed: Behavioral effects of dopamine agonists and antagonists: influence of estrous cycle, ovariectomy, and estrogen replacement in rats.
PubMed: Ultraviolet B suppresses vitamin D receptor gene expression in keratinocytes.
PubMed: Cholecystokinin peptides stimulate pancreatic secretion by multiple signal transduction pathways.
PubMed: Suppression of cholinergic activity via the dopamine D2 receptor in the rat striatum.
PubMed: Transient loss of dopamine autoreceptor control in the presence of highly potent dopamine agonists.
PubMed: Effect of the local anesthetics phenethyl alcohol and procaine on hns mutants of the acid-induced biodegradative arginine (adi) and lysine (cad) decarboxylases of Escherichia coli.
PubMed: Synthesis and antimicrobial activity of some new 1-[4-(4-fluorobenzoylamino)-benzoyl]-4-substituted thiosemicarbazides.
PubMed: Kairomone from dandelion,Taraxacum officinale, attractant for scarab beetleAnomala octiescostata.
PubMed: Inhibition of oxidative stress in HeLa cells by chemopreventive agents.
PubMed: Procaine, a local anesthetic, signals through the EnvZ receptor to change the DNA binding affinity of the transcriptional activator protein OmpR.
PubMed: High-performance liquid chromatographic measurement of (R)-4-[3-[(2-hydroxy-2-phenethyl)amino]-3-methylbutyl]benzamide monohydrochloride (LY195448) and its p-hydroxy metabolite in human plasma and urine.
PubMed: Effects of food preservatives and local anesthetics on synthesis of outer membrane proteins in Vibrio parahaemolyticus.
PubMed: Effects of antibiotics and other inhibitors on ATP-dependent protein translocation into membrane vesicles.
PubMed: Differential effects of procaine and phenethyl alcohol on excision repair of DNA in u.v.-irradiated Escherichia coli.
PubMed: Receptor binding sites of hypoglycemic sulfonylureas and related [(acylamino)alkyl]benzoic acids.
PubMed: Simultaneous determination of hydrocortisone and benzyl alcohol in pharmaceutical formulations by reversed-phase high-pressure liquid chromatography.
PubMed: Preferential suppression of normal exoenzyme formation by membrane-modifying agents.
PubMed: Aminobenzoic acid diuretics. 7. 3-Substituted 4-phenyl-, 4-arylcarbonyl-, and 4-arylmethyl-5-sulfamoylbenzoic acids and related compounds.
PubMed: The metabolism of phenethyl bromide, styrene and styrene oxide in the rabbit and rat.
Synonyms   Articles   Notes   Search   Top
click on the picture(s) below to
interact with the 3D model
Picture of molecule
Soluble in:
 alcohol
 water, 11.99 mg/L @ 25 °C (est)
Insoluble in:
 water
Stability:
 acid cleaner
 alcoholic lotion
 antiperspirant
 bleach
 deo stick
 detergent perborate
 fabric softener
 hard surface cleaner
 liquid detergent
 shampoo
 soap
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