benzyl acetone
4-phenylbutan-2-one
 
Notes:
None found
  • ACS International
    • ACS International GmbH
      Creativity Beyond Chemistry
      Production • Distribution • Sourcing • Logistics • Consulting
      Our hybrid business model, combining manufacturing with sourcing and exclusive distribution agreements, results in a superior level of purchasing power that when added to our global warehouse network with locations near all major flavor and fragrance industry compounding centers around the globe, make A.C.S. International your one-stop sourcing partner.
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      69904 Benzyl Acetone
       
  • Augustus Oils
    • Augustus Oils Ltd
      The Premier Supplier
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      A wealth of experience, expertise and knowledge has allowed Augustus to bridge the gulf in expectation and trust between growers and users of natural ingredients. The Company works in partnership with customers on the one hand, and growers, farmers and distillers on the other. Both users and producers can then focus on exactly what they do best, while skilled Augustus technicians closely monitor and control the delivered product. This ensures users can have the confidence that they will receive the best raw materials suited to their requirements.
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      Benzyl Acetone
       
  • Berjé
    • Berje Inc.
      Where the world comes to its senses
      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.
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  • BOC Sciences
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      Product(s):
      2550-26-7 Benzylacetone 97%
       
  • Global Essence
    • Global Essence Inc.
      Preferred Partner
      Accommodate each customers unique needs.
      Global Essence was founded in 1993 as a two person operation servicing regional customers in the New York/ New Jersey area. In the twenty years since, it has grown into a multinational operation with offices in the US, UK, and Singapore. These offices allow Global to provide regional support to its customers worldwide. As the world continues become more connected, this approach positions Global to continue to offer the highest quality products and experience to all of its customers.
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      Benzyl Acetone
       
  • 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.
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      BENZYL ACETONE
       
  • M&U International
    • M&U International LLC
      Steady supply & demand
      Meeting customers increasing demands at home as well as abroad.
      M&U dedicates itself to the development and production of new products as well as continuously promoting those new products. We’ve maintained a steady supply&demand relationship with a large number of manufacturers at home and abroad. We’ve developed an extensive network and because of our relationships with these manufacturers, we’re able to provide a stable supply of great quality materials. We’re located in China’s largest communications hub, Shanghai and in the U.S. near one of the largest sea ports on the East Coast. The strategic locations of our facilities ensure convenient, prompt and secure delivery of our products to our customers.
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      A0615 Benzyl Acetone
       
  • Moellhausen
  • OQEMA
    • OQEMA
      With a focus on providing the highest level of service
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      The guiding principles of OQEMA have always been to establish long term relationships with customers and suppliers alike to build sustainable and profitable business for all parties. Through OQEMA’s business divisions the company tailors products and services to better support and service our customers requirements. This structure also allows the company to focus its marketing campaigns more effectively to certain industries. Over the last decade OQEMA has achieved strong growth as a result of the expansion of our business model. Going forward, the company will be expanding this business model into existing and new strategic territories.
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      Benzyl Acetone
       
  • Pell Wall Perfumes
    • Pell Wall Perfumes
      Hand-made fragrances
      Pell Wall maintains a broad palette of ingredients & in order to keep stocks fresh & the options wide we also sell from our own stock.
      Pell Wall was founded by perfumer Chris Bartlett to provide exclusive hand-made fragrances to a select few people who love them. All our products are created using fine quality ingredients, many of which we also offer for sale to other perfumers and enthusiasts. Pell Wall make fragrances for men, for women and for the home.
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      Benzyl Acetone
      Arctander has some other suggestions: “floral-green odor, fresher than that of Benzylacetate, more lasting. Stable in soap. Suggested for use in perfumes as a modifier for Benzylacetate, particularly in soap fragrances. Its somewhat sharper character can at times bean advantage for the more robust job of perfuming a soap.”
       
       
  • Penta International
    • Penta International Corporation
      Chemistry innovation
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      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.
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      02-18000 BENZYL ACETONE
       
  • Prodasynth
    • Prodasynth
      PRODUCTEUR PAR ESSENCE
      Chemical specialist in manufacturing, distributing and sourcing of tailor-made ingredients for the Flavour & Fragrance industry.
      Today we are also proud to say, we have created an important range of Natural Molecules which can be found in our Raw Material Compendium. The versatility of our small but efficient structure is one of our main strengths when trying to fulfill our clients' requirements.
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      BENZYL ACETONE (> 99%)
       
  • 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.
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      BENZYL ACETONE
       
  • TCI AMERICA
    • TCI AMERICA
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      We continuously strive to advance our technology.
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      Tokyo Chemical Industry Co., Ltd. (TCI) is a leading worldwide manufacturer of specialty organic chemicals founded in 1946. TCI provides organic laboratory chemicals as well as pharmaceutical, cosmetic and functional materials. More than 70 years of synthesis experience and multi-purpose plants enable TCI to offer more than 30,000 products as well as custom synthesis.
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      B0405 4-Phenyl-2-butanone >95.0%(GC)
      SDS
       
  • Ernesto Ventós
  • Vigon International
    • Vigon International
      Passion for Simplicity
      Manufacturer and supplier of high quality flavor and fragrance ingredients.
      The growth and success of Vigon is due in large part to a unique corporate concept that Vigon has developed and established within the industry: Creative Partnerships. This partnership concept has been and continues to be the foundation and guiding principle for all of Vigon's activities.
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      502463 Benzyl Acetone
       
  • Zanos
    • Zanos Ltd.
      Distributor of Speciality Chemicals and Natural Ingredients
      Sourcing and supplying quality aroma chemicals and prestige natural ingredients for the flavour and fragrance industry.
      The flavour and fragrance industry's premier source for aroma chemicals and essential oils
      Zanos Ltd. is a B2B supplier of aroma chemicals, speciality chemicals, natural ingredients and vitamins to a diverse range of customers. In Autumn 2020, Stort Chemicals Limited completed their acquisition of Zanos Ltd. Combining our strengths, Stort and Zanos have boosted our respective portfolios of aroma chemicals, speciality chemicals and natural ingredients. With warehousing facilities across the UK, Rotterdam and Hamburg, Zanos is perfectly positioned to dispatch product throughout Europe.
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Synonyms   Articles   Notes   Search
Fragrance Demo Formulas
CAS Number: 2550-26-7Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 219-847-4
FDA UNII: UZM5QH16YW
Nikkaji Web: J31.102B
Beilstein Number: 1907123
MDL: MFCD00008790
CoE Number: 11182
XlogP3-AA: 1.80 (est)
Molecular Weight: 148.20484000
Formula: C10 H12 O
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome, Edge or firefox)
Category: 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
Pubchem Patents: Search
PubMed: Search
NCBI: Search
DG SANTE Food Flavourings: 07.194  4-phenylbutan-2-one
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance: colorless to yellow clear liquid to solid (est)
Assay: 99.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 0.98500 to 0.99100 @  25.00 °C.
Pounds per Gallon - (est).: 8.196 to  8.246
Refractive Index: 1.50900 to 1.51500 @  20.00 °C.
Melting Point: -13.00 °C. @ 760.00 mm Hg
Boiling Point: 233.00 to  235.00 °C. @ 760.00 mm Hg
Boiling Point: 115.00 °C. @ 13.00 mm Hg
Vapor Pressure: 0.056000 mmHg @ 25.00 °C. (est)
Flash Point: 208.00 °F. TCC ( 97.78 °C. )
logP (o/w): 1.963 (est)
Soluble in:
 alcohol
 water, 1625 mg/L @ 25 °C (est)
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: floral
 
Odor Strength: medium
 
Substantivity: 172 hour(s) at 100.00 %
 
 floral  balsamic  
Odor Description:
at 100.00 %. 
floral balsam
 
 
Flavor Type: fruity
 
 strawberry  
Taste Description:
strawberry
 
Odor and/or flavor descriptions from others (if found).
 
Vigon International
Benzyl Acetone
Odor Description: Floral, jasmine-Benzyl acetate, herbal, chemical aromatic
 
Moellhausen
BENZYL ACETONE
Odor Description: sweet aromatic, fruity
Taste Description: strawberry
 
Pell Wall Perfumes
Benzyl Acetone
Odor Description: Floral, balsamic, sweet, aromatic
Arctander has some other suggestions: “floral-green odor, fresher than that of Benzylacetate, more lasting. Stable in soap. Suggested for use in perfumes as a modifier for Benzylacetate, particularly in soap fragrances. Its somewhat sharper character can at times bean advantage for the more robust job of perfuming a soap.”
Taste Description: strawberry
 
Prodasynth
BENZYL ACETONE (> 99%)
Odor Description: FLORAL, HERBAL
Taste Description: strawberry
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
ACS International
Benzyl Acetone
Odor: Floral Balsamic
Operational Capabilities
Augustus Oils
Benzyl Acetone
Services
Berjé
Benzyl Acetone
Media
Best Value Chem
Benzyl Acetone
Odor: Sweet, herbal, floral with jasmine nuance
BOC Sciences
For experimental / research use only.
Benzylacetone 97%
Diffusions Aromatiques
BENZYL ACETONE
EMD Millipore
For experimental / research use only.
Benzylacetone
Ernesto Ventós
BENZYL ACETONE
Odor: FLORAL, HERBAL
Fuzhou Farwell
Benzyl Acetone
Global Essence
Benzyl Acetone
Indukern F&F
BENZYL ACETONE
Odor: AROMATIC, SWEET, FRUITY
Lluch Essence
BENZYL ACETONE
Odor: FRUITY, SWEET
M&U International
Benzyl Acetone
Moellhausen
BENZYL ACETONE
Odor: sweet aromatic, fruity
OQEMA
Benzyl Acetone
Pell Wall Perfumes
Benzyl Acetone
Odor: Floral, balsamic, sweet, aromatic
Use: Arctander has some other suggestions: “floral-green odor, fresher than that of Benzylacetate, more lasting. Stable in soap. Suggested for use in perfumes as a modifier for Benzylacetate, particularly in soap fragrances. Its somewhat sharper character can at times bean advantage for the more robust job of perfuming a soap.”
Penta International
BENZYL ACETONE
Prodasynth
BENZYL ACETONE
(> 99%)
Odor: FLORAL, HERBAL
Sigma-Aldrich: Aldrich
For experimental / research use only.
4-Phenyl-2-butanone 98%
SRS Aromatics
BENZYL ACETONE
TCI AMERICA
For experimental / research use only.
4-Phenyl-2-butanone >95.0%(GC)
Vigon International
Benzyl Acetone
Odor: Floral, jasmine-Benzyl acetate, herbal, chemical aromatic
Zanos
Benzyl Acetone
Odor: Floral, balsamic
Synonyms   Articles   Notes   Search   Top
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 38 - Irritating to skin.
S 02 - Keep out of the reach of children.
S 24 - Avoid contact with skin.
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.
Oral/Parenteral Toxicity:
oral-rat LD50  [sex: M] 3200 mg/kg
(Moreno, 1980j)

oral-mouse LD50  1590 mg/kg
Yaoxue Tongbao. Bulletin of Pharmacology. Vol. 15(5), Pg. 7, 1980.

intraperitoneal-mouse LD50  583 mg/kg
Yaoxue Tongbao. Bulletin of Pharmacology. Vol. 15(5), Pg. 7, 1980.

oral-rat LD50  3200 mg/kg
Food and Chemical Toxicology. Vol. 21, Pg. 647, 1983.

Dermal Toxicity:
skin-rabbit LD50 > 5000 mg/kg
Food and Chemical Toxicology. Vol. 21, Pg. 647, 1983.

Inhalation Toxicity:
Not determined
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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 benzyl acetone usage levels up to:
  2.0000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.0012 (μg/capita/day)
Modified Theoretical Added Maximum Daily Intake (mTAMDI): 1600 (μg/person/day)
Threshold of Concern:1800 (μg/person/day)
Structure Class: I
 
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): 3.0000015.00000
Fats and oils, and fat emulsions (type water-in-oil) (02.0): 2.0000010.00000
Edible ices, including sherbet and sorbet (03.0): 3.0000015.00000
Processed fruit (04.1): 2.0000010.00000
Processed vegetables (incl. mushrooms & fungi, roots & tubers, pulses and legumes), and nuts & seeds (04.2): --
Confectionery (05.0): 4.0000020.00000
Chewing gum (05.0): --
Cereals and cereal products, incl. flours & starches from roots & tubers, pulses & legumes, excluding bakery (06.0): 2.0000010.00000
Bakery wares (07.0): 5.0000025.00000
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): 1.000005.00000
Eggs and egg products (10.0): --
Sweeteners, including honey (11.0): --
Salts, spices, soups, sauces, salads, protein products, etc. (12.0): 2.0000010.00000
Foodstuffs intended for particular nutritional uses (13.0): 3.0000015.00000
Non-alcoholic ("soft") beverages, excl. dairy products (14.1): 2.0000010.00000
Alcoholic beverages, incl. alcohol-free and low-alcoholic counterparts (14.2): 4.0000020.00000
Ready-to-eat savouries (15.0): 5.0000025.00000
Composite foods (e.g. casseroles, meat pies, mincemeat) - foods that could not be placed in categories 01.0 - 15.0 (16.0): 2.0000010.00000
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):
Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) related to Flavouring Group Evaluation 16 (FGE.16): Aromatic ketones from chemical group 21 (Commission Regulation (EC) No 1565/2000 of 18 July 2000)
View page or View pdf
Flavouring Group Evaluation 16, Revision 1 (FGE.16Rev1)[1]: Aromatic ketones from chemical group 21- Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
View page or View pdf
Flavouring Group Evaluation 69, (FGE.69)[1] - Consideration of aromatic substituted secondary alcohols, ketones and related esters evaluated by JECFA (57th meeting) structurally related to aromatic ketones from chemical group 21 evaluated by EFSA in FGE.16 (2006) - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
View page or View pdf
Flavouring Group Evaluation 16, Revision 2 (FGE.16Rev2): Aromatic ketones from chemical group 21
View page or View pdf
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 2550-26-7
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 17355
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 1
 4-phenylbutan-2-one
Chemidplus: 0002550267
RTECS: EL9600000 for cas# 2550-26-7
Synonyms   Articles   Notes   Search   Top
References:
 4-phenylbutan-2-one
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 2550-26-7
Pubchem (cid): 17355
Pubchem (sid): 134982576
Pherobase: View
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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
CHEMBL: View
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 2914.39.9000
Typical G.C.
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
aromatic
(4E,9Z)-13-methyloxacyclopentadeca-4,9-dien-2-oneFR
balsamic
 bornyl formateFL/FR
isobornyl isobutyrateFL/FR
isobornyl phenyl acetateFL/FR
isobutyl benzoateFL/FR
 cinnamyl cinnamateFL/FR
 frankincense absoluteFL/FR
 khella oilFR
camphoreous
 camphor tree bark oilFL/FR
citrus
beta-bisabololFL/FR
2-heptanolFL/FR
floral
alpha-amyl cinnamaldehydeFL/FR
alpha-amyl cinnamaldehyde diethyl acetalFR
alpha-amyl cinnamaldehyde dimethyl acetalFL/FR
alpha-amyl cinnamyl acetateFL/FR
 amyl cyclopentenoneCS
 amyl salicylateFL/FR
isoamyl salicylateFL/FR
 benzyl formateFL/FR
 benzyl isobutyrateFL/FR
 benzyl phenyl acetateFL/FR
 butyl tiglateFR
 cananga oilFL/FR
 cananga oil chinaFL/FR
(E)-cinnamophenone 
 citronellyl acetoneFL/FR
 coriander seed oilFL/FR
2-para-cresyl oxyethyl acetateFR
 cyclohexyl salicylateFR
 dihydrogeranyl linaloolFR
 dihydrojasmoneFL/FR
 dimethyl benzyl carbinyl propionateFR
2,4-dimethyl-3-cyclohexene-1-methanolFR
 ethyl linaloolFR
 ethyl linalyl acetalFR
 floral undecenoneFR
 frangipani specialtyFR
 gelsone (IFF)FL/FR
 herbal pyranFR
 hexahydrofarnesyl acetoneFL/FR
(Z)-3-hexen-1-yl salicylateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 honeysuckle absoluteFR
beta-ionolFL/FR
 jasmin absolute (from pommade)FL/FR
 jasmin absolute china (from concrete)FL/FR
 jasmin absolute egypt (from concrete)FL/FR
 jasmin absolute india (from concrete)FL/FR
 jasmin absolute italy (from concrete)FL/FR
 jasmin absolute sambacFL/FR
 jasmin acetateFL/FR
 jasmin lactone (IFF)FL/FR
 jasmin pyranolFR
(Z)-jasmoneFL/FR
isojasmoneFL/FR
para-jasmoneFR
 karo karounde absoluteFR
 lavandula angustifolia flower oilFL/FR
 lavender oil franceFL/FR
 lavender oil greeceFL/FR
 linalool oxide (furanoid)FL/FR
 methyl dihydrojasmonateFL/FR
 methyl jasmonateFL/FR
 methyl phenoxyethanolFR
2-methyl-4-phenyl-1,3-dioxolaneFR
(Z)-beta-ocimeneFL/FR
2-pentadecanoneFL/FR
 pentenyl cyclopentanoneFR
2-pentyl cyclopentan-1-olFR
1-phenyl propyl alcoholFL/FR
1-phenyl propyl butyrateFL/FR
3-phenyl propyl propionateFL/FR
4-phenyl-3-buten-2-olFL/FR
(Z,E)-phytolFL/FR
isophytolFL/FR
 pittosporum specialtyFR
 prenyl salicylateFL/FR
2-isopropoxyethyl salicylateFR
 terpinyl isobutyrateFL/FR
 wallflower absoluteFR
 ylang ylang oil III fractionsFR
fruity
 benzyl propionateFL/FR
 cyclohexyl crotonateFR
 peach nitrileFR
(R)-styralyl acetateFL/FR
 styralyl butyrateFL/FR
(E,E)-5,6,7,7-tetramethyl-2,5-octadien-4-oneFR
green
holy basil leaf oilFL/FR
isobutyl benzyl carbinolFL/FR
 chrysanthemum oxideFL/FR
 heptyl benzoateFL/FR
 heptyl formateFL/FR
(Z)-3-hexen-1-yl benzoateFL/FR
 privet dioxaneFR
herbal
 carrot seed oil (daucus carota ssp. gummifer hook. fil.) spainFR
 chamomile isobutyrateFR
 chrysanthemum ketoneFR
 coriander seed absoluteFL/FR
 glyceryl tribenzoateCS
abrialis lavandin oilFL/FR
 lavender absolute bulgariaFL/FR
 lavender stem oil lithuaniaFR
 methyl cyclogeranate (Firmenich)FR
 methyl ortho-anisateFL/FR
 myrtle oilFL/FR
 rhododendron anthopogon leaf oilFR
 rosemary oil africaFL/FR
 rosemary oil corsicaFL/FR
 rosemary oil tunisiaFL/FR
pine
 bornyl benzoate 
spicy
alpha-amyl cinnamyl alcoholFL/FR
 carnation absoluteFR
 walnut leaf oilFR
woody
 cistus twig/leaf absoluteFR
2-decalinyl acetateFR
isolongifolene epoxideFR
 spruce needle oil canadaFL/FR
 woody acetateFR
 
For Flavor
 
No flavor group found for these
alpha-amyl cinnamaldehyde dimethyl acetalFL/FR
holy basil leaf oilFL/FR
 bornyl benzoate 
 bornyl formateFL/FR
isobornyl phenyl acetateFL/FR
(E)-cinnamophenone 
 citronellyl acetoneFL/FR
 heptyl benzoateFL/FR
 jasmin lactone (IFF)FL/FR
 linalool oxide (furanoid)FL/FR
 methyl ortho-anisateFL/FR
1-phenyl propyl butyrateFL/FR
3-phenyl propyl propionateFL/FR
isoquinolineFL
(R)-styralyl acetateFL/FR
 terpinyl isobutyrateFL/FR
amber
isobutyl benzyl carbinolFL/FR
aromatic
 amyl salicylateFL/FR
balsamic
isobornyl isobutyrateFL/FR
1-phenyl propyl alcoholFL/FR
(Z,E)-phytolFL/FR
camphoreous
 camphor tree bark oilFL/FR
 rosemary oil tunisiaFL/FR
citrus
beta-bisabololFL/FR
earthy
alpha-amyl cinnamyl acetateFL/FR
fatty
 heptyl formateFL/FR
(Z)-3-hexen-1-yl benzoateFL/FR
2-pentadecanoneFL/FR
floral
 cananga oilFL/FR
 cananga oil chinaFL/FR
 dihydrojasmoneFL/FR
beta-ionolFL/FR
pseudoiononeFL
 jasmin absolute (from pommade)FL/FR
 jasmin absolute china (from concrete)FL/FR
 jasmin absolute egypt (from concrete)FL/FR
 jasmin absolute india (from concrete)FL/FR
 jasmin absolute italy (from concrete)FL/FR
 jasmin absolute sambacFL/FR
 jasmin acetateFL/FR
 methyl dihydrojasmonateFL/FR
 methyl jasmonateFL/FR
fruity
 benzyl formateFL/FR
 benzyl isobutyrateFL/FR
 benzyl propionateFL/FR
isobutyl benzoateFL/FR
2-heptanolFL/FR
 styralyl butyrateFL/FR
green
isoamyl salicylateFL/FR
 chrysanthemum oxideFL/FR
 gelsone (IFF)FL/FR
 hexahydrofarnesyl acetoneFL/FR
(Z)-3-hexen-1-yl salicylateFL/FR
isojasmoneFL/FR
(Z)-beta-ocimeneFL/FR
herbal
 coriander seed absoluteFL/FR
 coriander seed oilFL/FR
abrialis lavandin oilFL/FR
 lavandula angustifolia flower oilFL/FR
 lavender absolute bulgariaFL/FR
 lavender oil franceFL/FR
 lavender oil greeceFL/FR
 prenyl salicylateFL/FR
 rosemary oil africaFL/FR
 rosemary oil corsicaFL/FR
honey
 benzyl phenyl acetateFL/FR
medicinal
 frankincense absoluteFL/FR
oily
isophytolFL/FR
spicy
alpha-amyl cinnamyl alcoholFL/FR
 cinnamyl cinnamateFL/FR
 myrtle oilFL/FR
tropical
alpha-amyl cinnamaldehydeFL/FR
waxy
alpha-hexyl cinnamaldehydeFL/FR
4-phenyl-3-buten-2-olFL/FR
woody
(Z)-jasmoneFL/FR
 spruce needle oil canadaFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 balsamFR
 blackberryFR
 currantFR
 jasminFR
 raspberryFR
 strawberryFR
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 agarwood oil @ 3.50%
Data  GC  Search  PMC Picture
 galangal root oil @ 0.03%
Data  GC  Search Trop  Picture
Synonyms   Articles   Notes   Search   Top
Synonyms:
 benzylacetone
2-butanone, 4-phenyl-
 methyl 2-phenyl ethyl ketone
 methyl 2-phenylethyl ketone
 methyl phenethyl ketone
 methyl phenyl ethyl ketone
 phenethyl methyl ketone
4-phenyl butan-2-one
beta-phenyl ethyl methyl ketone
4-phenyl-2-butanone
1-phenyl-3-butanone
4-phenyl-butan-2-one
4-phenylbutan-2-one
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed: A genomic search approach to identify carbonyl reductases in Gluconobacter oxydans for enantioselective reduction of ketones.
PubMed: Mutation of Thermoanaerobacter ethanolicus secondary alcohol dehydrogenase at Trp-110 affects stereoselectivity of aromatic ketone reduction.
PubMed: [GC-MS analysis of volatile oil components from Aquilariae Lignum Resinatum concreted by a new artificial method].
PubMed: Nematicidal activity of the essential oil of Rhododendron anthopogonoides aerial parts and its constituent compounds against Meloidogyne incognita.
PubMed: Cornflower (Centaurea cyanus L.) honey quality parameters: chromatographic fingerprints, chemical biomarkers, antioxidant capacity and others.
PubMed: Sedative effects of inhaled benzylacetone and structural features contributing to its activity.
PubMed: Acetophenone reductase with extreme stability against a high concentration of organic compounds or an elevated temperature.
PubMed: RNAi-mediated silencing of the HD-Zip gene HD20 in Nicotiana attenuata affects benzyl acetone emission from corollas via ABA levels and the expression of metabolic genes.
PubMed: Immobilization of Escherichia coli containing ω-transaminase activity in LentiKats®.
PubMed: The post-pollination ethylene burst and the continuation of floral advertisement are harbingers of non-random mate selection in Nicotiana attenuata.
PubMed: Synthesis and antimalarial activity of dihydroperoxides and tetraoxanes conjugated with bis(benzyl)acetone derivatives.
PubMed: Toxicity of Rhododendron anthopogonoides essential oil and its constituent compounds towards Sitophilus zeamais.
PubMed: A smart palladium catalyst in ionic liquid for tandem processes.
PubMed: Ionic liquid catalysed synthesis of β-hydroxy ketones.
PubMed: [Synthesis and investigation on antidiabetic activity of 4-(1-aryl-3-oxo-5-phenylpentylamino) benzenesulfonamide].
PubMed: Chemical composition of volatile oils of Aquilaria malaccensis (Thymelaeaceae) from Malaysia.
PubMed: A serine-type protease activity of human lens βA3-crystallin is responsible for its autodegradation.
PubMed: Composition of sulla (Hedysarum coronarium L.) honey solvent extractives determined by GC/MS: norisoprenoids and other volatile organic compounds.
PubMed: Changing pollinators as a means of escaping herbivores.
PubMed: Field experiments with transformed plants reveal the sense of floral scents.
PubMed: Plant science. The "invisible hand" of floral chemistry.
PubMed: Comparison of the volatile composition in thyme honeys from several origins in Greece.
PubMed: Total synthesis of natural product (R)-4-phenyl-2-O-[beta-D-xylopyranosyl(1-->6)-beta-D-glucopyranosyl]butane and its epimer.
PubMed: A Bax/Bak-independent mechanism of cytochrome c release.
PubMed: Asymmetric reduction and oxidation of aromatic ketones and alcohols using W110A secondary alcohol dehydrogenase from Thermoanaerobacter ethanolicus.
PubMed: Dakin-West synthesis of beta-aryl ketones.
PubMed: 4-Phenylbutan-2-one semicarbazone.
PubMed: Purification and characterization of PrbA, a new esterase from Enterobacter cloacae hydrolyzing the esters of 4-hydroxybenzoic acid (parabens).
PubMed: Reductive metabolism of an alpha,beta-ketoalkyne, 4-phenyl-3-butyn-2-one, by rat liver preparations.
PubMed: Reductive metabolism In vivo of trans-4-phenyl-3-buten-2-one in rats and dogs.
PubMed: Synthesis and immunotropic activity of some 2-aminobenzimidazoles, Part 4.
PubMed: Absorption, disposition, and metabolism of trans-methyl styryl ketone in female B6C3F1 mice.
PubMed: Camptothecin-induced apoptosis in p53-null human leukemia HL60 cells and their isolated nuclei: effects of the protease inhibitors Z-VAD-fmk and dichloroisocoumarin suggest an involvement of both caspases and serine proteases.
PubMed: A Plant Chloroplast Glutamyl Proteinase.
PubMed: Stereoselective catalysis of a retro-Michael reaction by class mu glutathione transferases. Consequences for the internal distribution of products in the active site.
PubMed: Big endothelin-converting enzyme activities in subcellular fractions of bovine aortic endothelial cells.
PubMed: Inhibition of pig liver esterase by trifluoromethyl ketones: modulators of the catalytic reaction alter inhibition kinetics.
PubMed: Semiochemical attractants ofDiabrotica undecimpunctata howardi barber, southern corn rootworm, andDiabrotica virgifera virgifera leconte, the western corn rootworm (Coleoptera: Chrysomelidae).
PubMed: Biotransformation of terodiline I. Identification of metabolites in dog urine by mass spectrometry.
PubMed: The mode of binding of potential transition-state analogs to acetylcholinesterase.
PubMed: The structure and function of acid proteases. VI. Effects of acid protease-specific inhibitors on the acid proteases from Aspergillus niger var. macrosporus.
PubMed: Enzymic and physicochemical properties of Streptomyces griseus trypsin.
PubMed: A new method for determining the absolute molarity of solutions of trypsin and chymotrypsin by using p-nitrophenyl N2-acetyl-N1-benzylcarbazate.
PubMed: Studies on the reaction of chymotrypsin and L-1-chloro-3-tosylamido-4-phenyl-2-butanone.
PubMed: New Synthetic Lures for the Male Melon Fly.
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