benzylidene acetone
4-phenyl-3-buten-2-one
 
Notes:
Flavouring ingredient. Present in hydrolysed soy protein
  • Alfrebro
    • Alfrebro LLC/ Archer Daniels Midland Company
      Let's get reacquainted
      Building great taste with aroma chemicals, extracts, and distillates
      The Alfrebro brand was established in the early 1900s by Alex Fries & Brothers, a Cincinnati Flavor Company. In 1980, the brand was re-launched as an aroma chemical manufacturer. Since its inception, Alfrebro’s primary focus has been to provide quality natural and high value synthetic chemicals.
      Email: Sarah Forbis
      Email: Sales
      Voice: 513-539-3021
      Fax: 513-539-7372
      US Voice: 513-539-7373
      Newsroom
      Product(s):
      4-PHENYL-3-BUTEN-2-ONE NATURAL
       
  • 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.
      Email: For Information
      Email: For Sales
      Voice: 973-748-8980
      Fax: 973-680-9618
      Flavor Ingredients
      Fragrance Ingredients
      Functional Ingredients
      Happening at Berje
      Products List: View
      Product(s):
      Benzylidene Acetone
       
  • BOC Sciences
    • BOC Sciences
      Best of Chemicals Supplier
      Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecule and chiral compounds.
      BOC Sciences provides a wide range of services to support the pharmaceutical industry through all stages of drug discovery including Custom Synthesis of those chemicals that are not in stock, Isotope Labeling Service, Chiral Synthesis and Resolution, Bioconjugation, PEGylation services, analytical services.
      BOC Sciences is a brand of BOCSCI Inc. We leverage our wide spectrum of business in the fields of development, manufacturing, marketing, and distribution to help you make best-informed decisions tailored to your evolving needs for premium chemicals. Our complete suite of CRO services spans the entire molecule development pipeline including contract research for target identification, building blocks, compound synthesis, biochemical and cellular analysis, preclinical animal tests, and clinical studies.
      Email: Marketing
      US Email: Marketing
      Email: Sales
      US Email: Sales
      Voice: 1-631-504-6093
      Fax: 1-631-614-7828
      US Voice: 1-631-504-6093
      US Fax: 1-631-614-7828
      Europe44-203-286-1088
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      Product(s):
      122-57-6 Warfarin Impurity (Benzalacetone)
      One of the impurities of Warfarin, which is a kind of Coumarin anticoagulant.
       
       
  • Charkit Chemical
    • Charkit Chemical Corporation
      The Specialty Chemical Specialists
      Explore this website to discover the products and services that Charkit provides for your industry and please contact us directly to find out how we can be of service to you.
      about: Since 1982, Charkit has been committed to expanding the markets we serve as our roster of products and services continues to grow with us. Our substantial portfolio of personal care ingredients now include a wide array of luxury and exotic components to compliment the key products we have always offered. We have expanded our offerings to the nutraceutical, industrial, and resin markets with a growing roster of versatile and unique ingredients. We continue to lead the way in our traditional markets such as Metal and Water Treatment, Imaging, Flavor & Fragrance, Aroma and Food. Our Pharmaceutical offerings continue to expand, still anchored by the Boronic Derivatives that meet the demands of Suzuki coupling reactions. Please contact us to learn how we can help you reach your goals.
      Email: Sales
      Voice: 203-299-3220
      Fax: 203-299-1355
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      Blog
      Products List: View
      Product(s):
      BENZYLIDENE ACETONE
       
  • CJ Latta & Associates
    • CJ Latta & Associates, LLC
      Extensive Line
      Aromatic Chemicals and Organic Acids.
      CJ Latta & Associates is a distributor of specialty aromatics and organic acids used in the formulation of flavors and fragrance manufactured worldwide. We pride ourselves on our reputation for, fair pricing, quality and reliability. We’ve built our business on successfully sourcing and developing many challenging specialty chemicals and fine ingredients for our clients.
      Email: Info
      US Email: Chip Latta
      Email: Sales
      US Email: Chip Latta
      Voice: (630) 240-8079
      Product(s):
      BENZYLIDENE ACETONE
       
  • 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
      Linkedin
      Product(s):
      BENZYLIDENE ACETONE
       
  • Moellhausen
  • 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):
      02-22000 BENZYLIDENE ACETONE
      02-22010 BENZYLIDENE ACETONE NATURAL
       
  • Sigma-Aldrich
  • TCI AMERICA
    • TCI AMERICA
      Moving Your Chemistry Forward
      We continuously strive to advance our technology.
      With East & West Coast distribution centers, count on TCI to deliver products quickly and reliably. Over 28,000 Reagents available today in benchtop to bulk quantities. Sign up for a TCI account today for fast and free shipping!
      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 60 years of synthesis experience and multi-purpose plants enable TCI to offer more than 28,000 products as well as custom synthesis. TCI has established overseas facilities in North America, Europe, China and India to serve customers worldwide.
      US Email: Sales
      Email: Technical Support
      Voice: 1-800-423-8616
      Fax: 1- 888-520-1075
      Facebook
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      Product(s):
      P0163 Benzalacetone >98.0%(GC)
       
  • 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
      History
      Product(s):
      Benzylidene Acetone
       
  • R C Treatt & Co Ltd
    • R C Treatt and Co Ltd
      Innovative ingredient solutions
      World-leading innovative ingredient solutions provider for the flavour, fragrance and FMCG industries.
      We offer innovative and trend-setting product concepts for our customers, collaborating with them to create true value for their products.
      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
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      Product(s):
      Benzylidene Acetone
       
  • Ernesto Ventós
Synonyms   Articles   Notes   Search
Fragrance Demo Formulas
CAS Number: 122-57-6Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 204-555-1
Beilstein Number: 0742047
MDL: MFCD00008779
CoE Number: 158
XlogP3: 2.10 (est)
Molecular Weight: 146.18890000
Formula: C10 H10 O
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Also(can) Contains: (E)-benzylidene acetone
 (Z)-benzylidene acetone
Category: flavoring 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
JECFA Food Flavoring: 820  4-phenyl-3-buten-2-one
FLAVIS Number: 07.024 (Old)
DG SANTE Food Flavourings: 07.024  4-phenylbut-3-en-2-one
FEMA Number: 2881  4-phenyl-3-buten-2-one
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):122-57-6 ; 4-PHENYL-3-BUTEN-2-ONE
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: white to yellow crystalline solid (est)
Assay: 97.00 to 100.00 % sum of isomers
Food Chemicals Codex Listed: No
Melting Point: 39.00 to  42.00 °C. @ 760.00 mm Hg
Boiling Point: 260.00 to  261.00 °C. @ 760.00 mm Hg
Boiling Point: 147.00 to  149.00 °C. @ 20.00 mm Hg
Congealing Point: 39.00 °C.
Vapor Pressure: 0.012000 mmHg @ 25.00 °C. (est)
Flash Point: 253.00 °F. TCC ( 122.78 °C. )
logP (o/w): 2.070
Soluble in:
 alcohol
 water, 1345 mg/L @ 25 °C (est)
Stability:
 bath foam
 hair spray
 non-discoloring
 shampoo
 soap
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: spicy
 
Odor Strength: medium ,
recommend smelling in a 1.00 % solution or less
 
Substantivity: 400 hour(s) at 20.00 %
 
 sweet  spicy  cinnamon  balsamic  rhubarb  creamy  floral  
Odor Description:
at 1.00 % in dipropylene glycol. 
sweet spice cinnamon balsam rhubarb creamy floral
Luebke, William tgsc, (1986)
 
 sweet  spicy  cinnamon  balsamic  anisic  powdery  phenolic  jammy  fruity  
Odor Description:
Sweet, spicy, cinnamon, balsamic, anisyl, powdery and phenolic with jammy, fruity notes
Mosciano, Gerard P&F 22, No. 3, 47, (1997)
 
 
Flavor Type: spicy
 
 spicy  cinnamyl  powdery  waxy  balsamic  
Taste Description:
at 30.00 ppm.  
Spicy, cinnamate-like with powdery and waxy balsamic nuances
Mosciano, Gerard P&F 22, No. 3, 47, (1997)
 
Odor and/or flavor descriptions from others (if found).
 
Sigma-Aldrich
Benzylideneacetone, ≥98%, FG
Odor Description: almond; anise; balsam; butter; cherry; cinnamon; creamy; jam; floral; herbaceous; sweet; vanilla; woody
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: not used anymore
Synonyms   Articles   Notes   Search   Top
Suppliers:
Alfrebro
4-PHENYL-3-BUTEN-2-ONE NATURAL
Odor: Sweet, Pungent, Creamy
Berjé
Benzylidene Acetone
Happening at Berje
BOC Sciences
For experimental / research use only.
Warfarin Impurity (Benzalacetone)
Odor: characteristic
Use: One of the impurities of Warfarin, which is a kind of Coumarin anticoagulant.
Charkit Chemical
BENZYLIDENE ACETONE
CJ Latta & Associates
BENZYLIDENE ACETONE
EMD Millipore
For experimental / research use only.
Benzylideneacetone
Ernesto Ventós
BENZYLIDENEACETONE
Odor: FLORAL, SLIGHTLY BUTTERY
Flavor: BUTTER-LIKE, CHEESSY, SLIGHT RASPBERRY
Inoue Perfumery
BENZYLIDENE ACETONE
Lluch Essence
BENZYLIDENE ACETONE
Moellhausen
BENZYLIDENE ACETONE
Penta International
BENZYLIDENE ACETONE NATURAL
Penta International
BENZYLIDENE ACETONE
R C Treatt & Co Ltd
Benzylidene Acetone
Reincke & Fichtner
Benzylidene Acetone
Santa Cruz Biotechnology
For experimental / research use only.
4-Phenyl-3-buten-2-one
Sigma-Aldrich
Benzylideneacetone, ≥98%, FG
Odor: almond; anise; balsam; butter; cherry; cinnamon; creamy; jam; floral; herbaceous; sweet; vanilla; woody
Certified Food Grade Products
TCI AMERICA
For experimental / research use only.
Benzalacetone >98.0%(GC)
The John D. Walsh Company
Benzylidene Acetone
Synonyms   Articles   Notes   Search   Top
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 36/37/38 - Irritating to eyes, respiratory system, and skin.
R 43 - May cause sensitisation by skin contact.
S 02 - Keep out of the reach of children.
S 22 - Do not breath dust.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 37/39 - Wear suitable gloves and eye/face protection.
 
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:
2 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
oral-rat LD50  2031 mg/kg
VASCULAR: REGIONAL OR GENERAL ARTERIOLAR OR VENOUS DILATION BEHAVIORAL: MUSCLE WEAKNESS SKIN AND APPENDAGES (SKIN): HAIR: OTHER
United States Environmental Protection Agency, Office of Pesticides and Toxic Substances. Vol. 8EHQ-0391-1194

intraperitoneal-mouse LD50  1210 mg/kg
Arzneimittel-Forschung. Drug Research. Vol. 19, Pg. 617, 1969.

intravenous-mouse LD50  112 mg/kg
Arzneimittel-Forschung. Drug Research. Vol. 19, Pg. 617, 1969.

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
Category: flavoring agents
IFRA Critical Effect: Dermal sensitization
IFRA: View Standard
Recommendation for benzylidene acetone usage levels up to:
 PROHIBITED: Should not be used as a fragrance ingredient.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 2.40 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 7.00 (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
Click here to view publication 3
 average usual ppmaverage maximum ppm
baked goods: -4.50000
beverages(nonalcoholic): -0.82000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: -0.20000
fish products: --
frozen dairy: -0.84000
fruit ices: -0.84000
gelatins / puddings: -2.10000
granulated sugar: --
gravies: --
hard candy: -3.70000
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: --
soups: --
sugar substitutes: --
sweet sauces: --
Synonyms   Articles   Notes   Search   Top
Safety References:
Flavor & Extract Manufacturers Association (FEMA) reference(s):
The FEMA GRAS assessment of aromatic substituted secondary alcohols, ketones, and related esters used as flavor ingredients. View pdf
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):
List of apha, beta-Unsaturated Aldehydes and Ketones representative of FGE.19 substances for Genotoxicity Testing [1] - Statement of the Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids (CEF)
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 215 (FGE.215): Seven a,-Unsaturated Cinnamyl Ketones from subgroup 3.2 of FGE.19
View page or View pdf
EPI System: View
Chemical Carcinogenesis Research Information System: Search
Cancer Citations: Search
Toxicology Citations: Search
Env. Mutagen Info. Center: Search
EPA Substance Registry Services (TSCA): 122-57-6
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 15909
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 1
 4-phenylbut-3-en-2-one
Chemidplus: 0000122576
RTECS: EN0330050 for cas# 122-57-6
Synonyms   Articles   Notes   Search   Top
References:
 4-phenylbut-3-en-2-one
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 122-57-6
Pubchem (cid): 15909
Pubchem (sid): 134973889
Pherobase: 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 Substances Added to Food (formerly EAFUS): View
CHEBI: View
CHEMBL: View
HMDB (The Human Metabolome Database): HMDB31617
FooDB: FDB008255
Export Tariff Code: 2914.39.9000
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
RSC Learn Chemistry: View
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
No odor group found for these
 dehydro-ar-ionene 
alpha-iononeFL/FR
acidic
 cyclohexyl acetic acidFL/FR
amber
 ambrette seed oilFL/FR
anise
 anise oleoresinFL/FR
 anise seed oilFL/FR
star anise seed oil chinaFL/FR
 anise seed oil colombiaFL/FR
star anise seed oil terpenelessFL/FR
sweet fennel absoluteFL/FR
sweet fennel oleoresinFL/FR
anisic
para-acetanisoleFL/FR
ortho-acetanisoleFL/FR
 amyl furoateFL/FR
ortho-anisaldehydeFL/FR
para-anisaldehydeFL/FR
para-anisyl phenyl acetateFL/FR
para-anisyl propanalFR
 dihydroanetholFL/FR
 ethyl para-anisateFL/FR
 ocimum basilicum herb oilFL/FR
 sassafras acetateFL/FR
balsamic
sumatra benzoin absoluteFL/FR
sumatra benzoin resinoidFL/FR
 benzophenoneFR
alpha-bisaboleneFL/FR
isobutyl benzoateFL/FR
isobutyl cinnamateFL/FR
 cinnamyl alcoholFL/FR
 cinnamyl benzoateFL/FR
 cinnamyl butyrateFL/FR
 cinnamyl cinnamateFL/FR
 copaiba balsam oilFL/FR
 ethyl cinnamateFL/FR
 frankincense absoluteFL/FR
(Z)-3-hexen-1-yl cinnamateFR
 linalyl cinnamateFL/FR
 myrrh resinoidFR
 octyl cinnamateFR
 opoponax oil (balsamodendron kafal)FL/FR
 opoponax resinoid (balsamodendron kafal)FR
 peru balsam oilFL/FR
 peru balsam resinoidFL/FR
2-phenoxyethyl formateFR
3-phenyl propyl acetateFL/FR
black poplar bud oleoresinFL/FR
 tetrahydrofurfuryl cinnamateFL/FR
 tolu balsam oilFL/FR
chocolate
 cocoa oleoresinFL/FR
 cocoa pentenalFL/FR
citrus
 citralFL/FR
 citronella oil ceylonFL/FR
 lemongrass oilFL/FR
 litsea cubeba fruit oilFL/FR
creamy
para-vanillic acidFL/FR
floral
 anise indeneFR
para-anisyl acetaldehydeFL/FR
 anisyl propanal / methyl anthranilate schiff's baseFR
 autumn carboxylateFR
 citronellalFL/FR
 dimethyl alpha-iononeFR
 dimethyl anthranilateFL/FR
 geranyl phenyl acetateFL/FR
 hawthorn acetateFR
 heliotropinFL/FR
 hydroxycitronellalFL/FR
(E)-beta-iononeFL/FR
alpha-iononeFL/FR
alpha-ironeFL/FR
ortho-methyl acetophenoneFL/FR
beta-isomethyl iononeFL/FR
alpha-isomethyl ionone (50% min.)FL/FR
alpha-isomethyl ionone (90% min.)FL/FR
 methyl ionyl acetateFL/FR
 orris rhizome resinoid (iris pallida)FL/FR
isopropyl phenyl acetateFL/FR
 rhodinolFL/FR
 rhodinyl phenyl acetateFL/FR
(E)-2,5,9-trimethyl-4,9-decadien-1-alFR
fruity
 acetyl methyl anthranilateFL/FR
para-anisyl methyl ketoneFL/FR
 berry hexanoateFR
 cherry oxyacetateFL/FR
 ethyl methyl-para-tolyl glycidateFL/FR
(E,E)-ethyl sorbateFL/FR
 peach pivalateFR
 tolualdehydes (mixed o,m,p)FL/FR
green
 diphenyl oxideFL/FR
para-methyl hydratropaldehydeFL/FR
 phenoxyethyl isobutyrateFL/FR
 tiglaldehydeFL/FR
herbal
american elder flower absoluteFR
 floral nitrileFR
licorice
(E)-anetholFL/FR
 clausena anisata leaf oil 
minty
 ethyl salicylateFL/FR
bitter fennel flower oil lithuania 
bitter fennel seed oil lithuaniaCS
musk
 cyclohexadecanoneFR
 ethylene brassylateFL/FR
 exaltone (Firmenich)FR
dextro,laevo-musconeFL/FR
 musk amberolFR
 musk indaneFR
 musk tetralinFR
omega-pentadecalactoneFL/FR
musty
 cocoa butenalFL/FR
naphthyl
para-methyl anisoleFL/FR
beta-naphthyl ethyl etherFL/FR
nutty
2,3,5-trimethyl pyrazineFL/FR
pine
white pine bark oilFL/FR
powdery
para-anisyl acetateFL/FR
para-anisyl alcoholFL/FR
alpha-methyl iononeFL/FR
spicy
 artemisia dracunculus herb oilFL/FR
 bay leaf oil terpenelessFL/FR
 benzyl isoeugenolFL/FR
 cassia bark oil chinaFL/FR
 cinnamyl acetateFL/FR
 cinnamyl propionateFL/FR
 clove bud oilFL/FR
 mace oil CO2 extractFL/FR
para-methoxy-alpha-methyl cinnamaldehydeFL/FR
para-methoxycinnamaldehydeFL/FR
alpha-methyl cinnamaldehydeFL/FR
 methyl heptadienoneFL/FR
alpha-methyl-(E)-cinnamaldehydeFL/FR
 myrtenalFL/FR
 nutmeg absoluteFL/FR
 nutmeg oil CO2 extractFL/FR
 spicy acetoacetateFL/FR
terpenic
alpha-terpineolFL/FR
 mint lactoneFL/FR
 tonka undecanoneFR
vanilla
 heliotropyl alcoholFL/FR
 vanillyl acetateFL/FR
 vanillylidene acetoneFL/FR
woody
 amber formateFR
 guaiacwood oilFL/FR
 patchouli ethanoneFR
(+)-alpha-santalyl acetateFL/FR
 timber propanolFR
 vetiveryl acetateFL/FR
 woody epoxideFR
 woody octeneFR
 
For Flavor
 
No flavor group found for these
 amyl furoateFL/FR
para-anisyl acetaldehydeFL/FR
alpha-bisaboleneFL/FR
 cinnamyl benzoateFL/FR
 clausena anisata leaf oil 
 dehydro-ar-ionene 
4-ethyl anisoleFL
bitter fennel flower oil lithuania 
2-furfurylidene butyraldehydeFL
 heliotropyl alcoholFL/FR
alpha-iononeFL/FR
para-methoxy-alpha-methyl cinnamaldehydeFL/FR
 methyl furfuracrylateFL
beta-isomethyl iononeFL/FR
white pine bark oilFL/FR
black poplar bud oleoresinFL/FR
(+)-alpha-santalyl acetateFL/FR
 tetrahydrofurfuryl cinnamateFL/FR
 vetiveryl acetateFL/FR
amber
 ambrette seed oilFL/FR
anise
(E)-anetholFL/FR
 anise oleoresinFL/FR
 anise seed oilFL/FR
star anise seed oil chinaFL/FR
 anise seed oil colombiaFL/FR
star anise seed oil terpenelessFL/FR
 ethyl para-anisateFL/FR
sweet fennel absoluteFL/FR
sweet fennel oleoresinFL/FR
anisic
para-acetanisoleFL/FR
ortho-anisaldehydeFL/FR
para-anisyl phenyl acetateFL/FR
ortho-methyl acetophenoneFL/FR
balsamic
sumatra benzoin resinoidFL/FR
isobutyl cinnamateFL/FR
 copaiba balsam oilFL/FR
 ethyl cinnamateFL/FR
 opoponax oil (balsamodendron kafal)FL/FR
 peru balsam oilFL/FR
 peru balsam resinoidFL/FR
3-phenyl propyl acetateFL/FR
 tolu balsam oilFL/FR
 vanillylidene acetoneFL/FR
cherry
 heliotropinFL/FR
para-methoxycinnamaldehydeFL/FR
chocolate
 cocoa oleoresinFL/FR
citrus
 citralFL/FR
 citronella oil ceylonFL/FR
 lemongrass oilFL/FR
 litsea cubeba fruit oilFL/FR
alpha-terpineolFL/FR
coconut
6-methyl coumarinFL
creamy
para-anisaldehydeFL/FR
 dihydrocoumarinFL
 mint lactoneFL/FR
para-vanillic acidFL/FR
floral
 cinnamyl propionateFL/FR
 citronellalFL/FR
 cocoa pentenalFL/FR
 geranyl phenyl acetateFL/FR
alpha-iononeFL/FR
alpha-isomethyl ionone (50% min.)FL/FR
alpha-isomethyl ionone (90% min.)FL/FR
 orris rhizome resinoid (iris pallida)FL/FR
 rhodinolFL/FR
fruity
 acetyl methyl anthranilateFL/FR
para-anisyl acetateFL/FR
para-anisyl alcoholFL/FR
isobutyl benzoateFL/FR
 cherry oxyacetateFL/FR
 dimethyl anthranilateFL/FR
 ethyl methyl-para-tolyl glycidateFL/FR
(E,E)-ethyl sorbateFL/FR
 linalyl cinnamateFL/FR
alpha-methyl iononeFL/FR
 tiglaldehydeFL/FR
 tolualdehydes (mixed o,m,p)FL/FR
green
 cinnamyl alcoholFL/FR
 cocoa butenalFL/FR
 diphenyl oxideFL/FR
 methyl heptadienoneFL/FR
para-methyl hydratropaldehydeFL/FR
 phenoxyethyl isobutyrateFL/FR
herbal
 dihydroanetholFL/FR
 ocimum basilicum herb oilFL/FR
honey
isopropyl phenyl acetateFL/FR
licorice
2-butyl-3-methyl pyrazineFL
meaty
ortho-thioguaiacolFL
medicinal
 frankincense absoluteFL/FR
minty
 ethyl salicylateFL/FR
(1R)-(-)-myrtenalFL
 myrtenalFL/FR
musk
 ethylene brassylateFL/FR
dextro,laevo-musconeFL/FR
musty
2,3,5-trimethyl pyrazineFL/FR
naphthyl
para-methyl anisoleFL/FR
nutty
 furfural acetoneFL
powdery
ortho-acetanisoleFL/FR
beta-naphthyl ethyl etherFL/FR
 powdery ketoneFL
spicy
para-anisyl methyl ketoneFL/FR
 artemisia dracunculus herb oilFL/FR
 bay leaf oil terpenelessFL/FR
sumatra benzoin absoluteFL/FR
 benzyl isoeugenolFL/FR
 cassia bark oil chinaFL/FR
 cinnamyl acetateFL/FR
 cinnamyl cinnamateFL/FR
 clove bud oilFL/FR
 galangal root oleoresinFL
 mace oil CO2 extractFL/FR
alpha-methyl cinnamaldehydeFL/FR
alpha-methyl-(E)-cinnamaldehydeFL/FR
 nutmeg absoluteFL/FR
 nutmeg oil CO2 extractFL/FR
 spicy acetoacetateFL/FR
sweet
 cyclohexyl acetic acidFL/FR
tarragon
 sassafras acetateFL/FR
vanilla
omega-pentadecalactoneFL/FR
 vanillyl acetateFL/FR
waxy
 hydroxycitronellalFL/FR
 rhodinyl phenyl acetateFL/FR
winey
 cinnamyl butyrateFL/FR
woody
 guaiacwood oilFL/FR
(E)-beta-iononeFL/FR
alpha-ironeFL/FR
 methyl ionyl acetateFL/FR
 
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Potential Uses:
 almondFL
 apple blossomFR
 blackberryFL
 castoreumFR
 cherryFL
 chocolate cocoaFL
 currantFR
 fernFR
 fixer 
 fruitFR
 grapeFL
 hawthornFR
 hay new mown hayFR
 heliotropeFR
 jonquilFR
 lavenderFR
 lemonFL
 lilacFR
 muskFR
 neroliFR
 nutFL
 pineFR
 raspberryFL
 rhubarbFR
 strawberryFL
 sweet peaFR
 vanillaFL
 violetFL
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Occurrence (nature, food, other): note
 coffee roasted coffee
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 soybean
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 tobacco virginia tobacco
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Synonyms:
 acetocinnamone
 benzal acetone
 benzalacetone
 benzylideneacetone
3-buten-2-one, 4-phenyl-
 methyl 2-phenyl vinyl ketone
 methyl beta-styryl ketone
 methyl styryl ketone
4-phenyl but-3-en-2-one
4-phenyl butenone
2-phenyl vinyl methyl ketone
4-phenyl-3-buten-2-one
4-phenylbut-3-en-2-one
4-phenylbutenone
 styryl methyl ketone
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed: Digallane with redox-active diimine ligand: dualism of electron-transfer reactions.
PubMed: Ferrous Carbonyl Dithiolates as Precursors to FeFe, FeCo, and FeMn Carbonyl Dithiolates.
PubMed: Additive-assisted regioselective 1,3-dipolar cycloaddition of azomethine ylides with benzylideneacetone.
PubMed: Protein preparation, crystallization and preliminary X-ray analysis of Polygonum cuspidatum bifunctional chalcone synthase/benzalacetone synthase.
PubMed: An entomopathogenic bacterium, Xenorhabdus nematophila, suppresses expression of antimicrobial peptides controlled by Toll and Imd pathways by blocking eicosanoid biosynthesis.
PubMed: (99m)Tc-labeled dibenzylideneacetone derivatives as potential SPECT probes for in vivo imaging of β-amyloid plaque.
PubMed: Metabolism of BYZX in human liver microsomes and cytosol: identification of the metabolites and metabolic pathways of BYZX.
PubMed: Engineering of plant type III polyketide synthases.
PubMed: Gas phase retro-Michael reaction resulting from dissociative protonation: fragmentation of protonated warfarin in mass spectrometry.
PubMed: Gas chromatography with flame ionization detection for determination of additives in an electrolytic Zn bath.
PubMed: Toxicology and carcinogenesis studies of methyl trans-styryl ketone (CAS NO 1896-62-4) in F344/N rats and B6C3F1 mice (feed and dermal studies).
PubMed: Phospholipase A2 inhibitors synthesized by two entomopathogenic bacteria, Xenorhabdus nematophila and Photorhabdus temperata subsp. temperata.
PubMed: A facile solvent free Claisen-Schmidt reaction: synthesis of α,α'-bis-(substituted-benzylidene)cycloalkanones and α,α'-bis-(substituted-alkylidene)cycloalkanones.
PubMed: On the accuracy of DFT methods in reproducing ligand substitution energies for transition metal complexes in solution: the role of dispersive interactions.
PubMed: Synthesis of the pyridinyl analogues of dibenzylideneacetone (pyr-dba) via an improved Claisen-Schmidt condensation, displaying diverse biological activities as curcumin analogues.
PubMed: Evaluation of hepatic glutathione transferase Mu 1 and Theta 1 activities in humans and mice using genotype information.
PubMed: Ni(II) and Pd(II) pyridinyloxazolidine-compounds: synthesis, X-ray characterisation and catalytic activities in the aza-Michael reaction.
PubMed: Bacterial metabolites of an entomopathogenic bacterium, Xenorhabdus nematophila, inhibit a catalytic activity of phenoloxidase of the diamondback moth, Plutella xylostella.
PubMed: A New Route to Azadithiolato Complexes.
PubMed: Pd-NHC catalyzed conjugate addition versus the Mizoroki-Heck reaction.
PubMed: Benzylideneacetone, an eicosanoid biosynthesis inhibitor enhances baculovirus pathogenicity in the diamondback moth, Plutella xylostella.
PubMed: A structure-based mechanism for benzalacetone synthase from Rheum palmatum.
PubMed: Synthesis and anti-inflammatory activity of novel (substituted)benzylidene acetone oxime ether derivatives: molecular modeling study.
PubMed: Quantitative structure-activity relationship modeling of antioxidant activities of hydroxybenzalacetones using quantum chemical, physicochemical and spatial descriptors.
PubMed: Highly enantioselective organocatalytic conjugate addition of nitromethane to benzylidene acetones.
PubMed: Crystallization and preliminary crystallographic analysis of a plant type III polyketide synthase that produces benzalacetone.
PubMed: Benzylideneacetone, an immunosuppressant, enhances virulence of Bacillus thuringiensis against beet armyworm (Lepidoptera: Noctuidae).
PubMed: New "green" approaches to the synthesis of pyrazole derivatives.
PubMed: Microbial production of 4-hydroxybenzylidene acetone, the direct precursor of raspberry ketone.
PubMed: Novel hydrido-ruthenium(II) complexes with histidine derivatives and their application in the hydrogenation of ketones.
PubMed: Phenolic Michael reaction acceptors: combined direct and indirect antioxidant defenses against electrophiles and oxidants.
PubMed: An entomopathogenic bacterium, Xenorhabdus nematophila, inhibits hemocyte phagocytosis of Spodoptera exigua by inhibiting phospholipase A(2).
PubMed: Structure function analysis of benzalacetone synthase from Rheum palmatum.
PubMed: Highly asymmetric Michael addition to alpha,beta-unsaturated ketones catalyzed by 9-amino-9-deoxyepiquinine.
PubMed: Concise asymmetric total synthesis of obolactone.
PubMed: Antioxidant effects of hydroxybenzalacetones on peroxynitrite-induced lipid peroxidation in red blood cell membrane ghost and SOS response in Salmonella typhimurium TA4107/pSK1002.
PubMed: Metabolism of the alpha,beta-unsaturated ketones, chalcone and trans-4-phenyl-3-buten-2-one, by rat liver microsomes and estrogenic activity of the metabolites.
PubMed: Reaction of metalated nitriles with enones.
PubMed: Solution and solid state structure and tautomerism of azo coupled enaminone derivatives of benzoylacetone.
PubMed: Highly enantioselective conjugate additions of potassium organotrifluoroborates to enones by use of monodentate phosphoramidite ligands.
PubMed: Quantitative structure-activity relationship analyses of antioxidant and free radical scavenging activities for hydroxybenzalacetones.
PubMed: Identification of an antibacterial compound, benzylideneacetone, from Xenorhabdus nematophila against major plant-pathogenic bacteria.
PubMed: Site-directed mutagenesis of benzalacetone synthase. The role of the Phe215 in plant type III polyketide synthases.
PubMed: Organocatalytic asymmetric conjugate addition of nitroalkanes to alpha,beta-unsaturated enones using novel imidazoline catalysts.
PubMed: Enzymatic formation of an unnatural C(6)-C(5) aromatic polyketide by plant type III polyketide synthases.
PubMed: Quantum chemical- and 3-D-QSAR (CoMFA) studies of benzalacetones and 1,1,1-trifluoro-4-phenyl-3-buten-2-ones.
PubMed: Reductive metabolism of an alpha,beta-ketoalkyne, 4-phenyl-3-butyn-2-one, by rat liver preparations.
PubMed: Role of 4-phenyl-3-buten-2-one in boar taint: identification of new compounds related to sensorial descriptors in pig fat.
PubMed: Potency of Michael reaction acceptors as inducers of enzymes that protect against carcinogenesis depends on their reactivity with sulfhydryl groups.
PubMed: Structure-antimutagenic activity relationships of benzalacetone derivatives against UV-induced mutagenesis in E. coli WP2uvrA and gamma-induced mutagenesis in Salmonella typhimurium TA2638.
PubMed: Production and elicitation of benzalacetone and the raspberry ketone in cell suspension cultures of Rubus idaeus.
PubMed: Structure-activity relationship in potentially anti-tumor promoting benzalacetone derivatives, as assayed by the epstein-barr virus early antigen activation.
PubMed: Microsomal carbonyl reductase responsible for reduction of 4-phenyl-3-buten-2-one in rats.
PubMed: Reductive metabolism In vivo of trans-4-phenyl-3-buten-2-one in rats and dogs.
PubMed: Anticandidial effect of phenylbutene derivatives and their interaction with ergosterol.
PubMed: The three-dimensional structure of an avian class-mu glutathione S-transferase, cGSTM1-1 at 1.94 A resolution.
PubMed: The inhibition by flavonoids of 2-amino-3-methylimidazo[4,5-f]quinoline metabolic activation to a mutagen: a structure-activity relationship study.
PubMed: Absorption, disposition, and metabolism of trans-methyl styryl ketone in female B6C3F1 mice.
PubMed: Antimutagenic effects of dehydrozingerone and its analogs on UV-induced mutagenesis in Escherichia coli.
PubMed: Oral and topical absorption, disposition kinetics, and the metabolic fate of trans-methyl styryl ketone in the male Fischer 344 rat.
PubMed: Glutathione transferase mimics: micellar catalysis of an enzymic reaction.
PubMed: Distribution of glutathione S-transferase isoforms in rat liver after induction by beta-naphthoflavone or 3-methylcholanthrene.
PubMed: Multiplicity of rat liver 15-ketoprostaglandin delta 13-reductases.
PubMed: Glutathione S-transferases in the Japanese quail: tissue distribution and purification of the liver isozymes.
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: The high non-enzymatic conjugation rates of some glutathione S-transferase (GST) substrates at high glutathione concentrations.
PubMed: Biochemical analysis of recombinant glutathione S-transferase of Fasciola hepatica.
PubMed: Rational reconstruction of the active site of a class mu glutathione S-transferase.
PubMed: Influences of dietary deoxycholic acid on progression of hepatocellular neoplasms and expression of glutathione S-transferases in rats.
PubMed: Reduced expression of glutathione S-transferase Yb2 during progression of chemically induced hepatocellular carcinomas in Fischer 344 rats.
PubMed: Effects of age and dietary restriction on liver glutathione transferase activities in Lobund-Wistar rats.
PubMed: Purification and kinetic mechanism of the glutathione S-transferase from C6/36, an Aedes albopictus cell line.
PubMed: Inter-individual variability of human hepatic glutathione S-transferase isozymes assessed by inhibitory capacity.
PubMed: Structure and function of the xenobiotic substrate binding site of a glutathione S-transferase as revealed by X-ray crystallographic analysis of product complexes with the diastereomers of 9-(S-glutathionyl)-10-hydroxy-9,10-dihydrophenanthrene.
PubMed: Human Mu-class glutathione S-transferases present in liver, skeletal muscle and testicular tissue.
PubMed: Purification and characterization of class mu glutathione S-transferase isozymes from rabbit hepatic tissue.
PubMed: Characterization of a novel microsomal glutathione S-transferase produced by Aspergillus ochraceus TS.
PubMed: Schistosoma mansoni: single-step purification and characterization of glutathione S-transferase isoenzyme 4.
PubMed: Contribution of tyrosine 6 to the catalytic mechanism of isoenzyme 3-3 of glutathione S-transferase.
PubMed: Are the histidine residues of glutathione S-transferase important in catalysis? An assessment by 13C NMR spectroscopy and site-specific mutagenesis.
PubMed: A novel glutathione transferase (13-13) isolated from the matrix of rat liver mitochondria having structural similarity to class theta enzymes.
PubMed: Hepatic glutathione S-transferases in mice fed on a diet containing the anticarcinogenic antioxidant butylated hydroxyanisole. Isolation of mouse glutathione S-transferase heterodimers by gradient elution of the glutathione-Sepharose affinity matrix.
PubMed: Variation in the expression of Mu-class glutathione S-transferase isoenzymes from human skeletal muscle. Evidence for the existence of heterodimers.
PubMed: The isolation and characterization of the major glutathione S-transferase from the squid Loligo vulgaris.
PubMed: Xenobiotic-inducible expression of murine glutathione S-transferase Ya subunit gene is controlled by an electrophile-responsive element.
PubMed: S-(1,2-dicarboxyethyl)glutathione and activity for its synthesis in rat tissues.
PubMed: Effect of aflatoxin B1 treatment in vivo on the in vitro activity of hepatic and extrahepatic glutathione S-transferase.
PubMed: Sex differences in the subunits of glutathione-S-transferase isoenzyme from rat and human kidney.
PubMed: Changes in hepatic cytosolic glutathione S-transferase enzymes induced by clotrimazole treatment in rats.
PubMed: Purification and properties of glutathione transferase from Issatchenkia orientalis.
PubMed: Differences in the influence of diet on hepatic glutathione S-transferase activity and glutathione content between young and old C57 black female mice.
PubMed: Xenobiotic metabolizing enzyme systems in test fish. III. Comparative studies of liver cytosolic glutathione S-transferases.
PubMed: Fluorometric determination of benzylideneacetone in fragrance products by liquid chromatography with post-column derivatization.
PubMed: Purification of three cytosolic glutathione S-transferases from adult Schistosoma mansoni.
PubMed: Halothane: inhibition and activation of rat hepatic glutathione S-transferases.
PubMed: Paradoxical inhibition of rat glutathione transferase 4-4 by indomethacin explained by substrate-inhibitor-enzyme complexes in a random-order sequential mechanism.
PubMed: Differential induction of rat hepatic glutathione S-transferase isoenzymes by hexachlorobenzene and benzyl isothiocyanate. Comparison with induction by phenobarbital and 3-methylcholanthrene.
PubMed: Sex- and substrate-dependent changes in hepatic cytosolic glutathione S-transferase enzymes produced by dietary choline-deficiency.
PubMed: The purification and characterization of glutathione S-transferase from the hepatopancreas of the blue crab, Callinectes sapidus.
PubMed: Synthesis and antiarrhythmic activity of new 3-[2-(omega-aminoalkoxy)phenoxy]-4-phenyl-3-buten-2-ones and related compounds.
PubMed: The major isozyme of rat cardiac glutathione transferases. Its correspondence to hepatic transferase X.
PubMed: Kinetic independence of the subunits of cytosolic glutathione transferase from the rat.
PubMed: Synthesis of 3-(4,4-dimethyl-2-piperidon-6-yl)methyl-2-pyrazoline derivatives.
PubMed: Effects of pH on weak and positive control mutagens in the Ames Salmonella plate assay.
PubMed: Antigenic competition in the induction of contact sensitivity in the guinea pig.
PubMed: Age-development and inducibility of hepatic glutathione S-transferase activities in mice, rats, rabbits and guinea-pigs.
PubMed: Purification and characterization of glutathione S-transferases P, S and N. Isolation from rat liver of Yb1 Yn protein, the existence of which was predicted by subunit hybridization in vitro.
PubMed: Mannich bases of 4-phenyl-3-buten-2-one: a new class of antiherpes agent.
PubMed: Regulation of epididymal glutathione S-transferases: effects of orchidectomy and androgen replacement.
PubMed: Purification of a new glutathione S-transferase (transferase mu) from human liver having high activity with benzo(alpha)pyrene-4,5-oxide.
PubMed: The presence and longitudinal distribution of the glutathione S-transferases in rat epididymis and vas deferens.
PubMed: Stoichiometric model of alpha-cyclodextrin complex formation.
PubMed: Glutathione S-transferases in earthworms (Lumbricidae).
PubMed: Isoelectric focusing of glutathione S-transferases from rat liver and kidney.
PubMed: [Halogenated 4-phenyl-3-buten-2-one Oximes (author's transl)].
PubMed: Distribution of enzymes that catalyse reactions of glutathione with alpha beta-unsaturated compounds.
PubMed: Enzymes catalysing conjugations of glutathione with alpha-beta-unsaturated carbonyl compounds.
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