alpha-damascone
Notes:
used in skin testing for immune competence.
  • 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):
      Damascone Alpha
       
  • 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):
      04-00300 DAMASCONE (ALPHA), Kosher
       
  • PerfumersWorld
    • PerfumersWorld Ltd.
      feeeel... the smell!
      The one-stop resource for the creative perfumer.
      No minimum orders. Aroma chemicals, essential oils, isolates, pheremones, absolutes, resinoids, FleuressenceTM key bases, PWx FactorTM, solubilizers, kits, creation systems, workshops, training, distance learning, The PerfumersWorld Perfumer's Studio, The Perfumer’s Formulation Bulletin, perfumery software, bespoke creation, analysis, consultancy, project counselling, trouble-shooting, unperfumed product bases, bottles, smelling strips, scales, distillation, equipment and inspiration!
      Email:Enquiries
      Email:Sales
      Voice:+66(0)2-99-800-80
      Fax:+66(0)2-99-800-80
      PerfumersWorld Skype Skype
      Software:Perfumer's Workbook
      Product(s):
      9IF02656 Damascone alpha-
      5IF07569 Damascone alpha- 10% in DPG
       
  • Phoenix Aromas & Essential Oils
    • Phoenix Aromas & Essential Oils, Inc.
      EXCEPTIONAL Flavor and Fragrance Ingredients
      Phoenix sources the finest flavor and fragrance ingredients for its customers.
      Phoenix Aromas & Essential Oils LLC was founded in 1994, grounded in a simple set of core values: provide top-quality products, cost-effective pricing and personalized attention to all our customers. After two decades, we remain committed to those values. With extensive market knowledge of our products, we anticipate, as opposed to merely react, to industry challenges. You can rely on us for all your flavor and fragrance ingredient needs. Customers benefit from Phoenix's long-standing relationships with experienced and reputable growers, processors and manufacturers in key global locations, who are committed to sustainability and green programs. With a strategically located 80,000 sq-ft facility, customers can rely on Phoenix to deliver quality products on time, and cost-effectively.
      Email:EU Info
      US Email:Info
      US Email:Kristina Streva
      Voice:+44(0) 208 532 1022
      Fax:+44(0) 208 532 1023
      US Voice:201-784-6100
      US Fax:201-784-8566
      Product(s):
      alpha-Damascone
       
  • 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):
      alpha-Damascone
       
 
Synonyms   Articles   Notes   Search
Fragrance Demo Formulas
1-(2,6,6-trimethyl-1-cyclohex-2-enyl)but-3-en-1-one (Click)
CAS Number: 43052-87-5
% from:98.00% to 100.00%
FDA UNII:UP5JTZ982I
FEMA Number:3659
CoE Number:11053
XlogP3-AA:3.20 (est)
Molecular Weight:192.30160000
Formula:C13 H20 O
NMR Predictor:Predict
Also(can) Contains:(E)-alpha-damascone 92.00% to 99.00%
 (Z)-alpha-damascone 4.00% to 8.00%
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
IBM Patents: Obtain
Pubchem Patents:Search
PubMed: Search
NCBI: Search
JECFA Food Flavoring:385  alpha-damascone
Flavis Number:07.134 (Old)
EU SANCO Food Flavourings:07.134  alpha-damascone

FEMA Number:3659  alpha-damascone
FDA Mainterm: ALPHA-DAMASCONE
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance:pale yellow clear liquid (est)
Assay: 98.00 to 100.00 % sum of isomers
Food Chemicals Codex Listed:No
Specific Gravity:0.92800 to 0.93800 @  25.00 °C.
Pounds per Gallon - (est).: 7.722 to  7.805
Refractive Index:1.49200 to 1.49900 @  20.00 °C.
Boiling Point: 267.13 °C. @ 760.00 mm Hg (est)
Acid Value: 1.00 max. KOH/g
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
Odor Type:floral
Odor Strength:high ,
recommend smelling in a 1.00 % solution or less
Odor Description:
at 1.00 % in dipropylene glycol. 
sweet floral metallic fruity apple spicy plum minty
Luebke, William tgsc, (1994)
Odor sample from:Ungerer & Company, Inc.
Odor Description:
Sweet, fruity, floral woody with a green berry nuance
Mosciano, Gerard P&F 16, No. 2, 49, (1991)
Taste Description:
at 30.00 ppm.  
Sweet, fruity, woody with a green seedy background
Mosciano, Gerard P&F 16, No. 2, 49, (1991)
Substantivity:66 hour(s) at 100.00 %
  
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: masking agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
Berjé
Damascone Alpha
PCW France
Damascone Alpha
Penta International
DAMASCONE (ALPHA), Kosher
PerfumersWorld
Damascone alpha- 10% in DPG
PerfumersWorld
Damascone alpha-
Odor: natural diffusive fruity floral woody
Phoenix Aromas & Essential Oils
alpha-Damascone
Tengzhou Jitian Aroma Chemiclal
4-(2.6.6-Trimethyl cyclohex-2-enyl)-but-2-en-4-one
Treatt
alpha-Damascone
Zhejiang Taizhou TU-POLY
a-Damascone
Synonyms   Articles   Notes   Search   Top
Safety Information:
Oral/Parenteral Toxicity:
  Not determined
Dermal Toxicity:
  Not determined
Inhalation Toxicity:
  Not determined
Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
0.0031 mg/kg/day (IFRA, 2002, 2003)
Category:flavor and fragrance agents
Maximised Survey-derived Daily Intakes (MSDI-EU):6.90 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA):0.40 (μg/capita/day)
Structure Class:I
Fragrance usage is IFRA RESTRICTED. View Standard for complete information.
Please review all IFRA documents for complete information.
IFRA categories: limits in the finished product: (For a description of the categories, refer to the IFRA QRA Information Booklet.)
Category 1:
See Note (1)
0.003 % (1)
Category 2: 0.02 %
Category 3: 0.02 %
Category 4: 0.02 %
Category 5: 0.02 %
Category 6: 0.07 % (1)
Category 7: 0.008 %
Category 8: 0.02 %
Category 9: 0.02 %
Category 10: 0.02 %
Category 11:See Note (2)
 Notes:
 

For this material, for pragmatic reasons, restrictive levels allowed by the QRA for certain categories but actually being higher than those already in place before applying the QRA, will temporarily not be implemented until the end of a 5 year monitoring phase. At the end of the 5 years the position will be reevaluated again.

 

(1) IFRA would recommend that any material used to impart perfume or flavour in products intended for human ingestion should consist of ingredients that are in compliance with appropriate regulations for foods and food flavourings in the countries of planned distribution and, where these are lacking, with the recommendations laid down in the Code of Practice of IOFI (International Organisation of the Flavor Industry). Further information about IOFI can be found on its website (www.iofi.org).

 

(2) Category 11 includes all non-skin contact or incidental skin contact products. Due to the negligible skin contact from these types of products there is no justification for a restriction of the concentration of this fragrance ingredient in the finished product.

use level in formulae for use in cosmetics:
  0.1200 %
Dermal Systemic Exposure in Cosmetic Products:
 
Recommendation for alpha-damascone flavor usage levels up to:
  25.0000 ppm in the finished product.
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):
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)
page or pdf
Flavouring Group Evaluation 210: alpha,beta-Unsaturated alicyclic ketones and precursors from chemical subgroup 2.4 of FGE.19[1]
page or pdf
EPI System:View
Chemicalize.org:Calculate predicted properties
Cancer Citations:Search
Toxicology Citations:Search
EPA ACToR:Toxicology Data
National Institute of Allergy and Infectious Diseases:Data
SCCNFP:opinion
WGK Germany:1
 1-(2,6,6-trimethyl-1-cyclohex-2-enyl)but-3-en-1-one
Chemidplus:0043052875
Synonyms   Articles   Notes   Search   Top
References:
Leffingwell:chirality
 1-(2,6,6-trimethyl-1-cyclohex-2-enyl)but-3-en-1-one
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:43052-87-5
Pubchem (cid):62002
Pubchem (sid):135019827
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:2914.29.0000
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
2-acetyl furanFL/FR
 allyl amyl glycolateFR
 allyl cyclohexyl propionateFL/FR
 allyl heptanoateFL/FR
 allyl propionateFL/FR
 amyl 2-methyl butyrateFL/FR
 amyl isobutyrateFL/FR
 amyl isovalerateFL/FR
isoamyl salicylateFL/FR
isoamyl valerateFL/FR
 amyris wood oilFL/FR
 angelica root oilFL/FR
para-anisaldehydeFL/FR
 anise seed oil colombiaFL/FR
para-anisyl alcoholFL/FR
 apple ketalFL/FR
 benzyl acetateFL/FR
 benzyl cinnamateFL/FR
 benzyl isovalerateFL/FR
 benzyl propionateFL/FR
blood orange oil italyFL/FR
 bois de rose oil brazilFL/FR
isobutyl cinnamateFL/FR
 butyl heptanoateFL/FR
 butyl isovalerateFL/FR
isobutyl isovalerateFL/FR
 caramel furanoneFL
 caraway seed oilFL/FR
 cassia bark oil chinaFL/FR
 cinnamyl alcoholFL/FR
 cistus twig/leaf oilFL/FR
 clary sage oil franceFL/FR
 clove bud oilFL/FR
 coriander seed oilFL/FR
para-cresyl isobutyrateFL/FR
para-cresyl isovalerateFL/FR
black currant bud absoluteFL/FR
 cyclamen aldehydeFL/FR
 cyclohexyl butyrateFL/FR
 cyclohexyl ethyl alcoholFL/FR
 cyclohexyl isovalerateFL/FR
(Z)-beta-damasconeFL/FR
beta-damasconeFL/FR
gamma-damasconeFR
gamma-decalactoneFL/FR
 decanal (aldehyde C-10)FL/FR
3-decen-2-oneFL/FR
 diethyl 1-malateFL
 dihydrojasmoneFL/FR
 dimethyl benzyl carbinyl butyrateFL/FR
 ethyl (E,Z)-2,4-decadienoateFL/FR
 ethyl 2-methyl butyrateFL/FR
 ethyl 3-methyl valerateFL/FR
 ethyl acetoacetateFL/FR
 ethyl cinnamateFL/FR
 ethyl decanoateFL/FR
 ethyl heptanoateFL/FR
 ethyl isovalerateFL/FR
 ethyl maltolFL/FR
 ethyl methyl mercaptopropionateFL/FR
 ethyl valerateFL/FR
isoeugenyl acetateFL/FR
 floral pyranolFR
 fruity ketalFL/FR
 galbasconeFR
 galbanum oilFL/FR
 geraniolFL/FR
 geranyl 2-methyl butyrateFL/FR
 geranyl acetateFL/FR
(E)-geranyl acetoneFL/FR
 geranyl isovalerateFL/FR
 grapefruit oil c.p. californiaFL/FR
 grapefruit pentanolFR
 green acetateFR
 heliotropinFL/FR
 heliotropyl acetoneFL/FR
 heptyl 2-methyl butyrateFL
 hexanal diethyl acetalFL/FR
(Z)-3-hexenal diethyl acetalFL/FR
(E)-2-hexenal dimethyl acetalFL
(Z)-3-hexenal dimethyl acetal 
(Z)-3-hexen-1-yl 2-methyl butyrateFL/FR
3-hexenyl 2-methyl butyrateFL/FR
(Z)-3-hexen-1-yl acetateFL/FR
(Z)-3-hexen-1-yl butyrateFL/FR
(Z)-3-hexen-1-yl isobutyrateFL/FR
(E)-2-hexen-1-yl propionateFL/FR
(Z)-3-hexen-1-yl propionateFL/FR
(Z)-3-hexen-1-yl salicylateFL/FR
(Z)-3-hexen-1-yl tiglateFL/FR
(E)-2-hexen-1-yl valerateFL/FR
(Z)-3-hexen-1-yl valerateFL/FR
 hexyl 2-methyl butyrateFL/FR
 hexyl acetateFL/FR
 hexyl butyrateFL/FR
alpha-hexyl cinnamaldehydeFL/FR
 hexyl formateFL/FR
 hexyl isobutyrateFL/FR
 hexyl tiglateFL/FR
(Z)-leaf acetalFL/FR
 leerallFR
 linaloolFL/FR
 linalool oxideFL/FR
 maltolFL/FR
 marine formateFR
 melon heptenalFL/FR
 melon nonenoateFL/FR
 buchu mercaptan acetateFL/FR
4-methoxy-2-methyl butane thiolFL/FR
4-methyl 4-mercaptopentan-2-one 1% solutionFL/FR
 methyl butyrateFL/FR
 methyl citronellateFL/FR
 methyl dihydrojasmonateFL/FR
 methyl heptine carbonateFL/FR
 methyl isovalerateFL/FR
 methyl octine carbonateFL/FR
 methyl ortho-anisateFL/FR
 methyl valerateFL/FR
 mimosa absolute franceFL/FR
 muguet octadienolFR
beta-naphthyl ethyl etherFL/FR
 nerolFL/FR
 nerolidolFL/FR
 neryl acetateFL/FR
(E,Z)-2,6-nonadien-1-olFL/FR
 nonanal (aldehyde C-9)FL/FR
(Z)-6-nonenalFL/FR
 nonyl isovalerateFL/FR
 ocean propanalFL/FR
(E)-2-pentenalFL/FR
 peony alcoholFR
 petitgrain oil paraguayFL/FR
 phenethyl acetateFL/FR
 phenethyl isobutyrateFL/FR
 phenethyl isovalerateFL/FR
 pineapple heptadienone 10%FR
isopropyl isobutyrateFL/FR
 propyl isovalerateFL/FR
isopropyl isovalerateFL/FR
 propyl tiglateFL/FR
 raspberry ketone methyl etherFL/FR
 rose butanoateFL/FR
 santallFR
 strawberry furanoneFL/FR
 strawberry glycidate 1 (aldehyde C-16 (so-called))FL/FR
alpha-terpineolFL/FR
para-tolualdehydeFL/FR
gamma-undecalactone (aldehyde C-14 (so-called))FL/FR
10-undecen-1-al (aldehyde C-11 undecylenic)FL/FR
10-undecen-1-olFL/FR
 vanilla bean absolute (vanilla planifolia)FL/FR
 vanillyl acetateFL/FR
 veramossFR
 violet leaf absoluteFL/FR
 violet methyl carbonateFR
 watermelon ketoneFR
(Z)-woody amyleneFR
 ylang ylang flower oilFL/FR
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 agrumen 
 aldehydicFR
 amberFR
 anais anais 
 angelicaFL/FR
 animalFR
 appleFR
 apple blossomFR
 apple brandy 
 apple crabapple 
 apple greenFR
 apple redFR
 apricotFR
 ash mountain ash berry 
 azzaro 
 bark 
 berryFR
 berry jamFR
 blossom tropical blossom 
 boxwood 
 bramble arctic bramble blackberry 
 cassis black currant budFL/FR
 cedar forestFR
 chamomileFR
 cheese ghee cheese 
 cherry blackFR
 christmas blendsFR
 chrysanthemum chrysanthemeFR
 cistusFL/FR
 citrusFR
 cloudberry bakeapple 
 crabapple blossomFR
 cranberryFR
 currant blackFR
 dateFR
 de bagatelle 
 drakkar 
 drakkar noir 
 eglantine sweet briarFR
 elder berryFR
 figFR
 floralFR
 fruitFR
 fruit dried fruit 
 fruit tropical fruit 
 ginger aleFL
 gooseberryFR
 grapeFR
 grape white grape 
 guavaFR
 herbalFR
 hibiscusFR
 honey mielFR
 honeysuckle chevrefeuilleFR
 hugonia 
 immortelle helichrysum everlastingFL/FR
 jardins de bagatelle 
 kiwiFR
 kiwi blossom 
 licorice red licorice 
 lycheeFR
 mangoFR
 mapleFR
 marigold tageteFL/FR
 marjoramFL/FR
 mateFL/FR
 melonFR
 montana 
 nahema 
 necterineFL
 pansyFR
 paris 
 passion blossomFR
 passion fruitFR
 pearFR
 pear bartlett pear 
 pear blossomFR
 pear emperor pear 
 pineappleFR
 plumFR
 plum greengage plum 
 plum mirabelleFR
 poison 
 pomegranateFR
 pruneFR
 raisinFR
 raspberryFR
 redwood 
 roseFR
 rose tea roseFR
 rose wild rose 
 rueFL/FR
 saint laurent 
 stephanotisFR
 tangerineFR
 tea 
 tea greenFR
 tobaccoFR
 toffeeFR
 tropicalFL
 watercress nasturtium 
 white linen 
 wineFR
 woodyFR
 wormwood absinthiumFL/FR
Synonyms   Articles   Notes   Search   Top
Natural Occurrence in: note
 rose
 tea
 tobacco
GRIN Trop Picture
Synonyms   Articles   Notes   Search   Top
Synonyms:
2-buten-1-one, 1-(2,6,6-trimethyl-2-cyclohexen-1-yl)-
 damarose alpha
 damascone (alpha)
 dihydro floriffone A
1-(2,6,6-trimethyl-1-cyclohex-2-enyl)but-3-en-1-one
1-(2,6,6-trimethyl-2-cyclohexen-1-yl)-2-butenone
4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-but-2-en-4-one
1-(2,6,6-trimethyl-2-cyclohexenyl)-2-buten-1-one
4-(2,6,6-trimethyl-2-cyclohexenyl)-2-buten-4-one
4-(2,6,6-trimethyl-2-cyclohexenyl)-2-butene-4-one
1-(2,6,6-trimethyl-cyclohex-2-enyl)-but-2-en-1-one
1-(2,6,6-trimethylcyclohex-2-en-1-yl)but-2-en-1-one
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed:Comparison of aroma active and sulfur volatiles in three fragrant rice cultivars using GC-olfactometry and GC-PFPD.
PubMed:Influence of triterpenoids present in apple peel on inflammatory gene expression associated with inflammatory bowel disease (IBD).
PubMed:Analytical and sensory characterization of the aroma of "Langhe D.O.C. Nebbiolo" wines: influence of the prefermentative cold maceration with dry ice.
PubMed:Characterization of volatiles and aroma-active compounds in honeybush (Cyclopia subternata) by GC-MS and GC-O analysis.
PubMed:Aromatic aldols and 1,5-diketones as optimized fragrance photocages.
PubMed:[Isoprenoids and phenylpropanoids from Saussurea deltoidea].
PubMed:Characterization of the bound volatile extract from baby kiwi (Actinidia arguta).
PubMed:Structural Analysis of CYP101C1 from Novosphingobium aromaticivorans DSM12444.
PubMed:Influence of the backbone structure on the release of bioactive volatiles from maleic acid-based polymer conjugates.
PubMed:Insecticidal potency of novel compounds on multiple insect species of medical and veterinary importance.
PubMed:Volatile composition screening of Salix spp. nectar honey: benzenecarboxylic acids, norisoprenoids, terpenes, and others.
PubMed:Identification of 3-hydroxy-beta-damascone and related carotenoid-derived aroma compounds as novel potent inducers of Nrf2-mediated phase 2 response with concomitant anti-inflammatory activity.
PubMed:Substrate promiscuity of RdCCD1, a carotenoid cleavage oxygenase from Rosa damascena.
PubMed:[Retention of components in a mixture of volatile organic substances by maltodextrins].
PubMed:Synthetic applications of enantioselective protonation and case study for (S)-alpha-damascone.
PubMed:Characterization of the most odor-active compounds in an American Bourbon whisky by application of the aroma extract dilution analysis.
PubMed:Fragrance material review on cis-beta-damascone.
PubMed:Fragrance material review on gamma-damascone.
PubMed:Fragrance material review on delta-damascone.
PubMed:Fragrance material review on alpha-damascone.
PubMed:Fragrance material review on trans-beta-damascone.
PubMed:Fragrance material review on cis-alpha-damascone.
PubMed:Fragrance material review on trans,trans-delta-damascone.
PubMed:[Investigation of the pyrolysis behavior of 4-oxo-beta-damascone by on-line pyrolysis gas chromatography-mass spectrometry].
PubMed:Glycosidically bound volatiles and flavor precursors in Laurus nobilis L.
PubMed:A simple and efficient highly enantioselective synthesis of alpha-ionone and alpha-damascone.
PubMed:A novel biomimetic route to the 3-acyl-5-hydroxy-3-pyrrolin-2-one and 3-acyl-3,4-epoxy-5-hydroxypyrrolidin-2-one ring systems.
PubMed:Investigation of bound aroma constituents of yellow-fleshed nectarines (Prunus persica L. Cv. Springbright). changes in bound aroma profile during maturation.
PubMed:Aroma composition of Vitis vinifera Cv. tannat: the typical red wine from Uruguay.
PubMed:Identification of (3S, 9R)- and (3S, 9S)-megastigma-6,7-dien-3,5,9-triol 9-O-beta-D-glucopyranosides as damascenone progenitors in the flowers of Rosa damascena Mill.
PubMed:Principles and methodology for identification of fragrance allergens in consumer products.
PubMed:Character impact odorants of the apple cultivars Elstar and Cox Orange.
PubMed:Volatile compounds released by enzymatic hydrolysis of glycoconjugates of leaves and grape berries from Vitis vinifera Muscat of Alexandria and Shiraz cultivars.
PubMed:Acid-catalyzed hydrolysis of alcohols and their beta-D-glucopyranosides.
PubMed:Identification of potent odorants in Japanese green tea (Sen-cha).
PubMed:C(13)-Norisoprenoid glucoconjugates from lulo (Solanum quitoense L.) leaves.
PubMed:Bioconversion of alpha-Damascone by Botrytis cinerea.
PubMed:Progress in synthesis of sensory important trace components of essential oils and natural flavours.
Synonyms   Articles   Notes   Search   Top
click on the picture(s) below to
interact with the 3D model
Picture of molecule
Soluble in:
 alcohol
 dipropylene glycol
 water, 10.31 mg/L @ 25 °C (est)
Insoluble in:
 water
Stability:
 alcoholic solution
 antiperspirant
 cream
 deodorant spray
 hair spray
 shampoo
 soap
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