(E)-6-decenal
trans-6-decenal
 
Notes:
Flavouring compound [Flavornet]
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CAS Number: 147159-48-6Picture of molecule3D/inchi
FDA UNII: ZR7BC83500
Nikkaji Web: J933.116F
XlogP3-AA: 2.90 (est)
Molecular Weight: 154.25266000
Formula: C10 H18 O
NMR Predictor: Predict (works with chrome or firefox)
Category: flavoring agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
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Google Scholar: with word "odor"Search
Perfumer and Flavorist: Search
Google Patents: Search
US Patents: Search
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Pubchem Patents: Search
PubMed: Search
NCBI: Search
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Physical Properties:
Appearance: colorless clear liquid (est)
Assay: 92.00 to 100.00 % 
Food Chemicals Codex Listed: No
Boiling Point: 214.00 to  216.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.151000 mmHg @ 25.00 °C. (est)
Flash Point: 175.00 °F. TCC ( 79.44 °C. )
logP (o/w): 3.544 (est)
Soluble in:
 alcohol
 water, 67.82 mg/L @ 25 °C (est)
Insoluble in:
 water
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Organoleptic Properties:
 
Odor Type: green
 
Odor Strength: high ,
recommend smelling in a 0.10 % solution or less
 
 cucumber  green  
Odor Description:
at 0.10 % in dipropylene glycol. 
green cucumber
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
Chemical Sources Association
Need This Item for Flavor/Food?: You can contact the CSA
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Safety Information:
 
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:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: flavoring agents
Recommendation for (E)-6-decenal usage levels up to:
 not for fragrance use.
 
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Safety References:
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 5283348
National Institute of Allergy and Infectious Diseases: Data
 (E)-dec-6-enal
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References:
 (E)-dec-6-enal
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 5283348
Pubchem (sid): 10546547
Flavornet: 147159-48-6
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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
HMDB (The Human Metabolome Database): Search
FooDB: FDB029706
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
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Potential Blenders and core components note
 
For Odor
aldehydic
aldehydic
 decanal (aldehyde C-10)FL/FR
 dodecanal (aldehyde C-12 lauric)FL/FR
 nonanal (aldehyde C-9)FL/FR
2-tridecenalFL/FR
 undecanalFL/FR
balsamic
 guaiyl acetateFL/FR
citrus
(E)-4-decenalFL/FR
 decanolFL/FR
3-decen-2-oneFL/FR
 methyl 2-hexenoateFL/FR
2-nonenalFL/FR
(E)-2-nonenalFL/FR
(E)-2-octenalFL/FR
2-octenalFL/FR
floral
 citronellyl formateFL/FR
fruity
 ethyl hexanoateFL/FR
 methyl 2-methyl butyrateFL/FR
 octen-1-yl cyclopentanoneFL/FR
 octyl formateFL/FR
 dodecanal dimethyl acetalFL/FR
 galbanum decatrieneFL/FR
 heptanal cyclic propylene acetalFL/FR
3-heptanoneFL/FR
(Z)-4-heptenalFL/FR
2-heptenalFL/FR
(Z)-4-heptenal diethyl acetalFL/FR
 heptyl formateFL/FR
2-heptyl furanFL/FR
 hexanal (aldehyde C-6)FL/FR
(Z)-3-hexen-1-yl pyruvateFL/FR
(Z)-3-hexenalFL/FR
 manzanate (Givaudan)FL/FR
 methyl heptine carbonateFL/FR
 methyl octine carbonateFL/FR
(E,Z)-2,6-nonadien-1-olFL/FR
3,6-nonadien-1-olFL/FR
2,6-nonadien-1-olFL/FR
(E,Z)-3,6-nonadien-1-olFL/FR
(Z,Z)-3,6-nonadien-1-olFL/FR
(E,Z)-2,6-nonadien-1-yl acetateFL/FR
2,6-nonadienalFL/FR
(E,Z)-2,6-nonadienalFL/FR
(E,Z)-2,6-nonadienal diethyl acetalFL/FR
(Z)-2-nonen-1-olFL/FR
 violet leaf absolute egyptFL/FR
melon
 melon heptenalFL/FR
(Z)-6-nonen-1-olFL/FR
(Z)-6-nonenalFL/FR
2,4-nonadien-1-olFL/FR
 
For Flavor
 
No flavor group found for these
 epoxy-2-decenalFL
 furfuryl hexanoateFL
 guaiyl acetateFL/FR
 heptanal cyclic propylene acetalFL/FR
2-heptenalFL/FR
 hexanal butane-2,3-diol acetalFL
 hexanal octane-1,3-diol acetalFL
 hexyl (E)-2-hexenoateFL
 methyl 2-hexenoateFL/FR
2,6-nonadienalFL/FR
2,4,6-nonatrienalFL
2-octenalFL/FR
2-propyl pyridineFL
(±)-3-(methyl thio) heptanalFL
aldehydic
 nonanal (aldehyde C-9)FL/FR
2-tridecenalFL/FR
apple
(E,Z)-2,6-nonadien-1-olFL/FR
cooling
 manzanate (Givaudan)FL/FR
fatty
2,4-decadienalFL
(E,E)-2,4-decadienalFL
(E,E)-2,4-heptadienalFL
 heptyl formateFL/FR
2-heptyl furanFL/FR
2,4-nonadien-1-olFL/FR
2,4-nonadienalFL
(Z)-2-nonen-1-olFL/FR
2-nonenalFL/FR
(E)-2-octenalFL/FR
fruity
 citronellyl formateFL/FR
 ethyl hexanoateFL/FR
 methyl 2-methyl butyrateFL/FR
 octen-1-yl cyclopentanoneFL/FR
green
3-decen-2-oneFL/FR
 dihydroxyacetophenone (mixed isomers)FL
 dodecanal dimethyl acetalFL/FR
 galbanum decatrieneFL/FR
(Z)-4-heptenalFL/FR
(Z)-4-heptenal diethyl acetalFL/FR
 hexanal (aldehyde C-6)FL/FR
(Z)-3-hexen-1-yl pyruvateFL/FR
(Z)-3-hexenalFL/FR
2-hexyl pyridineFL
 melon heptenalFL/FR
 methyl 2-undecynoateFL
 methyl heptine carbonateFL/FR
 methyl octine carbonateFL/FR
3-(5-methyl-2-furyl) butanalFL
(E,Z)-3,6-nonadien-1-olFL/FR
2,6-nonadien-1-olFL/FR
3,6-nonadien-1-olFL/FR
(E,Z)-2,6-nonadien-1-yl acetateFL/FR
(E,Z)-2,6-nonadienalFL/FR
(E,E)-2,6-nonadienalFL
(E,Z)-2,6-nonadienal diethyl acetalFL/FR
(Z)-6-nonenalFL/FR
(E)-2-nonenalFL/FR
(E,E)-2,4-octadienalFL
 octyl formateFL/FR
 violet leaf absolute egyptFL/FR
ketonic
3-heptanoneFL/FR
ripe
(E)-4-decenalFL/FR
soapy
 dodecanal (aldehyde C-12 lauric)FL/FR
waxy
 decanal (aldehyde C-10)FL/FR
 decanolFL/FR
(Z,Z)-3,6-nonadien-1-olFL/FR
(Z)-6-nonen-1-olFL/FR
 undecanalFL/FR
 
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Potential Uses:
 chamomileFR
 champacaFR
 cilantroFL/FR
 clary sage oil replacerFR
 genetFR
 greenFL
 linden flowerFR
 rose tea roseFR
 teaFL
 tea black teaFL
 tea china 
 tea herbal teaFL
 tea lemon teaFL
 yerba mateFL/FR
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Occurrence (nature, food, other): note
 parsley leaf
Search Trop  Picture
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Synonyms:
(E)-dec-6-enal
trans-dec-6-enal
(E)-6-decen-1-al
trans-6-decen-1-al
trans-6-decenal
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Articles:
PubMed: Simultaneous determination of ten taste and odor compounds in drinking water by solid-phase microextraction combined with gas chromatography-mass spectrometry.
PubMed: Effect of chemical form, heating, and oxidation products of linoleic acid on rumen bacterial population and activities of biohydrogenating enzymes.
PubMed: Flavour chemistry of chicken meat: a review.
PubMed: Food volatile compounds facilitating HII mesophase formation: solubilization and stability.
PubMed: Identification and formation of volatile components responsible for the characteristic aroma of mat rush (igusa).
PubMed: Exposure to polycyclic aromatic hydrocarbons (PAHs), mutagenic aldehydes and particulate matter during pan frying of beefsteak.
PubMed: Volatile composition of Catharanthus roseus (L.) G. Don using solid-phase microextraction and gas chromatography/mass spectrometry.
PubMed: Characterization of the most odor-active compounds in an American Bourbon whisky by application of the aroma extract dilution analysis.
PubMed: Effects of fatty acid oxidation products (green odor) on rumen bacterial populations and lipid metabolism in vitro.
PubMed: Analysis of FeII-mediated decomposition of a linoleic acid-derived lipid hydroperoxide by liquid chromatography/mass spectrometry.
PubMed: Liquid chromatography/mass spectrometry analysis of bifunctional electrophiles and DNA adducts from vitamin C mediated decomposition of 15-hydroperoxyeicosatetraenoic acid.
PubMed: A novel, inducible, citral lyase purified from spores of Penicillium digitatum.
PubMed: 4,5-Epoxy-2(E)-decenal-induced formation of 1,N(6)-etheno-2'-deoxyadenosine and 1,N(2)-etheno-2'-deoxyguanosine adducts.
PubMed: Quantification of key odorants formed by autoxidation of arachidonic acid using isotope dilution assay.
PubMed: Identification of potent odorants formed by autoxidation of arachidonic acid: structure elucidation and synthesis of (E,Z,Z)-2,4,7-tridecatrienal.
PubMed: Cytotoxic aldehydes as possible markers for childhood cancer.
PubMed: Induction of a wide range of C(2-12) aldehydes and C(7-12) acyloins in the kidney of Wistar rats after treatment with a renal carcinogen, ferric nitrilotriacetate.
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