EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

(E)-2-nonenal
trans-2-nonenal

Sponsors

Fragrance Demo Formulas
Name:(E)-non-2-enal
CAS Number: 18829-56-6Picture of molecule3D/inchi
% from:96.00% to 99.90%
ECHA EINECS - REACH Pre-Reg:242-609-6
FDA UNII:8VEO649985
Nikkaji Web:J110.528K
Beilstein Number:1722170
MDL:MFCD00007012
CoE Number:733
XlogP3-AA:3.10 (est)
Molecular Weight:140.22572000
Formula:C9 H16 O
NMR Predictor:Predict (works with chrome or firefox)
Also(can) Contains:(Z)-2-nonenal 0.10% to 3.50%
EFSA/JECFA Comments:
At least 92%; secondary component 3-4% 2-nonenoic acid. (CoE)
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
FLAVIS Number:05.072 (Old)
DG SANTE Food Flavourings:05.072 trans-2-nonenal
FEMA Number:3213 trans-2-nonenal
FDA:No longer provide for the use of these seven synthetic flavoring substances
 
Physical Properties:
Appearance:colorless to pale yellow clear liquid (est)
Assay: 92.00 to 100.00 sum of isomers
Food Chemicals Codex Listed: Yes
Specific Gravity:0.85500 to 0.86500 @ 25.00 °C.
Pounds per Gallon - (est).: 7.114 to 7.198
Refractive Index:1.45400 to 1.46000 @ 20.00 °C.
Boiling Point: 88.00 to 90.00 °C. @ 12.00 mm Hg
Boiling Point: 188.00 to 190.00 °C. @ 760.00 mm Hg
Acid Value: 5.00 max. KOH/g
Vapor Pressure:0.256000 mm/Hg @ 25.00 °C. (est)
Vapor Density:4.8 ( Air = 1 )
Flash Point: 184.00 °F. TCC ( 84.44 °C. )
logP (o/w): 3.319 (est)
Soluble in:
 alcohol
 dipropylene glycol
 fixed oils
 water, 204.9 mg/L @ 25 °C (est)
Insoluble in:
 water
 
Organoleptic Properties:
Odor Type: fatty
Odor Strength:high ,
recommend smelling in a 1.00 % solution or less
Substantivity: > 8 hour(s) at 100.00 %
fatty green cucumber aldehydic citrus
Odor Description:at 1.00 % in dipropylene glycol. fatty green cucumber aldehydic citrus
green cucumber aldehydic fatty citrus
Odor Description:Green, cucumber, aldehydic, fatty with a citrus nuance
Mosciano, Gerard P&F 16, No. 3, 79, (1991)
Flavor Type: green
green soapy cucumber melon aldehydic fatty
Taste Description: at 10.00 ppm. Green, soapy, cucumber / melon-like with an aldehydic / fatty nuance
Mosciano, Gerard P&F 16, No. 3, 79, (1991)
Odor and/or flavor descriptions from others (if found).
Bedoukian Research
trans-2-NONEN-1-AL ≥96.0% (trans), FCC, Kosher
Odor Description:Green, aldeydic, bright odor with persistent fatty, carrot leaf, and melon notes
Addition of traces to ionones and methyl ionones lends power and diffusion. Blends well with florals.
Taste Description:Sweet, fatty, citrus, melon
Citrus especially orange, melon especially cantaloupe.
Apiscent Labs
T2 NONENAL
Odor Description:Powerful fried fatty odor with citrus-like background
FCI SAS
TRANS-2-NONENAL
Odor Description:Powerful fried fatty odor with citrus like background
Taste Description:Slight oily fried taste with nutty background
 
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: perfuming agents
 
Suppliers:
Advanced Biotech
CUCUMBER ALDEHYDE WONF TYPE FLAVOR NATURAL
Advanced Biotech
NONENAL 1% IN ETOH NATURAL
Odor: Alcoholic, Fatty
Advanced Biotech
NONENAL 1% IN TRIACETIN NATURAL
Odor: Alcoholic, Fatty
Advanced Biotech
NONENAL 1% IN TRIETHYL CITRATE NATURAL
Advanced Biotech
NONENAL 10% OS NATURAL
Alfrebro
trans-2-NONENAL NATURAL 10% IN TRIACETIN
Odor: Fatty, Violet
Alfrebro
trans-2-NONENAL NATURAL10% IN MCTG
Apiscent Labs
T2 NONENAL
Odor: Powerful fried fatty odor with citrus-like background
Apple Flavor & Fragrance
trans-2-Nonen-1-al
Axxence Aromatic
TRANS-2-NONENAL 1% IN ETHANOL, Natural, Kosher
Sustainability
Axxence Aromatic
TRANS-2-NONENAL, Natural, Kosher
Bedoukian Research
trans-2-NONEN-1-AL
≥96.0% (trans), FCC, Kosher
Odor: Green, aldeydic, bright odor with persistent fatty, carrot leaf, and melon notes
Use: Addition of traces to ionones and methyl ionones lends power and diffusion. Blends well with florals.
Flavor: Sweet, fatty, citrus, melon
Citrus especially orange, melon especially cantaloupe.
Beijing Lys Chemicals
trans-2-Nonenal
BOC Sciences
For experimental / research use only.
trans-2-NONEN-1-AL FCC 97.0% (sum of isomers)
Excellentia International
trans-2-Nonenal Natural
FCI SAS
TRANS-2-NONENAL
Odor: Powerful fried fatty odor with citrus like background
Flavor: Slight oily fried taste with nutty background
Inoue Perfumery
TRANS-2-NONENAL
Lluch Essence
trans-2-NONENAL NATURAL
M&U International
Nat. Trans-2-Nonenal
Moellhausen
TRANS-2-NONEN-1-AL
Nagar Haveli Perfumes & Aromatics
Trans-2-Nonenal
Natural
Natural Advantage
trans-2 Nonenal Nat
Penta International
trans-2-NONENAL NATURAL 1% IN ETOH (EU & US NATURAL), Kosher
Penta International
trans-2-NONENAL NATURAL 5% IN ETOH (EU & US NATURAL), Kosher
Penta International
trans-2-NONENAL NATURAL 5% IN NATURAL ETHYL ACETATE (EU & US NATURAL), Kosher
Penta International
trans-2-NONENAL, Kosher
Reincke & Fichtner
trans-2-Nonenal
Riverside Aromatics
trans-2-NONENAL, NATURAL
Santa Cruz Biotechnology
For experimental / research use only.
trans-2-Nonenal 97%
Sigma-Aldrich
trans-2-Nonenal, ≥95%, FG
Odor: waxy; fatty
Certified Food Grade Products
Synerzine
trans-2-Nonenal
TCI AMERICA
For experimental / research use only.
trans-2-Nonenal >95.0%(GC)
The Perfumers Apprentice
Cucumber Aldehyde (Natural)
Odor: This Natural Cucumber Aldehyde is the experience of pure unadulterated crisp, green, fresh & light cucumber
 
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 36/38 - Irritating to skin and eyes.
S 02 - Keep out of the reach of children.
S 24/25 - Avoid contact with skin and eyes.
S 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:
4 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
oral-rat LD50 5000 mg/kg

Dermal Toxicity:
skin-rabbit LD50 3700 mg/kg

Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category: flavor and fragrance agents
Recommendation for (E)-2-nonenal usage levels up to:
  4.0000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.12 (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: 4
 average usual ppmaverage maximum ppm
baked goods: -0.20000
beverages(nonalcoholic): --
beverages(alcoholic): --
breakfast cereal: -0.20000
cheese: --
chewing gum: --
condiments / relishes: -0.20000
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: --
fruit ices: --
gelatins / puddings: --
granulated sugar: --
gravies: -0.20000
hard candy: --
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: -0.20000
milk products: -0.20000
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: -0.20000
sugar substitutes: --
sweet sauces: --
 
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):

EFSA Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids (CEF)
View page or View pdf

EPI System: View
Chemical Carcinogenesis Research Information System:Search
Env. Mutagen Info. Center:Search
NLM Developmental and Reproductive Toxicity:Search
EPA Substance Registry Services (TSCA):18829-56-6
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :5283335
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
(E)-non-2-enal
Chemidplus:0018829566
RTECS:RA8509050 for cas# 18829-56-6
 
References:
 (E)-non-2-enal
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:18829-56-6
Pubchem (cid):5283335
Pubchem (sid):134982395
Flavornet:18829-56-6
Pherobase:View
 
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
CHEBI:View
CHEMBL:View
HMDB (The Human Metabolome Database):HMDB31269
FooDB:FDB003312
YMDB (Yeast Metabolome Database):YMDB01794
Export Tariff Code:2912.19.9000
Typical G.C.
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View
RSC Learn Chemistry:View
 
Potential Blenders and core components note
For Odor
aldehydic
citronellyl oxyacetaldehyde
FL/FR
dodecanal (aldehyde C-12 lauric)
FL/FR
(Z)-4-
dodecenal
FL/FR
fresh carbaldehyde
FR
iso
freshal
FR
3-
methyl-4-(1-methyl hexyl oxy) butyraldehyde
FR
3-
methyl-4-heptyl oxybutyraldehyde
FR
nonanal (aldehyde C-9)
FL/FR
octanal (aldehyde C-8)
FL/FR
octane nitrile
FR
(Z)-8-
undecenal
FR
balsamic
guaiyl acetate
FL/FR
citrus
citrus limon peel oil expressed
FL/FR
citrus paradisi peel extract
FL/FR
curacao specialty
FR
(Z)-4-
decenal
FL/FR
(E)-4-
decenal
FL/FR
(Z)-7-
decenal
FR
lemon oil c.p. california
FL/FR
lemon oil c.p. furocoumarin reduced
FL/FR
mandarin specialty
FR
marine decadienal
FR
2-
methyl decanal (aldehyde C-11 MOA)
FL/FR
orange fruit oil
FL/FR
blood
orange oil italy
FL/FR
2-
tetradecenal
FL/FR
tetrahydrocitral
FL/FR
earthy
3-
octanol
FL/FR
fatty
(E,E)-2,4-
decadien-1-ol
FL/FR
2,4-
decadien-1-ol
FL/FR
3-
decen-2-one
FL/FR
(E,Z)-2,6-
dodecadienal
FL/FR
methyl 2-hexenoate
FL/FR
6-
methyl-5-hepten-2-one propylene glycol acetal
FL/FR
2-
nonen-1-ol
FL/FR
(Z)-2-
nonenal
CS
2-
nonenal
FL/FR
(E)-2-
octenal
FL/FR
2-
octenal
FL/FR
floral
citronellal
FL/FR
citronellyl formate
FL/FR
methoxymelonal
FL/FR
fruity
iso
amyl octanoate
FL/FR
dimethyl succinate
FL/FR
ethyl hexanoate
FL/FR
methyl 2-methyl butyrate
FL/FR
methyl 3-nonenoate
FL/FR
octen-1-yl cyclopentanone
FL/FR
propyl 2,4-decadienoate
FL/FR
(E)-2-
undecenal
FL/FR
green
cilantro leaf oil
FL/FR
cumin acetaldehyde
FL/FR
iso
cyclocitral (IFF)
FL/FR
green carbaldehyde
FR
heptanal (aldehyde C-7)
FL/FR
(Z)-4-
heptenal
FL/FR
2-
heptyl furan
FL/FR
hexanal (aldehyde C-6)
FL/FR
(Z)-3-
hexen-1-yl formate
FL/FR
(Z)-3-
hexen-1-yl oxyacetaldehyde
FR
(Z)-3-
hexen-1-yl pyruvate
FL/FR
(Z)-3-
hexenal
FL/FR
alpha-
hexyl cinnamaldehyde dimethyl acetal
FR
manzanate (Givaudan)
FL/FR
methyl heptine carbonate
FL/FR
methyl octine carbonate
FL/FR
methyl octine carbonate replacer
FR
3,6-
nonadien-1-ol
FL/FR
(Z,Z)-3,6-
nonadien-1-ol
FL/FR
2,6-
nonadien-1-ol
FL/FR
(E,Z)-3,6-
nonadien-1-ol
FL/FR
(E,Z)-2,6-
nonadien-1-ol
FL/FR
(E,Z)-3,6-
nonadien-1-yl acetate
FL/FR
3,6-
nonadien-1-yl acetate
FL/FR
2,6-
nonadienal
FL/FR
(E,Z)-2,6-
nonadienal
FL/FR
(E,Z)-2,6-
nonadienal diethyl acetal
FL/FR
(Z)-2-
nonen-1-ol
FL/FR
(E)-2-
nonen-1-ol
FL/FR
2-
nonene nitrile
FR
violet leaf absolute egypt
FL/FR
herbal
3-
octyl acetate
FL/FR
melon
melon carboxaldehyde
FR
(Z)-6-
nonen-1-yl acetate
FL/FR
(Z)-6-
nonenal
FL/FR
watermelon ketone
FR
muguet
4-iso
butyl 1-(3-methoxy-2-propen-1-yl) benzene
FR
4-
ethyl 1-(3-methoxy-2-propen-1-yl) benzene
FR
4-
methyl 1-(3-methoxy-2-propen-1-yl) benzene
FR
4-
propyl 1-(3-methoxy-2-propen-1-yl) benzene
FR
soapy
methyl anthranilate / hexyl cinnamaldehyde schiff's base
FR
spicy
cumin seed absolute
FL/FR
waxy
aldenal C-9
FR
9-
decenoic acid
FL/FR
heptyl octanoate
FL/FR
methyl octanoate
FL/FR
2,4-
nonadien-1-ol
FL/FR
(Z)-3-
nonen-1-ol
FL/FR
octyl isobutyrate
FL/FR
propyl decanoate
FL/FR
For Flavor
No flavor group found for these
(E,E)-2,4-
decadien-1-ol
FL/FR
9-
decen-2-one
FL
(Z)-6-
decenal
FL
(Z)-4-
dodecenal
FL/FR
furfuryl hexanoate
FL
guaiyl acetate
FL/FR
(E,E)-2,4-
heptadien-1-ol
FL
hexanal butane-2,3-diol acetal
FL
hexanal octane-1,3-diol acetal
FL
hexyl (E)-2-hexenoate
FL
methyl 2-hexenoate
FL/FR
6-
methyl octanal
FL
6-
methyl-5-hepten-2-one propylene glycol acetal
FL/FR
2,6-
nonadienal
FL/FR
2,4,6-
nonatrienal
FL
2-
octenal
FL/FR
propyl decanoate
FL/FR
2-
propyl pyridine
FL
2-
tetradecenal
FL/FR
tetrahydrocitral
FL/FR
(±)-3-(
methyl thio) heptanal
FL
aldehydic
aldehydic
nonanal (aldehyde C-9)
FL/FR
octanal (aldehyde C-8)
FL/FR
apple
(E,Z)-2,6-
nonadien-1-ol
FL/FR
citrus
cilantro leaf oil
FL/FR
citronellyl oxyacetaldehyde
FL/FR
citrus limon peel oil expressed
FL/FR
citrus paradisi peel extract
FL/FR
(Z)-4-
decenal
FL/FR
lemon oil c.p. california
FL/FR
lemon oil c.p. furocoumarin reduced
FL/FR
2-
methyl decanal (aldehyde C-11 MOA)
FL/FR
orange fruit oil
FL/FR
blood
orange oil italy
FL/FR
cooling
manzanate (Givaudan)
FL/FR
creamy
octyl isobutyrate
FL/FR
cucumber
2-
ethyl octine carbonate
FL
fatty
2,4-
decadien-1-ol
FL/FR
(E,E)-2,4-
decadienal
FL
2,4-
decadienal
FL
(E,E)-2,4-
heptadienal
FL
2-
heptyl furan
FL/FR
2,4-
nonadien-1-ol
FL/FR
(E,E)-2,4-
nonadienal
FL
2,4-
nonadienal
FL
2-
nonen-1-ol
FL/FR
(Z)-2-
nonen-1-ol
FL/FR
2-
nonenal
FL/FR
(E)-2-
octenal
FL/FR
floral
citronellal
FL/FR
fruity
iso
amyl octanoate
FL/FR
cantaloupe distillates
FL
citronellyl formate
FL/FR
dimethyl succinate
FL/FR
ethyl hexanoate
FL/FR
methoxymelonal
FL/FR
methyl (E)-3-nonenoate
FL
methyl 2-methyl butyrate
FL/FR
methyl 3-nonenoate
FL/FR
octen-1-yl cyclopentanone
FL/FR
green
cucumber distillates
FL
cumin acetaldehyde
FL/FR
iso
cyclocitral (IFF)
FL/FR
3-
decen-2-one
FL/FR
dihydroxyacetophenone (mixed isomers)
FL
(E,Z)-2,6-
dodecadienal
FL/FR
heptanal (aldehyde C-7)
FL/FR
(Z)-4-
heptenal
FL/FR
(E)-2-
heptenal
FL
(E,E)-2,4-
hexadienal
FL
2,4-
hexadienal
FL
hexanal (aldehyde C-6)
FL/FR
(Z)-3-
hexen-1-yl formate
FL/FR
(Z)-3-
hexen-1-yl pyruvate
FL/FR
(Z)-3-
hexenal
FL/FR
2-
hexyl pyridine
FL
methyl heptine carbonate
FL/FR
methyl octanoate
FL/FR
methyl octine carbonate
FL/FR
2,6-
nonadien-1-ol
FL/FR
3,6-
nonadien-1-ol
FL/FR
(E,Z)-3,6-
nonadien-1-ol
FL/FR
3,6-
nonadien-1-yl acetate
FL/FR
(E,Z)-3,6-
nonadien-1-yl acetate
FL/FR
(E,Z)-2,6-
nonadienal
FL/FR
(E,E)-2,6-
nonadienal
FL
(E,Z)-2,6-
nonadienal diethyl acetal
FL/FR
(E)-2-
nonen-1-ol
FL/FR
(Z)-6-
nonen-1-yl acetate
FL/FR
(Z)-6-
nonenal
FL/FR
2,4-
octadienal
FL
(E,E)-2,4-
octadienal
FL
3-
octyl acetate
FL/FR
violet leaf absolute egypt
FL/FR
melon
cantaloupe flavor
FL
propyl 2,4-decadienoate
FL/FR
musty
3-
octanol
FL/FR
ripe
(E)-4-
decenal
FL/FR
soapy
dodecanal (aldehyde C-12 lauric)
FL/FR
spicy
cumin seed absolute
FL/FR
waxy
9-
decenoic acid
FL/FR
heptyl octanoate
FL/FR
(Z,Z)-3,6-
nonadien-1-ol
FL/FR
(Z)-3-
nonen-1-ol
FL/FR
(E)-2-
undecenal
FL/FR
 
Potential Uses:
FRapple green apple
FRapricot
 bread crisp bread
FLbread crust
FLcarrot
FRcitrus
FRcoffee
FRcucumber
FRfilbert
FRfungus
FRgeranium
 grape brandy
FRhoneydew
FRlime
 melon watermelon muskmelon cantaloupe
FLolive
FRorange
FRorris
 pea green pea
FRpeanut
FRrose
FLsesame
FLtea
FLtomato
 
Occurrence (nature, food, other):note
 artichoke cooked artichoke
Search Trop Picture
 asparagus cooked asparagus
Search Trop Picture
 beer
Search PMC Picture
 bread white bread
Search PMC Picture
 butter
Search PMC Picture
 cantaloupe fruit
Search Trop Picture
 carrot
Search Trop Picture
 carrot leaf oil @ 3.22%
Data GC Search Trop Picture
 cassie absolute @ 0.20%
Data GC Search Trop Picture
 caviar
Search PMC Picture
 cheese
Search PMC Picture
 coffee
Search PMC Picture
 crithmum maritimum l. oil turkey @ 0.10%
Data GC Search Trop Picture
 cucumber
Search Trop Picture
 filbert roasted filbert
Search Trop Picture
 fish
Search PMC Picture
 ginger
Search Trop Picture
 grape
Search Trop Picture
 ham
PbMd Search PMC Picture
 hop
Search Trop Picture
 lovage root
Search Trop Picture
 lychee canned lychee
Search Trop Picture
 melon
Search PMC Picture
 milk
Search PMC Picture
 olive
Search Trop Picture
 orris
Search PMC Picture
 pea
Search Trop Picture
 peach fruit
Search Trop Picture
 peanut roasted peanut
Search Trop Picture
 potato chip
Search PMC Picture
 rice cooked rice
PbMd Search PMC Picture
 rugula herb
Search Trop Picture
 sesame seed roasted
Search Trop Picture
 soybean
Search Trop Picture
 strawberry wild strawberry fruit
Search Trop Picture
 tea
Search Trop Picture
 thyme oil wild or creeping france @ 0.05%
Data GC Search Trop Picture
 tomato
Search Trop Picture
 
Synonyms:
(E)-cucumber aldehyde natural
(E)-heptylidene acetaldehyde
(E)-3-hexyl acrolein
(E)-3-hexyl-2-propenal
(2E)-non-2-enal
(E)-non-2-enal
trans-non-2-enal
trans-2-nonen-1-al
(E)-2-nonen-1-al
trans-2-nonen-1-al
(2E)-nonenal
(2E)-2-nonenal
(E)-2-nonenal
T2 nonenal
trans-2-nonenal
trans-2-nonenal 1% in ethanol natural
trans-2-nonenal 1% in triethyl citrate natural
trans-2-nonenal 10% in liponate natural
trans-2-nonenal natural 1% in ETOH (EU & US natural)
trans-2-nonenal natural 5% in ETOH (EU & US natural)
trans-2-nonenal natural 5% in natural ethyl acetate (EU & US natural)
2-nonenal, (2E)-
2-nonenal, (E)-
2-nonenal, (trans)-isomer
 

Articles:

PubMed:Identification of Potent Odorants in a Novel Nonalcoholic Beverage Produced by Fermentation of Wort with Shiitake (Lentinula edodes).
PubMed:Ultrahigh performance liquid chromatography analysis of volatile carbonyl compounds in virgin olive oils.
PubMed:Cooked carrot volatiles. AEDA and odor activity comparisons. Identification of linden ether as an important aroma component.
PubMed:Influence of heating and acidification on the flavor of whey protein isolate.
PubMed:Influence of endogenous ferulic acid in whole wheat flour on bread crust aroma.
PubMed:Comparison of the flavor chemistry and flavor stability of mozzarella and cheddar wheys.
PubMed:Studies on the key aroma compounds in soy milk made from three different soybean cultivars.
PubMed:Volatile compounds with characteristic odour in moso-bamboo stems (Phyllostachys pubescens Mazel ex Houz. De ehaie).
PubMed:Identification and formation of volatile components responsible for the characteristic aroma of mat rush (igusa).
PubMed:Decrease of aged beer aroma by the reducing activity of brewing yeast.
PubMed:Binding of flavor compounds and whey protein isolate as affected by heat and high pressure treatments.
PubMed:Comparison of odor-active compounds from six distinctly different rice flavor types.
PubMed:Aroma components of American country ham.
PubMed:Instrumental and sensory characterization of heat-induced odorants in aseptically packaged soy milk.
PubMed:An assessment of the role played by some oxidation-related aldehydes in wine aroma.
PubMed:Characterization of aroma-active compounds in rainbow trout (Oncorhynchus mykiss) eliciting an off-odor.
PubMed:Characterization and semiquantitative analysis of volatiles in seedless watermelon varieties using solid-phase microextraction.
PubMed:Identification of a stale-beer-like odorant in extracts of naturally aged beer.
PubMed:The cytotoxic and genotoxic effects of conjugated trans-2-nonenal (T2N), an off-flavor compound in beer and heat processed food arising from lipid oxidation.
PubMed:Enzymatic hydrogenation of trans-2-nonenal in barley.
PubMed:Further insights into the role of methional and phenylacetaldehyde in lager beer flavor stability.
PubMed:Identification and sensory evaluation of volatile compounds in oxidized porcine liver.
PubMed:Determination of stale-flavor carbonyl compounds in beer by stir bar sorptive extraction with in-situ derivatization and thermal desorption-gas chromatography-mass spectrometry.
PubMed:Release of deuterated (E)-2-nonenal during beer aging from labeled precursors synthesized before boiling.
PubMed:How low pH can intensify beta-damascenone and dimethyl trisulfide production through beer aging.
PubMed:Quantitation of odor-active compounds in rye flour and rye sourdough using stable isotope dilution assays.
PubMed:Fresh cucumber flavor in refrigerated pickles: comparison of sensory and instrumental analysis.
PubMed:Relationships between antioxidant activity, color, and flavor compounds of crystal malt extracts.
PubMed:Determination of key aroma compounds in the crumb of a three-stage sourdough rye bread by stable isotope dilution assays and sensory studies.
PubMed:Solid-phase microextraction (SPME) technique for measurement of generation of fresh cucumber flavor compounds.
PubMed:Apparatus for the quantitative analysis of the aroma of french bread and its loss during storage.
PubMed:Aroma components of an oil-based grill flavoring by direct thermal desorption-gas chromatography-olfactometry and sample dilution analysis.
PubMed:In vitro antibacterial activity of some aliphatic aldehydes from Olea europaea L.
PubMed:Identification of character impact odorants of different soybean lecithins.
PubMed:Influence of variety and growing location on the development of off-flavor in precooked vacuum-packed potatoes.
PubMed:Release of deuterated nonenal during beer aging from labeled precursors synthesized in the boiling kettle.
PubMed:trans-2-Nonenal insect repellent, insecticide, and flavor compound in carrot roots, cell suspensions, and "hairy" root cultures.
 
Notes:
Enhances rose and geranium. Widespread in nature, in beer, coffee, watermelon, cucumbers, redcurrants, orris oil, palm oil, potatoes etc. Flavouring ingredient
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