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

2-methyl butyraldehyde
2-methylbutyraldehyde

Supplier Sponsors

Name:2-methylbutanal
CAS Number: 96-17-3Picture of molecule3D/inchi
Other:57456-98-1
ECHA EINECS - REACH Pre-Reg:202-485-6
FDA UNII:47H597M1YY
Nikkaji Web:J35.111C
Beilstein Number:1633540
MDL:MFCD00006984
CoE Number:575
XlogP3-AA:1.10 (est)
Molecular Weight:86.13390000
Formula:C5 H10 O
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome or firefox)
Category:flavor and fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar:Search
Google Books:Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Perfumer and Flavorist:Search
Google Patents:Search
US Patents:Search
EU Patents:Search
Pubchem Patents:Search
PubMed:Search
NCBI:Search
JECFA Food Flavoring:254 2-methylbutyraldehyde
FLAVIS Number:05.049 (Old)
DG SANTE Food Flavourings:05.049 2-methylbutyraldehyde
FEMA Number:2691 2-methylbutyraldehyde
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):96-17-3 ; 2-METHYLBUTYRALDEHYDE
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.
 
Physical Properties:
Appearance:colorless to pale yellow clear liquid (est)
Assay: 98.00 to 100.00 sum of isomers
Food Chemicals Codex Listed: No
Specific Gravity:0.80000 to 0.81000 @ 25.00 °C.
Pounds per Gallon - (est).: 6.657 to 6.740
Refractive Index:1.38600 to 1.39400 @ 20.00 °C.
Melting Point: 91.00 °C. @ 760.00 mm Hg
Boiling Point: 90.00 to 93.00 °C. @ 760.00 mm Hg
Acid Value: 5.00 max. KOH/g
Vapor Pressure:49.317001 mmHg @ 25.00 °C. (est)
Vapor Density:2.9 ( Air = 1 )
Flash Point: 40.00 °F. TCC ( 4.44 °C. )
logP (o/w): 1.267 (est)
Soluble in:
 alcohol
 water, 1.123e+004 mg/L @ 25 °C (est)
Stability:
 alkalis
 
Organoleptic Properties:
Odor Type: chocolate
Odor Strength:high ,
recommend smelling in a 1.00 % solution or less
Substantivity: > 1 hour(s) at 100.00 %
musty cocoa coffee nutty
Odor Description:at 1.00 % in dipropylene glycol. musty cocoa coffee nutty
Luebke, William tgsc, (1986)
Odor sample from: Sigma-Aldrich
musty chocolate nutty malty fermented
Odor Description:Musty, chocolate, nutty, furfural and iaovaleraldehyde-like with malty and fermented nuances
Mosciano, Gerard P&F 23, No. 1, 33, (1998)
Flavor Type: fusel
musty rummy nutty cereal caramellic fruity
Taste Description: at 10.00 ppm. Musty, furfural and rummy, with nutty and cereal notes, and caramel and fruity undernotes
Mosciano, Gerard P&F 23, No. 1, 33, (1998)
Odor and/or flavor descriptions from others (if found).
Bedoukian Research
2-METHYL BUTYRALDEHYDE ≥98.0%, FCC, Kosher
Odor Description:An extremely volatile cocoa or coffee-like
Used for lift in woody and cocoa topnote complexes.
Taste Description:Strong, cocoa powder notes
Useful for chocolate, cocoa, mocha/coffee flavors.
Frutarom
2-METHYLBUTYRALDEHYDE
Odor Description:Aldehydic, Berry, Choking, Cocoa, Musty
Suggested Uses: Apple, Bakery, Cheese, Chocolate, Coffee, Hard Fruits, Tomato
Taste Description:green fruity musty berry
Taytonn
2-Methylbutyraldehyde
Odor Description:Aldehydic/ Aldehyde, Cocoa, Fruity, Musty
 
Cosmetic Information:
CosIng:cosmetic data
Cosmetic Uses: perfuming agents
 
Suppliers:
Advanced Biotech
2 METHYL BUTYRALDEHYDE NATURAL
94% min.
Odor: Cocoa, Fruity, Slight
Alfrebro
2-METHYL BUTYRALDEHYDE NATURAL
Odor: Cocoa, Coffee on Dilution
Augustus Oils
2-Methyl Butanal
Services
Aurochemicals
2-METHYL BUTYRALDEHYDE, Natural
Bedoukian Research
2-METHYL BUTYRALDEHYDE
≥98.0%, FCC, Kosher
Odor: An extremely volatile cocoa or coffee-like
Use: Used for lift in woody and cocoa topnote complexes.
Flavor: Strong, cocoa powder notes
Useful for chocolate, cocoa, mocha/coffee flavors.
Beijing Lys Chemicals
2-Methylbutanal
Berjé
2-Methyl Butyraldehyde
Happening at Berje
BOC Sciences
For experimental / research use only.
2-METHYL BUTYRALDEHYDE FCC 98.0%
Charkit Chemical
METHYLBUTYRALDEHYDE, 2- M0800 FEMA 2691
Frutarom
2-METHYLBUTYRALDEHYDE
Odor: Aldehydic, Berry, Choking, Cocoa, Musty
Use: Suggested Uses: Apple, Bakery, Cheese, Chocolate, Coffee, Hard Fruits, Tomato
H. Interdonati, Inc.
2-Methylbutyraldehyde Natural, Kosher
Featured Products
Jiangyin Healthway
2-Methyl Butyraldehyde
New functional food ingredients
Kunshan Sainty
2-Methyl Butyraldehyde, Natural
Kunshan Sainty
2-Methylbutyraldehyde, Kosher
M&U International
NAT.2-METHYL BUTYRALDEHYDE, Kosher
Natural Advantage
Methylbutyraldehyde, 2- Nat
Flavor: aldehydic, fruity
Riverside Aromatics LTD.is the exclusive distributor for Europe in UK for any non-US based inquiries
O'Laughlin Industries
2-METHYLBUTYRALDEHYDE NATURAL
Pearlchem Corporation
Natural 2-Methyl Butyraldehyde
Penta International
2-METHYLBUTYRALDEHYDE NATURAL
Penta International
2-METHYLBUTYRALDEHYDE
R C Treatt & Co Ltd
2-Methylbutyraldehyde
Reincke & Fichtner
2-Methylbutyraldehyde natural
Reincke & Fichtner
2-Methylbutyraldehyde
Riverside Aromatics
2-METHYLBUTYRALDEHYDE, NATURAL
Santa Cruz Biotechnology
For experimental / research use only.
2-Methylbutyraldehyde
Sigma-Aldrich
2-Methylbutyraldehyde, ≥95%, FG
Odor: chocolate; coffee
Certified Food Grade Products
Sigma-Aldrich
2-Methylbutyraldehyde, natural, 98%
Sunaux International
2-Methylbutyaldehyde
Sunaux International
nat.2-Methyl Butyraldehyde
Synerzine
2-Methyl Butyraldehyde
Taytonn
2-Methylbutyraldehyde
Odor: Aldehydic/ Aldehyde, Cocoa, Fruity, Musty
TCI AMERICA
For experimental / research use only.
2-Methylbutyraldehyde >95.0%(GC)
The Perfumers Apprentice
Methylbutyraldehyde 1% (PG)
Vigon International
METHYL-2 BUTYRALDEHYDE
WEN International
2-METHYLBUTYRALDEHYDE Natural
WholeChem
2-Methylbutanal
 
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 11 - Highly flammable.
R 36/37/38 - Irritating to eyes, respiratory system, and skin.
R 53 - May cause long-term adverse effects in the aquatic wnvironment.
S 02 - Keep out of the reach of children.
S 16 - Keep away from sources of ignition - No Smoking.
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 36/37/39 - Wear suitable clothing, gloves and eye/face protection.
S 61 - Avoid release to the environment. Refer to special instructions/safety data sheet.
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
oral-rat LD50 6400 mg/kg
Food and Chemical Toxicology. Vol. 20, Pg. 739, 1982.

Dermal Toxicity:
skin-rabbit LD50 5730 ul/kg
Union Carbide Data Sheet. Vol. 10/5/1972

skin-guinea pig LD50 > 20000 mg/kg
Food and Chemical Toxicology. Vol. 20, Pg. 739, 1982.

Inhalation Toxicity:
inhalation-rat LC50 14000 ppm/4H
Union Carbide Data Sheet. Vol. 10/5/1972

 
Safety in Use Information:
Category: flavor and fragrance agents
Recommendation for 2-methyl butyraldehyde usage levels up to:
  0.3000 % in the fragrance concentrate.
 
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
 average usual ppmaverage maximum ppm
baked goods: -5.70000
beverages(nonalcoholic): 1.500002.00000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: 2.000008.00000
fruit ices: 2.000008.00000
gelatins / puddings: --
granulated sugar: --
gravies: --
hard candy: -6.60000
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: --
 
Safety References:
European Food Safety Authority (EFSA) reference(s):

Flavouring Group Evaluation 3, Revision 1 (FGE.03Rev1): Acetals of branched- and straight-chain aliphatic saturated primary alcohols and branched- and straight-chain saturated or unsaturated aldehydes, an ester of a hemiacetal and an orthoester of formic acid, from chemical groups 1, 2 & 4 Commission Regulation (EC) No 1565/2000 of 18 July 2000) [1] - Scientific Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC)on a request from the Commission
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):96-17-3
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :7284
National Institute of Allergy and Infectious Diseases:Data
WISER:UN 1989
WGK Germany:1
2-methylbutanal
Chemidplus:0000096173
RTECS:ES3400000 for cas# 96-17-3
 
References:
Leffingwell:Chirality or Article
 2-methylbutanal
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:96-17-3
Pubchem (cid):7284
Pubchem (sid):134972369
Flavornet:96-17-3
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
FDA Substances Added to Food (formerly EAFUS):View
CHEBI:View
CHEMBL:View
KEGG (GenomeNet):C02223
HMDB (The Human Metabolome Database):HMDB31526
FooDB:FDB008127
YMDB (Yeast Metabolome Database):YMDB00485
Export Tariff Code:2912.19.5000
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
No odor group found for these
sulfuryl octanoate
FL/FR
sulfuryl butyrate
FL/FR
sulfuryl decanoate
FL/FR
sulfuryl hexanoate
FL/FR
sulfuryl isobutyrate
FL/FR
sulfuryl propionate
FL/FR
valeraldehyde dibutyl acetal
FL/FR
valeraldehyde propylene glycol acetal
FL/FR
alcoholic
alcoholic
3-
hexanol
FL/FR
propyl alcohol
FL/FR
alliaceous
methyl furfuryl disulfide
FL/FR
balsamic
2-
acetyl furan
FL/FR
iso
amyl cinnamate
FL/FR
amyl cinnamate
FL/FR
amyl phenyl acetate
FL/FR
iso
amyl pyruvate
FL/FR
butyl cinnamate
FL/FR
prenyl benzoate
FL/FR
propyl benzoate
FL/FR
bready
coffee furanone
FL/FR
buttery
acetyl propionyl
FL/FR
3,4-
hexane dione
FL/FR
camphoreous
bornyl isobutyrate
FL/FR
caramellic
coffee dione
FL/FR
cyclotene
FL/FR
ethyl 2-hydroxy-2-methyl butyrate
FL/FR
ethyl cyclopentenolone
FL/FR
fenugreek oleoresin
FL/FR
iso
propenyl pyrazine
FL/FR
cereal
bran absolute
FR
chocolate
iso
amyl phenyl acetate
FL/FR
iso
butyl phenyl acetate
FL/FR
chocolate pyrazine A
FL/FR
cocoa hexenal
FL/FR
cocoa oleoresin
FL/FR
cocoa pentenal
FL/FR
2,5-
dimethyl pyrazine
FL/FR
2,6-
dimethyl pyrazine
FL/FR
2-
methoxypyrazine
FL/FR
2,4,5-
trimethyl thiazole
FL/FR
cocoa
2-iso
butyl-3,5-(and 3,6)-dimethyl pyrazine
FL/FR
coconut
alpha-
angelica lactone
FL/FR
gamma-
heptalactone
FL/FR
coffee
coffee difuran
FL/FR
furfuryl mercaptan
FL/FR
1-
hydroxy-2-butanone
FL/FR
2-
methyl-3-,5 or 6-(furfuryl thio) pyrazine
FL/FR
corn chip
popcorn pyrimidine
FL/FR
coumarinic
coumane
FL/FR
tonka bean resinoid
FR
creamy
butyl lactate
FL/FR
earthy
bean pyrazine
FL/FR
2-
ethyl-3-methoxypyrazine
FL/FR
ethereal
acetal
FL/FR
decyl propionate
FL/FR
ethyl acetate
FL/FR
ethyl pyruvate
FL/FR
1-
hexen-3-ol
FL/FR
(E)-
methyl tiglate
FL/FR
propyl formate
FL/FR
iso
propyl formate
FL/FR
fatty
coconut absolute
FL/FR
fermented
butyl laevo-lactate
FL/FR
ethyl (E)-2-crotonate
FL/FR
3-
methyl-1-pentanol
FL/FR
2-
pentanol
FL/FR
valeraldehyde
FL/FR
floral
alpha-
amyl cinnamyl acetate
FL/FR
amyl salicylate
FL/FR
boronia butenal
FR
para-
cresyl laurate
FL/FR
ethyl hydrocinnamate
FL/FR
ethyl phenyl acetate
FL/FR
linalyl propionate
FL/FR
fruity
allyl 2-ethyl butyrate
FL/FR
allyl hexanoate
FL/FR
iso
amyl nonanoate
FL/FR
berry pentadienoate
FL/FR
butyl acetoacetate
FL/FR
iso
butyl butyrate
FL/FR
butyl formate
FL/FR
cherry oxyacetate
FL/FR
cyclohexanone diethyl acetal
FL/FR
ethyl heptanoate
FL/FR
ethyl propionate
FL/FR
fruity carboxylate
FR
geranyl acetoacetate
FL/FR
3-
hexanone
FL/FR
methyl propionate
FL/FR
methyl valerate
FL/FR
3-
methyl-2-butenal
FL/FR
2-
phenyl propyl butyrate
FL/FR
prenyl formate
FL/FR
tetrahydrofurfuryl acetate
FL/FR
tropical thiazole
FL/FR
green
butyl 2-methyl butyrate
FL/FR
heptyl acetate
FL/FR
2-
heptyl furan
FL/FR
(E)-2-
hexen-1-yl formate
FL/FR
(E)-2-
hexen-1-yl phenyl acetate
FL/FR
(E,Z)-2,6-
nonadien-1-yl acetate
FL/FR
phenyl acetaldehyde
FL/FR
tiglaldehyde
FL/FR
herbal
white
cognac oil
FL/FR
saffron pyranone
FR
tricyclodecenyl isobutyrate
FR
gamma-
valerolactone
FL/FR
honey
allyl phenyl acetate
FL/FR
butyl phenyl acetate
FL/FR
phenyl acetic acid
FL/FR
jammy
ethyl 2-methyl-2-pentenoate
FR
medicinal
2,6-
xylenol
FL/FR
milky
laevo-
glutamine
CS
moldy
strawberry furanone methyl ether
FL/FR
musty
2-
acetyl pyrrole
FL/FR
3-
acetyl-2,5-dimethyl furan
FL/FR
cocoa butenal
FL/FR
hazelnut pyrazine
FL/FR
menthofuran
FL/FR
naphthyl
ortho-
methyl anisole
FL/FR
para-
methyl anisole
FL/FR
nutty
3-
acetyl pyridine
FL/FR
2-
acetyl-3-ethyl pyrazine
FL/FR
2-
acetyl-3-methyl pyrazine
FL/FR
2-
acetyl-3,5-dimethyl pyrazine
FL/FR
2-
acetyl-5-methyl furan
FL/FR
3,6-
cocoa pyrazine
FL/FR
3,5-
cocoa pyrazine
FL/FR
2,3-
dimethyl pyrazine
FL/FR
4,5-
dimethyl-2-ethyl-3-thiazoline
FL/FR
2-
ethyl pyrazine
FL/FR
2-
ethyl-4-methyl thiazole
FL/FR
filbert heptenone
FL/FR
filbert pyrazine
FL/FR
2,6-
lutidine
FL/FR
maraniol
CS
2-
methyl pyrazine
FL/FR
5-
methyl quinoxaline
FL/FR
2-
methyl thio-3,5 or 6-methyl pyrazine
FL/FR
2-
methyl-3-(methyl thio) pyrazine
FL/FR
2-
methyl-3-ethoxypyrazine
FL/FR
2-
methyl-3-propyl pyrazine
FL/FR
nutty cyclohexenone
FL/FR
nutty quinoxaline
FL/FR
shoyu pyrazine
FL/FR
2,3,5,6-
tetramethyl pyrazine
FL/FR
2,3,5-
trimethyl pyrazine
FL/FR
vinyl sulfurol
FL/FR
popcorn
2-
acetyl pyrazine
FL/FR
2-
acetyl thiazole
FL/FR
roasted
fenugreek resinoid
FL/FR
trigonella foenum-graecum seed oil CO2 extract
FL/FR
spicy
eugenyl acetate
FL/FR
3-(2-
furyl) acrolein
FL/FR
sulfurous
benzothiazole
FL/FR
furfuryl thioacetate
FL/FR
S-
furfuryl thioformate
FL/FR
2-
methyl 5-(methyl thio) furan
FL/FR
tobacco
veltonal (Bedoukian)
FR
tonka
coumarin
FR
tonka bean absolute
FR
whiskey lactone
FL/FR
vanilla
ethyl vanillin isobutyrate
FL/FR
vanillin
FL/FR
vanillyl isobutyrate
FL/FR
vegetable
1-
furfuryl pyrrole
FL/FR
mesityl oxide
FL/FR
waxy
ethyl nonanoate
FL/FR
phenethyl octanoate
FL/FR
For Flavor
No flavor group found for these
acetyl acetaldehyde dimethyl acetal
FL
2-
acetyl-6-methyl pyrazine
FL
amyl phenyl acetate
FL/FR
iso
amyl pyruvate
FL/FR
bean pyrazine
FL/FR
bornyl isobutyrate
FL/FR
butter nut rum flavor
FL
butyl 2-methyl butyrate
FL/FR
butyl acetoacetate
FL/FR
butyl cinnamate
FL/FR
butyl formate
FL/FR
2-iso
butyl-3,5-(and 3,6)-dimethyl pyrazine
FL/FR
2(4)-iso
butyl-4(2),6-dimethyl dihydro-4H-1,3,5-dithiazine
FL
butyramide
FL
chocolate pyrazine A
FL/FR
chocolate pyrazine B
FL
coumane
FL/FR
cyclohexanone diethyl acetal
FL/FR
cyclohexyl methyl pyrazine
FL
decyl propionate
FL/FR
2,5-
diethyl thiazole
FL
2,5-
diethyl-4-methyl thiazole
FL
6,7-
dihydro-2,3-dimethyl-5H-cyclopentapyrazine
FL
dimethyl dihydrocyclopentapyrazine
FL
2,5-
dimethyl thiazole
FL
4,5-
dimethyl-2-ethyl thiazole
FL
2,5-
dimethyl-3-thiofuroyl furan
FL
ethyl 2-hydroxy-2-methyl butyrate
FL/FR
ethyl hydrocinnamate
FL/FR
2-
ethyl-3-methoxypyrazine
FL/FR
(Z+E)-5-
ethyl-4-methyl-2-(2-butyl) thiazoline
FL
(Z+E)-5-
ethyl-4-methyl-2-(2-methyl propyl) thiazoline
FL
3-(2-
furyl) acrolein
FL/FR
geranyl acetoacetate
FL/FR
(E,E)-2,4-
heptadien-1-ol
FL
(E)-2-
hexen-1-yl phenyl acetate
FL/FR
2-
hexyl-5 or 6-keto-1,4-dioxane
FL
2-
methoxypyrazine
FL/FR
methyl 2-(methyl thio) acetate
FL
(E)-
methyl tiglate
FL/FR
2-
methyl-3-,5 or 6-(furfuryl thio) pyrazine
FL/FR
2-
methyl-3-(methyl thio) pyrazine
FL/FR
2-
methyl-3-ethoxypyrazine
FL/FR
peanut dithiazine
FL
prenyl benzoate
FL/FR
prenyl formate
FL/FR
2-
propyl pyridine
FL
para-
salicylic acid
FL
sulfuryl butyrate
FL/FR
sulfuryl decanoate
FL/FR
sulfuryl hexanoate
FL/FR
sulfuryl isobutyrate
FL/FR
valeraldehyde propylene glycol acetal
FL/FR
5-
acetyl-2,3-dihydro-1,4-thiazine
FL
sulfuryl formate
FL
sulfuryl octanoate
FL/FR
sulfuryl propionate
FL/FR
valeraldehyde dibutyl acetal
FL/FR
alcoholic
alcoholic
3-
hexanol
FL/FR
propyl alcohol
FL/FR
alliaceous
benzyl mercaptan
FL
dicyclohexyl disulfide
FL
2-
methyl thioacetaldehyde
FL
tropical thiazole
FL/FR
aromatic
amyl salicylate
FL/FR
balsamic
amyl cinnamate
FL/FR
bitter
cocoa pyrazines base (mixture of pyrazines)
FL
methyl ethoxypyrazine
FL
paullinia cupana seed extract
FL
bready
2-
propionyl thiazole
FL
brown
fenugreek oleoresin
FL/FR
1-
hydroxy-2-butanone
FL/FR
tetrahydrofurfuryl acetate
FL/FR
burnt
furfuryl alcohol
FL
2-
methyl quinoxaline
FL
iso
propenyl pyrazine
FL/FR
2,6-
xylenol
FL/FR
buttery
butyl laevo-lactate
FL/FR
butyroin
FL
3,4-
hexane dione
FL/FR
camphoreous
ortho-
methyl anisole
FL/FR
caramellic
caramel furanone
FL
cyclotene
FL/FR
fenugreek resinoid
FL/FR
pyruvaldehyde
FL
chocolate
cocoa oleoresin
FL/FR
cocoa propanal
FL
cocoa
iso
butyl phenyl acetate
FL/FR
butyraldehyde
FL
cocoa distillates
FL
cocoa hexenal
FL/FR
2-
methyl furan
FL
coffee
coffee difuran
FL/FR
coffee dione
FL/FR
coffee pyrazine
FL
difurfuryl ether
FL
diisoamyl thiomalate
FL
2,4-
dimethyl thiazole
FL
2-
ethyl-4-methyl thiazole
FL/FR
furfuryl mercaptan
FL/FR
methyl furfuryl disulfide
FL/FR
2-iso
propyl pyrazine
FL
2-
thiophene thiol
FL
corn chip
2-
acetyl thiazole
FL/FR
2-
acetyl-2-thiazoline
FL
popcorn pyrimidine
FL/FR
creamy
alpha-
angelica lactone
FL/FR
dairy
butyl lactate
FL/FR
earthy
alpha-
amyl cinnamyl acetate
FL/FR
difurfuryl sulfide
FL
1-
hexen-3-yl acetate
FL
2-
methyl-3-propyl pyrazine
FL/FR
ethereal
allyl 2-ethyl butyrate
FL/FR
ethyl acetate
FL/FR
fatty
coconut absolute
FL/FR
(E,E)-2,4-
decadienal
FL
2-
heptyl furan
FL/FR
(E,E)-2,4-
nonadienal
FL
fermented
methyl thio isovalerate
FL
fishy
4,5-
dimethyl thiazole
FL
floral
iso
amyl cinnamate
FL/FR
iso
amyl phenyl acetate
FL/FR
cocoa pentenal
FL/FR
phenyl acetic acid
FL/FR
fruity
allyl hexanoate
FL/FR
berry pentadienoate
FL/FR
iso
butyl butyrate
FL/FR
cherry oxyacetate
FL/FR
ethyl heptanoate
FL/FR
ethyl propionate
FL/FR
furfuryl propionate
FL
2,4-
hexadien-1-ol
FL
3-
hexanone
FL/FR
methyl propionate
FL/FR
methyl valerate
FL/FR
3-
methyl-2-butenal
FL/FR
phenethyl octanoate
FL/FR
propyl benzoate
FL/FR
iso
propyl formate
FL/FR
propyl formate
FL/FR
tiglaldehyde
FL/FR
fusel
white
cognac oil
FL/FR
green
cocoa butenal
FL/FR
dihydroxyacetophenone (mixed isomers)
FL
2,5-
dimethyl thiophene
FL
2-
ethyl butyraldehyde
FL
heptyl acetate
FL/FR
1-
hexen-3-ol
FL/FR
4-
methyl thiazole
FL
2-
methyl-5-isopropyl pyrazine
FL
(E,Z)-2,6-
nonadien-1-yl acetate
FL/FR
2-
vinyl pyrazine
FL
herbal
linalyl propionate
FL/FR
honey
allyl phenyl acetate
FL/FR
butyl phenyl acetate
FL/FR
ethyl phenyl acetate
FL/FR
phenyl acetaldehyde
FL/FR
jammy
ethyl cyclopentenolone
FL/FR
lactonic
gamma-
heptalactone
FL/FR
meaty
benzothiazole
FL/FR
2-
methyl 3-(methyl thio) furan
FL
moldy
strawberry furanone methyl ether
FL/FR
mustard
furfuryl methyl ether
FL
musty
2,5-
dimethyl pyrazine
FL/FR
2-
ethoxythiazole
FL
ethyl (E)-2-crotonate
FL/FR
hazelnut pyrazine
FL/FR
menthofuran
FL/FR
2-
methyl 5-(methyl thio) furan
FL/FR
2-
pentanol
FL/FR
propionaldehyde
FL
shoyu pyrazine
FL/FR
2,3,5-
trimethyl pyrazine
FL/FR
naphthyl
para-
methyl anisole
FL/FR
nutty
acetal
FL/FR
2-
acetyl furan
FL/FR
3-
acetyl pyridine
FL/FR
2-
acetyl pyrrole
FL/FR
3-
acetyl-2,5-dimethyl furan
FL/FR
2-
acetyl-3-ethyl pyrazine
FL/FR
2-
acetyl-3-methyl pyrazine
FL/FR
2-
acetyl-3,5-dimethyl pyrazine
FL/FR
2-
acetyl-5-methyl furan
FL/FR
aconitic acid
FL
3,5(6)-
cocoa pyrazine
FL
3,5-
cocoa pyrazine
FL/FR
3,6-
cocoa pyrazine
FL/FR
coffee furanone
FL/FR
3,5-
diethyl-2-methyl pyrazine
FL
2,5-
diethyl-3-methyl pyrazine
FL
2,6-
dimethyl pyrazine
FL/FR
2,3-
dimethyl pyrazine
FL/FR
4,5-
dimethyl-2-ethyl-3-thiazoline
FL/FR
2,4-
dimethyl-5-vinyl thiazole
FL
2-
ethyl pyrazine
FL/FR
1-
ethyl-2-acetyl pyrrole
FL
filbert heptenone
FL/FR
filbert pyrazine
FL/FR
european
hazelnut oleoresin
FL
2,6-
lutidine
FL/FR
2-
methyl pyrazine
FL/FR
5-
methyl quinoxaline
FL/FR
2-
methyl thio-3,5 or 6-methyl pyrazine
FL/FR
nutty cyclohexenone
FL/FR
nutty quinoxaline
FL/FR
nutty thiazole
FL
peanut oxazole
FL
2,3,5,6-
tetramethyl pyrazine
FL/FR
2,4,5-
trimethyl thiazole
FL/FR
vinyl sulfurol
FL/FR
onion
furfuryl isopropyl sulfide
FL
popcorn
2-
propionyl-2-thiazoline
FL
potato
mesityl oxide
FL/FR
roasted
2-
acetyl pyrazine
FL/FR
ethyl 3-(furfuryl thio) propionate
FL
furfuryl thioacetate
FL/FR
trigonella foenum-graecum seed oil CO2 extract
FL/FR
rummy
ethyl pyruvate
FL/FR
(E)-2-
hexen-1-yl formate
FL/FR
solvent
2-
ethyl furan
FL
spicy
eugenyl acetate
FL/FR
2-
phenyl propyl butyrate
FL/FR
sulfurous
butyl mercaptan
FL
ethyl methyl sulfide
FL
S-
ethyl thioacetate
FL
S-
furfuryl thioformate
FL/FR
furfuryl thiopropionate
FL
2-
thienyl mercaptan
FL
toasted
acetyl propionyl
FL/FR
tonka
gamma-
valerolactone
FL/FR
vanilla
ethyl vanillin isobutyrate
FL/FR
vanillin
FL/FR
vanillyl isobutyrate
FL/FR
vegetable
1-
furfuryl pyrrole
FL/FR
waxy
para-
cresyl laurate
FL/FR
ethyl nonanoate
FL/FR
whiskey
3-
methyl-1-pentanol
FL/FR
winey
iso
amyl nonanoate
FL/FR
5-
ethyl-2-methyl pyridine
FL
valeraldehyde
FL/FR
woody
whiskey lactone
FL/FR
 
Potential Uses:
FLapple
FLbanana
FLberry mixed berry
FLbread
FLcaramel
FLchocolate cocoa
FLcoffee
FLgrape
FLmalt
FLolive
FLpapaya
FLrum
FLtomato
FLtropical
FLwine
 
Occurrence (nature, food, other):note
 apple fruit
Search PMC Picture
 bay laurel leaf
Search Trop Picture
 cardamom
Search Trop Picture
 cayenne fruit
Search Trop Picture
 cheese @ 251.00 ± 43 µg%
Data GC Search PMC Picture
 cheese cheddar cheese
Search PMC Picture
 cheese swiss cheese
Search PMC Picture
 currant black currant fruit
Search Trop Picture
 fish
Search PMC Picture
 grape
Search Trop Picture
 kohlrabi
Search Trop Picture
 kohlrabi stem
Search Trop Picture
 lovage flower oil @ trace%
Data GC Search Trop Picture
 lovage leaf oil @ trace%
Data GC Search Trop Picture
 lovage root
Search Trop Picture
 mushroom giant puffball mushroom
Search PMC Picture
 onion bulb
Search Trop Picture
 papaya fruit
Search Trop Picture
 paprika
Search PMC Picture
 peanut roasted peanut
Search Trop Picture
 pepper bell pepper fruit
Search Trop Picture
 plum fruit
Search Trop Picture
 potato
Search Trop Picture
 rice cakes
PbMd Search PMC Picture
 rum
Search PMC Picture
 spearmint oil
Search Trop Picture
 truffle
Search Picture
 
Synonyms:
 acetaldehyde, ethylmethyl-
 butanal, 2-methyl-
 butyraldehyde, 2-methyl-
2-ethyl propanal
2-ethylpropanal
2-formyl butane
2-methyl butanal
alpha-methyl butanal
alpha-methyl butyraldehyde
nat.2-methyl butyraldehyde
2-methyl butyraldehyde natural
alpha-methyl butyric aldehyde
 methyl ethyl acetaldehyde
2-methyl-1-butanal
a-2-methyl-N-butanal
alpha-2-methyl-N-butanal
2-methylbutanal
a-methylbutanal
2-methylbutyraldehyde
a-methylbutyraldehyde
2-methylbutyraldehyde 99%, (naturals)
2-methylbutyraldehyde natural
2-methylbutyric aldehyde
a-methylbutyric aldehyde
alpha-methylbutyric aldehyde
 methylethyl acetaldehyde
 methylethylacetaldehyde
 

Articles:

PubMed:Identification and Characterization of the Aroma-Impact Components of Thai Fish Sauce.
PubMed:Severe drought stress is affecting selected primary metabolites, polyphenols, and volatile metabolites in grapevine leaves (Vitis vinifera cv. Pinot noir).
PubMed:Variation of volatile compounds among wheat varieties and landraces.
PubMed:Influence of storage on volatile profiles in roasted almonds (Prunus dulcis).
PubMed:Evaluation of volatile aldehydes as discriminating parameters in quality vinegars with protected European geographical indication.
PubMed:OH-initiated photooxidations of 1-pentene and 2-methyl-2-propen-1-ol: mechanism and yields of the primary carbonyl products.
PubMed:Characterisation of aroma profiles of commercial soy sauce by odour activity value and omission test.
PubMed:Quantitative volatile compound profiles in fungal cultures of three different Fusarium graminearum chemotypes.
PubMed:Lactose-hydrolyzed milk is more prone to chemical changes during storage than conventional ultra-high-temperature (UHT) milk.
PubMed:Characterization of important odorants in steamed male Chinese mitten crab (Eriocheir sinensis) using gas chromatography-mass spectrometry-olfactometry.
PubMed:Characterization of volatile aroma compounds in different brewing barley cultivars.
PubMed:Volatile constituents of commercial imported and domestic black-ripe table olives (Olea europaea).
PubMed:2-methylbutanal, a volatile biomarker, for non-invasive surveillance of Proteus.
PubMed:Characterization of protein hydrolysis and odor-active compounds of fish sauce inoculated with Virgibacillus sp. SK37 under reduced salt content.
PubMed:Characterization of the aroma signature of styrian pumpkin seed oil ( Cucurbita pepo subsp. pepo var. Styriaca) by molecular sensory science.
PubMed:[Difference of volatile constituents contained in female and male flowers of Trichosanthes kirilowii by HS-SPME-GC-MS].
PubMed:Thermochemistry of radicals formed by hydrogen abstraction from 1-butanol, 2-methyl-1-propanol, and butanal.
PubMed:Metabolic profiling of Lactococcus lactis under different culture conditions.
PubMed:Differentiation of fresh and frozen/thawed fish, European sea bass (Dicentrarchus labrax), gilthead seabream (Sparus aurata), cod (Gadus morhua) and salmon (Salmo salar), using volatile compounds by SPME/GC/MS.
PubMed:Headspace analysis of Italian and New Zealand parmesan cheeses.
PubMed:Tentative identification of volatile flavor compounds in commercial Budu, a Malaysian fish sauce, using GC-MS.
PubMed:Biosynthesis of rhodiocyanosides in Lotus japonicus: rhodiocyanoside A is synthesized from (Z)-2-methylbutanaloxime via 2-methyl-2-butenenitrile.
PubMed:Statistical thermodynamics of 1-butanol, 2-methyl-1-propanol, and butanal.
PubMed:Screening for emphysema via exhaled volatile organic compounds.
PubMed:Identification of chemical markers for the sensory shelf-life of saveloy.
PubMed:Sensory and physicochemical evolution of tropical cooked peeled shrimp inoculated by Brochothrix thermosphacta and Lactococcus piscium CNCM I-4031 during storage at 8°C.
PubMed:Use of Tetragenococcus halophilus as a starter culture for flavor improvement in fish sauce fermentation.
PubMed:Effect of enzyme activity and frozen storage on jalapeño pepper volatiles by selected ion flow tube-mass spectrometry.
PubMed:Biosynthesis of the cyanogenic glucosides linamarin and lotaustralin in cassava: isolation, biochemical characterization, and expression pattern of CYP71E7, the oxime-metabolizing cytochrome P450 enzyme.
PubMed:Effects of lipase, lipoxygenase, peroxidase and free fatty acids on volatile compound found in boiled buckwheat noodles.
PubMed:Influence of pre-cure freezing on the profile of volatile compounds during the processing of Iberian hams.
PubMed:Low-temperature catalytic oxidation of aldehyde mixtures using wood fly ash: kinetics, mechanism, and effect of ozone.
PubMed:Flavor variability and flavor stability of U.S.-produced whole milk powder.
PubMed:Kinetic modeling of the generation of 2- and 3-methylbutanal in a heated extract of beef liver.
PubMed:Release of volatile organic compounds from the lung cancer cell line NCI-H2087 in vitro.
PubMed:Super chilling enhances preservation of the freshness of salted egg yolk during long-term storage.
PubMed:Characterization of the most odor-active compounds in an American Bourbon whisky by application of the aroma extract dilution analysis.
PubMed:Biofiltration kinetics of a gaseous aldehyde mixture using a synthetic matrix.
PubMed:Characterization of the key aroma compounds in soy sauce using approaches of molecular sensory science.
PubMed:An assessment of the role played by some oxidation-related aldehydes in wine aroma.
PubMed:Quality and flavour stability of coffee substitute prepared by extrusion of wheat germ and chicory roots.
PubMed:Permeabilization and lysis induced by bacteriocins and its effect on aldehyde formation by Lactococcus lactis.
PubMed:Identification of the key aroma compounds in cocoa powder based on molecular sensory correlations.
PubMed:Critical aspects of the determination of pentafluorobenzyl derivatives of aldehydes by gas chromatography with electron-capture or mass spectrometric detection: Validation of an optimized strategy for the determination of oxygen-related odor-active aldehydes in wine.
PubMed:Electrophysiological and behavioral responses of a parasitic wasp to plant volatiles induced by two leaf miner species.
PubMed:Cell membrane damage induced by lacticin 3147 enhances aldehyde formation in Lactococcus lactis IFPL730.
PubMed:Volatiles released from bean plants in response to agromyzid flies.
PubMed:Analysis of volatile compounds from various types of barley cultivars.
PubMed:Interaction of soluble peptides and proteins from skeletal muscle with volatile compounds in model systems as affected by curing agents.
PubMed:Effect of the type of frying culinary fat on volatile compounds isolated in fried pork loin chops by using SPME-GC-MS.
PubMed:Branched-chain fatty acid biosynthesis in a branched-chain amino acid aminotransferase mutant of Staphylococcus carnosus.
PubMed:Identification by gas chromatography-mass spectrometry of the volatile organic compounds emitted from the wood-rotting fungi Serpula lacrymans and Coniophora puteana, and from Pinus sylvestris timber.
PubMed:Enhancement of 2-methylbutanal formation in cheese by using a fluorescently tagged Lacticin 3147 producing Lactococcus lactis strain.
PubMed:On-line monitoring of important organoleptic methyl-branched aldehydes during batch fermentation of starter culture Staphylococcus xylosus reveal new insight into their production in a model fermentation.
PubMed:Analysis of aldehydes in beer using solid-phase microextraction with on-fiber derivatization and gas chromatography/mass spectrometry.
PubMed:Effect of pH and temperature on the kinetics of odor oxidation using chlorine dioxide.
PubMed:Interactions of soluble peptides and proteins from skeletal muscle on the release of volatile compounds.
PubMed:Lacticin 3147 favours isoleucine transamination by Lactococcus lactis IFPL359 in a cheese-model system.
PubMed:Solvent-free asymmetric olefin hydroformylation catalyzed by highly cross-linked polystyrene-supported (R,S)-BINAPHOS-Rh(I) complex.
PubMed:Quantification of aroma compounds in Parmigiano Reggiano cheese by a dynamic headspace gas chromatography-mass spectrometry technique and calculation of odor activity value.
PubMed:NTP Toxicology and Carcinogenesis Studies of Isobutyraldehyde (CAS No. 78-84-2) in F344/N Rats and B6C3F1 Mice (Inhalation Studies).
PubMed:Volatile compounds of headspace gas in the Japanese fish sauce ishiru.
PubMed:Volatile compounds in Hispánico cheese manufactured using a mesophilic starter, a thermophilic starter, and bacteriocin-producing Lactococcus lactis subsp. lactis INIA 415.
PubMed:Effect of cultivar and storage time on the volatile flavor components of baked potato.
PubMed:Characterization of Ypr1p from Saccharomyces cerevisiae as a 2-methylbutyraldehyde reductase.
PubMed:Identification of distinctive volatile compounds in fish sauce.
PubMed:Quantitation of odor-active compounds in rye flour and rye sourdough using stable isotope dilution assays.
PubMed:Identification of aroma compounds in Parmigiano-Reggiano cheese by gas chromatography/olfactometry.
PubMed:Wet scrubber analysis of volatile organic compound removal in the rendering industry.
PubMed:Use of gas chromatography-olfactometry to identify key odorant compounds in dark chocolate. Comparison of samples before and after conching.
PubMed:Relationships between antioxidant activity, color, and flavor compounds of crystal malt extracts.
PubMed:Formation of volatile compounds during heating of spice paprika (Capsicum annuum) powder.
PubMed:Contribution of 3-methylthiopropionaldehyde to the worty flavor of alcohol-free beers.
PubMed:Volatile components of roots, stems, leaves, and flowers of Echinacea species.
PubMed:Quantification and sensory studies of character impact odorants of different soybean lecithins.
PubMed:Volatile flavor components of rice cakes.
PubMed:The biosynthesis of cyanogenic glucosides in seedlings of cassava (Manihot esculenta Crantz).
PubMed:Catalysis by cytochrome P-450 of an oxidative reaction in xenobiotic aldehyde metabolism: deformylation with olefin formation.
PubMed:Poisoning by 2-methylbutyraldehyde (isovaleraldehyde).
 
Notes:
None found
Please share your Comments.
Email Address:
Top of Page Home
Copyright © 1980-2018 The Good Scents Company (tgsc) ™ Disclaimer Privacy Policy