2-methyl butyraldehyde
  • Advanced Biotech
  • Alfrebro
    • Alfrebro LLC
      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
  • Bedoukian Research
    • Bedoukian Research, Inc.
      Constantly Improving
      Working closely with our customers to meet their requirements.
      Paul Bedoukian founded the company to fill a niche as a supplier of high quality specialty aroma and flavor ingredients. In 1975 the company began manufacturing insect pheromones which are chemically similar to flavor and fragrance ingredients. Today, Bedoukian Research offers more than 450 Aroma Chemicals and 50 Insect Pheromones, while also providing custom manufacturing services to the pharmaceutical, agrochemical, and specialty chemical industries.
      US Email: Customer Service
      US Voice: 1-203-830-4000
      US Fax: 1-203-830-4010
      Products List: View
      288 2-METHYL BUTYRALDEHYDE ≥98.0%, FCC, Kosher
      Used for lift in woody and cocoa topnote complexes.
      Useful for chocolate, cocoa, mocha/coffee flavors.
  • Beijing Lys Chemicals
    • Beijing Lys Chemicals Co, LTD.
      From Grams to Tons
      Fine chemical high-tech company which contains R&D, production, and sales.
      BEIJING LYS CHEMICALS CO, LTD, established in 2004, is a fine chemical high-tech company which contains R&D, production, and sales. We mainly engaged in export and technology development of flavor and fragrance materials and pharmaceutical intermediates. We have nearly 500 kinds of products, from grams to tons, exported to USA, Europe, South Asia and etc. And we custom manufacture new products according to customers’ needs, and serve good quality products and service. Our goal is to become a fine chemical enterprise which could provide special products and services.
      Email: Mr. Jia
      Email: Mr. Guo
      Voice: 86-10-68418738
      Fax: 86-10-68418739
      Mr. Guo86-10-68483445
      Mr. Guo86-10-68418739
      10468 2-Methylbutanal
  • 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
      Market Report
      2-Methyl Butyraldehyde
  • 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.
      Since 1982, Charkit has been committed to expanding the markets we serve and our roster of products and services continues to grow with us. Personal care ingredients now include a substantial array of luxury and exotic components. Substantial inroads have been made in the nutraceutical and resins markets, with a growing roster of versatile and unique ingredients. And 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.
      Email: Sales
      Voice: 203-299-3220
      Fax: 203-299-1355
      Products List: View
  • CTC Organics
    • CTC Organics
      For More Than 40 Year
      Your source for rare aroma chemicals for the flavor and fragrance industy.
      “The world is run by middle men.” The number of times I have heard Dr. Liu utter those words are innumerable. He loved reciting and recording famous quotes and had many of his own. Among his many talents, Dr. Liu had a unique genius in the area of chemistry. He had an uncanny understanding of the pulse of the chemical industry and was a superb salesman.
      US Email: Customer Service
      US Voice: (404) 524-6744
      US Fax: (404) 577-1651
      W1376 2-methyl butyraldehyde
  • Frutarom
    • Frutarom Ltd
      Discover Our Passion
      Your preferred partner for flavour and fragrance success.
      At Frutarom, we take pride in our expertise and knowledge of Flavour & Fragrance Ingredients and our thorough understanding of the needs of Flavourists, Perfumers and Food Technologists. Working closely with our customers we have a strong track record of providing unique solutions to fulfil requirements.
      US Email: Info- USA
      Email: Info - UK
      Voice: +44 (0) 1429 863 222
      US Voice: +1 513 870 4900
      Products List: View
      M0800-2 2-METHYLBUTYRALDEHYDE ≥95.00%, NI, Kosher
      Suggested Uses: Apple, Bakery, Cheese, Chocolate, Coffee, Hard Fruits, Tomato
  • H. Interdonati, Inc.
  • M&U International
    • M&U International LLC
      Steady supply & demand
      Meeting customers increasing demands at home as well as abroad.
      M&U dedicates itself to the development and production of new products as well as continuously promoting those new products. We’ve maintained a steady supply&demand relationship with a large number of manufacturers at home and abroad. We’ve developed an extensive network and because of our relationships with these manufacturers, we’re able to provide a stable supply of great quality materials. We’re located in China’s largest communications hub, Shanghai and in the U.S. near one of the largest sea ports on the East Coast. The strategic locations of our facilities ensure convenient, prompt and secure delivery of our products to our customers. We warmly welcome your inquiries, come witness our solemn commitment for yourself.
      Email: Sales
      US Email: Sales
      Voice: +86-21-32515501 60762991 60762992
      Fax: +86-21-32515502 64204960
      US Voice: 908-359-9000
      US Fax: 908-359-9002
  • Natural Advantage
    • Natural Advantage
      Manufacturer of natural flavor ingredients
      With over 25 years experience in the flavor and food ingredient industries.
      Natural Advantage was formed over seventeen years ago to supply the growing demand for natural food and flavor ingredients. We employ a wide range of multi-disciplined scientists who are dedicated to high quality service, customer satisfaction and creating an outstanding value for our clients.
      Email: Info
      Email: Customer service
      Voice: 318-215-1456
      Fax: 318-335-1579
      What We Do
      Products List: View
      2-Methylbutyraldehyde Nat
  • O'Laughlin Industries
    • O'Laughlin Industries Inc.
      Manufacturer of Aroma
      Leading the Flavor and Fragrance Industry since 1980.
      O'Laughlin was established in 1980 by its owner and chief executive Michael O'Laughlin, when he moved to Beijing, China and established a small office. Since then it has grown to be a world class producer of chemicals, with significant production facilities in China, and distribution and sales in all major world markets.
      Email: Sales
      US Email: Joe Schreiber
      Voice: (852) 2527-1031
      Fax: (852) 2529-0231
      US Voice: (973) 376-4600
      US Fax: (973) 376-4630
  • 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
      13-32200 2-METHYLBUTYRALDEHYDE, Kosher
  • Riverside Aromatics
    • Riverside Aromatics Ltd.
      Speciality Aroma Chemicals, Naturals and Synthetics
      Specialist raw material suppliers to the Flavour & Fragrance Industry.
      Peter Cannon & David Rowe established Riverside Aromatics in 2006 in Poole, UK, to offer a new type of specialist raw material supplier to the Flavour & Fragrance Industry. We bring together over 40 years of commercial & technical experience in the F&F industry which allows us to understand the needs of the Global F&F business and especially that of the West European Market.
      Email: Info
      Email: Peter Cannon (sales)
      Voice: +44 (0) 1202 679532
      Fax: +44 (0) 1202 679532
      Products List: View
      NM0500 2-Methylbutyraldehyde, Natural
  • Sigma-Aldrich
  • Sunaux International
  • Taytonn
      Supplying Asia Pacific
      We fully understand the demands of the F&F industry and we endeavour to supply quality products, with ready availability and a personalised service.
      Since 2001 TAYTONN has been distributing key ingredients to the Fragrance and Flavor industry in Asia. We work closely with customers, principals and vendors. Together we forecast demand and match it with supply of aroma chemicals, essential oils and natural isolates & extracts. Sourced from around the world, our F&F ingredient inventory in Singapore is ready to ship to any location in Asia and beyond. Time and again, we help our principals introduce new discoveries to the F&F market - stimulating creativity and bringing value added proposition to our customers.
      Email: Info
      Email: Sales
      Voice: + 65 - 6861 8113
      Fax: + 65 - 6861 8115
  • Treatt
    • Treatt PLC
      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
Synonyms   Articles   Notes   Search
2-methylbutanal (Click)
CAS Number: 96-17-3 57456-98-1
ECHA EINECS - REACH Pre-Reg: 202-485-6
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
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: 254  2-methylbutyraldehyde
Flavis Number: 05.049 (Old)
DG SANTE Food Flavourings: 05.049  2-methylbutyraldehyde
FEMA Number: 2691  2-methylbutyraldehyde
FDA Regulation:
Subpart F--Flavoring Agents and Related Substances
Sec. 172.515 Synthetic flavoring substances and adjuvants.
Synonyms   Articles   Notes   Search   Top
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 mm/Hg @ 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)
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
Odor Type: chocolate
Odor Strength: high ,
recommend smelling in a 1.00 % solution or less
 musty  cocoa  coffee  nutty  
Odor Description:
at 1.00 % in dipropylene glycol. 
musty cocoa coffee nutty
Luebke, William tgsc, (1986)
 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)
 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)
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
Synonyms   Articles   Notes   Search   Top
Advanced Biotech
94% min.
Odor: Cocoa, Fruity, Slight
Odor: Cocoa, Coffee on Dilution
Bedoukian Research
≥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-Methyl Butyraldehyde
Charkit Chemical
CTC Organics
2-methyl butyraldehyde
≥95.00%, NI, Kosher
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
Kunshan Sainty
2-Methyl Butyraldehyde, Natural
Kunshan Sainty
2-Methylbutyraldehyde, Kosher
M&U International
Natural Advantage
2-Methylbutyraldehyde Nat
O'Laughlin Industries
Pearlchem Corporation
Natural 2-Methyl Butyraldehyde
Penta International
Penta International
Reincke & Fichtner
2-Methylbutyraldehyde natural
Reincke & Fichtner
Riverside Aromatics
2-Methylbutyraldehyde, Natural
Santa Cruz Biotechnology
For experimental / research use only.
2-Methylbutyraldehyde, ≥95%, FG
Odor: chocolate; coffee
Certified Food Grade Products
2-Methylbutyraldehyde, natural, 98%
Sunaux International
Sunaux International
nat.2-Methyl Butyraldehyde
Odor: Aldehydic/ Aldehyde, Cocoa, Fruity, Musty
For experimental / research use only.
2-Methylbutyraldehyde >95.0%(GC)
The Perfumers Apprentice
Methylbutyraldehyde 1% (PG)
WEN International
Synonyms   Articles   Notes   Search   Top
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
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

Synonyms   Articles   Notes   Search   Top
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
Click here to view publication 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: --
Synonyms   Articles   Notes   Search   Top
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
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
Chemidplus: 0000096173
RTECS: ES3400000 for cas# 96-17-3
Synonyms   Articles   Notes   Search   Top
Leffingwell: chirality
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 96-17-3
Pubchem (cid): 7284
Pubchem (sid): 134972369
Flavornet: 96-17-3
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 Everything Added to Food in the United States (EAFUS): View
KEGG (GenomeNet): C02223
HMDB (The Human Metabolome Database): HMDB31526
YMDB (Yeast Metabolome Database): YMDB00485
Export Tariff Code: 2912.19.5000
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
RSC Learn Chemistry: View
Read: Under the conditions of intended use - New developments in the FEMA GRAS program and the safety assessment of flavor ingredients
Read: A GRAS assessment program for flavor ingredients
Read: Sensory testing for flavorings with modifying properties. Food Technology
Read: Criteria for the safety evaluation of flavoring substances
Read: A procedure for the safety evaluation of natural flavor complexes used as ingredients in food: essential oils
Read: FEMA Expert Panel: 30 Years of safety evaluation for the flavor industry
Read: Consumption ratio and food predominance of flavoring materials
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 acetyl acetaldehyde dimethyl acetalFL
2-acetyl furanFL/FR
 acetyl propionylFL/FR
2-acetyl pyrazineFL/FR
3-acetyl pyridineFL/FR
2-acetyl pyrroleFL/FR
2-acetyl thiazoleFL/FR
3-acetyl-2,5-dimethyl furanFL/FR
2-acetyl-3-ethyl pyrazineFL/FR
2-acetyl-3-methyl pyrazineFL/FR
2-acetyl-3,5-dimethyl pyrazineFL/FR
2-acetyl-5-methyl furanFL/FR
 aconitic acidFL
 allyl 2-ethyl butyrateFL/FR
 allyl hexanoateFL/FR
 allyl phenyl acetateFL/FR
 amyl cinnamateFL/FR
isoamyl cinnamateFL/FR
alpha-amyl cinnamyl acetateFL/FR
isoamyl nonanoateFL/FR
 amyl phenyl acetateFL/FR
isoamyl phenyl acetateFL/FR
isoamyl pyruvateFL/FR
 amyl salicylateFL/FR
alpha-angelica lactoneFL/FR
 benzyl mercaptanFL
 berry pentadienoateFL/FR
 bornyl isobutyrateFL/FR
 boronia butenalFR
 bran absoluteFR
 butyl 2-methyl butyrateFL/FR
 butyl acetoacetateFL/FR
isobutyl butyrateFL/FR
 butyl cinnamateFL/FR
 butyl formateFL/FR
 butyl lactateFL/FR
 butyl laevo-lactateFL/FR
 butyl mercaptanFL
 butyl phenyl acetateFL/FR
isobutyl phenyl acetateFL/FR
2-isobutyl-3,5-(and 3,6)-dimethyl pyrazineFL/FR
2(4)-isobutyl-4(2),6-dimethyl dihydro-4H-1,3,5-dithiazineFL
 caramel furanoneFL
 chocolate pyrazine AFL/FR
 chocolate pyrazine BFL
 cocoa butenalFL/FR
 cocoa hexenalFL/FR
 cocoa oleoresinFL/FR
 cocoa pentenalFL/FR
 cocoa propanalFL
3,5-cocoa pyrazineFL/FR
3,5(6)-cocoa pyrazineFL
3,6-cocoa pyrazineFL/FR
 coconut absoluteFL/FR
 coffee difuranFL/FR
 coffee dioneFL/FR
 coffee furanoneFL/FR
 coffee pyrazineFL
white cognac oilFL/FR
para-cresyl laurateFL/FR
 cyclohexanone diethyl acetalFL/FR
 cyclohexyl methyl pyrazineFL
 decyl propionateFL/FR
 dicyclohexyl disulfideFL
2,5-diethyl thiazoleFL
3,5-diethyl-2-methyl pyrazineFL
2,5-diethyl-3-methyl pyrazineFL
2,5-diethyl-4-methyl thiazoleFL
 difurfuryl etherFL
 difurfuryl sulfideFL
 dihydroxyacetophenone (mixed isomers)FL
 diisoamyl thiomalateFL
 dimethyl dihydrocyclopentapyrazineFL
2,3-dimethyl pyrazineFL/FR
2,5-dimethyl pyrazineFL/FR
2,6-dimethyl pyrazineFL/FR
2,4-dimethyl thiazoleFL
2,5-dimethyl thiazoleFL
4,5-dimethyl thiazoleFL
2,5-dimethyl thiopheneFL
4,5-dimethyl-2-ethyl thiazoleFL
2,5-dimethyl-3-thiofuroyl furanFL
2,4-dimethyl-5-vinyl thiazoleFL
 ethyl (E)-2-crotonateFL/FR
 ethyl 2-hydroxy-2-methyl butyrateFL/FR
 ethyl 2-methyl-2-pentenoateFR
 ethyl 3-(furfuryl thio) propionateFL
 ethyl acetateFL/FR
2-ethyl butyraldehydeFL
 ethyl cyclopentenoloneFL/FR
2-ethyl furanFL
 ethyl heptanoateFL/FR
 ethyl hydrocinnamateFL/FR
 ethyl methyl sulfideFL
 ethyl nonanoateFL/FR
 ethyl phenyl acetateFL/FR
 ethyl propionateFL/FR
2-ethyl pyrazineFL/FR
 ethyl pyruvateFL/FR
S-ethyl thioacetateFL
 ethyl vanillin isobutyrateFL/FR
1-ethyl-2-acetyl pyrroleFL
5-ethyl-2-methyl pyridineFL
2-ethyl-4-methyl thiazoleFL/FR
(Z+E)-5-ethyl-4-methyl-2-(2-butyl) thiazolineFL
(Z+E)-5-ethyl-4-methyl-2-(2-methyl propyl) thiazolineFL
 eugenyl acetateFL/FR
 fenugreek oleoresinFL/FR
 fenugreek resinoidFL/FR
 filbert heptenoneFL/FR
 filbert pyrazineFL/FR
 fruity carboxylateFR
 furfuryl alcoholFL
 furfuryl isopropyl sulfideFL
 furfuryl mercaptanFL/FR
 furfuryl methyl etherFL
 furfuryl propionateFL
1-furfuryl pyrroleFL/FR
 furfuryl thioacetateFL/FR
S-furfuryl thioformateFL/FR
 furfuryl thiopropionateFL
3-(2-furyl) acroleinFL
 geranyl acetoacetateFL/FR
 geranyl methyl tiglate 
european hazelnut oleoresinFL
 hazelnut pyrazineFL/FR
 heptyl acetateFL/FR
2-heptyl furanFL/FR
3,4-hexane dioneFL/FR
(E)-2-hexen-1-yl formateFL/FR
(E)-2-hexen-1-yl phenyl acetateFL/FR
1-hexen-3-yl acetateFL
2-hexyl-5 or 6-keto-1,4-dioxaneFL
 linalyl propionateFL/FR
 methyl 2-(methyl thio) acetateFL
2-methyl 3-(methyl thio) furanFL
2-methyl 5-(methyl thio) furanFL/FR
ortho-methyl anisoleFL/FR
para-methyl anisoleFL/FR
 methyl ethoxypyrazineFL
2-methyl furanFL
 methyl furfuryl disulfideFL/FR
S-methyl methioninium chloride 
 methyl propionateFL/FR
2-methyl pyrazineFL/FR
2-methyl quinoxalineFL
5-methyl quinoxalineFL/FR
4-methyl thiazoleFL
 methyl thio isovalerateFL
2-methyl thio-3,5 or 6-methyl pyrazineFL/FR
2-methyl thioacetaldehydeFL
(E)-methyl tiglateFL/FR
 methyl valerateFL/FR
2-methyl-3-,5 or 6-(furfuryl thio) pyrazineFL/FR
2-methyl-3-(methyl thio) pyrazineFL/FR
2-methyl-3-propyl pyrazineFL/FR
2-methyl-5-isopropyl pyrazineFL
(E,Z)-2,6-nonadien-1-yl acetateFL/FR
 nutty cyclohexenoneFL/FR
 nutty quinoxalineFL/FR
 nutty thiazoleFL
 peanut dithiazineFL
 peanut oxazoleFL
 phenethyl octanoateFL/FR
 phenyl acetaldehydeFL/FR
 phenyl acetic acidFL/FR
2-phenyl propyl butyrateFL/FR
 popcorn pyrimidineFL/FR
 prenyl benzoateFL/FR
 prenyl formateFL/FR
2-propionyl thiazoleFL
 propyl alcoholFL/FR
 propyl benzoateFL/FR
 propyl formateFL/FR
isopropyl formateFL/FR
2-isopropyl pyrazineFL
2-propyl pyridineFL
 saffron pyranoneFR
para-salicylic acidFL
 shoyu pyrazineFL/FR
 sulfuryl butyrateFL/FR
 sulfuryl decanoateFL/FR
 sulfuryl formateFL
 sulfuryl hexanoateFL/FR
 sulfuryl isobutyrateFL/FR
 sulfuryl octanoateFL/FR
 sulfuryl propionateFL/FR
 tetrahydrofurfuryl acetateFL/FR
2,3,5,6-tetramethyl pyrazineFL/FR
2-thienyl mercaptanFL
2-thiophene thiolFL
 veltonal (Bedoukian)FR
 tonka bean absoluteFR
 tonka bean resinoidFR
 tricyclodecenyl isobutyrateFR
2,3,5-trimethyl pyrazineFL/FR
2,4,5-trimethyl thiazoleFL/FR
 tropical thiazoleFL/FR
 valeraldehyde dibutyl acetalFL/FR
 valeraldehyde propylene glycol acetalFL/FR
 vanillyl isobutyrateFL/FR
2-vinyl pyrazineFL
 vinyl sulfurolFL/FR
 whiskey lactoneFL/FR
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 berry mixedFL
 chocolate cocoa 
Synonyms   Articles   Notes   Search   Top
Natural Occurrence in: note
 calvatia gigantea
GRIN Trop Picture
GRIN Trop Picture
 cheese cheddar cheese
GRIN Trop Picture
 cheese swiss cheese
GRIN Trop Picture
 currant black currant
GRIN Trop Picture
 lovage flower oil @ trace%
Data  GC  GRIN Trop Picture
 lovage leaf oil @ trace%
Data  GC  GRIN Trop Picture
 peanut roasted peanut
 rice cakes
 cheese @ 251.00 ± 43 µg%
Data  GC 
Synonyms   Articles   Notes   Search   Top
 acetaldehyde, ethylmethyl-
 butanal, 2-methyl-
 butyraldehyde, 2-methyl-
2-ethyl propanal
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-methylbutyraldehyde 99%, (naturals)
2-methylbutyraldehyde natural
2-methylbutyric aldehyde
a-methylbutyric aldehyde
alpha-methylbutyric aldehyde
 methylethyl acetaldehyde
Synonyms   Articles   Notes   Search   Top
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).
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Soluble in:
 water, 1.123e+004 mg/L @ 25 °C (est)
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