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
      Product(s):
      2-METHYL BUTYRALDEHYDE NATURAL
       
  • 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
      Product(s):
      288 2-METHYL BUTYRALDEHYDE ≥98.0%, FCC, Kosher
      MSDS
       
  • 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
      Product(s):
      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
      Product(s):
      2-Methyl Butyraldehyde
       
  • H. Interdonati, Inc.
    • H. Interdonati, Inc.
      Innovative products
      Because your flavors and fragrances are only as good as their source "Since 1952"
      H. Interdonati, Inc. began in 1952 with the tradition of delivering quality pharmaceuticals and fine chemical ingredients at competitive prices. The mission was simple: To provide the most reliable, personal service in the industry.
      Email: Info
      US Email: Info
      Email: Sales
      US Email: Andrew Interdonati (Sales)
      Voice: 800 367-6617
      Fax: 631 367-6626
      Product(s):
      2-Methylbutyraldehyde Natural, Kosher
       
  • 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
      Product(s):
      N0110 NAT.2-METHYL BUTYRALDEHYDE, Kosher
       
  • 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
      Products List: View
      Product(s):
      2-Methyl Butyraldehyde
       
  • 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
      Product(s):
      2-METHYLBUTYRALDEHYDE NATURAL
       
  • Penta International
    • Penta International Corporation
      Chemistry innovation
      At Penta, our products and services help businesses do business better.
      For over 30 years, Penta Manufacturing Company has played a growing role in worldwide chemistry innovations and applications. As an industry leader, Penta continues to pioneer chemistry-based solutions for practically every area of commerce. Our products and expertise have helped fuel technical advances in dozens of commercial applications including flavoring, coloring, fragrances and chemical processes.
      US Email: Technical Services
      US Email: Sales
      US Voice: (973) 740-2300
      US Fax: (973) 740-1839
      Product(s):
      13-32200 2-METHYLBUTYRALDEHYDE, Kosher
      13-32202 2-METHYLBUTYRALDEHYDE, NATURAL, 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
      Product(s):
      NM0500 2-Methylbutyraldehyde, Natural
       
  • SAFC Global
    • SAFC
      Complete Supply Chain
      The perfect blend of products and services that bring your creativity to life.
      Sigma-Aldrich is a leading Life Science and High Technology company dedicated to providing high-quality, safe and certified flavor ingredients with transparent and easily accessible documentation to customers around the globe. Sigma-Aldrich also provides a suite of analytical tools that allow food analysts to simplify sample preparation, cleanup and analysis steps, while increasing sensitivity to trace ingredients and harmful substances to meet regulations and quality standards.
      Email: Information
      US Email: Sales
      US Voice: 800-244-1173
      US Fax: 800-368-4661
      Product(s):
      W269107 2-Methyl butyraldehyde ≥90%, FG, Kosher
      MSDS
      W269101 2-Methyl butyraldehyde 90%, natural, US
      MSDS
       
  • Sunaux International
  • Treatt
    • Treatt PLC
      Full Range of Naturals
      World-leading, independent ingredients supplier to the flavour and fragrance industries.
      We are proud of our heritage in trading essential oils. Our founder Richard Court Treatt's charismatic and personable approach still embodies the spirit of Treatt today.
      Email: Enquiries
      US Email: Enquiries
      Voice: +44 (0) 1284 702500
      Fax: +44 (0) 1284 703809
      US Voice: +1 863 668 9500
      US Fax: +1 863 668 3388
      Product(s):
      2-Methylbutyraldehyde
       
 
Synonyms   Articles   Notes   Search
2-methylbutanal (Click)
CAS Number: 96-17-3 57456-98-1
ECHA EC Number: 202-485-6
FDA UNII: 47H597M1YY
Beilstein Number: 1633540
MDL: MFCD00006984
FEMA Number: 2691
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)
EU SANCO Food Flavourings: 05.049  2-methylbutyraldehyde

FEMA Number: 2691  2-methylbutyraldehyde
FDA Mainterm: 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.
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
Odor Description:
at 1.00 % in dipropylene glycol. 
musty cocoa coffee nutty
Luebke, William tgsc, (1986)
Odor sample from: SAFC
Odor Description:
Musty, chocolate, nutty, furfural and iaovaleraldehyde-like with malty and fermented nuances
Mosciano, Gerard P&F 23, No. 1, 33, (1998)
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
Suppliers:
Advanced Biotech
2-METHYL BUTYRALDEHYDE NATURAL
94% min.
Odor: Cocoa, Fruity, Slight
Alfrebro
2-METHYL BUTYRALDEHYDE NATURAL
Odor: Cocoa, Coffee on Dilution
Aurochemicals
2-METHYL BUTYRALDEHYDE, Natural
Bedoukian Research
2-METHYL BUTYRALDEHYDE
≥98.0%, FCC, Kosher
Beijing Lys Chemicals
2-Methylbutanal
Berjé
2-Methyl Butyraldehyde
Charkit Chemical
METHYLBUTYRALDEHYDE, 2-
CTC Organics
2-methyl butyraldehyde
Frutarom
2-METHYLBUTYRALDEHYDE
≥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
Kunshan Sainty
2-Methyl Butyraldehyde, Natural
Kunshan Sainty
2-Methylbutyraldehyde, Kosher
M&U International
NAT.2-METHYL BUTYRALDEHYDE, Kosher
Natural Advantage
2-Methyl Butyraldehyde
O'Laughlin Industries
2-METHYLBUTYRALDEHYDE NATURAL
Pearlchem Corporation
Natural 2-Methyl Butyraldehyde
Penta International
2-METHYLBUTYRALDEHYDE, Kosher
Penta International
2-METHYLBUTYRALDEHYDE, NATURAL, Kosher
Reincke & Fichtner
2-Methylbutyraldehyde natural
Reincke & Fichtner
2-Methylbutyraldehyde
Riverside Aromatics
2-Methylbutyraldehyde, Natural
SAFC Global
2-Methyl butyraldehyde
90%, natural, US
Odor: chocolate; coffee
SAFC Global
2-Methyl butyraldehyde
≥90%, FG, Kosher
Odor: chocolate; coffee
Santa Cruz Biotechnology
2-Methylbutyraldehyde
For experimental / research use only.
Sunaux International
2-Methylbutyaldehyde
Sunaux International
nat.2-Methyl Butyraldehyde
Taytonn
2-Methylbutyraldehyde
Odor: Aldehydic/ Aldehyde, Cocoa, Fruity, Musty
The Perfumers Apprentice
Methylbutyraldehyde 1% (PG)
Treatt
2-Methylbutyraldehyde
WEN International
2-METHYLBUTYRALDEHYDE Natural
Synonyms   Articles   Notes   Search   Top
Safety Information:
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

Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
Category: flavor and fragrance agents
Structure Class: I
Recommendation for 2-methyl butyraldehyde usage levels up to:
  0.3000 % in the fragrance concentrate.
Recommendation for 2-methyl butyraldehyde flavor usage levels up to:
  10.0000 ppm in the finished product.
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
Chemicalize.org: Calculate predicted properties
ECHA Data Sheet: View
Chemical Carcinogenesis Research Information System: Search
Env. Mutagen Info. Center: Search
EPA Substance Registry Services (TSCA): 96-17-3
EPA ACToR: Toxicology Data
National Institute of Allergy and Infectious Diseases: Data
WISER: UN 1989
WGK Germany: 1
 2-methylbutanal
DTP/NCI: 77077
Chemidplus: 0000096173
RTECS: ES3400000 for cas# 96-17-3
Synonyms   Articles   Notes   Search   Top
References:
Leffingwell: chirality
 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 Floral: 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
CHEBI: View
Export Tariff Code: 2912.19.9000
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 acetalFL/FR
 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-2-pyrrolineFL
2-acetyl thiazoleFL/FR
2-acetyl-2-thiazolineFL
5-acetyl-2,3-dihydro-1,4-thiazineFL
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
 benzothiazoleFL/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
 butyraldehydeFL
 butyramideFL
 butyroinFL
 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
 coumaneFL/FR
 coumarinFR
para-cresyl laurateFL/FR
 cyclohexanone diethyl acetalFL/FR
 cyclohexyl methyl pyrazineFL
 cycloteneFL/FR
(E,E)-2,4-decadienalFL
 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
6,7-dihydro-2,3-dimethyl-5H-cyclopentapyrazineFL
 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
4,5-dimethyl-2-ethyl-3-thiazolineFL/FR
2,5-dimethyl-3-thiofuroyl furanFL
2,4-dimethyl-5-vinyl thiazoleFL
2-ethoxythiazoleFL
 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-3-methoxypyrazineFL/FR
3-methyl-1-pentanolFL/FR
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 
laevo-glutamineCS
 hazelnut oleoresinFL
 hazelnut pyrazineFL/FR
(E,E)-2,4-heptadien-1-olFL
gamma-heptalactoneFL/FR
 heptyl acetateFL/FR
2-heptyl furanFL/FR
2,4-hexadien-1-olFL/FR
3,4-hexane dioneFL/FR
3-hexanoneFL/FR
(E)-2-hexen-1-yl formateFL/FR
(E)-2-hexen-1-yl phenyl acetateFL/FR
1-hexen-3-olFL/FR
1-hexen-3-yl acetateFL
2-hexyl-5 or 6-keto-1,4-dioxaneFL
1-hydroxy-2-butanoneFL/FR
 linalyl propionateFL/FR
2,6-lutidineFL/FR
 maraniolCS
 menthofuranFL/FR
2-methoxypyrazineFL/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
3-methyl-2-butenalFL/FR
2-methyl-3-,5 or 6-(furfuryl thio) pyrazineFL/FR
2-methyl-3-(methyl thio) pyrazineFL/FR
2-methyl-3-ethoxypyrazineFL/FR
2-methyl-3-propyl pyrazineFL/FR
2-methyl-5-isopropyl pyrazineFL
(E,E)-2,4-nonadienalFL
(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
 propionaldehydeFL
2-propionyl thiazoleFL
2-propionyl-2-thiazolineFL
 propyl alcoholFL/FR
 propyl benzoateFL/FR
 propyl formateFL/FR
isopropyl formateFL/FR
2-isopropyl pyrazineFL
2-propyl pyridineFL
 pyruvaldehydeFL
 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
 tiglaldehydeFL/FR
 tobacco butenalFR
 tonka bean absoluteFR
 tonka bean resinoidFR
 tricyclodecenyl isobutyrateFR
2,3,5-trimethyl pyrazineFL/FR
2,4,5-trimethyl thiazoleFL/FR
 tropical thiazoleFL/FR
 valeraldehydeFL/FR
 valeraldehyde dibutyl acetalFL/FR
 valeraldehyde propylene glycol acetalFL/FR
gamma-valerolactoneFL/FR
 vanillinFL/FR
 vanillyl isobutyrateFL/FR
2-vinyl pyrazineFL
 vinyl sulfurolFL/FR
 whiskey lactoneFL/FR
2,6-xylenolFL/FR
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 appleFL
 bananaFL
 berry mixedFL
 breadFL
 caramelFL
 chocolate cocoa 
 coffeeFL
 grapeFL
 malt 
 olive 
 papayaFL
 rumFL
 tomatoFL
 tropicalFL
 wineFL
Synonyms   Articles   Notes   Search   Top
Natural Occurrence in: note
 apple
 calvatia gigantea
GRIN Trop Picture
 cardamom
GRIN Trop Picture
 cheese cheddar cheese
GRIN Trop Picture
 cheese swiss cheese
GRIN Trop Picture
 currant black currant
GRIN Trop Picture
 fish
 grape
 kohlrabi
 lovage flower oil @ trace%
Data  GC  GRIN Trop Picture
 lovage leaf oil @ trace%
Data  GC  GRIN Trop Picture
 papaya
 paprika
 peanut roasted peanut
 plum
 potato
 rice cakes
PbMd 
 rum
 truffle
 cheese @ 251.00 ± 43 µg%
Data  GC 
Synonyms   Articles   Notes   Search   Top
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
Synonyms   Articles   Notes   Search   Top
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).
Synonyms   Articles   Notes   Search   Top
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interact with the 3D model
Picture of molecule
Soluble in:
 alcohol
 water, 1.123e+004 mg/L @ 25 °C (est)
Insoluble in:
 water
Stability:
 alkalis
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