2-methyl butyraldehyde
2-methylbutyraldehyde
 
Notes:
None found
  • 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
      Newsroom
      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
      News
      Products List: View
      Product(s):
      288 2-METHYL BUTYRALDEHYDE ≥98.0%, FCC, Kosher
      SDS
      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
      News
      Product(s):
      10468 2-Methylbutanal
       
  • Berjé
    • Berje 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
      Flavor Ingredients
      Fragrance Ingredients
      Functional Ingredients
      Happening at Berje
      Product(s):
      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
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      Products List: View
      Product(s):
      METHYLBUTYRALDEHYDE, 2- M0800 FEMA 2691
       
  • 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
      Resources
      History
      Product(s):
      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
      Product(s):
      M0800-2 2-METHYLBUTYRALDEHYDE ≥95.00%, NI, Kosher
      Suggested Uses: Apple, Bakery, Cheese, Chocolate, Coffee, Hard Fruits, Tomato
       
       
  • H. Interdonati, Inc.
  • Jiangyin Healthway
    • Jiangyin Healthway International Trade Co.
      Independent Ingredients Supplier
      We provide custom synthesis and contract manufacturing from milligrams to metric tonnes.
      Jiangyin Healthway International Trade Co., Ltd is a professional company, main engaged in manufacturing and exporting aroma chemicals ,food additives , cosmetic ingredient ,pharmaceutical intermediates & other fine chemicals; especially on aroma chemicals , as the major manufacturer of heterocyclic and sulphur aroma compounds , we are the leading independent ingredients supplier to the flavour and fragrance industries in China, can offer hundreds of different high quality aroma chemicals.
      Email: Info
      Email: Sales
      Voice: 86-510-86023169
      Fax: 86-510-86023170
      Mobile0086-13093133011
      Services
      Biochemical
      Natural Food Colour
      New functional food ingredients
      Product(s):
      HL0545 2-Methyl Butyraldehyde
       
  • 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
      News
      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
      What We Do
      Products List: View
      Product(s):
      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
      Product(s):
      771-2061 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
      Library
      Products List: View
      Product(s):
      NM0500 2-Methylbutyraldehyde, Natural
       
  • Sigma-Aldrich
  • Sunaux International
  • Taytonn
    • TAYTONN PTE LTD
      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
      Product(s):
      2-Methylbutyraldehyde
       
  • 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
      News
      Product(s):
      2-Methylbutyraldehyde
       
  • Vigon International
    • Vigon International, Inc.
      Passion for Simplicity
      Manufacturer and supplier of high quality flavor and fragrance ingredients.
      The growth and success of Vigon is due in large part to a unique corporate concept that Vigon has developed and established within the industry: Creative Partnerships. This partnership concept has been and continues to be the foundation and guiding principle for all of Vigon's activities.
      US Email: Sales
      US Voice: 570-476-6300
      US Fax: 570-476-1110
      Facebook
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      Blog
      Products List: View
      Product(s):
      507961 METHYL-2 BUTYRALDEHYDE
       
Synonyms   Articles   Notes   Search
2-methylbutanal (Click)
CAS Number: 96-17-3Picture of molecule
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
IBM Patents: Obtain
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 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)
Soluble in:
 alcohol
 water, 1.123e+004 mg/L @ 25 °C (est)
Stability:
 alkalis
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
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
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
Charkit Chemical
METHYLBUTYRALDEHYDE, 2- M0800 FEMA 2691
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
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
2-Methylbutyraldehyde Nat
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
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
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)
Treatt
2-Methylbutyraldehyde
Vigon International
METHYL-2 BUTYRALDEHYDE
WEN International
2-METHYLBUTYRALDEHYDE Natural
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
 
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
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
 2-methylbutanal
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: 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
CHEMBL: View
KEGG (GenomeNet): C02223
HMDB (The Human Metabolome Database): HMDB31526
FooDB: FDB008127
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
 
For Odor
No odor group found for these
 sulfuryl octanoateFL/FR
 sulfuryl butyrateFL/FR
 sulfuryl decanoateFL/FR
 sulfuryl hexanoateFL/FR
 sulfuryl isobutyrateFL/FR
 sulfuryl propionateFL/FR
 valeraldehyde dibutyl acetalFL/FR
 valeraldehyde propylene glycol acetalFL/FR
alcoholic
 propyl alcoholFL/FR
 methyl furfuryl disulfideFL/FR
balsamic
2-acetyl furanFL/FR
isoamyl cinnamateFL/FR
 amyl cinnamateFL/FR
 amyl phenyl acetateFL/FR
isoamyl pyruvateFL/FR
 butyl cinnamateFL/FR
 prenyl benzoateFL/FR
 propyl benzoateFL/FR
bready
 coffee furanoneFL/FR
buttery
 acetyl propionylFL/FR
3,4-hexane dioneFL/FR
camphoreous
 bornyl isobutyrateFL/FR
 coffee dioneFL/FR
 cycloteneFL/FR
 ethyl 2-hydroxy-2-methyl butyrateFL/FR
 ethyl cyclopentenoloneFL/FR
 fenugreek oleoresinFL/FR
cereal
 bran absoluteFR
chocolate
isoamyl phenyl acetateFL/FR
isobutyl phenyl acetateFL/FR
 chocolate pyrazine AFL/FR
 cocoa hexenalFL/FR
 cocoa oleoresinFL/FR
 cocoa pentenalFL/FR
2,6-dimethyl pyrazineFL/FR
2,5-dimethyl pyrazineFL/FR
2-methoxypyrazineFL/FR
2,4,5-trimethyl thiazoleFL/FR
cocoa
2-isobutyl-3,5-(and 3,6)-dimethyl pyrazineFL/FR
coconut
alpha-angelica lactoneFL/FR
gamma-heptalactoneFL/FR
coffee
 coffee difuranFL/FR
 furfuryl mercaptanFL/FR
1-hydroxy-2-butanoneFL/FR
2-methyl-3-,5 or 6-(furfuryl thio) pyrazineFL/FR
 popcorn pyrimidineFL/FR
coumarinic
 coumaneFL/FR
 tonka bean resinoidFR
creamy
 butyl lactateFL/FR
2-ethyl-3-methoxypyrazineFL/FR
ethereal
 acetalFL/FR
 decyl propionateFL/FR
 ethyl acetateFL/FR
 ethyl pyruvateFL/FR
1-hexen-3-olFL/FR
(E)-methyl tiglateFL/FR
isopropyl formateFL/FR
 propyl formateFL/FR
fatty
 coconut absoluteFL/FR
fermented
 butyl laevo-lactateFL/FR
 ethyl (E)-2-crotonateFL/FR
3-methyl-1-pentanolFL/FR
 valeraldehydeFL/FR
floral
alpha-amyl cinnamyl acetateFL/FR
 amyl salicylateFL/FR
 boronia butenalFR
para-cresyl laurateFL/FR
 ethyl hydrocinnamateFL/FR
 ethyl phenyl acetateFL/FR
 linalyl propionateFL/FR
fruity
 allyl 2-ethyl butyrateFL/FR
 allyl hexanoateFL/FR
isoamyl nonanoateFL/FR
 berry pentadienoateFL/FR
 butyl acetoacetateFL/FR
isobutyl butyrateFL/FR
 butyl formateFL/FR
 cyclohexanone diethyl acetalFL/FR
 ethyl heptanoateFL/FR
 ethyl propionateFL/FR
 fruity carboxylateFR
 geranyl acetoacetateFL/FR
 geranyl methyl tiglate 
3-hexanoneFL/FR
 methyl propionateFL/FR
 methyl valerateFL/FR
3-methyl-2-butenalFL/FR
2-phenyl propyl butyrateFL/FR
 prenyl formateFL/FR
 tetrahydrofurfuryl acetateFL/FR
 tropical thiazoleFL/FR
green
 butyl 2-methyl butyrateFL/FR
 heptyl acetateFL/FR
2-heptyl furanFL/FR
(E)-2-hexen-1-yl formateFL/FR
(E)-2-hexen-1-yl phenyl acetateFL/FR
(E,Z)-2,6-nonadien-1-yl acetateFL/FR
 phenyl acetaldehydeFL/FR
 tiglaldehydeFL/FR
herbal
white cognac oilFL/FR
 saffron pyranoneFR
 tricyclodecenyl isobutyrateFR
gamma-valerolactoneFL/FR
honey
 allyl phenyl acetateFL/FR
 butyl phenyl acetateFL/FR
 phenyl acetic acidFL/FR
jammy
 ethyl 2-methyl-2-pentenoateFR
malty
S-methyl methioninium chloride 
medicinal
2,6-xylenolFL/FR
musty
2-acetyl pyrroleFL/FR
3-acetyl-2,5-dimethyl furanFL/FR
 cocoa butenalFL/FR
 hazelnut pyrazineFL/FR
 menthofuranFL/FR
naphthyl
para-methyl anisoleFL/FR
ortho-methyl anisoleFL/FR
nutty
3-acetyl pyridineFL/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
3,5-cocoa pyrazineFL/FR
3,6-cocoa pyrazineFL/FR
2,3-dimethyl pyrazineFL/FR
4,5-dimethyl-2-ethyl-3-thiazolineFL/FR
2-ethyl pyrazineFL/FR
2-ethyl-4-methyl thiazoleFL/FR
 filbert heptenoneFL/FR
 filbert pyrazineFL/FR
2,6-lutidineFL/FR
2-methyl pyrazineFL/FR
5-methyl quinoxalineFL/FR
2-methyl thio-3,5 or 6-methyl pyrazineFL/FR
2-methyl-3-(methyl thio) pyrazineFL/FR
2-methyl-3-ethoxypyrazineFL/FR
2-methyl-3-propyl pyrazineFL/FR
 nutty cyclohexenoneFL/FR
 nutty quinoxalineFL/FR
 shoyu pyrazineFL/FR
2,3,5,6-tetramethyl pyrazineFL/FR
2,3,5-trimethyl pyrazineFL/FR
 vinyl sulfurolFL/FR
popcorn
2-acetyl pyrazineFL/FR
2-acetyl thiazoleFL/FR
 fenugreek resinoidFL/FR
spicy
 eugenyl acetateFL/FR
sulfurous
 benzothiazoleFL/FR
 furfuryl thioacetateFL/FR
S-furfuryl thioformateFL/FR
2-methyl 5-(methyl thio) furanFL/FR
tobacco
 veltonal (Bedoukian)FR
tonka
 coumarinFR
 tonka bean absoluteFR
 whiskey lactoneFL/FR
vanilla
 ethyl vanillin isobutyrateFL/FR
 vanillinFL/FR
 vanillyl isobutyrateFL/FR
vegetable
1-furfuryl pyrroleFL/FR
waxy
 ethyl nonanoateFL/FR
 phenethyl octanoateFL/FR
 
For Flavor
 
No flavor group found for these
 acetyl acetaldehyde dimethyl acetalFL
2-acetyl-2-pyrrolineFL
2-acetyl-3-methyl pyrazineFL/FR
 allyl 2-ethyl butyrateFL/FR
 amyl phenyl acetateFL/FR
isoamyl pyruvateFL/FR
 bornyl isobutyrateFL/FR
 butyl 2-methyl butyrateFL/FR
 butyl acetoacetateFL/FR
 butyl cinnamateFL/FR
 butyl formateFL/FR
 butyl mercaptanFL
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
 butyramideFL
 chocolate pyrazine AFL/FR
 chocolate pyrazine BFL
 coumaneFL/FR
 cyclohexanone diethyl acetalFL/FR
 cyclohexyl methyl pyrazineFL
 decyl propionateFL/FR
2,5-diethyl thiazoleFL
2,5-diethyl-4-methyl thiazoleFL
6,7-dihydro-2,3-dimethyl-5H-cyclopentapyrazineFL
 dimethyl dihydrocyclopentapyrazineFL
2,5-dimethyl thiazoleFL
4,5-dimethyl-2-ethyl thiazoleFL
2,5-dimethyl-3-thiofuroyl furanFL
 ethyl 2-hydroxy-2-methyl butyrateFL/FR
 ethyl 3-(furfuryl thio) propionateFL
 ethyl hydrocinnamateFL/FR
2-ethyl-3-methoxypyrazineFL/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
3-(2-furyl) acroleinFL
 geranyl acetoacetateFL/FR
(E,E)-2,4-heptadien-1-olFL
(E)-2-hexen-1-yl phenyl acetateFL/FR
2-hexyl-5 or 6-keto-1,4-dioxaneFL
2-methoxypyrazineFL/FR
 methyl 2-(methyl thio) acetateFL
2-methyl furanFL
 methyl propionateFL/FR
(E)-methyl tiglateFL/FR
2-methyl-3-,5 or 6-(furfuryl thio) pyrazineFL/FR
2-methyl-3-(methyl thio) pyrazineFL/FR
2-methyl-3-ethoxypyrazineFL/FR
 peanut dithiazineFL
 prenyl benzoateFL/FR
 prenyl formateFL/FR
2-propyl pyridineFL
para-salicylic acidFL
 sulfuryl butyrateFL/FR
 sulfuryl decanoateFL/FR
 sulfuryl hexanoateFL/FR
 sulfuryl isobutyrateFL/FR
 valeraldehyde propylene glycol acetalFL/FR
gamma-valerolactoneFL/FR
 sulfuryl formateFL
 sulfuryl octanoateFL/FR
 sulfuryl propionateFL/FR
 valeraldehyde dibutyl acetalFL/FR
alcoholic
 propyl alcoholFL/FR
alliaceous
 benzyl mercaptanFL
 dicyclohexyl disulfideFL
2-methyl thioacetaldehydeFL
 tropical thiazoleFL/FR
aromatic
 amyl salicylateFL/FR
bitter
 methyl ethoxypyrazineFL
bready
2-propionyl thiazoleFL
brown
 fenugreek oleoresinFL/FR
1-hydroxy-2-butanoneFL/FR
 tetrahydrofurfuryl acetateFL/FR
burnt
 furfuryl alcoholFL
2-methyl quinoxalineFL
2,6-xylenolFL/FR
buttery
 butyl laevo-lactateFL/FR
 butyroinFL
3,4-hexane dioneFL/FR
camphoreous
ortho-methyl anisoleFL/FR
caramellic
 caramel furanoneFL
 cycloteneFL/FR
 fenugreek resinoidFL/FR
 pyruvaldehydeFL
chocolate
 cocoa oleoresinFL/FR
 cocoa propanalFL
cocoa
 butyraldehydeFL
 cocoa hexenalFL/FR
coffee
 coffee difuranFL/FR
 coffee dioneFL/FR
 coffee pyrazineFL
 difurfuryl etherFL
 diisoamyl thiomalateFL
2,4-dimethyl thiazoleFL
2-ethyl-4-methyl thiazoleFL/FR
 furfuryl mercaptanFL/FR
 methyl furfuryl disulfideFL/FR
2-isopropyl pyrazineFL
2-thiophene thiolFL
corn chip
2-acetyl thiazoleFL/FR
2-acetyl-2-thiazolineFL
 popcorn pyrimidineFL/FR
creamy
alpha-angelica lactoneFL/FR
dairy
 butyl lactateFL/FR
earthy
alpha-amyl cinnamyl acetateFL/FR
 difurfuryl sulfideFL
1-hexen-3-yl acetateFL
2-methyl-3-propyl pyrazineFL/FR
ethereal
 ethyl acetateFL/FR
fatty
 coconut absoluteFL/FR
(E,E)-2,4-decadienalFL
2-heptyl furanFL/FR
(E,E)-2,4-nonadienalFL
fermented
 methyl thio isovalerateFL
fishy
4,5-dimethyl thiazoleFL
floral
isoamyl cinnamateFL/FR
isoamyl phenyl acetateFL/FR
 cocoa pentenalFL/FR
 linalyl propionateFL/FR
 phenyl acetic acidFL/FR
fruity
 allyl hexanoateFL/FR
 amyl cinnamateFL/FR
 berry pentadienoateFL/FR
isobutyl butyrateFL/FR
 ethyl heptanoateFL/FR
 ethyl propionateFL/FR
 furfuryl propionateFL
 geranyl methyl tiglate 
2,4-hexadien-1-olFL
3-hexanoneFL/FR
 methyl valerateFL/FR
3-methyl-2-butenalFL/FR
 phenethyl octanoateFL/FR
 propyl benzoateFL/FR
isopropyl formateFL/FR
 propyl formateFL/FR
 tiglaldehydeFL/FR
fusel
white cognac oilFL/FR
green
 cocoa butenalFL/FR
 dihydroxyacetophenone (mixed isomers)FL
2,5-dimethyl thiopheneFL
2-ethyl butyraldehydeFL
 heptyl acetateFL/FR
1-hexen-3-olFL/FR
4-methyl thiazoleFL
2-methyl-5-isopropyl pyrazineFL
(E,Z)-2,6-nonadien-1-yl acetateFL/FR
2-vinyl pyrazineFL
honey
 allyl phenyl acetateFL/FR
 butyl phenyl acetateFL/FR
 ethyl phenyl acetateFL/FR
 phenyl acetaldehydeFL/FR
jammy
 ethyl cyclopentenoloneFL/FR
lactonic
gamma-heptalactoneFL/FR
meaty
 benzothiazoleFL/FR
2-methyl 3-(methyl thio) furanFL
mustard
 furfuryl methyl etherFL
musty
2,3-dimethyl pyrazineFL/FR
2,5-dimethyl pyrazineFL/FR
2-ethoxythiazoleFL
 ethyl (E)-2-crotonateFL/FR
 hazelnut pyrazineFL/FR
 menthofuranFL/FR
2-methyl 5-(methyl thio) furanFL/FR
 propionaldehydeFL
 shoyu pyrazineFL/FR
2,3,5-trimethyl pyrazineFL/FR
naphthyl
para-methyl anisoleFL/FR
nutty
 acetalFL/FR
2-acetyl furanFL/FR
3-acetyl pyridineFL/FR
2-acetyl pyrroleFL/FR
5-acetyl-2,3-dihydro-1,4-thiazineFL
3-acetyl-2,5-dimethyl furanFL/FR
2-acetyl-3-ethyl pyrazineFL/FR
2-acetyl-3,5-dimethyl pyrazineFL/FR
2-acetyl-5-methyl furanFL/FR
 aconitic acidFL
3,5-cocoa pyrazineFL/FR
3,5(6)-cocoa pyrazineFL
3,6-cocoa pyrazineFL/FR
 coffee furanoneFL/FR
3,5-diethyl-2-methyl pyrazineFL
2,5-diethyl-3-methyl pyrazineFL
2,6-dimethyl pyrazineFL/FR
4,5-dimethyl-2-ethyl-3-thiazolineFL/FR
2,4-dimethyl-5-vinyl thiazoleFL
2-ethyl pyrazineFL/FR
1-ethyl-2-acetyl pyrroleFL
 filbert heptenoneFL/FR
 filbert pyrazineFL/FR
european hazelnut oleoresinFL
2,6-lutidineFL/FR
2-methyl pyrazineFL/FR
5-methyl quinoxalineFL/FR
2-methyl thio-3,5 or 6-methyl pyrazineFL/FR
 nutty cyclohexenoneFL/FR
 nutty quinoxalineFL/FR
 nutty thiazoleFL
 peanut oxazoleFL
2,3,5,6-tetramethyl pyrazineFL/FR
2,4,5-trimethyl thiazoleFL/FR
 vinyl sulfurolFL/FR
onion
 furfuryl isopropyl sulfideFL
popcorn
2-propionyl-2-thiazolineFL
roasted
2-acetyl pyrazineFL/FR
 furfuryl thioacetateFL/FR
rummy
 ethyl pyruvateFL/FR
(E)-2-hexen-1-yl formateFL/FR
solvent
2-ethyl furanFL
spicy
2-phenyl propyl butyrateFL/FR
sulfurous
 ethyl methyl sulfideFL
S-ethyl thioacetateFL
S-furfuryl thioformateFL/FR
 furfuryl thiopropionateFL
S-methyl methioninium chloride 
2-thienyl mercaptanFL
toasted
 acetyl propionylFL/FR
vanilla
 ethyl vanillin isobutyrateFL/FR
 vanillinFL/FR
 vanillyl isobutyrateFL/FR
vegetable
1-furfuryl pyrroleFL/FR
waxy
para-cresyl laurateFL/FR
 ethyl nonanoateFL/FR
whiskey
3-methyl-1-pentanolFL/FR
winey
isoamyl nonanoateFL/FR
5-ethyl-2-methyl pyridineFL
 valeraldehydeFL/FR
woody
 whiskey lactoneFL/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
Occurrence (nature, food, other): note
 apple fruit
Search  Picture
 bay laurel leaf
Search Trop  Picture
 cardamom
Search Trop  Picture
 cayenne fruit
Search Trop  Picture
 cheese @ 251.00 ± 43 µg%
Data  GC  Search  Picture
 cheese cheddar cheese
Search  Picture
 cheese swiss cheese
Search  Picture
 currant black currant fruit
Search Trop  Picture
 fish
Search  Picture
 grape
Search  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  Picture
 peanut roasted peanut
Search  Picture
 pepper bell pepper fruit
Search Trop  Picture
 plum fruit
Search  Picture
 potato
Search  Picture
 rice cakes
PbMd  Search  Picture
 rum
Search  Picture
 spearmint oil
Search Trop  Picture
 truffle
Search  Picture
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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