2-octanone
  • 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):
      METHYL HEXYL KETONE NATURAL
       
  • Apiscent Labs
    • Apiscent Labs, LLC
      Delivery of Quality
      Custom manufacturer and international supplier of fine ingredients.
      We believe inspired chemistry enriches lives. That's why our team is guided by a mission to provide fine ingredients to the worldwide pharmaceutical, flavor and fragrance markets with a primary focus on the manufacturing of value-added, research-based molecules. We're innovative problem solvers committed to excellence at every phase. Our work builds the foundation for our clients' continued success.
      Email: Info
      Email: Carl Sheeley
      Email: Customer Service
      Voice: +1 (414) 744 3993
      Fax: +1 (414) 744 7111
      Product(s):
      2 OCTANONE
       
  • Axxence Aromatic
    • Axxence Aromatic GmbH
      We bring nature to your flavour
      Dedicated to provide the best possible quality and supply service of natural aroma ingredients.
      Axxence Aromatic is entirely dedicated to provide the best possible quality and supply service of natural aroma ingredients to the Flavour & Fragrance Industry worldwide.
      Email: Service
      Voice: +49.2822.68561.0
      Fax: +49.2822.68561.39
      Products List: View
      Product(s):
      280200 METHYL HEXYL KETONE Natural Kosher
       
  • 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):
      601 METHYL HEXYL KETONE ≥97.5%, FCC, Kosher
      MSDS
      An interesting note for lilac compositions.
      Can be used in mushroom, dairy, apple and beer flavors.
       
       
  • 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):
      Methyl Hexyl Ketone
       
  • Firmenich
    • Firmenich Inc.
      We Create
      We create perfumes and flavors for the World's most desirable brands.
      Firmenich is the largest privately-owned company in the perfume and flavor business. Swiss and family owned, we have created many of the world’s favorite perfumes for over 100 years and produced a number of the most well known flavors we enjoy each day.
      US Email: Fred Keifer
      US Voice: +1 609 452 1000
      US Fax: +1 609 452 6077
      Product(s):
      958910 2-Octanone min. 98%, Kosher

      2-OCTANONE adds nice fruity, blue and parmesan cheese-like notes with mushroom and dairy nuances to dairy, fruit and cooked meat flavors.
       
       
  • fnfsurplus.com
    • fnfsurplus.com
      Surplus Stock Buy & Sell
      Distributors and Traders dealing in Fragrances, Flavors , Aroma Chemicals and Essential oils.
      fnfsurplus.com is online marketplace for surplus of raw materials, finished goods, packaging materials, capital goods and other items of use pertaining to Fragrances and Flavors industry. Our objective is to provide a convenient way to our members for Buying and Selling of surplus and obsolete inventories.
      Email: Nikunj Harlalka
      Email: Ramachandiran Tk
      Voice: +91 22 32545295
      Fax: +91 22 24716502
      Products List: View
      Product(s):
      2-Octanone
       
  • Indukern F&F
  • Lluch Essence
    • Lluch Essence S.L.
      A family company dedicated to sales and distribution
      Flexibility, availability, price and quality.
      Flexibility, availability, price and quality make LLUCH ESSENCE S.L. one of Europe’s references when it comes to essential oils and aroma chemicals, and it is now well known all around the world.
      Email: Info
      Voice: 34 93 379 38 49
      Fax: 34 93 370 65 04
      Product(s):
      METHYL HEXYL KETONE
      METHYL HEXYL KETONE NATURAL
       
  • 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):
      A0402 -METHYL HEXYL KETONE, Kosher
       
  • 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):
      13-51600 METHYL HEXYL KETONE 90, Kosher
      13-51602 METHYL HEXYL KETONE, NATURAL, Kosher
       
  • PerfumersWorld
    • PerfumersWorld Ltd.
      feeeel... the smell!
      The one-stop resource for the creative perfumer.
      No minimum orders. Aroma chemicals, essential oils, isolates, pheremones, absolutes, resinoids, FleuressenceTM key bases, PWx FactorTM, solubilizers, kits, creation systems, workshops, training, distance learning, The PerfumersWorld Perfumer's Studio, The Perfumer’s Formulation Bulletin, perfumery software, bespoke creation, analysis, consultancy, project counselling, trouble-shooting, unperfumed product bases, bottles, smelling strips, scales, distillation, equipment and inspiration!
      Email: Enquiries
      Email: Sales
      Voice: +66(0)2-99-800-80
      Fax: +66(0)2-99-800-80
      PerfumersWorld Skype Skype
      Software: Perfumer's Workbook
      Product(s):
      3LF00299 Methyl hexyl ketone
      Blends-well-with - +2-heptanone Herbaceous-notes
       
       
  • 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):
      W280208 2-Octanone ≥98%, Kosher
      MSDS
       
  • SRS Aromatics
    • SRS Aromatics Ltd
      For over 25 years
      Bringing flavour and fragrance into your world.
      As suppliers / distributors of ingredients to the fragrance and flavour industries, our goal is to provide high quality materials at competitive prices with an exceptional level of service. Established in 1984, SRS Aromatics Ltd is an independent family owned business which has become very well-respected within the fragrance and flavour industry as a reliable and trustworthy partner. Over the years this has allowed the company to develop strong relationships with many global manufacturers; several of whom we represent in the UK. A core aim of our business is to work extremely closely with both our suppliers and customers to maximise service levels with minimum disruption to supply.
      Email: Info
      Email: Sales
      Voice: +44 (0) 1284 704076
      Fax: +44 (0) 1284 760819
      Product(s):
      METHYL HEXYL KETONE
       
  • The John D. Walsh Company
    • The John D. Walsh Company, Inc
      Suppliers Since 1942
      Supplying the fragrance and flavor industry with high quality products.
      The John D. Walsh Company, Inc. has evolved from its beginnings as an agent/broker into a distributor of essential oils, aroma chemicals, concretes and absolutes. We currently represent the following companies, as their North American distributor: Destilerias Munoz Galvez, S.A. International Flavors & Fragrances PFW Aroma Chemicals B.V. Innospec Widnes Limited Hydrodiffusion de Guatemala, S. A. DSM Nutritional Products The John D. Walsh Company, Inc. is proud to be a founding member of IFEAT, an active member of IFRA, North America, and a corporate sponsor of the WFFC.
      Email: Information
      Email: Sales
      Email: Firmenich Flavor inquiries
      Voice: 973-962-1400
      Fax: 973-962-1557
      Firmenich Flavor Phone:973-962-1888
      Firmenich Flavor Fax:973-962-1898
      Product(s):
      Methyl Hexyl Ketone
      MSDS
       
  • 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-Octanone
       
  • Ernesto Ventós
 
Synonyms   Articles   Notes   Search
Fragrance Demo Formulas    Flavor Demo Formulas
octan-2-one (Click)
CAS Number: 111-13-7
ECHA EC Number: 203-837-1
FDA UNII: J2G84H29AF
Beilstein Number: 0635843
MDL: MFCD00009540
FEMA Number: 2802
CoE Number: 153
XlogP3: 2.40 (est)
Molecular Weight: 128.21472000
Formula: C8 H16 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: 288  2-octanone
Flavis Number: 07.019 (Old)
EU SANCO Food Flavourings: 07.019  octan-2-one

FEMA Number: 2802  2-octanone
FDA Mainterm: 2-OCTANONE
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: 95.00 to 100.00 % 
Food Chemicals Codex Listed: Yes
Specific Gravity: 0.81500 to 0.81700 @  25.00 °C.
Pounds per Gallon - (est).: 6.782 to  6.798
Refractive Index: 1.41400 to 1.41700 @  20.00 °C.
Melting Point: -16.00 to  -15.00 °C. @ 760.00 mm Hg
Boiling Point: 173.00 to  175.00 °C. @ 760.00 mm Hg
Boiling Point: 94.00 to  95.00 °C. @ 50.00 mm Hg
Acid Value: 1.00 max. KOH/g
Vapor Pressure: 1.725000 mm/Hg @ 25.00 °C. (est)
Vapor Density: 4.4 ( Air = 1 )
Flash Point: 145.00 °F. TCC ( 62.78 °C. )
logP (o/w): 2.370
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
Odor Type: earthy
Odor Strength: medium ,
recommend smelling in a 10.00 % solution or less
Odor Description:
at 10.00 % in dipropylene glycol. 
earthy weedy natural woody herbal
Odor Description:
Musty, ketonic, bleu and parmesan cheese-like with earthy and dairy nuances
Mosciano, Gerard P&F 21, No. 1, 33, (1996)
Taste Description:
at 10.00 ppm.  
Dairy, waxy, cheese, woody, mushroom and yeast
Mosciano, Gerard P&F 21, No. 1, 33, (1996)
Substantivity: 4 Hour(s)
  
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
Advanced Biotech
2-OCTANONE NATURAL
98% min.
Odor: Camphor, Bitter
Alfrebro
METHYL HEXYL KETONE NATURAL
Odor: Floral, Green, Herbaceous, Fruity
Apiscent Labs
2 OCTANONE
Associate Allied Chemicals
Methyl Hexyl Ketone
Odor: Green, herbaceous, fruity
Augustus Oils
Methyl Hexyl Ketone
Aurochemicals
2-OCTANONE, Natural
Axxence Aromatic
METHYL HEXYL KETONE Natural
Kosher
Bedoukian Research
METHYL HEXYL KETONE
≥97.5%, FCC, Kosher
Odor: sweet, earthy, weedy, 'natural'
Use: An interesting note for lilac compositions.
Flavor: cheesy
Can be used in mushroom, dairy, apple and beer flavors.
Berjé
Methyl Hexyl Ketone
CG Herbals
Methyl Hexyl Ketone
Odor: Pleasant Floral, But Bitter-Green Slightly Musty-Herbaceous
CTC Organics
2-octanone
Ernesto Ventós
METHYL HEXYL KETONE
Odor: GREEN,CAMPHOR,LAVENDER,FATTY
ExtraSynthese
2-Octanone (GC) ≥97.5%
For experimental / research use only.
Firmenich
2-Octanone
min. 98%, Kosher
Flavor: Intense blue cheese, fruity, mushroom and green notes
2-OCTANONE adds nice fruity, blue and parmesan cheese-like notes with mushroom and dairy nuances to dairy, fruit and cooked meat flavors.
fnfsurplus.com
2-Octanone
Global Essence
Methyl hexyl ketone
Indukern F&F
METHYL HEXYL KETONE
Odor: GREEN, HERBAL, FRUITY
Innospec
Laventerre
98% minimum
Inoue Perfumery
HEXYL METHYL KETONE
Kunshan Sainty
2-Octanone, Natural
Lluch Essence
METHYL HEXYL KETONE NATURAL
Lluch Essence
METHYL HEXYL KETONE
M&U International
-METHYL HEXYL KETONE, Kosher
Moellhausen
2-OCTANONE
Nature-identical
Odor: floral, green, herbaceous, fruity
Flavor: cheesy, sharp, ketonic (waxy note)
PCAS
Methyl Hexyl Ketone, Kosher
Penta International
METHYL HEXYL KETONE 90, Kosher
Penta International
METHYL HEXYL KETONE, NATURAL, Kosher
PerfumersWorld
Methyl hexyl ketone
Odor: sweet earthy weedy natural woody herbal green fruity wine floral green herbaceous fruity
Use: Blends-well-with - +2-heptanone Herbaceous-notes
Reincke & Fichtner
2-Octanone
SAFC Global
2-Octanone
≥98%, Kosher
Odor: green; herbaceous; floral; fruity
SRS Aromatics
METHYL HEXYL KETONE
Taytonn
Ketone C-8
Odor: Bitter, Floral, Fruity, Green, Herbal/ Herbaceous, Musk/ Musky
The John D. Walsh Company
Methyl Hexyl Ketone
The Perfumers Apprentice
Methyl Hexyl Ketone
Odor: earthy weedy woody herbal
Treatt
2-Octanone
Synonyms   Articles   Notes   Search   Top
Safety Information:
European information :
Most important hazard(s):
Xn - Harmful.
  R 21 - Harmful in contact with skin.
R 36/37/38 - Irritating to eyes, respiratory system, and skin.
S 02 - Keep out of the reach of children.
S 20/21 - When using do not eat, drink or smoke.
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.
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Human Experience:
 4 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
  oral-rat LD50  > 5000 mg/kg
(Katz et al., 1980)

oral-mouse LD50  [sex: M] 3823 mg/kg
(Tanii et al., 1986)

oral-mouse LD50  3870 mg/kg
(Tanii et al., 1986)

intraperitoneal-mouse LD50  800 mg/kg
"Patty's Industrial Hygiene and Toxicology," 3rd rev. ed., Clayton, G.D., and F.E. Clayton, eds., New York, John Wiley & Sons, Inc., 1978-82. Vol. 3 originally pub. in 1979; pub. as 2n rev. ed. in 1985.Vol. 2C, Pg. 4765, 1982.

oral-mouse LD50  3824 mg/kg
Toxicology Letters. Vol. 30, Pg. 13, 1986.

unreported-mouse LD50  1600 mg/kg
Journal of Medicinal Chemistry. Vol. 19, Pg. 1257, 1976.

intraperitoneal-rat LD50  800 mg/kg
"Patty's Industrial Hygiene and Toxicology," 3rd rev. ed., Clayton, G.D., and F.E. Clayton, eds., New York, John Wiley & Sons, Inc., 1978-82. Vol. 3 originally pub. in 1979; pub. as 2n rev. ed. in 1985.Vol. 2C, Pg. 4765, 1982.

oral-rat LD50  3089 mg/kg
Kodak Company Reports. Vol. #901875

Dermal Toxicity:
  skin-rabbit LD50 1337 mg/kg
Kodak Company Reports. Vol. #901875

Inhalation Toxicity:
  inhalation-rat LC50 2132 ppm/6hours
KODAK*
#901875

inhalation-rat LC50 > 2132 ppm/6H
Kodak Company Reports. Vol. #901875

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Safety in Use Information:
Category: flavor and fragrance agents
Maximised Survey-derived Daily Intakes (MSDI-EU): 93.00 (μg/capita/day)
Recommendation for 2-octanone usage levels up to:
  4.0000 % in the fragrance concentrate.
Recommendation for 2-octanone flavor usage levels up to:
  10.0000 ppm in the finished product.
Synonyms   Articles   Notes   Search   Top
Safety References:
European Food Safety Athority(efsa): Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...
European Food Safety Authority (EFSA) reference(s):
Opinion of the Scientific Panel on food additives, flavourings, processing aids and materials in contact with food (AFC) related to Flavouring Group Evaluation 7 (FGE.07): Saturated and unsaturated aliphatic secondary alcohols, ketones and esters of secondary alcohols and saturated linear or branched-chain carboxylic acids from chemical group 5
View page or View pdf
Flavouring Group Evaluation 7, Revision 1 (FGE.07Rev1): Saturated and unsaturated aliphatic secondary alcohols, ketones and esters of secondary alcohols and saturated linear or branched-chain carboxylic acids from chemical group 5 (Commission Regulation (EC) No 1565/2000 of 18 July 2000) - Scientific opinion of the 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
Flavouring Group Evaluation 7, Revision 2 (FGE.07Rev2) : Saturated and unsaturated aliphatic secondary alcohols, ketones and esters of secondary alcohols and saturated linear or branched-chain carboxylic acids from chemical group 5
View page or View pdf
EPI System: View
Chemicalize.org: Calculate predicted properties
NLM Hazardous Substances Data Bank: Search
Toxicology Citations: Search
Env. Mutagen Info. Center: Search
EPA Substance Registry Services (TSCA): 111-13-7
EPA ACToR: Toxicology Data
National Institute of Allergy and Infectious Diseases: Data
WISER: UN 1224
WGK Germany: 1
 octan-2-one
DTP/NCI: 3712
Chemidplus: 0000111137
RTECS: RH1484000 for cas# 111-13-7
Synonyms   Articles   Notes   Search   Top
References:
 octan-2-one
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 111-13-7
Pubchem (cid): 8093
Pubchem (sid): 134974863
Flavornet: 111-13-7
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
CHEMBL: View
Export Tariff Code: 2914.19.0000
Haz-Map: View
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Formulations/Preparations:
assay: 98% minimum
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 acetoin butyrateFL
 acetyl propionylFL/FR
 butyl butyryl lactateFL/FR
 butyric acidFL/FR
isobutyric acidFL/FR
 cyclohexyl acetic acidFL/FR
 cyclohexyl carboxylic acidFL/FR
2,4-dimethyl-2-pentenoic acidFL
 ethyl cyclohexyl carboxylateFL
 filbert hexenoneFL/FR
(E,E)-2,4-heptadien-1-olFL
2,3-heptane dioneFL/FR
4-heptanoneFL/FR
 herbal ketoneFR
 hexanoic acidFL/FR
(E)-2-hexenalFL/FR
(Z)-3-hexenoic acidFL
2-methyl 3-(methyl thio) furanFL
 methyl 4-(methyl thio) butyrateFL
 methyl 4-methyl valerateFL/FR
2-methyl butyl isovalerateFL/FR
2-methyl butyric acidFL/FR
2-methyl heptanoic acidFL/FR
2-methyl hexanoic acidFL/FR
5-methyl hexanoic acidFL
 methyl thio isovalerateFL
S-(methyl thio) butyrateFL/FR
2-methyl valeric acidFL/FR
3-methyl valeric acidFL
4-methyl valeric acidFL
2-methyl-2-hexenoic acidFR
2-methyl-4-pentenoic acidFL
 nonanoic acidFL/FR
2-nonanolFL/FR
2-nonanoneFL/FR
 nutty quinoxalineFL/FR
(E)-2-octenoic acidFL
 patchouli oilFL/FR
(E)-2-pentenoic acidFL
4-pentenoic acidFL
 prenyl hexanoateFL/FR
 sorbyl butyrateFL/FR
 undecanoic acidFL/FR
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 appleFR
 apricotFR
 bananaFR
 beerFL
 carawayFL/FR
 cheese blueFL
 cheese cheddarFL
 citrusFR
 coconutFR
 fern fougereFR
 floralFR
 fungus mushroomFR
 hay new mown hay foin coupeFR
 lavenderFR
 lilac lilas syringaFR
 milkFL
 peachFR
 plumFR
 reseda mignonetteFR
Synonyms   Articles   Notes   Search   Top
Natural Occurrence in: note
 banana
 beer
 butter
 cocoa
GRIN Trop Picture
 lavandin oil china @ 1.18%
Data  GC  GRIN Trop Picture
 mushroom
 osmanthus absolute @ trace%
Data  GC  GRIN Trop Picture
 peanut roasted peanut
 potato chip
 rue flower oil colombia @ 0.18%
Data  GC  GRIN Trop Picture
 rue oil china @ 0.24%
Data  GC  GRIN Trop Picture
 rue plant
GRIN Trop Picture
 yogurt
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Synonyms:
 hexyl methyl ketone
N-hexyl methyl ketone
 ketone, hexyl methyl
 laventerre
 methyl hexyl cetone
 methyl hexyl ketone
 methyl hexyl ketone 90
 methyl hexyl ketone, natural
 methyl N-hexyl ketone
 octan-2-one
2-oxooctane
 octane-2-one
2-octanon
2-octanone
2-octanone natural
Synonyms   Articles   Notes   Search   Top
Articles:
US Patents: 3,952,024 - Furfurylthioacetone
PubMed: Binding of carbonyl flavours to canola, pea and wheat proteins using GC/MS approach.
US Patents: 3,931,166 - Certain 2,5-dimethyl-3-thiopyrazines
PubMed: Communication: Coordination structure of bromide ions associated with hexyltrimethylammonium cations at liquid/liquid interfaces under potentiostatic control as studied by total-reflection X-ray absorption fine structure.
PubMed: Olfactory Sensitivity and Odor Structure-Activity Relationships for Aliphatic Ketones in CD-1 Mice.
PubMed: Characterization of aroma compounds of Chinese famous liquors by gas chromatography-mass spectrometry and flash GC electronic-nose.
PubMed: Brushed block copolymer micelles with pH-sensitive pendant groups for controlled drug delivery.
PubMed: Mass and Ion Transport in Ketones and Ketone Electrolytes: Comparison with Acetate Systems.
PubMed: Formation yields of C8 1,4-hydroxycarbonyls from OH + n-octane in the presence of NO.
PubMed: Brain phospholipase C, diacylglycerol lipase and monoacylglycerol lipase are involved in (±)-epibatidine-induced activation of central adrenomedullary outflow in rats.
PubMed: Analysis of quinolones by voltage-assisted liquid-phase microextraction combined with LC-MS.
PubMed: Fragrance material review on methyl hexyl oxo cyclopentanone carboxylate.
PubMed: Color, lipid oxidation, sensory quality, and aroma compounds of beef steaks displayed under different levels of oxygen in a modified atmosphere package.
PubMed: Electromembrane extraction of peptides--fundamental studies on the supported liquid membrane.
PubMed: Evaluation of parallel milliliter-scale stirred-tank bioreactors for the study of biphasic whole-cell biocatalysis with ionic liquids.
PubMed: Evaluation of the use of Syzygium cumini fruit extract as an antioxidant additive in orange juice and its sensorial impact.
PubMed: Controlling the facial selectivity of asymmetric [4+2] cyclo-additions: a concise synthesis of the cis-decalin core structure of superstolides A and B.
PubMed: Thermodynamics and activity coefficients at infinite dilution measurements for organic solutes and water in the ionic liquid N-hexyl-3-methylpyridinium tosylate.
PubMed: Comparison of volatile components in Chinese traditional pickled peppers using HS-SPME-GC-MS, GC-O and multivariate analysis.
PubMed: Solvent free oxidation of primary alcohols and diols using thymine iron(III) catalyst.
PubMed: Novel aspect of ketone action: β-hydroxybutyrate increases brain synthesis of kynurenic acid in vitro.
PubMed: Isolation and characterization of 4-tert-butylphenol-utilizing Sphingobium fuliginis strains from Phragmites australis rhizosphere sediment.
PubMed: Neurotoxicity of fungal volatile organic compounds in Drosophila melanogaster.
PubMed: Prolonged stimulus exposure reveals prolonged neurobehavioral response patterns.
PubMed: Hollow fiber-liquid-phase microextraction of fungicides from orange juices.
PubMed: Asymmetric [4+2] cycloadditions employing 1,3-dienes derived from (R)-4-t-butyldimethyl-silyloxy-2-cyclohexen-1-one.
PubMed: Purification and characterization of an anti-Prelog alcohol dehydrogenase from Oenococcus oeni that reduces 2-octanone to (R)-2-octanol.
PubMed: Widespread occurrence of estrogenic UV-filters in aquatic ecosystems in Switzerland.
PubMed: Ionic liquid based dispersive liquid-liquid microextraction for the extraction of pesticides from bananas.
PubMed: Gas chromatography-olfactometry analysis of the volatile compounds of two commercial Irish beef meats.
PubMed: Selective three-phase liquid phase microextraction of acidic compounds from foodstuff simulants.
PubMed: Chemical characterization of territorial marking fluid of male Bengal tiger, Panthera tigris.
PubMed: Templation of the excited-state chemistry of alpha-(n-alkyl) dibenzyl ketones: how guest packing within a nanoscale supramolecular capsule influences photochemistry.
PubMed: Optimization of chlorophyllase-catalyzed hydrolysis of chlorophyll in monophasic organic solvent media.
PubMed: Kinetic analysis of volatile formation in milk subjected to pressure-assisted thermal treatments.
PubMed: Glial-cytokine-neuronal interactions underlying the mechanisms of persistent pain.
PubMed: Purification, characterization, and gene cloning of glycerol dehydrogenase from Hansenula ofunaensis, and its expression for production of optically active diol.
PubMed: Anti-prelog reduction of prochiral carbonyl compounds by Oenococcus oeni in a biphasic system.
PubMed: Chemical boundaries for detection of eye irritation in humans from homologous vapors.
PubMed: Dominant role for calpain in thromboxane-induced neuromicrovascular endothelial cytotoxicity.
PubMed: Stability of immobilized soybean lipoxygenase in selected organic solvent media.
PubMed: Stereoselective synthesis of c3-c12 dihydropyran portion of antitumor laulimalide using copper-catalyzed oxonium ylide formation-[2,3] shift.
PubMed: 1,4-hydroxycarbonyl products of the OH radical initiated reactions of C5-C8 n-alkanes in the presence of NO.
PubMed: Bis{1-n-hexyl-3-methyl-4-[1-(phenylimino)propyl]-1H-pyrazol-5-olato}copper(II): a new copper(II) complex with a chelating alkylpyrazolone-based enamine.
PubMed: Characterization of French and Spanish dry-cured hams: influence of the volatiles from the muscles and the subcutaneous fat quantified by SPME-GC.
PubMed: Designing the "search pathway" in the development of a new class of highly efficient stereoselective hydrosilylation catalysts.
PubMed: High-yield conversion of (R)-2-octanol from the corresponding racemate by stereoinversion using Candida rugosa.
PubMed: Bimetallic isopropoxides M[Al(OC(3)H(i)(7))(4)](3) (M = Pr, Nd)--catalyzed reduction of 2-octanone and benzophenone.
PubMed: Controlled production of Camembert-type cheeses. Part II. Changes in the concentration of the more volatile compounds.
PubMed: Use of an ionic liquid in a two-phase system to improve an alcohol dehydrogenase catalysed reduction.
PubMed: Expression of adhesion molecules by sphingosine 1-phosphate and histamine in endothelial cells.
PubMed: Volatiles in a sausage surface model-influence of Penicillium nalgiovense, Pediococcus pentosaceus, ascorbate, nitrate and temperature.
PubMed: An efficient direct alpha-alkylation of ketones with primary alcohols catalyzed by [Ir(cod)Cl]2/PPh3/KOH system without solvent.
PubMed: Analysis of ketones by selected ion flow tube mass spectrometry.
PubMed: Synthesis of (4R,6S,7R)-7-hydroxy-4,6-dimethyl-3-nonanone and (3R,5S,6R)- 6-hydroxy-3,5-dimethyl-2-octanone, the pheromone components of the bostrychid beetle, Dinoderus bifoveolatus.
PubMed: Associative learning of complex odours in parasitoid host location.
PubMed: Relationship between molecular structure, concentration and odor qualities of oxygenated aliphatic molecules.
PubMed: Chlorpromazine inhibits the glucocorticoid receptor-mediated gene transcription in a calcium-dependent manner.
PubMed: Aroma active components in aqueous kiwi fruit essence and kiwi fruit puree by GC-MS and multidimensional GC/GC-O.
PubMed: Influence of lipid fraction, emulsifier fraction, and mean particle diameter of oil-in-water emulsions on the release of 20 aroma compounds.
PubMed: Selective Oxidation of Vinyl Ethers and Silyl Enol Ethers with Hydrogen Peroxide Catalyzed by Peroxotungstophosphate.
PubMed: An enantiospecific approach to tricyclic sesquiterpenes mayurone and thujopsenes.
PubMed: Asymmetric reduction of ketones with catecholborane using 2,6-BODOL complexes of titanium(IV) as catalysts.
PubMed: Interactions between artificial saliva and 20 aroma compounds in water and oil model systems.
PubMed: Signalling mechanisms underlying the myogenic response in human subcutaneous resistance arteries.
PubMed: Efficient oxidation of alcohols to carbonyl compounds with molecular oxygen catalyzed by N-hydroxyphthalimide combined with a Co species
PubMed: Interactions between methyl ketones and beta-lactoglobulin: sensory analysis, headspace analysis, and mathematical modeling.
PubMed: Blocking and the detection of odor components in blends.
PubMed: Interactions of flavor compounds with pectic substances.
PubMed: Oxidative cleavage of the octyl side chain of 1-(3,4-dichlorobenzyl)-5-octylbiguanide (OPB-2045) in rat and dog liver preparations.
PubMed: Effect of aeration during cell growth on ketone reactions by immobilized yeast.
PubMed: Interactions between aroma and edible films. 1. Permeability Of methylcellulose and low-density polyethylene films to methyl ketones.
PubMed: Solvent-modified solid-phase microextraction for the determination of diazepam in human plasma samples by capillary gas chromatography.
PubMed: An analysis of blocking in odorant mixtures: an increase but not a decrease in intensity of reinforcement produces unblocking.
PubMed: Neighboring Group Participation in a Regio- and Stereoselective Chlorination of a Bicyclo[2.2.2]octanone.
PubMed: Enhanced sensitivity to androstenone following regular exposure to pemenone.
PubMed: Effects of solvation on partition and dimerization of benzoic acid in mixed solvent systems.
PubMed: Ketone EC50 values in the Microtox test.
PubMed: Structure, stereochemistry, and thermal isomerization of the male sex pheromone of the longhorn beetle Anaglyptus subfasciatus.
PubMed: Immiscible organic solvent inactivation of urease, chymotrypsin, lipase, and ribonuclease: separation of dissolved solvent and interfacial effects.
PubMed: Juvenile hormone esterase purified by affinity chromatography with 8-mercapto-1,1,1-trifluoro-2-octanone as a rationally designed ligand.
PubMed: Sensory irritation and pulmonary irritation of n-methyl ketones: receptor activation mechanisms and relationships with threshold limit values.
PubMed: Effect of some metallic cations and organic compounds on the O-hexyl O-2,5-dichlorophenyl phosphoramidate hydrolysing activity in hen plasma.
PubMed: Competitive inhibition of lipolytic enzymes. VII. The interaction of pancreatic phospholipase A2 with micellar lipid/water interfaces of competitive inhibitors.
PubMed: Electroantennogram response of alfalfa seed chalcid,Bruchophagus roddi (Hymenoptera: Eurytomidae) to host- and nonhost-plant volatiles.
PubMed: Antidopaminergic effects of the stereoisomers of N-[(1-alkyl-2- pyrrolidinyl)methyl]-5-sulfamoylbenzamides and -2,3-dihydrobenzofuran-7-carboxamides.
PubMed: Inhibition of cathepsin B and papain by peptidyl alpha-keto esters, alpha-keto amides, alpha-diketones, and alpha-keto acids.
PubMed: Volatile methyl ketone seed-germination inhibitors fromAmaranthus palmeri S. Wats. Residues.
PubMed: Experimental study on the enhancement of the neurotoxicity of methyl n-butyl ketone by non-neurotoxic aliphatic monoketones.
PubMed: Neurophysiological studies on the relation between the structural properties and neurotoxicity of aliphatic hydrocarbon compounds in rats.
PubMed: Volatile constituents of wolf (Canis lupus) urine as related to gender and season.
PubMed: Further studies on ketone neurotoxicity and interactions.
PubMed: [An experimental study on the neurotoxicity of 2-octanone and 2-hexanol, a metabolite of n-hexane].
PubMed: Commercial-grade methyl heptyl ketone (5-methyl-2-octanone) neurotoxicity: contribution of 5-nonanone.
PubMed: Gas-chromatographic resolution of enantiomeric secondary alcohols. Stereoselective reductive metabolism of ketones in rabbit-liver cytosol.
PubMed: Cycloalkanones. 9. Comparison of analogues which inhibit cholesterol and fatty acid synthesis.
PubMed: Cycloalkanones. 7. Hypocholesterolemic activity of aliphatic compounds related to 2,8-dibenzylcyclooctanone.
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Soluble in:
 alcohol
 water, 900 mg/L @ 20 °C (exp)
Insoluble in:
 water
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