isobutyl methyl ketone
4-methyl-2-pentanone
 
Notes:
Present in orange, lemon, concord grape, vinegar, cheeses, cooked beef, roasted peanut and other foodstuffs. Flavouring ingredient Methyl isobutyl ketone (MIBK) is an organic solvent. MIBK is among the top ten most popular organic solvents used in industry. MIBK is occasionally found as a volatile component of urine. MIBK in urine is considered as a biological marker of occupational exposure to this solvent. Olfactory perception is significant but adaptation may occur. The typical toxicity effects of MIBK in humans exposed at 50 to 100 ppm are mucous membrane irritation and weak effects on the central nervous system (CNS) such as headache. Visual dysfunction has been reported in workers exposed to a mixture of organic solvents containing MIBK. Memory impairment was detected in clinical observation on a 44-year-old man who had been exposed to MIBK at 100 ppm for more than 10 years. Regarding to the route of absorption, skin penetration of MIBK is substantial. (PMID: 12592578, 17485256, 16464817, 5556886)
  • Alfrebro
    • Alfrebro LLC/ Archer Daniels Midland Company
      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):
      4-METHYL-2-PENTANONE NATURAL
       
  • ECSA Chemicals
    • ECSA Chemicals
      Human Chemistry
      ECSA Chemicals has been active since 1913 in the trading and international commerce of raw materials. With an organisation divided into industrial segments managed by specialists, it has become one of the largest distributors worldwide.
      ECSA Chemicals is the largest Swiss-owned company in terms of warehouses for the distribution of chemical products. We have been distributing chemical products for over 100 years and we have a special interest in protecting the environment and in the safety of our facilities and collaborators.
      Established in 1913 as a small grocery store, in its over 100 years of activity ECSA Chemicals has become one of the most important Swiss-owned distributors of chemical products. The company, which is active in international distribution and trading, is organised into industrial segments that are managed by teams of specialists and experts. They guarantee professional and customised consultancy and services. With our experience, we can rapidly and safely connect you with the best suppliers on the market, providing you with a complete search, consulting and assistance service. The focus of our approach and operations is you, our customers. We strive every day to find the best products that satisfy your needs as quickly as possible. Your satisfaction is our greatest success. WHY CHOOSE ECSA? EXPERIENCE We have been working for 100 years. QUALITY We have obtained many certifications (ISO, SQAS, GDP, Responsible Care, Bio-Inspecta, RSPO, etc.). We guarantee full compliance with the current laws and continuous training for our staff. SAFETY We constantly carry out risk analyses for each infrastructure, defining safety levels and implementing corrective measures promptly wherever they are needed. WIDESPREAD DISTRIBUTION We have warehouses in strategic locations to supply goods to Switzerland and to the rest of the world. STORAGE CAPACITY The 3 ECSA-owned warehouses guarantee considerable storage area and capacity in each warehouse, with full availability of products (base chemicals and speciality chemicals). SPEED Presence all over the country, staff dedicated to sourcing raw materials and considerable storage capacity guarantee that goods are rapidly obtained and supplied. CONSULTANCY Our specialists - in-depth knowledge of the market and products allows us to provide full consulting services, from the purchase to the supply of raw materials.
      Email: Info
      Email: Sales
      Email: Trading
      Email: Maintenance
      Email: Energy
      Voice: +41 91 695 88 00
      Fax: +41 91 695 88 01
      Linkedin
      Youtube
      RSS Feed
      ECSA Trade
      ECSA TRADE THE MOST UPDATED FINANCIAL PUBLICATION ON THE WORLD OF CHEMISTRY
      Products List: View
      Product(s):
      MP-010801 METHYL ISOBUTYL KETONE
      RE-461945 METHYL ISOBUTYL KETONE RPE-ACS-FOR ANALYSIS-
       
  • Glentham Life Sciences
  • Moellhausen
  • Pell Wall Perfumes
    • Pell Wall Perfumes
      Hand-made fragrances
      Pell Wall maintains a broad palette of ingredients & in order to keep stocks fresh & the options wide we also sell from our own stock.
      Pell Wall was founded by perfumer Chris Bartlett to provide exclusive hand-made fragrances to a select few people who love them. All our products are created using fine quality ingredients, many of which we also offer for sale to other perfumers and enthusiasts. Pell Wall make fragrances for men, for women and for the home.
      Email: Info
      Email: Sales
      Voice: +44 (0) 20 3745 0887
      Facebook
      Twitter
      Instagram
      Blog
      Product(s):
      Isobutyl Methyl Ketone
      Used to give an ethereal quality to fragrances, add ‘lift’ and is particularly useful where a fruity element is desired, where it can enhance the top note, giving a more juicy effect. Usage level is normally well below 1% of the fragrance concentrate.
       
       
  • 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):
      13-53200 METHYL ISOBUTYL KETONE
      13-53205 METHYL ISOBUTYL KETONE NATURAL
       
  • Sigma-Aldrich
  • TCI AMERICA
    • TCI AMERICA
      Moving Your Chemistry Forward
      We continuously strive to advance our technology.
      With East & West Coast distribution centers, count on TCI to deliver products quickly and reliably. Over 30,000 Reagents available today in benchtop to bulk quantities. We also offer custom synthesis solutions. Sign up for a TCI account today for fast and free shipping!
      Tokyo Chemical Industry Co., Ltd. (TCI) is a leading worldwide manufacturer of specialty organic chemicals founded in 1946. TCI provides organic laboratory chemicals as well as pharmaceutical, cosmetic and functional materials. More than 70 years of synthesis experience and multi-purpose plants enable TCI to offer more than 30,000 products as well as custom synthesis.
      US Email: Sales
      Email: Technical Support
      Voice: 1-800-423-8616
      Fax: 1- 888-520-1075
      Facebook
      Twitter
      Instagram
      Linkedin
      Product(s):
      M0389 4-Methyl-2-pentanone >99.5%(GC)
       
Synonyms   Articles   Notes   Search
CAS Number: 108-10-1Picture of molecule3D/inchi
Other(deleted CASRN): 1338234-91-5
ECHA EINECS - REACH Pre-Reg: 203-550-1
FDA UNII: U5T7B88CNP
Nikkaji Web: J2.861D
Beilstein Number: 0605399
MDL: MFCD00008938
CoE Number: 151
XlogP3: 1.30 (est)
Molecular Weight: 100.16084000
Formula: C6 H12 O
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: cosmetic, flavor and fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Perfumer and Flavorist: Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
JECFA Food Flavoring: 301  4-methyl-2-pentanone
DG SANTE Food Flavourings: 07.017  4-methylpentan-2-one
FEMA Number: 2731 4-methyl-2-pentanone
FDA:No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm (SATF):108-10-1 ; METHYL ISOBUTYL KETONE
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.


FDA PART 172 -- FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION
Subpart I--Multipurpose Additives
Sec. 172.842 Sorbitan monostearate.


FDA PART 175 -- INDIRECT FOOD ADDITIVES: ADHESIVES AND COMPONENTS OF COATINGS
Subpart B--Substances for Use Only as Components of Adhesives
Sec. 175.105 Adhesives.


FDA PART 176 -- INDIRECT FOOD ADDITIVES: PAPER AND PAPERBOARD COMPONENTS
Subpart B--Substances for Use Only as Components of Paper and Paperboard
Sec. 176.180 Components of paper and paperboard in contact with dry food.


FDA PART 176 -- INDIRECT FOOD ADDITIVES: PAPER AND PAPERBOARD COMPONENTS
Subpart B--Substances for Use Only as Components of Paper and Paperboard
Sec. 176.200 Defoaming agents used in coatings.


FDA PART 176 -- INDIRECT FOOD ADDITIVES: PAPER AND PAPERBOARD COMPONENTS
Subpart B--Substances for Use Only as Components of Paper and Paperboard
Sec. 176.210 Defoaming agents used in the manufacture of paper and paperboard.


FDA PART 177 -- INDIRECT FOOD ADDITIVES: POLYMERS
Subpart B--Substances for Use as Basic Components of Single and Repeated Use Food Contact
Sec. 177.1650 Polysulfide polymer-polyepoxy resins.
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance: colorless clear liquid (est)
Assay: 99.00 to 100.00 % 
Food Chemicals Codex Listed: Yes
Specific Gravity: 0.79600 to 0.79900 @  25.00 °C.
Pounds per Gallon - (est).: 6.624 to  6.648
Refractive Index: 1.39100 to 1.39600 @  20.00 °C.
Melting Point: -84.00 °C. @ 760.00 mm Hg
Boiling Point: 116.50 °C. @ 760.00 mm Hg
Acid Value: 2.00 max. KOH/g
Vapor Pressure: 19.900000 mmHg @ 25.00 °C.
Vapor Density: 3.5 ( Air = 1 )
Flash Point: 56.00 °F. TCC ( 13.33 °C. )
logP (o/w): 1.310
Soluble in:
 alcohol
 dipropylene glycol
 water, 1.90E+04 mg/L @ 25 °C (exp)
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: green
 
 sharp  solvent  green  herbal  fruity  dairy  spicy  
Odor Description:
at 10.00 % in dipropylene glycol. 
sharp solvent green herbal fruity dairy spice
 
 sharp  solvent  green  herbal  fruity  dairy  
Odor Description:
Sharp solvent-like with green, herbal, fruity and dairy nuances
Mosciano, Gerard P&F 21, No. 1, 33, (1996)
 
 
Flavor Type: green
 
 green  vegetable  herbal  fruity  dairy  
Taste Description:
Green, vegetative, herbal, fruity and dairy nuances
Mosciano, Gerard P&F 21, No. 1, 33, (1996)
 
Odor and/or flavor descriptions from others (if found).
 
Bedoukian Research
METHYL ISOBUTYL KETONE ≥99.0%, FCC, Kosher, Special Order
Odor Description: A sharp, green, herbal, fruity, spicy aroma
Used for its ethereal quality in fragrances.
Taste Description: green
Used in spice, apple, whiskey, fruit and ripe banana flavors.
 
Alfrebro
4-METHYL-2-PENTANONE NATURAL
Odor Description: Fruity, Ethereal, Spicy
 
Pell Wall Perfumes
Isobutyl Methyl Ketone
Odor Description: Sharp, solvent-like, ethereal, fruity, green. Diffusive
Used to give an ethereal quality to fragrances, add ‘lift’ and is particularly useful where a fruity element is desired, where it can enhance the top note, giving a more juicy effect. Usage level is normally well below 1% of the fragrance concentrate.
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: denaturants
perfuming agents
solvents
Synonyms   Articles   Notes   Search   Top
Suppliers:
Alfrebro
4-METHYL-2-PENTANONE NATURAL
Odor: Fruity, Ethereal, Spicy
Arkema
Methylisobutylketone
Odor: characteristic
Use: MIBK (Methylisobutylketone) is a stable, medium evaporating liquid and compatible with many organic materials, which makes it a good industrial solvent. MIBK can also be used in order to extract, separate and purify various products. It is used in the pharmaceutical, agrochemical industries, in fine chemistry…
Eastman Chemical
Eastman™ Methyl Isobutyl Ketone
Odor: characteristic
Use: Eastman™ Methyl Isobutyl Ketone (MIBK) is a medium-evaporating solvent. It is an active solvent for many synthetic resins including cellulosics, vinyl copolymers, acrylics, alkyds, polyesters, and epoxies. It is very useful in developing high-solids coatings because of its combination of high solvent activity and low density. In addition to its use as a solvent for inks, coatings, and adhesives, MIBK is used as an extraction agent in the dewaxing and deoiling of petroleum products. It is also used in the manufacture of germicides, fungicides, pharmaceuticals, electroplating solutions, and as a denaturant in many ethanol formulations.
ECSA Chemicals
METHYL ISOBUTYL KETONE RPE-ACS-FOR ANALYSIS-
ECSA TRADE THE MOST UPDATED FINANCIAL PUBLICATION ON THE WORLD OF CHEMISTRY
ECSA Chemicals
METHYL ISOBUTYL KETONE
EMD Millipore
For experimental / research use only.
isoButyl Methyl Ketone
Glentham Life Sciences
4-Methyl-2-pentanone
Inoue Perfumery
isoBUTYL METHYL KETONE
Moellhausen
METHYL ISOBUTYL KETONE
Odor: fresh, fruity, somewhat burnt; banana-like with dairy nuance
Pell Wall Perfumes
Isobutyl Methyl Ketone
Odor: Sharp, solvent-like, ethereal, fruity, green. Diffusive
Use: Used to give an ethereal quality to fragrances, add ‘lift’ and is particularly useful where a fruity element is desired, where it can enhance the top note, giving a more juicy effect. Usage level is normally well below 1% of the fragrance concentrate.
Penta International
METHYL ISOBUTYL KETONE NATURAL
Penta International
METHYL ISOBUTYL KETONE
Shiva Chemicals and Pharmaceuticals
Methyl Iso Butyl Ketone (MIBK)
Sigma-Aldrich
4-Methyl-2-pentanone, ≥99%, FCC
Odor: spicy; ethereal; fruity
Certified Food Grade Products
Silver Fern Chemical
Methyl Isobutyl Ketone (MIBK)
Odor: characteristic
Use: Methyl isobutyl ketone is primarily used as a solvent for paints, varnishes, nitrocellulose, lacquers, organic synthesis, and a denaturant for alcohol.
TCI AMERICA
For experimental / research use only.
4-Methyl-2-pentanone >99.5%(GC)
Wedor Corporation
METHYL ISOBUTYL KETONE
Synonyms   Articles   Notes   Search   Top
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xn - Harmful.
R 11 - Highly flammable.
R 20 - Harmful by inhalation.
R 36/37 - Irritating to eyes and respiratory system.
R 66 - Repeated exposure may cause skin dryness or cracking.
S 02 - Keep out of the reach of children.
S 09 - Keep container in a well-ventilated place.
S 16 - Keep away from sources of ignition - No Smoking.
S 29 - Do not empty into drains.
 
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  2080 mg/kg
(Smyth et al., 1951)

oral-mouse LD50  [sex: M] 2670 mg/kg
(Tanii et al., 1986)

oral-mouse LD50  1200 mg/kg
(McOmie & Anderson, 1949a)

intraperitoneal-guinea pig 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. 4748, 1982.

oral-guinea pig LD50  1600 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. 4748, 1982.

unreported-mammal (species unspecified) LD50  1396 mg/kg
Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 51(5), Pg. 61, 1986.

intraperitoneal-mouse LD50  268 mg/kg
Shell Chemical Company. Unpublished Report. Vol. -, Pg. 7, 1961.

oral-mouse LD50  1900 mg/kg
National Technical Information Service. Vol. OTS0535383

intraperitoneal-rat LD50  400 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. 4748, 1982.

oral-rat LD50  2080 mg/kg
Union Carbide Data Sheet. Vol. 4/25/1958

Dermal Toxicity:
skin-rabbit LD50 > 3000 mg/kg
National Technical Information Service. Vol. OTS0535383

Inhalation Toxicity:
inhalation-rat LC50 100000 mg/m3
National Technical Information Service. Vol. OTS0535383

inhalation-mouse LC50 23300 mg/m3
Gigiena Truda i Professional'nye Zabolevaniya. Labor Hygiene and Occupational Diseases. Vol. 17(11), Pg. 52, 1973.

inhalation-guinea pig LCLo 68900 mg/m3/3H
LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES CARDIAC: PULSE RATE SENSE ORGANS AND SPECIAL SENSES: OTHER: EYE
National Technical Information Service. Vol. OTS0535383

inhalation-man TCLo 2290 mg/m3
SENSE ORGANS AND SPECIAL SENSES: OTHER CHANGES: OLFACTION
National Technical Information Service. Vol. OTS0535383

Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
Category: cosmetic, flavor and fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for isobutyl methyl ketone usage levels up to:
  0.5000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 6.10 (μg/capita/day)
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: -6.30000
beverages(nonalcoholic): -6.30000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -6.30000
fruit ices: -6.30000
gelatins / puddings: --
granulated sugar: --
gravies: --
hard candy: -6.30000
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 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 63 (FGE.63): Consideration of aliphatic secondary alcohols, ketones and related esters evaluated by JECFA (59th meeting) structurally related to saturated and unsaturated aliphatic secondary alcohols, ketones and esters of secondary alcohols and saturated linear or branched-chain carboxylic acids evaluated by EFSA in FGE.07 (2005) (Commission Regulation (EC) No 1565/2000 of 18 July 2000)
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
EPA-Iris: IRIS
NIOSH International Chemical Safety Cards: search
NIOSH Pocket Guide: search
Chemical Carcinogenesis Research Information System: Search
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 108-10-1
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 7909
National Institute of Allergy and Infectious Diseases: Data
WISER: UN 1245
WGK Germany: 1
 4-methylpentan-2-one
Chemidplus: 0000108101
EPA/NOAA CAMEO: hazardous materials
RTECS: 108-10-1
Synonyms   Articles   Notes   Search   Top
References:
 4-methylpentan-2-one
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 108-10-1
Pubchem (cid): 7909
Pubchem (sid): 134972890
Pherobase: View
Synonyms   Articles   Notes   Search   Top
Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
FDA Substances Added to Food (formerly EAFUS): View
FDA Indirect Additives used in Food Contact Substances:View
CHEBI: View
CHEMBL: View
KEGG (GenomeNet): C19263
HMDB (The Human Metabolome Database): HMDB02939
FooDB: FDB008174
Export Tariff Code: 2914.19.0000
Typical G.C.
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
No odor group found for these
 tagete oil rwanda 
acidic
2-ethyl butyric acidFL/FR
aldehydic
 agrumen nitrileFR
 dibutyl sulfideFL/FR
 dipropyl disulfideFL/FR
animal
isobutyl quinolineFR
anisic
 amyl furoateFL/FR
 estragoleFL/FR
 ocimum basilicum leaf oil americaFL/FR
balsamic
siam benzoin absoluteFL/FR
 cinnamyl formateFL/FR
christmas pine fragranceFR
bready
 coffee furanoneFL/FR
caramellic
2-isobutyl-3-methyl pyrazineFL/FR
chocolate
2,4,5-trimethyl thiazoleFL/FR
citrus
(Z)-4-decenalFL/FR
isodecyl acetateFR
 methyl heptenoneFL/FR
 ocimene quintoxideFL/FR
coconut
alpha-angelica lactoneFL/FR
coumarinic
 phthalideFL/FR
earthy
 geosminFL/FR
(S)-1-octen-3-olFL/FR
 spathulenol 
ethereal
 butyl acetateFL/FR
 ethyl 4-pentenoateFL/FR
2-methyl valeraldehydeFL/FR
isopropyl formateFL/FR
fatty
2,4-decadien-1-olFL/FR
(E,E)-2,4-decadien-1-olFL/FR
2-octenalFL/FR
(E)-2-octenalFL/FR
floral
isoamyl angelateFL/FR
alpha-amyl cinnamaldehydeFL/FR
 cassis cyclohexeneFR
 cassis oxime 10%FR
 cilantro herb oil egyptFL/FR
 cymbopogon validus leaf oilFR
 dictamnus hispanicus oilFR
 dihydrocitronellyl ethyl etherFR
 dihydrorose oxideFR
 dimethyl benzyl carbinyl butyrateFL/FR
2,4-dimethyl-3-cyclohexene-1-methanolFR
2,4-dimethyl-alpha-allyl-3-cyclohexene methanol 
4,6-dimethyl-alpha-allyl-3-cyclohexene methanol 
 geranium oil africaFL/FR
 geranium oil egyptFL/FR
 jasmin absolute egypt (from concrete)FL/FR
 linden flower absoluteFR
 magnolia flower oil CO2 extractFL/FR
 melaleuca ericifolia leaf oilFR
 menthadienyl formateFR
para-methyl benzyl acetateFL/FR
 methyl benzyl acetate (mixed ortho-,meta-,para-)FL/FR
 neryl formateFL/FR
 nonan-3-yl acetateFL/FR
3-nonanoneFL/FR
2-pentyl cyclopentanoneFR
isophytolFL/FR
 prenyl salicylateFL/FR
 reseda absoluteFR
(Z)-rose oxideFL/FR
 rose pyranFR
5-tricyclodecenyl acetateFR
fruity
isoamyl acetateFL/FR
para-anisyl propionateFL/FR
 balsam specialtyFR
3-butyl bicyclo[3.2.1]-6-octen-2-oneFR
 ethyl 2-ethyl acetoacetateFL/FR
1-ethyl-2-methyl propyl chrysanthemumate 
2-methyl butyl isovalerateFL/FR
2-nonanoneFL/FR
sesquiphellandrene 
 propyl acetateFL/FR
 tropical indeneFR
garlic
4-methyl-2-[2-(methyl thio)ethyl]-1,3-oxathiane 
green
 acetaldehyde butyl phenethyl acetalFL/FR
 agrumen aldehydeFR
 birch leaf specialtyFR
isobutyl heptanoateFL/FR
 butyl heptanoateFL/FR
2-isobutyl thiazoleFL/FR
2-sec-butyl thiazoleFL/FR
S-sec-butyl thioisovalerateFL/FR
 carrot leaf oil (daucus carota ssp.maximus)FR
 chrysanthemum carbaldehydeFR
 cortex pyridineFL/FR
 dicyclopentadiene propionateFR
 galbanum decatrieneFL/FR
 heptanal (aldehyde C-7)FL/FR
1-heptanolFL/FR
 heptyl benzoateFL/FR
 herbal cyclohexaneFR
(Z)-4-hexen-1-olFL/FR
(E)-4-hexen-1-ol 
(Z)-2-hexen-1-olFL/FR
(Z)-3-hexen-1-yl tiglateFL/FR
3-hexenyl 2-methyl butyrateFL/FR
 hexyl hexanoateFL/FR
 hexyl tiglateFL/FR
english ivy leaf absoluteFR
(Z)-leaf acetalFL/FR
 marigold pot absoluteFL/FR
 methyl heptine carbonateFL/FR
6-methyl-3-hepten-2-oneFL/FR
 nerol oxideFL/FR
(Z,Z)-3,6-nonadien-1-olFL/FR
1-penten-3-olFL/FR
3-propyl bicyclo(3.2.1)-6-octen-2-oneFR
 seaweed absolute (fucus vesiculosus et serratus)FL/FR
 terpinyl propionateFL/FR
 triplal / ethyl anthranilate schiff's baseFR
herbal
6-acetoxydihydrotheaspiraneFL/FR
9-acetyl-5-methyl-tricyclo[6.2.1.0.sup.2,7 ]undec-4-ene 
alpha-amyl cinnamyl formateFL/FR
isoamyl heptanoateFL/FR
 anethum graveolens herb oilFL/FR
 anethum graveolens herb tinctureFL/FR
 anthemis nobilis flower extractFL/FR
 anthemis nobilis flower oil romanFL/FR
 apium graveolens seed oilFL/FR
 apium graveolens seed oil indiaFL/FR
 artemisia alba oilFR
 artemisia ludoviciana oilFR
sweet basil absoluteFL/FR
 buchu mercaptan acetateFL/FR
 butyl levulinateFL/FR
3-butylidene phthalideFL/FR
(+)-alpha-campholenic aldehydeFL/FR
 chamomile propionateFR
 chamomile valerateFR
 chrysanthemum ketoneFR
 coriander oleoresinFL/FR
 dill weed oil cubaFL/FR
 dill weed oil reunionFL/FR
 dimethyl benzyl carbinyl crotonateFL/FR
 dimethyl benzyl carbinyl formateFL/FR
2-(2,4-dimethyl-3-cyclohexene-1-yl)-4,4-dimethyl-1,3-oxathianeFR
cis-herbal cyclohexaneFR
 herbal dioxaneFR
 herbal heptaneFR
 hop absoluteFL/FR
 hop oilFL/FR
 lantana camara flower oilFR
 linalyl formateFL/FR
 linalyl octanoateFL/FR
 marigold oil mexicoFL/FR
 melaleuca leucadendron var. cajuputi leaf oilFL/FR
1-para-menthen-9-yl acetateFL/FR
1-(2-methyl allyl oxy) heptaneFR
 methyl hexyl etherFL/FR
(E)-6-methyl-3-hepten-2-oneFL/FR
 mistletoe absolute 
 monarda fistulosa oilFR
 myrtle oilFL/FR
 nonisyl formateFR
(E,Z)-3,5-octadien-2-one 
3-octanon-1-olFL/FR
1-octen-3-yl acetateFL/FR
 oregano specialtyFR
 origanum oilFL/FR
 origanum oil greeceFL/FR
curled parsley seed oilFL/FR
 perilla leaf oilFL/FR
 perillaldehydeFL/FR
 petroselinum crispum seed oil CO2 extractFL/FR
beta-sesquiphellandrene 
 phenyl acetaldehyde diisoamyl acetalFR
 prenyl senecioateFL/FR
3-propylidene phthalideFL/FR
 rosmarinus officinalis extractFL/FR
 rosmarinus officinalis tinctureFL/FR
 rue flower oil colombia 
 rue oilFL/FR
 rue oil cubaFL/FR
 tagete oil CO2 extractFL/FR
 tagete oil egyptFL/FR
 tagete oil south africaFL/FR
 tagete oil turkeyFL/FR
 tagete oil zambiaFL/FR
 theaspiraneFL/FR
 thyme absoluteFL/FR
 tricyclodecenyl isobutyrateFR
 tricyclodecenyl propionateFR
 tricyclodecyl acetateFR
 viridiflorolFL/FR
 wormwood oil americaFL/FR
 wormwood oil italyFL/FR
 wormwood oil polandFL/FR
minty
 carvyl acetateFL/FR
(-)-menthoneFL/FR
(-)-isopulegolFL/FR
mossy
 treemoss absoluteFR
musty
 cocoa butenalFL/FR
orris
 orris capronateFL/FR
soapy
 methyl anthranilate / hexyl cinnamaldehyde schiff's baseFR
spicy
 boldus leaf oilCS
isobutyl angelateFL/FR
trans-carveolFL/FR
(-)-cubenolFL/FR
 cuminaldehydeFL/FR
isocyclogeraniol (IFF)FR
 origanum majorana oilFL/FR
 outdoors specialtyFR
 spicy carbonateFR
3-(methyl thio) hexanolFL/FR
tonka
(±)-dihydromint lactoneFL/FR
waxy
 ethyl laurateFL/FR
2-nonanolFL/FR
woody
 cinnamyl tiglateFL/FR
 dalbergia sissoo leaf oilFR
2-decalinyl acetateFR
alpha-farneseneFL/FR
alpha-farnesene isomerFL/FR
 patchouli absoluteFR
alpha-thujene 
 verdoxanFR
yeasty
2-octen-4-oneFL/FR
 
For Flavor
 
No flavor group found for these
6-acetoxydihydrotheaspiraneFL/FR
4-acetyl-2-isopropenyl pyridineFL
9-acetyl-5-methyl-tricyclo[6.2.1.0.sup.2,7 ]undec-4-ene 
isoamyl angelateFL/FR
alpha-amyl cinnamyl formateFL/FR
 amyl furoateFL/FR
para-anisyl propionateFL/FR
 benzyl methyl tiglateFL
isobutyl heptanoateFL/FR
2-sec-butyl thiazoleFL/FR
4-butyl thiazoleFL
S-sec-butyl thioisovalerateFL/FR
trans-carveolFL/FR
 cinnamyl tiglateFL/FR
(±)-(cis+trans)-1,2-dihydroperillaldehydeFL
 dimethyl benzyl carbinyl crotonateFL/FR
 dimethyl benzyl carbinyl formateFL/FR
 ethyl 4-pentenoateFL/FR
1-ethyl-2-methyl propyl chrysanthemumate 
 fig leaf absoluteFL
 heptyl benzoateFL/FR
(E,E)-2,4-hexadien-1-olFL
 linalyl formateFL/FR
 magnolia flower oil CO2 extractFL/FR
 melaleuca leucadendron var. cajuputi leaf oilFL/FR
 methyl benzyl acetate (mixed ortho-,meta-,para-)FL/FR
4-methyl-2-[2-(methyl thio)ethyl]-1,3-oxathiane 
6-methyl-3-hepten-2-oneFL/FR
(E)-6-methyl-3-hepten-2-oneFL/FR
 mistletoe absolute 
 nonan-3-yl acetateFL/FR
(E,Z)-3,5-octadien-2-one 
3-octanon-1-olFL/FR
(S)-1-octen-3-olFL/FR
2-octenalFL/FR
3-octyl butyrateFL
 perilla leaf oilFL/FR
sesquiphellandrene 
beta-sesquiphellandrene 
 prenyl senecioateFL/FR
2-propyl thiazoleFL
 rue flower oil colombia 
 seaweed absolute (fucus vesiculosus et serratus)FL/FR
 spathulenol 
 tagete oil rwanda 
alpha-thujene 
ortho-vinyl anisoleFL
 viridiflorolFL/FR
 althaea officinalis root tinctureFL
acidic
2-ethyl butyric acidFL/FR
 propionic acidFL
alliaceous
 allyl thiopropionateFL
 dipropyl disulfideFL/FR
celery
3-butylidene phthalideFL/FR
cheesy
2-nonanoneFL/FR
citrus
(Z)-4-decenalFL/FR
cooling
 theaspiraneFL/FR
coumarinic
 phthalideFL/FR
creamy
 althaea officinalis root extractFL
alpha-angelica lactoneFL/FR
earthy
 geosminFL/FR
estery
 propyl acetateFL/FR
ethereal
 butyl acetateFL/FR
 methyl hexyl etherFL/FR
fatty
2,4-decadien-1-olFL/FR
(E,E)-2,4-decadien-1-olFL/FR
(E)-2-octenalFL/FR
floral
 dimethyl benzyl carbinyl butyrateFL/FR
4,6-dimethyl-alpha-allyl-3-cyclohexene methanol 
2,4-dimethyl-alpha-allyl-3-cyclohexene methanol 
 geranium oil africaFL/FR
 geranium oil egyptFL/FR
 jasmin absolute egypt (from concrete)FL/FR
fruity
isoamyl acetateFL/FR
 buchu mercaptan acetateFL/FR
 butyl heptanoateFL/FR
 ethyl 2-ethyl acetoacetateFL/FR
2,4-hexadien-1-olFL
 hexyl hexanoateFL/FR
 linalyl octanoateFL/FR
1-para-menthen-9-yl acetateFL/FR
para-methyl benzyl acetateFL/FR
2-methyl butyl isovalerateFL/FR
 neryl formateFL/FR
isopropyl formateFL/FR
 tagete oil CO2 extractFL/FR
 tagete oil south africaFL/FR
 tagete oil turkeyFL/FR
 tagete oil zambiaFL/FR
green
 acetaldehyde butyl phenethyl acetalFL/FR
 anethum graveolens herb tinctureFL/FR
isobutyl angelateFL/FR
2-isobutyl thiazoleFL/FR
2-isobutyl-3-methyl pyrazineFL/FR
(+)-alpha-campholenic aldehydeFL/FR
 celery distillatesFL
 cocoa butenalFL/FR
 cortex pyridineFL/FR
 dibutyl sulfideFL/FR
 dihydroxyacetophenone (mixed isomers)FL
alpha-farneseneFL/FR
alpha-farnesene isomerFL/FR
 galbanum decatrieneFL/FR
 heptanal (aldehyde C-7)FL/FR
 heptanal 2,3-butane diol acetalFL
(Z)-2-hexen-1-olFL/FR
(Z)-4-hexen-1-olFL/FR
(E)-4-hexen-1-ol 
(Z)-3-hexen-1-yl tiglateFL/FR
3-hexenyl 2-methyl butyrateFL/FR
2-hexyl pyridineFL
 hexyl tiglateFL/FR
 horseradish oilFL
(Z)-leaf acetalFL/FR
 marigold pot absoluteFL/FR
 methyl heptenoneFL/FR
 methyl heptine carbonateFL/FR
4-methyl thiazoleFL
 nerol oxideFL/FR
3-nonanoneFL/FR
 ocimene quintoxideFL/FR
1-octen-3-yl acetateFL/FR
4-penten-1-yl acetateFL
1-penten-3-olFL/FR
3-propylidene phthalideFL/FR
(Z)-rose oxideFL/FR
 terpinyl propionateFL/FR
herbal
isoamyl heptanoateFL/FR
 anethum graveolens herb oilFL/FR
 anthemis nobilis flower extractFL/FR
 anthemis nobilis flower oil romanFL/FR
 apium graveolens seed oilFL/FR
 apium graveolens seed oil indiaFL/FR
sweet basil absoluteFL/FR
 butyl levulinateFL/FR
 celery seed oleoresinFL
 cilantro herb oil egyptFL/FR
 coriander oleoresinFL/FR
 dill weed oil cubaFL/FR
 dill weed oil reunionFL/FR
 hop absoluteFL/FR
 hop oilFL/FR
 ilex paraguariensis leaf extractFL
 marigold oil mexicoFL/FR
 ocimum basilicum leaf oil americaFL/FR
 origanum majorana oilFL/FR
 origanum oilFL/FR
 origanum oil greeceFL/FR
curled parsley seed oilFL/FR
 petroselinum crispum seed oil CO2 extractFL/FR
 prenyl salicylateFL/FR
 rosmarinus officinalis extractFL/FR
 rosmarinus officinalis tinctureFL/FR
 rue oilFL/FR
 rue oil cubaFL/FR
 tagete oil egyptFL/FR
 thyme absoluteFL/FR
 wormwood oil americaFL/FR
 wormwood oil italyFL/FR
 wormwood oil polandFL/FR
lactonic
(±)-dihydromint lactoneFL/FR
licorice
 estragoleFL/FR
metallic
3-(methyl thio) hexanolFL/FR
minty
 carvyl acetateFL/FR
(-)-menthoneFL/FR
(-)-isopulegolFL/FR
nutty
 coffee furanoneFL/FR
2,4,5-trimethyl thiazoleFL/FR
oily
isophytolFL/FR
orris
 orris capronateFL/FR
seafood
1,4-dithianeFL
solvent
1-heptanolFL/FR
 methyl phenyl sulfideFL
spicy
siam benzoin absoluteFL/FR
 cinnamyl formateFL/FR
(-)-cubenolFL/FR
 cuminaldehydeFL/FR
 myrtle oilFL/FR
 perillaldehydeFL/FR
tropical
alpha-amyl cinnamaldehydeFL/FR
vegetable
2-methyl valeraldehydeFL/FR
2-octen-4-oneFL/FR
waxy
 ethyl laurateFL/FR
(Z,Z)-3,6-nonadien-1-olFL/FR
2-nonanolFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 appleFR
 bananaFR
 cherryFR
 creamFR
 dairyFL
 fruitFR
 grapeFR
 greenFR
 herbalFR
 mintFR
 orangeFR
 pearFR
 pineappleFR
 spiceFR
 whiskeyFL
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 beer
Search  PMC Picture
 coffee
Search  PMC Picture
 elder black elder flower oil
Search Trop  Picture
 ginger oil
Search Trop  Picture
 grape
Search Trop  Picture
 lavender oil spike spain @ 0.003%
Data  GC  Search Trop  Picture
 orange fruit
Search Trop  Picture
 strawberry fruit 0.40%
Search Trop  Picture
 tagete oil rwanda @ 0.03%
Data  GC  Search Trop  Picture
 vinegar
Search  Picture
Synonyms   Articles   Notes   Search   Top
Synonyms:
isobutylmethyl ketone
isohexanone
 hexone
 ketone, isobutyl methyl
 methyl 2-methylpropyl ketone
4-methyl 2-pentanone
 methyl iso-butyl ketone
 methyl isobutyl ketone
 methyl isobutyl ketone natural
4-methyl pentan-2-one
2-methyl propyl methyl ketone
4-methyl-2-oxopentane
4-methyl-2-pentanone
2-methyl-4-oxopentane
2-methyl-4-pentanone
 methyl-isobutylketone
4-methyl-pentan-2-one
 methylisobutylketone
4-methylpentan-2-one
2-methylpropyl methyl ketone
 mibk
2-pentanone, 4-methyl-
isopropyl acetone
Synonyms   Articles   Notes   Search   Top
Articles:
Info: Volatile Flavor Components in Bogyojosaeng and Suhong Cultivars of Strawberry (Fragaria ananassa Duch.)
PubMed: The Japan Flavour and Fragrance Materials Association's (JFFMA) safety assessment of acetal food flavouring substances uniquely used in Japan.
PubMed: Influence of manufacturing conditions and crop season on the formation of 4-mercapto-4-methyl-2-pentanone in Japanese green tea (sen-cha).
PubMed: Changes in analytical and volatile compositions of red wines induced by pre-fermentation heat treatment of grapes.
PubMed: Quantification of Polyfunctional Thiols in Wine by HS-SPME-GC-MS Following Extractive Alkylation.
PubMed: Volatile compounds responsible for aroma of Jutrzenka liquer wine.
PubMed: Hydrothermal conversion of bamboo: identification and distribution of the components in solid residue, water-soluble and acetone-soluble fractions.
PubMed: A powerful methodological approach combining headspace solid phase microextraction, mass spectrometry and multivariate analysis for profiling the volatile metabolomic pattern of beer starting raw materials.
PubMed: Influence of volatile thiols in the development of blackcurrant aroma in red wine.
PubMed: Inhalation two-generation reproductive toxicity study of methyl isobutyl ketone in rats.
PubMed: Developmental toxicity evaluation of inhaled methyl isobutyl ketone in Fischer 344 rats and CD-1 mice.
PubMed: Color, lipid oxidation, sensory quality, and aroma compounds of beef steaks displayed under different levels of oxygen in a modified atmosphere package.
PubMed: Sensory and chemical characterisation of the aroma of Prieto Picudo rosé wines: the differential role of autochthonous yeast strains on aroma profiles.
PubMed: Determination of cadmium, copper, and lead in sodium chloride food salts by flame atomic absorption spectroscopy.
PubMed: Determination of semduramicin in poultry feed additive, premixture and compound feed by liquid chromatography and UV spectrophotometric detection after post-column derivatisation.
PubMed: Identification of potent odorants in Japanese green tea (Sen-cha).
PubMed: Screening method for determination of high levels of cadmium, lead, and copper in foods by polarized Zeeman atomic absorption spectrometry using discrete nebulization technique.
PubMed: New factor characterizing the in-mouth release of odorants (volatile thiols): compositional changes in odorants exhaled from the human nose during drinking.
PubMed: Cobalt content of foods and diets in a Spanish population (short communication).
PubMed: Atomic absorption spectrophotometric method for determination of polydimethylsiloxane residues in pineapple juice: collaborative study.
PubMed: Aroma composition changes in early season grapefruit juice produced from thermal concentration.
PubMed: Occurrence of polyfunctional thiols in fresh lager beers.
PubMed: Combinatorial synthesis and sensorial properties of mercapto primary alcohols and analogues.
PubMed: Identification of potent odorants in different green tea varieties using flavor dilution technique.
PubMed: Determination of tin, vanadium, iron, and molybdenum in various matrices by atomic absorption spectrometry using a simultaneous liquid-liquid extraction procedure.
PubMed: Determination of tin in canned fruits and vegetables by atomic absorption spectrometry and liquid-liquid extraction.
PubMed: Atomic absorption spectrophotometric determination of chromium in foods.
PubMed: [Evaluation of heavy metal contamination of potatoes from various regions of Poland].
PubMed: Electrothermal atomic absorption spectrometric determination of selenium in foods and diets.
PubMed: Identification and characterization of bacteria isolated under selective pressure of volatile organic compounds.
PubMed: Quantitative evaluation of sensory irritating and neurobehavioural properties of aliphatic ketones in mice.
PubMed: Multiple microbial activities for volatile organic compounds reduction by biofiltration.
Synonyms   Articles   Notes   Search   Top
Please share your Comments.
Email Address:
 
 
 
 
Top of Page Home
Copyright © 1980-2021 Perflavory ™ Disclaimer Privacy Policy