2-methyl butyl 2-methyl butyrate
2-methylbutyl 2-methylbutyrate
 
Notes:
Flavouring ingredient. Present in essential oil of hops (Humulus lupulus) and odorous component of grapes Vaccinium vitis-idaea
  • 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-METHYLBUTYL-D-2-METHYLBUTYRATE NATURAL
       
  • 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):
      W1817 2-methylbutyl-2-methyl butyrate
       
  • ECSA Chemicals
    • ECSA Chemicals
      International trading and distribution
      ECSA Group offers its customers in these business segments a complete 'one-stop shopping' solution.
      A hundred years on from its establishment, the Emanuele Centonze Holding SA has developed a solid presence in Switzerland and in Europe. The Group currently includes: ECSA Chemicals AG/ECSA Italia SRL SocietÓ con Unico Socio – ECSA Maintenance AG – ECSA Energy SA – Porta Ticino Easy Stop SA. The Group operates in the distribution of chemical and petroleum products, in the international trading of commodities, and in the distribution of maintenance systems. With 285 employees, a consolidated turnover of 335 million Swiss Francs in 2015, and more than 15,000 active customers, the Group ranks among the top 500 companies in Switzerland. ECSA operates in Switzerland and the EU, and in particular has consolidated its geographical position on the main axis linking northern and southern Europe, thus creating a competitive and privileged logistical hub.
      Email: Info
      Email: Sales
      Email: Trading
      Email: Maintenance
      Email: Energy
      Voice: +41 91 695 88 00
      Fax: +41 91 695 88 01
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      Company Profile
      Products List: View
      Product(s):
      Methyl-2-butylmethyl Butyrate
       
  • 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
      Linkedin
      Product(s):
      2-METHYL BUTYL 2-METHYL BUTYRATE
       
  • 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):
      N0095 NAT.2-METHYLBUTYL 2-METHYLBUTYRATE, Kosher
      N0096 NAT.D-2-METHYLBUTYL 2-METHYLBUTYRATE, Kosher
       
  • Penta International
  • 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
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      Software: Perfumer's Workbook
      Product(s):
      4FD00001 2-Methylbutyl 2-Methylbutyrate
       
  • Sigma-Aldrich
  • 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
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      Product(s):
      METHYL 2 BUTYL 2 METHYL BUTYRATE
       
  • Sunaux International
Synonyms   Articles   Notes   Search
2-methylbutyl 2-methylbutanoate (Click)
CAS Number: 2445-78-5Picture of molecule
% from: 90.00% to 95.00%
ECHA EINECS - REACH Pre-Reg: 219-497-2
FDA UNII: HYC739X7BP
Nikkaji Web: J102.392F
MDL: MFCD00059395
CoE Number: 10773
XlogP3-AA: 3.20 (est)
Molecular Weight: 172.26780000
Formula: C10 H20 O2
NMR Predictor: Predict (works with chrome or firefox)
Also(can) Contains: 2-methyl butyl isovalerate 5.00% to 10.00%
EFSA/JECFA Comments: At least 90%; secondary component 5-7% 2-methylbutyl 3-methylbutyrate. (JECFA) (R) or (S) enantiomer not specified by CASrn in Register.
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: 212  2-methylbutyl 2-methylbutyrate
Flavis Number: 09.516 (Old)
DG SANTE Food Flavourings: 09.516  2-methylbutyl 2-methylbutyrate
FEMA Number: 3359  2-methylbutyl 2-methylbutyrate
FDA Mainterm: 2-METHYLBUTYL 2-METHYLBUTYRATE
Synonyms   Articles   Notes   Search   Top
Physical Properties:
Appearance: colorless to pale yellow clear liquid (est)
Assay: 90.00 to 100.00 % 
Additional Assay Information: 2-methylbutyl isovalerate 5% - 10%
Food Chemicals Codex Listed: No
Specific Gravity: 0.84700 to 0.85600 @  25.00 °C.
Pounds per Gallon - (est).: 7.048 to  7.123
Refractive Index: 1.40100 to 1.42000 @  20.00 °C.
Boiling Point: 70.00 to  72.00 °C. @ 11.00 mm Hg
Boiling Point: 184.00 to  187.00 °C. @ 760.00 mm Hg
Vapor Pressure: 0.713000 mm/Hg @ 25.00 °C. (est)
Flash Point: 153.00 °F. TCC ( 67.22 °C. )
logP (o/w): 3.530 (est)
Soluble in:
 alcohol
 water, 44.59 mg/L @ 25 °C (est)
Insoluble in:
 water
Similar Items: note
isoamyl 2-methyl butyrate
amyl 2-methyl butyrate
benzyl 2-methyl butyrate
bornyl 2-methyl butyrate
butyl 2-methyl butyrate
isobutyl 2-methyl butyrate
citronellyl 2-methyl butyrate
ethyl 2-hydroxy-2-methyl butyrate
(±)-ethyl 3-acetoxy-2-methyl butyrate
(±)-ethyl 3-hydroxy-2-methyl butyrate
ethyl 2-methyl butyrate
furfuryl 2-methyl butyrate
geranyl 2-methyl butyrate
heptyl 2-methyl butyrate
(E)-2-hexen-1-yl 2-methyl butyrate
(Z)-3-hexen-1-yl 2-methyl butyrate
3-hexen-1-yl 2-methyl butyrate
hexyl 2-methyl butyrate
methyl 3-acetoxy-2-methyl butyrate
methyl 2-methyl butyrate
octyl 2-methyl butyrate
propyl 2-methyl butyrate
isopropyl 2-methyl butyrate
propylene glycol di-2-methyl butyrate
propylene glycol mono-2-methyl butyrate
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
Odor Type: fruity
Odor Strength: medium ,
recommend smelling in a 10.00 % solution or less
 sweet  fruity  estery  berry  green  waxy  apple  
Odor Description:
at 10.00 % in dipropylene glycol. 
sweet fruity ester berry green waxy apple
 sweet  fruity  estery  green  waxy  
Odor Description:
Sweet, fruity, estry, with green waxy nuances
Mosciano, Gerard P&F 15, No. 3, 51, (1990)
 sweet  fruity  pineapple  green  waxy  woody  
Taste Description:
at 30.00 ppm.  
Sweet, fruity, pineapple character with green, waxy and woody nuances
Mosciano, Gerard P&F 15, No. 3, 51, (1990)
  
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
None found
Synonyms   Articles   Notes   Search   Top
Suppliers:
Alfrebro
2-METHYLBUTYL-D-2-METHYLBUTYRATE NATURAL
Odor: Fruity, Floral
Apple Flavor & Fragrance
2-Methylbutyl 2-methylbutyrate
CTC Organics
2-methylbutyl-2-methyl butyrate
ECSA Chemicals
Methyl-2-butylmethyl Butyrate
Company Profile
Grau Aromatics
METHYL-2-BUTYL-2-METHYLBUTYRATE
NI, Kosher
Inoue Perfumery
2-METHYL BUTYL 2-METHYL BUTYRATE
Kunshan Sainty
2-Methylbutyl 2-methylbutyrate, Natural
Kunshan Sainty
D-2-Methylbutyl 2-methylbutyrate, Natural
Lluch Essence
2-METHYL BUTYL 2-METHYL BUTYRATE
M&U International
NAT.2-METHYLBUTYL 2-METHYLBUTYRATE, Kosher
M&U International
NAT.D-2-METHYLBUTYL 2-METHYLBUTYRATE, Kosher
Mane
2-methyl butyl 2-methyl butyrate
Penta International
2-METHYLBUTYL-2-METHYL BUTYRATE, Kosher
Penta International
2-METHYLBUTYL-2-METHYL BUTYRATE, NATURAL, Kosher
PerfumersWorld
2-Methylbutyl 2-Methylbutyrate
Odor: sweet fruity ester green waxy sweet fruity fatty pineapple green waxy
Shanghai Vigen Fine Chemical
2-Methylbutyl 2-Methylbutyrate
Sigma-Aldrich
2-Methylbutyl 2-methylbutyrate, ≥95%, FG
Odor: apple
Certified Food Grade Products
Sigma-Aldrich
2-Methylbutyl 2-methylbutyrate, natural, ≥98%, FG
SRS Aromatics
METHYL 2 BUTYL 2 METHYL BUTYRATE
Sunaux International
nat.2-Methylbutyl 2-methylbutyrate
Sunaux International
nat.D-2-Methylbutyl 2-methylbutyrate
TCI AMERICA
For experimental / research use only.
2-Methylbutyl DL-2-Methylbutyrate >97.0%(GC)
Ungerer & Company
Methyl Butyl (2) 2 Methyl Butyrate
WEN International
2-METHYLBUTYL-2-METHYLBUTYRATE Natural
Synonyms   Articles   Notes   Search   Top
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
N - Dangerous for the environment.
R 51/53 - Toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment.
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:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
Synonyms   Articles   Notes   Search   Top
Safety in Use Information:
Category: flavor and fragrance agents
Recommendation for 2-methyl butyl 2-methyl butyrate usage levels up to:
  5.0000 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 3.00 (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: 6
Click here to view publication 6
 average usual ppmaverage maximum ppm
baked goods: -8.00000
beverages(nonalcoholic): -5.00000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -5.00000
fruit ices: -5.00000
gelatins / puddings: -5.00000
granulated sugar: --
gravies: --
hard candy: -8.00000
imitation dairy: --
instant coffee / tea: --
jams / jellies: -5.00000
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):
Flavouring Group Evaluation 1, Revision 1 (FGE.01Rev 1): Branched-chain aliphatic saturated aldehydes, carboxylic acids and related esters of primary alcohols and branched-chain carboxylic acids from chemical groups 1 and 2 (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 01 Rev2 (FGE.01 Rev2): Branched-chain aliphatic saturated aldehydes, carboxylic acids and related esters of primary alcohols and branched-chain carboxylic acids from chemical groups 1 and 2
View page or View pdf
EPI System: View
EPA Substance Registry Services (TSCA): 2445-78-5
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 17129
National Institute of Allergy and Infectious Diseases: Data
WISER: UN 3082
WGK Germany: 3
 2-methylbutyl 2-methylbutanoate
Chemidplus: 0002445785
Synonyms   Articles   Notes   Search   Top
References:
 2-methylbutyl 2-methylbutanoate
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 2445-78-5
Pubchem (cid): 17129
Pubchem (sid): 134981921
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
HMDB (The Human Metabolome Database): HMDB39218
FooDB: FDB018750
Export Tariff Code: 2915.60.5000
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: 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
(E)-5-nonen-2-oneFL/FR
aldehydic
 lily pentanalFR
2-methyl undecanal dimethyl acetalFR
alliaceous
 methyl furfuryl disulfideFL/FR
amber
 ambrette seed absoluteFL/FR
balsamic
isoamyl benzoateFL/FR
caramellic
 maltyl isobutyrateFL/FR
citrus
(E)-2-tetradecenalFL/FR
creamy
3-heptyl dihydro-5-methyl-2(3H)-furanoneFL/FR
ethereal
 propyl formateFL/FR
fatty
 allyl octanoateFL/FR
(E)-2-octenalFL/FR
floral
alpha-damasconeFL/FR
 geranyl acetateFL/FR
 hexyl 2-furoateFL/FR
 hydroxycitronellalFL/FR
 hydroxycitronellal dimethyl acetalFL/FR
beta-iononeFL/FR
 jasmin cyclopentanolFR
 nerolin fragarolFL/FR
 rose carboxylateFR
fruity
 allyl butyrateFL/FR
 allyl cyclohexyl acetateFL/FR
isoamyl hexanoateFL/FR
isoamyl isobutyrateFL/FR
3-benzyl-4-heptanoneFL/FR
 berry hexanoateFR
isobutyl hexanoateFL/FR
 butyl hexanoateFL/FR
 butyl isobutyrateFL/FR
 butyl isovalerateFL/FR
 butyl valerateFL/FR
 cherry pentenoateFL/FR
 cyclohexyl propionateFL/FR
 diethyl malonateFL/FR
 ethyl (E)-2-decenoateFL/FR
 ethyl 2-hydroxy-3-methyl valerateFL/FR
 ethyl 2-methyl butyrateFL/FR
 ethyl 2-octenoateFL/FR
 ethyl 3-hexenoateFL/FR
 ethyl 3,5,5-trimethyl hexanoateFR
 ethyl acetoacetateFL/FR
 ethyl levulinateFL/FR
 ethyl methyl-para-tolyl glycidateFL/FR
 grape butyrateFL/FR
 green acetateFR
 heliotropyl isobutyrateFL/FR
 hexyl (E)-tiglateFL/FR
 hexyl acetateFL/FR
beta-ionone epoxideFL/FR
 methyl 2-methyl butyrateFL/FR
 methyl 2-methyl valerateFL/FR
3-nonen-2-oneFL/FR
 osmanthus flower absoluteFL/FR
isopropenyl acetateFL/FR
 propyl hexanoateFL/FR
 styralyl butyrateFL/FR
 vanilla carboxylateFL/FR
 ethyl (E,Z)-2,4-decadienoateFL/FR
 heptyl formateFL/FR
(Z)-3-hexen-1-yl 2-methyl butyrateFL/FR
(Z)-3-hexen-1-yl butyrateFL/FR
(Z)-3-hexen-1-yl formateFL/FR
(E)-2-hexen-1-yl isovalerateFL/FR
 hexyl 2-methyl butyrateFL/FR
 hexyl octanoateFL/FR
 hexyl phenyl acetateFL/FR
 melon nonenoateFL/FR
 neryl butyrateFL/FR
3,6-nonadien-1-yl acetateFL/FR
(E,Z)-3,6-nonadien-1-yl acetateFL/FR
(E)-2-nonen-1-olFL/FR
 phenoxyethyl isobutyrateFL/FR
 phenyl acetaldehyde ethylene glycol acetalFR
 pineapple heptadienone 10%FR
 thiogeraniolFL/FR
herbal
 tagete oil indiaFL/FR
melon
(Z)-6-nonen-1-olFL/FR
mentholic
 menthyl acetate racemicFL/FR
soapy
 ambrettolideFL/FR
spicy
 cinnamyl isovalerateFL/FR
sulfurous
 blackberry thiophenoneFL/FR
 buchu mercaptanFL/FR
vegetable
1-furfuryl pyrroleFL/FR
waxy
 decanal diethyl acetalFL/FR
9-decenoic acidFL/FR
 methyl butyl phenyl acetateFL/FR
(E)-methyl geranateFL/FR
2-methyl heptanoic acidFL/FR
 methyl octanoateFL/FR
2-nonanolFL/FR
(Z)-3-nonen-1-olFL/FR
 octanolFL/FR
(E)-2-octen-1-yl butyrateFL/FR
 phenethyl octanoateFL/FR
 
For Flavor
 
No flavor group found for these
 allyl tiglateFL
 blackberry thiophenoneFL/FR
 ethyl 2-hydroxy-3-methyl valerateFL/FR
 heliotropyl isobutyrateFL/FR
2-hexenal diethyl acetalFL
 hydroxycitronellal dimethyl acetalFL/FR
beta-ionone epoxideFL/FR
 menthyl acetate racemicFL/FR
(E)-methyl geranateFL/FR
2-nonanolFL/FR
(Z)-3-nonen-1-olFL/FR
(E)-5-nonen-2-oneFL/FR
(E)-2-octen-1-yl butyrateFL/FR
(E)-2-octen-4-olFL
 osmanthus flower absoluteFL/FR
caramellic
 maltyl isobutyrateFL/FR
coffee
 methyl furfuryl disulfideFL/FR
estery
 ethyl acetoacetateFL/FR
ethereal
isopropenyl acetateFL/FR
fatty
 allyl octanoateFL/FR
 heptyl formateFL/FR
(E)-2-octenalFL/FR
fruity
 allyl cyclohexyl acetateFL/FR
isoamyl benzoateFL/FR
isoamyl hexanoateFL/FR
isoamyl isobutyrateFL/FR
3-benzyl-4-heptanoneFL/FR
 butyl hexanoateFL/FR
isobutyl hexanoateFL/FR
 butyl isobutyrateFL/FR
 butyl isovalerateFL/FR
 butyl valerateFL/FR
 cherry pentenoateFL/FR
 cinnamyl isovalerateFL/FR
 cyclohexyl propionateFL/FR
alpha-damasconeFL/FR
 diethyl malonateFL/FR
 ethyl (E)-2-decenoateFL/FR
 ethyl (E)-2-octenoateFL
 ethyl 2-methyl butyrateFL/FR
 ethyl 2-octenoateFL/FR
 ethyl 3-hexenoateFL/FR
 ethyl 3-oxohexanoateFL
 ethyl levulinateFL/FR
 ethyl methyl-para-tolyl glycidateFL/FR
 furfuryl isovalerateFL
3-heptyl dihydro-5-methyl-2(3H)-furanoneFL/FR
(E)-2-hexenal diethyl acetalFL
 hexyl acetateFL/FR
 hexyl phenyl acetateFL/FR
 methyl 2-methyl butyrateFL/FR
 methyl 2-methyl valerateFL/FR
 nerolin fragarolFL/FR
 phenethyl octanoateFL/FR
 propyl formateFL/FR
 propyl hexanoateFL/FR
 styralyl butyrateFL/FR
 vanilla carboxylateFL/FR
green
 allyl butyrateFL/FR
 geranyl acetateFL/FR
 grape butyrateFL/FR
(Z)-3-hexen-1-yl 2-methyl butyrateFL/FR
(Z)-3-hexen-1-yl butyrateFL/FR
(Z)-3-hexen-1-yl formateFL/FR
(E)-2-hexen-1-yl isovalerateFL/FR
 hexyl (E)-tiglateFL/FR
 hexyl 2-furoateFL/FR
 hexyl 2-methyl butyrateFL/FR
 hexyl octanoateFL/FR
 melon nonenoateFL/FR
 methyl octanoateFL/FR
4-methyl-2-pentenalFL
 neryl butyrateFL/FR
(E,Z)-3,6-nonadien-1-yl acetateFL/FR
3,6-nonadien-1-yl acetateFL/FR
(E)-2-nonen-1-olFL/FR
 phenoxyethyl isobutyrateFL/FR
herbal
 tagete oil indiaFL/FR
juicy
 ethyl (E,Z)-2,4-decadienoateFL/FR
leafy
 methyl butyl phenyl acetateFL/FR
minty
 thiogeraniolFL/FR
oily
3-nonen-2-oneFL/FR
soapy
 ambrettolideFL/FR
sulfurous
 buchu mercaptanFL/FR
vegetable
1-furfuryl pyrroleFL/FR
waxy
 decanal diethyl acetalFL/FR
9-decenoic acidFL/FR
 hydroxycitronellalFL/FR
2-methyl heptanoic acidFL/FR
(Z)-6-nonen-1-olFL/FR
 octanolFL/FR
(E)-2-tetradecenalFL/FR
woody
 ambrette seed absoluteFL/FR
beta-iononeFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 appleFR
 bananaFR
 berryFR
 grapeFR
 melon watermelon muskmelon cantaloupe 
 peachFR
 pineappleFR
 plumFR
 valerianFL/FR
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 apple fruit
Search  Picture
 apricot fruit
Search Trop  Picture
 chamomile garden chamomile plant
Search Trop  Picture
 chamomile roman chamomile oil
Search Trop  Picture
 cocoa bean
Search Trop  Picture
 cupuacu
Search  Picture
 feijoa fruit
Search Trop  Picture
 filbert roasted filbert
Search Trop  Picture
 heracleum paphlagonicum czeczott fruit oil turkey @ 0.10%
Data  GC  Search Trop  Picture
 hop oil
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 horsemint shoot
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 lovage leaf
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 melon
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 myrtle berry
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 myrtle leaf
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 peppermint oil mongolia @ 0.07%
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 spearmint oil
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Synonyms:
 butanoic acid, 2-methyl-, 2-methylbutyl ester
 butyric acid, 2-methyl-, 2-methylbutyl ester
 hops butyrate
2-methyl butanoic acid 2-methyl butyl ester
 methyl butyl (2) 2 methyl butyrate
2-methyl butyl 2-methyl butanoate
2-methyl butyl-2-methyl butyrate
2-methyl butyric acid 2-methyl butyl ester
 methyl-2-butyl-2-methylbutyrate
2-methylbutanoic acid 2-methylbutyl ester
2-methylbutanoic acid, 2-methylbutyl ester
2-methylbutyl 2-methylbutanoate
2-methylbutyl 2-methylbutyrate
D-2-methylbutyl 2-methylbutyrate
nat.2-methylbutyl 2-methylbutyrate
nat.D-2-methylbutyl 2-methylbutyrate
2-methylbutyl 2-methylbutyrate natural
2-methylbutyl DL-2-methylbutyrate
2-methylbutyl-2-methyl butyrate
2-methylbutyl-2-methyl butyrate natural
2-methylbutyl-2-methylbutyrate natural
2-methylbutyl-D-2-methylbutyrate
2-methylbutyric acid 2-methylbutyl ester
DL-2-methylbutyric acid 2-methylbutyl ester
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Articles:
PubMed: Biodegradation of C5-C 8 fatty acids and production of aroma volatiles by Myroides sp. ZB35 isolated from activated sludge.
PubMed: Effects of extracts of Humulus lupulus (hops) and Yucca schidigera applied alone or in combination with monensin on rumen fermentation and microbial populations in vitro.
PubMed: In-tube extraction and GC-MS analysis of volatile components from wild and cultivated sea buckthorn (Hippophae rhamnoides L. ssp. Carpatica) berry varieties and juice.
PubMed: Biodegradation of gasoline ether oxygenates.
PubMed: Fragrance material review on 2-methyl-4-phenyl-2-butyl acetate.
PubMed: Early leaf removal impact on volatile composition of Tempranillo wines.
PubMed: Volatile composition of four southern highbush blueberry cultivars and effect of growing location and harvest date.
PubMed: Pharmacological actions of oximino-propofol analogues at GABA(B) autoreceptors.
PubMed: Comparison of volatile components in Chinese traditional pickled peppers using HS-SPME-GC-MS, GC-O and multivariate analysis.
PubMed: Identification of a pheromone regulating caste differentiation in termites.
PubMed: Formulations of dietary supplements and herbal extracts for relaxation and anxiolytic action: Relarian.
PubMed: Impact of thermal and nonthermal processing technologies on unfermented apple cider aroma volatiles.
PubMed: Modulation of PPAR receptor subtype selectivity of the ligands: aliphatic chain vs aromatic ring as a spacer between pharmacophore and the lipophilic moiety.
PubMed: Eubacterium limosum activates isoxanthohumol from hops (Humulus lupulus L.) into the potent phytoestrogen 8-prenylnaringenin in vitro and in rat intestine.
PubMed: Effects of traditionally used anxiolytic botanicals on enzymes of the gamma-aminobutyric acid (GABA) system.
PubMed: Pathway analysis of branched-chain ester biosynthesis in apple using deuterium labeling and enantioselective gas chromatography-mass spectrometry.
PubMed: Evidence that the beta-acids fraction of hops reduces central GABAergic neurotransmission.
PubMed: Genes involved in the methyl tert-butyl ether (MTBE) metabolic pathway of Mycobacterium austroafricanum IFP 2012.
PubMed: Effects of beer and hop on ionotropic gamma-aminobutyric acid receptors.
PubMed: Aroma extract dilution analysis of cv. Meeker (Rubus idaeus L.) red raspberries from Oregon and Washington.
PubMed: Human adipocyte fatty acid-binding protein (aP2) gene promoter-driven reporter assay discriminates nonlipogenic peroxisome proliferator-activated receptor gamma ligands.
PubMed: A novel selective peroxisome proliferator-activated receptor alpha agonist, 2-methyl-c-5-[4-[5-methyl-2-(4-methylphenyl)-4-oxazolyl]butyl]-1,3-dioxane-r-2-carboxylic acid (NS-220), potently decreases plasma triglyceride and glucose levels and modifies lipoprotein profiles in KK-Ay mice.
PubMed: Medicinal chemistry and molecular pharmacology of GABA(C) receptors.
PubMed: Character impact odorants of the apple cultivars Elstar and Cox Orange.
PubMed: Effect of 1-methylcyclopropene on volatile emission and aroma in cv. Anna apples.
PubMed: Biosynthesis of strawberry aroma compounds through amino acid metabolism.
PubMed: Aromatic profile of aqueous banana essence and banana fruit by gas chromatography-mass spectrometry (GC-MS) and gas chromatography-olfactometry (GC-O).
PubMed: Biotransformation of MTBE, ETBE, and TAME after inhalation or ingestion in rats and humans.
PubMed: Toxicokinetics of methyl tert-butyl ether and its metabolites in humans after oral exposure.
PubMed: Metabolism of ethyl tiglate in apple fruits leads to the formation of small amounts of (R)-ethyl 2-methylbutanoate.
PubMed: Biotransformation and kinetics of excretion of methyl-tert-butyl ether in rats and humans.
PubMed: 13C(2)-Labeled methyl tert-butyl ether: toxicokinetics and characterization of urinary metabolites in humans.
PubMed: GC and GC-MS determination of fluoroacetic acid and phenoxy acid herbicides via triphasal extractive pentafluorobenzylation using a polymer-bound phase-transfer catalyst.
PubMed: Assimilation of volatiles from ripe apples by Sporidiobolus salmonicolor and Tilletiopsis washingtonensis.
PubMed: Inhibitory effect of antioxidants ethoxyquin and 2(3)-tert-butyl-4-hydroxyanisole on hepatic tumorigenesis in rats fed ciprofibrate, a peroxisome proliferator.
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