2-isobutyl thiazole
2-isobutylthiazole
 
Notes:
isolated from preorbital gland of the grey duiker, sylvicapra grimmia and the red duiker, cephalophus natalensis. Tomato volatile and flavouring ingredient. Liq. with tomato leaf odour
  • Advanced Biotech
  • Augustus Oils
    • Augustus Oils Ltd
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      A wealth of experience, expertise and knowledge has allowed Augustus to bridge the gulf in expectation and trust between growers and users of natural ingredients. The Company works in partnership with customers on the one hand, and growers, farmers and distillers on the other. Both users and producers can then focus on exactly what they do best, while skilled Augustus technicians closely monitor and control the delivered product. This ensures users can have the confidence that they will receive the best raw materials suited to their requirements.
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      2 Iso Butyl Thiazole
       
  • Beijing Lys Chemicals
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      From Grams to Tons
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      BEIJING LYS CHEMICALS CO, LTD, established in 2004, is a fine chemical high-tech company which contains R&D, production, and sales. We mainly engaged in export and technology development of flavor and fragrance materials and pharmaceutical intermediates. We have nearly 500 kinds of products, from grams to tons, exported to USA, Europe, South Asia and etc. And we custom manufacture new products according to customers’ needs, and serve good quality products and service. Our goal is to become a fine chemical enterprise which could provide special products and services.
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      10089 2-isoButylthiazole
       
  • BOC Sciences
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      Product(s):
      18640-74-9 2-isoButyl Thiazole 98%
       
  • Charkit Chemical
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      about: Since 1982, Charkit has been committed to expanding the markets we serve as our roster of products and services continues to grow with us. Our substantial portfolio of personal care ingredients now include a wide array of luxury and exotic components to compliment the key products we have always offered. We have expanded our offerings to the nutraceutical, industrial, and resin markets with a growing roster of versatile and unique ingredients. We continue to lead the way in our traditional markets such as Metal and Water Treatment, Imaging, Flavor & Fragrance, Aroma and Food. Our Pharmaceutical offerings continue to expand, still anchored by the Boronic Derivatives that meet the demands of Suzuki coupling reactions. Please contact us to learn how we can help you reach your goals.
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      ISOBUTYLTHIAZOLE, 2- 1% IN DPG
      ISOBUTYLTHIAZOLE, 2- FEMA 3134
       
  • Endeavour Specialty Chemicals
    • Endeavour Specialty Chemicals Ltd
      Expertise in high impact aroma chemicals
      Endeavour Speciality Chemicals offers high-impact aroma chemicals, at small to medium scale.
      Speciality Chemical has more than 25 years experience of manufacturing high-impact aroma chemicals. With our core expertise in sulfur and heterocyclic chemistries, Endeavours products have applications in a range of industry sectors including flavours and fragrances, pharmaceutical research and material sciences. Endeavour also offer custom synthesis and contract manufacturing services at their UK manufacturing site.
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      TZ0060 2-Isobutylthiazole 97% F&F
       
  • Frutarom
    • FRUTAROM USA INC,
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      441I110000 2-ISOBUTYLTHIAZOLE KOSHER
       
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      HL0145 2-IsoButyl Thiazole
       
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      2-ISOBUTYL THIAZOLE
       
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  • SRS Aromatics
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      THIAZYL 1% DPG
       
  • Sunaux International
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      H0067 2-isoButyl Thiazole
       
  • Synerzine
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      T712 2-isobutylthiazole nick-named Tomato Leaf Thiazole
       
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      2-isoButylthiazole
       
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      I0652 2-isoButylthiazole >97.0%(GC)
      SDS
       
  • 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.
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      Thiazyl 1% in DPG
      SDS
       
  • Tianjin Danjun International
    • Tianjin Danjun International Trade Co., LTD.
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      B-038 2-Isobutylthiazole
       
  • R C Treatt & Co Ltd
    • R C Treatt and Co Ltd
      Innovative ingredient solutions
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      2-Isobutylthiazole Halal, Kosher
      Odor threshold in water: 2-3.5 ppb.
      Effective in enhancing tomato juice at 25-50 ppb. Useful for enhancing Tomato flavor of condiments (e.g., Ketchup). This compound is essential to the flavor of Tomato. Normal use levels in finished consumer product: 0.02-1.0 ppm.
       
      2-Isobutylthiazole 1% in DPG Kosher
       
  • United International
    • Qingdao Free Trade Zone United International Co Ltd
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      2010 2-Isobutyl Thiazole
      2010N 2-Isobutyl Thiazole Nat.
       
  • Ernesto Ventós
  • Vigon International
    • Vigon International
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      501355 Isobutyl-2 Thiazole
       
  • WholeChem
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      Product(s):
      2-Isobutyl thiazole
       
Synonyms   Articles   Notes   Search
Fragrance Demo Formulas    Flavor Demo Formulas
CAS Number: 18640-74-9Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 242-470-1
FDA UNII: 7N03TDY75D
Nikkaji Web: J45.613F
MDL: MFCD00005334
CoE Number: 11618
XlogP3-AA: 2.60 (est)
Molecular Weight: 141.23667000
Formula: C7 H11 N S
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome, Edge or firefox)
Category: flavor and fragrance agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Perfumer and Flavorist: Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
JECFA Food Flavoring: 1034  2-isobutylthiazole
DG SANTE Food Flavourings: 15.013  2-isobutylthiazole
FEMA Number: 3134 2-isobutylthiazole
FDA:No longer provide for the use of these seven synthetic flavoring substances
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: 96.00 to 100.00 % 
Food Chemicals Codex Listed: No
Specific Gravity: 0.99500 to 0.99530 @  25.00 °C.
Pounds per Gallon - (est).: 8.279 to  8.282
Specific Gravity: 1.00000 to 1.00400 @  20.00 °C.
Pounds per Gallon - est.: 8.331 to 8.364
Refractive Index: 1.49400 to 1.49800 @  20.00 °C.
Refractive Index: 1.49000 to 1.49900 @  20.00 °C.
Boiling Point: 174.00 to  180.00 °C. @ 760.00 mm Hg
Vapor Pressure: 1.091000 mmHg @ 25.00 °C. (est)
Vapor Density: 4.8 ( Air = 1 )
Flash Point: 135.00 °F. TCC ( 57.22 °C. )
logP (o/w): 1.715 (est)
Soluble in:
 alcohol
 water, 255.2 mg/L @ 25 °C (est)
Insoluble in:
 water
Stability:
 stable in most media
Synonyms   Articles   Notes   Search   Top
Organoleptic Properties:
 
Odor Type: green
 
Odor Strength: high ,
recommend smelling in a 0.10 % solution or less
 
Substantivity: > 1 hour(s) at 100.00 %
 
 green  wasabi  privet  tomato leaf  earthy  vegetable  metallic  
Odor Description:
at 1.00 % in dipropylene glycol. 
green wasabi privet tomato leaf earthy vegetable metallic
Luebke, William tgsc, (2009)
 
 green  vegetable  musty  waxy  
Odor Description:
Green, vegetable, musty with a waxy nuance
Mosciano, Gerard P&F 17, No. 4, 33, (1992)
 
 
Flavor Type: green
 
 green  vegetable  tomato  raw  musty  
Taste Description:
at 2.00 ppm.  
Green, vegetable, tomato-like with raw musty nuances
Mosciano, Gerard P&F 17, No. 4, 33, (1992)
 
Odor and/or flavor descriptions from others (if found).
 
R C Treatt & Co Ltd
2-Isobutylthiazole Halal, Kosher
Odor Description: Green tomato leaf
Odor threshold in water: 2-3.5 ppb.
Taste Description: Green tomato
Effective in enhancing tomato juice at 25-50 ppb. Useful for enhancing Tomato flavor of condiments (e.g., Ketchup). This compound is essential to the flavor of Tomato. Normal use levels in finished consumer product: 0.02-1.0 ppm.
 
Pell Wall Perfumes
Isobutylthiazole
Odor Description: Green, tomato, earthy, vegetable, metallic. Extremely powerful
A very interesting material that, when sufficiently diluted gives an extremely realistic note of tomatoes – with the addition of other components it can easily be pushed in the direction of ripe tomato fruits or that characteristic smell of the tomato plant itself.
 
Perfumery Laboratory
Tomato leaf thiazol 0.1% in DPG PFW (Tomato leaf thiazole 0.1% PFW)
Odor Description: Powerful, fresh, natural, tomato, earthy
 
 
Synonyms   Articles   Notes   Search   Top
Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: perfuming agents
Synonyms   Articles   Notes   Search   Top
Suppliers:
Advanced Biotech
2-ISOBUTYL THIAZOLE NATURAL
Advanced Biotech
2-ISOBUTYL THIAZOLE
Odor: Tomato leaf
Advanced Biotech
ISO BUTYL THIAZOLE 1% ETOH NATURAL
Advanced Biotech
ISOBUTYL THIAZOLE 1% WS NATURAL
Odor: Tomato leaf
Ambles Nature et Chimie
2-ISOBUTYL THIAZOLE
Anhui Suzhou Jinli Aromatic Chemicals
2-isoButyl Thiazole
Odor: tomato
Augustus Oils
2 Iso Butyl Thiazole
Services
Beijing Lys Chemicals
2-isoButylthiazole
BOC Sciences
For experimental / research use only.
2-isoButyl Thiazole 98%
Charkit Chemical
ISOBUTYLTHIAZOLE, 2- 1% IN DPG
Charkit Chemical
ISOBUTYLTHIAZOLE, 2- FEMA 3134
DeLong Chemicals America
2-Isobutylthiazole, Kosher
Endeavour Specialty Chemicals
2-Isobutylthiazole 97% F&F
Speciality Chemical Product Groups
Ernesto Ventós
2-isoBUTYLTHIAZOLE
Odor: TOMATO LEAVES, MUSHROOM, EARTHY
Frutarom
2-ISOBUTYLTHIAZOLE
KOSHER
Flavor: Fresh, Green, Tomato, Vinous, Musty
CBD Offering
IFF
2-ISOBUTYLTHIAZOLE
KOSHER
Flavor: Fresh, Green, Tomato, Vinous, Musty
Indukern F&F
2-ISOBUTYL THIAZOLE
Odor: GREEN TOMATO LEAF, WOODY
Jiangyin Healthway
2-IsoButyl Thiazole
New functional food ingredients
Jinan Enlighten Chemical Technology(Wutong Aroma )
2-isoButyl thiazole, Kosherk
Kingchem Laboratories
2-ISOBUTYLTHIAZOLE
Odor: Tomato-like
Lluch Essence
2-ISOBUTYL THIAZOLE
Odor: WOODY, TOMATO-LEAF NOTES
M&U International
2-isoBUTYL THIAZOLE, Kosher
Natural Advantage
Isobutylthiazole Nat, 1% in Neobee
Flavor: green, musky, tomato
Riverside Aromatics LTD.is the exclusive distributor for Europe in UK for any non-US based inquiries
Natural Advantage
Isobutylthiazole Nat, 1% in OH
Flavor: green, musky, tomato
Natural Advantage
Isobutylthiazole Nat, 1% in PG
Flavor: green, musky, tomato
Natural Advantage
Isobutylthiazole Nat, 10% in Triacetin Nat USOC
Flavor: green, musky, tomato
Natural Advantage
Isobutylthiazole Nat, 10% in Triacetin
Flavor: green, musky, tomato
Natural Advantage
Isobutylthiazole
Flavor: green, musky, tomato
PCW France
Thiazyl 1% DPG
Steps to a fragranced product
Pearlchem Corporation
2-isoButyl Thiazole
Pell Wall Perfumes
Isobutylthiazole
Odor: Green, tomato, earthy, vegetable, metallic. Extremely powerful
Use: A very interesting material that, when sufficiently diluted gives an extremely realistic note of tomatoes – with the addition of other components it can easily be pushed in the direction of ripe tomato fruits or that characteristic smell of the tomato plant itself.
Penta International
2-ISOBUTYL THIAZOLE
Penta International
2-ISOBUTYLTHIAZOLE NATURAL
Perfumery Laboratory
Tomato leaf thiazol 0.1% in DPG PFW (Tomato leaf thiazole 0.1% PFW)
Odor: Powerful, fresh, natural, tomato, earthy
R C Treatt & Co Ltd
2-Isobutylthiazole 1% in DPG
Kosher
R C Treatt & Co Ltd
2-Isobutylthiazole
Halal, Kosher
Odor: Green tomato leaf
Use: Odor threshold in water: 2-3.5 ppb.
Flavor: Green tomato
Effective in enhancing tomato juice at 25-50 ppb. Useful for enhancing Tomato flavor of condiments (e.g., Ketchup). This compound is essential to the flavor of Tomato. Normal use levels in finished consumer product: 0.02-1.0 ppm.
Reincke & Fichtner
2-isoButylthiazole
Riverside Aromatics
2-isoBUTYLTHIAZOLE NATURAL 1% IN PG
Riverside Aromatics
2-ISOBUTYLTHIAZOLE, NATURAL
Riverside Aromatics
2-isoBUTYLTHIAZOLE
Robinson Brothers
2-IsoButylthiazole F&F
https://www.robinsonbrothers.uk/chemistry-competences
Santa Cruz Biotechnology
For experimental / research use only.
2-isoButylthiazole
Sigma-Aldrich
2-Isobutylthiazole, ≥99%, FG
Odor: green; vegetable
Certified Food Grade Products
SRS Aromatics
THIAZYL 1% DPG
Sunaux International
2-isoButyl Thiazole
Synerzine
2-isobutylthiazole
nick-named Tomato Leaf Thiazole
Taytonn ASCC
2-isoButylthiazole
Odor: Vinous, Green, Fresh, Tomato
TCI AMERICA
For experimental / research use only.
2-isoButylthiazole >97.0%(GC)
Tengzhou Jitian Aroma Chemiclal
2-isoButyl Thiazole
Tengzhou Xiang Yuan Aroma Chemicals
2-isoButyl Thiazole
The John D. Walsh Company
Thiazyl 1% in DPG
Tianjin Danjun International
2-Isobutylthiazole
United International
2-Isobutyl Thiazole Nat.
United International
2-Isobutyl Thiazole
Vigon International
Isobutyl-2 Thiazole
Odor: GREEN, NUTTY
WholeChem
2-Isobutyl thiazole
Synonyms   Articles   Notes   Search   Top
Safety Information:
Preferred SDS: View
European information :
Most important hazard(s):
Xi - Irritant
R 36/37/38 - Irritating to eyes, respiratory system, and skin.
S 02 - Keep out of the reach of children.
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.
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
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
Recommendation for 2-isobutyl thiazole usage levels up to:
  0.0800 % in the fragrance concentrate.
 
Maximised Survey-derived Daily Intakes (MSDI-EU): 3.00 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 0.40 (μg/capita/day)
Structure Class: II
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: 4
Click here to view publication 4
 average usual ppmaverage maximum ppm
baked goods: -1.00000
beverages(nonalcoholic): -1.00000
beverages(alcoholic): --
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -1.00000
fruit ices: -1.00000
gelatins / puddings: -1.00000
granulated sugar: --
gravies: -1.00000
hard candy: -1.00000
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: -1.00000
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: -1.00000
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: --
soups: -1.00000
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 21: Thiazoles, thiophene, thiazoline and thienyl derivatives from chemical group 29. Miscellaneous substances from chemical group 30. (Commission Regulation (EC) No 1565/2000 of 18 July 2000) - Opinion of the Scientific Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC)
View page or View pdf
Flavouring Group Evaluation 76, (FGE.76)[1] - Consideration of sulphur-containing heterocyclic compounds evaluated by JECFA (59th meeting) structurally related to thiazoles, thiophene, thiazoline and thienyl derivatives from chemical group 29, miscellaneous substances from chemical group 30 evaluated by EFSA in FGE.21 - Scientific Opinion of the Panel on Food Additives, Flavourings, Processing Aids and Materials in Contact with Food
View page or View pdf
Flavouring Group Evaluation 21, Revision 1 (FGE.21Rev1): Thiazoles, thiophene, thiazoline and thienyl derivatives from chemical group 29 Miscellaneous substances from chemical group 30
View page or View pdf
Scientific Opinion on the safety and efficacy of thiazoles, thiophene, thiazoline and thienyl derivatives (chemical group 29): 3-acetyl-2,5-dimethylthiophene when used as a flavouring for all animal species
View page or View pdf
Scientific Opinion on Flavouring Group Evaluation 76, Revision 1 (FGE.76Rev1): Consideration of sulphur-containing heterocyclic compounds evaluated by JECFA (59th meeting) structurally related to thiazoles, thiophene, thiazoline and thienyl derivatives from chemical group 29 and miscellaneous substances from chemical group 30 evaluated by EFSA in FGE.21Rev3
View page or View pdf
Safety and efficacy of thiazoles, thiophene and thiazoline belonging to chemical group 29 when used as flavourings for all animal species
View page or View pdf
EPI System: View
AIDS Citations: Search
Cancer Citations: Search
Toxicology Citations: Search
EPA Substance Registry Services (TSCA): 18640-74-9
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 62725
National Institute of Allergy and Infectious Diseases: Data
WISER: UN 1993
WGK Germany: 3
 2-(2-methylpropyl)-1,3-thiazole
Chemidplus: 0018640749
RTECS: XJ5103412 for cas# 18640-74-9
Synonyms   Articles   Notes   Search   Top
References:
 2-(2-methylpropyl)-1,3-thiazole
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 18640-74-9
Pubchem (cid): 62725
Pubchem (sid): 135021306
Flavornet: 18640-74-9
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
CHEMBL: View
HMDB (The Human Metabolome Database): HMDB31862
FooDB: FDB008546
YMDB (Yeast Metabolome Database): YMDB01585
Export Tariff Code: 2934.10.0090
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Synonyms   Articles   Notes   Search   Top
Potential Blenders and core components note
 
For Odor
alliaceous
 dibutyl sulfideFL/FR
 dipropyl disulfideFL/FR
amber
 amber furanFR
balsamic
 tetrahydrofurfuryl cinnamateFL/FR
caramellic
2-isobutyl-3-methyl pyrazineFL/FR
S-(methyl thio) butyrateFL/FR
chocolate
2,4,5-trimethyl thiazoleFL/FR
citrus
 methyl heptenoneFL/FR
 petitgrain combava oilFR
coumarinic
 phthalideFL/FR
ethereal
2-methyl valeraldehydeFL/FR
fatty
2-nonenalFL/FR
(Z)-2-octenal 
(E)-2-octenalFL/FR
floral
 allyl anthranilateFL/FR
 geranium dihydropyranFR
 methyl dihydrojasmonateFL/FR
bitter orangeflower absolute moroccoFL/FR
 petitgrain lemon oilFL/FR
 rose absolute (rosa damascena) bulgariaFL/FR
laevo-rose oxideFL/FR
(Z)-rose oxideFL/FR
fruity
2-hexen-1-olFL/FR
(E)-2-hexen-1-olFL/FR
 hexyl acetateFL/FR
gamma-undecalactone (aldehyde C-14 (so-called))FL/FR
green
 acetaldehyde butyl phenethyl acetalFL/FR
 acetaldehyde di-(Z)-3-hexen-1-yl acetalFL/FR
 acetaldehyde ethyl phenethyl acetalFL/FR
isobutyl methyl ketoneFL/FR
 cortex pyridineFL/FR
 cumin acetaldehydeFL/FR
3,5,6-neocyclocitralFR
 diphenyl oxideFL/FR
 galbanum decatrieneFL/FR
 galbanum oil terpenelessFL/FR
 galbanum oleoresinFL/FR
 geranium absoluteFL/FR
 geranium thiazoleFL/FR
1-hepten-3-olFL/FR
 heptyl cinnamateFL/FR
3-hexen-1-olFL/FR
(Z)-4-hexen-1-olFL/FR
(Z)-2-hexen-1-olFL/FR
(E)-4-hexen-1-ol 
(E)-2-hexen-1-yl acetateFL/FR
(Z)-3-hexen-1-yl benzoateFL/FR
(Z)-3-hexen-1-yl lactateFL/FR
(Z)-3-hexen-1-yl methyl carbonateFL/FR
(Z)-3-hexen-1-yl tiglateFL/FR
3-hexenalFL/FR
 hexoxyacetaldehyde dimethyl acetalFR
 hexyl heptanoateFL/FR
(Z)-leaf acetalFL/FR
 leafy acetalFL/FR
 leafy oximeFR
 methyl heptine carbonateFL/FR
 narcissus flower absoluteFR
 nerol oxideFL/FR
(Z,Z)-3,6-nonadien-1-olFL/FR
(E,Z)-2,6-nonadien-1-yl acetateFL/FR
 octanal dimethyl acetalFL/FR
(Z)-5-octen-1-yl propionateFL/FR
1-penten-3-olFL/FR
(E)-2-pentenalFL/FR
2-pentenalFL/FR
 phenoxyacetaldehyde 50% in benzyl alcoholFR
3-phenyl propionaldehydeFL/FR
isopropyl phenyl propionaldehydeFR
 rose leaf absolute (rosa centifolia)FL/FR
 styralyl acetateFL/FR
herbal
 anthemis nobilis flower oil romanFL/FR
sweet basil absoluteFL/FR
3-butylidene phthalideFL/FR
isodihydrolavandulalFL/FR
 herbal heptaneFR
 rosemary oleoresinFL/FR
malty
S-methyl methioninium chloride 
minty
isopulegyl formateFL/FR
musty
 cocoa butenalFL/FR
 shoyu pyrazineFL/FR
2,3,5-trimethyl pyrazineFL/FR
pine
 plectranthus glandulosus hook f. leaf oil cameroonFR
 dimethyl sulfideFL/FR
 ethyl methyl mercaptopropionateFL/FR
 methyl 3-(methyl thio) propionateFL/FR
3-(methyl thio) hexanolFL/FR
4-methyl-1,3-dithiolane 
tomato
 tomato essenceFL/FR
 tomato specialtyFR
vegetable
 methionalFL/FR
woody
alpha-farneseneFL/FR
alpha-farnesene isomerFL/FR
yeasty
2-octen-4-oneFL/FR
 
For Flavor
 
No flavor group found for these
 acetaldehyde di-(Z)-3-hexen-1-yl acetalFL/FR
 allyl anthranilateFL/FR
2-ethyl-4,5-dimethyl oxazoleFL
 heptyl cinnamateFL/FR
3-hexen-1-olFL/FR
2-hexenalFL
(E)-2-hexenalFL
 hexyl heptanoateFL/FR
3-methyl-3-pentanolFL
(Z)-2-octenal 
2-pentenalFL/FR
isopulegyl formateFL/FR
 tetrahydrofurfuryl cinnamateFL/FR
alliaceous
 allyl thiopropionateFL
 dipropyl disulfideFL/FR
aromatic
 leafy acetalFL/FR
celery
3-butylidene phthalideFL/FR
citrus
 petitgrain lemon oilFL/FR
coumarinic
 phthalideFL/FR
creamy
gamma-undecalactone (aldehyde C-14 (so-called))FL/FR
fatty
(Z)-3-hexen-1-yl benzoateFL/FR
1-methyl thio-3-octanoneFL
2-nonenalFL/FR
(E)-2-octenalFL/FR
fermented
 methyl thio isovalerateFL
floral
 methyl dihydrojasmonateFL/FR
bitter orangeflower absolute moroccoFL/FR
 rose absolute (rosa damascena) bulgariaFL/FR
laevo-rose oxideFL/FR
fruity
2,4-hexadien-1-olFL
2-hexen-1-olFL/FR
 hexyl acetateFL/FR
 styralyl acetateFL/FR
green
 acetaldehyde butyl phenethyl acetalFL/FR
 acetaldehyde ethyl phenethyl acetalFL/FR
isobutyl methyl ketoneFL/FR
2-isobutyl-3-methyl pyrazineFL/FR
 cocoa butenalFL/FR
 cortex pyridineFL/FR
 cumin acetaldehydeFL/FR
 dibutyl sulfideFL/FR
 dihydroxyacetophenone (mixed isomers)FL
 diphenyl oxideFL/FR
alpha-farneseneFL/FR
alpha-farnesene isomerFL/FR
 galbanum decatrieneFL/FR
 galbanum oil terpenelessFL/FR
 galbanum oleoresinFL/FR
 geranium absoluteFL/FR
 geranium thiazoleFL/FR
1-hepten-3-olFL/FR
(E)-2-hexen-1-olFL/FR
(Z)-2-hexen-1-olFL/FR
(E)-4-hexen-1-ol 
(Z)-4-hexen-1-olFL/FR
(E)-2-hexen-1-yl acetateFL/FR
(Z)-3-hexen-1-yl lactateFL/FR
(Z)-3-hexen-1-yl methyl carbonateFL/FR
(Z)-3-hexen-1-yl tiglateFL/FR
3-hexenalFL/FR
2-hexyl pyridineFL
 horseradish oilFL
(Z)-leaf acetalFL/FR
 methyl heptenoneFL/FR
 methyl heptine carbonateFL/FR
4-methyl thiazoleFL
 nerol oxideFL/FR
(E,Z)-2,6-nonadien-1-yl acetateFL/FR
 octanal dimethyl acetalFL/FR
(Z)-5-octen-1-yl propionateFL/FR
4-penten-1-yl acetateFL
1-penten-3-olFL/FR
(E)-2-pentenalFL/FR
3-phenyl propionaldehydeFL/FR
 propylene glycol acetone ketalFL
 rose leaf absolute (rosa centifolia)FL/FR
(Z)-rose oxideFL/FR
herbal
 anthemis nobilis flower oil romanFL/FR
sweet basil absoluteFL/FR
isodihydrolavandulalFL/FR
 rosemary oleoresinFL/FR
metallic
2,5-dihydroxy-1,4-dithianeFL
3-(methyl thio) hexanolFL/FR
musty
S-(methyl thio) butyrateFL/FR
 shoyu pyrazineFL/FR
2,3,5-trimethyl pyrazineFL/FR
nutty
2,4,5-trimethyl thiazoleFL/FR
onion
 methyl propyl disulfideFL
4-methyl-1,3-dithiolane 
sulfurous
 dimethyl sulfideFL/FR
 ethyl methyl mercaptopropionateFL/FR
 ethyl methyl sulfideFL
S-methyl methioninium chloride 
 potato butanoneFL
tomato
 methionalFL/FR
 tomato essenceFL/FR
vegetable
 methyl 3-(methyl thio) propionateFL/FR
2-methyl valeraldehydeFL/FR
2-octen-4-oneFL/FR
 potato butyraldehydeFL
 radish isothiocyanateFL
waxy
(Z,Z)-3,6-nonadien-1-olFL/FR
 
Synonyms   Articles   Notes   Search   Top
Potential Uses:
 apricotFR
 earthFR
 floralFR
 fungusFR
 greenFR
 leaf 
 muskFR
 peachFR
 tomatoFL
 tomato leafFR
 vegetableFL
 vine 
Synonyms   Articles   Notes   Search   Top
Occurrence (nature, food, other): note
 cantaloupe fruit
Search Trop  Picture
 tomato
Search Trop  Picture
Synonyms   Articles   Notes   Search   Top
Synonyms:
2-isobutyl-1,3-thiazole
isobutyl-2 thiazole
2-isobutylthiazole
isobutylthiazole
2-(2-methyl propyl) thiazole
2-(2-methylpropyl)-1,3-thiazole
2-(2-methylpropyl)thiazole
 thiazole, 2-(2-methylpropyl)-
 thiazole, 2-isobutyl-
 thiazyl (PFW)
 thiazyl 1% DPG (PFW)
 thiazyl 1% in DPG (PFW)
 tomato leaf thiazole
Synonyms   Articles   Notes   Search   Top
Articles:
PubMed: Impact of different distribution scenarios and recommended storage conditions on flavor related quality attributes in ripening fresh tomatoes.
PubMed: Dynamics of odorant binding to thin aqueous films of rat-OBP3.
PubMed: Flavor release of the tomato flavor enhancer, 2-isobutylthiazole, from whey protein stabilized model dressings.
PubMed: Population pharmacokinetic model for a novel oral hypoglycemic formed in vivo: comparing the use of active metabolite data alone versus using data of upstream and downstream metabolites.
PubMed: Discovery of a series of phosphonic acid-containing thiazoles and orally bioavailable diamide prodrugs that lower glucose in diabetic animals through inhibition of fructose-1,6-bisphosphatase.
PubMed: Fructose-1,6-bisphosphatase regulates glucose-stimulated insulin secretion of mouse pancreatic beta-cells.
PubMed: P2Y2 receptor-Gq/11 signaling at lipid rafts is required for UTP-induced cell migration in NG 108-15 cells.
PubMed: Comparison of tomatillo and tomato volatile compounds in the headspace by selected ion flow tube mass spectrometry (SIFT-MS).
PubMed: The peripheral benzodiazepine receptor ligand 1-(2-chlorophenyl-methylpropyl)-3-isoquinoline-carboxamide is a novel antagonist of human constitutive androstane receptor.
PubMed: Studies on the aroma of five fresh tomato cultivars and the precursors of cis- and trans-4,5-epoxy-(E)-2-decenals and methional.
PubMed: A potential endogenous ligand for the aryl hydrocarbon receptor has potent agonist activity in vitro and in vivo.
PubMed: MB06322 (CS-917): A potent and selective inhibitor of fructose 1,6-bisphosphatase for controlling gluconeogenesis in type 2 diabetes.
PubMed: Nitric oxide donating nonsteroidal anti-inflammatory drugs induce apoptosis in human prostate cancer cell systems and human prostatic stroma via caspase-3.
PubMed: First synthesis of an amythiamicin pyridine cluster.
PubMed: Absolute configuration of 2-sec-butyl-4,5-dihydrothiazole in male mouse urine.
PubMed: CYP3A induction by N-hydroxyformamide tumor necrosis factor-alpha converting enzyme/matrix metalloproteinase inhibitors use of a pregname X receptor activation assay and primary hepatocyte culture for assessing induction potential in humans.
PubMed: Differential effects of tomato (Lycopersicon esculentum mill) matrix on the volatility of important aroma compounds.
PubMed: Addition of heteroaromatics to alkylidenecyclopropanes catalyzed by palladium.
PubMed: Odorants of different chemical classes interact with distinct odorant binding protein subtypes.
PubMed: Synthesis and dopamine receptor modulating activity of substituted bicyclic thiazolidine lactam peptidomimetics of L-prolyl-L-leucyl-glycinamide.
PubMed: Mammalian pheromones VIII Chemical characterization of preorbital gland secretion of grey duiker,Sylvicapra grimmia (Artiodactyla: Bovidae).
PubMed: Mammalian pheromone studies, VII. Identification of thiazole derivatives in the preorbital gland secretions of the grey duiker, Sylvicapra grimmia, and the red duiker, Cephalophus natalensis.
PubMed: The odorant-sensitive adenylate cyclase of olfactory receptor cells. Differential stimulation by distinct classes of odorants.
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