Category: flavor and fragrance agents
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
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 |
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 |
|
|
Cosmetic Information:
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
|
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
|
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 ppm | average 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: | - | - |
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 |
References:
Other Information:
Potential Blenders and core components note
|
For Odor |
alliaceous |
| dibutyl sulfide | FL/FR |
| dipropyl disulfide | FL/FR |
amber |
| amber furan | FR |
balsamic |
| tetrahydrofurfuryl cinnamate | FL/FR |
caramellic |
2-iso | butyl-3-methyl pyrazine | FL/FR |
S-( | methyl thio) butyrate | FL/FR |
chocolate |
2,4,5- | trimethyl thiazole | FL/FR |
citrus |
| methyl heptenone | FL/FR |
| petitgrain combava oil | FR |
coumarinic |
| phthalide | FL/FR |
ethereal |
2- | methyl valeraldehyde | FL/FR |
fatty |
2- | nonenal | FL/FR |
(Z)-2- | octenal | |
(E)-2- | octenal | FL/FR |
floral |
| allyl anthranilate | FL/FR |
| geranium dihydropyran | FR |
| methyl dihydrojasmonate | FL/FR |
bitter | orangeflower absolute morocco | FL/FR |
| petitgrain lemon oil | FL/FR |
| rose absolute (rosa damascena) bulgaria | FL/FR |
laevo- | rose oxide | FL/FR |
(Z)- | rose oxide | FL/FR |
fruity |
2- | hexen-1-ol | FL/FR |
(E)-2- | hexen-1-ol | FL/FR |
| hexyl acetate | FL/FR |
gamma- | undecalactone (aldehyde C-14 (so-called)) | FL/FR |
green |
| acetaldehyde butyl phenethyl acetal | FL/FR |
| acetaldehyde di-(Z)-3-hexen-1-yl acetal | FL/FR |
| acetaldehyde ethyl phenethyl acetal | FL/FR |
iso | butyl methyl ketone | FL/FR |
| cortex pyridine | FL/FR |
| cumin acetaldehyde | FL/FR |
3,5,6-neo | cyclocitral | FR |
| diphenyl oxide | FL/FR |
| galbanum decatriene | FL/FR |
| galbanum oil terpeneless | FL/FR |
| galbanum oleoresin | FL/FR |
| geranium absolute | FL/FR |
| geranium thiazole | FL/FR |
1- | hepten-3-ol | FL/FR |
| heptyl cinnamate | FL/FR |
3- | hexen-1-ol | FL/FR |
(Z)-4- | hexen-1-ol | FL/FR |
(Z)-2- | hexen-1-ol | FL/FR |
(E)-4- | hexen-1-ol | |
(E)-2- | hexen-1-yl acetate | FL/FR |
(Z)-3- | hexen-1-yl benzoate | FL/FR |
(Z)-3- | hexen-1-yl lactate | FL/FR |
(Z)-3- | hexen-1-yl methyl carbonate | FL/FR |
(Z)-3- | hexen-1-yl tiglate | FL/FR |
3- | hexenal | FL/FR |
| hexoxyacetaldehyde dimethyl acetal | FR |
| hexyl heptanoate | FL/FR |
(Z)- | leaf acetal | FL/FR |
| leafy acetal | FL/FR |
| leafy oxime | FR |
| methyl heptine carbonate | FL/FR |
| narcissus flower absolute | FR |
| nerol oxide | FL/FR |
(Z,Z)-3,6- | nonadien-1-ol | FL/FR |
(E,Z)-2,6- | nonadien-1-yl acetate | FL/FR |
| octanal dimethyl acetal | FL/FR |
(Z)-5- | octen-1-yl propionate | FL/FR |
1- | penten-3-ol | FL/FR |
(E)-2- | pentenal | FL/FR |
2- | pentenal | FL/FR |
| phenoxyacetaldehyde 50% in benzyl alcohol | FR |
3- | phenyl propionaldehyde | FL/FR |
iso | propyl phenyl propionaldehyde | FR |
| rose leaf absolute (rosa centifolia) | FL/FR |
| styralyl acetate | FL/FR |
herbal |
| anthemis nobilis flower oil roman | FL/FR |
sweet | basil absolute | FL/FR |
3- | butylidene phthalide | FL/FR |
iso | dihydrolavandulal | FL/FR |
| herbal heptane | FR |
| rosemary oleoresin | FL/FR |
malty |
S- | methyl methioninium chloride | |
minty |
iso | pulegyl formate | FL/FR |
musty |
| cocoa butenal | FL/FR |
| shoyu pyrazine | FL/FR |
2,3,5- | trimethyl pyrazine | FL/FR |
pine |
| plectranthus glandulosus hook f. leaf oil cameroon | FR |
| dimethyl sulfide | FL/FR |
| ethyl methyl mercaptopropionate | FL/FR |
| methyl 3-(methyl thio) propionate | FL/FR |
3-( | methyl thio) hexanol | FL/FR |
4- | methyl-1,3-dithiolane | |
tomato |
| tomato essence | FL/FR |
| tomato specialty | FR |
vegetable |
| methional | FL/FR |
woody |
alpha- | farnesene | FL/FR |
alpha- | farnesene isomer | FL/FR |
yeasty |
2- | octen-4-one | FL/FR |
|
For Flavor |
|
No flavor group found for these |
| acetaldehyde di-(Z)-3-hexen-1-yl acetal | FL/FR |
| allyl anthranilate | FL/FR |
2- | ethyl-4,5-dimethyl oxazole | FL |
| heptyl cinnamate | FL/FR |
3- | hexen-1-ol | FL/FR |
2- | hexenal | FL |
(E)-2- | hexenal | FL |
| hexyl heptanoate | FL/FR |
3- | methyl-3-pentanol | FL |
(Z)-2- | octenal | |
2- | pentenal | FL/FR |
iso | pulegyl formate | FL/FR |
| tetrahydrofurfuryl cinnamate | FL/FR |
alliaceous |
| allyl thiopropionate | FL |
| dipropyl disulfide | FL/FR |
aromatic |
| leafy acetal | FL/FR |
celery |
3- | butylidene phthalide | FL/FR |
citrus |
| petitgrain lemon oil | FL/FR |
coumarinic |
| phthalide | FL/FR |
creamy |
gamma- | undecalactone (aldehyde C-14 (so-called)) | FL/FR |
fatty |
(Z)-3- | hexen-1-yl benzoate | FL/FR |
1- | methyl thio-3-octanone | FL |
2- | nonenal | FL/FR |
(E)-2- | octenal | FL/FR |
fermented |
| methyl thio isovalerate | FL |
floral |
| methyl dihydrojasmonate | FL/FR |
bitter | orangeflower absolute morocco | FL/FR |
| rose absolute (rosa damascena) bulgaria | FL/FR |
laevo- | rose oxide | FL/FR |
fruity |
2,4- | hexadien-1-ol | FL |
2- | hexen-1-ol | FL/FR |
| hexyl acetate | FL/FR |
| styralyl acetate | FL/FR |
green |
| acetaldehyde butyl phenethyl acetal | FL/FR |
| acetaldehyde ethyl phenethyl acetal | FL/FR |
iso | butyl methyl ketone | FL/FR |
2-iso | butyl-3-methyl pyrazine | FL/FR |
| cocoa butenal | FL/FR |
| cortex pyridine | FL/FR |
| cumin acetaldehyde | FL/FR |
| dibutyl sulfide | FL/FR |
| dihydroxyacetophenone (mixed isomers) | FL |
| diphenyl oxide | FL/FR |
alpha- | farnesene | FL/FR |
alpha- | farnesene isomer | FL/FR |
| galbanum decatriene | FL/FR |
| galbanum oil terpeneless | FL/FR |
| galbanum oleoresin | FL/FR |
| geranium absolute | FL/FR |
| geranium thiazole | FL/FR |
1- | hepten-3-ol | FL/FR |
(E)-2- | hexen-1-ol | FL/FR |
(Z)-2- | hexen-1-ol | FL/FR |
(E)-4- | hexen-1-ol | |
(Z)-4- | hexen-1-ol | FL/FR |
(E)-2- | hexen-1-yl acetate | FL/FR |
(Z)-3- | hexen-1-yl lactate | FL/FR |
(Z)-3- | hexen-1-yl methyl carbonate | FL/FR |
(Z)-3- | hexen-1-yl tiglate | FL/FR |
3- | hexenal | FL/FR |
2- | hexyl pyridine | FL |
| horseradish oil | FL |
(Z)- | leaf acetal | FL/FR |
| methyl heptenone | FL/FR |
| methyl heptine carbonate | FL/FR |
4- | methyl thiazole | FL |
| nerol oxide | FL/FR |
(E,Z)-2,6- | nonadien-1-yl acetate | FL/FR |
| octanal dimethyl acetal | FL/FR |
(Z)-5- | octen-1-yl propionate | FL/FR |
4- | penten-1-yl acetate | FL |
1- | penten-3-ol | FL/FR |
(E)-2- | pentenal | FL/FR |
3- | phenyl propionaldehyde | FL/FR |
| propylene glycol acetone ketal | FL |
| rose leaf absolute (rosa centifolia) | FL/FR |
(Z)- | rose oxide | FL/FR |
herbal |
| anthemis nobilis flower oil roman | FL/FR |
sweet | basil absolute | FL/FR |
iso | dihydrolavandulal | FL/FR |
| rosemary oleoresin | FL/FR |
metallic |
2,5- | dihydroxy-1,4-dithiane | FL |
3-( | methyl thio) hexanol | FL/FR |
musty |
S-( | methyl thio) butyrate | FL/FR |
| shoyu pyrazine | FL/FR |
2,3,5- | trimethyl pyrazine | FL/FR |
nutty |
2,4,5- | trimethyl thiazole | FL/FR |
onion |
| methyl propyl disulfide | FL |
4- | methyl-1,3-dithiolane | |
sulfurous |
| dimethyl sulfide | FL/FR |
| ethyl methyl mercaptopropionate | FL/FR |
| ethyl methyl sulfide | FL |
S- | methyl methioninium chloride | |
| potato butanone | FL |
tomato |
| methional | FL/FR |
| tomato essence | FL/FR |
vegetable |
| methyl 3-(methyl thio) propionate | FL/FR |
2- | methyl valeraldehyde | FL/FR |
2- | octen-4-one | FL/FR |
| potato butyraldehyde | FL |
| radish isothiocyanate | FL |
waxy |
(Z,Z)-3,6- | nonadien-1-ol | FL/FR |
|
Potential Uses:
Occurrence (nature, food, other): note
Synonyms:
2-iso | butyl-1,3-thiazole | iso | butyl-2 thiazole | 2-iso | butylthiazole | iso | butylthiazole | 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 |
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. |
|