24295-03-2

  • Product Name2-Acetylthiazole
  • MFC5H5NOS
  • Molecular Weight127.167
  • Purity99%
  • Appearancewhite to light yellow crystal powder
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Product Details

Quick Details

  • CasNo: 24295-03-2
  • MF: C5H5NOS
  • Appearance: white to light yellow crystal powder
  • Purity: 99%

Best Quality Manufacturer Supply Top Purity 99% 2-Acetylthiazole 24295-03-2 with Cheapest Price

  • Molecular Formula:C5H5NOS
  • Molecular Weight:127.167
  • Appearance/Colour:white to light yellow crystal powder 
  • Vapor Pressure:0.173mmHg at 25°C 
  • Melting Point:65.5 °C 
  • Refractive Index:n20/D 1.548(lit.)  
  • Boiling Point:212.509 °C at 760 mmHg 
  • PKA:0.05±0.10(Predicted) 
  • Flash Point:82.323 °C 
  • PSA:58.20000 
  • Density:1.227 g/cm3 
  • LogP:1.34570 
  • IDLH:1041 
  • IDLH:11726 
  • IDLH:3328 

2-Acetylthiazole(Cas 24295-03-2) Usage

Chemical Properties

2-Acetylthiazole is a colorless to pale yellow liquid with green onion, herbal, grassy, hazelnuts, roasted meat, caramel, corn, and butter odor. Natural products are found in beef broth. Slightly soluble with water, soluble in most organic solvents. It is used in foods as antioxidant, as appearance control agent, and as flavoring ingredient.

Occurrence

2-Acetylthiazole is naturally found in raw asparagus, cooked asparagus, kohlrabi, cooked or boiled potatoes, turkey (roasted), raw chicken, boiled and cooked beef, grilled and roasted beef, pork liver, beer, Finnish whiskey, heated beans, other varieties of mushroom, rice bran, maize, and other natural sources.

Uses

2-Acetylthiazole can be used as a flavoring agent in food industries. It may be used as a food additive in the preparation of ′fragrant′ rice. It also was used in the preparation of triazolothiazoles, chiral alcohols and in aldol condensation reactions.

Preparation

2-Acetylthiazole is formed by oxidation of the corresponding carbinol using dichromate.

Aroma threshold values

Detection at 4 ppb

Taste threshold values

Taste characteristics at 30 ppm: corn chip with slightly musty background

Synthesis Reference(s)

The Journal of Organic Chemistry, 53, p. 1748, 1988 DOI: 10.1021/jo00243a029

General Description

2-Acetylthiazole is a volatile flavoring substance generally formed by the Maillard reaction between an amino acid and carbonyl compounds. It is reported to occur in canned sweet corn products, cooked pine mushroom, cooked asparagus and roasted beef.

Purification Methods

Check NMR spectrum; if it is not too bad, distil it through an efficient column in a vacuum. The oxime sublimes at 140-145o, m 159o, and when crystallised from H2O has m 163-165.5o. [Erlenmeyer et al. Helv Chim Acta 31 1142 1948, Waisvisz et al. J Am Chem Soc 79 4524 1957, Menasseé et al. Helv Chim Acta 40 554 1957, Beilstein 27 IV 2617.]

Who Evaluation

Evaluation year: 2002

InChI:InChI=1/C5H5NOS/c1-4(7)5-6-2-3-8-5/h2-3H,1H3

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24295-03-2 Process route

L-Cysteine
52-90-4

L-Cysteine

[1-<sup>13</sup>C]ascorbic acid
178101-88-7

[1-13C]ascorbic acid

2,5-dihydro-thiophene
1708-32-3

2,5-dihydro-thiophene

thiophene
188290-36-0,8014-23-1,25233-34-5

thiophene

2-Methylthiophene
554-14-3

2-Methylthiophene

4,5-Dimethylthiazole
3581-91-7

4,5-Dimethylthiazole

4,5-Dihydro-2-methylthiophen-3-(2H)-on
74015-70-6,13679-85-1

4,5-Dihydro-2-methylthiophen-3-(2H)-on

2,4,5-trimethylthiazole
13623-11-5

2,4,5-trimethylthiazole

2-Acetylthiophene
88-15-3,97511-16-5

2-Acetylthiophene

2-Acetylthiazole
24295-03-2,260998-74-1

2-Acetylthiazole

2-acetyl-3-methylthiophene
13679-72-6

2-acetyl-3-methylthiophene

3-(vinylthio)thiophene
867253-51-8

3-(vinylthio)thiophene

Conditions
Conditions Yield
at 140 ℃; for 2h; pH=8; aq. phosphate buffer; Sealed vessel;
 
L-Cysteine
52-90-4

L-Cysteine

ascorbic acid
50-81-7,98966-42-8

ascorbic acid

2,5-dihydro-thiophene
1708-32-3

2,5-dihydro-thiophene

thiophene
188290-36-0,8014-23-1,25233-34-5

thiophene

2-Methylthiophene
554-14-3

2-Methylthiophene

4,5-Dimethylthiazole
3581-91-7

4,5-Dimethylthiazole

4,5-Dihydro-2-methylthiophen-3-(2H)-on
74015-70-6,13679-85-1

4,5-Dihydro-2-methylthiophen-3-(2H)-on

2,4,5-trimethylthiazole
13623-11-5

2,4,5-trimethylthiazole

2-Acetylthiophene
88-15-3,97511-16-5

2-Acetylthiophene

2-Acetylthiazole
24295-03-2,260998-74-1

2-Acetylthiazole

2-acetyl-3-methylthiophene
13679-72-6

2-acetyl-3-methylthiophene

3-(vinylthio)thiophene
867253-51-8

3-(vinylthio)thiophene

Conditions
Conditions Yield
at 140 ℃; for 2h; pH=8; aq. phosphate buffer; Sealed vessel;
 

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