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Home > Encyclopedia > 2,4,5-Trimethylthiazole

2,4,5-Trimethylthiazole

2,4,5-Trimethylthiazole structure

2,4,5-Trimethylthiazole 

structure
  • CAS No:

    13623-11-5

  • Formula:

    C6H9NS

  • Chemical Name:

    2,4,5-Trimethylthiazole

  • Synonyms:

    Thiazole,2,4,5-trimethyl-;Thiazole,trimethyl-;2,4,5-Trimethylthiazole;Trimethylthiazole;NSC 170614;2,4,5-Trimethyl-1,3-thiazole

  • Categories:

    Flavors and Fragrances  >  Synthetic Fragrances

Description

clear colourless to yellow liquid 2,4,5-Trimethyl thiazole has a cocoa, dark chocolate, nutty, coffee taste.ChEBI: A 1,3-thiazole that is thiazole in which all three hydrogens are replaced by methyl groups. A Maillard reaction product, it is a flavour component in many cooked foods, including cooked meats and potatoes.2,4,5-trimethyl thiazole has a cocoa, dark chocolate, nutty, coffee note. It is naturally found in cooked potatoes, cooked meat, coffee, black tea, and herbs. It is used as a flav


Clear colourless liquid; cocoa, dark chocolate, nutty, coffee-like odour


2,4,5-trimethylthiazole is a 1,3-thiazole that is thiazole in which all three hydrogens are replaced by methyl groups. A Maillard reaction product, it is a flavour component in many cooked foods, including cooked meats and potatoes. It has a role as a Maillard reaction product.

2,4,5-Trimethylthiazole Basic Attributes

127.21

127.21

107148

237-107-9

6393273PE0

170614

DTXSID5065564

29339900

Characteristics

41.1

2.2

Clear, colorless.

1.0327 g/cm3 @ Temp: 20 °C

213-215 °C @ Solvent: Ethanol

164-166 °C

133 °F

n 20/D 1.509(lit.)

slightly|Soluble in organic solvents|Miscible at room temperature (in ethanol)

Store in a cool, dry place. Keep container closed when not in use.

2.11mmHg at 25°C

Safety Information

III

3.2

UN 1993 3/PG 3

3

22-37/38-41-36/37/38

26-39-37/39-36-7/9

Xn,Xi

Stable under normal temperatures and pressures.

P261-P280-P305 + P351 + P338

H226-H302-H315-H318-H335

|Warning|H302 (97.59%): Harmful if swallowed [Warning Acute toxicity, oral]|P264, P270, P301+P312, P330, and P501|Aggregated GHS information provided by 1450 companies from 10 notifications to the ECHA C&L Inventory.

Drug Information

2,4,5-trimethylthiazole

2,4,5-Trimethylthiazole Use and Manufacturing

Methods of Manufacturing

It is formed by decarboxylation of 2, 4-dimethylthiazole-5-acetic acid. It is formed by the reaction of methyl-α-bromoethyl ketone and acetamide under the catalysis of phosphorus pentoxide.

Uses

Used as fragrance intermediate, organic synthesis reagent

Thiazole, 2,4,5-trimethyl-: ACTIVE

Food additives -> Flavoring Agents|Flavoring Agents -> JECFA Flavorings Index

Flavoring Agents

Computed Properties

Molecular Weight:127.21
XLogP3:2.2
Hydrogen Bond Acceptor Count:2
Exact Mass:127.04557046
Monoisotopic Mass:127.04557046
Topological Polar Surface Area:41.1
Heavy Atom Count:8
Complexity:84.6
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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