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Trimethyl thiazole

2,4,5-Trimethylthiazole

CAS: 13623-11-5

Molecular Formula: C6H9NS

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Trimethyl thiazole - Names and Identifiers

Name 2,4,5-Trimethylthiazole
Synonyms FEMA 3325
FEMA NUMBER 3325
TRIMETHYLTHIAZOLE
Trimethyl thiazole
2,4,5-trimethyl-thiazol
2,4,5-Trimethylthiazole
2,4,5-TRIMETHYLTHIAZOLE
TRIMETHYL(2,4,5-) THIAZOLE
2,4,5-Trimethyl-1,3-thiazole
CAS 13623-11-5
EINECS 237-107-9
InChI InChI=1/C6H9NS/c1-4-5(2)8-6(3)7-4/h1-3H3

Trimethyl thiazole - Physico-chemical Properties

Molecular FormulaC6H9NS
Molar Mass127.207
Density1.051g/cm3
Melting Point-32.4°C
Boling Point168.7°C at 760 mmHg
Flash Point56.1°C
Vapor Presure2.11mmHg at 25°C
AppearanceMorphological liquid
pKapK1:4.55 (25°C,μ=0.1)
Storage ConditionKeep in dark place,Inert atmosphere,Room temperature
Refractive Index1.527
Physical and Chemical PropertiesLiquid, with chocolate flavor.
boiling point 167 ℃
relative density 1.013g/cm3
refractive index 1.5090
UseUsed as a fragrance intermediate, organic synthesis reagent

Trimethyl thiazole - Risk and Safety

Hazard SymbolsXi - Irritant
Irritant
Risk CodesR36/37/38 - Irritating to eyes, respiratory system and skin.
Safety DescriptionS26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S37/39 - Wear suitable gloves and eye/face protection
UN IDsUN 1993 3/PG 3
WGK Germany3
TSCAYes
HS Code29339900
Hazard Class3.2
Packing GroupIII

Trimethyl thiazole - Upstream Downstream Industry

Raw MaterialsAcetamide
2,4-Dimethylthiazole
Thiazole, 5-ethyl-2-methyl-
5-ethyl-2,4-dimethylthiazole
1,2,4,5-Tetrathiane, 3,6-dimethyl-
2,5-Dihydro-alpha-2,4,5-tetramethyl-2-thiazolemethanethiolo]
(2,4-DIMETHYL-THIAZOL-5-YL)-ACETIC ACID
Tetramethylpyrazine
2,4,5-TRIMETHYLOXAZOLE
2,4,5-TriMethyl-4,5-dihydrothiazole
5-BROMO-2,4-DIMETHYL-1,3-THIAZOLE
N-(1-methyl-2-oxopropyl)acetamide
CHLORIDE STANDARD
3-Ethyl-2,5-diMethylpyrazine
3-BROMO-2-BUTANONE
Downstream Products2,5-Dihydrothiophene
2-Ethyl-4-methyl thiazole

Trimethyl thiazole - Uses and synthesis methods

Toxicity

GRAS(FEMA).

use limited

FEMA(mg/kg): cold drinks, candy, 2.0; Seasonings, pickles, meat products, meat soup, 6.0.

production method

It is decarboxylated from 2, 4-dimethylthiazol-5-acetic acid.

It is formed by the reaction of methyl-α-bromoethyl ketone and acetamide under the catalysis of phosphorus pentoxide.

Last Update:2024-04-09 21:21:28

Trimethyl thiazole - Nature

FEMA 3325 | 2,4,5-TRIMETHYLTHIAZOLE
Specific gravity 1.311.013
JECFA Number 1036
BRN 107148
NIST chemical information Thiazole, 2,4,5-trimethyl-(13623-11-5)
EPA chemical information Thiazole, trimethyl- (13623-11-5)
Last Update:2024-04-09 18:58:34
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View History
Trimethyl thiazole
trans,trans-3,7-Dimethyl-10-isopropylidene-3,7-cyclodecadien-1-one
argutone
1-octene-3-one
2,3-DINITROBENZOIC ACID
2,2-Cryptand
Cumene hydroperoxide
disodium dodecyl(sulphonatophenoxy)benzenesulphonate
阿昔洛韦侧链
葡萄糖酸氯已定
Raw Materials for Trimethyl thiazole
2,5-Dihydro-alpha-2,4,5-tetramethyl-2-thiazolemethanethiolo]
(2,4-DIMETHYL-THIAZOL-5-YL)-ACETIC ACID
Tetramethylpyrazine
2,4,5-TRIMETHYLOXAZOLE
5-BROMO-2,4-DIMETHYL-1,3-THIAZOLE
N-(1-methyl-2-oxopropyl)acetamide
CHLORIDE STANDARD
3-Ethyl-2,5-diMethylpyrazine
Downstream Products for Trimethyl thiazole
2,5-Dihydrothiophene
2-Ethyl-4-methyl thiazole
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