N-(Trimethylsilyl)imidazole (TSIM) CAS 18156-74-6 Purity >99.0% (GC) Factory Main Product

Short Description:

Chemical Name: N-(Trimethylsilyl)imidazole (TSIM)

CAS: 18156-74-6

Purity: >99.0% (GC)

Appearance: Colorless Clear Liquid

High Quality, Commercial Production

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Product Detail

Product Tags

Description:

Manufacturer Supply, High Purity, Commercial Production
Chemical Name: N-(Trimethylsilyl)imidazole (TSIM)
CAS: 18156-74-6

Chemical Properties:

Chemical Name	N-(Trimethylsilyl)imidazole
Synonyms	TSIM; 1-(Trimethylsilyl)imidazole; TMS-Imidazole; N-Trimethylsilylimidazole; 1-(Trimethylsilyl)-1H-Imidazole
CAS Number	18156-74-6
CAT Number	RF-PI978
Stock Status	In Stock, Production Scale Up to Tons
Molecular Formula	C6H12N2Si
Molecular Weight	140.26
Melting Point	-42℃
Boiling Point	93.0~94.0℃/14 mmHg (lit.)
Specific Gravity (20/20)	0.957 g/mL
Refractive Index	n20/D 1.4751~1.4780 (lit.)
Solubility	Soluble in Acetonitrile, Acetone, Pyridine
Brand	Ruifu Chemical

Specifications:

Item	Specifications
Appearance	Colorless Clear Liquid
Purity / Analysis Method	>99.0% (GC)
Total Impurities	<1.0%
Properties	Deliquescence Easily
Test Standard	Enterprise Standard
Usage	Silanizing Protectant; Silylation Reagents; for Gas Chromatography

Package & Storage:

Package: Bottle, 25kg/Barrel, or 180kg/Drum, or according to customer's requirement.

Storage Condition: Store in sealed containers at cool and dry place; Protect from light and moisture.

Advantages:

FAQ:

Application:

N-(Trimethylsilyl)imidazole (TSIM) (CAS: 18156-74-6) is a general silylating agent, particularly for alcohols. An intermediate for the synthesis of imidazole derivatives. Silylating reagent for the protection of hydroxyl groups in the presence of amine functionalities. N-(Trimethylsilyl)imidazole is a derivatisation agent used in gas chromatography/mass spectrometry applications. N-(Trimethylsilyl)imidazole is a silylating agent for alcohols and 1,3-dicarbonyl compounds; reaction with esters to give imidazolides; preparation of O-trimethylsilyl monothioacetals; aromatization of the A-ring of steroids. It participates in the reactions of Hydroxyl Silylation Reactions, Silyl Aminal Formation Reactions, Nitrogen Silylation Reactions, Acyl Imidazole Formation, Michael Addition Reactions, Substitution Reactions, Phosphoroimidazolidate Formation, and other uses.