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24589-78-4 | N-Methyl-N-(trimethylsilyl)trifluoroacetamide

24589-78-4 | N-Methyl-N-(trimethylsilyl)trifluoroacetamide

N-Methyl-N-(trimethylsilyl)trifluoroacetamide is an organic compound. It is soluble in many organic solvents such as chlorinated hydrocarbons and acetone.

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Product Introduction
Products Description

 

Properties:
- Appearance:N-Methyl-N-(trimethylsilyl)trifluoroacetamide is a colorless liquid.
- Stability: N-Methyl-N-(trimethylsilyl)trifluoroacetamide is stable to water and air, but hydrolysis reaction may occur under strong alkali conditions.

Among the derivatization reagents used for gas chromatography, the derivatization reaction of the silylation reagent and the sample compound is carried out by substituting the active hydrogen of the hydroxyl group, carboxyl group, mercapto group, amino group and imino group with silyl group.

24589-78-4
N-Methyl-N-(trimethylsilyl)trifluoroacetamide
Basic Info

 

ITEMS

SPECIFICATION

Melting point

98-100°C

vapor pressure

8.8 mm Hg ( 27 °C)

color

Clear colorless to light yellow

storage temp.

2-8°C

Fp

77 °F

refractive index

n20/D 1.383

form

Liquid

EPA Substance Registry System

Acetamide, 2,2,2-trifluoro-N-methyl-N-(trimethylsilyl)- (24589-78-4)

Water Solubility

reacts

density

1.075 g/mL at 25 °C(lit.)

Boiling point

130132°C

Specific Gravity

1.076

pka

-1.34

InChIKey

MSPCIZMDDUQPGJ-UHFFFAOYSA-N

Sensitive

Moisture Sensitive

vapor density

>1 (vs air)

BRN

1941550

Hydrolytic Sensitivity

7

 

N-Methyl-N-(trimethylsilyl)trifluoroacetamide, 97%

 

Uses & Description

 

Uses:
- As a reagent: N-Methyl-N-(trimethylsilyl)trifluoroacetamide is commonly used as a reagent and activator in organic synthesis.
- As a photosensitive polymer material: it may be used in the preparation of photosensitive polymers for use in photolithography and microelectronic manufacturing.

Description:

N-Methyl-N-(trimethylsilyl)trifluoroacetamide is an organic solvent used for the extraction of hydroxylated fatty acids from human serum. MSTFA is a derivative of trifluoroacetic acid and is used for the extraction of hydroxylated fatty acids. The derivatization reaction mechanism involves a nucleophilic substitution reaction between the amine group on MSTFA and the hydroxyl group on the fatty acid. This reaction occurs in aqueous solution and is greatly influenced by pH. To remove matrix effects, such as ionic strength and pH, it is necessary to use dispersive solid phase extraction for sample preparation.

 

Company Profile

 

Now our products are exported to more than 30 countries and regions such as Holland, India, Australia, etc., enjoying high reputation and popularity in the international arena. Our company has been developing rapidly and has now become a one-stop buyer and service provider for many customers around the world. 

 

2,2,2-Trifluoro-N-methyl-N-(trimethylsilyl)acetamide

 

N-Methyl-N-(trimethylsilyl)trifluoroacetamide, 97%

 

FAQ 

 

What is the lead time for delivery?

For most chemicals we have in stock, it takes about 1-3 days after payment confirmation.

How to control and quality assurance?

a. High-grade clean workshop.

b. inspection center equipped with instruments of HPLC, GC, etc, R&D, and QC for testing of each batch. Cooperated with third-party test agencies for testing heavy metals, pesticide residues, allergens, etc.

Can you produce customized products?

Please provide us with the specifications of the products you require and we will get back to you after evaluation.

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