N,O-Bis(diethylhydrogensilyl)trifluoroacetamide

85%

Reagent Code: #217696
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CAS Number 105384-38-1

science Other reagents with same CAS 105384-38-1

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scatter_plot Molecular Information
Weight 285.46 g/mol
Formula C₁₀H₂₂F₃NOSi₂
badge Registry Numbers
MDL Number MFCD00144992
inventory_2 Storage & Handling
Storage Room temperature, stored in inert gas

description Product Description

Used primarily as a silylating agent in analytical chemistry, especially in gas chromatography (GC) and mass spectrometry (MS). It efficiently introduces silyl groups to hydroxyl, amino, and other active hydrogen-containing functional groups in organic molecules, enhancing their volatility and thermal stability for better GC separation and detection. Its trifluoroacetamide structure increases reactivity compared to standard silylating reagents, allowing faster derivatization under mild conditions. Commonly applied in the analysis of steroids, drugs, and metabolites in biological samples. Also useful in protecting functional groups during multi-step organic synthesis due to the selectivity and ease of removal of the diethylsilyl group.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿3,060.00

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N,O-Bis(diethylhydrogensilyl)trifluoroacetamide
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Used primarily as a silylating agent in analytical chemistry, especially in gas chromatography (GC) and mass spectrometry (MS). It efficiently introduces silyl groups to hydroxyl, amino, and other active hydrogen-containing functional groups in organic molecules, enhancing their volatility and thermal stability for better GC separation and detection. Its trifluoroacetamide structure increases reactivity compared to standard silylating reagents, allowing faster derivatization under mild conditions. Common

Used primarily as a silylating agent in analytical chemistry, especially in gas chromatography (GC) and mass spectrometry (MS). It efficiently introduces silyl groups to hydroxyl, amino, and other active hydrogen-containing functional groups in organic molecules, enhancing their volatility and thermal stability for better GC separation and detection. Its trifluoroacetamide structure increases reactivity compared to standard silylating reagents, allowing faster derivatization under mild conditions. Commonly applied in the analysis of steroids, drugs, and metabolites in biological samples. Also useful in protecting functional groups during multi-step organic synthesis due to the selectivity and ease of removal of the diethylsilyl group.

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