N-(Trifluoromethanesulfonyl)trifluoroacetamide

≥98%

Reagent Code: #124815
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CAS Number 151198-85-5

science Other reagents with same CAS 151198-85-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.1 g/mol
Formula C₃HF₆NO₃S
thermostat Physical Properties
Melting Point 42-47°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a derivatization agent in analytical chemistry, particularly in gas chromatography-mass spectrometry (GC-MS) for the analysis of compounds like alcohols, phenols, and amines. Enhances the detection and separation of these compounds by converting them into more volatile and thermally stable derivatives. Also employed in organic synthesis as a reagent for introducing trifluoromethanesulfonyl (triflyl) groups, which can improve the biological activity and stability of pharmaceutical compounds. Its strong electron-withdrawing properties make it valuable in the development of advanced materials and catalysts.

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inventory 250mg
10-20 days ฿10,510.00

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N-(Trifluoromethanesulfonyl)trifluoroacetamide
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Used as a derivatization agent in analytical chemistry, particularly in gas chromatography-mass spectrometry (GC-MS) for the analysis of compounds like alcohols, phenols, and amines. Enhances the detection and separation of these compounds by converting them into more volatile and thermally stable derivatives. Also employed in organic synthesis as a reagent for introducing trifluoromethanesulfonyl (triflyl) groups, which can improve the biological activity and stability of pharmaceutical compounds. Its s

Used as a derivatization agent in analytical chemistry, particularly in gas chromatography-mass spectrometry (GC-MS) for the analysis of compounds like alcohols, phenols, and amines. Enhances the detection and separation of these compounds by converting them into more volatile and thermally stable derivatives. Also employed in organic synthesis as a reagent for introducing trifluoromethanesulfonyl (triflyl) groups, which can improve the biological activity and stability of pharmaceutical compounds. Its strong electron-withdrawing properties make it valuable in the development of advanced materials and catalysts.

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