N,N-Dimethyltrifluoroacetamide

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Reagent Code: #216864
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CAS Number 1547-87-1

science Other reagents with same CAS 1547-87-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 141.09 g/mol
Formula C₄H₆F₃NO
badge Registry Numbers
MDL Number MFCD00043555
thermostat Physical Properties
Boiling Point 132 °C
inventory_2 Storage & Handling
Density 1.23 g/cm3
Storage 2~8℃

description Product Description

Used primarily as a derivatization reagent in analytical chemistry, especially in gas chromatography-mass spectrometry (GC-MS). It introduces a trifluoroacetyl group to compounds containing active hydrogens, such as amines, alcohols, and amides, improving their volatility and thermal stability for better detection. Commonly applied in the analysis of pharmaceuticals, steroids, and forensic samples. Also serves as a reagent in organic synthesis for protection or modification of functional groups, particularly where fluorinated analogs are desired. Its use enhances sensitivity and resolution in detection due to the strong electron-withdrawing nature of the trifluoroacetyl group.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿780.00
inventory 25g
10-20 days ฿3,880.00
inventory 100g
10-20 days ฿11,710.00
inventory 500g
10-20 days ฿53,990.00

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N,N-Dimethyltrifluoroacetamide
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Used primarily as a derivatization reagent in analytical chemistry, especially in gas chromatography-mass spectrometry (GC-MS). It introduces a trifluoroacetyl group to compounds containing active hydrogens, such as amines, alcohols, and amides, improving their volatility and thermal stability for better detection. Commonly applied in the analysis of pharmaceuticals, steroids, and forensic samples. Also serves as a reagent in organic synthesis for protection or modification of functional groups, particul

Used primarily as a derivatization reagent in analytical chemistry, especially in gas chromatography-mass spectrometry (GC-MS). It introduces a trifluoroacetyl group to compounds containing active hydrogens, such as amines, alcohols, and amides, improving their volatility and thermal stability for better detection. Commonly applied in the analysis of pharmaceuticals, steroids, and forensic samples. Also serves as a reagent in organic synthesis for protection or modification of functional groups, particularly where fluorinated analogs are desired. Its use enhances sensitivity and resolution in detection due to the strong electron-withdrawing nature of the trifluoroacetyl group.

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