Valeraldehyde-O-pentafluorophenylmethyl-oxime

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Reagent Code: #245174
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CAS Number 932710-56-0

science Other reagents with same CAS 932710-56-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 281.2218 g/mol
Formula C₁₂H₁₂F₅NO
badge Registry Numbers
MDL Number MFCD03427479
thermostat Physical Properties
Boiling Point 270.6±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.26±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a derivatizing agent in analytical chemistry, particularly in gas chromatography-mass spectrometry (GC-MS) for the detection and identification of carbonyl compounds. It reacts selectively with aldehydes and ketones to form stable oxime derivatives, enhancing volatility and thermal stability for improved chromatographic separation. Its pentafluorophenyl group provides strong electron-capturing properties, making it highly suitable for electron capture detection (ECD) in trace analysis. Commonly applied in environmental and biological samples to detect low-concentration carbonyls such as pollutants, metabolites, or degradation products.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿48,000.00
inventory 100mg
10-20 days ฿28,800.00
inventory 1g
10-20 days ฿96,000.00
inventory 25mg
10-20 days ฿15,680.00

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Valeraldehyde-O-pentafluorophenylmethyl-oxime
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Used as a derivatizing agent in analytical chemistry, particularly in gas chromatography-mass spectrometry (GC-MS) for the detection and identification of carbonyl compounds. It reacts selectively with aldehydes and ketones to form stable oxime derivatives, enhancing volatility and thermal stability for improved chromatographic separation. Its pentafluorophenyl group provides strong electron-capturing properties, making it highly suitable for electron capture detection (ECD) in trace analysis. Commonly a

Used as a derivatizing agent in analytical chemistry, particularly in gas chromatography-mass spectrometry (GC-MS) for the detection and identification of carbonyl compounds. It reacts selectively with aldehydes and ketones to form stable oxime derivatives, enhancing volatility and thermal stability for improved chromatographic separation. Its pentafluorophenyl group provides strong electron-capturing properties, making it highly suitable for electron capture detection (ECD) in trace analysis. Commonly applied in environmental and biological samples to detect low-concentration carbonyls such as pollutants, metabolites, or degradation products.

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