2,3,4,5,6-Pentafluorophenoxyacetyl chloride

99%

Reagent Code: #132831
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CAS Number 55502-53-9

science Other reagents with same CAS 55502-53-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.55 g/mol
Formula C₈H₂ClF₅O₂
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MDL Number MFCD01320685
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used primarily as a derivatization reagent in analytical chemistry, especially in gas chromatography (GC) and mass spectrometry (MS). It introduces a highly fluorinated aromatic group to compounds containing active hydrogen atoms, such as alcohols, phenols, and amines, enhancing their volatility, thermal stability, and detection sensitivity. The pentafluorophenyl group improves electron-capture properties, making derivatized analytes easier to detect using electron capture detectors (ECD) or in negative ion chemical ionization (NICI) mass spectrometry. Commonly applied in environmental analysis, metabolomics, and pesticide residue testing due to its ability to increase selectivity and lower detection limits. Also employed in the synthesis of specialty agrochemicals and pharmaceuticals where fluorinated building blocks are needed to modulate lipophilicity and metabolic stability.

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inventory 5g
10-20 days ฿20,000.00

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2,3,4,5,6-Pentafluorophenoxyacetyl chloride
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Used primarily as a derivatization reagent in analytical chemistry, especially in gas chromatography (GC) and mass spectrometry (MS). It introduces a highly fluorinated aromatic group to compounds containing active hydrogen atoms, such as alcohols, phenols, and amines, enhancing their volatility, thermal stability, and detection sensitivity. The pentafluorophenyl group improves electron-capture properties, making derivatized analytes easier to detect using electron capture detectors (ECD) or in negative

Used primarily as a derivatization reagent in analytical chemistry, especially in gas chromatography (GC) and mass spectrometry (MS). It introduces a highly fluorinated aromatic group to compounds containing active hydrogen atoms, such as alcohols, phenols, and amines, enhancing their volatility, thermal stability, and detection sensitivity. The pentafluorophenyl group improves electron-capture properties, making derivatized analytes easier to detect using electron capture detectors (ECD) or in negative ion chemical ionization (NICI) mass spectrometry. Commonly applied in environmental analysis, metabolomics, and pesticide residue testing due to its ability to increase selectivity and lower detection limits. Also employed in the synthesis of specialty agrochemicals and pharmaceuticals where fluorinated building blocks are needed to modulate lipophilicity and metabolic stability.

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