4-(Dimethylamino)benzenesulfonylchloride

≥95%

Reagent Code: #179888
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CAS Number 19715-49-2

science Other reagents with same CAS 19715-49-2

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scatter_plot Molecular Information
Weight 219.69 g/mol
Formula C₈H₁₀ClNO₂S
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MDL Number MFCD19200057
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a derivatizing agent in analytical chemistry to enhance detection of compounds containing hydroxyl or amino groups. It reacts readily with alcohols, phenols, and amines to form sulfonate esters or sulfonamides, which are more stable and easier to analyze by techniques such as HPLC, GC, or mass spectrometry. Commonly applied in the modification of peptides and steroids to improve their chromophoric or fluorogenic properties for sensitive detection. Also employed in the synthesis of dyes and functional materials due to its electron-donating dimethylamino group and reactive sulfonyl chloride functionality.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,580.00
inventory 250mg
10-20 days ฿9,860.00
inventory 1g
10-20 days ฿27,380.00

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4-(Dimethylamino)benzenesulfonylchloride
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Used primarily as a derivatizing agent in analytical chemistry to enhance detection of compounds containing hydroxyl or amino groups. It reacts readily with alcohols, phenols, and amines to form sulfonate esters or sulfonamides, which are more stable and easier to analyze by techniques such as HPLC, GC, or mass spectrometry. Commonly applied in the modification of peptides and steroids to improve their chromophoric or fluorogenic properties for sensitive detection. Also employed in the synthesis of dyes

Used primarily as a derivatizing agent in analytical chemistry to enhance detection of compounds containing hydroxyl or amino groups. It reacts readily with alcohols, phenols, and amines to form sulfonate esters or sulfonamides, which are more stable and easier to analyze by techniques such as HPLC, GC, or mass spectrometry. Commonly applied in the modification of peptides and steroids to improve their chromophoric or fluorogenic properties for sensitive detection. Also employed in the synthesis of dyes and functional materials due to its electron-donating dimethylamino group and reactive sulfonyl chloride functionality.

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