6-(Dimethylamino)naphthalene-2-sulfonyl chloride

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Reagent Code: #130957
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CAS Number 60151-27-1

science Other reagents with same CAS 60151-27-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.75 g/mol
Formula C₁₂H₁₂ClNO₂S
badge Registry Numbers
MDL Number MFCD00467331
thermostat Physical Properties
Boiling Point 434.0±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.361±0.06 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Widely used in biochemistry and analytical chemistry for labeling primary and secondary amines due to its high fluorescence and sensitivity. Commonly employed to derivatize amino acids, peptides, and proteins, enabling their detection and quantification in techniques like HPLC and capillary electrophoresis. Frequently used in the synthesis of fluorescent probes and sensors, especially for monitoring enzymatic activity or studying molecular interactions. Its sulfonyl chloride group readily reacts with amine groups, forming stable sulfonamide bonds, making it ideal for covalent tagging in biological systems. Also utilized in the preparation of environment-sensitive dyes, where fluorescence properties change in response to polarity or binding events.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,950.00

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6-(Dimethylamino)naphthalene-2-sulfonyl chloride
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Widely used in biochemistry and analytical chemistry for labeling primary and secondary amines due to its high fluorescence and sensitivity. Commonly employed to derivatize amino acids, peptides, and proteins, enabling their detection and quantification in techniques like HPLC and capillary electrophoresis. Frequently used in the synthesis of fluorescent probes and sensors, especially for monitoring enzymatic activity or studying molecular interactions. Its sulfonyl chloride group readily reacts with ami

Widely used in biochemistry and analytical chemistry for labeling primary and secondary amines due to its high fluorescence and sensitivity. Commonly employed to derivatize amino acids, peptides, and proteins, enabling their detection and quantification in techniques like HPLC and capillary electrophoresis. Frequently used in the synthesis of fluorescent probes and sensors, especially for monitoring enzymatic activity or studying molecular interactions. Its sulfonyl chloride group readily reacts with amine groups, forming stable sulfonamide bonds, making it ideal for covalent tagging in biological systems. Also utilized in the preparation of environment-sensitive dyes, where fluorescence properties change in response to polarity or binding events.

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