(S)-(-)-NBD-Pro-COCl [=(S)-(-)-4-Nitro-7-(2-chloroformylpyrrolidin-1-yl)-2,1,3-benzoxadiazole]

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Reagent Code: #235305
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CAS Number 159717-68-7

science Other reagents with same CAS 159717-68-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.67 g/mol
Formula C₁₁H₉ClN₄O₄
badge Registry Numbers
MDL Number MFCD00191512
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a fluorescent derivatization reagent for chiral amino acids and amines in analytical chemistry. Its high sensitivity allows detection of trace enantiomers in complex mixtures, particularly in HPLC and capillary electrophoresis. The reagent selectively reacts with primary and secondary amines, forming highly fluorescent derivatives that enable precise stereochemical analysis. Widely applied in pharmaceutical quality control to determine enantiomeric purity of drug substances. Also employed in biochemical research for labeling and imaging amine-containing biomolecules with minimal interference due to its distinct excitation and emission wavelengths.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿890.00
inventory 50mg
10-20 days ฿2,035.00

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(S)-(-)-NBD-Pro-COCl [=(S)-(-)-4-Nitro-7-(2-chloroformylpyrrolidin-1-yl)-2,1,3-benzoxadiazole]
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Used as a fluorescent derivatization reagent for chiral amino acids and amines in analytical chemistry. Its high sensitivity allows detection of trace enantiomers in complex mixtures, particularly in HPLC and capillary electrophoresis. The reagent selectively reacts with primary and secondary amines, forming highly fluorescent derivatives that enable precise stereochemical analysis. Widely applied in pharmaceutical quality control to determine enantiomeric purity of drug substances. Also employed in bioc

Used as a fluorescent derivatization reagent for chiral amino acids and amines in analytical chemistry. Its high sensitivity allows detection of trace enantiomers in complex mixtures, particularly in HPLC and capillary electrophoresis. The reagent selectively reacts with primary and secondary amines, forming highly fluorescent derivatives that enable precise stereochemical analysis. Widely applied in pharmaceutical quality control to determine enantiomeric purity of drug substances. Also employed in biochemical research for labeling and imaging amine-containing biomolecules with minimal interference due to its distinct excitation and emission wavelengths.

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