(S)-N,N'-dibutyl-2-[(1-oxododecyl)amino]glutaramide

95%

Reagent Code: #235731
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CAS Number 63663-21-8

science Other reagents with same CAS 63663-21-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 439.68 g/mol
Formula C₂₅H₄₉N₃O₃
thermostat Physical Properties
Melting Point 155-163 ℃
Boiling Point 678.5 °C at 760 mmHg
inventory_2 Storage & Handling
Density 0.957±0.06 g/cm3
Storage 2-8°C

description Product Description

Used as a chiral derivatizing agent in analytical chemistry, particularly for the separation and detection of enantiomers in complex mixtures. Its structure allows selective interaction with chiral compounds, making it valuable in high-performance liquid chromatography (HPLC) and capillary electrophoresis. Commonly applied in pharmaceutical analysis to resolve racemic mixtures and assess enantiomeric purity during drug development. Also employed in studies involving asymmetric synthesis where monitoring stereochemical outcomes is critical.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿8,400.00
inventory 25g
10-20 days ฿29,380.00

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(S)-N,N'-dibutyl-2-[(1-oxododecyl)amino]glutaramide
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Used as a chiral derivatizing agent in analytical chemistry, particularly for the separation and detection of enantiomers in complex mixtures. Its structure allows selective interaction with chiral compounds, making it valuable in high-performance liquid chromatography (HPLC) and capillary electrophoresis. Commonly applied in pharmaceutical analysis to resolve racemic mixtures and assess enantiomeric purity during drug development. Also employed in studies involving asymmetric synthesis where monitoring

Used as a chiral derivatizing agent in analytical chemistry, particularly for the separation and detection of enantiomers in complex mixtures. Its structure allows selective interaction with chiral compounds, making it valuable in high-performance liquid chromatography (HPLC) and capillary electrophoresis. Commonly applied in pharmaceutical analysis to resolve racemic mixtures and assess enantiomeric purity during drug development. Also employed in studies involving asymmetric synthesis where monitoring stereochemical outcomes is critical.

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