58151AST

CHIRALPAK^® AGP (5 μm) HPLC Columns

L × I.D. 15 cm × 4 mm, HPLC Column

• UNSPSC Code: 41115700
• eCl@ss: 32110501
• NACRES: SB.52

Properties

• product name: CHIRALPAK^® AGP HPLC Column, 5 μm particle size, L × I.D. 15 cm × 4 mm
• material: stainless steel column
• Quality Level: 100
• Agency: suitable for USP L41
• product line: CHIRALPAK^®
• packaging: pkg of 1 ea
• manufacturer/tradename: CHIRALPAK^®
• parameter: 137 bar pressure (2000 psi); 20-30 °C temperature; 40 °C max. temp.
• technique(s): HPLC: suitable
• L × I.D.: 15 cm × 4 mm
• matrix: fully porous particle
• matrix active group: glycoprotein, alpha₁- phase
• particle size: 5 μm
• operating pH: 2-8
• separation technique: chiral
• storage temp.: 2-8°C

Description

General description

Hermansson described the use of natural proteins immobilized onto a silica support for chiral separations in 1983 (1). Proteins contain a large number of chiral centers of one configuration, and many other sites that contribute to the general retention process. CHIRALPAK AGP has the broadest range of selectivity of all protein phases currently available. CHIRALPAK AGP phase uses α₁-acid glycoprotein (AGP) as the chiral selector immobilized on spherical 5 μm silica particles. Bonded AGP is a very stable protein that tolerates pure organic solvents, elevated temperatures and pH values from 4 to 7. Operated in reversed-phase mode, CHIRALPAK AGP column separates enantiomers of an extremely broad range of drug substances, such as acids, amines and neutral compounds. The enantioselectivity and retention can easily be regulated by mobile phase pH and ionic strength, and the nature and concentration of the organic modifier.

Features:

• Direct reversed phase resolution of chiral molecules
• Stable with a variety of organic modifiers
• Available in analytical and semi-preparative sizes

(1) Hermansson, J. Direct liquid chromatographic resolution of racemic drugs using a1-acid glycoprotein as the chiral stationary phase. J. Chromatogr. A, 1983, 269, 71-80.

Application

• Evaluation of R- (-) and S- (+) Clenbuterol enantiomers during a doping cycle or continuous ingestion of contaminated meat using chiral liquid chromatography by LC-TQ-MS: This study demonstrates the use of a chiral HPLC column for the separation of clenbuterol enantiomers in biological samples, providing insights into the detection of doping substances or exposure to contaminated meat (Dolores et al., 2019).


• Stereochemical characterization of fluorinated 2-(phenanthren-1-yl)propionic acids by enantioselective high performance liquid chromatography analysis and electronic circular dichroism detection: This research highlights the capability of chiral HPLC columns to differentiate between the enantiomers of complex fluorinated compounds, offering a method for detailed analysis crucial in pharmaceutical studies (Bertucci et al., 2012).

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Legal Information

CHIRALPAK is a registered trademark of Daicel Corp.