Leírás és Paraméterek
Amylose-Based Chiral Phase for Enantioselective Reversed-Phase Chromatography
ReproSil Chiral-AM-R is a silica-based HPLC stationary phase coated with tris-(3,5-dimethylphenyl)carbamate amylose, specifically developed for enantioselective separations under reversed-phase conditions. This chiral amylose derivative enables multiple molecular interactions – such as hydrogen bonding, dipole–dipole, and π–π interactions – which result in excellent chiral recognition and high enantioselectivity for a wide variety of racemic compounds.
In contrast to the normal-phase version, ReproSil Chiral-AM-R is optimized for aqueous and polar mobile phases, providing high stability and reproducible retention under reversed-phase conditions. The phase is built on high-purity spherical silica, ensuring outstanding mechanical robustness and consistent performance even in gradient or high-pressure operation. ReproSil Chiral-AM-R is ideal for pharmaceutical, biochemical, and academic laboratories performing enantioselective analysis, method development, or quality control of chiral active ingredients and intermediates.
ReproSil Chiral-AM-R combines amylose-based chiral selectivity with reversed-phase compatibility – the dependable choice for efficient and reproducible enantioselective separations under aqueous chromatographic conditions.
Attractive alternative to CHIRALPAK® AD-RH (Daicel®).
| Particle Sizes |
|
|---|---|
| Pore Size | 1 000 Å |
| Surface Area | 30 m²/g |
| Phase/Modification | Tris-(3,5-dimethylphenyl)carbamat-Amylose |
| Particle Type | |
| Separation Modes | |
| USP Code | |
| Endcapping | No |
| pH Range | 2 to 8 |
Key Features:
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Silica-based stationary phase coated with tris-(3,5-dimethylphenyl)carbamate amylose
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Optimized for enantioselective separations in reversed-phase chromatography
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Excellent chiral recognition via hydrogen bonding, dipole–dipole, and π–π interactions
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Stable and reproducible under aqueous and polar mobile phase conditions
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Suitable for analytical and preparative chiral HPLC applications
Typical Applications:
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Enantioselective separation of chiral pharmaceuticals and intermediates
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Quality control and purity testing of optically active compounds
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Method development for chiral reversed-phase HPLC
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Analysis of chiral biomolecules and polar organic compounds