Leírás és Paraméterek
Immobilized Cellulose-Based Chiral Phase with Tris-(3-chloro-4-methylphenyl)carbamate for Enantioselective Normal-Phase Chromatography
ReproSil Chiral-MIZ is a silica-based HPLC stationary phase with immobilized tris-(3-chloro-4-methylphenyl)carbamate cellulose, developed for enantioselective separations under normal-phase conditions. The cellulose derivative, substituted with 3-chloro-4-methylphenyl carbamate groups, provides a well-balanced combination of electronic and steric effects, resulting in high chiral recognition capability and excellent resolution across a broad range of racemic compounds.
Chiral discrimination on ReproSil Chiral-MIZ occurs through multiple intermolecular interactions — including hydrogen bonding, π–π stacking, dipole–dipole interactions, and steric complementarity — between analyte molecules and the immobilized chiral selector. The chlorine and methyl substituents on the aromatic rings fine-tune the polarity and π-acceptor properties of the selector, giving the phase a distinct and versatile selectivity profile for compounds with varying functional groups.
The chiral selector is covalently immobilized onto high-purity spherical silica, ensuring exceptional chemical and mechanical stability. This immobilization allows the use of a wide range of mobile phases, including polar and non-standard solvent systems, without loss of enantioselectivity or phase integrity. As a result, ReproSil Chiral-MIZ offers outstanding flexibility for both method development and routine enantioseparations. With its robust design and reproducible performance, ReproSil Chiral-MIZ is ideally suited for pharmaceutical, biochemical, and chemical applications, providing precise, high-resolution separations of chiral compounds under demanding analytical or preparative conditions.
ReproSil Chiral-MIZ combines the proven chiral recognition of cellulose tris-(3-chloro-4-methylphenyl)carbamate with the durability of immobilized silica technology – the reliable choice for accurate, robust, and reproducible enantioselective separations in normal-phase chromatography.
| Particle Sizes |
|
|---|---|
| Pore Size | 1 000 Å |
| Surface Area | 30 m²/g |
| Phase/Modification | Tris-(3-chloro-4-methylphenyl)carbamat-Cellulose |
| Particle Type | |
| Separation Modes | |
| Endcapping | No |
| pH Range | 2 to 8 |
Key Features:
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Silica-based stationary phase with immobilized tris-(3-chloro-4-methylphenyl)carbamate cellulose
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Designed for enantioselective separations under normal-phase conditions
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Strong chiral recognition via hydrogen bonding, π–π stacking, and dipole–dipole interactions
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Unique selectivity influenced by chlorine and methyl substituents on the aromatic rings
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Covalent immobilization for enhanced chemical and solvent stability
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High mechanical strength and reproducible performance
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Suitable for analytical and preparative chiral HPLC applications
Typical Applications:
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Enantioselective separation of pharmaceuticals, intermediates, and fine chemicals
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Analysis of racemic mixtures containing aromatic or halogenated substituents
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Method development and chiral screening in normal-phase and polar-organic modes
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Stereochemical purity testing and quality control in pharmaceutical and chemical research