Provided is a separation method for amine, the separation method including performing liquid chromatography, wherein a separating agent in which a ligand having a crown ether-like cyclic structure is supported on a carrier is used as a stationary phase, and wherein a mobile phase contains an aqueous solution of at least one salt of a hydrophobic anion selected from the group consisting of a salt of a chaotropic anion and a salt of a hydrophobic organic acid.

A chiral stationary phase comprises a porous framework material and biomolecules. The porous framework material includes one of the metal-organic framework (MOF) material, the covalent organic framework (COF) material and the hydrogen-bonded organic framework (HOF) material. The biomolecules are biological chiral resolving agents. A pore size of the porous framework material is 0.2-15 nm. The porous framework material serves as a solid carrier. The biomolecules are loaded into the porous framework material. The porous framework material is modified with one or more of carboxyl, hydroxyl, amino, aldehyde, double bonds and mercapto groups.

The present disclosure provides methods for the separation and quantitation of enantiomers of vitamin E using supercritical fluid chromatography (SFC) or carbon dioxide-based chromatography on chiral columns. The disclosed methods may be used to quantitatively determine the concentration of RRR-α-tocopherol in foods, food ingredients, dietary supplements, vitamin premixes, nutritional formulas, and medicines. Further provided is a method of differentiating the source of α-tocopherol as natural or synthetic.

Provided is a separating agent for optical isomers, which is excellent in solvent resistance and has optical separating ability comparable to or higher than that of existing separating agents for optical isomers of chemical bonding type or physical adsorption type. In the separating agent for optical isomers, amylose (3-chloro-5-methylphenylcarbamate) is supported on a carrier through chemical bonding.

Provided are two-dimensional chromatography systems and methods for separating and/or analyzing complex mixtures of organic compounds. In particularly, a two-dimensional reversed-phase liquid chromatography (RPLC)—supercritical fluid chromatography (SFC) system is described including a trapping column at the interface which collects the analytes eluted from the first dimension chromatography while letting the RPLC mobile phase pass through. The peaks of interest from the RPLC dimension column are effectively focused as sharp concentration pulses on the trapping column, which is subsequently injected onto the second dimension SFC column. The system can be used for simultaneous achiral and chiral analysis of pharmaceutical compounds. The first dimension RPLC separation provides the achiral purity result, and the second dimension SFC separation provides the chiral purity result (enantiomeric excess).

Chiral polymer microspheres have a porous structure of a concentric multi-shell structure. Each layer of the multi-shell structure is optically and structurally anisotropic. The optical axes of adjacent layers have a sequential slight twist. All layers of the multi-shell structure generate a helix configuration and the chiral polymer microspheres are optically active. A method for preparing the chiral polymer microspheres, includes: forming a homogeneous liquid crystal mixture; dispersing the liquid crystal mixture into a continuous phase to form liquid crystal droplets through an emulsification process; polymerizing the reactive liquid crystal to form intermediate microspheres; and removing the one non-reactive liquid crystal and the chiral additive to form the chiral polymer microspheres. The chiral polymer microspheres have a porous structure and a swelling ability, and can be used as the stationary phase in chiral chromatograph, improving separation efficiency.

The present disclosure provides methods for the separation and quantitation of enantiomers of vitamin E using supercritical fluid chromatography (SFC) or carbon dioxide-based chromatography on chiral columns. The disclosed methods may be used to quantitatively determine the concentration of RRR-α-tocopherol in foods, food ingredients, dietary supplements, vitamin premixes, nutritional formulas, and medicines. Further provided is a method of differentiating the source of α-tocopherol as natural or synthetic.

Chiral polymer microspheres have a porous structure of a concentric multi-shell structure. Each layer of the multi-shell structure is optically and structurally anisotropic. The optical axes of adjacent layers have a sequential slight twist. All layers of the multi-shell structure generate a helix configuration and the chiral polymer microspheres are optically active. A method for preparing the chiral polymer microspheres, includes: forming a homogeneous liquid crystal mixture; dispersing the liquid crystal mixture into a continuous phase to form liquid crystal droplets through an emulsification process; polymerizing the reactive liquid crystal to form intermediate microspheres; and removing the one non-reactive liquid crystal and the chiral additive to form the chiral polymer microspheres. The chiral polymer microspheres have a porous structure and a swelling ability, and can be used as the stationary phase in chiral chromatograph, improving separation efficiency.

The present invention provides novel chromatographic materials, e.g., for chromatographic separations, processes for its preparation and separations devices containing the chromatographic material; separations devices, chromatographic columns and kits comprising the same; and methods for the preparation thereof. The chromatographic materials of the invention are high purity chromatographic materials comprising a chromatographic surface wherein the chromatographic surface comprises a hydrophobic surface group and one or more ionizable modifier.

The present invention provides novel chromatographic materials, e.g., for chromatographic separations, processes for its preparation and separations devices containing the chromatographic material; separations devices, chromatographic columns and kits comprising the same; and methods for the preparation thereof. The chromatographic materials of the invention are high purity chromatographic materials comprising a chromatographic surface wherein the chromatographic surface comprises a hydrophobic surface group and one or more ionizable modifier.