3A-Amino-3A-deoxy-(2AS,3AS)-α-cyclodextrin (CAS 121916-94-7)

3A-Amino-3A-deoxy-(2AS,3AS)-α-cyclodextrin, a modified form of cyclodextrin, has emerged as a valuable tool in scientific research, particularly in the fields of chemistry, materials science, and biotechnology. One of its primary mechanisms of action stems from its unique structure, which consists of a cyclic arrangement of glucose units with a cavity in the center. This cavity enables 3A-amino-3A-deoxy-(2AS,3AS)-α-cyclodextrin to encapsulate guest molecules of appropriate size and shape, forming inclusion complexes through non-covalent interactions such as hydrogen bonding and hydrophobic interactions. Researchers have exploited this property for various applications, including drug delivery, encapsulation of flavor and fragrance molecules, and separation and purification of biomolecules. Additionally, 3A-amino-3A-deoxy-(2AS,3AS)-α-cyclodextrin has been utilized in the synthesis of novel materials, such as nanoparticles and supramolecular assemblies, due to its ability to act as a versatile building block or scaffold. Furthermore, its chiral nature has facilitated applications in chiral separation and chromatography, enabling the resolution of enantiomers and stereoisomers in analytical and preparative chemistry. By harnessing the unique properties of 3A-amino-3A-deoxy-(2AS,3AS)-α-cyclodextrin, researchers continue to explore its diverse applications and potential contributions to advancing scientific knowledge and technological innovation.