6-O-alpha-D-Maltosyl-beta-cyclodextrin (CAS 104723-60-6 (anhydrous))

6-O-alpha-D-Maltosyl-beta-cyclodextrin, a modified cyclodextrin derivative, serves as a crucial tool in scientific research, particularly in the fields of chemistry, materials science, and biotechnology. Its mechanism of action revolves around its unique molecular structure, which consists of a cyclic arrangement of glucose units forming a truncated cone shape with a hydrophobic cavity. This cavity allows 6-O-alpha-D-Maltosyl-beta-cyclodextrin to encapsulate guest molecules, forming inclusion complexes through non-covalent interactions such as hydrogen bonding and hydrophobic interactions. Researchers leverage this property for various purposes, including drug delivery systems, encapsulation of bioactive compounds, and the separation and purification of biomolecules. Moreover, 6-O-alpha-D-Maltosyl-beta-cyclodextrin has demonstrated utility in the development of novel materials, such as nanoparticles and supramolecular assemblies, owing to its role as a versatile building block or scaffold. Additionally, its chiral nature facilitates applications in chiral separation and chromatography, enabling the resolution of enantiomers and stereoisomers in analytical and preparative chemistry. Through its distinctive properties and diverse applications, 6-O-alpha-D-Maltosyl-beta-cyclodextrin continues to advance scientific research across various disciplines.