Heptakis[6-(2-aminoethylamino)-6-deoxy]-β-cyclodextrin

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Heptakis[6-(2-aminoethylamino)-6-deoxy]-β-cyclodextrin

Catalog CD183069387

CAS Number 183069-38-7

Cyclodextrin Type Cyclodextrin derivatives

Packaging 2 g, 3 g, 5 g, 10 g

Storage Condition Store at room temperature, in tightly closed container

Shelf Life 1 year

Availability In stock

*On-demand pack size is available, please contact us for multi-kilograms pack sizes.

Product Description

Heptakis[6-(2-aminoethylamino)-6-deoxy]-β-cyclodextrin is a chemically modified derivative of β-cyclodextrin, a cyclic oligosaccharide composed of seven glucose units linked by α-1,4-glycosidic bonds. This particular modification involves the introduction of aminoethylamino groups at the 6-position of each glucose unit, replacing the hydroxyl groups to enhance the molecule's functional properties. The added amino groups make the cyclodextrin highly water-soluble and improve its ability to form inclusion complexes with various guest molecules, which is beneficial in applications such as drug delivery, catalysis, and supramolecular chemistry. By altering the solubility and binding characteristics, heptakis[6-(2-aminoethylamino)-6-deoxy]-β-cyclodextrin serves as a versatile agent in both research and industrial applications, offering novel solutions for improving the stability and solubility of hydrophobic compounds.

Specification

Applications

Heptakis[6-(2-aminoethylamino)-6-deoxy]-β-cyclodextrin has a range of applications across various fields due to its unique chemical structure and properties.

• Drug delivery. This modified cyclodextrin enhances the solubility, stability, and bioavailability of hydrophobic drug molecules. By forming inclusion complexes with drugs, it facilitates improved therapeutic efficacy and controlled release.

• Catalysis. The compound's ability to chelate transition metals makes it valuable in constructing artificial enzyme systems. It can complex with transition metals such as iron (Fe), cobalt (Co), nickel (Ni), and platinum (Pt), effectively catalyzing specific reactions.

• Supramolecular chemistry. The primary amines within the aminoethylamino groups serve as excellent linkers, capable of forming bonds with carboxylic acids, esters, anhydrides, aldehydes, ketones, and alkyl halides under mild conditions. Consequently, aminoethylamino-modified cyclodextrin acts as superb intermediate for constructing complex supramolecular architectures.

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