$1,995.00Original price was: $1,995.00.$995.00Current price is: $995.00.
Catalog Number: B2027546 (250 mg) Carboxymethyl-alpha-cyclodextrin sodium salt is an anionic cyclic oligosaccharide derivative composed of six alpha-1,4-linked D-glucose units functionalized with carboxymethyl sodium groups. Featuring a hydrophilic outer surface and a hydrophobic inner cavity, it offers enhanced water solubility and strong inclusion complexation capabilities. It is primarily utilized as a specialized reagent and carrier matrix to solubilize, stabilize, and…
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Catalog Number: B2027545 (250 mg) Mono-(2,3-di-O-benzyl)-heptakis-(2,3,6-tri-O-benzyl)-γ-Cyclodextrin is a selectively modified, perbenzylated derivative of γ-cyclodextrin featuring a single unfunctionalized hydroxyl group at the primary rim. This partially protected cyclic oligosaccharide serves as a versatile, site-specific building block for advanced supramolecular chemistry and host-guest functionalization. Custom bulk amounts of this product are available upon request. Live Chat enquiry about this product at:…
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Catalog Number: B2027544 (250 mg) 6-Monoamino-6-monodeoxy-γ-cyclodextrin hydrochloride is a selectively modified cyclic oligosaccharide derivative featuring a single amino substitution at the C-6 position of the γ-cyclodextrin ring. The introduced amino group provides a pH-dependent cationic charge and reactive site for targeted bioconjugation, while maintaining the characteristic hydrophobic cavity of γ-cyclodextrin. It serves as a versatile host molecule and building block…
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Catalog Number: B2027543 (250 mg) 6-Monoazido-6-monodeoxy-γ-Cyclodextrin is a selectively modified γ-cyclodextrin derivative containing a single azide functional group substituted at one of the C-6 primary hydroxyl positions on the macrocyclic ring. This monofunctionalized cyclodextrin serves as a versatile reactive building block for click chemistry applications, enabling bioorthogonal conjugation via copper-catalyzed azide-alkyne cycloaddition while preserving the native host-guest inclusion capabilities of…
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Catalog Number: B2027542 (250 mg) 6-Monoiodo-6-monodeoxy-γ-cyclodextrin is a selectively modified cyclic oligosaccharide derivative where a single primary hydroxyl group at the C-6 position of γ-cyclodextrin is replaced with an iodine atom. This mono-functionalized chemical serves as a versatile reactive intermediate for further site-specific modifications and nucleophilic substitution reactions. The compound is primarily utilized in advanced supramolecular chemistry and bioconjugation applications.…
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Catalog Number: B2027541 (250 mg) 6-Monomesyl-γ-Cyclodextrin is a selectively modified γ-cyclodextrin derivative featuring a single methanesulfonyl (mesyl) group at one of the primary C-6 hydroxyl positions. This regioselectively functionalized cyclic oligosaccharide acts as a key reactive intermediate, enabling nucleophilic displacement reactions to introduce various functional groups onto the γ-cyclodextrin macrocycle. It is widely utilized in chemical synthesis and supramolecular chemistry…
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Catalog Number: B2027540 (250 mg) Octakis-(2,3,6-tri-O-benzoyl)-γ-Cyclodextrin is a per-functionalized γ-cyclodextrin derivative in which all twenty-four hydroxyl groups at the C-2, C-3, and C-6 positions are esterified with benzoyl groups. This modification imparts strong hydrophobic character and high solubility in organic solvents, transforming the native cyclic oligosaccharide into a specialized hydrophobic host. It is widely utilized in supramolecular chemistry research and…
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Catalog Number: B2027539 (250 mg) Octakis-(2,3,6-tri-O-acetyl)-γ-cyclodextrin is a per-acetylated derivative of gamma-cyclodextrin in which all hydroxyl groups at the C-2, C-3, and C-6 positions across the eight glucopyranose units are converted to acetyl esters. This modification alters the hydrophilic-lipophilic balance, rendering the cyclic oligosaccharide derivative hydrophobic compared to parent γ-cyclodextrin. It is widely utilized as a specialized host molecule and…
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Catalog Number: B2027538 (250 mg) Octakis‐(2,3,6‐tri‐O‐benzyl)‐γ‐Cyclodextrin is a per-functionalized γ-cyclodextrin derivative in which all twenty-four hydroxyl groups across the C-2, C-3, and C-6 positions of the eight glucopyranose units are replaced with benzyl ether functional groups. This highly hydrophobic cyclic oligosaccharide features an expanded apolar cavity and hydrophobic exterior, making it a valuable chiral selector in chromatographic separations and a…
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Catalog Number: B2027537 (250 mg) Octakis-(2,3,6-tri-O-methyl)-γ-Cyclodextrin is a fully methylated derivative of γ-cyclodextrin in which all hydroxyl groups at the C-2, C-3, and C-6 positions are functionalized with methoxy groups. This chemical modification disrupts intramolecular hydrogen bonding, significantly altering its cavity properties and enhancing lipophilicity as well as organic solubility compared to native γ-cyclodextrin. It serves as a specialized macrocyclic…
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Catalog Number: B2027536 (250 mg) Octakis-(2,3,6-tri-O-methyl)-γ-Cyclodextrin is a per-methylated derivative of gamma-cyclodextrin in which the hydroxyl groups at the C-2, C-3, and C-6 positions of all eight glucopyranose units are replaced with methoxy groups. This hydrophobic modification alters its macrocyclic cavity environment, rendering it a useful supramolecular host for non-covalent inclusion complexation. It is extensively utilized as a chiral selector…
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Catalog Number: B2027535 (250 mg) Octakis-(2,3-di-O-acetyl-6-O-tert-butyldimethylsilyl)-γ-cyclodextrin is a derivatized cyclic oligosaccharide chiral selector featuring bulky tert-butyldimethylsilyl groups at the primary C-6 positions and acetyl groups at the C-2 and C-3 hydroxyl positions. Designed primarily for gas chromatography stationary phases, this modified gamma-cyclodextrin exhibits broad enantiorecognition capabilities through electron-donor-acceptor, hydrogen-bonding, and surface or inclusion interactions. It serves as a specialized analytical…