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(2‐Hydroxypropyl)‐β‐Cyclodextrin Bio‐Reagent

Original price was: $1,995.00.Current price is: $995.00.

Catalog Number: B2027561 (250 mg)
n-Butyl-β-cyclodextrin is a chemically modified cyclic oligosaccharide derivative composed of seven α-1,4-linked D-glucopyranose units functionalized with n-butyl ether groups. Featuring a hydrophobic inner cavity with modified surface characteristics relative to native β-cyclodextrin, it facilitates the encapsulation, solubilization, and controlled release of hydrophobic guest molecules. It is primarily utilized as a specialized reagent, carrier matrix, and complexation agent in biotechnological research. Custom bulk amounts of this product are available upon request.

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Product Description

5/5 - (1 vote)

(2‐Hydroxypropyl)‐β‐Cyclodextrin Bio‐Reagent
Catalog number: B2027561
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 250 mg
Molecular Weight or Concentration: ~1380
Supplied as: Powder
Storage: RT
Keywords: Hydroxypropyl-β-cyclodextrin, HP-β-CD, HPBCD, Hydroxypropylbetadex, 2-Hydroxypropyl-beta-cyclodextrin

References:
1. Nicolaescu, O. E., et al. Cyclodextrins: Enhancing Drug Delivery, Solubility and Bioavailability for Modern Therapeutics. Pharmaceutics, 2025.
2. Spiridon, I., et al. Cyclodextrins as Multifunctional Platforms in Drug Delivery and Beyond: Structural Features, Functional Applications, and Future Trends. Molecules, 2025.
3. Christaki, S., et al. Cyclodextrins for the Delivery of Bioactive Compounds from Natural Sources: Medicinal, Food and Cosmetics Applications. Pharmaceuticals, 2023.
4. Hubner, E. M., Steinkellner, P., Schmid, M. G. Novel NPS involving chiral substance classes by means of cyclodextrins. Journal of Pharmaceutical and Biopharmaceutical Research, 2022.
5. Szejtli, J. Formation of inclusion complexes with cyclodextrins for drug solubility. Chemical Reviews, 2004.
6. Koontz, J. L., Marcy, J. E. Formation of cyclodextrin inclusion complexes with natamycin. Journal of Agricultural and Food Chemistry, 2003.
7. Badawy, M. E. I., Rabea, E. I. Chitosan and its derivatives as antimicrobial agents. International Journal of Carbohydrate Chemistry, 2014.
8. van der Merwe, S. M., et al. Absorption enhancement of peptides using chitosan derivatives. European Journal of Pharmaceutics and Biopharmaceutics, 2004.
9. Kasaai, M. R. Determination of degree of deacetylation of chitosan. Carbohydrate Polymers, 2009.
10. Dubois, M., et al. Colorimetric method for determination of sugars and related substances. Analytical Chemistry, 1956.
(2‐Hydroxypropyl)‐β‐Cyclodextrin Bio‐Reagent

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Additional Information

Weight 0.15 oz
Dimensions 2 × 0.5 × 0.5 in
5/5 - (1 vote)

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