Date published: 2026-4-25

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Succinyl-(2-hydroxypropyl)-β-cyclodextrin

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Molecular Weight:
1767.59
Molecular Formula:
C70H110O51
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Succinyl-(2-hydroxypropyl)-β-cyclodextrin is a modified cyclodextrin used extensively in research to facilitate the delivery and solubility of hydrophobic compounds. This cyclodextrin derivative has a β-cyclodextrin backbone that is functionalized with succinyl and 2-hydroxypropyl groups, significantly improving its ability to form inclusion complexes with hydrophobic guest molecules. By encapsulating such molecules in its hydrophobic cavity, succinyl-(2-hydroxypropyl)-β-cyclodextrin increases their aqueous solubility, enhancing their transport and stability in biological systems. In research applications, this compound is crucial for studies involving poorly water-soluble drugs and molecular probes, enabling their effective delivery into cells and tissues. The succinyl and hydroxypropyl groups also offer additional interactions that can increase specificity and complexation strength with guest compounds. This makes it useful in evaluating how structural modifications to cyclodextrins affect their inclusion properties. Researchers utilize this compound to investigate drug delivery systems, controlled release mechanisms, and the encapsulation of bioactive molecules for molecular recognition studies. Moreover, the chemical′s interaction with lipids and proteins is valuable for exploring its influence on membrane permeability and protein stabilization. Its role in biocompatible formulations makes it a versatile agent in elucidating host-guest chemistry and enhancing biochemical assays in pharmaceutical and chemical research.


Succinyl-(2-hydroxypropyl)-β-cyclodextrin References

  1. Fisetin-In Search of Better Bioavailability-From Macro to Nano Modifications: A Review.  |  Szymczak, J. and Cielecka-Piontek, J. 2023. Int J Mol Sci. 24: PMID: 37762460
  2. Encapsulation of Prodan in beta-cyclodextrin environments: A critical study via electronic spectroscopy and molecular mechanics  |  Banerjee, A., Sengupta, B., Chaudhuri, S., Basu, K., & Sengupta, P. K. 2006. Journal of molecular structure. 794(1-3): 181-189.
  3. Encapsulation of 3-hydroxyflavone and fisetin in β-cyclodextrins: Excited state proton transfer fluorescence and molecular mechanics studies  |  Banerjee, A., & Sengupta, P. K. 2006. Chemical physics letters. 424(4-6): 379-386.
  4. Encapsulation of serotonin in β-cyclodextrin nano-cavities: Fluorescence spectroscopic and molecular modeling studies  |  Chaudhuri, S., Chakraborty, S., & Sengupta, P. K. 2010. Journal of Molecular Structure. 975(1-3): 160-165.
  5. Complex formation of flavonoids fisetin and geraldol with β-cyclodextrins  |  Sali, N., Csepregi, R., Kőszegi, T., Kunsági-Máté, S., Szente, L., & Poór, M. 2018. Journal of Luminescence. 194: 82-90.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Succinyl-(2-hydroxypropyl)-β-cyclodextrin, 1 g

sc-301845
1 g
$555.00