6-Monodeoxy-6-monothio-beta-cyclodextrin

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6-Monodeoxy-6-monothio-beta-cyclodextrin
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6-Monodeoxy-6-monothio-beta-cyclodextrin

Original price was: $1,795.00.Current price is: $895.00.

Catalog Number: B2027370 (100 mg)
6-Monodeoxy-6-monothio-beta-cyclodextrin is a modified cyclic oligosaccharide derivative featuring a thiol group substituted at the C-6 position of a glucopyranose unit. It retains the characteristic hydrophobic central cavity of beta-cyclodextrin for host-guest molecular encapsulation while offering a reactive sulfhydryl site for surface modification, bioconjugation, and catalysis. This compound is primarily utilized in scientific research, including chiral separation and biosensor development. Custom bulk amounts of this product are available upon request.

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Product Description

5/5 - (2 votes)

6-Monodeoxy-6-monothio-beta-cyclodextrin
Catalog number: B2027370
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 100 mg
Molecular Weight or Concentration: 1151
Supplied as: Chemicals
Storage: 2-8 ËšC
Keywords: Mono(6-mercapto-6-deoxy)-β-cyclodextrin, 6A-Thio-β-cyclodextrin, 6-Deoxy-6-mercapto-β-cyclodextrin, 6-Deoxy-6-thiol-β-cyclodextrin, Mono-6-deoxy-6-mercapto-β-cyclodextrin, Mono-6-mercapto-β-cyclodextrin

References:
1. Yang, H., Wei, W., Wang, C., Zhou, X., Liu, Y., Wang, Z., & Liu, S. (2020). Renewable electrochemical sensor based on host-guest recognition for the detection of PARP-1 activity. Biosensors and Bioelectronics, 148, 111810.
2. Xu, Y., et al. (2017). Efficient end-to-end assembly of gold nanorods via cyclodextrin-bisphenol A based supramolecular linker. Dyes and Pigments, 144, 168-172.
3. Ma, H., et al. (2021). Fabrication of polydopamine/hemin-cyclodextrin supramolecular assemblies for mimicking natural peroxidases and their sensitive detection of cholesterol. Journal of Molecular Liquids, 328, 115490.
4. Degirmenci, A., Sanyal, R., & Sanyal, A. (2023). Plug-and-Play Biointerfaces: Harnessing Host-Guest Interactions for Fabrication of Functional Polymeric Coatings. ACS Applied Materials & Interfaces, 15(34), 40120-40130.
5. Jicsinszky, L., & Cravotto, G. (2021). Nucleophilic Substitutions of 6I-O-Monotosyl-beta-cyclodextrin in a Planetary Ball Mill. ACS Sustainable Chemistry & Engineering, 9(24), 8123-8134.
6. Loftsson, T., & Duchene, D. (2007). Cyclodextrins and their pharmaceutical applications. International Journal of Pharmaceutics, 329(1-2), 1-11.
7. Szejtli, J. (1998). Introduction and general overview of cyclodextrin chemistry. Chemical Reviews, 98(5), 1743-1754.
8. Davis, M. E., & Brewster, M. E. (2004). Cyclodextrin-based pharmaceutics: past, present and future. Nature Reviews Drug Discovery, 3(12), 1023-1035.
9. Del Valle, E. M. (2004). Cyclodextrins and their uses: a review. Process Biochemistry, 39(9), 1033-1046.
10. Kurkov, S. V., & Loftsson, T. (2013). Cyclodextrins. International Journal of Pharmaceutics, 453(1), 167-180.
6-Monodeoxy-6-monothio-beta-cyclodextrin

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Additional Information

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

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