Acetyl-β-cyclodextrin (Highly Pure)
Catalog Number: B2012651 (100 mg)
Acetyl-β-cyclodextrin (Highly Pure) is a high quality glycosylation agent useful in the synthesis of polysaccharides, oligosaccharides, and monosaccharides. This product has been used as molecular tool for various biochemical applications. It has also been used in a wide array of other chemical and immunological applications. Custom bulk amounts of this product are available upon request.
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Acetyl-β-cyclodextrin (Highly Pure)
Catalog number: B2012651
Lot number: Batch Dependent
Expiration Date: Batch dependent
Amount: 100 mg
Molecular Weight or Concentration: 1,160.01 g/mol
Supplied as: Lyophilized Powder
Applications: molecular tool for various biochemical applications
Grade: Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity >18 MΩ-cm) and are filtered through 0.22 um.
1: Hirayama F, Mieda S, Miyamoto Y, Arima H, Uekama K. Heptakis(2,6-di-O-methyl-3-O-acetyl)-beta-cyclodextrin: A water-soluble cyclodextrin derivative with low hemolytic activity J Pharm Sci. 1999 Oct;88(10):970-5.
2: Chmurski K, Temeriusz A, Bilewicz R. Beta-cyclodextrin-based ferrocene-imprinted gold electrodes Anal Chem. 2003 Nov 1;75(21):5687-91.
3: Zappacosta R, Cornelio B, Pilato S, Siani G, Estour F, Aschi M, Fontana A. Effect of the Incorporation of Functionalized Cyclodextrins in the Liposomal Bilayer Molecules. 2019 Apr 9;24(7):1387.
4: Branch SK, Holzgrabe U, Jefferies TM, Mallwitz H, Matchett MW. Chiral discrimination of phenethylamines with beta-cyclodextrin and heptakis(2,3-di-O-acetyl)beta-cyclodextrin by capillary electrophoresis and NMR spectroscopy J Pharm Biomed Anal. 1994 Dec;12(12):1507-17.
5: Hägele JS, Hubner EM, Schmid MG. Chiral separation of cathinone derivatives using β-cyclodextrin-assisted capillary electrophoresis-Comparison of four different β-cyclodextrin derivatives used as chiral selectors Electrophoresis. 2019 Jul;40(14):1787-1794.
6: Cravotto G, Bicchi C, Tagliapietra S, Costa L, Di Carlo S, Nervi C. New chiral selectors: design and synthesis of 6-TBDMS-2,3-methyl beta-cyclodextrin 2-2′ thioureido dimer and 6-TBDMS-2,3-methyl (or 2-methyl-3-acetyl) beta-cyclodextrin bearing an (R) Mosher acid moiety Chirality. 2004 Oct;16(8):526-33.
7: Chankvetadze B, Lomsadze K, Burjanadze N, Breitkreutz J, Pintore G, Chessa M, Bergander K, Blaschke G. Comparative enantioseparations with native beta-cyclodextrin, randomly acetylated beta-cyclodextrin and heptakis-(2,3-di-O-acetyl)-beta-cyclodextrin in capillary electrophoresis Electrophoresis. 2003 Mar;24(6):1083-91.
8: Tutu E, Vigh G. Synthesis, analytical characterization and initial capillary electrophoretic use in an acidic background electrolyte of a new, single-isomer chiral resolving agent: heptakis(2-O-sulfo-3-O-methyl-6-O-acetyl)-β-cyclodextrin Electrophoresis. 2011 Oct;32(19):2655-62.
9: Lee KR, Nguyen NT, Lee YJ, Choi S, Kang JS, Mar W, Kim KH. Determination of the R-enantiomer of valsartan in pharmaceutical formulation by capillary electrophoresis Arch Pharm Res. 2015;38(5):826-33.
10: Hägele JS, Hubner EM, Schmid MG. Determination of the chiral status of different novel psychoactive substance classes by capillary electrophoresis and β-cyclodextrin derivatives Chirality. 2020 Sep;32(9):1191-1207.
Products Related to Acetyl-β-cyclodextrin (Highly Pure) can be found at Carbohydrates
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