Acetyl-β-cyclodextrin (Highly Pure)

Product Description

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
Storage: 2-8°C
Keywords: Cylcodextrins
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.

References:
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.

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