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β-Cyclodextrin, sulfated sodium salt

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For Research Use Only | Not For Clinical Use
CATAP37191698
CAS37191-69-8
Structure
MDL NumberMFCD00197857
Descriptionextent of labeling: 12-15 mol per mol β-CD
Autoignition Temperature770 °F
Size5G, 25G
1

Heptakis(2-O-methyl-3,6-di-O-sulfo)-beta-cyclodextrin: A Single Isomer, 14-sulfated Beta-Cyclodextrin for Use as a Chiral Resolving Agent in Capillary Electrophoresis

D K Maynard, G Vigh

Electrophoresis. 2001 Sep;22(15):3152-62.

PMID: 11589274

1

Stereospecific Synthesis of m-Hydroxymexiletine Enantiomers

Alessia Catalano, Alessia Carocci, Giovanni Lentini, Ivana Defrenza, Claudio Bruno, Carlo Franchini

Drug Metab Lett. 2012 Sep 1;6(3):182-6.

PMID: 23140556

1

Synthesis of a Single-Isomer Sulfated Beta-Cyclodextrin Carrying Nonidentical Substituents at All of the C2, C3, and C6 Positions and Its Use for the Electrophoretic Separation of Enantiomers in Acidic Aqueous and Methanolic Background Electrolytes. Part 2: Heptakis(2-O-methyl-6-O-sulfo) Cyclomaltoheptaose

M Brent Busby, Gyula Vigh

Electrophoresis. 2005 Oct;26(20):3849-60.

PMID: 16167310

1

Synthesis, Analytical Characterization and Capillary Electrophoretic Use of the Single-Isomer heptakis-(6-O-sulfobutyl)-beta-cyclodextrin

Milo Malanga, Ida Fejős, Erzsébet Varga, Gábor Benkovics, András Darcsi, Julianna Szemán, Szabolcs Béni

J Chromatogr A. 2017 Sep 8;1514:127-133.

PMID: 28760606

1

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

Edward Tutu, Gyula Vigh

Electrophoresis. 2011 Oct;32(19):2655-62.

PMID: 21983817

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