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Astec® CYCLOBOND II Chiral (5 μm) HPLC Columns

L × I.D. 25 cm × 4.6 mm, HPLC Column

Synonyme(s) :

Cyclodextrin-Based Chiral Column

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About This Item

Code UNSPSC :
41115700
eCl@ss :
32110501
Nomenclature NACRES :
SB.52

product name

Astec® Cyclobond II Chiral HPLC Column, 5 μm particle size, L × I.D. 25 cm × 4.6 mm

Matériaux

stainless steel column

Gamme de produits

Astec®

Conditionnement

pkg of 1 ea

Fabricant/nom de marque

Astec®

Paramètres

0-50 °C temperature
172 bar pressure (2500 psi)

Technique(s)

HPLC: suitable
LC/MS: suitable

L × D.I.

25 cm × 4.6 mm

Matrice

silica particle platform
fully porous particle

Groupe de la matrice active

cyclodextrin, gamma- phase

Taille des particules

5 μm

Dimension de pores

100 Å

pH de fonctionnement

3.5-7

Technique de séparation

chiral

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Catégories apparentées

Description générale

Consisting of eight glucopyranose units arranged in a truncated cone shape, CYCLOBOND II is an excellent chiral selector for multi-ring structures. It is useful for isomeric compounds based on anthracene, chrysene and pyrene type ring structures. CYCLOBOND II offers good selectivity and stability and is applicable to the polar organic mode of separation. Applications include steroids, porphyrins, FMOC amino acids.

  • Bonded phase: Underivatized, native γ-cyclodextrin

Resources:
CYCLOBOND FAQs
CYCLOBOND Reference Bibliography
Chiral Product Literature

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Informations légales

Astec is a registered trademark of Merck KGaA, Darmstadt, Germany

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Certificats d'analyse (COA)

Lot/Batch Number

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Separation and identification of sulfurized alkylphenols in oil by high-performance liquid chromatography with evaporative light scattering and mass spectrometric detection
Chen, Evan N., Jr., Nero, Vincent P.
Journal of Chromatography A, 549, 247-256 (1991)
Series of homologous displacers for preparative chiral displacement chromatographic separations on Cyclobond-II columns
Quintero,Gilberto, et al.
Journal of Chromatography A, 693 (1), 1-5 (1995)
A M Abushoffa et al.
Journal of chromatography. A, 700(1-2), 51-58 (1995-05-12)
The methods of separation of the enantiomers of the chiral drug oxamniquine are compared, between HPLC with either cyclodextrins and their related derivatives as chiral selectors in the mobile phase or immobilised in a chiral stationary phase (as Cyclobond I
Optical resolution of flavanones by high-performance liquid chromatography on various chiral stationary phases
Krause, Martin; Galensa, Rodolf
Journal of Chromatography A, 514, 147-159 (1990)
Baoguo Sun et al.
Journal of chromatography. A, 1271(1), 163-169 (2012-12-15)
Analytical methods were developed for a directed enzyme evolution research programme, which pursued high performance enzymes to produce high quality L-ribose using large scale biocatalytic reaction. A high throughput HPLC method with evaporative light-scattering detection was developed to test ribose

Contenu apparenté

CYCLOBOND is the name given to Astec technology for bonding cyclodextrins to a high purity silica gel through a stable ether linkage.

Chromatograms

application for HPLC

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