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Astec® CYCLOBOND II Chiral (5 μm) HPLC Columns

L × I.D. 15 cm × 4.6 mm, HPLC Column

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About This Item

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

product name

Astec® CYCLOBOND II Chiral HPLC Column, 5 μm particle size, L × I.D. 15 cm × 4.6 mm

material

stainless steel column

product line

Astec®

packaging

pkg of 1 ea

manufacturer/tradename

Astec®

parameter

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

technique(s)

HPLC: suitable
LC/MS: suitable

L × I.D.

15 cm × 4.6 mm

matrix

silica particle platform
fully porous particle

matrix active group

cyclodextrin, gamma- phase

particle size

5 μm

pore size

100 Å

operating pH

3.5-7

separation technique

chiral

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General description

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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Legal Information

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

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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

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