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Astec® CHIRALDEX™ GC Column Screening Kit

L × I.D. 30 m × 0.25 mm, pkg of 1 kit

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About This Item

UNSPSC Code:
41115710
NACRES:
SB.54

material

fused silica column

description

30 m kit

packaging

pkg of 1 kit

manufacturer/tradename

Astec®

parameter

-10-180 °C temperature (isothermal or programmed)

df

0.12 μm

technique(s)

gas chromatography (GC): suitable

L × I.D.

30 m × 0.25 mm

matrix active group

non-bonded; 2,3-di-O-methyl-6-t-butyl silyl derivative of β-cyclodextrin phase
non-bonded; 2,6-di-O-pentyl-3-methoxy derivative of β-cyclodextrin phase
non-bonded; 2,6-di-O-pentyl-3-trifluoroacetyl derivative of γ-cyclodextrin phase

column type

capillary chiral

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General description

CHIRALDEX column kit contains three GC CSPs that cover the widest possible range of enantioselectivity: G-TA, B-DM and B-DA, in the popular 30 m x 0.25 mm, 0.12 μm df dimensions. The G-TA separates the greatest number of enantiomers, often with high enantioselectivity. The B-DM separates the widest variety of different structural types. The B-DA is best suited for larger multi-ring structures. Eighty-five percent of analytes which exhibit enantioselectivity on cyclodextrin based chiral stationary phases will give enantioselectivity on one of these phases. Realize considerable savings over the columns purchased separately.

Kit contents: One 30 m × 0.25 mm I.D., 0.12 μm column of each type: CHIRALDEX G-TA, B-DM and B-DA

Other Notes

We offer a variety of chromatography accessories including analytical syringes

Legal Information

Astec is a registered trademark of Merck KGaA, Darmstadt, Germany
CHIRALDEX is a trademark of Sigma-Aldrich Co. LLC

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J Mydlová et al.
Journal of chromatography. A, 1150(1-2), 124-130 (2007-03-24)
The enantiomers of dialkyl 2,3-pentadienedioate undergo interconversion during gas chromatographic separation on chiral stationary phases. In this paper the on-column apparent interconversion kinetic and thermodynamic activation data were determined for dimethyl, diethyl, propylbutyl and dibutyl 2,3-pentadienedioate enantiomers by gas chromatographic
John H M Mommers et al.
Journal of chromatography. A, 1182(2), 215-218 (2008-02-02)
A new gas chromatography (GC) method is presented for analysing both the conversion and the enantiomeric excess (e.e.) of samples from alcohol dehydrogenase reactions. The chiral compounds studied were a series of saturated, straight chain alcohols, ranging from 2-butanol to
Jared L Anderson et al.
Journal of chromatography. A, 946(1-2), 197-208 (2002-03-05)
The separation of 17 chiral sulfoxides and eight chiral sulfinate esters by gas chromatography (GC) on four derivatized cyclodextrin chiral stationary phases (CSPs) (Chiraldex G-TA, G-BP, G-PN, B-DM) is presented. Many of these compounds are structural isomers or part of
Hoff et al.
Chirality, 11(10), 760-767 (1999-11-24)
Enantiomers of C-3 secondary alcohols, 3-hydroxybutanoates, and cyclic 1,3-dithioacetals were separated by chiral GLC using CP-Chirasil-Dex CB and Chiraldex G-TA columns. The former was most successful for analysis of n-alkyl esters of secondary alcohols and the separation depended on the
Ke Huang et al.
Tetrahedron, asymmetry, 17(19), 2821-2832 (2006-10-27)
The enantiomeric excess of chiral reagents used in asymmetric syntheses directly affects the reaction selectivity and product purity. In this work, 84 of the more recently available chiral compounds were evaluated to determine their actual enantiomeric composition. These compounds are
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