73023AST
Astec® CHIRALDEX™ B-TA Capillary GC Column
L × I.D. 30 m × 0.25 mm, df 0.12 μm
Synonym(s):
GC column, chiral, beta-dextran
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About This Item
UNSPSC Code:
41115710
NACRES:
SB.54
eCl@ss:
32110502
material
fused silica
description
GC capillary column
analyte chemical class(es)
alcohols, amino acids, amphetamines, ketones, terpenes
packaging
pkg of 1 ea
parameter
-10-180 °C temperature (isothermal or programmed)
Beta value
500
df
0.12 μm
technique(s)
gas chromatography (GC): suitable
L × I.D.
30 m × 0.25 mm
matrix active group
Chiral, non-bonded; 2,6-di-O-pentyl-3-trifluoroacetyl derivative of β-cyclodextrin phase
application(s)
agriculture
chemicals and industrial polymers
cleaning products
clinical
cosmetics
environmental
flavors and fragrances
food and beverages
forensics and toxicology
life science and biopharma
personal care
pharmaceutical (small molecule)
column type
capillary chiral
separation technique
chiral
General description
Incorporates a phase consisting of a 2,6-di-O-pentyl-3-trifluoroacetyl derivative of β-cyclodextrin. This phase exhibits high selectivity for oxygen-containing analytes in the form of alcohols, ketones, acids, aldehydes and lactones. It is also highly selective for halogenated compounds.
Features and Benefits
Temp. Limits:
- -10 °C to 180 °C isothermal and programmed
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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Enantioselective heterogeneous catalysis I. A working model for the catalyst:modifier:substrate interactions in chiral pyruvate hydrogenations
Augustine, Robert L.
Tetrahedron Asymmetry, 4 (8), 1803-1827 (1993)
Use of esterified and unesterified dipentylated y-, ?- and a-cyclodextrins as gas chromatographic stationary phases to indicate the structure of monoterpenoid constituents of volatile oils
Betts, Thomas.J.
Journal of Chromatography A, 672 (1-2), 254-260 (1994)
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 73023AST | 04061833540268 |