74033AST
Astec® CHIRALDEX™ G-PN Capillary GC Column
L × I.D. 30 m × 0.25 mm, df 0.12 μm
Synonym(s):
GC column, chiral, gamma-dextran
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About This Item
NACRES:
SB.54
UNSPSC Code:
41115710
material
fused silica
description
GC capillary column
analyte chemical class(es)
alcohols, amino acids, amphetamines, ketones, terpenes
packaging
1 ea of
parameter
-10-200 °C temperature (isothermal), -10-220 °C temperature (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-propionyl derivative of γ-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-propionyl derivative of γ-cyclodextrin. This phase exhibits high selectivity for lactones and aromatic amines. It is also suitable for epoxide separations. Additionally, the analysis of styrene oxide can be accomplished on this phase (this analyte degrades on the TA phases).
Features and Benefits
Temp. Limits:
- -10 °C to 200 °C isothermal, 220 °C 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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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)
Justyna M Płotka et al.
Journal of chromatography. A, 1347, 146-156 (2014-05-13)
The enantiomeric ratio of methylamphetamine (MAMP) is closely related to the optical activity of precursors and reagents used for the synthesis and this knowledge can provide useful information concerning the origins and synthetic methods used for illicit manufacture. The information
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 74033AST | 04061835553051 |