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74033AST

Supelco

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

UNSPSC Code:
41115710
NACRES:
SB.54

material

fused silica

description

GC capillary column

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

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

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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).

Chem/Phys Resistance

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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Certificates of Analysis (COA)

Lot/Batch Number
281671-04
281671-03
281671-02
281671-01
278324-04

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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
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
Thomas Kraemer et al.
Journal of analytical toxicology, 27(2), 68-73 (2003-04-03)
Prenylamine (R,S-N-(3,3-diphenylpropyl-methyl-2-phenethylamine), a World Health Organization class V calcium antagonist, is known to be metabolized to amphetamine. In this study, amphetamine concentrations after a single-dose administration of prenylamine were determined to check if they reached values that could be of

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