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Merck

73023AST

Supelco

Astec® CHIRALDEX B-TA Capillary GC Column

L × I.D. 30 m × 0.25 mm, df 0.12 μm

Synonym(e):

GC column, chiral, beta-dextran

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About This Item

UNSPSC-Code:
41115710
eCl@ss:
32110502
NACRES:
SB.54

Materialien

fused silica

Beschreibung

GC capillary column

Verpackung

pkg of 1 ea

Parameter

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

Beta-Wert

500

df

0.12 μm

Methode(n)

gas chromatography (GC): suitable

L × ID

30 m × 0.25 mm

Aktive Matrixgruppe

non-bonded; 2,6-di-O-pentyl-3-trifluoroacetyl derivative of β-cyclodextrin phase

Anwendung(en)

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)

Säulenart

capillary chiral

Trenntechnik

chiral

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Allgemeine Beschreibung

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.

Chemische/physikalische Beständigkeit

Temp. Limits:
  • -10 °C to 180 °C isothermal and programmed

Sonstige Hinweise

We offer a variety of chromatography accessories including analytical syringes

Rechtliche Hinweise

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

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Analysenzertifikate (COA)

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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

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