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76023AST

Supelco

Astec® CHIRALDEX™ B-PM Capillary GC Column

L × I.D. 30 m × 0.25 mm, df 0.12 μm

Sinónimos:

GC column, chiral, beta-dextran

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About This Item

Código UNSPSC:
41115710
eCl@ss:
32110502
NACRES:
SB.54

Materiales

fused silica

descripción

GC capillary column

envase

pkg of 1 ea

Parámetros

-10-200 °C temperature (isothermal)
-10-220 °C temperature (programmed)

Valor Beta

500

df

0.12 μm

técnicas

gas chromatography (GC): suitable

L × D.I.

30 m × 0.25 mm

grupo activo de la matriz

non-bonded; 2,3,6-tri-O-methyl derivative of β-cyclodextrin phase

aplicaciones

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)

tipo de columna

capillary chiral

técnica de separación

chiral

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Descripción general

The main difference between CHIRALDEX B-PM and the Supelco β-DEX 110 and Supelco β-DEX 120 phases is the concentration of the permethyl-derivatized cyclodextrin that is doped into the polysiloxane carrier. CHIRALDEX B-PM is a general-purpose column used for the separation of acids, alcohols, barbitals, diols, epoxides, esters, hydrocarbons, ketones, lactones and terpenes. Also, some underivatized alcohols and diols as well as some analytes with polar groups, i.e. tertiary amines, show excellent separation.

Resistencia química o física

Temp. Limits:
  • -10 °C to 200 °C isothermal, 220 °C programmed

Otras notas

We offer a variety of chromatography accessories including analytical syringes

Información legal

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

Aplicación

Referencia del producto
Descripción
Precios

G005035

GC Analysis of 1-Phenylethanol Enantiomers on Astec® CHIRALDEX™ B-PM, suitable for GC

G005036

GC Analysis of (R)-(+)-1-Phenylethanol on Astec® CHIRALDEX™ B-PM, suitable for GC

G005055

GC Analysis of β-Pinene Enantiomers on Astec® CHIRALDEX™ B-PM, suitable for GC

G005107

GC Analysis of 1-Phenylethylamine Enantiomers (N-Acetyl Derivatives) on Astec® CHIRALDEX™ B-PM, suitable for GC

G005143

GC Analysis of 1-Phenylethylamine Enantiomers (N-Chloroacetyl Derivatives) on Astec® CHIRALDEX™ B-PM, suitable for GC

G005116

GC Analysis of α-Pinene Enantiomers on Astec® CHIRALDEX™ B-PM, suitable for GC

Choose from one of the most recent versions:

Certificados de análisis (COA)

Lot/Batch Number
287223-04
287223-03
287223-02
287223-01
285743-04

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Visite la Librería de documentos

C Freissinet et al.
Journal of chromatography. A, 1306, 59-71 (2013-08-08)
The performances of several commercial chiral capillary columns have been evaluated with the aim of determining the one most suitable for enantiomeric separation in a gas chromatograph onboard a space probe. We compared the GC-MS response of three capillary columns
Synthesis of enantiopure ?2-homoalanine derivatives via rhodium catalyzed asymmetric hydrogenation
Luhr, Susan, et al.
Tetrahedron, 24 (7), 395-401 (2013)
Recent development of cationic cyclodextrins for chiral separation
Zhou, Jie, et al.
TrAC, Trends in Analytical Chemistry, 65, 22-29 (2015)
Izabela Kania-Korwel et al.
Journal of chromatography. A, 1278, 133-144 (2013-01-26)
Changes in the enantiomeric fraction of chiral polychlorinated biphenyls (PCBs) are a powerful tool to investigate the movement of PCBs in the environment, for example as part of source apportionment and ecological studies. Environmental studies typically employ a series of
Ionic cyclodextrins in ionic liquid matrices as chiral stationary phases for gas chromatography
Huang, Ke, et al.
Tetrahedron Asymmetry, 1217 (32), 5261-5273 (2010)

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