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73033AST

Supelco

Astec® CHIRALDEX™ G-TA Capillary GC Column

L × I.D. 30 m × 0.25 mm, df 0.12 μm

Synonim(y):

GC column, chiral, gamma-dextran

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About This Item

Kod UNSPSC:
41115710
NACRES:
SB.54

Materiały

fused silica

opis

GC capillary column

opakowanie

pkg of 1 ea

Parametry

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

Wartość beta

500

df

0.12 μm

metody

gas chromatography (GC): suitable

dł. × śr. wewn.

30 m × 0.25 mm

grupa aktywna macierzy

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

Zastosowanie

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)

typ kolumny

capillary chiral

metoda separacji

chiral

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Opis ogólny

Astec® CHIRALDEX G-TA is the first choice in the Group 1 CSPs (Surface Interactions, Complex Derivatives). This phase has been shown to be the most broadly-selective phase for the pharmaceutical industry, especially for the analysis of chiral intermediates and drug studies in various stages of clinical trials. Separations occur without the inclusion mechanism and are typically faster and more efficient than most chiral stationary phases. G-TA has also been used to separate parent drug enantiomers and their metabolites. G-TA has its highest selectivity for oxygen-containing analytes like alcohols, diols and polyols as the free alcohol and as an acyl derivative; amines as acyl derivatives; amino alcohols, halogens (Cl>Br>F), amino acids, hydroxy acids, lactones, furans and pyrans. It is also highly selective for halogenated compounds.

Zastosowanie

Astec® CHIRALDEX™ G-TA (2,6-di-O-pentyl-3-trifluoroacetyl-γ-cyclodextrin) derivatized cyclodextrin chiral stationary phase may be used in capillary gas chromatography for separation of four isomers from 7 racemic sulfinate esters. It was used in an experimental study done for cloning and characterization of three epoxide hydrolases identified by analyzing open reading frames (ORFs) of a marine bacterium, Erythrobacter litoralis HTCC2594. It was also used in HPLC and GC analyses of the conversion of epoxides during enantioselectivity of epoxide hydrolase from Agrobacterium radiobacter (EchA) using error-prone PCR and DNA shuffling.

Odporność chem./fiz.

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

Inne uwagi

We offer a variety of chromatography accessories including analytical syringes

Informacje prawne

Astec is a registered trademark of Merck KGaA, Darmstadt, Germany
CHIRALDEX is a trademark of Sigma-Aldrich Co. LLC
This page may contain text that has been machine translated.

Zastosowanie

Numer produktu
Opis
Cennik

G005039

GC Analysis of 2-Aminobutane (2-Butylamine) Enantiomers (N-Trifluoroacetyl Derivatives) on Astec® CHIRALDEX™ G-TA, suitable for GC

G005049

GC Analysis of 1-Methyl-3-Phenylpropylamine (4-Phenyl-2-Butylamine) Enantiomers (N-TFA Derivatives) on Astec® CHIRALDEX™ G-TA, suitable for GC

G005056

GC Analysis of β-Butyrolactone Enantiomers on Astec® CHIRALDEX™ G-TA, suitable for GC

G005061

GC Analysis of Methionine Methyl Ester Enantiomers (N-Trifluoroacetyl Derivatives) on Astec® CHIRALDEX™ G-TA, suitable for GC

G005064

GC Analysis of 2-Halohydrocarbon Enantiomers on Astec® CHIRALDEX™ G-TA, suitable for GC

G005067

GC Analysis of Mandelic Acid Methyl Ester Enantiomers on Astec® CHIRALDEX™ G-TA, suitable for GC

G005093

GC Analysis of 1,2-Alkyldiol Enantiomers (O-Trifluoroacetyl Derivatives) on Astec® CHIRALDEX™ G-TA, suitable for GC

G005122

GC Analysis of 2,5-Dimethoxytetrahydrofuran Enantiomers on Astec® CHIRALDEX™ G-TA, suitable for GC

G005096

GC Analysis of 2-Butanol Enantiomers (O-Acetyl Derivatives) on Astec® CHIRALDEX™ G-TA, suitable for GC

G005095

GC Analysis of 2-Butanol Enantiomers (O-Trifluoroacetyl Derivatives) on Astec® CHIRALDEX™ G-TA, suitable for GC

G005094

GC Analysis of 2-Butanol Enantiomers (Underivatized) on Astec® CHIRALDEX™ G-TA, suitable for GC

G005103

GC Analysis of 5-Amino-1,3,3-Trimethylcyclohexanemethylamine Enantiomers (N-TFA Derivatives) on Astec® CHIRALDEX™ G-TA, suitable for GC

G005131

GC Analysis of Glycidol Enantiomers on Astec® CHIRALDEX™ G-TA, suitable for GC

G005102

GC Analysis of Proline Methyl Ester Enantiomers (N-Acetyl Derivatives) on Astec® CHIRALDEX™ G-TA, suitable for GC

G005101

GC Analysis of Proline Methyl Ester Enantiomers (N-Trifluoroacetyl Derivatives) on Astec® CHIRALDEX™ G-TA, suitable for GC

G005076

GC Analysis of Verbenone Enantiomers on Astec® CHIRALDEX™ G-TA, suitable for GC

G005098

GC Analysis of Wieland-Miescher Ketone Enantiomers on Astec® CHIRALDEX™ G-TA, suitable for GC

G005111

GC Analysis of α-Hexachlorocyclohexane (α-HCH) Enantiomers on Astec® CHIRALDEX™ G-TA, suitable for GC

G005146

GC Analysis of δ-Decanolactone Enantiomers on Astec® CHIRALDEX™ G-TA, suitable for GC

G006117

GC Analysis of Volatile Flavor Compound Enantiomers on Astec® CHIRALDEX™ G-TA, suitable for GC

G006154

GC Analysis of D-Carvone Enantiomer in Caraway Essential Oil on Astec® CHIRALDEX™ G-TA, suitable for GC

G006155

GC Analysis of D-Carvone Enantiomer in Dill Seed Essential Oil on Astec® CHIRALDEX™ G-TA, suitable for GC

G006156

GC Analysis of D & L-Carvone Enantiomers in Caraway Essential Oil (Spiked with L-Carvone Enantiomer) on Astec® CHIRALDEX™ G-TA, suitable for GC

G006157

GC Analysis of D & L-Carvone Enantiomers in Dill Seed Essential Oil (Spiked with L-Carvone Enantiomer) on Astec® CHIRALDEX™ G-TA, suitable for GC

G006158

GC Analysis of D & L-Carvone Enantiomers in Native Spearmint Essential Oil (Spiked with D-Carvone Enantiomer) on Astec® CHIRALDEX™ G-TA, suitable for GC

G006159

GC Analysis of D & L-Carvone Enantiomers in Scotch Spearmint Essential Oil (Spiked with D-Carvone Enantiomer) on Astec® CHIRALDEX™ G-TA, suitable for GC

G006160

GC Analysis of D & L-Carvone Enantiomers on Astec CHIRALDEX™ G-TA, suitable for GC

G006162

GC Analysis of L-Carvone Enantiomer in Scotch Spearmint Essential Oil on Astec® CHIRALDEX™ G-TA, suitable for GC

Choose from one of the most recent versions:

Certyfikaty analizy (CoA)

Lot/Batch Number
281424-04
281424-03
281424-02
281424-01
281423-04

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Jung-Hee Woo et al.
Applied microbiology and biotechnology, 76(2), 365-375 (2007-06-02)
Previously, we reported that ten strains belonging to Erythrobacter showed epoxide hydrolase (EHase) activities toward various epoxide substrates. Three genes encoding putative EHases were identified by analyzing open reading frames of Erythrobacter litoralis HTCC2594. Despite low similarities to reported EHases
Bert van Loo et al.
Chemistry & biology, 11(7), 981-990 (2004-07-24)
The enantioselectivity of epoxide hydrolase from Agrobacterium radiobacter (EchA) was improved using error-prone PCR and DNA shuffling. An agar plate assay was used to screen the mutant libraries for activity. Screening for improved enantioselectivity was subsequently done by spectrophotometric progress
Catalytic asymmetric synthesis of Japonilure and its enantiomer
Xu, Hao, et al.
Tetrahedron Asymmetry, 25 (20-21), 1372-1375 (2014)
Investigation of a novel diamine based chiral auxiliary in the asymmetric alkylation of ketones
Clarke, Sarah L, et al.
Tetrahedron Asymmetry, 25 (4), 356-361 (2014)
Sequential kinetic resolution of (?)-2,3-butanediol in organic solvent using lipase from Pseudomonas cepacia.
Caron, Gaetan; Kazlauskas, R.J.
Tetrahedron Asymmetry, 4 (9), 1995-2000 (1993)
Wyświetl wszystkie powiązane dokumenty

Produkty

Proline Derivatization and Enantioresolution by Chiral GC

Amino acids are building blocks of peptides and proteins. Enantiomeric separation of these molecules can be performed through chromatography by chiral stationary phases. This article describes the chiral GC analysis of one amino acid, proline, after achiral derivatization.

Chiral GC Analysis of Carvone Enantiomers in Essential Oils

In this study we demonstrate the separation of D- and L-carvone enantiomers in samples of caraway seed, dill seed, native spearmint and scotch spearmint essential oils using an Astec CHIRALDEX G-TA capillary GC column.

Protokoły

GC Analysis of D-Carvone Enantiomer in Caraway Essential Oil on Astec® CHIRALDEX® G-TA

GC Analysis of D-Carvone Enantiomer in Caraway Essential Oil on Astec® CHIRALDEX® G-TA

Chromatograms

suitable for GCsuitable for GCsuitable for GCsuitable for GCPokaż więcej

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