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73032AST

Supelco

Astec® CHIRALDEX G-TA 毛细管GC色谱柱

L × I.D. 20 m × 0.25 mm, df 0.12 μm

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1 EA
$2,600.00

$2,600.00


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1 EA
$2,600.00

About This Item

UNSPSC代码:
41115710
NACRES:
SB.54

$2,600.00


请联系客服了解存货情况

物料

fused silica

描述

GC capillary column

包装

pkg of 1 ea

参数

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

β值

500

df

0.12 μm

技术

gas chromatography (GC): suitable

长度 × 内径

20 m × 0.25 mm

基质活性基团

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

应用

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)

色谱柱类型

capillary chiral

分离技术

chiral

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一般描述

Astec® CHIRALDEX G-TA 是第 1 组 CSP(表面相互作用,复合衍生物)的首选。该阶段已被证明是制药行业最广泛选择的阶段,特别是在临床试验的各个阶段中手性中间体和药物研究的分析。在没有包含机制的情况下发生分离,并且通常比大多数手性固定相更快且更有效。G-TA 也被用于分离母体药物对映体及其代谢物。G-TA 对含氧分析物的选择性最高,如醇、二醇和多元醇,作为游离醇和酰基衍生物;胺类作为酰基衍生物;氨基醇、卤素(Cl> Br> F)、氨基酸、羟基酸、内酯、呋喃和吡喃。它对卤化物也具有高选择性。

化学/物理抗性

温度限制:
  • -10 °C 至 180 °C 等温和程序的

其他说明

We offer a variety of chromatography accessories including analytical syringes

法律信息

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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The asymmetric hydrogenation of 2-phenethylacrylic acid as the key step for the enantioselective synthesis of Citralis Nitrile?
Scrivanti, Alberto, et al.
Tetrahedron Letters, 47 (52), 9261-9265 (2006)
Isolation of racemic 2,4-pentanediol and 2,5-hexanediol from commercial mixtures of racemic and meso isomers by way of cyclic sulfites.
Caron, Gaetan; Kazlauskas, R.J.
Tetrahedron Asymmetry, 5 (4), 657-664 (1994)
Asymmetric reduction of a-keto acetals with potassium 9-O-(1,2-isopropylidene-5-deoxy-D-xylofuranosyl)-9-boratabicyclo[3.3.1]nonane. Enantioselective synthesis of a-hydroxy acetals with high optical purities
Tae Cho, B; Sung Chun, Y;
Tetrahedron Asymmetry, 5 (7), 1147-1150 (1994)
Asymmetric conjugate addition to alkylidene malonates
Alexakis, Alexandre; Benhaim, Cyril;
Tetrahedron Asymmetry, 12 (8), 1151-1157 (2001)
The synthesis of enantioenriched a-hydroxy esters
Gu, Xin, et al.
Tetrahedron Asymmetry, 25 (24), 1573-1580 (2014)

商品

Chromatographic enantiomeric separation of amino acids, like proline, is described for chiral GC analysis after derivatization.

相关内容

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.

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.

Questions

1–2 of 2 Questions  
  1. What is the regeneration procedure for Chiraldex TA columns?

    1 answer
    1. The regeneration procedure for ChiraldexTA columns is located in Supelco brochure, T407123 (JCH), A Guide to Using Cyclodextrin Bonded Phases for Chiral Separations by Capillary Gas Chromatography, on pages 8 and 9.  These pages are attached.

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  2. What is the Department of Transportation shipping information for this product?

    1 answer
    1. Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.

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