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Merck
CN

73035AST

Supelco

Astec® CHIRALDEX G-TA 毛细管GC色谱柱

L × I.D. 50 m × 0.25 mm, df 0.12 μm

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别名:
GC column, chiral, gamma-dextran
UNSPSC代码:
41115710
NACRES:
SB.54

物料

fused silica

质量水平

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

50 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。

应用


  • Enantioselective gas chromatographic analysis of aqueous samples by on-line derivatisation. Application to enzymatic reactions.: This study explores the use of the Astec CHIRALDEX G-TA Capillary GC Column for enantioselective gas chromatographic analysis. The method involves on-line derivatization, enabling the analysis of aqueous samples and applying this technique to enzymatic reactions. This innovative approach highlights the column′s capability in achieving high selectivity and sensitivity for chiral compounds in complex matrices (Mommers et al., 2008).

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

我们提供各种色谱配件,包括分析注射器

法律信息

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

法规信息

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  1. Which document(s) contains shelf-life or expiration date information for a given product?

    If available for a given product, the recommended re-test date or the expiration date can be found on the Certificate of Analysis.

  2. How do I get lot-specific information or a Certificate of Analysis?

    The lot specific COA document can be found by entering the lot number above under the "Documents" section.

  3. How do I find price and availability?

    There are several ways to find pricing and availability for our products. Once you log onto our website, you will find the price and availability displayed on the product detail page. You can contact any of our Customer Sales and Service offices to receive a quote.  USA customers:  1-800-325-3010 or view local office numbers.

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

    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. 

  5. What is the regeneration procedure for Chiraldex TA columns? 

    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.

  6. My question is not addressed here, how can I contact Technical Service for assistance?

    Ask a Scientist here.

The synthesis of enantioenriched a-hydroxy esters
Gu, Xin, et al.
Tetrahedron Asymmetry, 25 (24), 1573-1580 (2014)
Organocatalysis using protonated 1,2-diamino-1,2-diphenylethane for asymmetric Diels?Alder reaction
Hoon Kim, Kyoung, et al.
Tetrahedron Letters, 46 (36), 5991-5994 (2005)
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)
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)
Asymmetric conjugate addition to alkylidene malonates
Alexakis, Alexandre; Benhaim, Cyril;
Tetrahedron Asymmetry, 12 (8), 1151-1157 (2001)

商品

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

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