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Merck

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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About This Item

UNSPSC代码:
41115710
NACRES:
SB.54

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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访问文档库

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)
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)
The synthesis of enantioenriched a-hydroxy esters
Gu, Xin, et al.
Tetrahedron Asymmetry, 25 (24), 1573-1580 (2014)
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.

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

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

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

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