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Merck
CN

12023AST

Supelco

Astec® CHIROBIOTIC® T Chiral (5 μm) HPLC Columns

L × I.D. 15 cm × 4.6 mm, HPLC Column

别名:

Chiral Stationary Phase Column T

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About This Item

UNSPSC代码:
41115700
eCl@ss:
32110501
NACRES:
SB.52

product name

Astec® CHIROBIOTIC® T 手性 HPLC 色谱柱, 5 μm particle size, L × I.D. 15 cm × 4.6 mm

物料

stainless steel column

质量水平

Agency

suitable for USP L63

描述

HPLC column

产品线

Astec®

包装

pkg of 1 ea

制造商/商品名称

Astec®

参数

0-45 °C temperature
241 bar pressure (3500 psi)

技术

HPLC: suitable
LC/MS: suitable

长度 × 内径

15 cm × 4.6 mm

基质

High-purity silica gel particle platform
fully porous particle

基质活性基团

teicoplanin glycopeptide phase

粒径

5 μm

孔径

100 Å

operating pH range

3.8-6.8

分离技术

chiral

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相关类别

一般描述

CHIROBIOTIC® T和T2具有替考拉宁作为手性选择剂。它们对许多类别的分子可提供独特的选择性,特别是未衍生化的α, β, γ以及环氨基酸、N-衍生氨基酸、羟基-羧基酸,酸性化合物包括羧基酸及酚、小肽、中性芳香族分析物及环状芳香族和脂肪族胺。通常在手性的冠醚或配体交换型CSP上获得的分离也可能发生在CHIROBIOTIC®T和T2上,但是是在大为简单的移动相如水-乙醇中。此外,所有已知的β-阻滞剂(氨醇)以及二氢香豆素都已被分解。CHIROBIOTIC® T和T2在它们的键化学和支持颗粒的孔径上存在差别,分别赋予了它们不同的选择和制备能力。

  • 键合相:替考拉宁
  • 操作pH范围:3.8 - 6.8
  • 粒子直径:5、10或16 μm
  • 孔径:100 Å (CHIROBIOTIC® T)或200 Å (CHIROBIOTIC® T2)

CHIROBIOTIC FAQ
CHIROBIOTIC 参考书目
Chiral产品文献

应用



  • Chiral liquid chromatography-mass spectrometry (LC-MS/MS) method development for the detection of salbutamol in urine samples.: This study details the application of chiral liquid chromatography coupled with mass spectrometry for detecting salbutamol in urine, highlighting the column′s utility in sensitive biomedical assays ( Chan et al., 2016).


  • High-performance liquid chromatographic enantioseparation of 2-aminomono- and dihydroxycyclopentanecarboxylic and 2-aminodihydroxycyclohexanecarboxylic acids on macrocyclic glycopeptide-based phases.: This research demonstrates the column′s effectiveness in enantioseparating specific cyclical amino acids, proving its versatility and importance in chiral separations ( Berkecz et al., 2009).


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法律信息

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

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Zahid Ali et al.
Journal of chromatography. A, 1052(1-2), 199-204 (2004-11-06)
The solvation parameter model is used to characterize the retention properties of a 3-aminopropylsiloxane-bonded (Alltima amino), three 3-cyanopropylsiloxane-bonded (Ultrasphere CN, Ultremex-CN and Zorbax SB-CN), a spacer bonded propanediol (LiChrospher DIOL) and a multifunctional macrocyclic glycopeptide (Chirobiotic T) silica-based stationary phases
Balázs Visegrády et al.
Journal of biochemical and biophysical methods, 53(1-3), 15-24 (2002-10-31)
This contribution deals with comparative studies on the chiral separation of thiazide diuretics using cellulose tris(3,5-dimethylphenylcarbamate) (Chiralcel OD-RH), cellulose tris(4-methylbenzoate) (Chiralcel OJ-R) and teicoplanin (Chirobiotic T) phases. All columns showed good chiral recognition ability for this class of compounds. Out
Felikss Mutulis et al.
Bioorganic & medicinal chemistry, 15(17), 5787-5810 (2007-07-10)
Two hundred and ten tertiary amides were prepared on solid phase. Diamines were coupled to activated carboxylated Wang polymer, and the polymeric substituted benzyloxycarbonyl protected diamines obtained were reacted with aldehydes or ketones in trimethyl orthoformate giving resin attached Schiff
D Abd el-Hady et al.
Journal of pharmaceutical and biomedical analysis, 37(5), 919-925 (2005-05-03)
A simple, sensitive and selective high performance liquid chromatographic method with UV detection for the chiral separation of racemic methotrexate (rac-Mtx) and enantiomeric purity of L-methotrexate in pharmaceutical formulations was developed and validated. The chiral separation was optimized studying both
Berit P Jensen et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 865(1-2), 48-54 (2008-03-07)
A stereoselective liquid chromatography-tandem mass spectrometry assay was developed and validated for quantification of S- and R-metoprolol at concentrations of 0.5-50 microg/L in human plasma. Metoprolol was extracted from plasma by liquid-liquid extraction with ethyl acetate (82% recovery). Chromatographic separation

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