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UNSPSC Code:
41115700
eCl@ss:
32110501
NACRES:
SB.52
L × i.d.:
25 cm × 10 mm
Particle size:
5 μm
Matrix active group:
teicoplanin glycopeptide phase
Pore size:
100 Å
Matrix:
High-purity silica gel particle platform
fully porous particle
fully porous particle
产品名称
Astec® CHIROBIOTIC® T 手性 HPLC 色谱柱, 5 μm particle size, L × I.D. 25 cm × 10 mm
material
stainless steel column
agency
suitable for USP L63
description
HPLC column
product line
Astec®
packaging
pkg of 1 ea
manufacturer/tradename
Astec®
parameter
0-45 °C temperature
241 bar pressure (3500 psi)
technique(s)
HPLC: suitable
LC/MS: suitable
L × I.D.
25 cm × 10 mm
matrix
High-purity silica gel particle platform
fully porous particle
matrix active group
teicoplanin glycopeptide phase
particle size
5 μm
pore size
100 Å
operating pH range
3.8-6.8
separation technique
chiral
Quality Level
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Application
- Chiral liquid chromatography-mass spectrometry (LC-MS/MS) method development for the detection of salbutamol in urine samples.:开发使用Astec® CHIROBIOTIC® T手性HPLC色谱柱的手性LC-MS/MS方法,检测尿液中的沙丁胺醇对映体,涉及兴奋剂控制和分析化学应用。研究证明该柱子可准确、选择性地检测复杂生物基质中的手性分子(Chan et al., 2016)。
- High-performance liquid chromatographic enantioseparation of 2-aminomono- and dihydroxycyclopentanecarboxylic and 2-aminodihydroxycyclohexanecarboxylic acids on macrocyclic glycopeptide-based phases.:该研究突出了Astec® CHIROBIOTIC® T手性HPLC色谱柱的多用性,使用该柱手性分离环状氨基酸,对新药开发和生化研究有重要意义。柱子可有效分离复杂手性酸,证明了它在药物研究和手性化学分析中的重要性(Berkecz et al., 2009)。
General description
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。
CHIROBIOTIC FAQ
CHIROBIOTIC 参考书目
Chiral产品文献
- 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
Legal Information
Astec is a registered trademark of Merck KGaA, Darmstadt, Germany
CHIROBIOTIC is a registered trademark of Sigma-Aldrich Co. LLC
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
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
Mohamed M Hefnawy et al.
Talanta, 61(5), 667-673 (2008-10-31)
A new analytical method for the separation and determination of R-(-)- and S-(+)- baclofen enantiomers in human plasma by high-performance liquid chromatography (HPLC) with UV detection was developed. Enantioselective resolution of the baclofen enantiomers was achieved by using teicoplanin macrocyclic
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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