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Merck
CN

59586-U

Supelco

Discovery® Cyano (5 µm) HPLC Columns

L × I.D. 2 cm × 4 mm Supelguard Guard Cartridge, pkg of 2 ea, Guard Cartridge holder required for use

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

product name

Discovery® 氰基 Supelguard 保护柱芯, 5 μm particle size, L × I.D. 2 cm × 4 mm

物料

stainless steel column

质量水平

Agency

suitable for USP L10

描述

Supelguard Cartridge

产品线

Discovery®

特点

endcapped

包装

pkg of 2 ea

技术

HPLC: suitable

长度 × 内径

2 cm × 4 mm

表面积

200 m2/g

基质

fully porous particle

基质活性基团

cyano phase

粒径

5 μm

孔径

180 Å

工作pH值

2-8

应用

food and beverages

分离技术

hydrophilic interaction (HILIC)
normal phase
reversed phase

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包装

适用于 4.0mm 内径和 4.6mm 内径的分析柱。

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法律信息

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

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E F Nemeth et al.
The Journal of pharmacology and experimental therapeutics, 299(1), 323-331 (2001-09-19)
Despite the discovery of many ions and molecules that activate the Ca2+ receptor, there are no known ligands that block this receptor. Reported here are the pharmacodynamic properties of a small molecule, NPS 2143, which acts as an antagonist at
Aaron D Milstein et al.
Trends in pharmacological sciences, 29(7), 333-339 (2008-06-03)
Presynaptic glutamate release elicits brief waves of membrane depolarization in neurons by activating AMPA receptors. Depending on its precise size and shape, current through AMPA receptors gates downstream processes like NMDA receptor activation and action potential generation. Over a decade
Alessandro Stella et al.
Bioorganic & medicinal chemistry, 21(5), 1209-1218 (2013-01-26)
A series of novel pyrimidine analogues were synthesized and evaluated for immunosuppressive activity in the Mixed Lymphocyte Reaction assay, which is well-known as the in vitro model for in vivo rejection after organ transplantation. Systematic variation of the substituents at
Aleem Gangjee et al.
Journal of medicinal chemistry, 53(22), 8116-8128 (2010-10-27)
Two classes of molecules were designed and synthesized based on a 6-CH(3) cyclopenta[d]pyrimidine scaffold and a pyrrolo[2,3-d]pyrimidine scaffold. The pyrrolo[2,3-d]pyrimidines were synthesized by reacting ethyl 2-cyano-4,4-diethoxybutanoate and acetamidine, which in turn was chlorinated and reacted with the appropriate anilines to
Graciela B Arhancet et al.
Journal of medicinal chemistry, 53(16), 5970-5978 (2010-08-03)
A new 1,4-dihydropyridine 5a, containing a cyano group at the C3 position, was recently reported to possess excellent mineralocorticoid receptor (MR) antagonist in vitro potency and no calcium channel-blocker (CCB) activity. In the present study, we report the structure-activity relationships

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