505137
Discovery® C18 (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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关于此项目
UNSPSC Code:
41115700
eCl@ss:
32110501
NACRES:
NB.21
L × i.d.:
2 cm × 4 mm
Particle size:
5 μm
Matrix active group:
C18 (octadecyl) bonding phase
Pore size:
180 Å
产品名称
Discovery® C18 Supelguard 保护柱, 5 μm particle size, L × I.D. 2 cm × 4 mm, pkg of 2 ea
agency
suitable for USP L1
packaging
pkg of 2 ea
technique(s)
HPLC: suitable
L × I.D.
2 cm × 4 mm
matrix active group
C18 (octadecyl) bonding phase
particle size
5 μm
pore size
180 Å
application(s)
food and beverages
separation technique
reversed phase
Quality Level
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General description
Discovery® C18 Supelguard保护柱芯 [5 μm 颗粒尺寸，L × I.D. 2 cm × 4 mm]的 2 cm 不锈钢柱体中含有Discovery®填料，封闭在聚醚醚酮（PEEK）包裹的不锈钢筛板（2 μm孔隙度）中。Supelguard套件（一个柱芯，两个独立的保护套，管道和2个螺母和套圈）让您可以配合任何分析柱使用该柱芯。直接式保护柱芯套可以将Supelguard柱芯和Supelco分析柱直接连接。3.0 mm柱芯只有两只装，需要单独购买独立式或模块式保护套。低容积的3.0 mm内径柱芯是保护含μm颗粒分析柱的良好选择。
Legal Information
Discovery is a registered trademark of Merck KGaA, Darmstadt, Germany
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Journal of pharmaceutical and biomedical analysis, 38(1), 173-179 (2005-05-24)
A simple, precise and accurate isocratic reverse-phase liquid chromatography method with programmed wavelength detection has been validated to quantify DRF-4367 and Phenol red, simultaneously for application in rat in situ single pass intestinal perfusion study to assess intestinal permeability of
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Journal of chromatography. A, 1095(1-2), 27-39 (2005-11-09)
The adsorption isotherms of an ionizable compound, nortriptyline, were accurately measured by frontal analysis (FA) on a C(18)-Discovery column, first without buffer (in an aqueous solution of acetonitrile at 15%, v/v of ACN), then with a buffer (in 28%, v/v
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This study presents the optimization of a simple HPLC-UV method for the determination of metformin in human plasma. Ion pair separation followed by UV detection was performed on deproteinized human plasma samples. The separation was carried out on a Discovery
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A novel isocratic reversed-phase high performance liquid-chromatography/ultraviolet detection method for simultaneous determination of cefdinir and cefixime in human plasma was developed and validated after optimization of various chromatographic conditions and other experimental parameters. Sample preparation based on a simple extraction
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Modafinil, adrafinil and their related substances were synthesized and analyzed by RP-LC with ESI-MS/MS. The ionization mode, polarity, cone voltage, and chromatographic conditions were evaluated. The optimum LC-MS conditions to obtain fragment ions indispensable for identification of the structures were
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