Shim-pack FC ODS
Shim-pack FC-ODS is an ideal column to shorten your analysis time using conventional HPLC. Its innovative surface structure and optimized packing method also enable outstanding resolution. Particle size is 3 μm, but the performance of a Shim-pack FC-ODS is equivalent to a 2 μm column while the resolution is twice as that of a 5 μm column. Therefore, Shim-pack FC-ODS can not only shorten analysis times, but also provide a higher number of theoretical plates.
Shim-pack FC-ODS separates components by hydrophobic interaction like other ODS columns. It is possible to change to Shim-pack FC-ODS from other ODS columns under...
High Speed Analysis of 2,4-DNPH derivatized aldehydes / ketones
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Determination of heterocyclic oxygen compounds in Citrus essential oils by Supercritical fluid chromatography-tandem mass spectrometry
New Nexera UC Prep Semi-Preparative Supercritical Fluid Chromatography System
Semi-Preparative Supercritical Fluid Chromatography System
New Nexera UC Supercritical Fluid Extraction / Supercritical Fluid Chromatograph
Nexera UC improves your analytical workflow by utilizing a completely new separation technology, Unified Chromatography, which unites sample separation, analysis with various separation modes, and high-sensitivity detection.
New Nexera Prep Preparative Purification Liquid Chromatograph
The Nexera Prep Purification System provides optimal solutions for your laboratory needs.
Shimadzu has released the Shim-pack™ SUR-Na Columns for Ligand Exchange Chromatography.
Shim-pack™ SUR-Na, a ligand exchange chromatography column, offers excellent performance by combining size exclusion mode and sodium-based ligand exchange mode to provide superior separation of sugar components. Pure water can be used for the mobile phase, resulting in less effort to prepare for the analysis.
Efficient Method Development by automated pH Screening with LabSolutions MD
This article describes an example of using LabSolutions MD, a dedicated software for supporting method development, to automate pH screening by varying the mobile phase pH from 2.5 to 8.5 to evaluate the optimal pH level for separating 12 small-molecule drugs.