Application Notes

Described in this application note are the details for an investigation of basic compound peak shape across four different alkyl C18 stationary phases that are all based upon the same core-shell HPLC/UHPLC particle morphology.

In this application, is the investigation into the relative selectivity of four different C18 stationary phases when applied to the reversed phase retention of six extremely polar artificial sweeteners.

For this analysis, we developed a fast, robust, and efficient separation on a Kinetex 2.6µm Polar C18 phase. This is a highly robust, core-shell stationary phase capable of providing increased efficiency over fully porous products. The Kinetex Polar C18 functionality provides unique polar selectivity that was critical in effectively retaining and separating these phenolic antioxidants.

For Developed is a rapid method analyzing 16 major cannabinoids with great resolution and low backpressures.

A straightforward separation of 10 closely related forms of vitamin E with a Kinetex 2.6 µm F5 HPLC column and under reversed-phase conditions. The 10 closely related structures were chromatographically separated by the multiple selectivity interaction mechanisms of the Kinetex F5 phase and Water/Methanol mobile phase.

For this application study, the alkaloid compound berberine was selected to help demonstrate the Kinetex PS C18 HPLC/UHPLC column’s unique multi-modal selectivity and improved chromatographic performance when applied to the analysis of polar basic compounds.

For this application study, the alkaloid compound berberine was selected to help demonstrate the Kinetex PS C18 HPLC/UHPLC column’s unique multi-modal selectivity and improved chromatographic performance when applied to the analysis of polar basic compounds.

A HPLC/UHPLC poster that ranks different stationary phases by 5 primary mechanism of reversed-phase selectivity.

This application is an alternative HPLC method for the analysis of 13 carbonyls without the use of any derivatization agent. The method uses the combined polar and non-polar selectivity of a Kinetex Biphenyl stationary phase to achieve improved chromatographic results.

For this analysis, we developed a fast, robust, and efficient separation on a Kinetex 2.6µm Polar C18 phase. This is a highly robust, core-shell stationary phase capable of providing increased efficiency over fully porous products. The Kinetex Polar C18 functionality provides unique polar selectivity that was critical in effectively retaining and separating these phenolic antioxidants.

This application is an alternative HPLC method for the analysis of 13 carbonyls without the use of any derivatization agent. The method uses the combined polar and non-polar selectivity of a Kinetex Biphenyl stationary phase to achieve improved chromatographic results.

This method presents the reversed-phase retention and detection of 7 polar Neonicotinoids and 4 deuterated-internal standards by LC-MS/MS and with a Kinetex 2.6 Biphenyl HPLC column. The Kinetex Biphenyl phase demonstrated significant polar compound retention and selectivity.

For Developed is a rapid method analyzing 16 major cannabinoids with great resolution and low backpressures.

A HPLC/UHPLC poster that ranks different stationary phases by 5 primary mechanism of reversed-phase selectivity.

Described in this application note are the details for an investigation of basic compound peak shape across four different alkyl C18 stationary phases that are all based upon the same core-shell HPLC/UHPLC particle morphology.

In this application, is the investigation into the relative selectivity of four different C18 stationary phases when applied to the reversed phase retention of six extremely polar artificial sweeteners.

Significantly reduce time to develop antibodies by combining titer and glycan screening using Bio-Layer Interferometry. Save on FTE costs and perform more projects.

This note describes a new method for simple, rapid determination of Aroclors and organochlorine pesticides using MRM analysis by GC-MS/MS.

Discover the Agilent QuickProbe GC/MS technology for a straightforward, quick workflow for drug analysis without sample preparation.

This application note demonstrates that SEC/MS and HIC/UV can be effectively used to characterize the drug-to-antibody ratio profile of antibody drug conjugates.

* How USP affects data integrity generated by a chromatography datasystem. * The role of quality assurance in providing oversight on the data-integrityprocess. * The cost of non-compliance

Create a new form in MJH DL and Publish on the live LCGC site using MMH Alfresco

See a simple and fast SPE method for the LC-MS/MS analysis of glyphosate, AMPA, and glufosinate in red wine without derivatization using AFFINIMIP® SPE Glyphosate.

Create a new form in MJH DL and Publish on the live LCGC site using MMH Alfresco

A first step to understanding and validating data is proper application of appropriate statistics and understanding the use and terminology of analytical processes.

A straightforward separation of 10 closely related forms of vitamin E with a Kinetex 2.6 µm F5 HPLC column and under reversed-phase conditions. The 10 closely related structures were chromatographically separated by the multiple selectivity interaction mechanisms of the Kinetex F5 phase and Water/Methanol mobile phase.

This method presents the reversed-phase retention and detection of 7 polar Neonicotinoids and 4 deuterated-internal standards by LC-MS/MS and with a Kinetex 2.6 Biphenyl HPLC column. The Kinetex Biphenyl phase demonstrated significant polar compound retention and selectivity.

Described in this application note are the details for an investigation of basic compound peak shape across four different alkyl C18 stationary phases that are all based upon the same core-shell HPLC/UHPLC particle morphology.

In this application, is the investigation into the relative selectivity of four different C18 stationary phases when applied to the reversed phase retention of six extremely polar artificial sweeteners.

For this analysis, we developed a fast, robust, and efficient separation on a Kinetex 2.6µm Polar C18 phase. This is a highly robust, core-shell stationary phase capable of providing increased efficiency over fully porous products. The Kinetex Polar C18 functionality provides unique polar selectivity that was critical in effectively retaining and separating these phenolic antioxidants.