Agilent ZORBAX SB-C8 Separation of Deoxy Ribonucleosides Application Note

This document introduces a high-efficiency method for separating nucleosides using reversed-phase separation with protected-bonded-phase columns.


Agilent ZORBAX SB-C8 Separation of Deoxy Ribonucleosides Application Note - cover page
Brand
Agilent
Category
Other
Document type
Application Note
Language
English
Pages
2
File format
PDF
File size
1 MB
Published
03 July, 2012
Updated
30 September, 2023
MD5 checksum
C98BFAE59A956962331FA6819D26D61E

About this manual

This document details a high-speed, high-resolution separation method for nucleosides, specifically Cytidine, 2 Deoxycytidine, Inosine, Guanosine, 2'- Deoxyinosine, Adenosine, and 2'- Deoxyguanosine. The method utilizes reversed-phase separation with sterically protected bonded-phase columns to achieve good peak shapes and high column efficiencies.

What's inside

  • Biochemical
  • Separation of Deoxy and Ribonucleosides
  • Highlights
  • Conditions
  • ZORBAX SB-C8
  • Mobile Phase
  • Flow
  • Detection

Specifications

Column Part Number866953-906
Column Dimensions4.6 x 75 mm
Mobile Phase Composition5% methanol, 95% phosphate buffer
Flow Rate2.0 mL/min
Detection Wavelength254 nm
Injection Volume1.6 pg each

Frequently asked questions

What is the recommended column size for this separation?

The recommended column size is 4.6 x 75 mm.

What is the recommended flow rate for this separation?

The recommended flow rate is 2.0 mL/min.

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