Agilent Mass-based Fraction Collection Application Note

This Application Note briefly describes the advantages of mass-based fraction collection compared to time and peak based fraction collection in combination with the Agilent 1200 Series purification system and the Agilent 6100 Single Quadrupole LC/MS


Agilent Mass-based Fraction Collection Application Note - cover page
Brand
Agilent
Document type
Application Note
Language
English
Pages
4
File format
PDF
File size
327 KB
Published
02 July, 2012
Updated
30 September, 2023
MD5 checksum
56958017370CF77FA6AB458FB27F1ED7

About this manual

The document explains that modern automated purification systems offer various ways to collect fractions, including manual, time-based, peak-based, and mass-based methods. It focuses on comparing these techniques in the context of drug discovery and preparative HPLC.

Mass-based fraction collection is highlighted as a highly specific method where the fraction collector is triggered by a single quadrupole MSD based on a known target mass (e.g., [M+H]+). The note details that this approach typically results in only one fraction per sample, eliminating the need for subsequent analysis to identify which fraction contains the compound of interest. However, it notes that purity may be slightly lower than peak-based collection if isomers with identical masses are present.

What's inside

  • Introduction
  • Manual fraction collection
  • Time-based fraction collection
  • Peak-based fraction collection
  • Mass-based fraction collection
  • Advantages and Disadvantages

Frequently asked questions

What systems are used for mass-based fraction collection?

The Agilent 1200 Series purification system in combination with the Agilent 6100 Single Quadrupole LC/MS.

What specific systems are combined to perform mass-based fraction collection?

The Agilent 1200 Series purification system is used in combination with the Agilent 6100 Single Quadrupole LC/MS.

What is required to use mass-based fraction collection?

The user must know the mass of the target compound before starting the process.

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