Agilent Improving Compound Integrity Application Note

This document discusses methods for improving the extraction and purification of pharmaceutical compounds, as well as the use of FlowTrap columns to address issues caused by TFA acid.


Agilent Improving Compound Integrity Application Note - cover page
Brand
Agilent
Category
Other
Document type
Application Note
Language
English
Pages
3
File format
PDF
File size
729 KB
Published
11 June, 2012
Updated
28 September, 2023
MD5 checksum
060769B86D47052D7F58D4DB2C27005D

About this manual

This document addresses the issue of compound isolation bottlenecks in the pharmaceutical industry caused by the evaporation of large volumes of HPLC fractions containing non-volatile eluents like trifluoroacetic acid (TFA). The text explains that TFA can pose risks of hydrolysis during evaporation and introduces FlowTrap columns as a solution for capturing and releasing small pharmaceutical molecules.

What's inside

  • Introduction
  • Materials and Reagents
  • TFA Removal from Caffeine and Metronidazole
  • Loading Conditions
  • Wash Conditions
  • Results and Discussion
  • Conclusion

Specifications

Detection wavelengthUV 280 nm
Trapping Column dimensions4.6 x 150 mm
Column part numberPL1560-3M07
Loading Eluent volume12 mL
Water Flow Rate4 mL/min
Base wash concentration2M NH3
Elution solvent100% CH3CN

Frequently asked questions

How effective is the base wash protocol at removing TFA?

The base wash protocol yielded freebase samples with no detectable TFA in the NMR analysis, removing more than 99% of TFA.

What is the benefit of in situ freebasing?

In situ freebasing results in a cleaner and narrower back elution peak profile, allowing for tighter elution volumes in sample collection.

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