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Chemical Compound Review: 

PubChem9299     2,3,4,5,6-pentafluoropyridine

Synonyms: SureCN188694, SureCN876026, ACMC-1BL6P, AG-K-65692, ANW-35818, ...
 
 
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Psychiatry related information on EINECS 211-839-9

  • The derivatization conditions including the phase-transfer catalyst, the amount of pentafluoropyridine, the reaction time, the concentration of NaOH and organic solvent were optimized [1].
 

High impact information on EINECS 211-839-9

  • The ion pairs, ammonium phenolates, formed on the C18 solid phase, were eluted with a solvent containing the derivatizing reagent, pentafluoropyridine, and completely derivatized during the elution [2].
  • The phenols adsorbed on Oasis MAX as phenolate ions were desorbed after derivatization with pentafluoropyridine [3].

References

  1. Determination of 4-alkylphenols by novel derivatization and gas chromatography-mass spectrometry. Kojima, M., Tsunoi, S., Tanaka, M. Journal of chromatography. A. (2003) [Pubmed]
  2. Ion-pair solid-phase extractive derivatization of 4-alkylphenols with pentafluoropyridine for gas chromatography-mass spectrometry. Kojima, M., Matsui, N., Tsunoi, S., Tanaka, M. Journal of chromatography. A. (2005) [Pubmed]
  3. High performance solid-phase analytical derivatization of phenols for gas chromatography-mass spectrometry. Kojima, M., Tsunoi, S., Tanaka, M. Journal of chromatography. A. (2004) [Pubmed]
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