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avoiding keto enol tautomerism in a compound in HPLC analysi

Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.

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We have been working hard on a compound which exhibits keto-enol tautomerism but we are unable to avoid it. can anyone suggest some tips to avoid this keto enol tautomerism while analysing by HPLC
Increase the temperature to speed things up so that you will be looking at the "average" configuration.
-- Tom Jupille
LC Resources / Separation Science Associates
tjupille@lcresources.com
+ 1 (925) 297-5374
I don't think you'll ever entirely be rid of it, but pH can play a role too. Assaying for avobenzone works much better at pH ~2.2 than at ~3.0 for this reason.
http://the-ghetto-chromatographer.blogspot.com/
3 posts Page 1 of 1

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