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How about basic buffers in positive mode?

Discussions about GC-MS, LC-MS, LC-FTIR, and other "coupled" analytical techniques.

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How about adjusting the pH to below 8-9, and operate the MS in positive mode? Possible or just poor ionization effiency? I am working with neutral compounds with low ionization effiency, but want to get rid of interfering substances.

Or could I adjust pH of the mobile phase during a run? Which is best?

if I understand correctly, you have to be pH 8-9 to get the separation adn wsnt M+.

I guess you may be still able to get Na adduct.

If not, do postcolumn addition
Excel

You loose some ionization efficiency, but it still works well. We went to pH 10 for analytes like amitriptyline and were surprised that we still got a good signal. The signal was around 2 to 3 times less than at pH 3, but this is not a big deal if you can get around other problems, such as ion suppression from interferences.
3 posts Page 1 of 1

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