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- Posts: 36
- Joined: Tue Jun 10, 2008 6:49 pm
I'd prefer to remain at a neutral pH so the compounds are deprotonated for detection by negative mode by ESI-MS. I have a GC or LC available to me. I didn't see much on the GC. I know that they are somewhat unstable molecules, and I prefer to not derivatize the compounds. Is there a better HPLC packing/separation approach I could try? I have lots of references on synthesis and degradation, but I haven't found much on analysis of these compounds.
Thank you in advance.
