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- Posts: 2
- Joined: Fri Apr 15, 2011 4:22 pm
I analyse soil lipid extracts by GC and typically methylate samples first with diazomethane (to methylate any acids) before drying and treating with BSTFA (+1% TMCS) 100 ul, a couple of drops of pyridine and some DCM (if needed to solublise the sample) and reacting at 60oC for 1.5 h to silylate any alcohols.
The problems i have been experiencing are twofold;
1) Sometimes, upon drying the sample under N2 to remove excess BSTFA, white crystals form of what i can only assume to be polysiloxanes. These do not dissolve well in DCM. Has anyone else experienced this problem and know why it happens and how it can be avoided?
2) when re-silylating a sample for a repeat analysis where, in the first analysis all my fatty acids were present in the GC chromatogram as single peaks corresponding to their methyl esters, i get the appearance of additional silyl esters analogues. I am sure that this is not down to incomplete methylation of the sample, however, trans esterification of FAMEs seems unlikely without a considerable kick from some acid. Does anyone have any advice to offer on this problem?
Thanks,
Matt
