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- Posts: 17
- Joined: Fri Feb 26, 2010 11:05 am
There are several topics on the effect of pore size, and I see the recommendation for Uwe Neue's book, so I will pursue that. However, is it possible to answer the following question simply? No problem if not, just let me know.
We are supplied with a compound by a company who use and HPLC chromatogram as their method of choice for purity estimation. The compound is the TFA salt of a cyclodextrin, and the column is a 4.6 x 150mm Vydac C18 run at room temperature. They run a gradient of acetonitrile in 0.1% TFA (10-50% ACN over 30mins) and calculate the area under the curve. I can't give any more information on the method, sorry, I don't know it.
The last two batches (of what should be the same material) have eluted at 20mins and 24mins respectively. The only difference I can see between methods is that the first column has a pore size of 100A and the second has a pore size of 300A.
So the question is, can the pore size make that much difference to a small molecule separation?
Overall though, I think the better approach will be to go back and ask them to run the same column each time.
Thanks in advance.
