Does anyone know the pH range that dimethyloctylamine can be used in? Is it compatable with LC-MS?
I am having a bad tailing problem with one of my first eluting peaks. My injection volume is 20 ul & the buffer I use now is 25 mM ammonium acetate at pH 6. TEA doesn't help, washing the column with a strong solvent doesn't help. Any suggestions?
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By Anonymous on Friday, March 30, 2001 - 11:24 am:
DMOA can be used at pH<7 or better pH<6, otherwhise t is not water-soluble. Once, I used it with good results for peaks with bad tailing, but that was 10 years ago. I think you can solve the problem by changing the column.
Have you tried another column (low metal silica, like Phenomenex Luna or Waters Symmetry)?
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By Uwe Neue on Friday, March 30, 2001 - 03:14 pm:
You can fix the solubility problem of dimethyloctylamine in water by adding some organic solvent to your buffer. However, I doubt that it is good for LC/MS. What happens to your peak when you change the pH?
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By Brian on Monday, April 9, 2001 - 05:01 pm:
In my experience, dimethyloctylamine does not work significantly better than triethylamine. Furthermore, it is not as soluble. I like Anonymous' idea of trying a different column. If I knew what the compound was it would be easier to suggest solutions.
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By Anonymous on Wednesday, April 11, 2001 - 05:31 pm:
Thanks for the responses. I used a Luna column a while ago, but choose the Zorbax SB for a specific separation problem. Now that I look back at the data, the tailing is much improved on the Luna (1 compared to 3!) If I can maintain the separation with the Luna,I'll be all set!
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