Chromatography Forum

Posted: **Sat Oct 28, 2006 5:10 pm**

Bruce,
Thank you for your information.

Posted: **Sun Oct 29, 2006 12:06 pm**

Hi Members,
What would you do if inpurity peaks starting to merge with the main peak? (the initial resolution between imputiry and main peak is about 1.5) column: Waters xterrra C8, mobile phase H2O and ACN, gradient 90% water to 10% water after 40 minutes. The main compound is testosterone palmitate and the impurity is a little tiny unknown peak. I noticed the same behavior in two "new" Waters C8 columns (about a month old). I had no choice but to buy another two columns

to complete the validation work.
Thanks in advance,

Posted: **Sun Oct 29, 2006 12:07 pm**

Hi Members,
What would you do if impurity peaks starting to merge with the main peak? (the initial resolution between impurity and main peak is about 1.5) column: Waters xterrra C8, mobile phase H2O and ACN, gradient 90% water to 10% water after 40 minutes. The main compound is testosterone palmitate and the impurity is a little tiny unknown peak. I noticed the same behavior in two "new" Waters C8 columns (about a month old). I had no choice but to buy another two columns

to complete the validation work.
Thanks in advance,

Posted: **Sun Oct 29, 2006 12:27 pm**

Hi Mav,
Opps! I don't mean to steal

your post. I will "void" mine

Best regards,

Chromatography Forum

Fronting peaks with PFPP column