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rosiglitazone

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10 posts Page 1 of 1
Hi everybody,

Can anyone give any suggestion about the hplc method for Rosiglitazone?
I'm just starting...
NH4CH3COO 0.01M pH=7 60% CH3CN 40%.
Column Phenomenex Hexyl-Phenyl
Detector UV 254 nm
Good resolution... Anyway I'd like to know if anyone has developed anything to compare and make it better.
Thanks.

Don't start with ammonium acetate at pH 7, start with a buffer, i.e. ammonium acetate at pH 4.75.

thanks, Hue.

I'll try soon.

sorry.. I meant Uwe.

First of all, Uwe's suggestion is a very important rule of thumb. Always use a "controlled" buffer system and avoid a solution with stuff you might not control.

Second, like in football, if you have a good team, don't change it! And if you have a team good enough to win the championship, do not expend a fortune with a galactic player... chromatography translation: if you have a good separation with the right eluent system - preferably isocratic - STUCK TO IT! :D

Hi Rafael,

Good to hear from you..
I thought that NH4AcO buffer strength is max at around 7 because of the Ammonium, while if I had used Na+ it would have been 4.8.
Anyway, I found that the separation has to be improved.
I'm going to try 4.8 soon... I thought I'd sorted it out too soon.
If you have any suggestion please let me know.
Thanks.

Rafael,

Do you mind if I e-mail you?
Thank you.

I thought that NH4AcO buffer strength is max at around 7 because of the Ammonium, while if I had used Na+ it would have been 4.8.
The pKa of ammonium (ammonia) is 9.2 and acetate is 4.8... Buffer is only effective within ±1 pH unit from its pKa. How could Zompa said that NH4OAc buffer strength is max at around 7?

Rafael,

Do you mind if I e-mail you?
Thank you.
No problem... since I made my e-mail "public", I do not mind any contact either by e-mail or MSM

Sorry everybody,

I was talking nonsense about the buffer power..

Zompa.
10 posts Page 1 of 1

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