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pH buffer 5.2 which can be evaporated
Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.
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						I would like to desalt peptides from its buffer (100ml scale or so). I would prefer to use a buffer that can be evaporated, maybe ammonium acetate. However, it nedds to buffer at around pH 5.2 - I think ammonium acetate buffers at pH7.
					
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						Ammonium acetate should be just fine at pH 5.2 as acetate's buffer range is approximately 3.6-5.6 if memory serves.
Good luck!
									Good luck!
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						Thanks,
I think pH 3.6-5.6 or so is for acetate/ acetic acid. NH4 CH3COO is a salt of a weak acid and a waek base, the buffering should good at around pH 7 or so.
Andre
									I think pH 3.6-5.6 or so is for acetate/ acetic acid. NH4 CH3COO is a salt of a weak acid and a waek base, the buffering should good at around pH 7 or so.
Andre
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						The pKa of HOAc is ~4.6, that of NH4+ is ~9.2, so the other "useful"  buffering  range of NH4OAc is ~8.2 - 10.2, not 7.
					
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						You could try a 2:8 v/v mixture of AcOH:NH4AcOH - just make sure
the acid and salt are the same ionic strength (i.e., 2:8 20mM AcOH:20mM NH4AcOH).
If you need more buffering capacity - increase the concentration of the acid and salt.
NH4AcOH has weak ionic strength - but it's worth a shot if you need something volatile at that pH.
									the acid and salt are the same ionic strength (i.e., 2:8 20mM AcOH:20mM NH4AcOH).
If you need more buffering capacity - increase the concentration of the acid and salt.
NH4AcOH has weak ionic strength - but it's worth a shot if you need something volatile at that pH.
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						Bryan, what do you mean with "ionic strength" here?
					
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						Hi Hans -
I just wanted to say that NH4AcOH is a weak buffer.
Thank you.
									I just wanted to say that NH4AcOH is a weak buffer.
Thank you.
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						Bryan, OK, think I can follow you now: If you dissolve a "pure"  NH4OAC in good H2O you get a pH ~7,  where there is little buffering as mentioned above.  
The source of my trouble stems from labeling mixtures of NH4+ and AcO- at pH of, lets say, 4.6 or 9.2 as NH4OAc buffers, and good ones at that.
									The source of my trouble stems from labeling mixtures of NH4+ and AcO- at pH of, lets say, 4.6 or 9.2 as NH4OAc buffers, and good ones at that.
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