What is the difference between purge septum flow and column flow in gas chromatography?
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Why we inject a standard 6 times for Related substances by HPLC and 5 times for Assay?
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is ther any guidline is available for limt of peak fronting.and what is the limt of peak fronting.
why we get only one peak in assay by hplc but in rs by hplc get more peaks
I have 1 gram of Diphenylamine and want to make a 10,000 or 1000 ppm solution in methanol. How do I make this?
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which detector is used in IR
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why base line not start from zoro in GC Chromatograme.