If we are getting split peak in Chromatogram,what we can do?
Answer Posted / n.s.r
In Method development time or already validated method first we conform that already validated method it's ok but in development time we go on peak purity and finalise column problem or if any impurities is present in main peak.Thank you ANY WAY YOU WILL answer that question.
Is This Answer Correct ? | 0 Yes | 6 No |
Post New Answer View All Answers
how can I make the copper get white bye any salt or acit?
WHICH STANDARD WE USE IN SILICA ANALYSIS IN SILICA-GEL METHOD FOR SOLID SAMPLE
How doing qbd practically?
can we use the same detector in HPLC as well GC and what could be the differences we can find in the final chromato graph in any aspects?
which situation gc hs and gc als require to use?
What is the formula to determine the concentration of M of a solution given the % transmittance? Use %T = 43.7 as an example.
Hi sir if any product monograph not given known impurities (may be 5 impurities) specifications then how we require to proceed for inhouse formulation?
how can give the expiry period and restadardisation of volumetric solution
why require the ph, buffer during hplc mobile phase?
what is the importance of peak purity in HPLC and how we can calculate through manul(not software)?
How we choose the mobile phase for method development.?
on saturation solubility study data how we can find out the bcs class of drug?
how to select short coloum and long coloumn for new molecule
why we are using hexane in calibration of number of drop per mL
why salisylic acid not using now days for disdolution calibration?