Why dissolution test apparatus calibration with salycilic acid tablets was stopped by FDA&USP from the year of 2009?
1 9293Post New Analytical Chemistry Questions
how to select short coloum and long coloumn for new molecule
How do we fix the sample concentaryion in hplc method development. What is the basis?
what is the difference between potentiometric titration and karl fischer titration?
How will u perform degradation study in detectors other thann PDA in HPLC Methodology
why lactose has less charges when packed in steel containers when compared with packing of lactose in polyamide material?
what is third integration
if peak get problamatic then what require to do?
how to selecet an exact coloumn for an new molecule development by hplc how to select exact salt as buffer for new molecule development by hplc what is the the process to select the mode of saparation of compoundes by hplc what is the use of ph of buffer what is use of buffer,ph,organic phase,ans methods how the molecules get saparated in coloumn,
WHY pKa value is more important than pH value of the mobile phase in HPLC?
in which situation require to use paddle and basket?
In which situation we require to prepare the standard solution from sample in Related substance method?
in which situation ion pair agent require to use?
In BP2013, Loperamid HCl monograph. Assay by titration with 0.1N sodium hydroxide using hydrocloric acid 0.01N and reading the volume added between the 2 points of inflexion. I have a question that if the diluent solvent is ethanol is certainly consumed a amount of volume of titrant, so this volume must be eliminated on the result calculation or not apart from first point which is subtracted above.
USP methodology, EP methodology, IP methodology, among three if possible to use one methodology for qualify working standard to use USP, EP, IP ? Please explain...
How to know the estimated LOQ concentration in ppm