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Which is the best mobile phase to separate organic acids using C8 column. And how should the samples be prepared for hplc?
1 5196Why we used in n-butyl acetate water content terminology while in ethyl acetate we used moisture content terminology?
IDA,
1903How to calculation of residual solvent methanol (3000 ppm) standard solution, and how many quantity used of test sample
3329Post New Analytical Chemistry Questions
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,
In which situation we require to analytical method validation of excipient?
Many times I don't got a caffeine peak in calibration of hplc using guard column ❓
How do we fix the sample concentaryion in hplc method development?
what is biorelivent dissolution media?
in which situation require to use paddle and basket?
how to decide for one product require water content or LOD?
if you get peak in blank then what require to do?
What is control room temperature and which guide line says?
how require to interprit the method precision data of hptlc?
what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
if peak get problamatic then what require to do?
From where require to take the RLD sample?
1.What is the difference between method validation and method verification 2.Which guidelines proposed to method transfer
If inhouse hplc related substance method is completly diffrent from Usp for finished proďuct with diffrent impurities then how require to prove method equivalecy?
