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[3/28, 20:52] Manoj P Venkatpurwar: how many impurities require to inject in assay specificity that how we can find out? and in Rs also how?
746How we can identify process related and degradation impurity in single method with short period?
758Post New Analytical Chemistry Questions
1.What is the difference between method validation and method verification 2.Which guidelines proposed to method transfer
which one is better separation in high pressure liquide chromatogram orlowpressure chromato gram in hplc
1)What's the meaning of Absorption,give a example. 2)What's the meaning of Adsorption,give a example. 2)what is the difference between Absorption and Adsorption.
Why we used in n-butyl acetate water content terminology while in ethyl acetate we used moisture content terminology?
how to calculate elemental impurities?
Why acetonitrile and water are used as extraction solvent when analysis melamine? I thought they are miscible and won't be able to separate...
Principle of single pan analytical balance
Which parameter require to do for analytical method equivalency?
effect of pore size, pore volume, partical size, column length, carbon load on retention time? what is carbon load? what is the use?
identification is for unknown? qualification for known? reporting for LOQ?
what is biorelivent dissolution media?
what is definition of validation? which components are followed give detail?
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?
How require to develop GC method? how to select diluent, GAS, column selection and other chromatographic conditions?
