please explian me about area normalisation method,diluted standard method,impurity vs impurity and which one has to be selected in method development
1628How they found 1mL of K.F reagent is equivalent to 5mg of water and if we change the composition of K.F reagent, is it can neutralize more amount of water?
1778Why acetonitrile and water are used as extraction solvent when analysis melamine? I thought they are miscible and won't be able to separate...
1689In HPLC calibration, caffeine is used as primary standard for wave length calibration due to caffeine is having dual maxima at 273 & 205 nm and one minima at 245 nm. Any body can give reference of these details from any pharmacopeia (with chapter no.) or any other authentic guideline?
1973Post New Analytical Chemistry Questions
please explian me about area normalisation method,diluted standard method,impurity vs impurity and which one has to be selected in method development
if tech transfer fails whay require to do?
If suppose 10 methods of dissolution given in pharmacopoeial for single content product then which method out of 10? or all 10 require to follow?
in api coa contains only process impurities and in product coa contains degradation impurities?
process of Diclofenac sodium,IP.
how to develop the icp ms method? Application of icp ms?
Ratio of Water and Acetonitrile(diluent) is not recommended to use in cleaning method validation,why?
Qc interview questions
Which type of column should i use to check the purity of high molecular weight protein using HPLC reverse phase column chromatography? Hi everyone. I wanna to check the purity of high molecular weight protein (collagen) with MW of ~130 kDa using a HPLC. I know C18
please explain about aluminium hydroxide assay
for inorganic molecules require to do RS, Assay and disso?
what is procedure of actual procedure for registration of drug?
[3/30, 13:29] Manoj P Venkatpurwar: How hplc column selection according to structure? How mobile phase buffer selection on molecule structure?
what is the importance of peak purity in HPLC and how we can calculate through manul(not software)?
How can the GC or HPLC method is selected to determine the impurity profile in drug product?