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why we are using benzene, anyline in acetic anhdride assay titration method?
How to calculation of residual solvent methanol (3000 ppm) standard solution, and how many quantity used of test sample
how require to set assay concentration for standard and sample?
What is the formula for relative diffrence for standard solution in solution stability in validation?
please explian me about area normalisation method,diluted standard method,impurity vs impurity and which one has to be selected in method development
What are usp limits for theoritical plats,resoution,tailing factor,peak to valley ratio
Why only hydroxy naphthol blue indicator is used for standardisation of 0.05M EDTA solution instead of solochrome Black T or Euriochrome Black T indicator which is used for all sample analysis with 0.05M EDTA solution?
what is the principle involved in turbidometry and nephelometry ?
From where require to take the RLD sample?
how to select short coloum and long coloumn for new molecule
In HPLC Calibration, On which basis RSD Limit of noise test is fixed (NMT 33.0 % )
Difference between the quantitative analysis and qualitative analysis?
why should we perform dissolution PVT calibration only by UV spectrometer, not by HPLC ?
what is the difference between potentiometric titration and karl fischer titration?
if you get peak in blank then what require to do?
