WHY given much noise PDA dector then VWD
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What is control room temperature and which guide line says?
How can the GC or HPLC method is selected to determine the impurity profile in drug product?
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.
AT WHAT CONDITIONS WILL YOU ANALYSE A SAMPLE,WHICH ARE PRESERVED AT OTHER THAN THE AMBIENT CONDITIONS?(ie COLD STORAGE SAMPLES BELOW 20* CENTIGRADE?
why chiral separation?
what is internal standard define
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what does optical rotation and specific rotataion means,difference between them
how to Calibrate FID IN GC
What is the limit for single maximum impurity limit as per USP??
why should we do limit of stray light in UV calibration and why should use potassium chloride
how to calibrate AAS ? give me the procedure?