Answer Posted / nilesh gharge
1%=1gm/100 ml
1gm=1000mg
1% solution=1000/100x1ooo = 10000 ppm
Is This Answer Correct ? | 1 Yes | 0 No |
Post New Answer View All Answers
How to fix the sample conc. in Related substances test by HPLC?
How require to develop GC method? how to select diluent, GAS, column selection and other chromatographic conditions?
Principle of single pan analytical balance
As per ICH related substances stability trend limit from initial to shelf life
What is shaking level in GC?
In which situation we require to analytical method validation of excipient?
for heavy metal test lead used in which form pure form or any other form for preparation of lead standard sol
What is related substance by HPLC impurity limits as per USP?
what is classification of elemental impurities? what is risk assement in elemental impurities?
If change in specification which parameter require to do for validation? if change in chromtographic condition then which parameter? if api change then which parameter? if change composition then which parameter? if old method not work out then whicj parameter? if additional one impurity added then which parameter of validation require to do on above each conditions? elaborate separately
how to calibrate hplc & gc
EXPLAIN THE CALCULATION PART OF AN KF TITRATOR CALIBRATION WITH SUITABLE EXAMPLE
What are modes of quantification in related substances
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.
If we have 5 strength which is not dose proportinate and excipients also diffrent in each strength then how we can proceed for Force degradation? and excipient are same but not dose propotinate the how FD?