how can delete the impurity in 1-(2:6 dichloro phenyl)-2-indolenone.and desolving the impurity in which solvent but does not desolve product in solvent.
1 3051in determination of(acetone) moister content we are using methanol replaced by pyredine.what hapend in that reaction.
2 9396what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
2592WHEN AN UN KNOWN SAMPLE IS GIVEN TO U,HOW WILL U START THE ANALYSIS(ie FIRST WHICH TEST TO BE DONE,NEXT,THEN NEXT),HOW WILL U DECIDE WHICH TYPE OF ANALYSIS TO BE DONE FOR IT?
2 10858Post New Analytical Chemistry Questions
Hi sir if any product monograph not given known impurities (may be 5 impurities) specifications then how we require to proceed for inhouse formulation?
in which situation require to take incident in validation?
Why only Copper standard is used to calibrate Atomic Absorption spectrophotometer?
Why sodium hydroxide used for maintain pH of phosphate buffer
what is the purge flow & how to calculate
WHAT IS THE USE OF STARTER ?????????
what is partion and column chromatography
AT WHAT CONDITIONS WILL YOU ANALYSE A SAMPLE,WHICH ARE PRESERVED AT OTHER THAN THE AMBIENT CONDITIONS?(ie COLD STORAGE SAMPLES BELOW 20* CENTIGRADE?
What is similarity factor and its use in api strength?
what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
how require to interprit the method precision data of hptlc?
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 calculation of residual solvent methanol (3000 ppm) standard solution, and how many quantity used of test sample
How to determine the EDTA content by potentiometry titration in Ceftriaxine sodium