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 2452in determination of(acetone) moister content we are using methanol replaced by pyredine.what hapend in that reaction.
2 8280what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
2208WHEN 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 9977Post New Analytical Chemistry Questions
How to calibration of the uv spectroscopy and its test?
mode of absorption in alimentary canal?
What is the acceptance criteria for moisture balance when calibrated with sodium sulfate
Many times I don't got a caffeine peak in calibration of hplc using guard column ❓
What is the Formula for coreletion coefficient in plhplc calibration
What is aggregate and fragments in SEC?
Tell me about analytical method validation in QC
how you start RS method development when for new product?
effect of pore size, pore volume, partical size, column length, carbon load on retention time? what is carbon load? what is the use?
what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?
Related substance method equivalency on control sample or spiked sample?
How we performed the force degradation for drug substance, is any specific guideline is available for each parameter(Acidic, basic, oxidation,heat)? what conditions you mentained for above parameters.
WHAT IS THE PURPOSE WE USE HCL, CHOPPER, BURNER, MONOCHROMATOR in AAS? PLEASE EXPLAIN BRIEFLY
What is related substance by HPLC impurity limits as per USP?
on the basis of bcs class how to proceed the solubility?
