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 1195
What is blank titration of potentiometrically.2 7367
which solution used for detecting factor of k.f.titroter except water3 6361
in dissolution why pool sample needed? in which type of drug pool sample need?1808
in determination of(acetone) moister content we are using methanol replaced by pyredine.what hapend in that reaction.2 6171
what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.1026
What is the difference between spectro meter and spectro photo meter?1 8406
How do u differentiate primary1 1288
WHEN 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 7533
WILL YOU DRY DST BEFORE FACTOR DETERMINATION BY USING KARL FISHER TITRATOR4 7664
How to start the dissolution development for unknown tab?
How we can determine water content in piperazine
In Karl Fischer titration,What is the situation if the material tested is only soluble in water,and not soluble in the common solvents used such as methanol ?? [e.g. Iron III Hydroxide polymaltose]
Principle of single pan analytical balance
Which type of column should i use to check the purity of high molecular weight protein using HPLC reverse phase column chromatography? Hi everyone. I wanna to check the purity of high molecular weight protein (collagen) with MW of ~130 kDa using a HPLC. I know C18
What is control room temperature and which guide line says?
why should we perform dissolution PVT calibration only by UV spectrometer, not by HPLC ?
if you have given a blank water how you analyse by general analytical techniques?
Did anybody have method for acetyl cysteine effervescnce tablet
In performance Check of GC Why Hexadecane Peak is Considered
what is the importence and role of LCMS and LCMS/MS and their applications? which type of compounds are analysis by lcms?
I have compare C2H2-air and C2H2-N2O flame AAS on determination calcium. Both use same range of std to plot calibration curve. (2-6ppm) When i measure the sample with phosphate, KCl and LaCl, C2H2-N2O flame give false positive result, around 0.5ppm. When i measure the sample with phosphste, KCl and EDTA. C2H2-N2O flame also give 0.5ppm false positive. But both above mentioned sample would not give false positive when measured by C2H2-air flame. What is the reason?
what is separation techniques.
What is gelatinization?