which effect is mainly responsible for chromatographic separation when silica is the statinary phase at TLC? thanks in advance
1 3958what is different when impergnated silica plates are used in separation of azo dyes using column chromatography?
2078Why we are having specification 100% above in case of assay as there is only 100% of compound?
2 6163While performing TOC sst analysis Zero shift disabled & sample analysis zero shift enabled why?
2901which one is better separation in high pressure liquide chromatogram orlowpressure chromato gram in hplc
2213what is the concept for adjustment of pH in HPLC buffer solution ? a. Common ion effect b. Counter ion effect and explain me, how we adapt this principles & what is the role of these principles in our method
1 3575Post New Analytical Chemistry Questions
why does used dry caffien in HPLC calibration?
inhouse product is in capsule form in combination and RLD is in tablet form then can we proceed for multimedia CDP? in inhouse capsule product disso is paddle with sinker in release media is there then RLD product in tablet form then with same as paddle with sinker we can proceed n.a.?
some product having water content method with pyridine and ethylene glycol mixture instead of methanol? how they are selecting and methanol is not suitable solvent how ?
What is aggregate and fragments in SEC?
acceptance criteria for lod & loq by standard deviation of response and slope??
in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
How to decide assay range for non pharmacopeial API analysis by HPLC? Could you give me any reference for same e.g Guidelines or Paper publications?
For standardization of volumetric solutions, acceptance limit for concentration is considered as 10% of nominal concentration and %RSD as NMT 0.2% (for appropriate no. of replicates). But , if %RSD has not met, what should be further action?
For titration in anhydrous media with perchloric acide, if lack of titrator, Which indicator is been used for replacement. How calculate pH of test solution to choose suitable indicator?
How to know the estimated LOQ concentration in ppm
how you fix the limits of impurities?
please explian me about area normalisation method,diluted standard method,impurity vs impurity and which one has to be selected in method development
Describe your field experience sample type collected,sample techniques,field measurements taken and equipment used?
How would you decide dissolution medium for NCE compound of class I drug
iam usig ph buffers merk. manually how to prepare ?