In pharmacopeal solibility parameter of a material, is et essential to test all paramete? If 70-75% parameter passes can we assess that the material is satisfactory or not?
1 5345Why triethylamine and o-phosphoric acid used while setting pH of mobile phase during HPLC Analysis?
6 33659why RID detector is used for selective materials like Mannitol, Hydroxyethyl Starch and Sorbitol?
5 12510For Dissolution test why we are Performing 6 Bowls why not more.any were mentioned or in what basis we are performing? --------Veerabhadrarao.M
2 12173In Number of Theoretical Plates (N) = 16 (tr/w)2. where tr: retention time, and W: peak width. My Question is here in formula what is 16.Can u explain briefly? ---Veerabhadrarao.M
3 19488A new drug substance found fail to meet specification for an unknown Impurity during stability study(Specific change),how would further proceed?
2 7367Post New Analytical Chemistry Questions
What is viod volume and peak purity in HPLC?
how to calibrate hplc & gc
What is the difference between purge septum flow and column flow in gas chromatography?
which batch require to use for analytical method validation?
why are measure gas flow " ml " in Gas chromatography
how can give the expiry period and restadardisation of volumetric solution
Why only hydroxy naphthol blue indicator is used for standardisation of 0.05M EDTA solution instead of solochrome Black T or Euriochrome Black T indicator which is used for all sample analysis with 0.05M EDTA solution?
How can we confirm the HPLC column is end-capped or not? Is it possible to identify by physical appearance?
why we are using hexane in calibration of number of drop per mL
what is lod and loq ?,why use k2cr2o7 , kcl h2so4 in uv calibration ?,why use benzophenone & caffene acetone in hplc calibration ?,what is leading peak in hplc ?why we do the calibration of limit of stry light in hplc & uv ?
How doing qbd practically?
How would you decide dissolution medium for NCE compound of class I drug
in DMF having extra impurities and in api COA also having extra imp than USP or BP product then how require to proceed?
How can the GC or HPLC method is selected to determine the impurity profile in drug product?