Analytical Chemistry Interview Questions
Questions Answers Views Company eMail

what is diffrence between shelf life and expiry date?

1 1035

how you start RS method development when for new product?

337

how you establish the LOQ?

362

in which situation require to use paddle and basket?

345

what is mean by dissolution hydrodynamics?

428

column washing procedure for normal phase and reverse phase?

1 984

how to convert normal phase hplc to reverse phase and vice versa?

1 1912

if your impurity coeluting with each other in that situation how require to set specification? is it acceptable?

442

what is mean by extactable and leachable study?

642

how to calculate elemental impurities?

623

how you fix the limits of impurities?

451

what is mean by nitrosamine impurities?

610

if instrument calibration fails then what require to do?

513

why require the ph, buffer during hplc mobile phase?

468

is it nessesary to do solution stability for 7 days?

379


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Un-Answered Questions { Analytical Chemistry }

WHAT IS THE USE OF STARTER ?????????

1980


what you do when compound having dwel wavelength?

360


identification is for unknown? qualification for known? reporting for LOQ?

357


if you get peak in blank then what require to do?

545


Why sometime potassium ortho phosphate mix with acetone use for sample preparation for hplc

1058






What is the accrptance criteria in RSD for RS method precision on basis of impurity percentages?

382


What should be the level/ Percentage of Arsenic in Arsenic free zinc.

1828


In Assy by potentio metry titration method how select MET U ,DET U, SET U,

1420


how much mass should be there in volumetric flask while in preparation of sample for assay? 

2126


we are performed SOR for a particular product the limit is -6 to -10.We face particular bathes it is not meeting the specification.we performed diffrent instrument diffrent analyst we are getting diffrent diffrent results.solvent is dimethyl sulfoxide what could be the reasion

1431


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?

3065


sop of a uv visible spectrophotometer double beam elico model

5440


What are the primary considerations in extractables and Leachables ?

1849


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 ?

3276


how to decide for one product require water content or LOD?

404