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what r the parts calibrated in gc
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for inorganic molecules require to do RS, Assay and disso?
why we are using hexane in calibration of number of drop per mL
Why we used in n-butyl acetate water content terminology while in ethyl acetate we used moisture content terminology?
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 ?
what are the standard methods for HPLC?
what is mean by 40 in the dissolution basket mesh size?
in which situation ion pair agent require to use?
What is stray light in uv what are units for stray light
What is the principle of HPLC, GC, LCMS, GCMS,LC QQQ, GC QQQ, LC Q TOF and GC Q TOF. What are the applications and Specificity?
Hi sir if any product monograph not given known impurities (may be 5 impurities) specifications then how we require to proceed for inhouse formulation?
on the basis of bcs class how to proceed the solubility?
how you start RS method development when for new product?
Please tell me about the pH of Polycaboxylic ether is it in the 5-6 range ever or more than 6
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
how you fix the limits of impurities?
