In burette calibration of Karl fischer Instrument, the multiplication factor 1.00693 is using for how much ml of water dispenced. why
1 4348In UV-VIS spectrophotometer:My diluent is methanol even though i corrected base line for methanol,In my sample scan i found methanol peak.what is the reason?
2 10124What is the diffrence between the performing of LOD ordinary drying at voven and vaccum method.
Apex,
4 10712how a particular wavelength can be different for a particular compund while analysing by uv and by HPLC.
2250in hplc calibration we are using 0.05% acetone why we are using that one and what happen when its conc increases or decreases
4 31906what is the different in Total ash, sulphated ash, acid insoluble ash, alcoholic or non alcoholic ash?
9931Post New Analytical Chemistry Questions
for heavy metal test lead used in which form pure form or any other form for preparation of lead standard sol
what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
mode of absorption in alimentary canal?
why lactose has less charges when packed in steel containers when compared with packing of lactose in polyamide material?
If suppose 10 methods of dissolution given in pharmacopoeial for single content product then which method out of 10? or all 10 require to follow?
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 guidelines for analytical method validations?
Why we use potassium dichromate in uv calibration Exact reason behind it??
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?
Why six unit used for precision?
what is mean by extactable and leachable study?
Ratio of Water and Acetonitrile(diluent) is not recommended to use in cleaning method validation,why?
How will u perform degradation study in detectors other thann PDA in HPLC Methodology
how you start RS method development when for new product?
What is a difference between potency and purity?