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Chemistry AllOther (190) In the test for control of absorbance in UV calibration why do we use only potassium dichromate and what is purpose of taking a specified amount of 57.0-63.0mg?
8 58539In the test for control of absorbance in UV calibration why do we use only potassium dichromate and what is purpose of taking a specified amount of 57.0-63.0mg?
1 9936How 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?
NCL,
3304How to compare XRD graphs against standard and carry polymorpism study of API's by powder XRD method?
NCL,
3821
What is chemical oxygen demand?
Why purity angle should be less than purity threshold in peak purity
What is the process for the removal of salts from brackish water or seawater to make it usable?
What is the role of stannous chloride?
How require to develop GC method? how to select diluent, GAS, column selection and other chromatographic conditions?
how many types of balance calibration test?
What is a proteic unit?
Any one is alembic pharmaceutical ltd. On starting to job ?
Give lewis dot structure for HBrO4?
If inhouse hplc related substance method is completly diffrent from Usp for finished proďuct with diffrent impurities then how require to prove method equivalecy?
if tech transfer fails whay require to do?
What is the difference between chromatographic purity and related substances?
pharma industries oriented
What is a difference between potency and purity?
If change in specification which parameter require to do for validation? if change in chromtographic condition then which parameter? if api change then which parameter? if change composition then which parameter? if old method not work out then whicj parameter? if additional one impurity added then which parameter of validation require to do on above each conditions? elaborate separately