why sre you used Potassium hydrogen phthalate in standarisation of 1N NaOH and 0.1 N Perchloric Acid?
Cipla, Elder, Vamsi Labs,
1 9724why we are using 6 dosage units in dissolution, and why we are using 6 tablets in disintegation test.is there any scientific reason beyond 6?
1 22083Post New Analytical Chemistry Questions
How to set analyticl specification for combination products?
how pda detector works over uv?
What are usp limits for theoritical plats,resoution,tailing factor,peak to valley ratio
Why we check moisture,ash & AIA in product
if peak get problamatic then what require to do?
what is the origin to prepare standard operating procedure
Why Ethanol is Used for Standardization of GC Head space?
in gas chromatography what is the difference between gas flow rate and average linear velocity ?
effect of pore size, pore volume, partical size, column length, carbon load on retention time? what is carbon load? what is the use?
what is the purge flow & how to calculate
How do we get end points and how many end points are possible for citric acid and di-acid not theorotically answer should be given practically.
How to start the dissolution development for unknown tab?
My question about gas chromatography sulfur chemiluminsecence detector. I test unknown sample gas by GC-SCD (calibrated ) and the result of *H2S is 279 PPM , *but when I test the same sample with the GC-TCD (calibrated ) the value of *H2S is 2500 PPM . I'd like to inform you that both GCs are calibrated and have very good operation conditions with stable parameters . the question is if the sample gas with higher H2S over detection limits of SCD detector (1000 ppm). why the result it 279 ppm Best regards
Why we select scan range from higer wavelength to lower wavelength in uv visible spectroscopy and ftir spectroscopy ? .
give clarity of linearity and range in method validation