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Chemistry AllOther (190) How long we can use hygroscopic reference standard in terms of water absorb.I mean in line with respective monograph's specification or more than that?
1 3202What is use of LOD and LOQ in validtion and give range and in calculation why we use 3.3* LOD here why we use 3.3
2 6998In the method validation proceedure,lod & loq calculation we use the formulae for LOD=3.3*SD/slope and for LOQ=10*SD/slope,why we use 3.3 & 10 in the formulae?
1 11136In HPLC Chromatographic separation Resolution equation is Rs = 1.18 (tR2 –tR1)/wh1+Wh2, Where, tR2 and tR1 is run time of eluent ratios of the distances from the point of application to the centers of the spots and the distance travelled by the solvent front from the point of application (retardation factor), and Wh1and Wh2 , is peak width of at half height. What is 1.18 ?
1 7475
What are the advantages of conductometric titration over visual or potentiometric titration?
on the basis of bcs class how to proceed the solubility?
what happens to the unit particles of a solute when it dissolves on a liquid?
Why are the titration involving edta carried out slowly towards the end point?
What is chemical oxygen demand?
What are the two most abundant elements in the universe?
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
How hydrate is forming along with API?
write short note on steroids,terpenes,prostagladins,and phospholipids.
What is the bluish white precipitate formed after adding ammonia solution?
How to convert -40 of into centigrade?
Write the equation of photosynthesis?
how you start RS method development when for new product?
in api coa analytical method given as Ph Europe which api used in formulation in this api coa method given Ph Europe so for Analytical methic for finished product we require to refer Ph Europe monograph ok n.a.? So any extra impurities which is given in USP monograph of api or finished product need not require to monitor on above case n.a.? but how require to do specificity?
what are the guidelines for analytical method validations?