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what is the purpose of Buffer in any titration?Ex:In determination of hardness of water we use ammonia ammoniachloride buffer in titration with EDTA.Why?
13 91919why KF factor is between 4.5 to 7.5 mg/ml ? why ? why sometime pyridine is used in analysis like in raw material solvent like acetone etc?
11 72080what is the importance of peak purity in HPLC and how we can calculate through manul(not software)?
4488When performing Moisture content how to you say only Methanol react with water not product Explain?
2 10368How we develop a method by HPLC for unknown compound,if we got three peaks with same response then how we can find out which one is our desired compound's peak without taking help of LC MS.
4 15014In case of dissolution test, if there is variation within 6 individual units however the batch is complying as per S1 criteria, is it necessary to do investigation for the same? What should be the criteria for such variation?
2 5646What is the difference between bulk property detectors and Solute property detectors vivimed labs limited
3 17556IF THE COMPOUND PKA IS 5.3 WHY WE ARE ADJUSTING PH+/-2 OF THE COMPOUNDS PKA. WHAT IS THE CONDITION
2 10439IN DISSOLUTION TEST S1AND S2 AND S3 CONDITIONS ALL ARE FAILED THEN WHAT IS THE DESSICION U CAN TAKE
12 28632Post New Analytical Chemistry Questions
Why irmoisture balance is used for corrugated box moisture testing
What is the main difference between ODS1 and ODS2 Hplc column.
what are risk assement in the analytical qbd?
Related substance method equivalency on control sample or spiked sample?
For standardization of volumetric solutions, acceptance limit for concentration is considered as 10% of nominal concentration and %RSD as NMT 0.2% (for appropriate no. of replicates). But , if %RSD has not met, what should be further action?
which situation gc hs and gc als require to use?
mode of absorption in alimentary canal?
from where i get mortar pastle for glass bottle crush? it's required for testing of it?
can we use the same detector in HPLC as well GC and what could be the differences we can find in the final chromato graph in any aspects?
What are modes of quantification in related substances
USP methodology, EP methodology, IP methodology, among three if possible to use one methodology for qualify working standard to use USP, EP, IP ? Please explain...
What is the difference between chromatographic purity and related substances?
which are the diffrent batches in the pharmaceuticals?
What is the purpose of octyl silane columns?
How to know the estimated LOQ concentration in ppm
