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Chemistry AllOther (190) If inhouse hplc related substance method is completly diffrent from Usp for finished proďuct with diffrent impurities then how require to prove method equivalecy?
751analytical method validation require to with respect to release specification or shelf life specification?
755in monograph 7 imp are there but in vendor showing 5 imp do not req to include 2 imp for that what will be justification?
690In which situation we require to prepare the standard solution from sample in Related substance method?
736Hi sir if any product monograph not given known impurities (may be 5 impurities) specifications then how we require to proceed for inhouse formulation?
672
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.
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 viod volume and peak purity in HPLC?
Explain what is the net charge of a non-ionized atom?
From where require to take the RLD sample?
Which form of Sucores is harmfull to humans ?
Comosition of bell metal
in gas chromatography what is the difference between gas flow rate and average linear velocity ?
Observe the following number to four significant figures and express the result in standard exponential notation: 0.006543210?
Explain how do you extract ephedrine from a mineral block?
Protactinium has potential applications in nuclear reactors. Could you elaborate on its role in enhancing reactor efficiency or safety?
Explain why acetic has less conductivity than hcl?
How to convert 673 kelvin into degrees centigrade?
What is electrode potential? : Electrochemistry Corrosion
Protactinium-231 decays to Uranium-235. How is this decay used in radiometric dating and the determination of geological ages?