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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?
773analytical method validation require to with respect to release specification or shelf life specification?
793in monograph 7 imp are there but in vendor showing 5 imp do not req to include 2 imp for that what will be justification?
723In which situation we require to prepare the standard solution from sample in Related substance method?
777Hi sir if any product monograph not given known impurities (may be 5 impurities) specifications then how we require to proceed for inhouse formulation?
707
Define electrochemical series? : Electrochemistry Corrosion
What are the products formed after cod analysis?
Why sometime potassium ortho phosphate mix with acetone use for sample preparation for hplc
What is glacial acetic acid? What are its uses?
Observe the following number to four significant figures and express the result in standard exponential notation: 0.006543210?
Comosition of bell metal
Why graphite rod is used in nuclear reactor?
How is the accuracy of the method determined?
in which situation require to change rs specification?
graphaite has higher melting point than fularine
1.What is the difference between method validation and method verification 2.Which guidelines proposed to method transfer
What is the role of a catalyst? : Polymer Chemistry
2. Two grams of Benzoic acid are dissolved in 200 ml of water and extracted with 200 ml of diethyl ether. The distribution coefficient of benzoic acid is 100, and its dissociation constant is 6.5 10-5. Calculate the distribution ratio (D) of benzoic acid at pH 2, 5, and 6. 3. Calculate D at pH 2 to 10 (1 unit apart) in the above problem, and plot D versus pH.
how you start RS method development when for new product?
how will you do the prep for unstable componds?