why in hplc peaks are in positive side(it means upside) not in
negative side?
Answer Posted / sagar mhaske
BEZ we are taking reading in mv,not in transmittance so all peak in hplc on positive side..
if we are taking reading in transmittance then automatically goes negative side.
| Is This Answer Correct ? | 6 Yes | 4 No |
Post New Answer View All Answers
What is shaking level in GC?
UV and PDA detector, which have less signal to noise ratio?
How can I develope method of dissolution by HPLC OR UV
In the HPLC Calibration done wavelength accuracy done between 200nm-280nm .but not done remaining 300-400nm not done ?
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?
about method developement in hplc
how can give the expiry period and restadardisation of volumetric solution
Identify problem faced when mass spectroscopy is used with HPLC system ?
WHY given much noise PDA dector then VWD Dector
what are risk assement in the analytical qbd?
how you start the solubility study?
Why do we use KMnO4 in the test of control of obsorbance ? and why do we take specific quantity i.e 57-63mg?
How to start the dissolution development for unknown tab?
how we can identify the impurity is coming below loq at transfering site?
We use Potassium Dichromate solution for the calibration of UV-Visible Spectrophotometer in UV region. My question is to calibrate visible region which solution could be used in photometric accuracy