Interested to Buy Any Domain ? << Click Here >> for more details...
What r the limitatoins of uv visible spectroscopy ? Why
Water use in blank standard for uv visible spectroscopy ?
- 4 Answers
- 41514 Views
- Cipla, Reddy Labs, I also Faced
- E-Mail Answers
Answer Posted / naveen kumar
UV is not applicable for the high concentration solutions means 0.01M Nd it is not applicable for suspensions emulsions coagulated products Nd florescence substances
| Is This Answer Correct ? | 3 Yes | 0 No |
Post New Answer View All Answers
about method developement in hplc
what is the purge flow & how to calculate
Which is the highly polar and highly non polar column in HPLC?
for heavy metal test lead used in which form pure form or any other form for preparation of lead standard sol
if you have given one product then how you determine the impurity in that?
what is difference in ods I ods II is this is realy from sorbent / packing characteristics or from other means
What is related substance by HPLC impurity limits as per USP?
what is definition of validation? which components are followed give detail?
Why to use propyl paraben in HPLC gradient calibration
1)What's the meaning of Absorption,give a example. 2)What's the meaning of Adsorption,give a example. 2)what is the difference between Absorption and Adsorption.
I have compare C2H2-air and C2H2-N2O flame AAS on determination calcium. Both use same range of std to plot calibration curve. (2-6ppm) When i measure the sample with phosphate, KCl and LaCl, C2H2-N2O flame give false positive result, around 0.5ppm. When i measure the sample with phosphste, KCl and EDTA. C2H2-N2O flame also give 0.5ppm false positive. But both above mentioned sample would not give false positive when measured by C2H2-air flame. What is the reason?
What should be the level/ Percentage of Arsenic in Arsenic free zinc.
how the compound separate in coulunm,explain
If inhouse hplc related substance method is completly diffrent from Usp for finished proďuct with diffrent impurities then how require to prove method equivalecy?
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?
