Interested to Buy Any Domain ? << Click Here >> for more details...
If we are getting split peak in Chromatogram,what we can do?
- 7 Answers
- 18483 Views
- I also Faced
- E-Mail Answers
Answer Posted / g.balaji
Main cause : That means u r column is contaminated
absorbant ion of impurites in the column.
Solution :
1)Wash calumn:-By polar solvent -> semi polar solvent -> non
polar solvent ->semi polar solvent -> polar solvent.
2)Check column performance
3)Replace column
| Is This Answer Correct ? | 0 Yes | 3 No |
Post New Answer View All Answers
Why a1% value is used for some product ? What is the criteria for selection a1% value ?
Which type of column should i use to check the purity of high molecular weight protein using HPLC reverse phase column chromatography? Hi everyone. I wanna to check the purity of high molecular weight protein (collagen) with MW of ~130 kDa using a HPLC. I know C18
what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.
What is the diffrence in japan mkt requirement in analytical method validation over US?
what is biorelivent dissolution media?
in api coa contains only process impurities and in product coa contains degradation impurities?
which batch require to use for analytical method validation?
How do we fix the sample concentaryion in hplc method development. What is the basis?
How to start the dissolution development for unknown tab?
Difference between hlaf and rlaf
UV and PDA detector, which have less signal to noise ratio?
if content uniformity passing but dissolution varrying then what is next step?
WHAT IS THE PURPOSE WE USE HCL, CHOPPER, BURNER, MONOCHROMATOR in AAS? PLEASE EXPLAIN BRIEFLY
in OSD forms require to use gas chromatography?
CAN WE DETERMINE THE PEAK PURITY IN GAS CHROMATOGRAPHY ANALYSIS?
