Golgappa.net | Golgappa.org | BagIndia.net | BodyIndia.Com | CabIndia.net | CarsBikes.net | CarsBikes.org | CashIndia.net | ConsumerIndia.net | CookingIndia.net | DataIndia.net | DealIndia.net | EmailIndia.net | FirstTablet.com | FirstTourist.com | ForsaleIndia.net | IndiaBody.Com | IndiaCab.net | IndiaCash.net | IndiaModel.net | KidForum.net | OfficeIndia.net | PaysIndia.com | RestaurantIndia.net | RestaurantsIndia.net | SaleForum.net | SellForum.net | SoldIndia.com | StarIndia.net | TomatoCab.com | TomatoCabs.com | TownIndia.com
Interested to Buy Any Domain ? << Click Here >> for more details...

How you will select column for HPLC development depends on
nature of compound and how it will work explain in brief?

Answer Posted / debananda mishra

Polar compounds can be analysed throgh polar stationary
phase and nonpolar compouds can separated through nonpolar
stationary phase but mobile phase used is vice versa.

Is This Answer Correct ?    4 Yes 1 No



Post New Answer       View All Answers


Please Help Members By Posting Answers For Below Questions

What is the difference between spectro meter and spectro photo meter?

11618


why cone formation during dissolution?

847


Why Ethanol is Used for Standardization of GC Head space?

4270


what are the standard methods for HPLC?

2831


which situation gc hs and gc als require to use?

838


on saturation solubility study data how we can find out the bcs class of drug?

956


what is impurity profile. how to interpret this impurity profile to a drug product or drug substance.

2680


Why potassium dichromate is used in calibration of uv?

2038


identification is for unknown? qualification for known? reporting for LOQ?

777


on the basis of bcs class how to proceed the solubility?

831


what is turbidimetric titration?Give 2 examples.

2733


in sampling of raw material which side is pasted sampled labels

1887


If change in specification which parameter require to do for validation? if change in chromtographic condition then which parameter? if api change then which parameter? if change composition then which parameter? if old method not work out then whicj parameter? if additional one impurity added then which parameter of validation require to do on above each conditions? elaborate separately

908


what is definition of validation? which components are followed give detail?

2448


pharma industries oriented

2295