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...

In UV-VIS spectrophotometer:My diluent is methanol even
though i corrected base line for methanol,In my sample scan
i found methanol peak.what is the reason?

Answer Posted / tpa lab

My diluent is only methanol(AR Grade).i got peak at 205nm
which is of AR Grade methanol.We are all very well know
that we get the peak for AR Methanol about 205nm and for
commercial methanol about 210nm.

Is This Answer Correct ?    1 Yes 1 No



Post New Answer       View All Answers


Please Help Members By Posting Answers For Below Questions

using gradient pressure in gas chromatography are not ?using gradient pressure why

3333


what is third integration

1931


How can we confirm the HPLC column is end-capped or not? Is it possible to identify by physical appearance?

3155


Why do we use KMnO4 in the test of control of obsorbance ? and why do we take specific quantity i.e 57-63mg?

2779


If vendor having more imp than monograph then how to proceed? and how to set spec?

848


What is the diffrence in japan mkt requirement in analytical method validation over US?

676


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

2585


1.What is the difference between method validation and method verification 2.Which guidelines proposed to method transfer

1792


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

799


Related substance method equivalency on control sample or spiked sample?

714


If we have 5 strength which is not dose proportinate and excipients also diffrent in each strength then how we can proceed for Force degradation? and excipient are same but not dose propotinate the how FD?

761


how you start RS method development when for new product?

661


what is the importance of peak purity in HPLC and how we can calculate through manul(not software)?

4422


if you have given a blank water how you analyse by general analytical techniques?

1977


In Dissolution Test why limit is define Q+5% what is the role of +5%.

3045