WILL YOU DRY DST BEFORE FACTOR DETERMINATION BY USING KARL
FISHER TITRATOR
Answer Posted / sanjeev.r
You should not dry the DST , because the hydrated water
malocules will gets off if you do so.
| Is This Answer Correct ? | 14 Yes | 1 No |
Post New Answer View All Answers
if rsd failed then what require to do?
What is the use of tlc and hplc? And when and where use?
My question about gas chromatography sulfur chemiluminsecence detector. I test unknown sample gas by GC-SCD (calibrated ) and the result of *H2S is 279 PPM , *but when I test the same sample with the GC-TCD (calibrated ) the value of *H2S is 2500 PPM . I'd like to inform you that both GCs are calibrated and have very good operation conditions with stable parameters . the question is if the sample gas with higher H2S over detection limits of SCD detector (1000 ppm). why the result it 279 ppm Best regards
how much mass should be there in volumetric flask while in preparation of sample for assay?
in OSD forms require to use gas chromatography?
why glutent are detected in the rice cereal baby food product even manufacturer claimed that they are using rice and milk only?we have using ELISA to do the test,and rice supposed not containing any glutent,rite?We already repeat the test so many times and it still detected.just wondering where the glutent came from?
why we use a particular hplc column for a particular compound give reasons?please
What if impurity area in control sample coming more as compared to LOQ level of impurity ?
For titration in anhydrous media with perchloric acide, if lack of titrator, Which indicator is been used for replacement. How calculate pH of test solution to choose suitable indicator?
using gradient pressure in gas chromatography are not ?using gradient pressure why
inhouse product is in capsule form in combination and RLD is in tablet form then can we proceed for multimedia CDP? in inhouse capsule product disso is paddle with sinker in release media is there then RLD product in tablet form then with same as paddle with sinker we can proceed n.a.?
Why do we use KMnO4 in the test of control of obsorbance ? and why do we take specific quantity i.e 57-63mg?
which are the sizes of capsules?
UV and PDA detector, which have less signal to noise ratio?
how a particular wavelength can be different for a particular compund while analysing by uv and by HPLC.