Answer Posted / ram krishna
Primary standard are highly purify and none degradable
| Is This Answer Correct ? | 0 Yes | 0 No |
Post New Answer View All Answers
Why we used in n-butyl acetate water content terminology while in ethyl acetate we used moisture content terminology?
why multimedia dissolution require to do?
What is the calibration of uv process and preparation
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
give clarity of linearity and range in method validation
how to select short coloum and long coloumn for new molecule
what is turbidimetric titration?Give 2 examples.
What are usp limits for theoritical plats,resoution,tailing factor,peak to valley ratio
How to set analyticl specification for combination products?
what is mean by peak intigrity?
which one is better separation in high pressure liquide chromatogram orlowpressure chromato gram in hplc
why salisylic acid not using now days for disdolution calibration?
what is mean by 40 in the dissolution basket mesh size?
acceptance criteria for lod & loq by standard deviation of response and slope??
How to establish relative response factor for hplc. Why it is required?