RIFAXIMIN IMPURITY, RIFAXIMIN EP IMPURITY, RIFAXIMIN REFERENCES STANDARD IS PHARMACOPIA IMPURITY STANDARD AND RIFAXIMIN RELATED COMPOUND IS UNITED STATES PHARMACOPEIA (USP) REFERENCE STANDARD.
RIFAXIMIN
CAT No : ALL-RIF-1948
Chemical Name : (2S,16Z,18E,20S,21S,22R,23R,24R,25S,26R,27S,28E)-5,6,21,23-Tetrahydroxy-27-methoxy-2,4,11,16,20,22,24,26-octamethyl-1,15-dioxo-1,2-dihydro-2,7-(epoxypentadeca[1,11,13]trienoimino)[1]benzofuro[4,5-e] pyrido[1,2-a] benzimida
Molecular Formula : C43H51N3O11
Molecular Weight : 785.88
CAS Number : 80621-81-4
Solubility : Methanol, DMSO
Storage : 2-8 °C
Keywords : PHARMACEUTICAL IMPURITIES LIKE RIFAXIMIN EP IMPURITY, PHARMACOPIAL IMPURITY STANDARD PRESENT IN DRUG RIFAXIMIN WITH OTHER CLARITHROMYCIN IMPURITIES AS PER EP AND USP PHARMACOPIA
ALLMPUS PROVIDE PRODUCT RIFAXIMIN IMPURITY WITH ALL RELATED DOCUMENTS INCLUDING MSDS/SDS, SER REPORT, COA, HPLC, and MASS, 13CNMR, 1HNMR AND TGA POTENCY (TGA UPTO 800 DEG C)
AND ARE ACCEPTABLE TO ALL REGULATORY AGENCIES & ALSO USED FOR ANDA FILING /DMF FILING AND GENOTOXIC STUDY