This impurity is related to Rifaximin EP Impurity H is provided with comprehensive characterization data in accordance with regulatory guidelines. It is suitable for use in analytical method development, method validation (AMV), Quality Control (QC) applications for Abbreviated New Drug Applications (ANDA) and commercial production of Asenapine.
Rifaximin EP Impurity H is used as a reference standard in analytical research. It ensures consistency of formulations.
Chemical Name:(2S,16Z,18E,20S,21S,22R,23R,24R,25S,26R,27S,28E)-5,6,21,23-tetrahydroxy-16-(hydroxymethyl)-27-methoxy-2,4,11,20,22,24,26-heptamethyl-1,15-dioxo-1,2-dihydro2,7-(epoxypentadeca[1,11,13]trienoimino)[1]benzofuro[4,5-e]pyrido[1,2-a]benzimidazol-25-yl acetate (16-desmethyl-16-(hydroxymethyl)rifaximin).Country of Origin: India Product Category: Impurity Reference StandardAPI NAME: Rifaximin Molecular Formula: C43H51N3O12
Molecular Weight: 801.9
Storage: Store in a cool, dry place.