Rifaximin EP Impurity H | CAS 1210022-90-4 - Request Quote
Rifaximin EP Impurity H
| SZ CAT No: | SZ-R027009 |
| CAS No | 1210022-90-4 |
| Mol.F. | C43H51N3O12 |
| Mol.Wt. | 801.9 |
| Inv. Status | Synthesis on demand |
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Rifaximin EP Impurity H is chemically (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 (as per EP). It is also known as 16-Desmethyl-16-(hydroxymethyl)Rifaximin (as per EP). Rifaximin EP Impurity H is supplied with detailed characterization data compliant with regulatory guideline. Rifaximin EP Impurity H can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Rifaximin.
The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.
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Rifaximin EP Impurity H for Method Validation
Rifaximin Reference Standard
Rifaximin EP Impurity H for ANDA Filing
Rifaximin EP Impurity H for Forced Degradation Studies
Rifaximin EP Impurity H Identification Standards
Rifaximin EP Impurity H for DMF Filing
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