Category
Rifaximin
CAS Number
NA
Molecular Formula
C43H49N3O12
Molecular Weight
799.9 g/mol
Synonym

Rifaximin Y ; [(7S,11S,12R,13S,14R,15S,16S,18R)-2,15,18,36-tetrahydroxy-11-methoxy-3,7,12,14,16,18,22,30-octamethyl-6,17,23-trioxo-8,37-dioxa-24,27,33-triazahexacyclo[23.10.1.14,7.05,35.026,34.027,32]heptatriaconta-1(35),2,4,9,19,21,25(36),26(34),28,30,32-undecaen-13-yl] acetate;

Keywords
Chiral standards
Pharmaceutical Standards
Intermediates
Fine Chemicals
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Purity:

Above - 95.0%

Technical Data:

We will provide complete documentation support for every Standard Material. All analytical reports such as ¹H NMR, ¹³C NMR, Mass, FT-IR, HPLC Purity/GC Purity/QNMR Purity, Water content by KF/ Loss on Drying/TGA (Thermo-gravimetric Analysis). Certificate of Analysis with potency report. Each Standard Material SER (Structure Elucidation Report) with NMR, Mass, IR spectral interpretation. This whole analytical document can be included in eCTD, ANDA, DMF submissions to regulatory agencies.

Rifaximin EP Impurity D is used as a reference standard in HPLC or other analytical methods to detect and quantify impurities in rifaximin. It ensures pharmaceutical batches meet European Pharmacopoeia impurity limits for safety and quality.