Product Details
Place of Origin: China
Brand Name: Sunshine
Certification: ISO,COA
Model Number: 80621-81-4
Payment & Shipping Terms
Minimum Order Quantity: Negotiation
Price: Negotiation
Packaging Details: Aluminum Foil Bag, Drum
Delivery Time: 7-15DAY
Payment Terms: L/C,D/P,T/T,MoneyGram,Western Union,D/A
Supply Ability: G,KG,TON
Appearance:: |
Red-orange Crystalline Powder |
CAS NO:: |
80621-81-4 |
Molecular Formula:: |
C43H51N3O11 |
Molecular Weight:: |
785.87900 |
EINECS NO:: |
617-130-4 |
MDL NO:: |
MFCD00864973 |
Appearance:: |
Red-orange Crystalline Powder |
CAS NO:: |
80621-81-4 |
Molecular Formula:: |
C43H51N3O11 |
Molecular Weight:: |
785.87900 |
EINECS NO:: |
617-130-4 |
MDL NO:: |
MFCD00864973 |
Product Description:
Product Name: Rifaximin CAS NO: 80621-81-4
Synonyms:
2s-acetyloxy-5,6,21,23-tetrahydroxy-27-m-ethoxy-2,4,11, 16,20,22,24,26-octamethyl-2,7-(epoxypentoeleca(1,11,13)trienimino)benzofuro[4,5-e]pyride[1,2-a]benzimidazole-1,15(2h)-dione;
ole-1,15(2h)-dione,25-(acetyloxy)-5,6,21,23-tetrahydroxy-27-m-ethoxy-2,4,11,16;
Chemical & Physical Properties:
Appearance: Red-orange crystalline powder
Assay :≥99.0%
Density: 1.366 g/cm3
Melting Point: 200-205℃(dec)
Refractive Index: 1.633
Storage Condition: 0-6℃
Solubility: ethanol: soluble1mg/mL
Safety Information:
RTECS: KD1576000
WGK Germany: 2
Toxicity: LD50 orally in rats: >2000 mg/kg (Borelli, Bertoli)
Rifaximin (trade names:RCIFAX, Rifagut, Xifaxan, Zaxine) is a semisynthetic antibiotic based on rifamycin. It has poor oral bioavailability, meaning that very little of the drug will be absorbed into the blood stream when it is taken orally. Rifaximin is used in the treatment of traveler's diarrhea, irritable bowel syndrome, and hepatic encephalopathy, for which it received orphan drug status from the U.S. Food and Drug Administration in 1998. It is used in the treatment of traveler's diarrhea and hepatic encephalopathy, for which it received orphan drug status from the U.S. Food and Drug Administration in 1998. Rifaximin interferes with transcription by binding to the β-subunit of bacterial RNA polymerase. This results in the blockage of the translocation step that normally follows the formation of the first phosphodiester bond, which occurs in the transcription process.
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