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ChemicalBook--->CAS DataBase List--->14897-39-3

14897-39-3

14897-39-3 Structure

14897-39-3 Structure
IdentificationBack Directory
[Name]

Rifamycin Sodium
[CAS]

14897-39-3
[Synonyms]

Rifamycin SV s
RIFAMYCIN SODIUM
Rifamycinsodiumsal
RIFAMYCIN SV-SODIUM
Rifamycin sodium CRS
RIFAMPICIN SV SODIUM
rifamycin sodium salt
Rifamycin Na USP/EP/BP
Rifamycin SV Monosodium
RIFAMYCIN,MONOSODIUMSALT
RIFAMYCIN SV SODIUM SALT
Rifamycin Sodium USP/EP/BP
RifaMycin SV MonosodiuM salt
RifaMycin, sodiuM salt (1:1)
Rifamycin SV sodium, >=900 IU/mg
RIFAMYCIN SV SODIUM SALT HEXAHYDRATE
Rifamycin SV hexahydrate sodium salt
Rifamycin SV Sodium Salt (Rifaximin EP Impurity C Sodium Salt)
5,6,9,17,19,21-Hexahydroxy-23-Methoxy-2,4,12,16,18,20,22-heptaMethyl-
2,7-(Epoxypentadeca(1,11,13)trienimino)naphtho(2,1-b)furan-1,11(2H)-dione, 5,6,9,17,19,21-hexahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-, 21-acetate, monosodium salt
(2S,12Z,14E,16S,17S,18R,19R,20R,21S,22R,23S,24E)-21-(Acetyloxy)-5,6,9,17,19-pentahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-2,7-(epoxypentadeca[1,11,13]trienimino)naphtho[2,1-b]furan-1,11(2H)-dione sodium salt
[EINECS(EC#)]

238-965-7
[Molecular Formula]

C37H46NNaO12
[MDL Number]

MFCD00056847
[MOL File]

14897-39-3.mol
[Molecular Weight]

719.75
Chemical PropertiesBack Directory
[Melting point ]

>215°C (dec.)
[storage temp. ]

-20°C Freezer
[solubility ]

ethanol: soluble50mg/mL
[form ]

powder
[color ]

Dark Red
[Water Solubility ]

Soluble in water, alcohol and dimethyl sulfoxide.
[Merck ]

13,8302
Safety DataBack Directory
[Safety Statements ]

22-24/25
[WGK Germany ]

3
[RTECS ]

KD1922500
[F ]

8-10-23
Raw materials And Preparation ProductsBack Directory
[Raw materials]

RIFAMYCIN SV
Hazard InformationBack Directory
[Chemical Properties]

Dark Red Solid
[Uses]

Semi-synthetic antibiotic derived from Rifamycin S. Antibacterial. Potency >900 units (dry basis).
[Biological Activity]

Rifamycin SV inhibits selective (E. coliB. subtilis) bacterial DNA-dependent RNA polymerase by binding to the polymerase β-subunita mechanism similar to rifabutin. It acts as a selective cytochrome P450 3A4 inducer. It is active against Gram-positive bacteria and is moderately active against Gram-negative organisms.
Spectrum DetailBack Directory
[Spectrum Detail]

Rifamycin Sodium(14897-39-3)1HNMR
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