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CAS:55297-96-6 C32H51NO8S Tiamulin fumarate

CAS NO.55297-96-6

  • Min.Order: 500 Gram
  • Payment Terms: L/C,T/T,
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Product Details

Keywords

  • CAS:55297-96-6 C32H51NO8S Tiamulin fumarate
  • CAS:55297-96-6 C32H51NO8S
  • CAS:55297-96-6

Quick Details

  • ProName: CAS:55297-96-6 C32H51NO8S Tiamulin fum...
  • CasNo: 55297-96-6
  • Molecular Formula: C32H51NO8S
  • Appearance: white poweder
  • Application: CAS:55297-96-6 C32H51NO8S Tiamulin fum...
  • DeliveryTime: 5 working days after cash deposit
  • PackAge: Plastic vacuum packaging bag or bucket
  • Port: depend on clients require
  • ProductionCapacity: 1 Metric Ton/Day
  • Purity: 99%
  • Storage: under the cool and dry area
  • Transportation: by express or by sea
  • LimitNum: 500 Gram
  • Grade: Industrial Grade,Pharma Grade

Superiority

Tiamulin fumarate Basic information
Product Name: Tiamulin fumarate
Synonyms: ((2-(DIETHYLAMINO)ETHYL)THIO)ACETIC ACID 8-ESTER WITH (3AS,4R,5S,6S,8R,9R,9AR,10R)-OCTAHYDRO-5,8-DIHYDROXY-4,6,9,10-TETRAMETHYL-6-VINYL-3A,9-PROPANO-3AH-CYCLOPENTACYCLOOCTEN-1(4H)-ONE FUMARATE;DENAGARD;,10-tetramethyl-1-oxo-3-alpha,9-propano-3-alpha-h-cyclopentacycloocten-8-yles;14-deoxy-14-((2-diethylaminoethyl)-mercaptoacetoxy)-mutilinhydrogenfumarate;14-desossi-14-((2-dietilaminoetil)mercapto-acetossi)mutilinidrogenofumarato;81723hfu;dynamutilin;sandoz81723hfu
CAS: 55297-96-6
MF: C32H51NO8S
MW: 609.81
EINECS: 259-581-6
Product Categories: Amines;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Sulfur & Selenium Compounds;API;We have in stock now.
Mol File: 55297-96-6.mol
Tiamulin fumarate Structure
 
Tiamulin fumarate Chemical Properties
mp  147-148°C
storage temp.  2-8°C
Merck  13,9495
CAS DataBase Reference 55297-96-6(CAS DataBase Reference)
 
Safety Information
Hazard Codes  Xn
Risk Statements  22
Safety Statements  36
RIDADR  UN2811 6.1/PG 3
RTECS  AG9560000
MSDS Information
 
 
Tiamulin fumarate Usage And Synthesis
Chemical Properties White Solid
Usage Tiamulin is a semi–synthetic analogue of pleuromutilin in which the hydroxyacetyl side chain is replaced with a larger diethylaminoethylthioacetyl moiety, providing greater hydrophobicity. The hemi-fumarate provides a stable salt with improved water solubility. Tiamulin is a potent and highly selective antibiotic active against a range of Gram positive bacteria, with no cross resistance to existing antibiotic classes due to its unique mode of action of inhibiting protein synthesis by binding to domain V of 23S rRNA.
Usage A derivative of Pleuromutilin. Antibacterial.

 

Details

Tiamulin fumarate Basic information
Product Name: Tiamulin fumarate
Synonyms: ((2-(DIETHYLAMINO)ETHYL)THIO)ACETIC ACID 8-ESTER WITH (3AS,4R,5S,6S,8R,9R,9AR,10R)-OCTAHYDRO-5,8-DIHYDROXY-4,6,9,10-TETRAMETHYL-6-VINYL-3A,9-PROPANO-3AH-CYCLOPENTACYCLOOCTEN-1(4H)-ONE FUMARATE;DENAGARD;,10-tetramethyl-1-oxo-3-alpha,9-propano-3-alpha-h-cyclopentacycloocten-8-yles;14-deoxy-14-((2-diethylaminoethyl)-mercaptoacetoxy)-mutilinhydrogenfumarate;14-desossi-14-((2-dietilaminoetil)mercapto-acetossi)mutilinidrogenofumarato;81723hfu;dynamutilin;sandoz81723hfu
CAS: 55297-96-6
MF: C32H51NO8S
MW: 609.81
EINECS: 259-581-6
Product Categories: Amines;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Sulfur & Selenium Compounds;API;We have in stock now.
Mol File: 55297-96-6.mol
Tiamulin fumarate Structure
 
Tiamulin fumarate Chemical Properties
mp  147-148°C
storage temp.  2-8°C
Merck  13,9495
CAS DataBase Reference 55297-96-6(CAS DataBase Reference)
 
Safety Information
Hazard Codes  Xn
Risk Statements  22
Safety Statements  36
RIDADR  UN2811 6.1/PG 3
RTECS  AG9560000
MSDS Information
 
 
Tiamulin fumarate Usage And Synthesis
Chemical Properties White Solid
Usage Tiamulin is a semi–synthetic analogue of pleuromutilin in which the hydroxyacetyl side chain is replaced with a larger diethylaminoethylthioacetyl moiety, providing greater hydrophobicity. The hemi-fumarate provides a stable salt with improved water solubility. Tiamulin is a potent and highly selective antibiotic active against a range of Gram positive bacteria, with no cross resistance to existing antibiotic classes due to its unique mode of action of inhibiting protein synthesis by binding to domain V of 23S rRNA.
Usage A derivative of Pleuromutilin. Antibacterial.

 

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