26116-56-3 (9S)-9-A...

26116-56-3 (9S)-9-Amino-9-deoxoerythromycin

26116-56-3 (9S)-9-Amino-9-deoxoerythromycin

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1 Kilogram

FOB Price: USD 1000.0000

  • Min.Order :1 Kilogram
  • Purity: 99%
  • Payment Terms : L/C,T/T

Keywords

26116-56-3 (9S)-9-Amino-9-deoxoerythromycin (9S)-9-Amino-9-deoxoerythromycin

Quick Details

  • Appearance:white powder
  • Application:pharma
  • PackAge:as clients needs
  • ProductionCapacity:1|Metric Ton|Day
  • Storage:RT
  • Transportation:sea

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Our company was built in 2009 with an ISO certificate.In the past 6 years, we have grown up as a famous fine chemicals supplier in China and we had established stable business relationships with Samsung,LG,Merck,Thermo Fisher Scientific and so on.Our main business covers the fields below:
 
 
 
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Details:

(9S)-9-Amino-9-deoxoerythromycin Chemical Properties
Melting point 123-127°C
storage temp. -20°C Freezer
Safety Information
Hazard Codes Xi,N
Risk Statements 41-50/53
Safety Statements 26-39-60-61
MSDS Information
(9S)-9-Amino-9-deoxoerythromycin Usage And Synthesis
Chemical Properties White Solid
Uses Erythromycylamine is a semi-synthetic analogue of erythromycin prepared by reduction of erythromycin oxime. Erythromycyclamine is a potent antibiotic, however the introduction of the amino- moiety increases the compound’s polarity and is disadvantageous for in vivo use. This limitation was overcome by the synthesis of dirithromycin, a Schiff base pro-drug that dissociates in vivo to erythromycylamine.
Uses Erythromycylamine is a semi-synthetic analogue of erythromycin prepared by reduction of erythromycin oxime. Erythromycylamine is a potent antibiotic, however the introduction of the amino- moiety increases the compound’s polarity and is disadvantageous for in vivo use. This limitation was overcome by the synthesis of dirithromycin, a Schiff base pro-drug that dissociates in vivo to erythromycylamine.
Uses A metabolite of Dirithromycin; an antibiotic
Definition ChEBI: A macrolide antibiotic that is erythromycin A in which the ketone group has been converted to the corresponding imine and then reduced to give the corresponding amino compound (the 9S diastereoisomer).

 

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