26116-56-3 (9S)-9-Amino-9-deoxoerythromycin CAS NO.26116-56-3
- FOB Price: USD: 1,000.00-1,000.00 /Metric Ton Get Latest Price
- Min.Order: 1 Kilogram
- Payment Terms: L/C,T/T
- Available Specifications:
pharma(0-1)Metric Ton
- Product Details
Keywords
- 26116-56-3
- (9S)-9-Amino-9-deoxoerythromycin
- (9S)-9-Amino-9-deoxoerythromycin
Quick Details
- ProName: 26116-56-3 (9S)-9-Amino-9-deoxoerythro...
- CasNo: 26116-56-3
- Molecular Formula: C37H70N2O12
- Appearance: white powder
- Application: pharma
- DeliveryTime: prompt
- PackAge: as clients needs
- Port: Shanghai,QingdaoTianjin,Guangzhou
- ProductionCapacity: 1 Metric Ton/Day
- Purity: 99%
- Storage: RT
- Transportation: sea
- LimitNum: 1 Kilogram
- Moisture Content: N/A
- Impurity: N/A
- N/A: N/A
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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).