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6-[2-(Diethylamino)ethylsulfonyl]-21-hydroxy-11,19-dimethyl-10-propan-2-yl-9,26-dioxa-3,15,28-triazatricyclo[23.2.1.03,7]octacosa-1(27),12,17,19,25(28)-pentaene-2,8,14,23-tetrone

Base Information
  • Chemical Name:6-[2-(Diethylamino)ethylsulfonyl]-21-hydroxy-11,19-dimethyl-10-propan-2-yl-9,26-dioxa-3,15,28-triazatricyclo[23.2.1.03,7]octacosa-1(27),12,17,19,25(28)-pentaene-2,8,14,23-tetrone
  • CAS No.:112362-50-2
  • Molecular Formula:C34H50 N4 O9 S
  • Molecular Weight:690.85
  • Hs Code.:
  • Wikipedia:Dalfopristin
  • NCI Thesaurus Code:C47468
  • Mol file:112362-50-2.mol
6-[2-(Diethylamino)ethylsulfonyl]-21-hydroxy-11,19-dimethyl-10-propan-2-yl-9,26-dioxa-3,15,28-triazatricyclo[23.2.1.03,7]octacosa-1(27),12,17,19,25(28)-pentaene-2,8,14,23-tetrone

Synonyms:26-(2-diethylaminoethyl)sulfonylpristamycin IIB;dalfopristin;RP 54476;RP-54476

Suppliers and Price of 6-[2-(Diethylamino)ethylsulfonyl]-21-hydroxy-11,19-dimethyl-10-propan-2-yl-9,26-dioxa-3,15,28-triazatricyclo[23.2.1.03,7]octacosa-1(27),12,17,19,25(28)-pentaene-2,8,14,23-tetrone
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • ChemScene
  • Dalfopristin 98.34%
  • 5mg
  • $ 1032.00
  • ChemScene
  • Dalfopristin 98.34%
  • 10mg
  • $ 1800.00
  • ChemScene
  • Dalfopristin 98.34%
  • 1mg
  • $ 312.00
  • Cayman Chemical
  • Dalfopristin (mesylate) ≥98%
  • 1mg
  • $ 275.00
  • Cayman Chemical
  • Dalfopristin (mesylate) ≥98%
  • 5mg
  • $ 899.00
  • Biosynth Carbosynth
  • Dalfopristin
  • 2 mg
  • $ 3603.60
  • Biosynth Carbosynth
  • Dalfopristin
  • 1 mg
  • $ 1982.00
  • Biosynth Carbosynth
  • Dalfopristin
  • 5 mg
  • $ 6552.00
  • ApexBio Technology
  • Dalfopristin(mesylate)
  • 1mg
  • $ 381.00
  • ApexBio Technology
  • Dalfopristin(mesylate)
  • 5mg
  • $ 1246.00
Total 17 raw suppliers
Chemical Property of 6-[2-(Diethylamino)ethylsulfonyl]-21-hydroxy-11,19-dimethyl-10-propan-2-yl-9,26-dioxa-3,15,28-triazatricyclo[23.2.1.03,7]octacosa-1(27),12,17,19,25(28)-pentaene-2,8,14,23-tetrone
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:~150° 
  • Boiling Point:940.5°C at 760 mmHg 
  • PKA:13.18±0.70(Predicted) 
  • Flash Point:522.6°C 
  • PSA:184.80000 
  • Density:1.27g/cm3 
  • LogP:3.61680 
  • XLogP3:2.2
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:11
  • Rotatable Bond Count:7
  • Exact Mass:690.32985036
  • Heavy Atom Count:48
  • Complexity:1340
Purity/Quality:

99%, *data from raw suppliers

Dalfopristin 98.34% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCN(CC)CCS(=O)(=O)C1CCN2C1C(=O)OC(C(C=CC(=O)NCC=CC(=CC(CC(=O)CC3=NC(=CO3)C2=O)O)C)C)C(C)C
  • Uses A Viiginiamycin M1 (V672810) derivative. A streptogramin antibiotic used to treat infections by staphylococci and by vancomycin-resistant Enterococcus faecium. Dalfopristin is a semi-synthetic analogue of ostreogyrcin A (virginiamycin M, pristinamycin IIA, streptogramin A) formed by addition of diethylaminoethylthiol to the 2-pyrroline group of ostreogyrcin, followed by oxidation to the sulphone. The structural changes provide a more hydrophobic compound with a readily ionisable group for generating a salt. Dalfopristin is used commercially in synergistic combination with quinupristin (70:30). There is little published data on the synthesis, biological or antibiotic activity of dalfopristin alone, however the combination product is highly effective, including activity against antibiotic resistant strains. Dalfopristin is a semi-synthetic analogue of ostreogrycin A (virginiamycin M, pristinamycin IIA, streptogramin A) formed by addition of diethylaminoethylthiol to the 2-pyrroline group of ostreogrycin, followed by oxidation to the sulfone. The structural changes provide a more hydrophobic compound with a readily ionisable group for generating a salt. Dalfopristin is used commercially in synergistic combination with quinupristin (70:30). There is little published data on the synthesis, biological or antibiotic activity of dalfopristin alone, however the combination product is highly effective, including activity against antibiotic resistant strains.
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