Pefloxacin

CAS Number 70458-92-3
Molecular Formula C17H20FN3O3
Molecular Weight 333.363 g/mol
InChI Key FHFYDNQZQSQIAI-UHFFFAOYSA-N
LogP 0.27
Synonyms
  • Pefloxacin
  • 1-Ethyl-6-fluoro-7-(4-methylpiperazin-1-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
  • 3-Quinolinecarboxylic acid, 1-ethyl-6-fluoro-1,4-dihydro-7-(4-methyl-1-piperazinyl)-4-oxo-
  • 70458-92-3
  • 3-Quinolinecarboxylic acid, 1-ethyl-6-fluoro-1,4-dihydro-7-(4-methyl-1-piperazinyl)-4-oxo-
  • Abactal
  • Abaktal
  • Globacin
  • N'-Methylnorfloxacin
  • Peflacine
  • pefloxacine
  • pefloxacino
  • BRN 0567618
  • EINECS 274-611-8
  • 1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(4-methyl-1-piperazinyl)-3-quinolinecarboxylic acid
  • Pefloxacinum
  • UNII-2H52Z9F2Q5
  • PFLX
  • perfloxacin

Applications:


HPLC Separation of a Complex of Quinolone Antibiotics
Quinolones are a group of synthetic broad-spectrum antibiotics with a wide variety of applications in medicine and veterinary sciences. Some quinolones have been found in food products including fish and shrimp. Primesep 100 was used to separate a mixture of quinolones and achieve baseline separation. Retention was controlled by adjusting acetonitrile in the mobile phase.

Condition

Column Primesep 100, 4.6x150 mm, 5 µm, 100A
Mobile Phase MeCN
Buffer H2SO4
Flow Rate 1.0 ml/min
Detection UV, 270 nm
 

Description

Class of Compounds Drug, Acid, Quinolone Antibiotics, Hydrophilic, Ionizable, Vitamin, Supplements
Analyzing Compounds Oxolinic Acid, Flumequine, Ciprofloxacin, Enrofloxacin, Pefloxacin
 

Application Analytes:

Ciprofloxacin
Enrofloxacin
Flumequine
Oxolinic acid
Pefloxacin