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

Ciprofloxacin
Enrofloxacin
Flumequine
Oxolinic acid
Pefloxacin

Applications:

HPLC Separation of a Complex of Quinolone Antibiotics

Condition

Description