Oxolinic acid

Oxolinic acid structural formula

CAS Number14698-29-4
Molecular FormulaC13H11NO5
Molecular Weight261.234
InChI KeyKYGZCKSPAKDVKC-UHFFFAOYSA-N
LogP0.94
Synonyms
  • Oxolinic acid
  • 5-Ethyl-8-oxo-5,8-dihydro-2H-[1,3]dioxolo[4,5-g]quinoline-7-carboxylic acid
  • 1,3-Dioxolo[4,5-g]quinoline-7-carboxylic acid, 5-ethyl-5,8-dihydro-8-oxo-
  • 14698-29-4
  • 1,3-Dioxolo[4,5-g]quinoline-7-carboxylic acid, 5-ethyl-5,8-dihydro-8-oxo-
  • 1-Ethyl-1,4-dihydro-6,7-methylenedioxy-4-oxo-3-quinolinecarboxylic acid
  • 1-Ethyl-6,7-methylenedioxy-4-quinolone-3-carboxylic acid
  • 5-Ethyl-5,8-dihydro-8-oxo-1,3-dioxolo[4,5-g]quinoline-7-carboxylic acid
  • Acide oxolinique
  • acido oxolinico
  • Dioxacin
  • Emyrenil
  • Gramurin
  • Nidantin
  • NSC 110364
  • Oxolininsaure
  • Prodoxal
  • Prodoxol
  • Starner
  • Starner 20WP
  • Ultibid
  • Uritrate
  • Uro-Alvar
  • Urotrate
  • BRN 0620635
  • EINECS 238-750-8
  • 5-Ethyl-5,8-dihydro-8-oxo-1,3-dioxolo(4,5-g)quinoline-7-carboxylic acid
  • NSC-110364
  • Oksaren
  • Oxolinic
  • Tiurasin
  • Cistopax
  • Orthurine
  • Acido ossolico
  • Acidum oxolinicum
  • UNII-L0A22B22FT
  • 5-Ethyl-5,8-dihydro-8-oxo-1,3-dioxolo(4,5-g)quinoline-7-carboxylic acid
  • OA

Applications:

HPLC Separation of a Complex of Quinolone Antibiotics

May 27, 2015

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, 4.6×150 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 Column

Primesep 100

The Primesep family of mixed-mode columns offers a wide variety of stationary phases, boasting unprecedented selectivity in the separation of a broad array of chemical compounds across multiple applications. Corresponding Primesep guard columns, available with all stationary phases, do not require holders. SIELC provides a method development service available to all customers. Inquire about our specially-tailored custom LC-phases for specific separations.

Select options
Application Analytes:
Ciprofloxacin
Enrofloxacin
Flumequine
Oxolinic acid
Pefloxacin
Application Detection:
UV Detection
SIELC Technologies usually develops more than one method for each compound. Therefore, this particular method may not be the best available method from our portfolio for your specific application. Before you decide to implement this method in your research, please send us an email to research@sielc.com so we can ensure you get optimal results for your compound/s of interest.