Indapamide

Indapamide structural formula

CAS Number26807-65-8
Molecular FormulaC16H16ClN3O3S
Molecular Weight365.830
InChI KeyNDDAHWYSQHTHNT-UHFFFAOYSA-N
LogP1.95
Synonyms
  • Indapamide
  • 4-Chloro-N-(2-methyl-2,3-dihydro-1H-indol-1-yl)-3-sulfamoylbenzamide
  • Benzamide, 3-(aminosulfonyl)-4-chloro-N-(2,3-dihydro-2-methyl-1H-indol-1-yl)-
  • 26807-65-8
  • 5-20-06-00348
  • Benzamide, 3-(aminosulfonyl)-4-chloro-N-(2,3-dihydro-2-methyl-1H-indol-1-yl)-
  • (.+-.)-Indapamide
  • 3-(Aminosulfonyl)-4-chloro-N-(2,3-dihydro-2-methyl-1H-indol-1-yl)benzamide
  • Bajaten
  • Benzamide, 4-chloro-N-(2-methyl-1-indolinyl)-3-sulfamoyl-
  • Benzamide,3-(aminosulfonyl)-4-chloro-N-(2,3-dihydro-2-methyl-1H-indol-1-yl)-
  • Flubest
  • Flupamid
  • Indaflex
  • Indamide
  • Indamol
  • Indapamid
  • indapamida
  • Natrilix
  • Noranat
  • Racemic indapamide
  • Tertensif
  • Veroxil
  • BRN 1604026
  • 4-Chloro-N-(2-methyl-1-indolinyl)-3-sulfamoylbenzamide
  • EINECS 248-012-7
  • Pressurai
  • Indapamidum
  • UNII-F089I0511L

Applications:

HPLC Method for Analysis of Indapamide

April 29, 2016

Chr_1047

 

Indapamide is an indole derivative of chlorosulphonamide and a sulfamyl diuretic with antihypertensive activity. It exerts its diuretic effect by inhibiting reabsorption of sodium and chloride, primarily as a result of action on the cortical diluting segment of the renal distal tubule. Indapamide is also used in the treatment of hypertension. Primesep 200, a reverse phase column, contains embedded acidic ionizable groups and can retain Indapamide. The method is UV compatible and can be used as a general approach for analyzing similar compounds.

Condition

Column Primesep 200, 3.2×100 mm, 5 µm, 100A
Mobile Phase Gradient MeCN – 5-50%
Buffer Gradient H3PO4 – 0.05-0.3%, 5 min, 4 min hold
Flow Rate 0.5 ml/min
Detection UV, 270 nm

 

 

Description

Class of Compounds
Drug,  Acid, Hydrophilic, Ionizable,
Analyzing Compounds Indapamide

Application Column

Primesep 200

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:
Indapamide

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.