Furosemide

Furosemide structural formula

CAS Number54-31-9
Molecular FormulaC12H11ClN2O5S
Molecular Weight330.740
InChI KeyZZUFCTLCJUWOSV-UHFFFAOYSA-N
LogP2.03
Synonyms
  • Furosemide
  • 4-Chloro-2-{[(furan-2-yl)methyl]amino}-5-sulfamoylbenzoic acid
  • Benzoic acid, 5-(aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]-
  • 54-31-9
  • 5-18-09-00555
  • Benzoic acid, 5-(aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]-
  • 2-Furfurylamino-4-chloro-5-sulfamoylbenzoic acid
  • 4-Chloro-N-(2-furylmethyl)-5-sulfamoylanthranilic acid
  • 4-Chloro-N-furfuryl-5-sulfamoylanthranilic acid
  • 4-Chloro-N-furfuryl-5-sulfamylanthranilic acid
  • 5-(Aminosulfamyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoic acid
  • 5-(Aminosulfonyl)-4-chloro-2-[(2-furanylmethyl)amino]benzoic acid
  • Aisemide
  • Aluzine
  • Anfuramaide
  • Anthranilic acid, 4-chloro-N-furfuryl-5-sulfamoyl-
  • Apo-Frusemide
  • Apo-Furosemide
  • Aquamide
  • Aquarid
  • Aquasin
  • Arasemide
  • Beronald
  • Bioretic
  • Cetasix
  • Desdemin
  • Discoid
  • Disemide
  • Diuretic salt
  • Diurolasa
  • Diusemide
  • Dryptal
  • Durafurid
  • Errolon
  • Eutensin
  • Fluidrol
  • Frumide
  • Frusedan
  • Frusema
  • Frusemide
  • Frusemin
  • Frusenex
  • Frusetic
  • Fuluvamide
  • Furanthril
  • Furanthryl
  • Furantril
  • Furanturil
  • Furesis
  • Furetic
  • Furo-Basan
  • Furocot
  • Furodiurol
  • Furomen
  • Furomex
  • Furomide M.D.
  • Furo-Puren
  • Furorese
  • Furosan
  • Furosedon
  • Furosem
  • Furosemid
  • furosemida
  • Furosix
  • Furoter
  • Furovite
  • Hissuflux
  • Hydro-rapid
  • Impugan
  • Kofuzon
  • Lasemid
  • Lasiletten
  • Lasilix
  • Lasix Retard
  • Lowpston
  • Lowpstron
  • Macasirool
  • Marsemide
  • Nephron
  • Nicorol
  • NSC 269420
  • Odemase
  • Oedemex
  • Prefemin
  • Profemin
  • Promedes
  • Promide
  • Radisemide
  • Radonna
  • Rosemide
  • Salinex
  • Salurid
  • Seguril
  • Selectofur
  • Transit
  • Trofurit
  • Uremide
  • Zafurida
  • 5-(Aminosulfonyl)-4-chloro-2-((2-furanylmethyl)amino)benzoic acid
  • BRN 0840915
  • 4-Chloro-5-sulfamoyl-N-furfuryl-anthranilic acid
  • EINECS 200-203-6
  • Endural
  • Furosemide mita
  • Furoside
  • Fursemid
  • Fursemide
  • Hydroled
  • Moilarorin
  • NCI-C55936
  • Neo-renal
  • Novosemide
  • Puresis
  • Sigasalur
  • Urosemide
  • Aldalix
  • Diurapid
  • Frusemid
  • Fuluvamine
  • Furobeta
  • Furodrix
  • Furosemidum
  • Furosemix
  • Furosifar
  • Fursemida
  • Jenafusid
  • less Diur
  • Logirene
  • Polysquall A
  • Protargen
  • Radouna
  • Salurex
  • Spirofur
  • Synephron
  • Zafimida
  • Chlor-N-(2-furylmethyl)-5-sulfamylanthranilsaeure
  • Furosemidu
  • UNII-7LXU5N7ZO5
  • Furosemide oral

Applications:

Alltesta HPLC Method for Analysis of Furosemide (Tablet Dosage) on Primesep B

October 7, 2024

Alltesta HPLC Method for Furosemide on Primesep B4 by SIELC Technologies

HPLC Method for Analysis of Furosemide on Primesep B Column by SIELC Technologies


 High Performance Liquid Chromatography (HPLC) Method for Analysis of Furosemide

Furosemide is a loop diuretic commonly used to treat conditions like edema (fluid retention) and hypertension (high blood pressure).

Furosemide can be retained, and analyzed using a Primesep B mixed-mode stationary phase column. The analysis utilizes an isocratic method with a simple mobile phase consisting of water, acetonitrile (MeCN), and sulfuric acid as a buffer. Detection is achieved using UV at 275 nm

ColumnPrimesep B4, 4.6 x 150 mm, 5 µm, 100 A
Mobile PhaseMeCN/H2O – 50/50%
BufferH3PO4 -0.1%
Flow Rate1.0 ml/min
DetectionUV 275 nm

Class of Compounds
Diuretic
Analyzing CompoundsFurosemide

You can view examples of chromatograms obtained using the Allesta instrument and Sielc columns by clicking here.

Application Column

Primesep B4

Column Diameter: 4.6 mm
Column Length: 150 mm
Particle Size: 5 µm
Pore Size: 100 A

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Application Analytes:
Furosemide

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.

HPLC Method for Analysis of Furosemide on Primesep B Column

February 1, 2024

HPLC Method for Analysis of Furosemide on (Column not found) by SIELC Technologies

HPLC Method for Analysis of Furosemide on Primesep B Column
HPLC Method for Analysis of Furosemide on Primesep B Column by SIELC Technologies


 High Performance Liquid Chromatography (HPLC) Method for Analysis of Furosemide

Furosemide is a medication commonly used to treat conditions such as edema (fluid retention) and hypertension (high blood pressure). It belongs to a class of drugs known as loop diuretics. Furosemide works by increasing the excretion of water and salts (sodium and chloride) from the kidneys.

Mechanism of Action: Furosemide inhibits the reabsorption of sodium and chloride ions in the ascending loop of Henle in the kidneys. This leads to increased urine production and helps reduce fluid retention.

Uses: Furosemide is commonly prescribed for conditions such as edema associated with congestive heart failure, liver cirrhosis, and renal disease. It is also used to treat hypertension.

 Furosemide can be retained, and analyzed using a Primesep B mixed-mode stationary phase column. The analysis utilizes an isocratic method with a simple mobile phase consisting of water, acetonitrile (MeCN), and sulfuric acid as a buffer. Detection is achieved using UV 235 nm

Column(Column variation not found)
Mobile PhaseMeCN/H2O – 40%
BufferH2SO4 – 0.1%
Flow Rate1.0 ml/min
DetectionUV 235 nm

Class of Compounds
Sulfonamides, sulphonamides, loop diuretics
Analyzing CompoundsFurosemide
Application Analytes:
Furosemide

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.

Separation of Furosemide on Newcrom R1 HPLC column

February 16, 2018
Separation of Furosemide on Newcrom C18 HPLC column

Furosemide can be analyzed by this reverse phase (RP) HPLC method with simple conditions. The mobile phase contains an acetonitrile (MeCN), water, and phosphoric acid. For Mass-Spec (MS) compatible applications the phosphoric acid needs to be replaced with formic acid. Smaller 3 µm particles columns available for fast UPLC applications. This liquid chromatography method is scalable and can be used for isolation impurities in preparative separation. It also suitable for pharmacokinetics.

Application Column

Newcrom R1

The Newcrom columns are a family of reverse-phase-based columns. Newcrom A, AH, B, and BH are all mixed-mode columns with either positive or negative ion-pairing groups attached to either short (25 Å) or long (100 Å) ligand chains. Newcrom R1 is a special reverse-phase column with low silanol activity.

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Application Analytes:
Furosemide
The result was obtained by a proprietary SIELC algorithm. It may deviate from the actual experimental data. The experimental data are available upon request. Contact us by e-mail: support@sielc.com or by phone: 847-229-2629.