Nimesulide

Nimesulide structural formula

CAS Number51803-78-2
Molecular FormulaC13H12N2O5S
Molecular Weight308.310
InChI KeyHYWYRSMBCFDLJT-UHFFFAOYSA-N
LogP2.60
Synonyms
  • Nimesulide
  • N-(4-Nitro-2-phenoxyphenyl)methanesulfonamide
  • Methanesulfonamide, N-(4-nitro-2-phenoxyphenyl)-
  • 51803-78-2
  • Methanesulfonamide, N-(4-nitro-2-phenoxyphenyl)-
  • 2-Phenoxy-4-nitromethanesulfonanilide
  • 4'-Nitro-2'-phenoxymethanesulfonanilide
  • 4-Nitro-2-phenoxymethanesulfonanilide
  • Mesulid
  • N-(4-Nitro-2-phenoxyphenyl)methanesulfonamide
  • Nimepast
  • Nimesulid
  • nimesulida
  • Nimulid
  • Nise*Gel
  • Nisulid
  • Orthobid
  • Sulidene
  • BRN 2421175
  • EINECS 257-431-4
  • Flogovital
  • 4-Nitro-2-phenoxy-methanesulfonanilide
  • 4'-Nitro-2'-phenoxymethansulfonanilid
  • Nimesulidum
  • UNII-V4TKW1454M

Applications:

HPLC – MS Method for Analysis of  Nimesulide on Newcrom R1 Column

October 4, 2023

HPLC Method for Analysis of Nimesulide on Newcrom R1 by SIELC Technologies

HPLC - MS Method for Analysis of  Nimesulide on Newcrom R1 Column  by SIELC Technologies
HPLC Method for Analysis of Nimesulide on Newcrom R1 Column by SIELC Technologies


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

Nimesulide is a non-steroidal anti-inflammatory drug (NSAID) that possesses analgesic and antipyretic properties. Below is some information about Nimesulide:

Mechanism of Action:

  • COX Inhibition: Nimesulide inhibits the enzyme cyclooxygenase, specifically COX-2, which is responsible for the synthesis of prostaglandins, compounds that play a key role in promoting inflammation, pain, and fever.

Clinical Uses:

  • Pain Management: Used to manage acute pain.
  • Osteoarthritis: Utilized in the treatment of pain and inflammation associated with osteoarthritis.
  • Primary Dysmenorrhea: Sometimes prescribed for managing pain during menstruation.

Safety Note:

  • Due to concerns regarding liver toxicity, the use of Nimesulide is restricted or banned in some countries.
  • It is important to use Nimesulide under medical supervision and strictly adhere to the prescribed dosage to minimize potential risks.

Synthesis:

  • Nimesulide is synthesized via various chemical routes which generally involve the condensation of 4-nitro-2-phenoxyaniline with formaldehyde and subsequent sulfonation of the resulting methylene intermediate.

Nimesulide can be retained, separated and analyzed on a Newcrom R1 reverse phase stationary phase column using an isocratic analytical method with a simple mobile phase of water, Acetonitrile (MeCN), and a ammonium format as a buffer. This analysis method can be detected using UV at 300 nm, an Evaporative Light Scattering Detector (ELSD), or any other evaporative detection method (CAD, ESI-MS)

ColumnNewcrom R1, 2.1 x 100 mm, 5 µm, 100 A
Mobile PhaseMeCN – 50%,
BufferAmmonium Formate pH 3.0-20 mM
Flow Rate0.2 ml/min
DetectionUV 300 nm, SIM 307.2-
Spray Voltage:1.5 kV
Nebulizing gas:1.5 L/min
Drying gas:15 L/min
 DL temp:250 ˚C
Heat Block:400 ˚C

Class of Compounds
Drug
Analyzing CompoundsNimesulide

Application Column

Newcrom R1

Column Diameter: 2.1 mm
Column Length: 100 mm
Particle Size: 5 µm
Pore Size: 100 A

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Application Analytes:
Nimesulide

Application Detection:
LC MS 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 Nimesulide on Newcrom R1 HPLC column

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

Nimesulide 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:
Nimesulide
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.