Sulfamethoxazole

85

CAS Number723-46-6
Molecular FormulaC10H11N3O3S
Molecular Weight253.276
InChI KeyJLKIGFTWXXRPMT-UHFFFAOYSA-N
LogP0.9
Synonyms
  • Sulfamethoxazole
  • Sulphamethoxazole
  • Sulfisomezole
  • Gantanol
  • Sulfamethoxazol
  • Metoxal
  • Sulfamethylisoxazole
  • Simsinomin
  • Radonil
  • Sinomin
  • Sulphamethoxazol
  • Sulpha-methoxizole
  • Sulfamethalazole
  • Azo-gantanol
  • 4-Amino-N-(5-methyl-3-isoxazolyl)benzenesulfonamide
  • Sulphamethylisoxazole
  • Urobak
  • Sulfamethoxizole
  • 3-Sulfanilamido-5-methylisoxazole
  • Gantanol-DS
  • 4-amino-N-(5-methylisoxazol-3-yl)benzenesulfonamide
  • Bactrimel
  • Gamazole
  • Azo gantanol
  • Sulfametoxazol
  • Sulphisomezole
  • Solfametossazolo
  • Sulfamethoxazolum
  • 5-Methyl-3-sulfanilamidoisoxazole
  • Ro 4-2130
  • MS 53
  • 3-Sulphanilamido-5-methylisoxazole
  • Benzenesulfonamide, 4-amino-N-(5-methyl-3-isoxazolyl)-
  • 5-Methyl-3-sulphanil-amidoisoxazole
  • 3-(p-Aminophenylsulfonamido)-5-methylisoxazole
  • 5-Methyl-3-sulfanylamidoisoxazole
  • N'-(5-Methyl-3-isoxazolyl)sulfanilamide
  • N1-(5-Methyl-3-isoxazolyl)sulfanilamide
  • N'-(5-Methylisoxazol-3-yl)sulphanilamide
  • EINECS 211-963-3
  • 129378-89-8
  • 3-(p-Aminobenzenesulfonamido)-5-methylisoxazole
  • BRN 0226453
  • NSC 147832
  • 4-Amino-N-(5-methyl-3-isoxazolyl)benzensulfonamide
  • Gantanol (TN)
  • 723-46-6
  • 3-(para-Aminophenylsulphonamido)-5-methylisoxazole
  • UNII-JE42381TNV
  • sulfametoxazol
  • N(sup 1)-(5-Methyl-3-isoxazolyl)sulphanilamide
  • Sulfanilamide, N(1)-(5-methyl-3-isoxazolyl)-
  • Sulfanilamide, N1-(5-methyl-3-isoxazolyl)-
  • 4-Amino-N-(5-methyl-1,2-oxazol-3-yl)benzene-1-sulfonamide
  • SMX

Applications:

Uv-Vis Spectrum of Sulfamethoxazole

January 14, 2026
Access the UV-Vis Spectrum SIELC Library
UV-Vis Spectrum of Sulfamethoxazole.

If you are looking for optimized HPLC method to analyze Sulfamethoxazole check our HPLC Applications library

For optimal results in HPLC analysis, it is recommended to measure absorbance at a wavelength that matches the absorption maximum of the compound(s) being analyzed. The UV spectrum shown can assist in selecting an appropriate wavelength for your analysis. Please note that certain mobile phases and buffers may block wavelengths below 230 nm, rendering absorbance measurement at these wavelengths ineffective. If detection below 230 nm is required, it is recommended to use acetonitrile and water as low UV-transparent mobile phases, with phosphoric acid and its salts, sulfuric acid, and TFA as buffers.
For some compounds, the UV-Vis Spectrum is affected by the pH of the mobile phase. The spectra presented here are measured with an acidic mobile phase that has a pH of 3 or lower.

 

Application Analytes:
Sulfamethoxazole
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 Sulfamethoxazole and Trimethoprim on Primesep 100 Column

March 22, 2022

HPLC Method for Trimethoprim, Sulfamethoxazole on Newcrom R1 by SIELC Technologies

High Performance Liquid Chromatography (HPLC) Method for Analysis of Trimethoprim, Sulfamethoxazole.

Sulfamethoxazole, also written as SMZ and SMX, is an antibiotic with the chemical formula C10H11N3O3S.  It is used primarily to treat bacterial infections including but not limited to bronchitis, prostatitis, urinary tract infections, as well as gam negative and positive bacteria. You can find detailed UV spectra of Sulfamethoxazole and information about its various lambda maxima by visiting the following link.

Trimethoprim, also written as TMP, is an antibiotic with the chemical formula C14H18N4O3. It is used primarily to treat bladder infections as well as middle ear infections and travelers’ diarrhea. People with HIV/AIDS might take it to treat Pneumocystis pneumonia. It works through binding to dihydrofolate reductase and inhibiting the production of dihydrofolic and tetrahydrofolic acid. You can find detailed UV spectra of Trimethoprim and information about its various lambda maxima by visiting the following link.

Trimethoprim, Sulfamethoxazole can be retained and analyzed using the Newcrom R1 stationary phase column. The analysis utilizes an isocratic method with a simple mobile phase consisting of water and acetonitrile (MeCN) with a sulfuric acid buffer. Detection is performed using UV.

Condition

Column Primesep 100, 4.6 x 150 mm, 5 µm, 100 A, dual ended
Mobile Phase MeCN/H2O – 40/60%
Buffer H2SO4 – 0.4%
Flow Rate 1.0 ml/min
Detection UV, 200 nm,

Description

Class of Compounds
Drug
Analyzing Compounds Trimethoprim, Sulfamethoxazole

Application Column

Primesep 100

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

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Newcrom R1

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

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Application Analytes:
Sulfamethoxazole
Trimethoprim
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 Antibiotics in Mixed-mode chromatography

May 11, 2015

 

A complex mixture of sulphonamide, macrolide, tetracycline and fluoroquinolone antibiotics were separated in one run using mixed-mode chromatography with LC/MS -compatible conditions. All compounds are separated based on reversed-phase and/or ion-exchange mechanism. Method can be used for analysis of various classes of antibiotics and related impurities in different sample matrices (blood, urine, soil, waste water).

 

Condition

Column Obelisc R, 2.1×150 mm, 5 µm, 100A
Mobile Phase Gradient MeCN – 0-25%, 6 min, 25-70% 14 min
Buffer Gradient Formic Acid – 0.05%-0.3%, 10 min, 14 min hold
Flow Rate 1.0 ml/min
Detection UV, 270 nm

 

Description

Class of Compounds
 Antibiotic, Drug, Hydrophobic, Ionizable
Analyzing Compounds Sulphanilamide, Sulphaguanidine, Oxytetracycline, Marbofloxacin, Sulphadiazine, Chlortetracycline, Nofloxacin, Spiramycin, Cefalonium, Tylosin, Josamycin, Sulphamethoxazole, Dapsone, Sulphaquinoxalline, Flumequine

 

Application Column

Obelisc R

SIELC has developed the Obelisc™ columns, which are mixed-mode and utilize Liquid Separation Cell technology (LiSC™). These cost-effective columns are the first of their kind to be commercially available and can replace multiple HPLC columns, including reversed-phase (RP), AQ-type reversed-phase, polar-embedded group RP columns, normal-phase, cation-exchange, anion-exchange, ion-exclusion, and HILIC (Hydrophilic Interaction Liquid Chromatography) columns. By controlling just three orthogonal method parameters - buffer concentration, buffer pH, and organic modifier concentration - users can adjust the column properties with pinpoint precision to separate complex mixtures.

Select options
Application Analytes:
Carboxymethylcysteine
Chlortetracycline
Dapsone
Flumequine
Josamycin
Marbofloxacin
Norfloxacin
Oxytetracycline
Spiramycin
Sulfamethoxazole
Sulfonamides
Sulphadiazine
Sulphaguanidine
Sulphanilamide
Sulphaquinoxaline
Tetracycline
Tylosin

Application Detection:
ELSD 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.