Date published: 2025-10-17

1-800-457-3801

SCBT Portrait Logo
Seach Input

4-Nitro Sulfamethoxazole (CAS 29699-89-6)

0.0(0)
Write a reviewAsk a question

Alternate Names:
Nitrosulfamethoxazole
Application:
4-Nitro Sulfamethoxazole is a Sulfamethoxazole metabolite
CAS Number:
29699-89-6
Molecular Weight:
283.26
Molecular Formula:
C10H9N3O5S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

4-Nitro Sulfamethoxazole is a Sulfamethoxazole metabolite. it is a sulfonamide compound that contains a 4-nitrosophenyl group attached to the sulfur atom and a 1,2-oxazol-3-yl group attached to the nitrogen atom. It serves as both a metabolite and an allergen. This compound belongs to the class of isoxazoles and is classified as a sulfonamide and a nitroso compound. It is functionally associated with sulfamethoxazole and sulfanilamide.


4-Nitro Sulfamethoxazole (CAS 29699-89-6) References

  1. Formation of diclofenac and sulfamethoxazole reversible transformation products in aquifer material under denitrifying conditions: batch experiments.  |  Barbieri, M., et al. 2012. Sci Total Environ. 426: 256-63. PMID: 22534360
  2. Direct photolysis of human metabolites of the antibiotic sulfamethoxazole: evidence for abiotic back-transformation.  |  Bonvin, F., et al. 2013. Environ Sci Technol. 47: 6746-55. PMID: 23186099
  3. Phototransformation of sulfamethoxazole under simulated sunlight: Transformation products and their antibacterial activity toward Vibrio fischeri.  |  Gmurek, M., et al. 2015. Sci Total Environ. 538: 58-63. PMID: 26298248
  4. Thermo activated persulfate oxidation of antibiotic sulfamethoxazole and structurally related compounds.  |  Ji, Y., et al. 2015. Water Res. 87: 1-9. PMID: 26378726
  5. Enhanced sulfamethoxazole degradation through ammonia oxidizing bacteria co-metabolism and fate of transformation products.  |  Kassotaki, E., et al. 2016. Water Res. 94: 111-119. PMID: 26938496
  6. Fate of sulfamethoxazole in groundwater: Conceptualizing and modeling metabolite formation under different redox conditions.  |  Rodríguez-Escales, P. and Sanchez-Vila, X. 2016. Water Res. 105: 540-550. PMID: 27676388
  7. Microbial degradation of sulfamethoxazole in the environment.  |  Wang, J. and Wang, S. 2018. Appl Microbiol Biotechnol. 102: 3573-3582. PMID: 29516143
  8. Non-activated peroxymonosulfate oxidation of sulfonamide antibiotics in water: Kinetics, mechanisms, and implications for water treatment.  |  Ji, Y., et al. 2018. Water Res. 147: 82-90. PMID: 30300784
  9. Free nitrous acid (FNA) induced transformation of sulfamethoxazole in the enriched nitrifying culture.  |  Sun, F., et al. 2019. Water Res. 149: 432-439. PMID: 30472545
  10. The Role of Reactive Nitrogen Species in Sensitized Photolysis of Wastewater-Derived Trace Organic Contaminants.  |  Scholes, RC., et al. 2019. Environ Sci Technol. 53: 6483-6491. PMID: 31082223
  11. Whole genome sequencing identifies genetic variants associated with co-trimoxazole hypersensitivity in Asians.  |  Wang, CW., et al. 2021. J Allergy Clin Immunol. 147: 1402-1412. PMID: 32791162
  12. Degradation of sulfamethoxazole using PMS activated by cobalt sulfides encapsulated in nitrogen and sulfur co-doped graphene.  |  Wang, S., et al. 2022. Sci Total Environ. 827: 154379. PMID: 35263608
  13. Isotopically labeled ozone: A new approach to elucidate the formation of ozonation products.  |  Sierra-Olea, M., et al. 2023. Water Res. 233: 119740. PMID: 36822109

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-Nitro Sulfamethoxazole, 5 mg

sc-210124
5 mg
$306.00

4-Nitro Sulfamethoxazole, 50 mg

sc-210124A
50 mg
$2448.00