Date published: 2025-10-17

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N-Hydroxy Sulfamethoxazole (CAS 114438-33-4)

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Alternate Names:
4-(Hydroxyamino)-N-(5-methyl-3-isoxazolyl)-benzenesulfonamide
Application:
N-Hydroxy Sulfamethoxazole is a sulfamethoxazole metabolite
CAS Number:
114438-33-4
Molecular Weight:
269.28
Molecular Formula:
C10H11N3O4S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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N-Hydroxy Sulfamethoxazole, a metabolite of sulfamethoxazole, finds application in diverse scientific research endeavors. As a member of the sulfonamide family, it contributes to the synthesis of various molecules and serves as a intermediate in the creation of pharmaceuticals, pesticides, and other compounds. Its utility extends to the creation of peptides, peptidomimetics, and peptidomimetic analogs. Additionally, it facilitates the synthesis of organometallic compounds like palladium and platinum complexes. Acting as a nucleophile during molecule synthesis, N-Hydroxy Sulfamethoxazole interacts with various functional groups such as alkenes, alkynes, and aryl halides. It also engages with oxidizing agents like hydrogen peroxide and sodium hypochlorite. This reaction is believed to follow a radical mechanism, where the N-Hydroxy Sulfamethoxazole radical abstracts a hydrogen atom from the substrate, leading to the formation of an intermediate. Subsequently, a series of rearrangements occur to yield the desired product.


N-Hydroxy Sulfamethoxazole (CAS 114438-33-4) References

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  3. Mass spectrometric investigation of the mechanism of inactivation of hamster arylamine N-acetyltransferase 1 by N-hydroxy-2-acetylaminofluorene.  |  Guo, Z., et al. 2004. Chem Res Toxicol. 17: 275-86. PMID: 15025497
  4. 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
  5. Exogenous cofactors for the improvement of bioremoval and biotransformation of sulfamethoxazole by Alcaligenes faecalis.  |  Zhang, YB., et al. 2016. Sci Total Environ. 565: 547-556. PMID: 27203516
  6. Improving the bioremoval of sulfamethoxazole and alleviating cytotoxicity of its biotransformation by laccase producing system under coculture of Pycnoporus sanguineus and Alcaligenes faecalis.  |  Li, X., et al. 2016. Bioresour Technol. 220: 333-340. PMID: 27591519
  7. Emergent contaminants: Endocrine disruptors and their laccase-assisted degradation - A review.  |  Barrios-Estrada, C., et al. 2018. Sci Total Environ. 612: 1516-1531. PMID: 28915546
  8. Accurate Quantification of Sulfonamide Metabolites in Goat Meat: A New Strategy for Minimizing Interaction between Sheep Serum Albumin and Sulfonamide Metabolites.  |  Jia, W., et al. 2021. J Agric Food Chem. 69: 6556-6568. PMID: 34080416
  9. Multiclass target analysis of contaminants of emerging concern including transformation products, soil bioavailability assessment and retrospective screening as tools to evaluate risks associated with reclaimed water reuse.  |  Beretsou, VG., et al. 2022. Sci Total Environ. 852: 158391. PMID: 36049679

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

N-Hydroxy Sulfamethoxazole, 2.5 mg

sc-212217
2.5 mg
$400.00