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Hydroxylamine solution (CAS 7803-49-8)

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Alternate Names:
Oxammonium; Nitroxide
Application:
Hydroxylamine solution is an inorganic compound used in organic synthesis and as a reducing agent
CAS Number:
7803-49-8
Molecular Weight:
33.03
Molecular Formula:
H3NO
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Hydroxylamine solution is a compound that functions as a reducing agent in various chemical reactions. Its mode of action involves the donation of hydrogen atoms to other molecules, leading to the reduction of those molecules and the oxidation of hydroxylamine itself. Hydroxylamine solution is particularly useful in the conversion of aldehydes and ketones to oximes, as well as in the synthesis of hydroxamic acids from esters and amides. Hydroxylamine solution also may play a role in the preparation of hydroxamic acid-based chelating agents and in the production of pharmaceuticals and agrochemicals. Its ability to react with carbonyl compounds and form stable oxime derivatives may be useful in organic synthesis and chemical research. Hydroxylamine solution can participate in the synthesis of heterocyclic compounds and in the modification of biomolecules, contributing to the advancement of various scientific fields.


Hydroxylamine solution (CAS 7803-49-8) References

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  2. Bead injection for surface enhanced Raman spectroscopy: automated on-line monitoring of substrate generation and application in quantitative analysis.  |  Cañada, MJ., et al. 2002. Analyst. 127: 1365-9. PMID: 12430611
  3. [Biochemical and immunochemical analyses of the protein components of the cell wall in group-A streptococci isolated by a sparing chemical method].  |  Blinnikova, EI. and Shikhman, AR. 1992. Zh Mikrobiol Epidemiol Immunobiol. 2-5. PMID: 1284507
  4. Tunable surface-enhanced infrared absorption on au nanofilms on si fabricated by self-assembly and growth of colloidal particles.  |  Huo, SJ., et al. 2005. J Phys Chem B. 109: 15985-91. PMID: 16853028
  5. Spectrophotometric determination of micro amounts of hydrazine and hydroxylamine alone and in the presence of each other.  |  Dias, F., et al. 1979. Talanta. 26: 47-9. PMID: 18962372
  6. Synthesis and application of N-[1-(4-(4-fluorophenyl)-2,6-dioxocyclohexylidene)ethyl] (Fde)-protected amino acids for optimization of solid-phase peptide synthesis using gel-phase (19)F NMR spectroscopy.  |  Pudelko, M., et al. 2009. J Pept Sci. 15: 264-71. PMID: 19235188
  7. [Construction of expression vectors for efficient expression of soluble recombinant proteins].  |  Jiang, Y., et al. 2010. Sheng Wu Gong Cheng Xue Bao. 26: 121-9. PMID: 20353102
  8. A simple spectrophotometric determination of meptyldinocap by its hydrolysis.  |  Kurup, S. and Pillai, AK. 2013. Acta Chim Slov. 60: 81-6. PMID: 23841335
  9. Integrated calibration and serum iron in situ analysis into an array microfluidic paper-based analytical device with smartphone readout.  |  Dortez, S., et al. 2023. Talanta. 253: 123914. PMID: 36103750
  10. The reaction of hydroxylamine with 4-thiouridine.  |  Iida, S., et al. 1973. Biochim Biophys Acta. 308: 198-204. PMID: 4196222
  11. Effect of hydroxylamine on photon-like events during dark adaptation in toad rod photoreceptors.  |  Leibrock, CS. and Lamb, TD. 1997. J Physiol. 501 (Pt 1): 97-109. PMID: 9174997
  12. Spectrophotometric determination of parathion and paraoxon using alkaline hydroxylamine solution for the liberation of 4-nitrophenol.  |  Ramakrishna, N. and Ramachandran, BV. 1976. Analyst. 101: 528-32. PMID: 952403
  13. Molecular basis of dark adaptation in rod photoreceptors.  |  Leibrock, CS., et al. 1998. Eye (Lond). 12 (Pt 3b): 511-20. PMID: 9775211

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Hydroxylamine solution, 100 ml

sc-250136
100 ml
$71.00