Date published: 2025-12-1

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8-Hydroxyquinoline hemisulfate salt hemihydrate (CAS 207386-91-2)

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Alternate Names:
8-Quinolinol hemisulfate
Application:
CAS Number:
207386-91-2
Purity:
≥98%
Molecular Weight:
406.42
Molecular Formula:
C18H14N2O2•H2SO4•H2O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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8-Hydroxyquinoline hemisulfate salt hemihydrate, a compound of interest in scientific research, has been extensively studied for its diverse applications, particularly in the fields of coordination chemistry and materials science. Its chemical structure features a hydroxyquinoline moiety, which imparts unique properties that make it valuable in various research endeavors. One significant area of investigation involves its role as a chelating ligand in coordination chemistry. Due to the presence of nitrogen and oxygen donor atoms, 8-hydroxyquinoline hemisulfate salt hemihydrate exhibits strong coordination abilities towards metal ions, forming stable complexes. These metal complexes have been explored for their potential applications in catalysis, luminescent materials, and molecular recognition. Moreover, researchers have utilized 8-hydroxyquinoline hemisulfate salt hemihydrate as a building block in the synthesis of functionalized organic molecules and supramolecular assemblies. Its ability to participate in various chemical reactions, such as coordination, hydrogen bonding, and π-π interactions, has enabled the design and fabrication of novel materials with tailored properties for applications in sensors, optoelectronics, and biotechnology. Continued research efforts aim to further explain its chemical reactivity and explore its potential in emerging fields, contributing to advancements in molecular design and materials science.


8-Hydroxyquinoline hemisulfate salt hemihydrate (CAS 207386-91-2) References

  1. Organic copper complexes as a new class of proteasome inhibitors and apoptosis inducers in human cancer cells.  |  Daniel, KG., et al. 2004. Biochem Pharmacol. 67: 1139-51. PMID: 15006550
  2. Cross-talk between lipid and protein carbonylation in a dynamic cardiomyocyte model of mild nitroxidative stress.  |  Griesser, E., et al. 2017. Redox Biol. 11: 438-455. PMID: 28086193
  3. Homocysteine directly interacts and activates the angiotensin II type I receptor to aggravate vascular injury.  |  Li, T., et al. 2018. Nat Commun. 9: 11. PMID: 29296021

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

8-Hydroxyquinoline hemisulfate salt hemihydrate, 100 g

sc-227132
100 g
$44.00