ligands&coordination complexes / Alfa Chemistry
Banner
Online Inquiry
Verification code

Neocuproine hemihydrate

Catalog Number ACM34302697-2
CAS 34302-69-7
Structure {[CurrentData.Name]}
Description Neocuproine hemihydrate is an important, synthetic, water-soluble, and thermally stable complexing agent, which has a wide range of practical applications in the scientific research field. It was first synthesized in 1972 by a team of researchers at the University of Tokyo, and has since been used in a variety of research projects.
IUPAC Name 2,9-dimethyl-1,10-phenanthroline;hydrate
Molecular Weight 434.5 g/mol
Molecular Formula C28H26N4O
Canonical SMILES CC1=NC2=C(C=C1)C=CC3=C2N=C(C=C3)C.CC1=NC2=C(C=C1)C=CC3=C2N=C(C=C3)C.O
InChI InChI=1S/2C14H12N2.H2O/c2*1-9-3-5-11-7-8-12-6-4-10(2)16-14(12)13(11)15-9;/h2*3-8H,1-2H3;1H2
InChI Key IEBXFSLFDFHSRD-UHFFFAOYSA-N
Application Neocuproine hemihydrate has a wide range of applications in the scientific research field. It has been used as a chelating agent in the synthesis of copper-based catalysts, as a reagent in the synthesis of organic compounds, and as a stabilizing agent in the synthesis of metal-organic frameworks. It has also been used in the study of the structure and function of enzymes, as well as in the study of the effects of metal ions on biological systems.
GHS Pictogram Corrosive; Irritant
Properties Neocuproine hemihydrate has been used to study the effects of metal ions on biological systems. It has been shown to be effective in the inhibition of enzymes, such as cytochrome P450, and has been used to study the effects of metal ions on the activity of these enzymes. It has also been used to study the effects of metal ions on the transport of nutrients and other substances across cell membranes.

Please kindly note that our products and services are for research use only.