19319-88-1

Basic information

• Product Name: DINITRATO(1,10-PHENANTHROLINE)COPPER(II)
• Synonyms: DINITRATO(1,10-PHENANTHROLINE)COPPER(II);Dinitrato(1,10-phenanthroline)copper(II),96%
• CAS NO: 19319-88-1
• Molecular Formula: C12H8CuN4O6
• Molecular Weight: 367.76
• Product Categories: Catalysis and Inorganic Chemistry;Chemical Synthesis;Copper
• Mol File: 19319-88-1.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 343.5°Cat760mmHg
• Flash Point: 219.4°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 7.01E-05mmHg at 25°C
• CAS DataBase Reference: DINITRATO(1,10-PHENANTHROLINE)COPPER(II)(CAS DataBase Reference)
• NIST Chemistry Reference: DINITRATO(1,10-PHENANTHROLINE)COPPER(II)(19319-88-1)
• EPA Substance Registry System: DINITRATO(1,10-PHENANTHROLINE)COPPER(II)(19319-88-1)

Safety Data

• Hazard Codes: O,Xn
• Statements: 8-20/21/22-36/37/38
• Safety Statements: 17-26-36/37/39
• RIDADR: UN 1479 5.1/PG 2
• WGK Germany: 3
• HazardClass: 5.1
• PackingGroup: III
• Hazardous Substances Data: 19319-88-1(Hazardous Substances Data)

Usage

General Description

Dinitrato(1,10-phenanthroline)copper(II) is a chemical compound that is formed by combining copper(II) with 1,10-phenanthroline and nitrate ions. It is commonly used in chemical reactions and materials science applications to catalyze various reactions. The compound has a bright blue color and is often used as a dye or pigment in various industries. It is also used in analytical chemistry as a reagent for detecting and measuring other substances, particularly in the presence of reducing agents. Dinitrato(1,10-phenanthroline)copper(II) is known for its stability and solubility in organic solvents, making it a versatile and valuable compound in many different scientific fields.

InChI:InChI=1/C12H10N2.Cu.2HNO3/c1-3-9-5-6-10-4-2-8-14-12(10)11(9)13-7-1;;2*2-1(3)4/h1-6H,7-8H2;;2*(H,2,3,4)/q-2;+2;;

Upstream product

• 14783-09-6 dichloro(1,10-phenanthroline) copper(II) 

Relevant articles and documents

A copper diimine-based honeycomb-like porous network as an efficient reduction catalyst

Nitrophenols are among the widely used industrial chemicals worldwide; however, their hazardous effects on environment are a major concern nowadays. Therefore, the conversion of environmentally detrimental p-nitrophenol (PNP) to industrially valuable p-aminophenol (PAP), a prototype reaction, is an important organic transformation reaction. However, the traditional conversion of PNP to PAP is an expensive and environmentally unfriendly process. Here, we report a honeycomb-like porous network with zeolite-like channels formed by the self-organization of copper, 1,10-phenanthroline, 4,4′-bipyridine, and water. This porous network effectively catalyzed the transformation of hazardous PNP to pharmaceutically valued PAP. In the presence of complex, PNP to PAP conversion occurred in a few minutes, which is otherwise a very sluggish process. To assess the kinetics, the catalytic conversion of PNP to PAP was studied at five different temperatures. The linearity of lnCt/Co versus temperature plot indicated pseudo-first-order kinetics. The copper complex with zeolite like channels may find applications as a reduction catalyst both on laboratory and industrial scales and in green chemistry for the remediation of pollutants.