92798-16-8

Basic information

• Product Name: 1,10-Phenanthroline, mono(4-methylbenzenesulfonate)
• Synonyms: 1,10-Phenanthroline, mono(4-methylbenzenesulfonate);PHENANTHROLINETOLUENESULFONIC ACID);1,10-phenanthroline-p-toluenesulfonic acid salt
• CAS NO: 92798-16-8
• Molecular Formula: C19H16N2O3S
• Molecular Weight: 352.41
• Mol File: 92798-16-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 365.1°Cat760mmHg
• Flash Point: 164.8°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 3.38E-05mmHg at 25°C
• CAS DataBase Reference: 1,10-Phenanthroline, mono(4-methylbenzenesulfonate)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,10-Phenanthroline, mono(4-methylbenzenesulfonate)(92798-16-8)
• EPA Substance Registry System: 1,10-Phenanthroline, mono(4-methylbenzenesulfonate)(92798-16-8)

Safety Data

• Hazardous Substances Data: 92798-16-8(Hazardous Substances Data)

Usage

General Description

1,10-Phenanthroline, mono(4-methylbenzenesulfonate) is a chemical compound that consists of a phenanthroline molecule with a mono(4-methylbenzenesulfonate) group attached. It is commonly used as a chelating agent in chemical and biological research, where it can bind to metal ions and form stable complexes. These complexes are often used in analytical chemistry, electrochemistry, and as catalysts in various chemical reactions. 1,10-Phenanthroline, mono(4-methylbenzenesulfonate) is also utilized in the pharmaceutical industry in the synthesis of certain drugs and as a ligand in coordination chemistry. It is a commercially available reagent with a variety of applications in scientific and industrial settings.

InChI:InChI=1/C12H8N2.C7H8O3S/c1-3-9-5-6-10-4-2-8-14-12(10)11(9)13-7-1;1-6-2-4-7(5-3-6)11(8,9)10/h1-8H;2-5H,1H3,(H,8,9,10)

Upstream product

• 66-71-7 1,10-Phenanthroline 
• 104-15-4 toluene-4-sulfonic acid 

Relevant articles and documents

Proton-gradient-transfer acid complexes and their catalytic performance for the synthesis of geranyl acetate

Special proton-gradient-transfer acid complexes (PGTACs) in which the bonded protons are not equivalent and have gradients in transfer ability, acidity, and reactivity were reported. The acidity gradient of the protons gave the PGTACs excellent catalytic activity and selectivity in the esterification of terpenols. These PGTACs are “reaction-induced self-separation catalysts” and can be easily reused. The kinetics with PGTACs as catalyst in the esterification of geraniol were also studied for use in engineering design.