14254-17-2

Basic information

• Product Name: [2-[[4-[(2-chloro-4-nitrophenyl)azo]phenyl]ethylamino]ethyl]trimethylammonium] methyl sulphate
• Synonyms: Ethanaminium, 2-((4-(2-(2-chloro-4-nitrophenyl)diazenyl)phenyl)ethylamino)-N,N,N-trimethyl-, methyl sulfate (1:1); 2-((4-((2-Chloro-4-nitrophenyl)azo)phenyl)ethylamino)-N,N,N-trimethylethanaminium methyl sulfate; 2-(N-Ethyl-N-(4-((2-chloro-4-nitrophenyl)azo)phenyl)-N,N,N-trimethylethanaminium, methyl sulfate; (2-((4-((2-Chloro-4-nitrophenyl)azo)phenyl)ethylamino)ethyl)trimethylammonium methyl sulphate; Ethanaminium, 2-((4-((2-chloro-4-nitrophenyl)azo)phenyl)ethylamino)-N,N,N-trimethyl-, methyl sulfate; 2-[{4-[(E)-(2-chloro-4-nitrophenyl)diazenyl]phenyl}(ethyl)amino]-N,N,N-trimethylethanaminium methyl sulfate
• CAS NO: 14254-17-2
• Molecular Formula: C₂₀H₂₈ClN₅O₆S
• Molecular Weight: 501.9842
• EINECS: 238-129-1
• Mol File: 14254-17-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [2-[[4-[(2-chloro-4-nitrophenyl)azo]phenyl]ethylamino]ethyl]trimethylammonium] methyl sulphate(CAS DataBase Reference)
• NIST Chemistry Reference: [2-[[4-[(2-chloro-4-nitrophenyl)azo]phenyl]ethylamino]ethyl]trimethylammonium] methyl sulphate(14254-17-2)
• EPA Substance Registry System: [2-[[4-[(2-chloro-4-nitrophenyl)azo]phenyl]ethylamino]ethyl]trimethylammonium] methyl sulphate(14254-17-2)

Safety Data

• Hazardous Substances Data: 14254-17-2(Hazardous Substances Data)

Usage

General Description

The chemical "[2-[[4-[(2-chloro-4-nitrophenyl)azo]phenyl]ethylamino]ethyl]trimethylammonium] methyl sulphate" is a quaternary ammonium compound that contains a methyl sulphate group. It consists of a complex arrangement of nitrogen, carbon, hydrogen, chlorine, and nitrogen atoms, along with a nitro and azo functional group. The compound is a water-soluble salt that is commonly used in various industrial and laboratory applications, including as a dye, pigment, and biological stain. It is also utilized as a surfactant and as a component in pharmaceutical products. The compound's chemical structure makes it suitable for a wide range of uses, and it is important to handle it with care due to its potential reactivity and toxicity.

Relevant articles and documents

Process for dry quaternization of azo compounds

Certain solid dye bases which are precursors of acrylic fiber dyes and which contain a tertiary nitrogen atom are effectively quaternized in high yield and purity in a "dry state" quaternization process comprising contacting the dye base with an essential