3618-73-3

Basic information

• Product Name: 2,2'-[[5-acetamido-4-[(2-chloro-4,6-dinitrophenyl)azo]-2-methoxyphenyl]imino]diethyl diacetate
• Synonyms: 2,2'-[[5-acetamido-4-[(2-chloro-4,6-dinitrophenyl)azo]-2-methoxyphenyl]imino]diethyl diacetate;C.I. Disperse Blue 79 press cake;N-[5-[bis[2-(acetyloxy)ethyl]amino]-2-[(2-chloro-4,6-dinitrophenyl)azo]-4-methoxyphenyl]-Acetamide;Acetamide, N-[5-[bis[2-(acetyloxy)ethyl] amino]-2-[(2-chloro-4,6-dinitrophenyl)azo]-4-methoxyphenyl ]-;5'-Bis(2-acetoxyethyl)amino-2'-(2-chloro-4,6-dinitrophenylazo)-4'-methoxyacetanilide;Disperse Blue 79:1;2-[[5-acetamido-4-(2-chloro-4,6-dinitro-phenyl)diazenyl-2-methoxy-phenyl]-(2-acetyloxyethyl)amino]ethyl ethanoate;2-[5-acetamido-N-(2-acetyloxyethyl)-4-(2-chloro-4,6-dinitrophenyl)diazenyl-2-methoxyanilino]ethyl acetate
• CAS NO: 3618-73-3
• Molecular Formula: C₂₃H₂₅ClN₆O₁₀
• Molecular Weight: 580.9318
• EINECS: 222-814-7
• Product Categories: Organics
• Mol File: 3618-73-3.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 784.5°Cat760mmHg
• Flash Point: 428.2°C
• Appearance: /
• Density: 1.46g/cm³
• PKA: 13.49±0.70(Predicted)
• CAS DataBase Reference: 2,2'-[[5-acetamido-4-[(2-chloro-4,6-dinitrophenyl)azo]-2-methoxyphenyl]imino]diethyl diacetate(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2'-[[5-acetamido-4-[(2-chloro-4,6-dinitrophenyl)azo]-2-methoxyphenyl]imino]diethyl diacetate(3618-73-3)
• EPA Substance Registry System: 2,2'-[[5-acetamido-4-[(2-chloro-4,6-dinitrophenyl)azo]-2-methoxyphenyl]imino]diethyl diacetate(3618-73-3)

Safety Data

• Hazardous Substances Data: 3618-73-3(Hazardous Substances Data)

Usage

General Description

2,2'-[[5-acetamido-4-[(2-chloro-4,6-dinitrophenyl)azo]-2-methoxyphenyl]imino]diethyl diacetate is a complex, synthetic chemical compound, the structure of which features a variety of chemical groups. It has the presence of an azo group (-N=N-) which often contributes to making a compound colorful, hence, such compounds are often used in the production of dyes. Its structure also includes several acetate and nitro groups, as well as a single chloro group. It is derived from phenol - specifically a dinitrophenyl derivative, and contains the functional group of an imino. This complex compound might be used in various industrial or laboratory processes, but specific applications are not generally known without additional context.

Upstream product

• 3531-19-9 2-chloro-4,6-dinitroaniline 
• 23128-51-0 3-N,N-bis-β-acetoxyethylamino-4-methoxyacetanilide 

Relevant articles and documents

Diazotization method of wet nitroaniline

The invention provides a diazotization method of wet nitroaniline, and relates to the field of dye synthesis. The diazotization method comprises following steps: step one, evenly stirring sulfuric acid (98%) and nitrosyl sulfuric acid (40%) in a diazotization reactor; and step two, adding wet nitroaniline into the diazotization reactor at a controlled temperature of -10 to 40 DEG C to obtain diazotization salts, wherein the mole ratio of sulfuric acid to nitrosyl sulfuric acid to diazotization component is 1.0-6: 1.02-1.1: 1. The quality of the provided wet dye is the same as that of a dry product, the diazotization component does not need to be dried, and the provided dye is energy saving and environmentally friendly.