16472-24-5

Basic information

• Product Name: 1,4-bis[[4-(2-hydroxyethoxy)phenyl]amino]anthraquinone
• Synonyms: 1,4-bis[[4-(2-hydroxyethoxy)phenyl]amino]anthraquinone;1,4-Bis[[4-(2-hydroxyethoxy)phenyl]amino]-9,10-anthracenedione;Einecs 240-529-6
• CAS NO: 16472-24-5
• Molecular Formula: C₃₀H₂₆N₂O₆
• Molecular Weight: 510.53724
• EINECS: 240-529-6
• Mol File: 16472-24-5.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 764.4°C at 760 mmHg
• Flash Point: 416.1°C
• Appearance: /
• Density: 1.39g/cm³
• Vapor Pressure: 1.43E-24mmHg at 25°C
• Refractive Index: 1.707
• CAS DataBase Reference: 1,4-bis[[4-(2-hydroxyethoxy)phenyl]amino]anthraquinone(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-bis[[4-(2-hydroxyethoxy)phenyl]amino]anthraquinone(16472-24-5)
• EPA Substance Registry System: 1,4-bis[[4-(2-hydroxyethoxy)phenyl]amino]anthraquinone(16472-24-5)

Safety Data

• Hazardous Substances Data: 16472-24-5(Hazardous Substances Data)

Usage

Type of Compound

Synthetic organic compound

Molecular Structure

Complex

Usage

Coloring agent in the textile industry

Key Component

Anthraquinone

Characteristics of Anthraquinone

Vibrant and long-lasting colors

Presence of Hydroxyethoxy and Phenyl Groups

Contributes to solubility in various solvents and ability to bind to different types of fabrics

Amino Groups

Make it suitable for use in dyes and pigments for a wide range of applications

Safety and Environmental Impact

Proper handling and disposal procedures should be followed to ensure safety and minimize environmental impact

InChI:InChI=1/C30H26N2O6/c33-15-17-37-21-9-5-19(6-10-21)31-25-13-14-26(32-20-7-11-22(12-8-20)38-18-16-34)28-27(25)29(35)23-3-1-2-4-24(23)30(28)36/h1-14,31-34H,15-18H2

Upstream product

• 602-25-5 1,4-dichloroanthraquinone 
• 123-30-8 4-amino-phenol 
• 15939-83-0 1,4-bis(4-hydroxyphenylamino)anthraquinone 
• 540-51-2 2-bromoethanol 
• 2905-61-5 2,5-dichlorobenzoyl chloride 
• 106-46-7 para-dichlorobenzene 

Downstream Products

• 1439439-88-9 1,4-bis(4-((2-methacryloxyethyl)oxy)phenylamino)anthraquinone 

Relevant articles and documents

Polymerization of novel methacrylated anthraquinone dyes

A new series of polymerizable methacrylated anthraquinone dyes has been synthesized by nucleophilic aromatic substitution reactions and subsequent methacrylation. Thereby, green 5,8-bis(4-(2-methacryloxyethyl)phenylamino)-1,4- dihydroxyanthraquinone (2), blue 1,4-bis(4-((2-methacryloxyethyl)oxy) phenylamino)anthraquinone (6) and red 1-((2-methacryloxy-1,1- dimethylethyl)amino)anthraquinone (12), as well as 1-((1,3-dimethacryloxy-2- methylpropan-2-yl)amino)anthraquinone (15) were obtained. By mixing of these brilliant dyes in different ratios and concentrations, a broad color spectrum can be generated. After methacrylation, the monomeric dyes can be covalently emplaced into several copolymers. Due to two polymerizable functionalities, they can act as cross-linking agents. Thus, diffusion out of the polymer can be avoided, which increases the physiological compatibility and makes the dyes promising compounds for medical applications, such as iris implants.