12217-92-4

Basic information

• Product Name: DISPERSE VIOLET 17
• Synonyms: Red Violet 17
• CAS NO: 12217-92-4
• Molecular Formula: C14H8BrNO3
• Molecular Weight: 318.12222
• Mol File: 12217-92-4.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: DISPERSE VIOLET 17(CAS DataBase Reference)
• NIST Chemistry Reference: DISPERSE VIOLET 17(12217-92-4)
• EPA Substance Registry System: DISPERSE VIOLET 17(12217-92-4)

Safety Data

• Hazardous Substances Data: 12217-92-4(Hazardous Substances Data)

Usage

Description

DISPERSE VIOLET 17 is a synthetic dye that exhibits a range of colors from blue light to pink, red, and purple. It is commonly used in the dyeing of polyester and blended fabrics, as well as acetate and cellulose acetate. It is also suitable for transfer printing and can be used as an intermediate for the production of dispersed and solvent dyes.

Uses

Used in Textile Industry:
DISPERSE VIOLET 17 is used as a dye for the coloring of polyester and blended fabrics. It provides good ironing fastness, light fastness, perspiration fastness, and washing fastness, making it a popular choice for various textile applications.
Used in Printing Industry:
DISPERSE VIOLET 17 is used as a dye for transfer printing, allowing for the creation of vibrant and long-lasting prints on various materials.
Used in Dye Production:
DISPERSE VIOLET 17 can be used as an intermediate in the production of dispersed and solvent dyes, contributing to the development of a wide range of colors and applications in various industries.

Preparation

1-Aminoanthracene-9,10-dione of bromine?bromide?with fuming sulfuric acid?and boric acid?hydrolysis.

Standard

Ironing Fastness

Fading

Stain

Upstream product

• 81-49-2 1-amino-2, 4-dibromoanthraquinone 
• 116-85-8 4-hydroxy-1-aminoanthraquinone 
• 116-83-6 1-amino-4-methoxyanthraquinone 
• 102184-28-1 1-amino-2-bromo-4-phenoxy-9,10-antraquinone 
• 76924-08-8 5-bromo-6-oxo-6H-anthra<1,9-cd>isoxazole 
• 82827-33-6 3-bromo-5-hydroxyanthra<1,9-cd>isoxazol-6-one 
• 74386-37-1 1-azido-4-bromoanthraquinone 
• 7664-93-9 sulfuric acid 
• 82840-40-2 3,5-dibromo-6-oxo-6H-anthra<1,9-cd>isoxazole 
• 106960-84-3 3-bromo-5-phenoxy-6-oxo-6H-anthra<1,9-cd>isoxazole 
• 82827-32-5 1-azido-2-bromo-4-hydroxyanthraquinone 
• 50981-12-9 sulfuric acid monohydrate 
• 82-45-1 1-amino-9,10-anthracenedione 

Downstream Products

• 79609-80-6 1-amino-4-hydroxy-2-p-tolylsulfanyl-anthraquinone 
• 38920-11-5 N-[4-(1-Amino-4-hydroxy-9,10-dioxo-9,10-dihydro-anthracen-2-yloxy)-3-methyl-phenyl]-acetamide 
• 38912-95-7 N-[3-(1-Amino-4-hydroxy-9,10-dioxo-9,10-dihydro-anthracen-2-yloxy)-4-chloro-phenyl]-acetamide 
• 38924-13-9 1-[3-(1-Amino-4-hydroxy-9,10-dioxo-9,10-dihydro-anthracen-2-yloxy)-phenyl]-3-phenyl-urea 
• 38919-98-1 N-[4-(1-Amino-4-hydroxy-9,10-dioxo-9,10-dihydro-anthracen-2-yloxy)-phenyl]-acetamide 
• 38920-13-7 N-[4-(1-Amino-4-hydroxy-9,10-dioxo-9,10-dihydro-anthracen-2-yloxy)-2-chloro-phenyl]-acetamide 
• 38912-94-6 N-[3-(1-Amino-4-hydroxy-9,10-dioxo-9,10-dihydro-anthracen-2-yloxy)-phenyl]-4-methyl-benzenesulfonamide 
• 38924-11-7 1-[4-(1-Amino-4-hydroxy-9,10-dioxo-9,10-dihydro-anthracen-2-yloxy)-phenyl]-3-phenyl-urea 
• 38924-15-1 1-[4-(1-Amino-4-hydroxy-9,10-dioxo-9,10-dihydro-anthracen-2-yloxy)-phenyl]-3-cyclohexyl-urea 
• 38924-14-0 1-[4-(1-Amino-4-hydroxy-9,10-dioxo-9,10-dihydro-anthracen-2-yloxy)-phenyl]-3-(4-chloro-phenyl)-urea 
• 38924-16-2 1-[4-(1-Amino-4-hydroxy-9,10-dioxo-9,10-dihydro-anthracen-2-yloxy)-phenyl]-3-hexadecyl-urea 
• 38924-17-3 1-[3-(1-Amino-4-hydroxy-9,10-dioxo-9,10-dihydro-anthracen-2-yloxy)-phenyl]-3-hexadecyl-urea 
• 36966-31-1 N-[3-(1-Amino-4-hydroxy-9,10-dioxo-9,10-dihydro-anthracen-2-yloxy)-phenyl]-acetamide 
• 1338810-38-0 4-amino-9,10-dioxo-3-(phenylethynyl)-9,10-dihydroanthracen-1-yl acetate 

Relevant articles and documents

COLORED CHARGED SILSESQUIOXANES

The present invention provides compounds of Formula (1A), wherein Formula (II) is Formula (III) and Formula (1B) wherein Formula (IV) is Formula (V) and electrophoretic devices comprising the compounds of formula (1A) or (1B).

CHARACTERISTICS OF THE ALKOXYLATION OF HALOGENO-6-OXO-6H-ANTHRAISOXAZOLES

The alkylation of 6-oxo-6H-anthraisoxazoles containing a chlorine or bromine atom at position 3 and also a bromine at position 5 takes place with substitution of the halogen or hydrogen, depending on the structure of the alkoxide ion and the type of halogen.

Process for the preparation of 1-amino-2-bromo-4-hydroxyanthraquinone

1-Amino-2-bromo-4-hydroxyanthraquinone is obtained in good yields and in an environmentally acceptable manner by bromination of 1-aminoanthraquinone in 2 to 5 times the quantity by weight of 80 to 98% strength sulphuric acid and using 1.1-1.5 mole of bromine under elevated pressure.