82-27-9

Basic information

• Product Name: 2-amino-1-chloroanthraquinone
• Synonyms: 2-amino-1-chloro-9,10-anthraquinone;2-azanyl-1-chloro-anthracene-9,10-dione;2-amino-1-chloroanthracene-9,10-dione
• CAS NO: 82-27-9
• Molecular Formula: C₁₄H₈ClNO₂
• Molecular Weight: 257.67182
• EINECS: 201-407-8
• Mol File: 82-27-9.mol

Chemical Properties

• Boiling Point: 500.9 °C at 760 mmHg
• Flash Point: 256.7 °C
• Appearance: /
• Density: 1.486 g/cm³
• Vapor Pressure: 3.64E-10mmHg at 25°C
• Refractive Index: 1.711
• CAS DataBase Reference: 2-amino-1-chloroanthraquinone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-1-chloroanthraquinone(82-27-9)
• EPA Substance Registry System: 2-amino-1-chloroanthraquinone(82-27-9)

Safety Data

• Hazardous Substances Data: 82-27-9(Hazardous Substances Data)

Usage

Uses

Used in Textile Industry:
2-Amino-1-chloroanthraquinone is used as a pigment in the textile industry for coloring fabrics due to its high color fastness and resistance to fading. Its unique properties make it particularly effective for dyeing applications, providing long-lasting and vibrant colors to textiles.
Used in Dye and Pigment Production:
In the dye and pigment production industry, 2-Amino-1-chloroanthraquinone is utilized in the manufacture of vat dyes, which are water-insoluble pigments known for their superior coloring capabilities. These dyes are essential for creating a wide range of colors in various materials, including textiles and plastics.
Used in Organic Synthesis:
2-Amino-1-chloroanthraquinone is also used as a starting material in organic synthesis, where it can be further modified to produce a variety of other chemical compounds with different properties and applications.
Used as a Pharmaceutical Intermediate:
Furthermore, 2-amino-1-chloroanthraquinone has been studied for its potential use as a pharmaceutical intermediate, indicating its possible role in the development of new drugs and therapeutic agents.

InChI:InChI=1/C14H8ClNO2/c15-12-10(16)6-5-9-11(12)14(18)8-4-2-1-3-7(8)13(9)17/h1-6H,16H2

Upstream product

• 85-44-9 phthalic anhydride 
• 117-79-3 2-aminoanthraquinone 
• 42983-73-3 1-chloro-2-acetylaminoanthraquinone 
• 7664-93-9 sulfuric acid 
• 859494-63-6 N-(1-chloro-9,10-dioxo-9,10-dihydro-[2]anthryl)-toluene-4-sulfonamide 
• 82-44-0 1-chloroanthracene-9,10-dione 

Downstream Products

• 81-77-6 6,15-dihydroanthrazine-5,9,14,18-tetrone 
• 71143-08-3 methyl violet 2B 
• 117-79-3 2-aminoanthraquinone 
• 1594-46-3 1,2-dichloro-anthraquinone 
• 6337-00-4 2-amino-3-bromoanthraquinone 
• 6374-73-8 2-amino-1-mercaptoanthraquinone 
• 330439-34-4 1-chloro-2-(2-chloro-benzoylamino)-anthraquinone 
• 43046-98-6 2-amino-1-(toluene-4-sulfonylamino)-anthraquinone 
• 102170-94-5 1-chloro-2-(4-nitro-anilino)-anthraquinone 
• 36339-31-8 2-phenylaminoanthraquinone 
• 68637-94-5 1-chloro-2-phenylaminoanthraquinone 
• 78692-25-8 1-chloro-2-(diphenylamino)anthraquinone 
• 78679-96-6 N,N'-diphenylindanthrene 
• 475-71-8 flavanthrone 

Relevant articles and documents

PHOTOCHEMICAL REACTION OF 9,10-ANTHRAQUINONE AND ITS DERIVATIVES WITH PYRIDINE

The previously unknown photochemical reaction of 9,10-anthraquinone with pyridine in an atmosphere of argon takes place with formation of 2-(1,2-dihydropyridino)- or 2-(1,4-dihydropyridino)-9,10-anthraquinone, which is converted by the action of alkali into 2-aminoanthraquinone.In the presence of atmospheric oxygen the reaction product after treatment whith alkali is 1-aminoanthraquinone in addition to 2-aminoanthraquinone.The 1- and 2-methoxyanthraquinones and chloroanthraquinones react with pyridine in the light and form, after treatment with alkali, substituted aminoanthraquinones.