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83-62-5

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83-62-5 Usage

Description

1-amino-9,10-dihydro-9,10-dioxoanthracene-2-sulphonic acid is a complex chemical compound that belongs to the anthraquinone dyes class. It features an amino group, a dihydroanthracene backbone, and a sulphonic acid group, which contribute to its water solubility and make it suitable for use as a dye.

Uses

Used in Textile Industry:
1-amino-9,10-dihydro-9,10-dioxoanthracene-2-sulphonic acid is used as a dyeing agent for textiles, providing vibrant and long-lasting colors to fabrics.
Used in Paper Industry:
In the paper industry, 1-amino-9,10-dihydro-9,10-dioxoanthracene-2-sulphonic acid is used as a coloring agent to impart desired shades to paper products.
Used in Plastics Industry:
1-amino-9,10-dihydro-9,10-dioxoanthracene-2-sulphonic acid is used as a pigment in the production of colored plastics, enhancing their visual appeal and durability.
Used in Pharmaceutical Manufacturing:
1-amino-9,10-dihydro-9,10-dioxoanthracene-2-sulphonic acid may have applications in the manufacturing of pharmaceuticals, potentially serving as an active ingredient or a component in drug formulations.
Used as a Chemical Intermediate:
1-amino-9,10-dihydro-9,10-dioxoanthracene-2-sulphonic acid can also be used as a chemical intermediate in the synthesis of other compounds, contributing to the development of new products and materials across various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 83-62-5 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 8 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83-62:
(4*8)+(3*3)+(2*6)+(1*2)=55
55 % 10 = 5
So 83-62-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H9NO5S/c15-12-10(21(18,19)20)6-5-9-11(12)14(17)8-4-2-1-3-7(8)13(9)16/h1-6H,15H2,(H,18,19,20)

83-62-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-amino-9,10-dioxoanthracene-2-sulfonic acid

1.2 Other means of identification

Product number -
Other names 1-Amino-9,10-dihydro-9,10-dioxo-2-anthracenesulfonic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:83-62-5 SDS

83-62-5Relevant articles and documents

1-amino anthraquinone sulfonation process for bromamine acid production

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Paragraph 0020; 0021; 0028-0062, (2021/03/13)

The invention relates to the technical field of organic synthesis, and discloses a 1-amino anthraquinone sulfonation process for bromamine acid production, which has the advantages of mild reaction conditions, no pollution, meeting of the concept of green chemistry, simplicity and convenience in operation, and high-efficiency synthesis of a precursor 1-amino anthraquinone-2-sulfonic acid product of bromamine acid by regulating and controlling a recrystallized benign solvent and a poor solvent. The purity is high and the yield is high.

Process for synthesizing 1-amino-anthraquinone-2-sulfonic acid through solid-phase method

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Paragraph 0033; 0037; 0041, (2018/07/06)

The invention provides a method for synthesizing 1-amino-anthraquinone-2-sulfonic acid from 1-amino-anthraquinone. The method comprises the following steps: generating a sulfate solid of 1-amino-anthraquinone through reaction of the 1-amino-anthraquinone and sulfuric acid, and then performing transposition on the sulfate solid of the 1-amino-anthraquinone to generate the 1-amino-anthraquinone-2-sulfonic acid. A process of synthesizing the 1-amino-anthraquinone-2-sulfonic acid by a sulfuric acid method is fundamentally improved; the sulfate of the 1-amino-anthraquinone is efficiently subjectedto transposition reaction under a solid-phase condition without a solvent after generated water is removed, so that the reaction yield is high, and no side effects are caused; furthermore, no 1-amino-4-chloroant-2-sulfonic acid is generated, and no wastewater, waste gas and waste residues are generated; an obtained product is further synthesized into bromamine acid, and the purity of the obtainedbromamine acid is close to 100 percent; the quality and the yield of the bromamine acid are both higher than the quality and the yield of bromamine acid synthesized by a chlorosulfonic acid method, afuming sulfuric acid method and a conventional sulfuric acid method.

OPTIMIZATION OF THE OXIDATIVE BROMINATION OF 1-AMINOANTHRAQUINONE-2-SULFONIC ACID

Gerasimov, S. V.,Filimonov, V. D.

, p. 928 - 930 (2007/10/03)

An efficient method of synthesis of 1-amino-4-bromoanthraquinone-2-sulfonic acid using bromination of the corresponding aminoathraquinonesulfonic acid with bromine in the presence of hydrogen peroxide has been proposed.The optimum conditions of synthesis, with a yield of the target product of 68percent, have been found.

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