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4-hydroxy-5-[(phenylsulphonyl)amino]naphthalene-2,7-disulphonic acid, also known as Reactive Blue 19, is a chemical compound that belongs to the class of naphthalene sulfonic acid dyes. It is commonly used as a dye in the textile industry for coloring fabrics and other materials. Reactive Blue 19 contains hydroxyl and sulphonyl functional groups and has a chemical structure consisting of two naphthalene rings with two sulphonate groups attached. This dye is known for its high affinity for cellulose fibers, making it suitable for dyeing cotton and other plant-based textiles.

83-22-7

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83-22-7 Usage

Uses

Used in Textile Industry:
4-hydroxy-5-[(phenylsulphonyl)amino]naphthalene-2,7-disulphonic acid is used as a dye for coloring fabrics and other materials. Its high affinity for cellulose fibers makes it suitable for dyeing cotton and other plant-based textiles. As a water-soluble and reactive dye, it allows for easy application and excellent color fastness properties.
It is important to handle Reactive Blue 19 with care, as it may cause skin and eye irritation and is harmful if ingested or inhaled.

Check Digit Verification of cas no

The CAS Registry Mumber 83-22-7 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, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 83-22:
(4*8)+(3*3)+(2*2)+(1*2)=47
47 % 10 = 7
So 83-22-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H13NO9S3/c18-15-9-13(29(24,25)26)7-10-6-12(28(21,22)23)8-14(16(10)15)17-27(19,20)11-4-2-1-3-5-11/h1-9,17-18H,(H,21,22,23)(H,24,25,26)

83-22-7SDS

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 4-(benzenesulfonamido)-5-hydroxynaphthalene-2,7-disulfonic acid

1.2 Other means of identification

Product number -
Other names EINECS 201-459-1

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:83-22-7 SDS

83-22-7Downstream Products

83-22-7Relevant academic research and scientific papers

Development of a One-Step Synthesis of 5-Amino-1 H-imidazole-4-carboxamide

Qi, Ji,Yin, Jingjun,Li, Donghong,Chen, Song,Liu, Zhenguo

, p. 591 - 596 (2021/04/05)

An innovative and efficient synthesis of 5-amino-1H-imidazole-4-carboxamide (AIC) from commercially available hypoxanthine (~$30/kg) is described. The development of the key hydrolysis step and a practical isolation enables a highly efficient one-step manufacturing process for AIC with minimal environmental impact and significant reduction of production cost.

PROCESS FOR THE PREPARATION OF TETRAZINE DERIVATIVES

-

, (2011/10/10)

The present invention provides a process for the preparation of a tetrazine derivative of formula (I), or a pharmaceutically acceptable salt thereof wherein R1 represents a hydrogen atom, a straight or branched C1-C6 alkyl group, C2-C6 alkenyl group or C2-C6 alkynyl group, which C1-C6 alkyl group, C2-C6 alkenyl group and C2-C6 alkynyl group is unsubstituted or substituted with 1, 2 or 3 substituents selected from halogen atoms, straight or branched C1-C4 alkoxy groups, C1-C4 alkylthio groups, C1-C4 alkylsulphinyl groups, C1-C4 alkylsulphonyl groups and phenyl groups, which phenyl groups are unsubstituted or substituted with one or more substituents selected from C1-C4 alkyl groups, C1-C4 alkoxy groups and nitro groups; or R1 represents a C3-C8 cycloalkyl group; and R2 represents a group of formula —(C═O)NR3R4, wherein R3 and R4 are independently selected from hydrogen atoms, C1-C4 alkyl groups, C2-C4 alkenyl groups and C3-C8 cycloalkyl groups, which process comprises: i) providing a compound N of formula (III), wherein R1 is as defined; R1—N═C═O ii) absorbing the compound of formula (III) into a solvent to obtain a solution of the compound of formula (III); iii) adding to the thus obtained solution a compound of formula (II), to obtain a compound of formula (I), as defined above, wherein R2 is as defined above; iv) decomposing any excess compound of formula (III) remaining by addition of water; and v) optionally salifying the thus obtained compound with a pharmaceutically acceptable acid, or base.

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