64981-00-6

Basic information

• Product Name: sodium 1-amino-9,10-dihydro-4-[[(4-methylphenyl)sulphonyl]amino]-9,10-dioxoanthracene-2-sulphonate
• Synonyms: sodium 1-amino-9,10-dihydro-4-[[(4-methylphenyl)sulphonyl]amino]-9,10-dioxoanthracene-2-sulphonate;Sodium 1-amino-9,10-dihydro-4-[[(4-methylphenyl) sulphonyl]amino]-9,10-dioxoanthracene-2-sulphonate Sodium 1-amino-9,10-dihydro-4-[[(4-methylphenyl)sulphonyl]amino]-9,10-dioxoanthracene-2-sulphonate;1-Amino-9,10-dihydro-4-[[(4-methylphenyl)sulfonyl]amino]-9,10-dioxo-2-anthracenesulfonic acid sodium salt
• CAS NO: 64981-00-6
• Molecular Formula: C₂₁H₁₅N₂O₇S₂*Na
• Molecular Weight: 494.47277
• EINECS: 265-297-3
• Mol File: 64981-00-6.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: sodium 1-amino-9,10-dihydro-4-[[(4-methylphenyl)sulphonyl]amino]-9,10-dioxoanthracene-2-sulphonate(CAS DataBase Reference)
• NIST Chemistry Reference: sodium 1-amino-9,10-dihydro-4-[[(4-methylphenyl)sulphonyl]amino]-9,10-dioxoanthracene-2-sulphonate(64981-00-6)
• EPA Substance Registry System: sodium 1-amino-9,10-dihydro-4-[[(4-methylphenyl)sulphonyl]amino]-9,10-dioxoanthracene-2-sulphonate(64981-00-6)

Safety Data

• Hazardous Substances Data: 64981-00-6(Hazardous Substances Data)

Usage

General Description

Sodium 1-amino-9,10-dihydro-4-[[(4-methylphenyl)sulphonyl]amino]-9,10-dioxoanthracene-2-sulphonate is a chemical compound that is used as a fluorescent dye and staining reagent in biological and biomedical research. It is often used to label antibodies and DNA for visualization under a fluorescence microscope. sodium 1-amino-9,10-dihydro-4-[[(4-methylphenyl)sulphonyl]amino]-9,10-dioxoanthracene-2-sulphonate is water-soluble and has a high degree of photostability, making it a valuable tool for various imaging applications. Additionally, it is also utilized in the study of protein interactions, cell morphology, and other cellular processes.

InChI:InChI=1/C21H16N2O7S2.Na/c1-11-6-8-12(9-7-11)31(26,27)23-15-10-16(32(28,29)30)19(22)18-17(15)20(24)13-4-2-3-5-14(13)21(18)25;/h2-10,23H,22H2,1H3,(H,28,29,30);/q;+1/p-1

Relevant articles and documents

Preparation process for aminoanthraquinone derivatives

A process for the preparation of aminoanthraquinone derivatives comprises reacting (A) bromaminic acid or a metal salt thereof with (B) an amine or amide in an aqueous alkaline medium in the presence of a copper (I) salt formed by in situ reduction of a copper (II) salt.