149-46-2

Usage

Uses

Used in Analytical Chemistry:
4,5-dihydroxybenzene-1,3-disulphonic acid is used as an analytical reagent for the determination of copper and hydrogen peroxide due to its ability to form complexes with these substances, enabling their detection and quantification.
Used in Dye and Pigment Production:
In the chemical industry, 4,5-dihydroxybenzene-1,3-disulphonic acid is used as a precursor in the synthesis of various dyes and pigments, contributing to their color properties and stability.
Used in Research and Development:
4,5-dihydroxybenzene-1,3-disulphonic acid is utilized in the field of research and development for the study of its chemical properties, potential applications, and interactions with other compounds.
Used in Industrial Product Manufacturing:
This chemical compound is also employed in the manufacture of various industrial products, where its properties may be leveraged for specific technical or functional requirements.
Safety Note:
It is important to handle 4,5-dihydroxybenzene-1,3-disulphonic acid with care and according to safe laboratory practices due to its potential health hazards, ensuring the safety of individuals and the environment.

InChI:InChI=1/C6H6O8S2/c7-4-1-3(15(9,10)11)2-5(6(4)8)16(12,13)14/h1-2,7-8H,(H,9,10,11)(H,12,13,14)

Upstream product

• 7134-09-0 3,4-dihydroxybenzenesulfonic acid 
• 120161-24-2 5-chloro-4-hydroxy-benzene-1,3-disulfonic acid 
• 121208-92-2 5-bromo-4-hydroxy-benzene-1,3-disulfonic acid 
• 120-80-9 benzene-1,2-diol 
• 35857-70-6 2,3-dihydroxybenzene-1-sulfonic acid 
• 7790-94-5 chlorosulfonic acid 
• 7664-93-9 sulfuric acid 
• 5930-44-9 phenol-2,4,6-trisulfonic acid 
• 149-45-1 tiron 

Downstream Products

• 120-80-9 benzene-1,2-diol 
• 47836-89-5 ferroin 
• 1120368-95-7 iron(II)tris(5,6-Me₂-phen)⁽²⁺⁾ 
• 15226-32-1 tris(5-methyl-1,10-phenanthroline)iron(II) 
• 1379458-90-8 C₆H₄O₉S₂ 

Relevant academic research and scientific papers

Novel Full Hydrogenation Reaction of Methyl Esters of Palm Kernel and Sunflower Oils Into Methyl Stearate Catalyzed by Rhodium, Ruthenium and Nickel Complexes of Bidentate Hexasulfonated o-Phenylendiphosphite Ligands

High catalytic activities (TOF = 8680?h?1) have been achieved by novel rhodium catalysts modified with the chelating sulfonated phosphite ligand hexasulfonated o-phenylendiphosphite in the hydrogenation reaction of renewable methyl esters of sunflower oil under mild reaction conditions and a low rhodium concentration of 50?ppm in methanol. Graphical Abstract: [Figure not available: see fulltext.].

Sulfonation and sulfation on reaction of 1,2-dihydroxybenzene and its methyl ethers in concentrated aqueous sulfuric acid

The homogeneous sulfonation of 1,2-dihydroxybenzene (1), its monomethyl (2) and dimethyl ether (3) in concentrated aqueous sulfuric acid at 25 deg C has been studied and isomer distributions, as well as rate coefficients for the sulfonation of 1-3 and their monosulfonic acids, have been determined.In 73.5-87.5percent H2SO4, 1 yields the 3- and 4-sulfonic acids in a ratio of 25:75, 2 yields the 4-, 5- and 6-sulfonic acids in a ratio of 46:36:18 in 73.5percent H2SO4 and 50:39:11 in 87.5percent H2SO4, whereas 3 yields only the 4-sulfonic acid.The remarkable absence of the 3-sulfonic acid (87.5percent H2SO4, the 4-sulfonic acid of 1 and the 5-sulfonic acid of 2 are present in part in the form of their hydrogen sulfate.In that acid region, the 3- and 4-sulfonic acids of 1 both yield the 3,5-disulfonic acid, the 4- and 6-sulfonic acids of 2 both yield the 4,6-disulfonic acid and the 4-sulfonic acid of 3 mainly yields the 4,6- together with some 4,5-disulfonic acid.