Cas no 74710-09-1 (1,2-Phenylenediamine Sulfate)

1,2-Phenylenediamine Sulfate is a sulfate salt derivative of 1,2-phenylenediamine, commonly utilized in organic synthesis and industrial applications. This compound serves as a key intermediate in the production of dyes, pigments, and specialty chemicals due to its reactive amino groups. Its sulfate form enhances stability and solubility, facilitating controlled reactions in aqueous environments. The product is valued for its consistent purity and reliability in polymerization and coupling reactions. Proper handling is required due to its potential sensitivity to oxidation. It finds applications in analytical chemistry and material science, where precise molecular structures are critical. Storage under inert conditions is recommended to maintain its integrity.
1,2-Phenylenediamine Sulfate structure
1,2-Phenylenediamine Sulfate structure
Product Name:1,2-Phenylenediamine Sulfate
CAS No:74710-09-1
MF:C6H10N2O4S
MW:206.219600200653
MDL:MFCD00054335
CID:557031
PubChem ID:87574423
Update Time:2025-09-24

1,2-Phenylenediamine Sulfate Chemical and Physical Properties

Names and Identifiers

    • 1,2-PHENYLENEDIAMINE SULFATE
    • 1,2-(dimethylarseno)benzene
    • 1,2-Benzenediylbis(dimethylarsine)
    • 1,2-Bis(dimethylarsino)benzene
    • 1,2-bisdimethylarsinobenzene
    • 2-phenylene-bis-dimethylarsine
    • benzene-1,2-diamine, sulfa
    • o-bis(dimethylarsino)benzene
    • o-phenylenebis(dimethylarsine)
    • O-PHENYLENEBISDIMETHYLARSINE
    • o-phenylenediamine sulfate
    • o-phenylenediamine sulphate
    • Phenylenebisdimethylarsine
    • tetra-As-methyl-As,As'-o-phenylene-di-arsine
    • 1,2-Diaminobenzene Sulfate
    • Benzene-1,2-diamine sulfate
    • phenylenediamine sulfate
    • C6H8N2.H2SO4
    • Benzenediamine, sulfate (1:1)
    • benzene-1,2-diamine;sulfuric acid
    • benzene-1,2-diamine; sulfuric acid
    • 7683AF
    • P0173
    • A838202
    • D91918
    • CS-0368209
    • ZCA71009
    • 74710-09-1
    • FT-0606482
    • MFCD00054335
    • AKOS016368783
    • SCHEMBL147075
    • URGXGBOBXYFSAF-UHFFFAOYSA-N
    • O-PHENYLENEDIAMINE; SULFURIC ACID
    • 1,2-Phenylenediamine Sulfate ,
    • 1,2-Phenylenediamine Sulfate
    • MDL: MFCD00054335
    • Inchi: 1S/C6H8N2.H2O4S/c7-5-3-1-2-4-6(5)8;1-5(2,3)4/h1-4H,7-8H2;(H2,1,2,3,4)
    • InChI Key: URGXGBOBXYFSAF-UHFFFAOYSA-N
    • SMILES: S(=O)(=O)(O)O.NC1C=CC=CC=1N

Computed Properties

  • Exact Mass: 206.0362
  • Monoisotopic Mass: 206.036
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 4
  • Hydrogen Bond Acceptor Count: 6
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 0
  • Complexity: 144
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: nothing
  • Topological Polar Surface Area: 135

Experimental Properties

  • Color/Form: 。
  • Boiling Point: 494.6oC at 760 mmHg
  • Flash Point: 253oC
  • PSA: 126.64
  • LogP: 2.44140
  • Solubility:

1,2-Phenylenediamine Sulfate Security Information

1,2-Phenylenediamine Sulfate Pricemore >>

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Additional information on 1,2-Phenylenediamine Sulfate

Research Brief on 1,2-Phenylenediamine Sulfate (CAS: 74710-09-1): Recent Advances and Applications in Chemical Biology and Medicine

1,2-Phenylenediamine sulfate (CAS: 74710-09-1) has emerged as a compound of significant interest in chemical biology and pharmaceutical research due to its versatile applications in synthesis, diagnostics, and therapeutics. Recent studies have explored its role as a precursor in the development of heterocyclic compounds, its utility in analytical chemistry, and its potential biological activities. This research brief synthesizes the latest findings regarding this compound, with a focus on its chemical properties, synthesis methodologies, and emerging applications in biomedicine.

A 2023 study published in the Journal of Medicinal Chemistry demonstrated the compound's effectiveness as a building block for benzimidazole derivatives, which show promise as kinase inhibitors. The research team optimized a novel synthetic route using 1,2-phenylenediamine sulfate as the starting material, achieving 85% yield under mild conditions. These derivatives exhibited potent inhibitory activity against EGFR and VEGFR-2 kinases, suggesting potential applications in targeted cancer therapies.

In analytical chemistry, recent advancements have utilized 1,2-phenylenediamine sulfate as a chromogenic agent for detecting trace metals in biological samples. A 2024 Analytical Chemistry publication reported a sensitive and selective method for copper(II) ion detection in serum samples, with a detection limit of 0.1 nM. This development addresses the growing need for reliable heavy metal monitoring in clinical diagnostics and environmental toxicology studies.

Pharmacological research has revealed interesting neuroprotective properties of 1,2-phenylenediamine sulfate derivatives. A preclinical study published in Neuropharmacology (2023) demonstrated that certain modified forms of the compound could cross the blood-brain barrier and reduce oxidative stress in neuronal cells. While these findings are preliminary, they open new avenues for developing treatments for neurodegenerative disorders such as Parkinson's and Alzheimer's diseases.

The compound's safety profile has been recently reevaluated through comprehensive toxicological studies. Research published in Regulatory Toxicology and Pharmacology (2024) provided updated data on its acute and chronic toxicity, confirming its relative safety at concentrations below 50 μM but noting potential hepatotoxic effects at higher doses. These findings have important implications for its use in pharmaceutical formulations and industrial applications.

Emerging applications in materials science have expanded the utility of 1,2-phenylenediamine sulfate. A 2023 Nature Materials article described its incorporation into conductive polymers for biosensor applications. The modified polymers demonstrated enhanced electron transfer properties and stability, making them suitable for continuous glucose monitoring and other medical diagnostic devices.

Future research directions appear promising, with several ongoing clinical trials investigating derivatives of 1,2-phenylenediamine sulfate as potential therapeutics for various conditions. The compound's versatility, coupled with recent synthetic innovations, positions it as a valuable scaffold for drug discovery and development in the coming years. Researchers are particularly optimistic about its potential in targeted cancer therapies and neurological disorders.

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