Cas no 54914-98-6 (1,3,6-Naphthalenetrisulfonicacid, 7-amino-, sodium salt (1:3))

1,3,6-Naphthalenetrisulfonic acid, 7-amino-, sodium salt (1:3) is a water-soluble aromatic sulfonic acid derivative with three sulfonate groups, enhancing its solubility and reactivity in aqueous systems. The presence of an amino group at the 7-position allows for further functionalization, making it useful as an intermediate in dye synthesis, fluorescent probes, and other specialty chemicals. Its high solubility and stability under various pH conditions make it suitable for applications in analytical chemistry, catalysis, and material science. The trisulfonate structure contributes to strong ionic character, facilitating interactions with cationic species, which is advantageous in ion-exchange processes and surface modification applications.
1,3,6-Naphthalenetrisulfonicacid, 7-amino-, sodium salt (1:3) structure
54914-98-6 structure
Product Name:1,3,6-Naphthalenetrisulfonicacid, 7-amino-, sodium salt (1:3)
CAS No:54914-98-6
MF:C10H6NNa3O9S3
MW:449.320251941681
CID:374726
PubChem ID:170454
Update Time:2025-05-20

1,3,6-Naphthalenetrisulfonicacid, 7-amino-, sodium salt (1:3) Chemical and Physical Properties

Names and Identifiers

    • 1,3,6-Naphthalenetrisulfonicacid, 7-amino-, sodium salt (1:3)
    • Trisodium 7-aminonaphthalene-1,3,6-trisulphonate
    • Trisodium 7-amino-1,3,6-naphthalenetrisulfonate
    • trisodium 7-aminonaphthalene-1,3,6-trisulfonate
    • 1,3,6-Naphthalenetrisulfonic acid, 7-amino-, sodium salt (1:?)
    • sodium 7-aminonaphthalene-1,3,6-trisulphonate
    • Trisodium 2-amino-3,6,8-naphthalenetrisulfonate
    • Sodium 7-aminonaphthalene-1,3,6-trisulfonate
    • 2-Naphthylamine-3,6,8 trisulfonic acid, sodium salt
    • 7-Aminonaphthalene-1,3,6-trisulphonic acid, sodium salt
    • EINECS 259-396-0
    • trisodium;7-aminonaphthalene-1,3,6-trisulfonate
    • JHV5STQ48N
    • DTXSID10970245
    • 1,3,6-Naphthalenetrisulfonic acid, 7-amino-, sodium salt (1:3)
    • 1,3,6-Naphthalenetrisulfonic acid, 7-amino-, trisodium salt
    • 1,3,6-Naphthalenetrisulfonic acid, 7-amino-, sodium salt
    • 41016-61-9
    • EINECS 255-177-9
    • 54914-98-6
    • JNVDPZMCBPFWKR-UHFFFAOYSA-K
    • G70124
    • Inchi: 1S/C10H9NO9S3.3Na/c11-8-4-7-5(2-10(8)23(18,19)20)1-6(21(12,13)14)3-9(7)22(15,16)17;;;/h1-4H,11H2,(H,12,13,14)(H,15,16,17)(H,18,19,20);;;/q;3*+1/p-3
    • InChI Key: JNVDPZMCBPFWKR-UHFFFAOYSA-K
    • SMILES: S(C1C=C(C=C2C=C(C(=CC2=1)N)S(=O)(=O)[O-])S(=O)(=O)[O-])(=O)(=O)[O-].[Na+].[Na+].[Na+]

Computed Properties

  • Exact Mass: 448.88988
  • Monoisotopic Mass: 448.89
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 10
  • Heavy Atom Count: 26
  • Rotatable Bond Count: 0
  • Complexity: 716
  • Covalently-Bonded Unit Count: 4
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 223A^2

Experimental Properties

  • Boiling Point: °Cat760mmHg
  • Flash Point: °C
  • PSA: 197.62

1,3,6-Naphthalenetrisulfonicacid, 7-amino-, sodium salt (1:3) Pricemore >>

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Additional information on 1,3,6-Naphthalenetrisulfonicacid, 7-amino-, sodium salt (1:3)

1,3,6-Naphthalenetrisulfonic Acid, 7-Amino-, Sodium Salt (1:3)

The compound 1,3,6-naphthalenetrisulfonic acid, 7-amino-, sodium salt (1:3), with CAS No. 54914-98-6, is a highly specialized chemical entity that has garnered significant attention in various scientific and industrial domains. This compound is derived from the naphthalene framework, a polycyclic aromatic hydrocarbon, which serves as a versatile platform for the synthesis of numerous functionalized derivatives. The presence of three sulfonic acid groups at positions 1, 3, and 6 of the naphthalene ring system imparts unique chemical properties, while the amino group at position 7 introduces additional functional versatility. The sodium salt form (1:3) indicates a specific stoichiometric ratio of the compound with sodium ions, which is critical for its stability and application in different chemical environments.

Recent advancements in synthetic chemistry have enabled the precise control over the synthesis of such complex molecules. Researchers have employed various methodologies to optimize the yield and purity of 1,3,6-naphthalenetrisulfonic acid derivatives. For instance, studies have demonstrated the use of microwave-assisted synthesis to accelerate reaction rates while minimizing side reactions. This approach has been particularly beneficial in producing high-purity samples of 7-amino-1,3,6-naphthalenetrisulfonic acid sodium salt, which is essential for its application in sensitive analytical techniques such as chromatography and electrophoresis.

The naphthalene framework has long been recognized for its aromatic stability and electronic properties. The introduction of sulfonic acid groups significantly enhances the compound's water solubility and ion exchange capabilities. This makes it an ideal candidate for applications in ion-exchange resins and detergents. Furthermore, the amino group at position 7 introduces nucleophilic character, enabling the compound to participate in various condensation reactions. Recent studies have explored its potential as a precursor for synthesizing advanced materials such as conductive polymers and metal-organic frameworks (MOFs), where its sulfonate groups can act as coordinating ligands.

In the field of materials science, 1,3,6-naphthalenetrisulfonic acid derivatives have been investigated for their role in creating stimuli-responsive materials. For example, researchers have developed hydrogels incorporating these compounds that exhibit pH-responsive swelling behavior. Such materials hold promise in drug delivery systems and biosensors due to their ability to respond dynamically to environmental changes. The sodium salt form further enhances these properties by ensuring optimal ion mobility within the material matrix.

The application of 7-amino-1,3,6-naphthalenetrisulfonic acid sodium salt extends into the pharmaceutical industry as well. Its unique structure allows it to serve as a scaffold for drug design targeting specific biological pathways. Recent studies have highlighted its potential as a lead compound in anti-inflammatory drug development due to its ability to modulate key inflammatory enzymes. Additionally, its sulfonate groups facilitate efficient absorption and bioavailability when administered orally or parenterally.

From an environmental perspective, this compound has been studied for its role in wastewater treatment technologies. Its ion-exchange capabilities make it effective in removing heavy metal ions from contaminated water sources. Recent research has focused on optimizing its performance under varying pH conditions and incorporating it into scalable filtration systems.

In conclusion, 1,3,6-naphthalenetrisulfonic acid, 7-amino-, sodium salt (CAS No. 54914-98-6) is a multifaceted compound with applications spanning across chemistry, materials science, pharmaceuticals, and environmental engineering. Its unique structural features and functional groups make it a valuable tool for advancing cutting-edge research and industrial innovations. As scientific understanding continues to evolve, this compound is poised to play an even more significant role in shaping future technologies.

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