Cas no 304671-69-0 (1-Naphthalenesulfonicacid, 4-hydroxy-, sodium salt, hydrate (1:1:1))

1-Naphthalenesulfonic acid, 4-hydroxy-, sodium salt, hydrate (1:1:1) is a water-soluble organic compound commonly used as an intermediate in the synthesis of dyes, pigments, and other specialty chemicals. Its structure features a sulfonate group and a hydroxyl group on the naphthalene ring, enhancing its reactivity and solubility in aqueous systems. The sodium salt form ensures improved stability and handling, while the hydrate component contributes to consistent crystalline properties. This compound is valued for its role in producing high-purity derivatives and its compatibility with industrial processes requiring precise pH control. Its consistent composition makes it suitable for applications demanding reliable performance in chemical synthesis and formulation.
1-Naphthalenesulfonicacid, 4-hydroxy-, sodium salt, hydrate (1:1:1) structure
304671-69-0 structure
Product Name:1-Naphthalenesulfonicacid, 4-hydroxy-, sodium salt, hydrate (1:1:1)
CAS No:304671-69-0
MF:C10H9NaO5S
MW:264.230232954025
CID:299561
PubChem ID:329754980
Update Time:2025-08-05

1-Naphthalenesulfonicacid, 4-hydroxy-, sodium salt, hydrate (1:1:1) Chemical and Physical Properties

Names and Identifiers

    • 1-Naphthalenesulfonicacid, 4-hydroxy-, sodium salt, hydrate (1:1:1)
    • 4-Hydroxy-1-naphthalenesulfonic acid
    • 4-Hydroxy-1-naphthalenesulfonic acid sodium salt hydrate, technical grade, ~70%
    • SCHEMBL4075590
    • 4-Hydroxy-1-naphthalenesulfonic acid sodium salt hydrate
    • 304671-69-0
    • MDL: MFCD00150296
    • Inchi: 1S/C10H8O4S.Na.H2O/c11-9-5-6-10(15(12,13)14)8-4-2-1-3-7(8)9;;/h1-6,11H,(H,12,13,14);;1H2/q;+1;/p-1
    • InChI Key: OIKKPHLQUZYWQL-UHFFFAOYSA-M
    • SMILES: S(C1C=CC(=C2C=CC=CC2=1)O)(=O)(=O)[O-].[Na+].O

Computed Properties

  • Exact Mass: 264.00683884g/mol
  • Monoisotopic Mass: 264.00683884g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 15
  • Rotatable Bond Count: 1
  • Complexity: 319
  • Covalently-Bonded Unit Count: 1
  • 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: 2
  • XLogP3: nothing
  • Topological Polar Surface Area: 86.8?2

Experimental Properties

  • Color/Form: powder
  • Solubility: Not determined

1-Naphthalenesulfonicacid, 4-hydroxy-, sodium salt, hydrate (1:1:1) Security Information

  • Hazardous Material transportation number:NONH for all modes of transport
  • WGK Germany:3
  • Safety Instruction: 22-24/25

1-Naphthalenesulfonicacid, 4-hydroxy-, sodium salt, hydrate (1:1:1) Pricemore >>

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Additional information on 1-Naphthalenesulfonicacid, 4-hydroxy-, sodium salt, hydrate (1:1:1)

1-Naphthalenesulfonic Acid, 4-Hydroxy-, Sodium Salt, Hydrate (1:1:1) - CAS No. 304671-69-0

The compound 1-Naphthalenesulfonic Acid, 4-Hydroxy-, Sodium Salt, Hydrate (1:1:1), identified by the CAS number 304671-69-0, is a significant chemical entity with diverse applications in various industries. This compound is a derivative of naphthalene, a polycyclic aromatic hydrocarbon, and is characterized by the presence of a sulfonic acid group at the 1-position and a hydroxyl group at the 4-position. The sodium salt form of this compound is often used in its hydrated state, making it suitable for a wide range of chemical processes.

Naphthalenesulfonic acids are known for their versatility in chemical synthesis due to their ability to undergo various reactions such as sulfonation, hydroxylation, and ring-opening reactions. The sodium salt form of this compound is particularly valuable in pharmaceutical and agrochemical industries due to its enhanced solubility in water and its ability to act as an intermediate in the synthesis of more complex molecules. Recent studies have highlighted the potential of this compound as a precursor in the development of novel pharmaceutical agents targeting specific biological pathways.

The hydrate form of 1-Naphthalenesulfonic Acid, 4-Hydroxy-, Sodium Salt ensures stability during storage and transportation, which is crucial for maintaining its chemical integrity. This property makes it an ideal candidate for use in large-scale manufacturing processes where consistent quality is paramount. Furthermore, the sodium salt form facilitates its use in aqueous solutions, which is essential for many industrial applications such as dyeing agents and chemical intermediates.

Recent advancements in green chemistry have led to innovative methods for synthesizing naphthalenesulfonic acids with improved yields and reduced environmental impact. Researchers have explored catalytic systems that enable selective sulfonation of naphthalene derivatives under mild conditions. These methods not only enhance the efficiency of production but also align with global sustainability goals by minimizing waste and energy consumption.

In the context of material science, naphthalenesulfonic acids have been investigated for their potential as building blocks in the synthesis of advanced materials such as conductive polymers and hybrid materials. Their unique electronic properties make them suitable for applications in organic electronics and optoelectronics. For instance, studies have demonstrated that derivatives of this compound can be incorporated into polymer blends to enhance their electrical conductivity without compromising mechanical properties.

The sodium salt hydrate form of this compound also finds application in pharmaceutical formulations where controlled release mechanisms are required. Its ability to form stable salts with other active pharmaceutical ingredients makes it a valuable component in drug delivery systems. Recent research has focused on optimizing the crystallization process to achieve uniform particle sizes, which is critical for ensuring consistent drug performance.

In summary, 1-Naphthalenesulfonic Acid, 4-Hydroxy-, Sodium Salt, Hydrate (1:1:1) is a multifaceted compound with significant potential across various industries. Its unique chemical properties, combined with advancements in synthetic methodologies and green chemistry practices, position it as a key player in the development of novel materials and pharmaceutical agents. As research continues to uncover new applications and optimize existing processes, this compound will likely remain at the forefront of chemical innovation.

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