Cas no 19437-42-4 (1,3,6-Naphthalenetrisulfonicacid, sodium salt (1:?))

1,3,6-Naphthalenetrisulfonic acid, sodium salt (1:?) is a water-soluble aromatic sulfonate compound characterized by its three sulfonic acid groups, which enhance its solubility and reactivity in aqueous solutions. The sodium salt form improves stability and handling, making it suitable for applications in dye synthesis, surfactants, and as an intermediate in organic chemistry. Its high sulfonation degree contributes to strong anionic properties, useful in dispersing and solubilizing agents. The compound’s rigid naphthalene backbone provides structural integrity, while the sulfonate groups facilitate interactions with cationic species. This combination of properties makes it valuable in industrial processes requiring precise molecular interactions.
1,3,6-Naphthalenetrisulfonicacid, sodium salt (1:?) structure
19437-42-4 structure
Product Name:1,3,6-Naphthalenetrisulfonicacid, sodium salt (1:?)
CAS No:19437-42-4
MF:C10H7NaO9S3
MW:390.341950654984
CID:202595
PubChem ID:23678425
Update Time:2025-06-13

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

Names and Identifiers

    • 1,3,6-Naphthalenetrisulfonicacid, sodium salt (1:?)
    • 1,3,6-NAPHTHALENETRISULFONIC ACID, SODIUM SALT, HYDRATE, MIXTURE OF ISOMERS
    • 1,3,6-NapthaleneTrisulfonicAcidTrisodiumSalt
    • naphthalene-1,3,6-trisulphonic acid, sodium salt
    • 1-amino-4-hydroxy-2-{4-[(2-oxoazepan-1-yl)methyl]phenoxy}-9,10-anthraquinone
    • EINECS 243-068-9
    • 1,3,6-Naphthalenetrisulfonic acid, sodium salt
    • 1,3,6-Naphthalenetrisulfonic acid, sodium salt (1:?)
    • DTXSID6066494
    • NS00083153
    • 19437-42-4
    • sodium;3,6-disulfonaphthalene-1-sulfonate
    • Inchi: 1S/C10H8O9S3.Na/c11-20(12,13)7-1-2-9-6(3-7)4-8(21(14,15)16)5-10(9)22(17,18)19;/h1-5H,(H,11,12,13)(H,14,15,16)(H,17,18,19);/q;+1/p-1
    • InChI Key: BERQWQSQOIEUMA-UHFFFAOYSA-M
    • SMILES: S(C1C=C(C=C2C=C(C=CC2=1)S(=O)(=O)O)S(=O)(=O)O)(=O)(=O)[O-].[Na+]

Computed Properties

  • Exact Mass: 433.87900
  • Monoisotopic Mass: 389.91498960g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 9
  • Heavy Atom Count: 23
  • Rotatable Bond Count: 3
  • Complexity: 726
  • 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
  • XLogP3: Not available
  • Topological Polar Surface Area: 166

Experimental Properties

  • Color/Form: Not available
  • PSA: 196.74000
  • LogP: 2.79450
  • Solubility: Not available

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

Comprehensive Overview of 1,3,6-Naphthalenetrisulfonic acid, sodium salt (1:?) (CAS No. 19437-42-4)

1,3,6-Naphthalenetrisulfonic acid, sodium salt (1:?), identified by its CAS No. 19437-42-4, is a highly versatile organic compound widely utilized in industrial and research applications. This sodium salt derivative of naphthalene trisulfonic acid is renowned for its exceptional solubility in water and its role as a key intermediate in the synthesis of dyes, surfactants, and specialty chemicals. Its unique molecular structure, featuring three sulfonic acid groups, enhances its reactivity and compatibility with various chemical processes, making it a valuable component in modern chemistry.

In recent years, the demand for 1,3,6-Naphthalenetrisulfonic acid, sodium salt (1:?) has surged due to its applications in environmentally friendly formulations. With growing consumer interest in sustainable chemistry and green manufacturing, this compound has gained attention as a potential alternative to traditional, less eco-friendly chemicals. Researchers are exploring its use in biodegradable detergents and low-impact textile dyes, aligning with global trends toward reducing environmental footprints. Searches for "eco-friendly sulfonic acid derivatives" and "water-soluble naphthalene compounds" have increased significantly, reflecting this shift in priorities.

The compound's CAS No. 19437-42-4 is frequently referenced in academic and industrial databases, underscoring its importance in chemical research. Its three sulfonate groups contribute to its high polarity, enabling it to act as an effective dispersant or solubilizing agent in aqueous systems. This property is particularly valuable in the formulation of advanced materials, such as conductive polymers and nanoparticle coatings, which are pivotal in electronics and nanotechnology. Online queries like "applications of naphthalene trisulfonates" and "sodium salts in material science" highlight the compound's relevance in cutting-edge technologies.

Another area of interest is the role of 1,3,6-Naphthalenetrisulfonic acid, sodium salt (1:?) in pharmaceutical intermediates. While not a drug itself, its structural features make it a useful building block for synthesizing more complex molecules. The compound's ability to improve solubility and bioavailability has prompted investigations into its potential for drug delivery systems. Searches such as "sulfonic acid salts in pharmaceuticals" and "naphthalene derivatives in medicine" demonstrate the growing curiosity about its biomedical applications.

From a commercial perspective, CAS No. 19437-42-4 is often sought after by manufacturers of specialty chemicals and industrial additives. Its compatibility with other anionic and non-ionic compounds allows for flexible formulation designs, catering to diverse industry needs. Additionally, its stability under various pH conditions makes it suitable for use in water treatment processes, where it can assist in controlling scale formation and corrosion. Popular search terms like "industrial uses of naphthalene sulfonates" and "water treatment chemicals" reflect these practical applications.

In conclusion, 1,3,6-Naphthalenetrisulfonic acid, sodium salt (1:?) (CAS No. 19437-42-4) is a multifaceted compound with significant industrial and scientific value. Its adaptability to emerging trends, such as green chemistry and advanced material development, ensures its continued relevance. As research progresses, this compound is likely to find even broader applications, further solidifying its position as a critical component in modern chemical innovation.

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