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CAS_5182 30 9

Trisodium naphthalene-1,3,6-trisulphonate

CAS NO.:5182-30-9

Trisodium naphthalene-1,3,6-trisulphonate (CAS: 5182-30-9) is a highly water-soluble naphthalene sulfonate derivative widely used in fields such as dyes, polymers, and chemical synthesis. Its sulfonate groups enable strong ionic interactions, making it effective as a dispersing, solubilizing, or functionalizing agent, and allowing incorporation into a variety of downstream formulations and materials.

 

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Product Name Trisodium naphthalene-1,3,6-trisulphonate
Synonyms SODIUMNAPHTHALENE-1,3,6-TRISULFONATE;SODIUM-1,3,6-NAPHTHALENETRISULFONATE;NAPHTHALENE-1,3,6-TRISULFONICACIDTRISODIUMSALT;1,3,6-Naphthalene-Trisulphonate;Sodium1,3,Chemicalbook6-naphthalenetrisulfonatetribasichydrate;trisodiumnaphthalene-1,3,6-trisulphonate;1,3,6-NaphthaleneTrisulfonicAcidTrisodium;trisodiumnaphthalene-1,3,6-trisulfonate
CAS NO 5182-30-9
Purity 98%
Appearance White to pale yellow to pale orange powder crystals
MF C10H5Na3O9S3
MW 434.31
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Trisodium naphthalene-1,3,6-trisulphonate (CAS: 5182-30-9) is a multifunctional sulfonated aromatic compound containing a naphthalene core substituted with three sulfonate groups. It primarily serves as an important functional intermediate in fields such as dyes, polymers, and materials science. Its specific applications are as follows:


1. Dye & Pigment Chemistry

Dispersing Agent:


The sulfonate groups provide strong ionic character, allowing it to act as a dispersant for insoluble dyes and pigments in aqueous systems.

Applications:

  • Dispersing agents in reactive, acid, or direct dye formulations

  • Stabilization of pigment suspensions for coatings and inks

  • Preparation of water-soluble dye intermediates

Effect:


Improves solubility, uniformity, and stability of dye formulations, while reducing aggregation in pigment dispersions.


2. Polymer & Materials Science

Functional Modifier:


Its ionic and aromatic structure enables incorporation into polymer systems to modify solubility, charge density, or surface properties.

Applications:

  • Water-soluble polymer additives

  • Ionic crosslinkers or functional monomers in polyelectrolytes

  • Surfactants for emulsion polymerization and colloidal stabilization

Effect:


Enhances compatibility with aqueous systems, improves dispersion, and contributes to controlled polymer network properties.


3. Chemical Synthesis & Versatility

Reactivity:


The sulfonate groups can participate in salt formation, ion-exchange reactions, or act as leaving groups in sulfonation-related transformations.

Applications:

  • Synthesis of sulfonated intermediates or functional materials

  • Formation of salts or complexes for specialty applications

  • Research in ionic or water-soluble aromatic compounds

Effect:


Expands molecular diversity and allows the design of functional water-soluble derivatives.


4. Points to Note

Stability:


Generally stable under standard laboratory conditions but hygroscopic; storage in a dry environment is recommended.

Usage Scope:


Primarily used in research and specialty formulations; large-scale industrial use depends on specific application needs.


Summary

The core value of trisodium naphthalene-1,3,6-trisulphonate lies in its water-soluble, multifunctional sulfonated structure, which enables its use as a dispersant, functional polymer additive, and intermediate in dye or specialty material synthesis. It is a versatile building block for aqueous systems, polymer engineering, and functional material design.

Packaging information: 1KG; 25KG; 100KG

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