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HS Code |
941398 |
| Chemical Name | Disodium 3,6-Dihydroxynaphthalene-2,7-Disulphonate |
| Molecular Formula | C10H6Na2O8S2 |
| Molecular Weight | 404.26 g/mol |
| Appearance | Yellow to brown powder |
| Solubility | Soluble in water |
| Cas Number | 1655-43-2 |
| Synonyms | Disodium salt of 3,6-dihydroxy-2,7-naphthalenedisulfonic acid |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Odor | Odorless |
| Ph Of 1 Percent Solution | Approximately 6.0-8.0 |
| Melting Point | Decomposes before melting |
| Uses | Intermediate in dyes and pigments manufacturing |
As an accredited Disodium 3,6-Dihydroxynaphthalene-2,7-Disulphonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of Disodium 3,6-Dihydroxynaphthalene-2,7-Disulphonate packaged in a sealed, labelled amber glass bottle for laboratory use. |
| Shipping | **Shipping Description:** Disodium 3,6-dihydroxynaphthalene-2,7-disulphonate should be shipped in tightly sealed containers, protected from moisture and light. Store and transport at room temperature. Ensure compliance with local and international chemical handling regulations. Label containers clearly with hazard information, and include safety data sheets with all shipments. Avoid release to the environment. |
| Storage | Disodium 3,6-dihydroxynaphthalene-2,7-disulphonate should be stored in a tightly sealed container in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Ensure the storage area is equipped to contain spills and labeled appropriately. Follow all relevant safety guidelines for handling and storage of chemical substances. |
Applications of Disodium 3,6-Dihydroxynaphthalene-2,7-Disulphonate in Industrial ManufacturingAs a direct manufacturer, we supply high-purity disodium 3,6-dihydroxynaphthalene-2,7-disulphonate to key industries where its sulfonated structure and reactivity drive specialized downstream processes. Below, we detail major application scenarios, focusing on compliance, dosage, integration in customer production lines, and resulting finished goods. 1. Synthetic Dye Manufacturing for TextilesTextile dye producers incorporate this intermediate in the diazo coupling step when producing reactive and direct dyes, especially for cotton and cellulosic fibers. The rigid aromatic framework supports strong chromophore development, enabling high washfastness and color depth. Formulators optimize input rates based on shade targets and process bath dynamics within their automated dye reactors. Industry compliance standards
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2. Electroplating Intermediate for Conductive CoatingsSpecialists in electroplated and conductive coatings use our product as an additive to improve bath stability and metal ion dispersion, enhancing deposit uniformity for electronic and hardware surface finishing. The compound’s sulfonate functionalities enhance complexation, improving metallic brightness and reducing hydrogen embrittlement in automated plating chains. Industry compliance standards
Typical usage ratio
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3. Color Developer in Thermal Paper ManufacturingThermal paper converters rely on this compound as a key color-developing agent in direct thermal imaging coatings for point-of-sale and logistics labels. Its naphthalene core reacts with leuco dyes under localized heat, forming crisp, high-contrast markings with durability under varying environmental exposures. Industry compliance standards
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4. Dye Intermediate for Leather ColorantsLeather finishing chemical manufacturers employ this intermediate during synthesis of metal-complex dye molecules. Its hydroxyl and sulphonate groups facilitate metal chelation, allowing the resulting colorants to provide controlled penetration and outstanding waterfastness on chrome-tanned hides. The precision in reaction timing and ratio impacts gloss retention and consistency in leather batch coloration. Industry compliance standards
Typical usage ratio
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5. Polymerization Retarder for Styrene-Based ResinsProducers of styrene and acrylic copolymers introduce this compound as a polymerization retarder to control molecular weight and minimize runaway reactions, particularly in continuous bulk and suspension polymerization systems. Its dihydroxynaphthalene core moderates free radical activity at trace levels, allowing precise product engineering during high-throughput monomer-to-polymer transformations. Industry compliance standards
Typical usage ratio
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6. Photographic Chemistry for Developer FormulationsManufacturers of photographic developer concentrates adopt this material as a secondary developing agent for black-and-white and color print chemistry. Its unique diazo-reactive moieties enhance midtone gradation and process stability during silver halide reduction stages, supporting consistent results across large-format and high-speed automated processors. Industry compliance standards
Typical usage ratio
Downstream process integration
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