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2-Naphthylamine-4,6,8-Trisulfonic Acid

    • Product Name 2-Naphthylamine-4,6,8-Trisulfonic Acid
    • Alias Hoesch reaction acid
    • Einecs 217-437-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    599875

    Chemicalname 2-Naphthylamine-4,6,8-Trisulfonic Acid
    Molecularformula C10H9N(SO3H)3
    Molarmass 369.35 g/mol
    Casnumber 134-67-8
    Appearance Orange to brown powder
    Solubility Soluble in water
    Meltingpoint Decomposes before melting
    Ph Acidic in aqueous solution
    Synonyms Naphtylamine Acid G, Acid Yellow 99
    Storageconditions Store in a cool, dry place, tightly closed

    As an accredited 2-Naphthylamine-4,6,8-Trisulfonic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a sealed, amber glass bottle containing 100 grams of 2-Naphthylamine-4,6,8-Trisulfonic Acid, labeled for laboratory use.
    Shipping 2-Naphthylamine-4,6,8-Trisulfonic Acid should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Handle with appropriate personal protective equipment. Transport according to local, national, and international regulations for chemicals. Store in a cool, dry place and label clearly as a hazardous material if required by regulatory guidelines.
    Storage 2-Naphthylamine-4,6,8-trisulfonic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Protect it from direct sunlight, moisture, and incompatible substances such as strong oxidizers. Clearly label the storage area, and ensure access is restricted to trained personnel. Wear suitable protective equipment when handling to avoid direct contact or inhalation.
    Application of 2-Naphthylamine-4,6,8-Trisulfonic Acid

    Applications of 2-Naphthylamine-4,6,8-Trisulfonic Acid in Industrial Manufacturing

    2-Naphthylamine-4,6,8-Trisulfonic Acid supports highly specialized sectors in chemical manufacturing, enabling precise color formulation, advanced chemical synthesis, and analytical processes. The following scenarios detail its direct integration and process requirements for distinct downstream industries.

    1. Azo Dye Synthesis for Textile Colorants

    Our material acts as a core diazo component in the production of direct and acid azo dyes for polyester, nylon, and cellulose fibers. Facilities utilize the trisulfonic acid group to increase water solubility and enhance dye exhaustion on hydrophilic substrates. Technical staff adjust the mixing protocol depending on the shade and target substrate. Color matching lines require consistent batch quality and tight pH adjustment during coupling to ensure repeatable dye characteristics and fastness properties.

    Industry compliance standards

    • OEKO-TEX® Standard 100 – Restricted Substances List
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 105-C06:2010 (Textile - Tests for Colour Fastness)
    • REACH Annex XVII restrictions in EU textile dyes

    Typical usage ratio

    • 10–30% of total diazo salt batch weight (dosed against coupling component molarity and desired color depth)
    • Adjusted in line with shade intensity and fastness targets

    Downstream process integration

    • Introduced in the diazotization reactor stage prior to coupling reaction
    • Monitored for pH 4–5 and maintained under chilled conditions to prevent premature decomposition
    • Filtered and concentrated before spray-drying of final dye powder

    Final product types

    • Direct dyes for cotton fabrics
    • Acid dyes for wool, silk, and nylon
    • Colorants for industrial uniforms and technical textiles
    • Specialty paper dyes

    2. Intermediates for Colorimetric Analytical Reagents

    Laboratory and diagnostic reagent manufacturers utilize our raw material to produce stable chromogenic reagents for trace metal detection and quantitative water analysis. The bulk of production requires strict process control over sulfonation levels to ensure reproducibility of color response in end-use kits. High-purity protocols support trace analysis requirements, while downstream QC teams verify the consistency of absorption spectra for regulatory submission.

    Industry compliance standards

    • ISO 3696:1987 (Water for Analytical Laboratory Use)
    • USP/NF (if used in analytical procedures related to pharmaceuticals)
    • EN 1483 (Water quality — Determination of mercury)
    • ISO/IEC 17025:2017 (Testing and calibration laboratory processes)

    Typical usage ratio

    • 2–7% in reagent concentrate (depends on analytical sensitivity and end-user dilution rate)
    • Calculated based on calibration curve linearity during formulation

    Downstream process integration

    • Dissolved in deionized water with buffer at controlled pH (commonly 6.5–7.5) before reagent blending
    • Stabilized with preservative additives for extended kit shelf life
    • Filled into aliquots for portable test kit assembly

    Final product types

    • Water hardness and trace metals colorimetric test kits
    • Field-use reagent ampoules
    • Calibration standards for lab spectrophotometry
    • Customized indicator solutions for research diagnostics

    3. Lightfast Pigment Precursors for Technical Coatings

    Coatings manufacturers leverage the compound for synthesis of sulfonated pigment intermediates, particularly where water-based dispersions or high-solubility pigment pastes are required. Its use enhances pigment stability against photodegradation and chemical weathering in architectural, automotive, or industrial surface coatings. Quality control protocols focus on monitoring sulfonic group content, ensuring pigment compatibility with waterborne acrylic or polyurethane resin systems.

    Industry compliance standards

    • EN 71-3:2019 (Toy Safety - Migration of Certain Elements, for coatings on children's furniture or toys)
    • ASTM D3022 (Color and Gloss Retention)
    • ISO 12944-6:2018 (Paints and coatings — Protective paint systems)
    • REACH SVHC list, pigment content restrictions

    Typical usage ratio

    • 3–12% of pigment precursor mix (modified by target shade strength and resin compatibility)
    • Scaling varies with binder type and dispersion process

    Downstream process integration

    • Introduced during the aqueous pigment synthesis step
    • Blended under high-shear mixing before pigment precipitation
    • Filtered, dried, and milled before letdown into formulated coating

    Final product types

    • Waterborne decorative paints
    • UV-cured coating systems
    • High-durability pigment dispersions for industrial finishes
    • Colorants for plastics and composites

    4. Catalytic Organic Synthesis in Advanced Chemical Processing

    Synthetic chemistry operations use the trisulfonic compound as a ligand precursor or functional additive for specialized aromatic coupling reactions. It modulates electronic properties in palladium- or copper-mediated processes, enabling controlled reactivity for high-value intermediates. Technical teams focus on purity, by-product management, and precise stoichiometry to maintain process efficiency for pharmaceutical or fine chemical synthesis lines.

    Industry compliance standards

    • GMP guidelines (if used in pharma intermediate steps: ICH Q7, 21 CFR Part 211)
    • ISO 9001:2015 (Quality management in batch chemical processing)
    • Process-specific registrations under REACH for European production
    • Internal corporate QC protocols for impurity tracking (HPLC/GC analysis)

    Typical usage ratio

    • 0.2–1.5 equivalent molar ratio, precise calibration per reaction pathway
    • Determined by catalytic selectivity and downstream purification efficiency

    Downstream process integration

    • Added to pre-mixed base solution before metal catalyst introduction
    • Operated under inert gas atmosphere to minimize unwanted side reactions
    • Extracted post-reaction by aqueous workup and crystallization of target intermediate

    Final product types

    • Pharmaceutical synthesis intermediates
    • Agrochemical actives
    • Bespoke aromatic building blocks for specialty chemicals
    • Research-grade coupling agents
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