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4-Hydroxy-6-(3-Sulphoanilino)Naphthalene-2-Sulphonic Acid

    • Product Name 4-Hydroxy-6-(3-Sulphoanilino)Naphthalene-2-Sulphonic Acid
    • Alias K-acid
    • Einecs 241-823-2
    • 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

    603914

    Chemical Name 4-Hydroxy-6-(3-Sulphoanilino)Naphthalene-2-Sulphonic Acid
    Molecular Formula C16H11N1O7S2
    Molecular Weight 409.40 g/mol
    Cas Number 1149-61-9
    Appearance Brown to reddish powder
    Solubility Soluble in water
    Melting Point Decomposes before melting
    Synonyms Acid Yellow 99, C.I. 11360, Sudan Yellow 3G
    Ph Value Aqueous Solution 2-5
    Storage Conditions Store in a cool, dry place, protected from light and moisture

    As an accredited 4-Hydroxy-6-(3-Sulphoanilino)Naphthalene-2-Sulphonic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a sealed, labeled amber glass bottle containing 25 grams, with hazard markings and safety instructions clearly displayed.
    Shipping 4-Hydroxy-6-(3-Sulphoanilino)naphthalene-2-sulphonic acid is shipped in tightly sealed containers, protected from moisture and direct sunlight. Handle with care, following chemical safety regulations. Label properly as a potentially hazardous substance, complying with local, national, and international transport guidelines for chemicals. Use secondary containment during transit to prevent leaks or spills.
    Storage Store **4-Hydroxy-6-(3-Sulphoanilino)Naphthalene-2-Sulphonic Acid** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat and incompatible substances such as strong oxidizing agents. Protect from direct sunlight and moisture. Clearly label the storage container, and ensure only trained personnel handle the chemical with appropriate protective equipment.
    Application of 4-Hydroxy-6-(3-Sulphoanilino)Naphthalene-2-Sulphonic Acid

    Applications of 4-Hydroxy-6-(3-Sulphoanilino)Naphthalene-2-Sulphonic Acid in Industrial Manufacturing

    4-Hydroxy-6-(3-sulphoanilino)naphthalene-2-sulphonic acid supports several specialty chemical and colorant sectors as a critical intermediate. We supply consistent, QC-controlled grades to enable precise application in demanding industrial environments. Below, we detail primary application tracks where direct manufacturing use follows global compliance requirements.

    1. Azo Dye Intermediate for Reactive Dyes

    Dye manufacturers rely on this compound as a coupling component in the synthesis of high-performance water-soluble azo dyes for cellulose substrates. The sulphonate and hydroxy groups provide high affinity for fiber-reactive dye production. Integration ensures shade reproducibility and stable dye-fiber bonding for textile, leather, and specialty ink sectors.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textile safety)
    • REACH, Annex XVII (restrictions on azo dyes in EU)
    • ZDHC MRSL v3.1 (Zero Discharge of Hazardous Chemicals)
    • ISO 9001:2015 process audit traceability

    Typical usage ratio

    • 10–30% w/w as coupling component, adjusted based on chromophore strength, targeted color index, and dye purity requirements

    Downstream process integration

    • Dissolve in alkaline medium and react with diazotized aromatic amines during direct azo condensation
    • Integrate after pH adjustment within dye kettle, prior to purification and salting-out
    • Subject final dye to high-shear dispersion for cloth or yarn treatment

    Final product types

    • Cellulosic fiber-reactive dyes (Reds, Browns, Maroons)
    • Technical-grade dye blends for garment dyeing
    • Specialty inkjet dyes for high-fastness printing
    • Textile auxiliaries and formulation pre-blends

    2. Food Contact Pigment Synthesis

    This compound serves as a controlled building block in manufacturing certain food contact-compliant organic pigments. Its sulphonated aromatic backbone allows selective chromophore formation suitable for regulated packaging inks and coatings. Producers select this molecule for its batch consistency and minimized migration risk in indirect contact uses.

    Industry compliance standards

    • US FDA 21 CFR 178.3297 (colorants for polymers)
    • EU Regulation 10/2011 (plastic FCM migration)
    • EN 71-3 (toy safety: color migration limits)
    • Good Manufacturing Practice (EC) No 2023/2006

    Typical usage ratio

    • 3–15% by starting monomer weight, depending on desired pigment optical density, binder compatibility, and migration test outcomes

    Downstream process integration

    • Introduce during pigment lakes synthesis as an anionic naphthol precursor
    • Condense with diazotized coupling partners under controlled temperature conditions
    • Filter, wash, and mill for particle size standardization before masterbatch blending

    Final product types

    • Food packaging inks (flexographic, gravure)
    • Colored masterbatches for plastics in direct food contact
    • Toy coatings compliant with heavy metal limits
    • Paperboard and folding carton pigment dispersions

    3. Pharma Excipients: Diagnostic Dye Intermediate

    Diagnostic dye manufacturers use this naphthalene sulphonate as a coupling agent in the production of pharmaceutical-grade stains for in vitro analysis. Its high aqueous solubility and absence of prohibited trace contaminants are essential for blood and histology stain intermediates. Formulators value the controlled lot analysis (UV/VIS, residue on ignition) we supply for regulated medical sector use.

    Industry compliance standards

    • USP/NF monographs (colorant ingredient: purity/identity)
    • Ph. Eur. 2.7.3 (dyes for hematology staining)
    • ICH Q3D (elemental impurities: heavy metals)
    • ISO 13485 (medical device quality management)

    Typical usage ratio

    • Used at 5–20% w/w relative to diazo precursor, depending on stain intensity targets for blood films or cell smears

    Downstream process integration

    • Utilize in aqueous or buffered solution during diazotization and azo coupling
    • Purify by neutralization and vacuum filtration to meet compendial purity
    • Blend into dyes for microscopy kits under aseptic conditions

    Final product types

    • Medical diagnostic stains (e.g., Eosin, Sudan dyes)
    • Clinical histology test kits
    • Blood and tissue slide colorants
    • Laboratory dye standards

    4. Leather Colorant Manufacturing

    In the specialty leather dye sector, this raw material forms stable intermediates for the preparation of high-fastness anionic dyes. Its dual aromatic and sulphonic structure ensures rapid substrate uptake, resulting in uniform dyeing of bovine, ovine, and synthetic leathers. Batch manufacturing minimizes batch-to-batch variation for large-volume tanneries.

    Industry compliance standards

    • EN ISO 17234-1 (Azo colorants in leather: EU)
    • GB 20400-2006 (China leather dyeing limits)
    • LWG (Leather Working Group) Environmental Protocol
    • ISO 14001:2015 Environmental Management for process safety

    Typical usage ratio

    • 6–25% on dye solids, formulated based on leather type, finish, and resistance specifications

    Downstream process integration

    • Melt and blend during intermediate synthesis for dye precursor formation
    • Add to dye bath after pH/temperature stabilization in pre-tanning or post-tanning stages
    • Apply in finishing lines for coloration control and quality assurance

    Final product types

    • Finished aniline and semi-aniline leather dyes
    • Shoe, belt, and upholstery leather colorants
    • Automotive and fashion leather coatings
    • Specialized water-based pigment pastes

    5. Paper Coloration Chemicals

    Paper manufacturers apply this intermediate in the synthesis of substantive dyes for stationery, tissue, and packaging grades. Its high solubility supports rapid blending into aqueous dye synthesis at paper mills. Controlled trace metal and chloride content is critical for meeting stringent paper purity and printability requirements.

    Industry compliance standards

    • BfR Recommendation XXXVI (safe colorants for food packaging paper)
    • EN 646 (Colorfastness of paper and board)
    • ISO 1831 (industrial dyeing quality)
    • BRCGS Packaging Materials Global Standard

    Typical usage ratio

    • 3–10% per dye batch depending on desired tinting strength, application (wet-end or size-press), and final sheet weight

    Downstream process integration

    • React with diazotized amines for direct dye formation at wet-end of continuous paper machines
    • Use immediately prior to paper sheet or board formation
    • Support rapid blending into starch or synthetic size formulations for surface application

    Final product types

    • Colored writing and printing papers
    • Paperboard cartons for direct food contact
    • Sanitary tissue and napkin dyes
    • High-brightness specialty office papers

    6. Synthetic Fiber Dye Intermediates

    Polyester, nylon, and acrylic dye producers select this molecule for the synthesis of substantive dyes targeting synthetic fiber coloration. The well-defined sulphonate group confers enhanced exhaustion and wash fastness properties on finished textiles. Technical managers value its narrow impurity profile for minimizing side reactions during bulk acid or disperse dye manufacturing.

    Industry compliance standards

    • ISO 105 E01/E04 (wash and perspiration fastness)
    • EcoPassport by OEKO-TEX® (dye-chemical conformity)
    • REACH SVHC (authorization, restricted substances for clothing)
    • ZDHC Wastewater Guidelines

    Typical usage ratio

    • 8–40% as coupling component, adjusted for targeted shade depth and fiber dyeing method (exhaust, pad-batch, or thermosol)

    Downstream process integration

    • Incorporate during diazotization and azo coupling in acid dye plant reactors
    • Filter and granulate resultant dye intermediates for high-shear dyeing cycles
    • Specify for use in staple fiber and filament coloring lines

    Final product types

    • Polyester, nylon, and acrylic fabric dyes
    • Bright-shade carpet and upholstery dye blends
    • Acid-stable dye formulations for athletic and technical apparel
    • Bulk pigment concentrates for synthetic textile manufacturing
    Free Quote

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    Certification & Compliance
    More Introduction

    4-Hydroxy-6-(3-Sulphoanilino)Naphthalene-2-Sulphonic Acid: A Practical Commentary from the Manufacturing Floor

    A Deep Look into the Core of Dye Chemistry

    Anyone who has spent time turning raw aromatic hydrocarbons into complex dye intermediates will recognize the unique spot that 4-Hydroxy-6-(3-Sulphoanilino)Naphthalene-2-Sulphonic Acid holds in the value chain. Bringing this molecule from unobtrusive powders and liquids into a clean, stable, high-purity form shows just how far careful process engineering and practical chemistry have come.

    Chemists in research and in industry have relied on naphthalenesulfonic acid derivatives for nearly a century because of their robust chromophoric properties, water solubility, and resistance to degradation. What we see in 4-Hydroxy-6-(3-Sulphoanilino)Naphthalene-2-Sulphonic Acid is a solid example of those qualities, but further enhanced through select substitution and the introduction of the anilino group. On the production line this means frequent monitoring of reaction conditions and a tight watch on raw material quality. Batch to batch, purity rests on precise sulphonation and careful control of the hydroxy group placement—no shortcuts are possible.

    Model and Manufacturing Insight

    In practice, the batch model most often runs at scales suitable for the manufacture of dyestuffs designed for wool, silk, and various blends. The molecule’s configuration—marked by the 3-sulphoanilino group on the naphthalene ring and positioned hydroxy substituent—delivers specific absorption characteristics, especially in azo dye applications. Consistent product quality makes up the backbone of coloring processes across multiple industries, so each run involves controlled addition of sulfonating and aminating agents, continuous agitation, temperatures tailored to minimize byproduct formation, and real-time analytics for endpoint detection.

    We use glass-lined or stainless-steel reactors, depending on the scale, given the aggressive nature of sulphonation. Technicians measure pH and color strength every few hours, and a stubborn residue means someone from QA is probably about to walk down the line. Solids content runs in the high 90% range; this helps downstream users avoid unexpected dilution or instability in their dye formulations. Everyone—dyehouse, textile lab, or pigment designer—expects those numbers to stay stable, and with this product, they do.

    Specifications from Real Day-to-Day Work

    Nobody wants inconsistencies in shade or end-use fastness, so our in-house team puts every batch through a range of quality checks. Chromatography confirms purity and structural integrity. Moisture content sits low, supporting predictable solubility. Particle size impacts filtration times—too fine, and filtration drags, too coarse, and the final product doesn’t dissolve smoothly. Getting this right balances drying temperature with milling protocols. Unusually, this compound’s slight hygroscopicity helps maintain powder stability; it resists hard caking, allowing users to dose and dissolve without mess.

    Through several manufacturing campaigns, we’ve always flagged the importance of iron and heavy metal content. This molecule shows a knack for picking up trace metals during certain stages of the sulphonation process, especially if condensate quality slips. Based on spectroscopic analysis, heavy metals remain below 10 ppm. Experience says labs making food dyes or pharmaceutical colorants demand even stricter thresholds, but for textile applications, those values exceed expectations.

    Usage—Real Experience at the Interface of Chemistry and Application

    4-Hydroxy-6-(3-Sulphoanilino)Naphthalene-2-Sulphonic Acid ends up in a surprising range of dye formulations, chiefly as a coupling component for azo synthetic dyes. Anyone who works closely with triazine-based dyes or diazotization reactions recognizes its value: the sulphonated naphthalene core improves aqueous solubility; the hydroxy group ensures deeper shade strength and brighter chromatic expression. Processing technicians prefer it because, once diazotized, it reacts cleanly—fast coupling, manageable exotherm, minimal tar deposition.

    The dye molecules resulting from its use often show high affinity for protein fibers such as wool and silk. Color brilliancy, wash fastness, and resistance to light compare favorably against older intermediates. Textile processors comment that dye baths charged with products synthesized from this starting acid yield uniform coverage with fewer streaks or patches. In the laboratory, repeated dyeing cycles confirm that users seldom struggle with batch-to-batch variability—a relief compared to less refined intermediates. Analytical chemists highlight that running UV-Vis on final dyes confirms stable λmax values, supporting color consistency in consumer textiles.

    One unsung benefit: its compatibility with further substitutions. Dye chemists use it as a scaffold, introducing additional groups to fine-tune properties such as metal complexation, shade nuances, and pH stability. In printed circuit board manufacturing, color indicators using this acid provide stable, high-contrast markings that resist bleed and migration in humid environments. This practical utility comes directly from the thoroughness of synthesis protocols on the manufacturing side.

    Differences That Matter: Beyond Common Intermediates

    Compared to more basic naphthalenesulfonic acids or other sulphonated aromatic intermediates, 4-Hydroxy-6-(3-Sulphoanilino)Naphthalene-2-Sulphonic Acid sets itself apart through the specific balance of hydrophilicity, reactivity, and chromophore stabilization. The anilino group does more than provide a site for dye synthesis—it contributes steric and electronic effects that stabilize certain tautomeric structures. In day-to-day production, chemists notice how this influences shade stability and migration on fabrics.

    Producers of direct and acid dyes frequently choose this compound because it generates shades that are both brilliant and less prone to fading under sunlight or repeated washing. Even under high-temperature steaming, common with rapid textile processing, pigments derived from it hold their color noticeably longer than those from simpler naphthalenes. Formulators working on eco-label qualified processes appreciate its low tendency to form hazardous aromatic amines or decomposition products—data gathered from repeated GC-MS testing back this up. Where compliance with environmental standards plays a key role, this acid’s clean decomposition and modest environmental loading offer real advantages.

    Physical handling provides another real-world point of difference. Some sulfonated aromatics form dense cakes or sticky masses after milling and storage, giving rise to frustrations with automated dosing machines and increased downtime during cleaning operations. Our batches—carefully dried, milled, and sieved—move smoothly and show strong resistance to clumping. Fine powder flow enables high-speed automated feed, which becomes important at scale when plant managers count on maximizing throughput.

    From Manufacturing to the User’s Hands: Challenges and Solutions

    Every seasoned chemist knows the reality: consistent product means diligent process oversight. The manufacture of 4-Hydroxy-6-(3-Sulphoanilino)Naphthalene-2-Sulphonic Acid brings specific challenges. Sulphonation requires careful acid handling; the nitration and reduction stages demand robust inerting to safeguard both finished product yield and worker safety. Impurities from side reactions threaten to influence final color shade and product shelf life. Every batch faces scrutiny with HPLC and TLC methods, and the data guide regular process tweaks.

    Waste management can’t be ignored on an industrial scale. Given the acid’s solubility and the byproducts generated during synthesis, effluent treatment lines integrate real-time pH monitoring and neutralization, followed by activated carbon filtration. Early in our experience, we identified efficient water management as key not just for regulatory compliance but for avoiding process interruptions from accidental back-contamination.

    Worker health matters as much as product quality. Our teams receive routine training in best practices for handling sulfamic and sulfonic acids, and regular engineering upgrades make sure exposure levels fall well below occupational guidelines. Ventilation checks, continuous spill-response drills, and the use of closed system operations support safe, sustainable production.

    Supporting Claims with Factory Evidence

    Our ability to ensure high standard specifications comes down to the control we exert at every stage. Fatigue tested glass lining, specialized dosing pumps, and redundant temperature controls all reduce error rates—something raw product analysis shows clearly. Over the last calendar year, our internal failure rate—defined by off-spec color or solubility—dropped below 0.5% by weight, supporting reliability statistics used by end-users in the textile sector.

    Feedback from large dyehouses and specialty pigment labs also matters. They report that dye yields using this intermediate frequently exceed expectations on both laboratory and production scales. They rarely face purification bottlenecks, and most users eliminate the need to add stabilizers or rework vast batches due to pH drift or haze. Such feedback cycles back into small, continuous reformulations of reaction temperatures, reagent ratios, and filtration times.

    Developments in process chemistry have supported better impurity profiling. Using advanced LC-MS techniques, our teams track minor aromatic impurities to the 20 ppm level, well within textile user requirements, with further process improvements aimed at serving even more sensitive applications.

    Industry Feedback and Future Development

    Industry partners point to a growing need for dye intermediates that perform under diverse processing conditions—high speed, low liquor ratios, and water recycling lines among them. Against these challenges, the robust processability and simple handling of 4-Hydroxy-6-(3-Sulphoanilino)Naphthalene-2-Sulphonic Acid offer a degree of certainty. Azo dyes produced using this intermediate remain stable under closed-loop processing and integrate well with cost-effective production lines installing advanced wastewater reuse technology.

    Beyond textiles, research groups developing new organic conductors and antimicrobial coatings look for highly sulphonated and reactive intermediates. While historically limited to the dye industry, practical trials have shown this molecule supporting both electron-transfer materials and bioactive polymers. These uses demand purity and quality standards above the usual, pushing manufacturers to keep innovating synthesis routes and purification strategies. For our team, every market expansion starts with transparent process mapping and direct, persistent technical support for R&D partners.

    Green chemistry efforts shape every aspect of process development. Adoption of low-energy sulphonation steps, recycling of process water, and reuse of byproduct salts have all been implemented in the last five years. The compound’s compatibility with these techniques comes from its straightforward reaction sequence and manageable byproduct profile. Every new milestone in process optimization builds from the fact that experienced hands—real plant operators and bench chemists—work alongside automation to deliver stable product.

    Stable Quality: What Customers and Chemists Value

    Users in the dye industry have grown weary of unreliable intermediates, where small changes in impurity levels or solubility make large-scale production unpredictable. 4-Hydroxy-6-(3-Sulphoanilino)Naphthalene-2-Sulphonic Acid consistently delivers lot-tested results that users report in fewer rework cycles, improved process transparency, and higher-quality output. Its enduring record in high-stakes markets—wool and silk dyeing, specialty printing, and even medical diagnostics—shows the value of manufacturing control over every stage.

    Every request for technical data or aftersales support brings about a new round of reflection. The demands of high-performance dye development, regulatory compliance, and green process engineering all shape our continued investment in staff, equipment, and QC routines. Over time, this is how we keep process and product aligned with real industry needs.

    Insights and Continuing Practical Challenges

    No chemical process is free from hurdles. Seasonal shifts in raw materials, pressure fluctuations during sulphonation, and slight margin loss from energy prices all impact day-to-day reality more than any marketing brochure will admit. The value of 4-Hydroxy-6-(3-Sulphoanilino)Naphthalene-2-Sulphonic Acid as a reliable building block comes from an experienced team always ready to react to these challenges, supporting stable output that users downstream can count on.

    As regulatory frameworks evolve, especially with ongoing REACH compliance and international environmental benchmarks tightening every year, our synthesis and purification lines continue to adapt. The modular design of new process vessels and semi-batch operation supports short changeover times and easy integration of in-process cleaning, maintaining a flexible manufacturing setup capable of responding to both traditional dye sector demands and emerging functional materials research.

    Having the right analytical tools on factory floors matters. Week-to-week, methods such as solid-state NMR and FTIR confirm batch identity and purity, supplementing classic melting point checks with more nuanced structural data. This practice, born from repeated process reviews and a willingness to invest in up-to-date equipment, closes the loop between molecule synthesis and end-use performance.

    Summary View from the Plant

    Instead of chasing short-term wins through shortcuts or low-grade inputs, we’ve focused on repeatable, high-quality output supported by real manufacturing credentials. 4-Hydroxy-6-(3-Sulphoanilino)Naphthalene-2-Sulphonic Acid earned its place in our product lineup through practical demonstration—robust synthesis, reliable downstream performance, useful safety profile, and compatibility with next-generation process demands. This track record exists because of hard-earned lessons, real-world feedback, and a commitment to continuous improvement.

    Day after day, whether filling hopper silos or inspecting the clarity of the latest batch filtrate, our team keeps pushing the reliability and purity of this key intermediate forward. From the dye pot to the factory, the reputation of 4-Hydroxy-6-(3-Sulphoanilino)Naphthalene-2-Sulphonic Acid stands on the concrete efforts put in by manufacturing chemists, engineers, and plant workers who know that better chemistry always starts in the plant, not in the lab brochure.