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4-Iodobenzenesulphonic Acid

    • Product Name 4-Iodobenzenesulphonic Acid
    • Alias Benzenesulfonic acid, 4-iodo-
    • Einecs 220-936-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    657532

    Productname 4-Iodobenzenesulphonic Acid
    Casnumber 636-97-5
    Molecularformula C6H5IO3S
    Molecularweight 284.08 g/mol
    Appearance White to light yellow crystalline powder
    Meltingpoint 245-247 °C
    Solubility Soluble in water
    Purity Typically ≥98%
    Density 2.3 g/cm³
    Boilingpoint Decomposes before boiling
    Synonyms 4-Iodobenzene-1-sulfonic acid
    Storageconditions Store in a cool, dry place, tightly closed

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

    Packing & Storage
    Packing The 250g 4-Iodobenzenesulphonic Acid is securely packaged in a sealed amber glass bottle with a chemical-resistant screw cap.
    Shipping **Shipping for 4-Iodobenzenesulphonic Acid**: This chemical is shipped in tightly sealed containers to prevent moisture ingress and contamination. Packaging complies with relevant hazardous material regulations, incorporating labeling for oxidation and health hazards. Typically transported via ground or air freight, it requires cool, dry, and well-ventilated storage during shipment.
    Storage 4-Iodobenzenesulphonic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong bases and oxidizing agents. Protect it from moisture, direct sunlight, and sources of ignition. Properly label the container and use secondary containment to prevent accidental spills or environmental contamination. Store following all applicable safety regulations.
    Application of 4-Iodobenzenesulphonic Acid

    Applications of 4-Iodobenzenesulphonic Acid in Industrial Manufacturing

    As an established manufacturer of 4-Iodobenzenesulphonic Acid, we support downstream industries with consistent, high-purity material tailored for demanding synthesis processes. Our customers leverage this specialty intermediate across several precise sectors, where rigorous formulation, compliance, and production discipline are essential to yield value-added chemical products. Below we outline the key industrial segments and the unique parameters associated with each field.

    1. Pharmaceutical Active Intermediate Manufacturing

    Pharmaceutical companies apply 4-Iodobenzenesulphonic Acid as a critical halogenated aromatic intermediate during multi-step syntheses of certain anti-infective, antihypertensive, and central nervous system (CNS) active pharmaceutical ingredients (APIs). The unique iodine and sulphonic acid substitution allows for high selectivity in coupling, cyclization, and further functionalization stages within regulated API synthesis flows.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP), ICH Q7
    • European Pharmacopoeia (Ph. Eur.) and United States Pharmacopeia (USP) guidance for intermediate use
    • EMA and US FDA guidelines for solvent and impurity control
    • ISO 9001 quality management

    Typical usage ratio

    • 0.2–1.2 molar equivalents per synthetic stage, adjusted based on pathway step and conversion efficiency; subject to API-specific route optimization results

    Downstream process integration

    • Introduced in key halogenation, sulfonation, or Suzuki–Miyaura coupling steps
    • Charged as a crystalline solid or solution under nitrogen during 1,4-aryl iodide activation or ring closure phases

    Final product types

    • Anti-infective API intermediates
    • Antihypertensive drug key building blocks
    • Precursors for CNS-active molecules
    • Registered pharmaceutical substances completed via downstream purification

    2. Azo Dye and Pigment Synthesis

    Producers of performance dyes and high-stability pigments use 4-Iodobenzenesulphonic Acid to construct diazo compounds with unique colorfast properties. The sulpho group enhances water solubility and affinity for textile fibers, while the iodine substituent enables advanced coupling and controlled shade development for technical textile and ink applications.

    Industry compliance standards

    • OEKO-TEX® Eco Passport certification for restricted substance lists
    • REACH Annex XVII and SVHC compliance for aromatic amines
    • ISO 9001 for continuous pigment and dye production
    • ZDHC Manufacturing Restricted Substances List (MRSL) for dyehouses

    Typical usage ratio

    • 3–7% wt in diazotization bath, modulated for targeted chromophore intensity and solubilization profile

    Downstream process integration

    • Direct feed into diazotization reactors for subsequent azo coupling reactions
    • Post-coupling sulphonation or metal complexation for enhanced fastness

    Final product types

    • Disperse and reactive textile dyes
    • Complex metal pigment formulations for digital inks
    • High-performance colorants for plastics and fiber blends
    • Water-soluble pigment intermediates

    3. Specialty Polymer Functionalization

    Producers in the advanced polymer segment include 4-Iodobenzenesulphonic Acid during monomer functionalization for sulphonated aryl polymer and ionomer production. The molecule’s dual functionality facilitates targeted post-polymer modification, delivering sulfonic acid groups and halogen handle sites for subsequent crosslinking, conductivity improvement, or membrane customization.

    Industry compliance standards

    • ISO 14001 for environmental management in polymer plants
    • ASTM D3866 and D7981 for sulfonated polymers in membranes and composites
    • RoHS Directive (2011/65/EU) for electrical and electronic product polymers
    • ISO 9001 QC protocols for specialty polymer production

    Typical usage ratio

    • 0.5–5% by mass relative to base aromatic monomer, customized for ion exchange capacity or hydrophilicity targets

    Downstream process integration

    • Dissolved into aromatic monomer stream before suspension, emulsion, or solution polymerization
    • Utilized in sulphonation reactors or as a post-polymer grafting agent in extrusion/blending steps

    Final product types

    • Sulfonated poly(arylene ether sulfone) (SPAES) membranes
    • Ion-exchange resins for water treatment
    • Conductive membranes for fuel cells
    • Specialty functionalized copolymers for engineering plastics

    4. Electronic Chemical Synthesis (Liquid Crystal and Conductive Material Intermediates)

    The electronics industry integrates 4-Iodobenzenesulphonic Acid into fine chemical syntheses for advanced liquid crystal precursors, display additives, and select conductive polymer intermediates. Its precise substitution pattern enables fine-tuning of dielectric and optical properties in downstream assembly lines for flat-panel displays and flexible electronics.

    Industry compliance standards

    • IPC-4101 laminated material qualification for electronics
    • IEC 62474 for declarable substances in electronics manufacturing
    • ISO 14644 cleanroom control during chemical handling
    • JPCA guidelines for electronics chemical traceability

    Typical usage ratio

    • 0.8–2.0 equiv per coupling or substitution step; formulation tailored per dielectric specification or LC design

    Downstream process integration

    • Charged into palladium-catalyzed cross-coupling reactors under strictly moisture-controlled atmospheres
    • Fed to condensation or substitution synthesis lines for tailoring side-chain functionality

    Final product types

    • Liquid crystal intermediates for TFT-LCD panels
    • Precursors for OLED display chemicals
    • Functionalized aryl sulphonates for conductive adhesives
    • Additives for dielectric layer formulation

    5. Fine Chemical Catalyst Preparation

    Catalyst manufacturers employ 4-Iodobenzenesulphonic Acid as a ligand precursor during the synthesis of complex metal catalysts used in carbon–carbon coupling and specialty polymerization reactions. The sulpho and iodo moieties improve ligand coordination, catalyst solubility, and precise electron transfer characteristics crucial for downstream selectivity in high-value chemical production.

    Industry compliance standards

    • ISO 17025 for analytical laboratories validating catalyst performance
    • ISO 9001 for catalyst batch manufacture
    • Responsible Care® environmental stewardship
    • REACH registration for advanced catalyst intermediates

    Typical usage ratio

    • 0.1–0.5 molar equivalents per target metal center, precisely metered to achieve defined ligand-to-metal ratios specific to catalyst design

    Downstream process integration

    • Introduced during ligand complexation with palladium, platinum, or ruthenium salts in reflux or inert atmosphere conditions
    • Charged post-purification in catalyst support impregnation stages

    Final product types

    • Palladium-based cross-coupling catalysts
    • Ruthenium complexes for olefin metathesis
    • Supported organometallic catalysts for specialty polymerizations
    • Fine chemical hydrogenation catalysts
    Free Quote

    Competitive 4-Iodobenzenesulphonic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    4-Iodobenzenesulphonic Acid: Manufacturer's Insights on Value and Application

    Understanding 4-Iodobenzenesulphonic Acid through Practical Manufacturing

    From years spent on the production floor, it’s immediately clear: specialty chemicals such as 4-iodobenzenesulphonic acid cannot be treated as mere commodities. Our daily work with this organic compound has taught us that consistent purity and controlled physical characteristics make all the difference between a research grade reagent and a reliable industrial input. This chemical, recognizable by its molecular formula C6H4IO3S, appears as an off-white to pale brown crystalline solid. In our facilities, we strive for material with minimal off-color and consistently manages moisture to low levels, helping researchers and industrial chemists avoid surprises during sensitive reactions.

    Our 4-iodobenzenesulphonic acid is produced via direct sulphonation of iodobenzene, relying on precise control of reaction conditions and purification steps. This process reflects hard-earned expertise: too mild, and the conversion lags, giving low yields. Excessive heat, and you open the door to byproducts that can spoil downstream chemistry or throw off stoichiometry. The final material targets an iodine content above 35%, as lower grades disrupt demanding processes where every atom matters. The pH after dissolution typically hovers near zero, thanks to a tightly controlled sulphonation route that limits inorganic residue.

    Where 4-Iodobenzenesulphonic Acid Makes a Difference

    The most frequent question from direct users is often straightforward: How does this product improve my synthesis or workflow? Unlike more basic arenesulfonic acids, the iodo group in our compound is prized for cross-coupling chemistry, such as Suzuki or Sonogashira pathways. The C–I bond activates the ring, lowering the activation energy in metal-catalyzed couplings and making the sulfophenyl substrate particularly amenable to downstream functionalization, whether you’re building pharmaceutical scaffolds or custom ligands for catalysis.

    We regularly ship this material to medicinal chemistry labs developing kinase inhibitor cores, where sulphonate functionality imparts water solubility and the iodo position allows late-stage introduction of a variety of aromatic partners under gentle conditions. Even subtle differences in lot-to-lot iodine incorporation or trace metal content will impact both reaction yield and ease of chromatographic purification, a challenge we meet through multiple recrystallizations and rigorous in-process checks.

    What Sets This Compound Apart from Similar Reagents

    4-Iodobenzenesulphonic acid shouldn’t be confused with less substituted benzenesulfonic acids or with common halobenzenes. Its synthesis combines the challenge of regioselective sulphonation with the cost and handling complexities of iodine, which remains pricier and more hydrophobic compared to other halogens like chlorine or bromine. In real-world terms, this means the market does not flood with generic versions. Technical details matter: we keep residual inorganic salts far lower than what’s offered through many secondary sources, since these contaminate hydrogenation or palladium-catalyzed steps and often show up as unwelcome spots on TLC or HPLC.

    Our production teams spend significant effort optimizing dehydration of the final product, as excessive water content dissolves subtle functional groups from glassware labels to catalyst supports. This compound also differs in its safety and environmental profile. Unlike some sulfonated aromatic intermediates, the presence of the iodo group slightly lowers volatility but increases toxicity risk if inhaled or ingested at high concentrations. By producing at controlled scale and supporting comprehensive QC documentation, we help downstream users comply with BPR and REACH standards.

    Applications Gained from Real World Feedback

    Listening to feedback has taught us where our compound matters most. Recent years have seen increased interest in iodoarene-mediated C–C and C–N bond formation, as well as the role of sulfonate groups in tuning electronic effects during aromatic substitution. Specialty dye developers rely on our material for its predictable electrophilic behavior, enabling fine-tuned substitution patterns that single-halide or non-functionalized benzenesulfonic acids simply can’t match. In polymer synthesis, direct sulfonation yields performance additives that improve ionic conductivity, especially where thermal or oxidative stability is critical, such as in proton-exchange membranes.

    We’ve also noticed several contract research organizations switching from home-made 4-iodobenzenesulphonic acid to our manufactured material. Their main reason: repeatability. Self-synthesized batches, often prepared through less controlled routes, suffer unpredictable yields and residue. Our investment in process optimization leads to fewer rejected batches and measurable time savings for chemists focused on speed to publication or regulatory submission.

    Meeting Challenges: From Sourcing to Safe Delivery

    Reliable access to high-purity iodine, matched with strong relationships with raw material vendors, supports our consistent production. Seasonal fluctuations in iodine price or availability occasionally cause headaches for the market, but by stocking moderate reserves and qualifying multiple sources, we buffer against the most severe supply shocks. While not a silver bullet, routine supplier audits and dual-source strategies mean that downstream users rarely encounter unplanned gaps when scaling up projects.

    Safe packaging must not be an afterthought. 4-Iodobenzenesulphonic acid, because of its acidity and sensitivity to moisture, demands substantial quality in both the inner liner and external drums. Our operations team worked with chemical engineers to select HDPE containers with airtight seals, reducing risk of hydration or accidental contact during storage and transit. This focus on containment is not just compliance. It reflects direct experience with user complaints over clumped or hydrolyzed shipments in the early days, lessons that still inform our procedures.

    Looking Beyond Quality: Regulatory and Analytical Commitment

    Chemical compliance grows more complicated each year, with tracking, documentation, and certification now part of every shipment. We collaborate with our in-house analytical department to support every batch with validated HPLC, NMR, and elemental analysis, in addition to standard IR fingerprinting. Some customers need certified metal content below 10ppm, particularly where trace palladium or copper could poison catalytic steps. Each certificate reflects hard data, not assumptions, a practice encouraged both by regulatory oversight and our own reputation among experienced chemists.

    Regulatory expertise is always evolving. The sulfonic acid group in our compound means it falls under regional registration requirements, in some cases demanding justification of both toxicological and ecological studies. Our compliance team maintains a constantly reviewed dossier, ensuring quick turnaround for clients needing pre-research exemption statements or full REACH registration support. By keeping our own production exclusively in-house, oversight over every kilogram shipped supports both traceability and real-world confidence when audits arise.

    Economic and Industry Reality: Customization, Not Over-Specification

    Customization in chemical manufacturing frequently involves a delicate balance between laboratory perfection and industrial reality. Pharmaceutical research partners occasionally request unusual purities or tailored salt-free forms. Unless they can justify the benefit over our standard, most users find diminishing returns above 99% HPLC purity, not to mention the significant cost nudge. In practice, what researchers truly need is robust supply, consistent characteristics, and complete analytics—not a catalog of hypothetical grades.

    At scale, throughput and process safety trump idealized specification. We’ve built small- and mid-scale lines, so we can adapt to development-stage pilot projects just as readily as we can commit to regular bulk clients. Having close direct relationships with end users means we avoid complications typical when working through third-party traders, from simple misunderstanding on grade selection to much more serious concerns about warehousing stability or adulteration.

    Environmental Responsibility: Practical Challenges, Measured Steps

    Production of halogenated organics faces valid scrutiny for sustainability. Concentrated sulphuric acid and iodine-based waste both create handling burdens. Over the years, our team invested in recovery systems for spent acids and recycling methods for iodine, reducing landfill burden by more than half over the previous decade. True green chemistry for aryl iodides remains an ongoing struggle: each kilogram saved from waste counts, yet no process can claim zero footprint.

    For each improvement, from deionized final washes to lower-energy drying steps, we lean on both in-house expertise and collaborative networks. We join industry-led efforts on best practices for effluent treatment, demonstrating commitment to potable water safety and regulatory discharge compliance. Responsible stewardship, not only for our workforce but also for the regions hosting our production facilities, stays at the core of our operations.

    Addressing User Concerns: Common Pitfalls and Direct Responses

    Direct customers often seek advice on storage conditions or shelf life. Our experience shows that tightly sealed, cool, and dry environments perform best. While sulphonated aromatics resist slow oxidation, exposure to high humidity leads to cakes or colored films. We’re upfront about recommended storage: avoid wide temperature swings, keep containers closed when not in use, and transfer with clean, dry tools.

    On the equipment side, stainless steel valves and glass-lined reactors prevent unwanted metal leaching during manufacture as well as storage. Occasionally, labs run into trouble with polymer impurities when dissolving in non-aqueous solvents—a challenge minimized by controlling quench times and proper product washing. We welcome technical feedback; often, customer comments help us further minimize minor trace contaminants that, over time, enhance both reputation and product lifecycle.

    Comparing 4-Iodobenzenesulphonic Acid to Alternative Aromatic Sulfonates

    Chemists often ask whether it’s preferable to use the iodo compound versus its bromo- or chloro- analogues. In catalytic cross-coupling, the iodo variant reacts under milder conditions and with faster rates—advantageous when handling valuable or sensitive partners. Compared to bromo-derivatives, iodinated species reduce the need for excess base or higher reaction temperatures, which can erode precious starting material or complicate purification. Chlorinated aromatics, while cheaper, require harsh reagents for coupling and frequently generate competing side reactions.

    The higher price of the iodo compound comes with real value in process reliability and efficiency. Additionally, the strong electron withdrawing character provided by the sulphonate further activates the aromatic ring for palladium catalysis, distinguishing this material from non-sulphonated halobenzenes. The result is smoother libraries of target molecules for drug discovery or advanced materials, fewer aspects of process optimization, and higher overall yields.

    Supporting the Next Generation of Development

    Our manufacturing process has evolved alongside waves of change in synthetic chemistry. Increasingly, customers focus on complex, multi-step syntheses and need reliable starting points that streamline their route. We supply regular technical briefings and collaborate on pilot routes for unique downstream transformations, facilitating shorter project timelines and keeping costs predictable for research budgets.

    We also prioritize new requests for improved environmental profiles or substitutions where regulations limit certain functionalities. Our R&D team investigates upgraded purification pathways and greener solvents without compromising yield or stability. Any modifications undertaken respond to clear user needs, not speculative trends.

    Why Direct Manufacturing Expertise Matters

    Too often, buyers encounter repackaged material or inconsistent batches from market intermediaries. As the direct producer, we maintain full documentation and can answer detailed questions about physical and chemical properties traceable to every lot shipped. This transparency extends to shelf life studies, impurity profiling, and post-shipment support. Customers benefit from a partner with skin in the game for every kilogram handled, not a sales-only operation cutting corners where it’s least visible.

    Whether refining pharmaceutical pathways or scaling up for new polymers, chemists count on genuine, batch-documented supply chains with technical support rooted in practical production—not filtered through abstract marketing bluster. Our experience brings hard-earned perspective to each order, so every user receives not just a sample or bottle but confidence in the material’s performance, safety, and compliance with international best practices.

    Summary of Our Product Difference

    4-Iodobenzenesulphonic acid represents more than a mere chemical—each batch signals careful process management, transparency from synthesis to shipment, and a practical orientation toward tough regulatory and operational demands. We don’t just meet purity numbers; we solve real workflow problems for chemists who expect both technical performance and responsive support. Our commitment to material quality, reliable logistics, environmental responsibility, and open communication anchors every kilogram produced and shipped. The value emerges not from a theoretical catalog, but from daily hands-on work and steady collaboration with the people putting this compound to its full use.