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4-Iodobenzoic Acid

    • Product Name 4-Iodobenzoic Acid
    • Alias p-Iodobenzoic acid
    • Einecs 209-992-9
    • 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
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    Specifications

    HS Code

    868421

    Product Name 4-Iodobenzoic Acid
    Cas Number 619-58-9
    Molecular Formula C7H5IO2
    Molecular Weight 248.02 g/mol
    Appearance White to off-white powder
    Melting Point 275-277 °C
    Solubility In Water Slightly soluble
    Density 2.1 g/cm3
    Purity Typically ≥98%
    Synonyms p-Iodobenzoic acid, 4-Carboxyiodobenzene
    Smiles C1=CC(=CC=C1C(=O)O)I
    Inchi Key ZJIOYQPZTZVVMW-UHFFFAOYSA-N
    Storage Temperature Room temperature

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

    Packing & Storage
    Packing 4-Iodobenzoic Acid, 25g, is packaged in a clear, sealed glass bottle with a white screw cap and safety labeling.
    Shipping 4-Iodobenzoic Acid is shipped in tightly sealed, chemical-resistant containers to prevent contamination and moisture exposure. Packages are clearly labeled with hazard information and handled following safety regulations for laboratory chemicals. Shipping complies with relevant international and local transport guidelines for hazardous materials, ensuring safe and secure delivery.
    Storage 4-Iodobenzoic acid should be stored in a tightly closed container, kept in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect it from moisture and direct sunlight. Store at room temperature, avoiding extreme temperatures. Proper chemical labeling and secure storage are important to prevent accidental exposure or spills.
    Application of 4-Iodobenzoic Acid

    Applications of 4-Iodobenzoic Acid in Industrial Manufacturing

    As a direct producer of 4-Iodobenzoic Acid, we supply this specialty intermediate for several regulated and technically demanding downstream sectors. The following sections detail distinct industrial applications, specifying compliance, composition, production methods, and the final manufactured outputs in each area.

    1. Pharmaceutical API Synthesis

    4-Iodobenzoic Acid serves as a key building block in the synthesis of several pharmaceutical active ingredients, primarily for iodine-containing antimicrobials and thyroid-related compounds. It is introduced at early reaction stages to facilitate aromatic iodination, which is essential for the biological activity of target APIs. Process control requires batch-specific QC to ensure compliance with trace impurity limits mandated by both regulatory authorities and international pharmacopoeias.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP/NF Monographs for intermediates
    • European Pharmacopoeia (Ph. Eur.) Section 5.10 on starting materials
    • 21 CFR Part 211 current Good Manufacturing Practice for Finished Pharmaceuticals

    Typical usage ratio

    • Used at 0.2–1.2 molar equivalents relative to target API synthesis batch size; precise quantity based on stoichiometric iodine requirement and desired degree of substitution.

    Downstream process integration

    • Charged into controlled halogenation or Suzuki coupling reactors after preformulation checks
    • Participates in closed-system synthesis under inert atmosphere
    • Removed via filtration or solvent partition step before final API purification stages

    Final product types

    • Antithyroid agents (e.g., iopanoic acid derivatives)
    • Iodinated contrast media precursors
    • Antimicrobial intermediates

    2. Agrochemical Intermediates Production

    Agrochemical producers incorporate 4-Iodobenzoic Acid in the multi-step synthesis of high-performance herbicides and fungicides, especially those with benzoyl or halogenated aromatic motifs. The selection of this intermediate assists in achieving precise substitution patterns required for crop protection chemistry. Its controlled addition supports product consistency across production cycles vital for global regulatory registrations.

    Industry compliance standards

    • ISO 9001:2015 certified quality management
    • FAO/WHO Specifications for Agricultural Pesticides
    • REACH registration requirements (European Union) for chemical intermediates
    • US EPA PRN 98-10 for inert ingredient use in pesticide production

    Typical usage ratio

    • Incorporated at 0.5–4% weight of total product batch, subject to target molecule substitution and downstream process yield optimization.

    Downstream process integration

    • Fed into acylation or aromatic coupling reactors in liquid phase under controlled pH
    • Subjected to in-process analytical verification for residual iodide and benzoic acid
    • Spent ion removal and crystallization before downstream formulation blending

    Final product types

    • Iodinated herbicides for cereals and broadleaf crops
    • Specialty fungicide intermediates
    • Precursors for plant growth regulators

    3. Performance Polymer and Resin Modification

    Chemical companies add 4-Iodobenzoic Acid during the synthesis of specialty polyesters, polyamides, or epoxy resins to introduce iodine functional groups for enhanced thermal or UV resistance. This contributes to tailored compounding in advanced engineering thermoplastics, including materials for electronics, filtration membranes, and specialty coatings. Batch records specify entry at controlled polymerization steps to regulate degree of end-group modification.

    Industry compliance standards

    • EN ISO 9001:2015 for chemical manufacturing
    • UL 94 for polymer flame resistance (final product verification)
    • RoHS Directive 2011/65/EU for electronic materials
    • ASTM D256 for impact resistance of plastics (downstream QC)

    Typical usage ratio

    • 0.3–2 parts per hundred resin (phr), adjusted according to polymer matrix and iodine content specification in the finished material.

    Downstream process integration

    • Dosed during in situ polymerization or as a masterbatch additive
    • Blended in monomer feed or melt phase with in-line viscosity monitoring
    • Chain termination or functional modification by subsequent curing or crosslinking

    Final product types

    • Flame-retardant thermoplastics
    • Iodine-functional polyesters
    • High-performance epoxy coatings for electronics

    4. Dyes and Pigments Synthesis

    Dye manufacturers rely on 4-Iodobenzoic Acid for specialty halogenated pigment synthesis, enabling selective iodination of aromatic colorants used in textile, inkjet, and plastic dyeing. Its purity profile is critical for achieving consistent batch shade and metamerism resistance. Handling protocol requires strict control of by-product formation and maintenance of color strength per end-user specification sheets.

    Industry compliance standards

    • Oeko-Tex Standard 100 for textile chemicals
    • REACH Annex XVII for dye safety in Europe
    • ISO 9001 certification for manufacturing quality control
    • EN 71-3 compliance for pigments in toys and children’s products

    Typical usage ratio

    • 0.8–2.5 molar equivalents, adjusted to final dye structure and degree of halogenation required; dosage tailored for maximizing color yield and performance.

    Downstream process integration

    • Introduced into halogenation reactors at initial condensation step
    • Utilized as an intermediate before coupling or diazotization reactions
    • Purified via chromatographic or crystallization separation to ensure hue consistency

    Final product types

    • Halogenated azo dyes
    • Iodinated pigments for specialty inks
    • Colorants for temperature-resistant plastics

    5. Specialty Chemical Synthesis for Electronics

    Electronics material producers employ 4-Iodobenzoic Acid in the fabrication of advanced fine chemicals, particularly in the production of iodinated crosslinkers and aromatic ligands for organic semiconductors. The raw material’s controlled reactivity supports high-purity routes for optoelectronic material synthesis, where trace contaminants affect end-use device performance. Typical end-users require documentation on traceability and purity for every lot supplied.

    Industry compliance standards

    • ISO 14001:2015 for environmental management in chemical production
    • IEC 61249-2-21 Halogen-free material compliance (where applicable)
    • RoHS Directive for controlled substance traceability
    • Customer-specific QPL (Qualified Product List) for major electronics OEMs

    Typical usage ratio

    • 0.1–0.8 molar equivalents, set by the requirements of the electronic substrate or semiconductor product; closely monitored for high selectivity reactions.

    Downstream process integration

    • Introduced at the aromatic halogenation or crosslinking initiation step
    • Fed into ligand-coupling reactions for material functionalization
    • Purity inspected via HPLC and trace heavy metal analysis before shipment

    Final product types

    • Iodinated aromatic crosslinkers for printed electronics
    • Ligands for organic light-emitting diodes (OLEDs)
    • Microelectronic installation materials

    6. Laboratory and Diagnostic Reagents

    Producers of laboratory reagents and clinical diagnostics integrate 4-Iodobenzoic Acid as a defined matrix material or radiolabel precursor. In this segment, material traceability, documentation, and lot-specific analysis reports are required. The acid enters reagent supply chains where strict contamination limits guarantee compatibility with sensitive analytical systems and validated toxicological profiles.

    Industry compliance standards

    • ISO 13485:2016 for medical device and diagnostic reagent manufacturing
    • FDA Quality System Regulation (21 CFR 820) for in vitro diagnostic devices
    • CLSI C24-A2 specimen collection and handling standards
    • USP <1047> for analytical standards and reagents

    Typical usage ratio

    • 0.02–0.3% by weight in reagent formulation; varies by detection method and target sensitivity.

    Downstream process integration

    • Dissolved or suspended in buffer systems for conjugation or binding assays
    • Radiolabeled by nucleophilic substitution for tracer synthesis
    • Packaged under argon or nitrogen to avoid oxidative degradation

    Final product types

    • Standardized calibration reagents for analytical instruments
    • Iodinated labeling kits for immunoassays
    • Diagnostic radiotracers
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    Certification & Compliance
    More Introduction

    4-Iodobenzoic Acid: Direct from the Manufacturer’s Perspective

    Understanding the Core Features of 4-Iodobenzoic Acid

    Working in the field of fine chemical manufacturing for decades, some substances stand out due to their reliability and practical value. Among halogenated aromatics, 4-Iodobenzoic Acid distinguishes itself by a particular blend of stability, reactivity, and adaptability in synthesis. Its molecular structure (C7H5IO2, CAS 619-58-9) attracts attention from researchers and production teams who value clean conversions and consistent outcomes. Our production lines focus on achieving a product purity above 99%, which supports sensitive reaction conditions and scale-up processes alike.

    Working hands-on with aromatic iodides every day, some differences become clear over time. 4-Iodobenzoic Acid carries an iodo group at the para position on the benzoic acid ring, setting it apart from both o- and m-iodobenzoic acids, as well as from other substituted benzoic acids. This placement changes not just its melting point and solubility, but also the way it activates the aromatic ring for further chemical transformations. Compared to non-halogenated analogues, the iodine atom’s size and polarizability provide unique leverage in cross-coupling reactions, especially in Suzuki, Sonogashira, and Heck reactions. This has practical implications for chemists aiming to introduce complex groups onto aromatic systems without excessive byproducts or harsh conditions. Day in and out, requests from medicinal chemistry labs and crop science R&D units confirm this real-world demand.

    As a manufacturer, we deal with the gritty details: handling, packaging, and verifying every batch that leaves our facility. To keep production efficient and safe, we choose chemical-grade glass or high-integrity HDPE bottles for packaging, with nitrogen overlays where oxygen-sensitive applications call for it. Free-flowing, crystalline nature reduces dust generation, easing transfer during research and kilo-scale projects. We’ve taken pride in making sure shipment matches the needs of both small synthesis labs and large-scale contract manufacturing. Over years of feedback, we refined our sieving and drying protocols to prevent caking, ensuring seamless handling upon arrival.

    Specification Overview: What Sets Our 4-Iodobenzoic Acid Apart

    People sometimes overlook the difference between a reagent that “should work” and one that gives repeatable, clean results. To avoid waste and extra purifications, chemists look for not just high assay purity, but also low levels of heavy metals, moisture content below 0.5%, and virtual absence of trace halides. From our experience, benzoic acids contaminated by bromide, chloride, or even trace organic residues can poison catalysts or introduce side products. Our process minimizes these contaminants through slow crystallization and targeted washes, using solvents rigorously tested for compatibility and extractive strength. We test the product’s physical form using modern particle inspection techniques and validate it batch-by-batch by HPLC, GC-MS, and classic titrations.

    The competing products that reach the market through traders or repackers often show black specks, off-odors, or broad melting points. We take daily pride in shipping 4-Iodobenzoic Acid that holds a snow-white, nearly odorless quality, with a sharp, consistent melting range close to 255°C—this reflects proper handling from synthesis to finish. Seasoned chemists immediately notice whether a crystalline product pours freely, dissolves cleanly in analytical solvents, and leaves little residue in round-bottom flasks. Those are the marks of care invested at every stage of real chemical manufacturing, not just bulk repackaging.

    Typical Uses in Laboratory and Industry

    Many research projects begin with an idea, but they live or die on the ability to reliably source quality reagents. 4-Iodobenzoic Acid continues to find a place at the very start of varied target-oriented syntheses. Its carboxylic acid group opens the door for amide coupling, ester formation, and further derivatizations, while its iodo group sets the stage for direct introduction of aryl, alkenyl, or alkynyl fragments. In my daily interactions with small molecule discovery teams, 4-Iodobenzoic Acid remains a staple in late-stage diversification—particularly for scaffolds used in pharmaceutical lead optimization.

    The same qualities make it attractive to those working on specialty polymers or advanced materials. For instance, its high-purity profile makes it suitable for manufacturing liquid crystals and specialty resins, where trace ionic contaminants can undermine performance. In the development of imaging agents or contrast media, direct halogen-substituted aromatics serve as backbone components, and 4-Iodobenzoic Acid proves efficient for such transformations. Its chemistry reduces the need for extra purification steps, especially when sensitive downstream coupling reactions are involved. This spares time, cuts costs, and streamlines process development—a fact hard-earned through communication with customer R&D departments tasked with lean, reproducible syntheses.

    In academic circles, graduate students lean on this acid for method development or as a starting block in teaching advanced organic synthesis, often to demonstrate site-selective C–C or C–N bond formation. The reliable, sharp melting range and clear spectral characteristics simplify laboratory instruction and grading, avoiding confusion from impure or degraded starting materials.

    How Manufacturing Approach Influences Consistency

    Scaling 4-Iodobenzoic Acid isn’t only about chemistry—it pulls in years of experience with equipment care, process monitoring, and batch record-keeping. A glass-lined reactor jacketed for temperature control and fitted with in-line sample ports stands at the heart of our approach. We use high-purity iodine sources and maintain excess acid scavengers to divert ortho- and meta-substituted byproducts. Our filtration systems use inert atmospheres and minimal handling between crystallization and drying to minimize both hydrolysis and oxidation by environmental oxygen.

    Instrumental checks ensure each lot respects published specifications for purity and moisture. These aren’t just paperwork or box-checking exercises—they prevent downstream headaches in cross-coupling or amidation steps. By managing crystallization rates closely, we lock in batch-to-batch reproducibility of particle size and density, so researchers and production chemists don’t battle unexpected solubility or sedimentation quirks. In response to customer input, we offer technical bulletins with advice on storage conditions, solubility charts, and recommendations for opening sealed containers to avoid contamination spikes.

    Contrast with Other Halogenated Benzoic Acids and Interchangeability

    Direct user feedback over years of supply has made clear how often substituent position and choice of halogen change practical chemistry. 4-Iodobenzoic Acid offers greater reactivity in palladium-catalyzed coupling reactions than its brominated or chlorinated counterparts, due to ease of oxidative addition at the C–I bond. It also presents cleaner reaction profiles compared with o- or m-iodobenzoic acid derived intermediates, which sometimes trigger unwanted side-reactions or additional isomeric products. For most arylation methodologies, chemists prefer the para isomer for both steric and electronic reasons.

    Users sometimes ask why not begin with less expensive bromo or chloro analogs. In reality, iodobenzoic acids command a higher price due to elevated raw material and processing costs. Despite that, for those reactions where catalyst lifetimes matter, or where yield and purity are tightly monitored, the extra investment pays dividends in fewer repeated runs, shorter work-up times, and less waste. We have seen in practice how higher loading in coupling reactions, or more forceful activation conditions, actually lead to more column chromatography, extra time, and raw material loss—things no manufacturing chemist enjoys battling.

    Common Pitfalls in Sourcing and Handling

    End-users in research and production often share frustrations. One recurring theme is the disappointment of buying what looks like a good deal, only to spend days purifying a poorly made lot. Black specks typically signal metal contamination. Broad, lower melting points may reflect incomplete drying or solvent traces. Recurrent off-odors sometimes mean organic decomposition, indicating a storage or packaging failure. From our side, it’s clear that robust, factory-controlled production makes a real difference, even more so when labs are pressed to meet deadlines or regulatory requirements.

    We go further than most to train our personnel in best-in-class handling and packing. Repeated investments in drying ovens, desiccant systems, and on-site analytical labs make batch consistency possible. Ongoing maintenance of our reactors, filtration equipment, and analytical tools justifies the confidence our users show by returning for repeat orders. Our team always welcomes technical queries, and we draw on case histories and empirical results accumulated over many years to answer them in detail—not just with data, but also with practical tactics for recovery, purification, or process improvement.

    Supporting Sustainable and Safe Chemical Practices

    Responsible manufacturing of fine chemicals leads to less environmental impact, lower waste, and safer conditions for workers and users. Our 4-Iodobenzoic Acid line features closed-drain systems, minimized solvent loss, and routine recycling of cleaning solutions to reduce environmental burdens. We have adopted real-time monitoring for effluent streams, using both in-line and at-line sensors. In practice, this means our finished product doesn’t merely meet regulatory standards—it stays ahead of future compliance changes.

    Our storage advice comes from daily reality, not just technical guidelines. Keep containers in a dry, cool area, ideally under inert gas if using over many weeks. Open only what’s required; reseal immediately. This keeps both quality high and risks low for handlers. Old habits die hard, so we use site walk-throughs and internal audits to encourage best practices and reduce accidental exposure. Customers benefit from these steps through increased shelf life and less variability between orders, saving time and reducing stress for supply chain managers.

    Troubleshooting and Real-World Problem Solving

    No fine chemical lives in a vacuum. Sourcing and working with 4-Iodobenzoic Acid brings occasional curveballs: variable solubility in planned solvents, unexpected impurities from aggressive reaction partners, or challenging filtrations in process scale-ups. Because we work with these complications ourselves, we gather and share advice that saves time and cost. Recent process development in an agrochemical project called for pentafluorophenyl coupling—the team ran into reproducibility issues with third-party 4-Iodobenzoic Acid, but when supplied our consistently produced acid, yields shot up and purification time fell by nearly half.

    Across synthesis platforms, the key to reduction in side products often lies in minimizing input impurities. Our technical support won’t just cite numbers but dives into raw analytical traces and practical post-run work-ups. We have advised users on gentle heating strategies to aid dissolution and have developed application notes on simple solvent screening for optimal reactivity. Such support goes beyond selling a commodity—it’s part of an ongoing partnership with working chemists who prize real, results-driven advice.

    Continuous Improvement through Industry Collaboration

    Our manufacturing processes do not stay still. Driven by both regulatory trends and evolving applications in chemical and pharmaceutical industries, we routinely review reaction throughput, downstream equipment, and supply chain logistics. Bench chemists and plant operators contribute practical feedback, which feeds into site improvements. This hands-on approach fosters upgrades to drying technologies, better yield management through crystal seeding, and often sparks innovation in waste stream reduction. Direct engagement with end-users provides the impetus to improve, not just to meet existing demand but to anticipate new ones—such as requirements from green chemistry initiatives or more demanding specifications from medicinal chemistry consortia.

    Over time, we’ve forged ongoing collaborations with university researchers and industrial consortia. These connections help us stay ahead of technical challenges—such as demand for ultra-high purity, specialty particle sizes, or tighter controls on trace metal content. These collaborative projects enrich our own manufacturing know-how and allow us to refine every batch, meaning newer and more challenging targets are just as achievable as the everyday jobs.

    Looking Ahead: Evolving Demands and Manufacturing Responses

    In today’s environment, demand for 4-Iodobenzoic Acid is no longer limited to traditional organic synthesis or pharmaceutical intermediates. We see emerging interest from the electronics sector, where specific halogen substitution patterns modulate material properties in advanced coatings or microfabrication. These users challenge us to reach ever-lower levels of unwanted ionic contaminants. In response, we continuously invest in purification equipment, expand analytical capacity, and seek feedback on downstream challenges seen by our customers.

    Flexible order sizes accommodate research or process chemistry—allowing cost-effective piloting of new reactions or the supply of production campaigns that might stretch into metric tons. Our experience informs packing line choices and shelf-life monitoring. Site visits by regulatory inspectors or third-party auditors are welcomed; we regularly demonstrate robust traceability, from batch synthesis logs to finished-product analyses.

    Key Takeaways on the Value of Direct-from-Manufacturer Supply

    Buying 4-Iodobenzoic Acid directly from the producer closes the gap between what chemists expect and what arrives at their bench. Contact with daily operational realities shapes how we approach custom requests or evolving specifications. Consistent supply, technical transparency, and real-world troubleshooting support contribute to trust over the long haul. As chemical manufacturing keeps stepping up to new regulatory and technical benchmarks, we stay invested in the details and distinctions that separate a quality reagent from just another commodity.

    Future challenges will surely arise, from tighter impurity controls to new downstream coupling strategies, but these are familiar territory for a manufacturer who goes beyond simply making a chemical. Our commitment lies in providing more than a product: every gram of 4-Iodobenzoic Acid that leaves our doors has behind it the experience, focus, and pride of those who made it. We invite practical, technical conversations because those exchanges improve both our craft and the work done by customers who trust and rely on us.