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2,5-Diiodobenzoic Acid

    • Product Name 2,5-Diiodobenzoic Acid
    • Alias 2,5-DIB
    • Einecs 217-961-7
    • 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

    720372

    Product Name 2,5-Diiodobenzoic Acid
    Cas Number 13329-12-7
    Molecular Formula C7H4I2O2
    Molecular Weight 389.92 g/mol
    Appearance White to off-white powder
    Melting Point 249-253 °C
    Solubility In Water Slightly soluble
    Density 2.73 g/cm3
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, in a dry place
    Synonyms 2,5-Diiodobenzoic acid, Benzoic acid, 2,5-diiodo-
    Smiles C1=CC(=C(C=C1I)C(=O)O)I
    Inchi InChI=1S/C7H4I2O2/c8-5-1-2-6(7(10)11)4(9)3-5/h1-3H,(H,10,11)

    As an accredited 2,5-Diiodobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for 2,5-Diiodobenzoic Acid, 25 grams, is a sealed amber glass bottle with a secure screw cap and hazard labeling.
    Shipping 2,5-Diiodobenzoic Acid is shipped in tightly sealed containers, protected from light and moisture, and labeled according to regulations for hazardous chemicals. It is handled with care to avoid breakage or spillage. Appropriate safety documents, such as the Safety Data Sheet (SDS), accompany each shipment to ensure safe and compliant transport.
    Storage 2,5-Diiodobenzoic acid should be stored in a tightly sealed container, away from moisture and incompatible materials such as strong oxidizers. Keep it in a cool, dry, and well-ventilated area, preferably in a chemical storeroom. Protect from light and store at room temperature. Ensure that the container is clearly labeled and follow all standard laboratory safety protocols.
    Application of 2,5-Diiodobenzoic Acid

    Applications of 2,5-Diiodobenzoic Acid in Industrial Manufacturing

    2,5-Diiodobenzoic acid supports multiple advanced chemical value chains as a unique iodine-containing benzoic acid derivative. Our manufacturing expertise ensures consistent quality, meeting varied industrial standards for specialized synthesis, formulation, and integrated production workflows. Below we detail focused downstream application sectors with technical specificity suited to actual industrial processing.

    1. Active Pharmaceutical Ingredient (API) Synthesis: Intermediate in Antithyroid Drug Manufacturing

    This compound functions as a key intermediate during multi-step synthesis of antihyperthyroid APIs—such as propylthiouracil derivatives—particularly where controlled iodine introduction is critical for pharmaceutical efficacy and regulatory submissions. We supply material with batch consistency tailored for scale-up, supporting direct integration into cGMP synthesis protocols for regulated API facilities. Materials pass low-residue and trace metal screening based on pharmaceutical requirements. Downstream operators adjust reaction stoichiometry based on protocol: variations hinge on specific molecule design and in-process analytics.

    Industry compliance standards

    • ICH Q7 for Good Manufacturing Practice of APIs
    • US FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) synthesis monographs
    • USP General Chapter <761> NMR, <467> Residual Solvents Control

    Typical usage ratio

    • 0.5–1.2 molar equivalents relative to primary core structure; adjustment per synthetic route and yield optimization data

    Downstream process integration

    • Input to stepwise iodination or Suzuki coupling in closed reactor systems under nitrogen to avoid unwanted oxidation; feeds directly into crystallization or purification step

    Final product types

    • Antithyroid tablets (e.g., propylthiouracil derivatives)
    • Iodinated contrast agents (for diagnostic imaging APIs)
    • Experimental thyroid hormone analogs for clinical pipelines

    2. Halogenated Agrochemical Intermediates: Synthesis of Selective Herbicides

    High-purity 2,5-Diiodobenzoic acid finds established use as a halogen-donating intermediate for selective herbicide actives where aromatic iodination is mandatory for chemical performance and patent-specific formulations. Our material targets formulators requiring reliable iodine source for constructing bioactive benzoic acid derivatives, especially for new-generation herbicides compliant with international registration. Applications focus on batch and continuous flow processes, integrated with real-time purity monitoring.

    Industry compliance standards

    • FAO Specifications for Plant Protection Products
    • EPA 40 CFR Part 180—Tolerances and Exemptions for Pesticide Chemicals
    • REACH Regulation (EC) No. 1907/2006 for chemical safety assessment
    • ISO 9001:2015-certified QC batch release documentation

    Typical usage ratio

    • 0.8–1.0 equivalents per mole of target agrochemical core; slight excess used to drive completion in scale batches

    Downstream process integration

    • Dosed during early-stage halogenation or as an electrophilic aromatic source in coupling cascades for herbicide active structure production

    Final product types

    • Iodinated benzoic herbicide actives
    • Pre-mix pesticide intermediates
    • Custom wettable powder and emulsifiable concentrate herbicide formulations

    3. Advanced Materials: Precursor for Organic Electronic Components

    Our 2,5-Diiodobenzoic acid supports functionalization of aromatic monomers and oligomers in organic electronics, where controlled iodination optimizes electrical and optoelectronic properties. Manufacturers use this compound as a building block for liquid crystal display materials and research prototypes. Rigid batch specifications—ensuring trace halide and heavy metal levels—enable downstream integration with sensitive polymerization and microelectronic device fabrication.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for electronics
    • IEC 61249-2-21 (halogen-free electronic materials standards)
    • ISO/TS 80004-8:2013 (nanomaterials for electronic applications)
    • Internal QC protocols for microcontaminant thresholds

    Typical usage ratio

    • 0.3–1.0 mol equivalents per synthetic step, modulated depending on end-use polymer chain length and functionalization density

    Downstream process integration

    • Feeds into initial coupling or halogen-exchange stages of functional monomer and prepolymer synthesis, prior to spin-coating or device assembly

    Final product types

    • Liquid crystal display (LCD) precursor materials
    • Organic light-emitting diode (OLED) active layers
    • Specialty conductive polymers for electronic ink or sensors

    4. Specialty Chemical Synthesis: Precursor in Custom Dye Production

    Chemical producers utilize 2,5-Diiodobenzoic acid as a tailored intermediate when synthesizing halogenated dyes for textile, inkjet, and imaging applications. Integration centers on steps where controlled aromatic substitution is needed to attain color fastness or spectral tuning. Material purity and lot traceability are tailored for regulated manufacturers with closed-cycle colorant synthesis processes, using validated analytical controls for halogen ratios in the final formulations.

    Industry compliance standards

    • Oeko-Tex Standard 100: hazardous substances in textiles
    • EN 71-3:2019 (Safety of Toys—Migration of Certain Elements; for ink formulations)
    • REACH Annex XVII: restrictions on azo dyes and halogen-based colorants
    • ISO 1833-series for textile compositional analysis

    Typical usage ratio

    • 0.7–1.0 molar ratio to parent dye forming core structure; calibrated according to specific chromatic property targets and waste minimization

    Downstream process integration

    • Direct substrate in diazotization or subsequent coupling stages, then transitions into pigment isolation, milling, and blending lines

    Final product types

    • Iodinated textile dyes for high-performance fibers
    • Halogenated inkjet printer pigments
    • Special effect imaging dyes for security marking
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    Competitive 2,5-Diiodobenzoic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2,5-Diiodobenzoic Acid: A Manufacturer’s Perspective on Quality and Application

    Solid Foundation in Synthesis: Our Experience with 2,5-Diiodobenzoic Acid

    Over the years in our plant, we have handled many types of iodinated benzoic acids, but 2,5-Diiodobenzoic Acid—often identified by its structure where two iodine atoms attach to positions 2 and 5 on the benzoic acid ring—provides a set of advantages that keep chemists coming back to it in research and production. At the bench and in reactors, the compound appears as off-white crystalline powder, and it offers unique reactivity in both laboratory and industrial conditions. We take pride in supplying a product that meets the exact expectations of organic synthesis, pharmaceutical intermediates, and research projects requiring high-purity reagents.

    Physical Properties That Matter in Daily Operations

    Production relies on repeatability, and chemists rely on predictability. 2,5-Diiodobenzoic Acid melts in the range of 270–272°C, which speaks to stability during temperature-dependent processes. Its low solubility in water makes it simple to isolate by crystallization, eliminating the guesswork during product recovery. Most tasks do not require this product to dissolve quickly in water, so that works as an advantage rather than a limitation. Instead, the high density and solid form support smooth, container-to-reactor transfer with minimal product loss, keeping raw material costs down.

    Purity, Contaminants, and Real-World Results

    In our own runs, we saw that off-colors or cloudiness quickly signalled trace impurities, especially in such a heavily substituted aromatic system. Running careful controls at each stage, our finished 2,5-Diiodobenzoic Acid always tests greater than 98 percent by HPLC, which we find sufficient for most organic transformations, including complex cross-coupling reactions and advanced pharmaceutical syntheses. Iron, chloride, and sulfate contents receive just as much attention as the iodine assay, because even trace amounts can interfere with cerium, palladium, or silver catalysts. We monitor residual solvents thoroughly so downstream yields and safety remain unaffected. This is not just a lab concern. Unwanted side products in large-batch processes can increase rework, eat supply budgets, and slow scale-up.

    The Manufacturing Pathway: From Raw Material to Final Crystals

    Our facility’s batch reactors handle both benzoic acid iodination and post-reaction purification with reliability. By fine-tuning stoichiometry and temperature control, we ensure we achieve consistent iodine placement at the 2 and 5 ring locations, minimizing di- or tri-iodination at wrong positions. Filtration and pH control remain constant themes in our daily operations. To reduce mother liquor impurities, we rely on multistage crystallization. Once precipitated, our team inspects each batch visually and spectroscopically to confirm retention of fine, easily handled crystals. We use analytical tools such as NMR and GC-MS to confirm structure and purity. Our operators have learned to spot clumping, an early sign that ambient humidity or mechanical stresses have interfered somewhere along the drying process.

    Why 2,5-Diiodobenzoic Acid Stands Apart Compared to Other Iodinated Benzoic Acids

    Comparisons with 4-iodobenzoic acid or 3,5-diiodobenzoic acid come up often in our customer conversations. Single-iodine analogs simply cannot match the reactivity in Suzuki and Sonogashira coupling reactions that our 2,5 compound offers. Positioning iodine atoms at 2 and 5 opens up symmetrical substitution patterns, which proves valuable in synthesizing advanced materials or imaging agents. In our own experience, the double iodine on a single aromatic ring presents more selective modification options for medicinal chemistry and agricultural discovery work. For reactions sensitive to steric hindrance, our compound provides a structured yet reactive profile that supports higher yields than densely substituted alternatives like 2,4,6-triiodobenzoic acid.

    Proven Track Record in Key Industries

    We’ve shipped thousands of kilos to academic groups and production plants, most aiming to use 2,5-Diiodobenzoic Acid in small molecule synthesis, radiolabeling, and catalyst development. Many research teams cite its predictable behavior in oxidative aromatic substitutions and its suitability as a precursor for functionalized benzoic acids with electron-withdrawing characteristics. Some drug discovery platforms choose it as a scaffold for coupling reactions, benefiting from the selective reactivity at the ortho and para positions relative to the carboxyl group. In recent years, several electronics firms have drawn on its iodine content for experiments in organic semiconducting material synthesis, where the regular spacing of iodine atoms supports targeted bandgap engineering.

    Challenges in Handling, Shipping, and Storage

    We face our share of difficulties moving a material this dense and iodine-rich. In high-humidity regions and during summer months, caking risks increase, so we have established a packaging line that seals material under nitrogen before closing. Glass containers provide better performance over plastic as they do not interact with iodine and prevent unwanted contamination. Our warehouse stores product below 25°C, and airflow monitoring is standard protocol. By investing in these safeguards, we avoid reductions in shelf life or purity that can arise if crystals sit exposed to atmospheric moisture. During ocean freight, we coordinate temperature-controlled logistics partners, as heat buildup inside a container can shift melting range and degrade product quality.

    Application in Coupling Reactions and Beyond

    From the perspective of synthetic chemists, 2,5-Diiodobenzoic Acid gives straightforward activation for a variety of catalytic cycles. In house, we routinely supply partners developing cross-coupling reactions, especially those using palladium or copper systems. Its diiodo structure allows for stepwise introduction of different functional groups, producing valuable intermediates for active pharmaceutical ingredients and dye chemistry. Many customers report consistent results when switching from other iodinated acids; they appreciate the lower halogen-related by-product formation compared to alternatives with more crowded substitution patterns. The carboxylic acid group anchors the molecule for further derivatization, supporting both amidation and esterification pathways with minimal side product generation.

    Environmental and Regulatory Experience

    Working with iodine-based reagents requires care to prevent waste and manage effluents responsibly. In our plant, closed systems keep process emissions low. We recycle mother liquors for reprocessing, which cuts down both waste and raw material costs. Our wastewater treatment unit neutralizes residual halides and organic compounds before discharge. Authorities focus increasingly on minimizing persistent organic pollutants and halogenated waste streams, so we stay ahead by maintaining full chain-of-custody documentation and supporting every batch with traceability records. Our experience tells us industry can combine performance and environmental stewardship with the right engineering controls in place.

    Supporting Research and Scale-Up

    Some of our earliest partnerships began by sending gram samples to university labs interested in new cross-coupling conditions. Over time, those collaborations scaled to multi-kilo quantities. What separates a successful manufacturing operation in this field is willingness to supply both research and commercial volumes without loss in consistency. Many of our long-term customers return with higher order values after running small-lot tests that show our product works reliably. We engage directly with R&D teams to tune product granularity, packaging, or analytical specification as project needs shift. In every case, repeatable purity and physical integrity make a difference from lab scale to pilot plant output.

    Differences That Chemists Notice: User Experience

    Years of direct feedback shape how we continue to produce and package 2,5-Diiodobenzoic Acid. Several customers have pointed out that our crystalline form handles better—easier to weigh, pour, and dissolve in organic solvents. Fine powder-form products sourced elsewhere sometimes form clumps or static-laden clouds that delay formulation steps in their labs. Our team focuses on crystal habit as much as purity assays, using slow recrystallization to secure ideal morphology. This avoids issues common with amorphous or needle-shaped forms. Chemical structure alone does not guarantee real-world performance. Granules that flow easily through dosing units help reduce downtime and material loss, especially in automated synthesis setups.

    Packaging and Usability in the Field

    Many chemicals start to degrade once exposed to air or transferred multiple times. We take packaging seriously, using UV-blocking amber glass containers sealed under inert gas and tamper-evident closures. For bulk shipments, we provide containers with built-in humidity absorbers, which helps preserve integrity during customs or long ocean freight legs. We have learned some research groups prefer single-use vials for small-scale synthesis work, while scale-up partners choose bulk bottles for uninterrupted campaign runs. The goal is always the same—give every end user a clean, consistent experience from start to finish.

    Why Quality Matters for Fine Chemical Intermediates

    As manufacturers, we know purity and reliability directly impact how customers’ products perform downstream. The secondary effects can show up as improved yields in coupling reactions, sharper peaks in chromatography, or fewer purification cycles. For those in regulated industries such as pharmaceuticals, impurities—even below tolerance—can trigger repeat testing or require additional validation steps. We remain committed to strict in-process monitoring using modern equipment—HPLC, NMR, ICP-MS—rather than relying solely on post-production spot checks. This approach helps us catch variations early and avoid batch failures that cost both time and reputation.

    Upgrade Paths: Beyond Simple 2,5-Substitution

    A growing trend sees researchers using 2,5-Diiodobenzoic Acid as a jumping-off point for more complex targets. By employing selective coupling or nucleophilic aromatic substitution, customers prepare advanced materials and compounds with tailored properties. For example, adding boronic acids or alkynes at the diiodo positions enables the construction of multi-functional, high-value scaffolds for OLEDs, agrochemicals, or non-linear optical materials. Crucially, the symmetrical substitution pattern yields predictable reactivity, reducing the guessing game for subsequent steps.

    Global Sourcing and Customer Collaboration

    We serve partners in North America, Europe, and Asia, each with distinct logistical and regulatory challenges. Logistics teams work proactively with import/export authorities to ensure paperwork, classification, and documentation align with evolving international standards. By collaborating directly with chemists at the end use site, we address their requirements for particle size, residual solvent content, or packaging modifications—matching our production cycle with their development timelines. This reduces supply disruptions and shortens the bench-to-market cycle for new molecules built on our compound.

    Our Commitment to Continuous Improvement

    Every batch of 2,5-Diiodobenzoic Acid produced in our facility undergoes regular review. Operators receive ongoing training in best laboratory and industrial practices. We invest in technology that supports both quality and safety—such as improved dust collection, automated monitoring of key process steps, and batch traceability software. These measures keep both customer confidence and employee safety high. We listen to input from researchers and sourcing managers to drive upgrades in process and logistics.

    Conversations with End Users: What Drives Demand

    In our discussions with chemistry teams, demand for 2,5-Diiodobenzoic Acid centers on three factors: reliable reactivity, consistent availability, and assurance of purity. Some mention its status as a “workhorse” intermediate in developing specialty chemicals or new drug candidates. Others stress how a shortage or unexpected impurity can slow down whole project timelines. We find that close supplier-user communication keeps both sides ahead of potential delays, and this feedback loops into our scheduling, quality, and inventory management practices.

    Conclusion: The Human Element in Chemical Manufacturing

    Our staff understand that chemical production is both a science and a craft. Each day, we refine how we source raw iodine, optimize reaction conditions, and complete packaging to deliver material that serves more than a formula on a label. Year by year, we expand our ability to support advanced synthesis, reliable shipping, and technical collaboration, rooted in both hands-on manufacturing and a commitment to long-term success for everyone using 2,5-Diiodobenzoic Acid in their work.