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2-Bromo-5-Iodobenzoic Acid

    • Product Name 2-Bromo-5-Iodobenzoic Acid
    • Alias 2-Bromo-5-iodobenzoic acid
    • Einecs 261-950-2
    • 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

    725825

    Product Name 2-Bromo-5-Iodobenzoic Acid
    Cas Number 6937-35-1
    Molecular Formula C7H4BrIO2
    Molecular Weight 326.92
    Appearance White to off-white powder
    Melting Point 222-226°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 2.33 g/cm³ (approximate)
    Storage Conditions Store at room temperature, keep container tightly closed
    Smiles C1=CC(=C(C=C1C(=O)O)Br)I
    Inchi InChI=1S/C7H4BrIO2/c8-5-2-1-4(7(10)11)3-6(5)9/h1-3H,(H,10,11)

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

    Packing & Storage
    Packing Amber glass bottle with a screw cap, labeled with product details; contains 25 grams of 2-Bromo-5-Iodobenzoic Acid.
    Shipping 2-Bromo-5-Iodobenzoic Acid is shipped in secure, airtight containers to prevent moisture and contamination. The chemical is classified as hazardous; thus, it requires handling by trained personnel following all relevant safety and transportation regulations. Shipping documentation includes hazard identification and safety instructions to ensure safe and compliant delivery.
    Storage 2-Bromo-5-Iodobenzoic Acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from light and moisture. Store at room temperature, avoiding excessive heat. Proper labeling and secure shelving are essential to prevent spills and accidental contact.
    Application of 2-Bromo-5-Iodobenzoic Acid

    Applications of 2-Bromo-5-Iodobenzoic Acid in Industrial Manufacturing

    2-Bromo-5-Iodobenzoic Acid is widely used as a functional intermediate in pharmaceutical synthesis, agrochemical development, fine chemical processing, and advanced material research. As a manufacturer, we supply this compound to specialized industries requiring precise molecular transformations and high-purity raw materials.

    1. Pharmaceutical Intermediates for API Synthesis

    Major pharmaceutical companies use 2-Bromo-5-Iodobenzoic Acid to build key intermediates for active pharmaceutical ingredient (API) manufacturing, especially in targeted oncology therapies and selective enzyme inhibitors. Its halo-substitution pattern enables regioselective coupling reactions, facilitating downstream modifications such as Suzuki-Miyaura and Buchwald-Hartwig cross-coupling processes. Typically, manufacturers rely on this material in multi-step synthetic pathways under cGMP-controlled environments where trace metal and halide content are strictly monitored to guarantee final API quality.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP General Chapter <923> Residual Solvents)
    • EU Guidelines on Impurities in New Drug Substances (ICH Q3A)
    • FDA 21 CFR Parts 210/211 (cGMP)

    Typical usage ratio

    • 0.03–0.12 mol equivalent relative to the core pharmaceutical scaffold, adjusted according to target molecule complexity and process yield optimization

    Downstream process integration

    • Introduced post-core skeleton assembly, utilized in halogen exchange, palladium-catalyzed couplings, or as a termination agent in sequence-controlled synthesis

    Final product types

    • Kinase inhibitors
    • Anti-cancer small molecules
    • Advanced generics and patent API development candidates
    • Custom intermediates for CRO/CDMO partners

    2. Agrochemical Intermediate Synthesis

    R&D and production teams in agrochemical firms integrate 2-Bromo-5-Iodobenzoic Acid into routes for constructing selective herbicides and specialized insecticides. The compound's dual halogen functionality opens site-selective transformations, enabling rapid library expansion for efficacy and stability testing. Consistent batch quality ensures reproducible activity screening and regulatory approval for commercial crop protection products.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • ISO 9001:2015 Quality Management Systems
    • OECD Principles of Good Laboratory Practice (GLP) for R&D scale

    Typical usage ratio

    • 8–18% by weight in intermediate reaction mixtures, dependent on target ring assembly and substitution strategy

    Downstream process integration

    • Deployed in early or mid-stage synthesis, enabling halogen exchange or aryl functionalization before stabilization and final formulation for agrochemical actives

    Final product types

    • Pre-emergence and post-emergence herbicides
    • Specialty insecticide actives
    • Fungicide intermediates with halogenated benzoic acid motifs
    • Lead compounds for structure-activity-relationship (SAR) studies

    3. Specialty Dye and Pigment Manufacturing

    Producers of high-performance dyes and pigments employ this material as a starting point for synthesizing advanced N-heterocyclic and aromatic chromophores with tailored optical properties. The electron-withdrawing bromine and iodine groups increase color fastness and tune absorption wavelengths, essential for niche dye applications in electronics and textile coatings.

    Industry compliance standards

    • REACH Regulation (EC) No. 1907/2006 for chemical registration
    • ISO 14001:2015 Environmental Management
    • CENELEC colorant safety guidelines for industrial use
    • OEKO-TEX® Standard 100 (where applicable for textile finishes)

    Typical usage ratio

    • 5–13% of total dye-batch mass, adjusted as per chromophore backbone design and desired pigment strength

    Downstream process integration

    • Integrated during primary condensation reactions in dye synthesis or introduced in halogenation steps prior to coupling with azo, anthraquinone, or perylene intermediates

    Final product types

    • Electronic display colorants
    • Technical textile dyes
    • Photoactive pigment powders
    • Fluorescent standards for analytical applications

    4. Advanced Material and Polymer Additive Research

    Chemical research groups and advanced materials manufacturers utilize 2-Bromo-5-Iodobenzoic Acid in the controlled modification of polymer backbones and as a functional anchor for supramolecular assemblies. Its presence facilitates cross-linking or grafting, enhancing thermal stability or introducing specific reactivity. Reliable supply at high purity supports investigational studies and pilot-scale material development.

    Industry compliance standards

    • ISO 9001:2015 for manufacturing and quality assurance
    • ISO 10993 for preliminary biocompatibility testing (when polymers intended for medical use)
    • RoHS Directive (2011/65/EU) for electronics applications
    • Internal R&D qualification protocols

    Typical usage ratio

    • 0.5–4.5% by weight relative to monomer or polymer feed, varies with degree of functionalization sought in polymers or coatings

    Downstream process integration

    • Grafted onto polymer chains by post-polymerization modification, or co-polymerized under controlled conditions to introduce desired active sites or cross-linked domains

    Final product types

    • High-performance engineering plastics
    • Functional surface-modified films
    • Responsive coating systems
    • Precursor blocks for supramolecular assemblies
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    Certification & Compliance
    More Introduction

    2-Bromo-5-Iodobenzoic Acid: A Chemical Manufacturer’s Perspective

    An Honest Look at 2-Bromo-5-Iodobenzoic Acid

    In the world of specialty chemicals, consistency, transparency, and attention to detail separate quality manufacturers from the rest. 2-Bromo-5-Iodobenzoic Acid, with a molecular formula of C7H4BrIO2 and a CAS number of 63069-13-8, represents a case study in reliable, careful production. As a manufacturer engaged in its preparation for years, I’ve watched chemists and formulators try countless approaches to halogenated benzoic acids. Every step during production—the order of addition, the selectivity of halogenation, the purification—matters for labs and downstream intermediates.

    Why Chemists Select 2-Bromo-5-Iodobenzoic Acid

    Demand for precise halogenated benzoic acids comes from real-world challenges in fine chemicals, pharmaceutical intermediates, and advanced materials. The custom substitutions on the aromatic ring open doors to reactions conventional benzoic acids cannot tackle. Iodine and bromine placements at the 2 and 5 positions don’t just fill a gap on the periodic table—they enable cross-coupling, custom ligand synthesis, and scaffold modifications where side-reactions can cost valuable time and raw materials. Over years of manufacturing, I have seen this product chosen for Suzuki, Sonogashira, and Heck reactions where selectivity and yield rise or fall on trace contaminants or batch integrity.

    Chemical Purity Backed by Experience

    Control during multi-step synthesis makes or breaks a batch of 2-Bromo-5-Iodobenzoic Acid. Subtle changes in raw material suppliers, temperature stability, and solvent choice show up in purity trends and impurity profiles. Many users demand 98% minimum purity, but manufacturers know the goal goes beyond a single HPLC peak. Color, handling during crystallization, residual moisture, and storage stability all influence downstream results. I can trace plenty of user complaints about reaction failures or column fouling to minor differences in synthetic batches from traders or low-cost importers who don’t understand how every fraction or endpoint matters. Our own internal standards check for heavy metals, halogen balance, and trace organics—often above and beyond a typical certificate of analysis. Feedback from downstream labs often picks up minute impurities like 2-Iodo-5-bromobenzoic acid isomers or poly-halogenated byproducts formed by uncontrolled conditions. Years of hands-on production have taught us to spot trends within our plant before clients pick up the phone.

    Real Uses, Real Challenges

    The utility of 2-Bromo-5-Iodobenzoic Acid goes far beyond a printed chemical catalog. For instance, contract research organizations and medicinal chemistry labs often request it for constructing biaryls via palladium-catalyzed coupling, where position-selective halogen removal is a key step. Some bioconjugation pathways depend specifically on this regioisomer, not simply any bromo- or iodo-benzoic acid. I’ve seen scale-up runs where a tiny side product from early-stage commercial batches blocked crucial downstream transformations. Formulators using it for advanced material functionalization or microelectronics also report that even trace levels of ortho-para swapped isomers compromise end-product integrity. These lessons drive how we handle purification, recheck analytical data, and approach every drum and bottle that leaves site.

    In contrast, more basic halogenated benzoic acids—such as 2-bromobenzoic acid or 5-iodobenzoic acid—lack the unique reactivity of dual halogen sites. Without both bromine and iodine in specific positions, chemists lose the stepwise selectivity that enables regiospecific coupling or fine-tuned functionalization. We regularly answer questions from new or cost-conscious clients debating whether a less complex isomer could replace 2-Bromo-5-Iodobenzoic Acid. Our experience shows time and again that once a project moves past the screening stage, inferior regiospecificity or poor downstream reaction yields lead clients back to our product, looking for batch-to-batch consistency and fewer synthetic headaches.

    The Subtleties of Handling and Packaging

    Even the packaging of 2-Bromo-5-Iodobenzoic Acid offers lessons in chemical stewardship. Its crystalline form, off-white to pale yellow in color, might seem stable but reacts unkindly to excessive moisture or prolonged light exposure. Glass or high-density polyethylene containers with tight closures prevent hygroscopic clumping or surface darkening. Over the years, we shifted away from metal containers after fielding reports of slow decomposition or contamination when improperly lined tins contacted moist samples. Dosing from poorly sealed bulk drums can seed dust and handling losses; something we’ve tackled with custom-packed aliquots for clients with process sensitivity.

    Shipping presents its own headaches, especially during hot and humid seasons. Insulated shipping or dry desiccants fight caking—a small investment with a large payoff for our customers. A client once returned an entire shipment after particles fused into hard lumps during overseas transit. Since then, we verify every lot’s flowability before it leaves the warehouse, then log temperature records during shipment for traceability. Nobody working with this compound wants to troubleshoot solvated clumps that skew their weighing scale.

    Analytical Controls and Traceability

    Manufacturing a specialty halogenated compound isn’t a “set and forget” job. In my day-to-day work, I rely on a combination of classical titration, NMR, LC-MS, and ICP-OES to keep tabs on batch quality. It’s one thing to hit a purity target; it’s another to track and minimize byproducts like 3,5-dibromobenzoic acid or iodine-rich fractions. Clients in pharmaceutical R&D rely on guarantee—not just hope—that every batch matches previous lots without silent profile shifts. Full traceability from raw materials to final packaging remains essential. We keep years’ worth of production and QC records for every lot, along with retains for offsite inspection. No amount of documentation replaces personal responsibility: more than once, I’ve insisted on holding back a questionable batch that “looked fine on paper” but didn’t match our own in-plant experience.

    Supply Chain Realities

    Careful manufacturing doesn’t end at our gate. Upstream, we source bromine and iodine from proven suppliers who share transparency on trace impurities, origin, and supply continuity. A global shortage in either raw material throws timelines into chaos and exposes everyone to substitution risks. Some years, a late monsoon or export tailback in Asia restricts import volume, testing our contingency planning and inventory control. I’ve watched traders enter the market during shortages promising “identical” lots, only for downstream users to report changes in yield, handling, or analytical readings. Sticking to established sources means less troubleshooting—and fewer headaches for researchers and pilot-scale plants who depend on reliable materials.

    We regularly interact with solvers tackling new synthesis pathways or regulatory approvals. In those cases, documentation and supply chain transparency transition from “nice to have” to “mission critical.” It isn’t rare for a regulatory review committee to ask about sources of halogen, full supply chain mapping, or heavy metal content. Responding with full, documented traceability shortens review cycles and fosters trust. Especially for projects scaling up to GMP or pharmaceutical-grade uses, our adherence to batch documentation and validated cleaning cycles reduces risk at every stage.

    Environmental and Handling Considerations

    Manufacturers working with halogenated aromatics owe their community responsible handling and environmental stewardship. Waste minimization, fume treatment, and responsible solvent recovery aren’t just verbal commitments—they show up in energy bills, effluent quality, and employee safety. Our team practices zero-discharge protocols for mother liquors and halogen-containing residues. For every kilogram made, we track solvent and by-product throughput to minimize the load on downstream treatment systems. Strict adherence to waste management makes regulatory audits smoother and lowers our insurance costs—a reality any manufacturer ignores at their own peril.

    Employee training matters here as much as process equipment. Mistakes during filtration or drying introduce the risk of occupational halogen exposure or accidental release. Regular safety drills, PPE maintenance, and monthly process reviews keep risk in check. We’ve found that small investments in spill response equipment and real-time air quality monitoring pay off in employee confidence and incident prevention. Repeatedly, process improvements that lower exposure also lower defect rates—reminding us that operator experience is just as valuable as reactor automation.

    Comparison with Similar Chemicals

    Those new to this chemistry sometimes ask if bromo- or iodo-benzoic acid alone do the job. Over multiple production cycles and customer feedback loops, it’s become clear that nothing substitutes the dual placement of bromine and iodine in controlling synthetic routes. Mono-halogenated acids miss the mark by failing to provide the necessary leaving group diversity for cross-coupling or multistep derivatization. Other isomers—placing halogens at positions 3 or 4—lack the pattern-recognition and selectivity chemists rely on for certain molecular architectures. We’ve repeatedly seen clients switch from single-halogen products after failed attempts at selective activation or functionalization. In one particular case, a pharmaceutical research group conducted side-by-side trials with 2-bromo-5-fluorobenzoic acid, only to return to our product due to superior conversion rates and lower side product formation.

    Every year brings new publications and patents employing 2-Bromo-5-Iodobenzoic Acid as a key intermediate for drug candidates, conjugated polymers, or advanced materials. Its unique reactivity profile drives its adoption by research and development teams who prize speed, selectivity, and predictability. We regularly monitor the literature for emerging uses, enabling us to anticipate new analytical needs or property tweaks. These conversations flow both ways—what starts as a custom request today often sets a new internal production standard a year later.

    What We’ve Learned: A Manufacturer’s Wisdom

    Perfection in chemical manufacturing never really belongs to the next batch, the next project, or the new piece of equipment. It comes from learning from every cycle, talking openly to clients who run reactions all night or trouble-shoot columns at 4 am. 2-Bromo-5-Iodobenzoic Acid, as routine as it may seem in catalog listings, remains a technically challenging, detail-rich product. Production doesn’t tolerate shortcuts. There’s no replacement for disciplined controls, nor for doing the hard work of following a batch from start to finish.

    I’ve overseen runs where a small error in the addition order caused colored impurities that only revealed themselves after application. Some clients have traced unexplained bioactivity losses to barely-detectable impurity shifts, which sent us back through weeks of in-depth analysis and process tinkering. Years on, I know that every bottle we pack stands for the hours of attention, repair, and open communication built into our operation. Mistakes can’t be hidden—nor can pride in a batch that holds tight to rigorous standards and empowers real chemists to solve unsolved problems.

    Looking Ahead: Partnerships and Progress

    As industry trends swing toward more sophisticated drug candidates and electronic materials, the appetite for specialty halogenated building blocks keeps growing. Regulations tighten, supply chains feel every jolt, and synthetic chemists push the limits of selectivity and scale. For manufacturers, this shift means doubling down on analytical transparency, investing in plant upgrades, and partnering closely with clients from early-stage ideas to commercial drum deliveries. True difference isn’t found in bland lists of purity or yield percentage, but in the documented, lived expertise and open, responsive support we provide.

    Through economic cycles, regulatory shifts, and an ever-expanding library of synthetic needs, 2-Bromo-5-Iodobenzoic Acid remains a microcosm of the constant effort, skill, and care that define specialty chemical manufacturing. Our commitment hasn’t wavered. Every batch reflects the blend of science, craft, and service that enable chemists, engineers, and researchers worldwide to build a safer, smarter, and more productive future.