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3-Bromo-4-Iodotoluene

    • Product Name 3-Bromo-4-Iodotoluene
    • Alias 3-Bromo-4-iodo-1-methylbenzene
    • Einecs 837-059-6
    • 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

    764116

    Cas Number 60456-29-1
    Molecular Formula C7H6BrI
    Molecular Weight 312.93 g/mol
    Appearance White to off-white solid
    Melting Point 53-57°C
    Density 2.1 g/cm³ (approximate)
    Purity Typically ≥97%
    Smiles Cc1ccc(I)c(Br)c1
    Inchi InChI=1S/C7H6BrI/c1-5-2-3-6(8)7(9)4-5/h2-4H,1H3
    Solubility Slightly soluble in organic solvents

    As an accredited 3-Bromo-4-Iodotoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 3-Bromo-4-Iodotoluene, tightly sealed with a chemical-resistant cap and labeled for safety.
    Shipping 3-Bromo-4-Iodotoluene is shipped as a hazardous chemical under standard chemical transport regulations. It is securely packed in appropriate, labeled containers to prevent leakage or contamination. The package includes safety data sheets and complies with international guidelines for the transportation of hazardous substances. Handle with care during transit and storage.
    Storage 3-Bromo-4-Iodotoluene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizing agents. Protect from light and moisture. Store at room temperature, preferably in a chemical storage cabinet designed for hazardous organic compounds. Properly label the container and follow standard laboratory safety protocols.
    Application of 3-Bromo-4-Iodotoluene

    Applications of 3-Bromo-4-Iodotoluene in Industrial Manufacturing

    3-Bromo-4-Iodotoluene serves as a crucial halogenated aromatic intermediate in specialty and bulk chemical synthesis. Our in-house production supports consistent supply for multiple downstream sectors reliant on high-purity inputs for advanced product development. Below, we detail core industrial application fields, production context, regulatory compliance, typical usage ratios, process integration points, and primary final product categories.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers use this material as a building block in the synthesis of complex APIs, especially for small-molecule drugs where controlled halogenation facilitates targeted functional group introduction. Synthesis routes for antihypertensives and anticancer drugs often require strict structure-activity modulation, where precise substitution patterns delivered by this compound become essential for final molecular configuration and bioactivity. Quality consistency, traceability, and impurity management are tightly controlled during scale-up and qualification.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • European Pharmacopoeia monograph references
    • US FDA 21 CFR 211 cGMP
    • Chinese Pharmacopoeia 2020 (ChP-2020)

    Typical usage ratio

    • 0.2–1.5 molar equivalents as halogenated intermediate based on total yield required for each batch; fine-tuned according to downstream coupling efficiency, API route, and impurity profile targets.

    Downstream process integration

    • Fed during organometallic cross-coupling (Suzuki, Stille, or Sonogashira reactions) after initial protection steps, prior to final deprotection or salt formation stages.

    Final product types

    • Targeted kinase inhibitors
    • Antiviral agents
    • Specialty antihypertensive compounds
    • Research pharmaceuticals in clinical development

    2. Agrochemical Intermediate Synthesis

    Producers in crop protection and pest control markets utilize this compound for selective halogenation when preparing active ingredients or fine-tuning intermediate reactivity. Formulation scientists deploy it for new-generation herbicide molecule branches and for intermediates in the construction of pyrazole, triazole, or benzimidazole rings critical in broad-spectrum fungicides. Process engineers manage reaction selectivity to control environmental residue and toxicity limits.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Chemical Manufacturing
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • Chinese GB 2763 Food Safety National Standards (MRLs)
    • REACH Regulation (EC) No 1907/2006 — Annex XVII

    Typical usage ratio

    • 5–20% by mass in preparative reactions, calculated relative to precursor aromatic moiety, modulated depending on targeted bioactive skeleton and scale of synthetic route validation.

    Downstream process integration

    • Introduced post-nitration and prior to alkylation or amination steps in multi-stage flow or batch synthesis systems preparing advanced intermediates for active ingredient manufacture.

    Final product types

    • Herbicidal active substances
    • Fungicide pre-cursors
    • Novel insecticide intermediates
    • Field-use agrichemical finished products

    3. Electronic Chemicals and OLED Material Synthesis

    Producers in the electronics sector source this material for its defined halogenation pattern, which contributes to high-performance organic semiconductors required in OLED display manufacturing and next-generation photonic applications. Its aromatic structure enables downstream coupling for multi-aryl core assembly pathways, forming parts of hole transporting layers or electron injection segments. Thorough trace metal and particle control remains critical for process compatibility and device reliability.

    Industry compliance standards

    • IEC 61249-2-21 (Halogen-Free Electronic Material Specs)
    • China RoHS 2.0 (SJ/T 11364-2014)
    • SEMATECH purity standards (sub-ppb metallic residue)

    Typical usage ratio

    • 0.1–0.3 units per device precursor batch, based on mole ratios for targeted aryl coupling reactions; level determined by emission layer architecture and required optical gap tuning.

    Downstream process integration

    • Loaded into palladium-catalyzed cross-coupling reactors, supporting formation of high-purity functionalized arenes for vacuum deposition processes or solution-based coating lines.

    Final product types

    • OLED emitter compounds
    • Hole transporting materials (HTMs)
    • Light extraction layer intermediates
    • Small molecule semiconductors for flexible displays

    4. Dye and Pigment Manufacturing

    Dye manufacturers employ this intermediate in formulations where specific halogen substitutions are required to modify absorption maxima and colorfastness, especially in the development of specialty azo or anthraquinone dyes. Its predictable reactivity profile provides tight control over substitution during late-stage synthesis, helping ensure reliable shade reproducibility and batch-to-batch quality. Environmental and worker safety compliance is a focus during production and blending.

    Industry compliance standards

    • OEKO-TEX® Standard 100 Restricted Substance List
    • EN 71-3:2019 (Migration of Certain Elements in Toys)
    • EU REACH Annex XVII (Azo Dyes Restrictions)
    • US EPA TSCA Regulation Compliance

    Typical usage ratio

    • 8–22% of dye batch mass, ratio optimized for chromatographic purity, substitution degree, and achieved hue; adjusted for process scale and desired final pigment strength.

    Downstream process integration

    • Reacted mid-route in diazotization or electrophilic aromatic substitution steps before final coupling, sulfonation, or metallization procedures in dye synthesis production lines.

    Final product types

    • Disperse and reactive textile dyes
    • Industrial pigments for coatings and plastics
    • High-performance inkjet colorants
    • Specialty coloring agents for fiber and film applications
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    Certification & Compliance
    More Introduction

    Building High-Value Chemistry With 3-Bromo-4-Iodotoluene: Insights from the Manufacturer

    Getting Closer to the Core of Fine Chemical Synthesis

    We have been working with aromatic halides for decades, watching the evolution of pharmaceutical and agrochemical research push ever more demanding chemical requests. Out of the broad family of halogenated toluenes, 3-Bromo-4-Iodotoluene stands out in our production lineup for a simple reason—its ability to anchor complexity. Each lot of this compound that leaves our reactors carries the story of a process tuned over years, drawing on feedback from labs that challenge us to push beyond standard purity and consistency.

    Under the Hood: Model, Purity, and What Sets Ours Apart

    Offering 3-Bromo-4-Iodotoluene as a raw material means putting forward a well-defined structural combination: a single toluene ring with bromine at position 3, iodine at position 4, and a methyl group attached. The molecular structure alone doesn’t capture the significance. The journey starts with careful selection of raw precursors—before any halogenation step, we monitor impurity levels in our starting toluenes, choosing lots with the cleanest baseline spectra. Any deviation here can throw off a whole synthesis run, resulting in a waste of resources and extended downtime.

    We supply this product at laboratory and kilogram scales, with typical purity exceeding 98% by GC and HPLC. Truthfully, only tight controls through both small and large batches can maintain these standards, given how sensitive halogen substitution reactions are to micro-impurities and water content. Each batch is tested rigorously not just for major contaminants, but for residual isomers and side products like 2-bromo-4-iodotoluene or diiodo-toluenes—byproducts that would complicate downstream transformations for our customers.

    Why 3-Bromo-4-Iodotoluene Remains a Favourite Among Synthetic Chemists

    After years on the production floor and in technical support, we’ve noticed R&D teams come back with the same feedback: this molecule handles coupling reactions with a flexibility that’s hard to match. The dual halogen pattern allows chemists to carry out highly selective reactions—palladium-catalyzed cross-coupling on one position, leaving the other for further functionalization.

    Once, a customer in the early stages of drug discovery showed us side-by-side performance with related compounds. 3-Bromo-4-Iodotoluene consistently led to higher yields when introducing new aryl or alkynyl groups. Part of this comes down to the difference in bond activation energies between iodine and bromine—the iodine position undergoes oxidative addition under milder conditions, but the bromine acts as a solid backup for orthogonal chemistry. Such versatility has made it a staple in routes towards anti-cancer and antiviral agents. Agrochemical teams ask for it to trim synthesis steps off complex pesticide intermediates.

    Our technical team has helped troubleshoot bottlenecks that stemmed from suppliers with inconsistent halide ratios. Once, a pharmaceutical partner struggled for weeks chasing a problematic impurity that resulted from co-elution of a dibromotoluene. Consistent feedback like this drives us to keep refining our analytical methods with improved NMR and mass spectrometry protocols, so we can pinpoint even minor divergences batch-to-batch.

    Distinguishing 3-Bromo-4-Iodotoluene from Lookalike Halogenated Toluenes

    Understanding the practical differences between close structural analogues isn’t just a theoretical exercise. We make and supply other monohalogenated and dihalogenated toluenes as well, including 3-bromotoluene, 4-iodotoluene, and 2-bromo-4-iodotoluene. Through customer case studies, it’s clear that swapping positions on the aromatic ring or using a different halogen source changes everything—from reactivity to byproduct formation to final yield.

    In multi-step organic syntheses, the choice between 3-bromo-4-iodotoluene and its isomers can define feasibility. Substitutions at the 2-position come with different steric hindrance and electronic effects, introducing complications in regioselective coupling. Meanwhile, the 3-bromo-4-iodo pattern manages to strike a sweet spot: minimal ortho hindrance and easier access for both nucleophilic and electrophilic partners. Our close ties to med-chemists and process developers have shown us how a seemingly small shift in substitution can spell the difference between a one-pot sequence that works reliably or a drawn-out purification ordeal.

    Our years of direct feedback show that some suppliers treat all dihalogenated toluenes as interchangeable, blending isomers or cutting corners on purification. We have to correct misconceptions, helping customers decipher subtle differences during troubleshooting. Some projects only got past critical roadblocks after switching to our single-isomer 3-Bromo-4-Iodotoluene, which shaved days off iterative optimization cycles.

    Downstream Uses: More Than Just a Building Block

    Pharmaceutical groups rely on 3-bromo-4-iodotoluene most frequently in the construction of complex aromatic scaffolds. With its ortho and para directing effects, it offers control over the placement of new functional groups. Our collaborations have helped custom-synthesis firms reduce the number of protection and deprotection steps by starting with a more functionally dense intermediate. The same attributes translate smoothly into the agrochemical sector, where rapid iteration on core structures is essential for patent circumvention and efficacy improvements.

    Some academic labs working on material sciences request 3-bromo-4-iodotoluene as a precursor for advanced conjugated systems or polymers. The bromine and iodine substituents open the door to cross-coupling strategies that build long, high-purity chains. Our batches support these demanding applications by keeping trace metals and micro-impurities far below industry-accepted thresholds, since even minute contamination changes photophysical properties in these advanced materials.

    Over time, we’ve watched demand shift towards more sustainable chemistry. We are adjusting manufacturing protocols to minimize solvent use, increase recycling, and cut down on halogenated byproducts. Much of this work happens quietly, long before the product reaches a customer’s bench. Still, it impacts the final result; the cleaner the production cycle, the easier tech transfer becomes when labs try to scale up new syntheses from milligrams to pilot batches.

    Production Challenges and Long-Term Reliability

    Manufacturing dihalogenated aromatics requires more than routine reaction setups. Each lot of 3-bromo-4-iodotoluene traces back to multi-stage halogenations, controlled quenching, and careful workup to remove trace acids, halides, and residual solvents. Any variability can mean months of downstream troubleshooting for clients, which is why we invest so heavily in process stability. Raw material sourcing forms the backbone here. Sourcing high-purity toluene starting materials and halogenation reagents cuts total impurity load dramatically, a step that cheaper options skip, leading to grim purification headaches later.

    Constant monitoring and adjustment are the reality. We have set up in-line analytical controls during synthesis and downstream work-up, using GC-MS and HPLC along every key checkpoint. These checkpoints help us catch trace contaminants before they are locked into the matrix of the final product. For every kilo that leaves our plant, analytical documentation follows. The result: our partners avoid sudden surprises during development and regulatory audits.

    Supporting Solutions for Chemists and Development Teams

    We’ve seen enough failed projects to know that troubleshooting support should not stop at the point of sale. Our technical team works with process chemists to adapt this intermediate to unique synthetic routes. In one project, a team working on kinase inhibitors hit a wall because their previous supplier’s product had up to 1% co-eluting dibromo impurity. Through several calls and data exchanges, we dialed the specification tighter, isolating a pure 3-bromo-4-iodotoluene that enabled successful coupling—ultimately, they landed a new lead compound.

    We support solvent selection and reaction parameter adjustments based on years running analogous reactions in our own lab. With real world project timelines in mind, we commit to stockholding and rush shipments, preventing production interruptions for teams on deadline. Rapid response for urgent needs is something we take pride in—having walked in the shoes of chemists relying on timely delivery of niche intermediates.

    Beyond the bench, we collaborate with regulatory consultants and quality assurance teams to make sure shipments measure up to evolving European, American, and Asian quality standards. Experience has taught us how even small variances in impurity profiles show up in regulatory documentation, affecting final product registrations. We proactively offer full characterization data with every batch, including NMR, GC, HPLC, and residual solvents, saving time at the point of filing.

    Safeguarding People, Environment, and Product Integrity

    Production, handling, and shipping of 3-bromo-4-iodotoluene brings direct safety and environmental considerations. Years on the production floor have shown our operations team the practical value of investing in closed-system handling and fume extraction. Iodine compounds, in particular, present unique containment challenges. We train our staff accordingly and regularly upgrade infrastructure to minimize losses and emissions.

    Waste management cannot be left to chance. We neutralize halogenated byproducts with a closed-loop system, marrying regulatory compliance with real environmental responsibility. Proper handling is as much about protecting our own teams as it is about safeguarding global ecosystems against accidental releases.

    Shipping requires close attention to temperature control and secure packaging. Some customers run pilot projects in remote locations, so we work with trusted carriers only, selecting packaging that maintains the compound’s integrity during extreme conditions. Our logistics support team maintains traceability and handles customs and compliance challenges, cutting the risk of costly delays or regulatory issues.

    Dynamics of a Volatile Supply Chain

    Sourcing iodine and high-purity bromination agents faces volatile pricing and supply disruption risks, as global events and environmental regulations shift market dynamics. Because this affects our ability to offer stable pricing and secure long-term contracts, we work directly with upstream producers, not just resellers, to maintain traceability all the way back through the supply chain. Advanced planning and multi-source agreements let us hold safety stock, smoothing out supply crunches for our partners and shielding delicate research timelines from sudden interruptions.

    In the last couple of years, increasing scrutiny of halogenated intermediates has also led to new compliance hurdles—ranging from REACH registration in Europe to chemical control laws elsewhere. Our compliance teams stay on the leading edge, preparing and updating dossiers, helping customers avoid regulatory setbacks.

    Building the Future with Reliable Partnerships

    Developing and manufacturing 3-bromo-4-iodotoluene has always demanded real technical investment and close ties to scientists in the field. Over decades, our relationships with universities, pharmaceutical innovators, and contract research organizations have taught us which improvements matter most. It comes down to providing a consistently pure, well-characterized material, backed by responsive technical support, reliable delivery, and a commitment to safety and sustainability that starts long before shipping.

    With each order, we draw on years of practical experience, combining modern analytical technology with hard-earned manufacturing know-how. Our approach reflects a belief that even complex chemistry can be made accessible and scalable for teams focused on moving faster—from invention all the way through to scale-up and market launch.

    Continual reinvestment in our people and processes shapes the reputation of this product line. We keep improving reactor design, analytical controls, waste treatment, and data management. Open channels with customers mean we detect emerging needs and pivot quickly when the field asks for new specifications or even rarer analogues. Our experience confirms the message from countless successful projects: well-made building blocks like 3-bromo-4-iodotoluene shorten innovation cycles, cut hidden costs, and unlock new chemistry. That’s the perspective we’ve earned, grounded in the realities of modern chemical manufacturing and a deep respect for the downstream inventors.