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2-Bromo-4-Iodopyridine

    • Product Name 2-Bromo-4-Iodopyridine
    • Alias 2-Bromo-4-iodo-pyridine
    • Einecs 823-311-7
    • 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
    VTB
    Specifications

    HS Code

    181623

    Chemical Name 2-Bromo-4-Iodopyridine
    Molecular Formula C5H3BrIN
    Molecular Weight 299.89 g/mol
    Cas Number 226677-35-6
    Appearance White to off-white solid
    Melting Point 66-70°C
    Density 2.37 g/cm³
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥97%
    Smiles C1=CN=C(C=C1I)Br
    Inchi InChI=1S/C5H3BrIN/c6-4-1-2-5(7)8-3-4/h1-3H
    Storage Conditions Store at room temperature, in a tightly closed container
    Synonyms 4-Iodo-2-bromopyridine

    As an accredited 2-Bromo-4-Iodopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2-Bromo-4-Iodopyridine (5g) is supplied in a sealed amber glass bottle with a printed hazard label and screw cap.
    Shipping 2-Bromo-4-Iodopyridine is shipped in tightly sealed containers, protected from light and moisture. It is classified as a hazardous material and handled according to relevant chemical transport regulations. The packaging ensures leak-proof containment, with proper labeling and documentation provided for safe and compliant delivery. Use appropriate personal protective equipment during handling.
    Storage 2-Bromo-4-iodopyridine should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Store at room temperature and avoid excessive heat. Use personal protective equipment when handling to prevent skin and eye contact, and follow local safety regulations.
    Application of 2-Bromo-4-Iodopyridine

    Applications of 2-Bromo-4-Iodopyridine in Industrial Manufacturing

    2-Bromo-4-Iodopyridine serves as a valuable halogenated heterocycle, taking on specialized functions across fine chemical manufacturing value chains. Our direct production and quality management ensure each batch supports critical downstream synthesis steps, especially in pharmaceutical, agrochemical, and advanced material sectors. Explore how our material fits precisely into these select industrial applications.

    1. Pharmaceutical API Intermediate for Oncology Compounds

    Our material is frequently integrated into the creation of targeted cancer drug intermediates, where its halogen substitution patterns enable nucleophilic aromatic substitution and cross-coupling reactions crucial for constructing active pharmaceutical ingredient (API) cores. Pharmaceutical innovators rely on this intermediate to streamline process development, facilitate late-stage functionalization, and maintain batch-to-batch consistency for regulatory filing.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211: FDA cGMP for Finished Pharmaceuticals
    • USP–NF Monographs (relevant intermediates and final APIs)
    • EDQM CEP Guidelines for API intermediates

    Typical usage ratio

    • Usage level typically ranges from 0.8 to 1.2 mole equivalents relative to the core pyridine assembly, with specific ratios determined by the targeted coupling or substitution transformation and impurity profile requirements in the synthetic route.

    Downstream process integration

    • Material is introduced after initial pyridine ring formation, acting as a key substrate in Suzuki, Buchwald-Hartwig, or nucleophilic aromatic substitution reactions to introduce side chains or functional groups forming the API precursor structure; it is purified prior to final API conversion and isolation.

    Final product types

    • Small-molecule kinase inhibitors (e.g., for oncology indications)
    • Antiviral pyridine-based APIs
    • Generic and innovator pharmaceutical compounds containing functionalized pyridine rings
    • Patented investigational oncology drugs

    2. Agricultural Chemical Synthesis: Pyridine-Based Herbicide Intermediate

    2-Bromo-4-Iodopyridine acts as a pivotal halogenated intermediate in the multi-step synthesis of novel heterocyclic herbicides. Agrochemical formulators value this building block for its unique electronic properties, which promote subsequent functionalization leading to selective and potent weed control compounds intended for both crop and non-crop uses with well-defined residue profiles.

    Industry compliance standards

    • FAO/WHO Guidelines for the Quality Control of Pesticides (FAO Specification Manual)
    • ISO 9001:2015 Quality Management for Chemical Synthesis
    • EU Regulation 1107/2009 (Authorization of Plant Protection Products)
    • OECD Principles of Good Laboratory Practice

    Typical usage ratio

    • Addition amount ranges from 0.95 to 1.05 molar equivalents relative to pyridine-comprising ring system formation, with ratio fine-tuned to minimize impurities and maximize conversion yield in palladium-catalyzed coupling stages.

    Downstream process integration

    • Introduced following initial pyridine base synthesis, this raw material participates in halogen exchange and cross-coupling reactions that form the active herbicidal core; subsequent steps include selective oxidation, alkylation, and formulation for field application testing.

    Final product types

    • N-heterocyclic herbicide actives for pre-emergent or post-emergent use
    • Crop-specific herbicide formulations
    • Specialty weed control products for industrial or municipal land management
    • Herbicide-tolerant seed treatment compounds

    3. Electronic Material Precursors: OLED and Liquid Crystal Development

    Manufacturers of advanced display and semiconductor devices employ this heteroaromatic compound for high-purity precursor synthesis during the fabrication of organic light-emitting diode (OLED) emitter materials and customized liquid crystal additives. Its dual halogen functionality enables precise scaffold modifications essential for optimizing charge-transport and emission properties in final display technologies.

    Industry compliance standards

    • JEITA ET-7304: Standards for Electronic Grade Organic Materials
    • ISO 9001:2015 (quality system for materials supplied to electronics sector)
    • IEC QMS 80000:2016 (Electronics Quality Management System Requirements)
    • RoHS Directive (EU 2011/65 restrictions for hazardous substances in electronics)

    Typical usage ratio

    • Usually charged at 1.0 molar equivalent in aromatic coupling stages; exact dosing tailored based on the degree of subsequent halogen exchange or substitution required for electronic properties modification.

    Downstream process integration

    • Material is deployed within the early stage of organic electroluminescent material synthesis, often as a coupling partner for formation of substituted pyridine emitter core, prior to downstream functionalization, purification by recrystallization, and integration into device-grade layer precursors.

    Final product types

    • OLED small molecule emitters
    • Pyridine-based charge transporter intermediates
    • Customized liquid crystal dopants for high-resolution displays
    • Functional dyes and specialty organic thin-film semiconductors

    4. Custom Fine Chemical Synthesis: Halogen Exchange and Ligand Construction

    Our high-purity material supports leading catalyst development groups and custom synthesis firms as a precision halogenated scaffold in ligand and coordination compound assembly. The site-selective functionalization enabled by the bromo and iodo substituents assists in creating advanced metal-ligand complexes and specialty reagents required in high-performance technical and analytical applications.

    Industry compliance standards

    • ISO 17025:2017 for analytical and testing laboratory processes
    • REACH Regulation (EC) No 1907/2006 for technical chemical intermediates
    • AIChE Center for Chemical Process Safety Guidelines
    • ISO 9001:2015 for batch traceability in custom synthesis

    Typical usage ratio

    • Batchwise input ranges from 0.2 to 1.0 mole equivalent depending on complexity of the ligand architecture or degree of functional group interconversion required for the customer’s custom synthesis campaign.

    Downstream process integration

    • Integrated during initial scaffold assembly for selective halogen-metal exchange followed by attachment of functional moieties; downstream flows involve palladium or copper catalysis, followed by chromatographic purification and isolation for analytical validation.

    Final product types

    • Pyridine-based phosphine ligand intermediates
    • Transition metal catalyst complexes for selective hydrogenation or coupling
    • Analytical-grade specialty reagents
    • Screening libraries for pharmaceutical, agrochemical, or material science research
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    Certification & Compliance
    More Introduction

    2-Bromo-4-Iodopyridine: A Perspective from the Manufacturing Floor

    A Closer Look at 2-Bromo-4-Iodopyridine

    From years of mixing and refining specialty pyridine derivatives, we pay close attention to what chemists ask for in their day-to-day work. 2-Bromo-4-Iodopyridine (CAS 19849-88-4) is a staple among halogenated pyridines because of its unique profile. The molecular structure of C5H3BrIN blends two reactive halogen sites—bromine and iodine—on a pyridine ring, delivering a compound that unlocks multiple pathways for future transformations.

    Our process achieves a fine white to pale yellow crystalline powder, with no signs of contamination or problematic moisture. Each batch meets strict standards for identity, purity above 98.0%, and low residue on ignition. We track melting point consistently in the expected range, under controlled atmospheric conditions, eliminating guesswork when you receive your shipment. Not every lab-grade source can promise uniform texture and robust shelf life—two characteristics critical to smooth, consistent chemical reactions.

    Why 2-Bromo-4-Iodopyridine Draws a Crowd

    Demand for this particular derivative grows steadily year after year for a reason. Synthesis managers in pharmaceutical R&D, electronic materials, and fine chemical plants recognize 2-Bromo-4-Iodopyridine as an efficient intermediate. Its halogen layout enables chemists to introduce diversity at the 2 and 4 positions more readily than with mono-substituted analogues. One team can perform selective cross-coupling at the iodo position using less aggressive catalysts. Another group might pursue nucleophilic substitutions on the bromo group, building out new scaffolds for active pharmaceutical ingredients or specialty heterocycles.

    Our experience shows a broad difference in reactivity between the iodine and bromine sites. The carbon–iodine bond, relatively weaker, reacts readily under mild palladium-catalyzed coupling. The bromine gives reliable activation with different ligands and conditions, delivering greater flexibility in multi-step syntheses. Having both functionalities on a single ring streamlines route design and reduces waste, which end users appreciate in process development.

    Usage Insights from Direct Manufacturing

    Working on the manufacturing line, it becomes evident which steps require extra supervision for this compound. 2-Bromo-4-Iodopyridine tends to shine in Suzuki–Miyaura coupling reactions, a go-to choice for creating biaryls and aryl–heteroaryl linkages. Electron flow on the ring supports clean, high-yielding conversions. We hear from partners in pesticide and herbicide research who rely on it as a cornerstone intermediate, often favoring it over the monohalides for its precise control during stepwise substitution. Medicinal chemists mention it as a quick entry to libraries of pyridine analogs, skipping complicated protection and deprotection steps.

    2-Bromo-4-Iodopyridine handles well under common lab storage conditions, provided sealed containers and minimal exposure to light. Its solid state resists caking and lump formation, easing both manual and automated weighing. Skilled operators appreciate this subtle, behind-the-scenes detail: handling losses stay low, and measurement translates more predictably from formulation trials to kilo lab scale.

    Why Differentiation Matters: Not All Pyridine Derivatives Compare

    Many newcomers ask why not simply use 2-bromopyridine or 4-iodopyridine. In practical synthesis, each substituent brings distinct challenges. The 2-position on pyridine resists modification compared to the 4-position. Loading both a bromine at C2 and an iodine at C4 provides a strategic advantage; reaction designers gain choices. By starting with our product, medicinal chemists accelerate their search for active compounds, picking the order and nature of further substitutions. Fewer synthetic steps save both money and time.

    In side-by-side tests, yields run higher with 2-Bromo-4-Iodopyridine during two-step arylations or heteroarylations than from singly halogenated sources. Process engineers highlight improved selectivity, reduced byproduct levels, and extended catalyst life. As a manufacturer, these differences show up in our own waste profiles. We’ve seen reductions in both solvent consumption and byproduct streams with dual-functionalized intermediates. Since every reduction in waste lowers environmental impact, these practical gains translate directly into smaller footprints for pilot and production runs.

    Manufacturing Realities: Purity, Scale, and Customer Requirements

    Every gram matters to the end user. Multi-step organic syntheses can stall from hidden contaminants as minor as half a percent. We operate multi-stage purification flows using recrystallization and column chromatography, verified with HPLC and GC-MS, to guarantee a clean product each time. No shortcut can match the security that comes from rigorous in-process monitoring and batch-level tracking. Having walked through scale-up headaches ourselves, we plan residue removal into the workflow from day one.

    Assemblers working at different batch sizes—from a few grams in drug discovery, up to dozens of kilograms for pilot plants—inspect materials under diverse protocols. We tailor particle size distribution and solvent residuals based on the customer's technical requirements, not just standard formats. Smaller pharma shops require tight packaging for easy weighing on the bench. Larger buyers in agrochemicals or electronics lean toward drum or process-ready tote blends. Both groups expect batch-to-batch consistency that shows up across analytical spectra, from NMR to mass spectrometry.

    Factual Comparison: 2-Bromo-4-Iodopyridine, Halogenated Analogues, and Application Success

    Unlike 2-chloro-4-iodopyridine or 2-bromo-4-chloropyridine, the bromine-iodine combination on 2-Bromo-4-Iodopyridine offers more differentiated leaving group abilities and cross-coupling reactivity. This structural feature matters for teams racing to assemble complex scaffolds for trial batches. More predictable reactivity and consistent activation of the halide positions mean fewer purification headaches and more reliable troubleshooting in method development. Over the years, we have noted that projects built with 2-Bromo-4-Iodopyridine tend to require fewer process adjustments as scale increases.

    In contrast to plain pyridine, installing dual electron-withdrawing halogens at the 2 and 4 positions tunes the electron density, affecting not just reactivity but end-use properties such as solubility and stability. Our quality audits include accelerated aging studies to verify stability in sealed, amber containers. We catch degradation issues before they reach research teams. Purity and long-term shelf life count for more than a theoretical yield metric—easy to forget until a time-sensitive project faces unexpected setbacks from failed material.

    Real World Applications: What Chemists Accomplish

    Customers use 2-Bromo-4-Iodopyridine in areas as distinct as kinase inhibitor development and new OLED materials formulation. We work with pharmaceutical firms who build kinase inhibitor cores via selective Suzuki coupling, skipping multiple labor-intensive protecting group sequences by taking advantage of the built-in selectivity and reactivity of each halide. In materials science, the push for more stable, high-performing organic semiconductors relies on assembling library compounds rapidly, something made less cumbersome by using bifunctional pyridine handles.

    Feedback from university groups affirms these results. Students have less difficulty with non-specific side reactions or intractable column purifications when starting with our batches. Analytical chemists at large multinationals confirm better recovery of target compounds compared to products sourced from inconsistent suppliers. Over time, these incremental benefits add up—shorter project timelines, fewer troubleshooting cycles, and less waste overall.

    Quality Across Batches: Our Manufacturing Experience

    Each run through our reactors receives full attention from our experienced technical staff. We train operators to identify minor deviations in color or particle texture before they reach the packing line. HPLC purity readings above 98.0% are routine, but we also verify absence of related halogenated pyridines, avoiding unknown side products common in less controlled production. Water content and residual solvent data receive independent verification, so delivered product matches request, not just specification sheet promises.

    We adjust process parameters such as stirring intensity, induction times, and separation methods based on outcomes observed in prior batches. This hands-on approach prevents drift in physical properties, giving chemists peace of mind every time a new container arrives. With shipping handled promptly after quality checks, shelf life remains optimal, and powder flow properties stay reliable.

    Handling, Storage, and Safety Advice from the Source

    Direct work with this molecule, day in and day out, teaches respect for its reactivity. All production staff wear nitrile gloves and respirators, observing normal precautions for low molecular weight organohalides. Dust-tight containers and desiccant pouches guard against moisture absorption. Our warehouse keeps ambient humidity below 40%, providing extra insurance against clumping and unwanted hydrolysis. A cool, dark shelf and intact packaging prevent any drop in melting point or discoloration over time.

    Experienced users store opened containers in well-sealed bags and limit air exposure, preserving stability for months. If any question arises regarding handling or reactivity, our process chemists provide practical, firsthand insights built up from running many kilograms through pilot and plant equipment. Direct answers, not theoretical suggestions, based on actual experience moving material from storage bin to laboratory scale-up.

    Potential Challenges and Solutions from a Manufacturer's View

    No chemical production flows without challenges. Scale-up brings new worries: batch consistency, yield loss, off-color product in summer, or variation across glassware surfaces. We address these by tracking process temperatures and environmental controls, adjusting solvent swaps or recrystallization procedures as seasons change. Our maintenance team reviews key equipment failures after every campaign, resetting seals and agitator speeds to ward off contamination.

    One recurring issue relates to packing under high humidity. Early batches from years ago showed sticking or softening of crystals. Now every fill zone passes a dew point check before a drum gets sealed. This improved protocol reduced customer complaints and improved long-haul shipping outcomes. Direct review of QC analytics after each shipment allows us to spot trends before they become expensive remediation projects, not waiting for outside audits or delayed customer feedback.

    Transparency and Traceability

    We build documentation around our production history for every order. Each batch links back to technician logs, temperature charts, and raw material analysis. Traceability means knowing both what went right and what demands improvement. Technical support includes full spectral data, so customers can run side-by-side comparisons in their own labs.

    If a question arises about an impurity or an unexpected analytical signal, our records provide the clarity necessary for quick troubleshooting. Over the years, these direct conversations with chemists have led us to adjust not just manufacturing protocols, but analytical calibrations and packing formats as well. Improvement rarely shows up in specs, but quality-minded customers know when they're working with a manufacturer who learns from feedback.

    Environmental Responsibility: Saving Resources in Practice

    Every step we take to minimize solvent use or recycle halide reagents shows benefits downstream for our buyers. Less solvent in your drum means easier disposal. Careful monitoring of halide uptake in early reaction steps lets us control byproducts; what doesn't start doesn’t require cleaning up later. Filtration by-products are collected, separated, and sent to appropriate specialty waste handlers. Even our internal audits focus as much on resource efficiency as cost controls—these goals align naturally for manufacturers who work directly with global research teams facing tighter regulatory and cost limits.

    Supply chain reviews now regularly cover new sources for bromine and iodine, balancing security of delivery with overall ethics and traceability. As more end users require evidence of origin, we track raw materials to their source, avoiding “conflict” minerals and prioritizing reliable logistics. Every minor improvement in transparency or waste handling protects future users, not just the current customer.

    What Buyers Gain from Direct Manufacturer Relationships

    New customers often comment on the predictability of our product from batch to batch. The extra work to control particle size, solvent traces, and shelf life means smaller gaps between research, pilot, and commercial stages. Procurement teams face fewer unexpected costs from repeat purifications or underperforming material. That reliability—the product arriving at expected purity, with all analytics up to spec—backs up laboratory progress at every stage.

    Direct communication also helps buyers solve problems unique to their process. If a customer encounters an unforeseen impurity, our in-house techs can help identify causes and propose solutions based on direct experience, not guesswork. This saves precious time and avoids costly project delays. Over the years, we’ve found that a closer connection leads to less wasted effort for everyone who touches the compound.

    Looking Ahead: Innovations Based on Experience

    Development doesn’t stop for us. Every year brings subtle changes in feedstock sources, regulatory limits, or new application routes. Our R&D team tracks these trends and tunes parameters to fit emerging expectations for cleaner, safer, more cost-effective production. Recent improvements in solvent recycling reduced waste by double digits over 24 months. User feedback on powder flow, handling, and purity prompted a tweak to our final crystallization process, leading to even greater reproducibility.

    While academic literature and patent filings track expected applications, the real success stories come from teams who push boundaries in the laboratory and pilot plant. Our best ideas often emerge from direct conversations with scientists working to build new pharmaceuticals, crop protection agents, or high-performance materials. These partnerships ensure that each batch of 2-Bromo-4-Iodopyridine reflects both technical rigor and the real-world demands of modern chemistry.

    Conclusion: Reliable Quality for demanding chemistry

    Hands-on manufacturing brings us face to face with the practical needs of innovators every day. 2-Bromo-4-Iodopyridine provides the versatility and predictability researchers want, supported by a manufacturer who treats production as a continuous, evolving science. Our daily experience with the compound—from synthesis through packing and analytics—remains the backbone of our commitment to quality and customer trust. That commitment appears at every step, from the clean bench in our plant to your next project milestone.