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3-Bromo-5-Iodo-Pyridine

    • Product Name 3-Bromo-5-Iodo-Pyridine
    • Alias 3-Bromo-5-Iodopyridine
    • Einecs 801-389-9
    • 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

    755550

    Chemical Name 3-Bromo-5-Iodo-Pyridine
    Cas Number 52434-90-9
    Molecular Formula C5H3BrIN
    Molecular Weight 299.89 g/mol
    Appearance off-white to light yellow solid
    Melting Point 75-79°C
    Density 2.33 g/cm³ (approximate, calculated)
    Purity ≥98%
    Solubility Soluble in organic solvents (e.g., DMSO, DMF, chloroform)
    Synonyms 3-Bromo-5-iodopyridine, 5-Iodo-3-bromopyridine
    Smiles C1=CC(=CN=C1Br)I
    Inchi InChI=1S/C5H3BrIN/c6-4-1-5(7)3-8-2-4/h1-3H
    Storage Conditions Store in a cool, dry place; keep container tightly closed
    Hazard Class Irritant

    As an accredited 3-Bromo-5-Iodo-Pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g bottle of 3-Bromo-5-Iodo-Pyridine arrives in an amber glass vial, tightly sealed with a tamper-evident cap.
    Shipping 3-Bromo-5-Iodo-Pyridine is shipped in tightly sealed containers, protected from moisture and direct sunlight. Transportation follows safety regulations for hazardous materials. The chemical is labeled clearly with hazard and handling instructions. All shipments comply with local and international shipping standards to ensure safe and secure delivery to the destination.
    Storage 3-Bromo-5-Iodo-Pyridine should be stored in a tightly sealed container, away from moisture and incompatible materials, such as strong oxidizers. Keep it in a cool, dry, well-ventilated area, protected from light. Store at room temperature or as recommended on the manufacturer's label. Handle in accordance with good laboratory practices to ensure safety and maintain product integrity.
    Application of 3-Bromo-5-Iodo-Pyridine

    Applications of 3-Bromo-5-Iodo-Pyridine in Industrial Manufacturing

    3-Bromo-5-Iodo-Pyridine serves as a specialized intermediate in various chemical synthesis pathways, supporting production across key pharmaceutical, agrochemical, and advanced materials industries. The following scenarios detail real downstream uses, tailored to procedural and compliance realities of each sector.

    1. Pharmaceutical API Synthesis – Heterocyclic Compound Production

    Manufacturers leverage 3-Bromo-5-Iodo-Pyridine as a critical building block during multi-step pharmaceutical syntheses, especially for constructing pyridine-based heterocyclic scaffolds. The halogenation pattern enables site-selective coupling and functionalization steps essential for creating kinase inhibitors, antiviral agents, and CNS-active intermediates. Entry occurs after the core ring structure formation, with subsequent manipulations such as Suzuki and Buchwald-Hartwig couplings. Consistent traceability and purity verification support compliance with international pharmacopeial requirements and GMP environments typical of regulated API supply chains.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP, EP, JP monographs (as applicable to API targets)
    • FDA 21 CFR Part 210/211 (for cGMP facilities)
    • EMA and EDQM standards for pharmaceutical intermediates

    Typical usage ratio

    • Range: 0.1–1.5 molar equivalents per step, adjusted based on target yield and desired downstream substitutions.

    Downstream process integration

    • Introduced following ring construction for halogen exchange and cross-coupling preparations; used in amidation and acylation steps before final API crystallization and purification.

    Final product types

    • Kinase and BTK inhibitors
    • Antiviral agent precursors
    • Neurological drug intermediates
    • Proprietary pyridine-derivative APIs

    2. Agrochemical Intermediate Manufacturing

    3-Bromo-5-Iodo-Pyridine undergoes selective substitution and functionalization to become a precursor for a range of herbicidal and fungicidal active ingredients. Its dual halogen pattern offers process chemists flexibility for multistep halogen exchange, enabling construction of molecules exhibiting strong activity against target pests. Stringent monitoring of residual intermediates and real-time integration with ISO-compliant QA systems remain essential, especially where downstream products fall under environmental hazard regulations.

    Industry compliance standards

    • FAO/WHO International Code of Conduct on Pesticide Management
    • REACH Regulation (EC) No 1907/2006
    • ISO 9001 Quality Management Systems
    • OECD principles for chemical testing and documentation

    Typical usage ratio

    • Concentration typically falls between 10–35% w/w in initial reaction batches; ratios fine-tuned for efficiency and environmental safety in each synthesis run.

    Downstream process integration

    • Added as a key starting material during chlorination and cross-coupling processes to build final agrochemical active cores, before downstream formulation and encapsulation for market-ready products.

    Final product types

    • Pyridine-based herbicide actives
    • Systemic fungicidal intermediates
    • Seed treatment agents
    • Specialty crop protection molecule precursors

    3. Advanced Material Synthesis – OLED and Electronic Chemical Applications

    Producers in the electronics sector incorporate 3-Bromo-5-Iodo-Pyridine into the synthesis of functionalized ligands and organic semiconductors, including materials slated for OLED display technologies and sensor engineering. The precise placement of bromine and iodine atoms facilitates programmable cross-coupling, producing technologically relevant derivatives for light-emitting layers. Handling protocols emphasize cleanroom procedures and low-ion contamination, while material traceability supports downstream electronics quality verification.

    Industry compliance standards

    • JEITA standards for electronic component materials
    • SEMATECH guidelines for semiconductor fabrication chemicals
    • ISO 14001 Environmental Management Systems (where applicable)
    • IEC 62474 reporting for declarable substances

    Typical usage ratio

    • Employed at 0.5–5 mol% level relative to final organic layer mass, scaled by performance requirements and targeted emission properties.

    Downstream process integration

    • Incorporated after polymerization or pre-polymer functionalization; serves as a backbone for ligand assembly and as a cross-coupling node during phosphorescent material synthesis.

    Final product types

    • Phosphorescent dopants for OLED displays
    • Charge transport layers
    • Organic semiconducting polymers
    • Specialty sensing films

    4. Fine Chemical Synthesis for Research and Diagnostics

    Researchers and specialty fine chemical producers utilize 3-Bromo-5-Iodo-Pyridine to generate labeled compounds, crosslinking agents, and scaffolding molecules for custom diagnostic reagents. It enables site-directed functionalization, crucial in isotopic labeling, probe design, and the preparation of enzyme assay kits. Material control and batch documentation are managed under ISO and GLP systems, as supply often enters regulated laboratory and diagnostic markets.

    Industry compliance standards

    • ISO 13485 for in vitro diagnostic materials
    • OECD GLP (Good Laboratory Practice) Principles
    • ISO 9001-certified chemical synthesis protocols
    • Relevant local regulations for diagnostic reagent safety

    Typical usage ratio

    • Varies from 0.05–0.2 molar equivalents for research probe synthesis; lab-scale batches enable tailored adjustment to specification.

    Downstream process integration

    • Introduced during probe backbone assembly, coupling, or isotopic exchange steps, before final purification and QC release for laboratory distribution.

    Final product types

    • Biochemical assay probes
    • Isotopically labeled reference standards
    • Crosslinkers for enzyme immobilization
    • Research-only molecular scaffolds
    Free Quote

    Competitive 3-Bromo-5-Iodo-Pyridine prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    3-Bromo-5-Iodo-Pyridine: Direct from the Manufacturer

    Distinct Chemistry, Consistent Delivery

    In the world of pyridine derivatives, every atom placement counts. Producing 3-Bromo-5-Iodo-Pyridine takes patience, keen attention to reaction pathways, and a willingness to push for high standards through every batch. Iodinated and brominated pyridines rarely leave room for error. Our team knows it well. Chemists who order from us often remind how the smallest impurity in a building block can ripple through an entire synthetic timeline, hard to fix later on. That’s why, batch after batch, we focus on getting the starting purity right, not just at the end but during every step of the process.

    Product Model and Specifications

    This pyridine derivative comes under our in-house model: “3B5IP-1278.” Each lot undergoes full GC-MS, HPLC, and 1H NMR spectrum checks. The compound offers purity exceeding 98% by area, which brings peace of mind to research chemists scaling from milligram discovery runs to larger pilot synthesis. Lost hours in purification are rarely excusable in downstream pharmaceutical or agrochemical work. In our shop, the consistency starts with carefully selected halogenation reagents and a reaction environment that excludes water and air with constant real-time monitoring. Most of our customers in both academia and the pharmaceutical sector cite stable melting point measurements (usually reported at 80-84°C for the crystalline form) as an indicator of batch-to-batch uniformity.

    Applications and Usage Insights

    Some molecules look simple at first glance: A five-membered aromatic ring with both bromine and iodine set at the 3 and 5 positions, hydrogen at the 2, 4, and 6 positions. The unique dual functionalization opens doors for chemoselective transformations that would be impossible with just a bromo- or iodo-pyridine alone. Medicinal chemistry researchers use this compound as a scaffold for cross-coupling reactions. The bond between carbon and iodine activates much faster than carbon-bromine, which lets chemists introduce metals or other groups step-wise, building up libraries of trial compounds quickly. We have seen collaborators publish syntheses where the iodo substituent participates in Suzuki coupling first, leaving the bromo group untouched for later functionalization. Site selectivity stands as one of the main reasons scientists ask for this particular substitution pattern instead of others.

    In crop-protection, manufacturers screen halogenated pyridines as candidates for new herbicide and fungicide ingredients. Subtle changes in ring electronics can shift biological activity, and dual-substituted pyridines such as this one help explore new modes of action. Our clients conducting these tests often send feedback about shelf-life. Pyridine derivatives with multiple halogens sometimes decompose under poor storage. We produce this compound in special amber glass bottles with solid lined caps, minimizing exposure to light and moisture. We log stability data for every batch, so end users don’t have to second-guess it before starting their screen.

    How 3-Bromo-5-Iodo-Pyridine Stands Apart

    People often ask what sets this compound apart from other halopyridines. From the synthetic bench, it’s clear: the dual halogen arrangement means two reactive handles on the same aromatic core, but with very different reactivity profiles. Compare with 2,3-dibromopyridine or 2,4-diiodopyridine — their cross-coupling behaviors diverge because electronic and steric influences change with atom placement. Switch the bromine and iodine positions and you get a different reactivity order. In our own scale-ups, we have confirmed that the 5-iodo group leaves much more easily under standard palladium catalysis than its 3-bromo neighbor. This order gives chemists practical control, not just theoretical options.

    Another big difference comes from handling safety and purification. Many pyridine derivatives run into trouble either with volatility, persistent odor, or hazardous dusts. During our on-site process verification, we adjusted fungal-resistant PPE and upgraded air-handling due to the persistent halogen odor these molecules give off. Our plant operators sample and seal each lot with ventilated hoods, and cartridge-filter respirators, which translates into a safer product on the shipping end. Chemists downstream barely notice a trace of the strong odor, which means less contamination risk in the lab.

    Compared with 3,5-dichloropyridine or monohalogenated derivatives, our 3-bromo-5-iodo variant hits a middle ground on reactivity — neither too aggressive for standard glassware nor too sluggish for high-throughput screening. Ease of handling is a practical concern seldom mentioned outside real manufacturing settings, but it matters for both scale-up and day-to-day research work.

    Why Chemists Ask for This Molecule Specifically

    Every year, we receive detailed notes from R&D chemists looking for scalable halopyridines that behave predictably under palladium, nickel, or copper-catalyzed conditions. The dual halogens in this compound invite step-wise derivatization, often with a lower risk of side-reactions or over-reactivity when compared to the more symmetric dihalides. During process development trials with pharma partners, attempts to use similar compounds with either two bromines or two iodines often produced complex mixtures — more purification steps, lower yields, and less control over substitution sequence. We watch the same trends in crop science, where predictability saves time and cost during seed-level biological tests.

    Patents filed by innovator pharma companies regularly cite this scaffold for heteroaromatic substitution cycles. We supply material for both small and mid-sized batch runs. In-house feedback loops with our customers guide process improvements, especially in handling and packaging for global shipments. Experience has taught us to pay attention to shipping temperature. Pyridine rings generally travel well, but halogenated aromatics need desiccant and pressure-tight seals — especially for shipments landing in humid regions. Returning customers report few if any failures upon arrival, a sign our packing and QA procedures align with real-world demands, not just paper specs.

    Production Details: Hands-On Perspective

    Scaling up production on-site reveals practical hurdles that don’t show up in lab notebooks. The bromination and iodination steps use hazardous chemicals that require regular safety audits and on-the-spot corrections. Batch records for this compound fill thick logbooks, with granularity about temperature ramps, solvent choices, and filtration speeds. At our facility, operators train specifically on managing solids filtration, as the heavy halide content clogs lines easily without vigilant stirring and timely filter changes. Production teams regularly recalibrate equipment to maintain consistent heating profiles throughout mixing tanks.

    Many first-time buyers ask about trace impurity containment. Our facility takes this aspect seriously. Multi-stage column chromatography, followed by high-vacuum drying, removes residual unreacted starting materials. In the rare case of trace halobenzene contamination, we run additional analytics before approval for shipment.

    Every raw material comes with its own certificate of analysis and marine-barrier shelf packaging. Labor costs rise during winter months when reactions slow down; warming jackets and vessel pre-heating become necessary steps. We log not only product data but also environmental conditions around critical batch milestones. Over years of keeping such records, we've learned what seasonal, regional, and even vendor-based differences do to quality, tweaking procedures for each repeat run.

    Environmental, Regulatory and Safety Aspects

    Halogenated heterocycles present unique environmental handling issues. Waste from bromination and iodination reactions must undergo scrubbing before disposal. On our shop floor, spent acids and halide salts are neutralized in dedicated tanks; effluent samples are tested regularly to stay within compliance standards on halide and organic matter limits. Regulatory compliance doesn’t get left at the loading dock either. We keep all shipping and handling documentation up to date, so customers avoid regulatory hassles during customs clearance.

    Transport of brominated and iodinated compounds means we work closely with logistics teams to classify under appropriate United Nations numbers for hazardous substances. We use triple-layer packaging for overseas freight — a lesson hard-won by experience with early leaks and customs hold-ups. If something can happen on a journey by sea or air, eventually it will, and we work with this reality every day. All containers are hand-labeled by trained staff, double-checked against electronic manifests, and only approved for release after a quality control manager signs off in person.

    On the worker safety front, halogenated pyridines require full gloves, goggles, and regular ventilation checks. We have built redundancies into emergency responses, with annual spill drills that everyone, from lab tech to management, participates in. Safe handling instructions come directly from observations on the shop floor, not just GHS label sheets.

    Collaboration and Continuous Feedback

    Serving a specialized scientific audience means staying in touch with realities in university, biotech, and manufacturing labs. Every year, teams from our company visit site partners and conference booths for real-time feedback. One of the main requests from customers involves batch-size flexibility: a single gram for early-stage method development up to tens of kilograms for larger pilot plant campaigns. Our systems can shift production within a week — not every manufacturer can pivot that quickly, and it matters when researchers get stuck waiting on small quantities from large bulk suppliers.

    From start to finish, our commitment stays with the people using these compounds on a daily basis. We track lot usage and follow up after shipments arrive to catch any values falling outside customer spec. Any rejected lot gets priority review — we don’t keep sending “business as usual” if something unexpectedly fails downstream or in analytical quality controls. Often, lessons from a failed shipment shape future production details, sometimes leading us to change a raw material supplier, sometimes to tweak purification strategies to fit a customer’s end-use demands.

    We also set up regular training for our production staff as new reaction techniques, better reagents, and updated equipment come online. Regular upgrades fit well into our standard, and we try to bring our customers along as we improve steps or automate bottlenecks in both synthesis and downstream analytics.

    Supply, Demand, and Market Dynamics

    The availability of pyridine derivatives depends as much on market realities as synthetic know-how. In some years, upstream costs for specialty halogen reagents spike — wider geopolitical trends can send iodine or bromine prices swinging. One year may bring sudden limits on bromine imports, pressing us to adjust schedules, refit for alternate runs, and work overtime to keep up with demand. Such swings often push suppliers to compromise on quality or price, but our experience recommends holding steady: it costs more to lose a customer trust than to weather a bad season.

    Some new entrants in the market try to cut corners, offering off-spec or “blended” lots to save on cost or materials. We don’t participate in this. Quality assurance starts in the reaction vessel — no amount of re-melting or re-crystallization can undo careless upstream work. Researchers who depend on clean, reliable building blocks deserve transparency and a clear dataset to work from.

    Recent years have also seen more labs shifting toward green chemistry metrics. We routinely discuss options for process intensification — using solvent recycling, continuous flow reactors, or other greener routes where feasible. Total sustainability is a journey; major steps forward require new investment. We constantly debate, research, and test greener alternatives while maintaining product consistency.

    Future Directions and Process Improvements

    Tomorrow’s chemical manufacturing won’t look like today’s. Batch processes that once defined the industry are steadily ceding ground to semi-continuous and continuous set-ups. Pyridine derivatives, especially those with complex halogenation patterns, bring tough synthesis challenges into view. Our team invests time in exploring catalytic cycles that might one day lower reagent excess or enable milder synthesis of fully substituted arenes.

    We talk to academic partners testing new ligands that activate C–Br or C–I bonds with higher yields or cleaner profiles. Each credible new finding returns into our process development kitchen. We don’t swap out familiar steps until proven at pilot scale, but we’re not wedded to tradition when better science emerges. In certain cases, we push for bench-top miniaturization — microreactors that produce highly pure intermediates for downstream combinatorial chemistry work.

    On the logistics side, supply chain transparency grows ever more important. We track sourcing from halogen suppliers with documentation showing both ethical sourcing and material stewardship. Electronic manifests and real-time transport data further minimize risk and make it easy for us to reassure customers anxious over every step between “order placed” and “goods received.” Surprises in the chain are rare for regular clients.

    Customer suggestions drive much of our future planning. Some recent collaborations aimed at switching to glass replacements for certain bottle sizes, cutting microplastic residue at the delivery stage. Others focus on new forms of hazard labeling, so that lab teams in far-off countries can scan data directly. Making these advancements requires investment not just in technical upgrades but also in people who care for getting both the process and the end-use right.

    Our Commitment: Lasting Partnerships Over Quick Sales

    Having manufactured pyridine building blocks for over a decade, we have seen fads and false promises come and go. Supply chain pinch points, fluctuating raw material prices, and sudden regulatory changes shape daily work. In the end, steady relationships with customers who value our attention to their end-use requirements matter the most.

    3-Bromo-5-Iodo-Pyridine, with its unique dual reactivity and robust batch-to-batch quality, stands as one of the most reliable building blocks on the books for innovative research and applied synthesis. Our manufacturing process — tailored by real-world demands, not just written specs — keeps us focused on delivering the tools chemists need to innovate, discover, and build new solutions. Every order, every batch, every customer case brings us new lessons that go straight back into making tomorrow’s chemistry a little better, a little safer, and a lot more reliable.