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3-Bromo-2,5-Dichloropyridine

    • Product Name 3-Bromo-2,5-Dichloropyridine
    • Alias 3-Bromo-2,5-dichloro-pyridine
    • Einecs 629-794-1
    • 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

    273109

    Chemicalname 3-Bromo-2,5-Dichloropyridine
    Casnumber 745783-00-6
    Molecularformula C5H2BrCl2N
    Molecularweight 242.39 g/mol
    Appearance White to off-white solid
    Meltingpoint 62-66°C
    Purity Typically >98%
    Solubility Soluble in organic solvents like DMSO and dichloromethane
    Density 1.84 g/cm³
    Smiles C1=CC(=NC(=C1Cl)Br)Cl
    Inchi InChI=1S/C5H2BrCl2N/c6-3-1-4(7)9-5(8)2-3/h1-2H
    Storagetemperature Store at 2-8°C
    Synonyms 2,5-Dichloro-3-bromopyridine

    As an accredited 3-Bromo-2,5-Dichloropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 3-Bromo-2,5-Dichloropyridine is packaged in a sealed 25g amber glass bottle with a tamper-evident cap and safety labeling.
    Shipping 3-Bromo-2,5-Dichloropyridine is shipped in tightly sealed containers, protected from moisture and direct sunlight. Transport occurs under standard ambient temperature with appropriate labeling. As a hazardous material, it follows all relevant chemical shipping regulations to ensure safety. Suitable protective measures are taken to prevent spillage or accidental contact during transit.
    Storage 3-Bromo-2,5-Dichloropyridine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep it separated from incompatible substances such as strong oxidizing agents. Store at room temperature, and ensure proper labeling. Use personal protective equipment when handling, and avoid exposure to moisture and extreme temperatures.
    Application of 3-Bromo-2,5-Dichloropyridine

    Applications of 3-Bromo-2,5-Dichloropyridine in Industrial Manufacturing

    As the original manufacturer, we supply 3-Bromo-2,5-Dichloropyridine to global B2B clients whose downstream processes rely on specialized halogenated pyridine intermediates. Our consistent QC, documentation, and process control support its integration in select, high-value industrial sectors. Below, we provide detailed information on real application scenarios, with technical specifications for compliance, formulation, finished goods, and process integration.

    1. Pharmaceutical API Intermediate Synthesis

    Major pharmaceutical manufacturers utilize 3-Bromo-2,5-Dichloropyridine as a halogenated pyridine intermediate within active pharmaceutical ingredient (API) synthesis pathways. Its unique substitution pattern allows direct incorporation into heterocyclic scaffolds for neuropathic pain management compounds, antibacterial agents, and oncology drug leads. Sourcing directly from our facility provides upstream traceability for regulatory audits and seamless documentation needed for finished API registration.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) general chapter 2034
    • USP General Chapter <1078> GMP
    • FDA 21 CFR Part 211: Finished Pharmaceuticals

    Typical usage ratio

    • 0.4–2.5 molar equivalents per target API batch; precise ratio depends on downstream pyridinyl core structural requirements and pathway conversion yield

    Downstream process integration

    • Introduced during early-stage synthesis as a building block in Suzuki-Miyaura or Buchwald-Hartwig coupling cycles; steps include halogen-metal exchange, dehalogenation, and further N-functionalization transformations

    Final product types

    • Neuroactive drugs (e.g., antiepileptics under patent)
    • Anti-infective compounds (candidate pipeline molecules)
    • Oncology research chemicals for structure–activity relationship studies

    2. Agrochemical Active Ingredient Manufacturing

    Leading agrochemical producers employ this substituted pyridine derivative within custom synthetic routes for pyridinyl-based herbicides and fungicides. The halogenation pattern supports downstream reactivity in nucleophilic aromatic substitution and directed metalation, enhancing field efficacy of the final crop protection products while simplifying impurity profiling at industrial scale.

    Industry compliance standards

    • FAO/WHO Manual on Development and Use of FAO and WHO Specifications for Pesticides
    • ISO 9001:2015 for agrochemical production
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • China GB/T 1604 pesticide standards

    Typical usage ratio

    • 5–15% by weight of active ingredient synthetic starting material; actual ratio depends on target herbicide or fungicide structural complexity

    Downstream process integration

    • First halogenated pyridine input within multi-step catalytic synthesis, followed by O- and N-alkylation reactions and purification via distillation and crystallization units

    Final product types

    • Pyridinyl-based herbicides for cereals and legumes
    • Fungal disease control agents for rice and cotton crops
    • Custom pesticide active ingredients supplied as technical concentrates

    3. Fine Chemical Synthesis for Specialty Electronic Materials

    Manufacturers in specialty electronics formulate halogenated aromatic compounds based on our product to produce advanced intermediates used in OLED materials, liquid crystal displays, and electron-transporting agents. The halogen and nitrogen atom configuration provides solution-phase reactivity compatible with high-purity requirement synthesis for the electronics industry.

    Industry compliance standards

    • IEC 62474 Material Declaration Standard for the Electrical and Electronics Industry
    • REACH (EC) No 1907/2006 Registration
    • JIS G 0321 Japanese Materials Standard
    • RoHS Directive 2011/65/EU constraints on hazardous halogen content

    Typical usage ratio

    • 1–8% by total weight of specialty fine chemical batch; adjusted according to electronic performance target and downstream yield optimization

    Downstream process integration

    • Input within cyclization, cross-coupling, and high-vacuum distillation stages to obtain ultrapure aromatic intermediates for device-grade deposition precursors

    Final product types

    • OLED emitter and electron-transporting material intermediates
    • Precursors for aligning layers in TFT-LCD panels
    • Electronic-grade fine chemicals for advanced display manufacturers

    4. Custom Synthesis for Research & Development Reagents

    Analytical chemistry and university R&D laboratories source this compound for development of new pyridine-based scaffolds and as a reference standard during synthesis route exploration. The halogenated pyridine structure facilitates controlled reactivity studies, directed halogen exchange, and validation for structure elucidation in heterocyclic research.

    Industry compliance standards

    • ISO/IEC 17025:2017 Laboratory Competence Standard
    • ACS Analytical Reagent Specifications
    • GLP (Good Laboratory Practice) for chemical research
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • 0.01–0.5 g per reaction scale; chemists adjust proportion for small molecule screening, reference synthesis, or analytical spike introduction

    Downstream process integration

    • Dissolved as a core reactant for halogenation, Suzuki coupling, and nucleophilic substitution test reactions; also serves as calibration standard in HPLC/GC-MS method development

    Final product types

    • Research-grade heterocyclic reference compounds
    • Library screening building blocks for new molecular discovery pipelines
    • Analytical standards for trace detection of halogenated pyridines
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    Competitive 3-Bromo-2,5-Dichloropyridine prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    3-Bromo-2,5-Dichloropyridine: A Practical Look from the Manufacturer’s Bench

    Everyday Work With 3-Bromo-2,5-Dichloropyridine

    Chemists working in the production halls know the importance of precision and responsibility when it comes to handling sensitive intermediates. 3-Bromo-2,5-dichloropyridine holds a steady presence in our daily workflow, not because it’s the fanciest or most publicized pyridine derivative, but because of its consistent performance and versatility. In our factory, the value of a substance comes out not just in the lab, but also at scale—how it behaves across dozens of batches, how controllable it is, how cleanly it reacts with other building blocks, how predictable the outcome for downstream chemistry.

    The Role of Structure in Performance

    With the molecular formula C5HCl2BrN, and registered under CAS number 97963-53-8, 3-Bromo-2,5-dichloropyridine stands out for its unique substitution pattern. The two chlorine atoms at positions 2 and 5, plus a bromine at the 3-position, produce electron withdrawing effects. Over repeated campaigns, we’ve noticed that this substitution unlocks special reactivity for subsequent cross-coupling, especially Suzuki and Stille reactions. The molecule responds reliably to palladium-catalyzed coupling, offering a clean bridge to a wide range of aryl, alkynyl, or alkyl partners. Our chemists appreciate the way this combination of halides lets them tune downstream reactions—some customers require selectivity, others need flexibility. Comparing countless analogues, not many others match both the range and the control this compound provides.

    Batch Manufacturing Realities

    On the production floor, everything begins with sourcing. Reasonably pure starting materials, mostly upstream halopyridines and halogenating agents, set the tone for purity later on. We watched, over the years, how even a subtle change in solvent source or a difference in drying conditions can throw off the downstream purity or even crystal habit. Each kilogram we manufacture runs through stages of purification and quality checks—liquid chromatography, melting point determination, and NMR analysis. Consistent results have taught us the limits: this pyridine derivative comes off as a light beige crystalline powder, with purity above 98% by GC or HPLC. Impurities show up early; production teams respond by adjusting the isolation protocol or tweaking temperatures at the crystallization step.

    Specifications Reflect What Works

    Though the market offers several pyridines with similar substitution patterns, they often bring different challenges in reactivity or handling. 3-Bromo-2,5-dichloropyridine, for us, maintains a manageable melting range (typically around 70-74°C, as observed repeatedly in our lab), handles air and moisture in standard storage, and moves easily in glassware. Packing the product follows standard safety rules for halogenated aromatic compounds: polyethylene-lined fiber drums or strong sealed bags inside sturdy cardboard containers. Our warehouse staff highlights that it doesn’t cling, clump, or form static the way some analogues do—a simple but important detail for anyone filling, weighing, or dispensing during downstream processing.

    How Customers Use It

    Feedback from longtime partners—both large pharma synthesis teams and smaller custom research groups—echoes similar themes. 3-Bromo-2,5-dichloropyridine enters as a starting point for more complicated scaffolds, especially for medicinal chemistry and agrochemical discovery. Many rely on its dual halogen functionality to block certain positions, then selectively manipulate others. The structure helps in preparing derivatives that explore the properties of potential new APIs or crop protectants. We’ve watched over the years how those downstream transformations rely heavily on the initial halide orientation. Colleagues from other companies occasionally experiment with one-chlorine or three-chlorine pyridines, but the pattern of reactivity for this 2,5-dichloro-3-bromo variant keeps coming up for the right blend of activity and selectivity.

    Direct Experience with Handling and Storage

    We store the product under ambient indoor conditions, with a simple desiccant. While some pyridine derivatives absorb water or degrade, our own aging tests show this compound remains stable for over a year in the right packaging. Over our years of production, only minor issues arising from defective seals have triggered sweating or color change; adjustments in packaging materials solved these problems effectively. Even so, warehouse and logistics teams always treat it with respect. It has a pungent, but tolerable, odor characteristic of many halogenated pyridines, and requires only the usual PPE—nitrile gloves, safety glasses, and a lab coat—for safe handling. Routine spills are easy to control, as it’s non-volatile and settles quickly.

    Consistency Across Large Campaigns

    The leap from pilot-scale batches to consistent multi-kilogram runs took its toll on our staff’s patience years ago. Scaling up means addressing issues that small batches rarely reveal: uneven heating, mixing inefficiencies, small differences in cooling rates. Our production engineers recall checking each large batch against the same reference chromatograms to ensure that the bromide and chloride content landed squarely within spec. The pressure to deliver uniform material—lot after lot—to demanding multinational customers forced us to refine our procedures to the point where even minor off-spec readings call for root cause investigation. Once a customer working on a critical synthesis flagged a trace impurity—the result of a barely detectible byproduct from the halogenation step. Adjusting reagent concentration and reaction sequence solved it for good.

    Comparison With Related Pyridines

    The world of halopyridines carries its own routines and quirks. We’ve routinely worked with 2,3,5-trichloropyridine, 3-bromo-5-chloropyridine, and 2,6-dichloro-3-bromopyridine. Each brings pros and cons, but the 2,5-dichloro-3-bromo arrangement gives better coupling reactivity at the 4-position and more stability than certain mono-bromo or mono-chloro variants. Researchers notice that for selective further substitutions or metalations, this variant avoids competing side reactions that sometimes turn up in other halopyridine isomers. Syntheses that stall, form tars, or generate a mess of inseparable isomers on other derivatives tend to proceed more cleanly using this compound. In that sense, actual usage across repeated projects—instead of theoretical comparisons—guides both us and our clients toward this molecule.

    Process Upsets and Everyday Solutions

    Real production doesn’t always run as planned. Occasional raw material contaminants, batch contamination from outside sources, or shipment delays put added stress on the team. We’ve learned to maintain backup supplies of our key starting pyridines, and often run rapid test reactions and isolation checks to catch potential out-of-spec products at the earliest possible stage. Teams from analytical chemistry work side by side with operators, sometimes running samples as soon as a batch is filtered instead of waiting for the normal schedule. All of this cuts down on wasted time and lost revenue later. Establishing a culture of open reporting—where a team member can call out a cloudy batch before it ever leaves the reactor—stems from years of producing compounds like this and dealing with the fallout of missed problems.

    How We Approach Quality and Safety

    Producing halogenated pyridines carries both rewards and risks. The best lessons in handling triangular-shaped molecular structures with halides at multiple sites have come from direct encounters with toxicity concerns and scale-specific hazards. Chlorinated and brominated aromatics have environmental and safety implications; every step must get documented and monitored under strict internal and governmental regulations. Our teams have learned not just to comply but to improve year by year, reducing waste solvent volumes, improving energy use during reaction and washing cycles, and capturing exhaust streams for proper treatment. Actual reductions show up both as cost savings and in regulatory audits. A close partnership with waste handlers and regular reviews of our waste streams make sure residues of compounds like 3-Bromo-2,5-dichloropyridine don’t present downstream problems.

    Reflections on Market Demand and Trends

    Shifts in market demand always matter for a small set of specialist chemicals. We see pharma moving steadily toward more halogenated heterocycles, especially in early stage research, which directly affects run schedules and storage planning. As drug candidates become more complex, the requests for more jejune intermediates like 3-Bromo-2,5-dichloropyridine rise. Certain agricultural research groups also keep this compound in their toolkit, especially for protecting groups or for preparing lead candidates with higher lipophilicity. A noticeable trend is the growing demand for higher-purity material, driven by tightening regulatory scrutiny of trace metal and non-halide byproducts. We’ve adapted testing protocols to meet these requirements—sometimes ahead of regulation, simply to satisfy customer expectations.

    Support for Research-Scale Through Commercial Orders

    Manufacturing doesn’t stand alone. Researchers often ask for minor modifications in packaging, documentation, or testing, all depending on their downstream needs. Sometimes a new project requires a re-validation of existing certificates or the addition of new impurity profiles. Our approach is to make small-lot material available for method development in addition to regular production orders. The lessons learned from supporting relatively small-scale, high-variability requests have actually helped improve bulk production, since identifying customer pain points leads quickly to process improvement and better outcomes for all involved.

    The Role of Traceability

    Years of experience in the chemical sector highlights the value of traceability for each kilogram leaving our storage. Each drum, each inner bag, every analytical report links back to actual production records and operator logs. This practice doesn’t just support internal quality; customers rely on full provenance to validate their own processes. Researchers, production engineers, and procurement specialists consistently ask about batch histories, stability trials, and lot-specific data—especially if a downstream synthesis hits a snag. Open records, accessible via electronic logs and actual retention samples, translate directly into trust. We see it every year in the form of long-term contracts, repeat projects, and technical inquiries that go beyond the standard fare.

    Regulatory Reality and Compliance

    Handling halogenated heterocycles such as 3-Bromo-2,5-dichloropyridine obligates us to meet evolving regulatory standards. Governments and auditors ask for more stringent documentation every year—not limited to product quality, but covering staff training, waste disposition, air and water emissions, and transportation. Our technical, EHS, and documentation teams collaborate to anticipate new requirements and to ensure not only compliance, but efficient operation. Detailed records of solvent consumption, reagent shipments, and product turnover reduce the risk of audits resulting in headaches or downtime. It becomes clear that regulatory expectations also drive process improvements, as compliance becomes another way to demonstrate capability and integrity with our partners.

    Looking at Environmental Impact

    Production of halogenated aromatics brings the tough question of environmental footprint. Our customers, especially in pharma, now ask about carbon accounting, water use, and end-of-life disposal even for early intermediates. Over time, we’ve invested in solvent recycling and energy recovery, as well as measures to contain fugitive emissions. On several occasions, customer audits cover not just material traces but life cycle assessments and waste management records. We’ve learned to see these demands as opportunities to document good practice and to uncover possible areas for progress—be it by modifying a cleaning procedure or investing in updated scrubbers. Taking these extra steps means more than checking boxes; they help us make the case for continued cooperation with environmentally conscious partners.

    Continuous Improvement Driven by End Use

    Practical insight comes directly from regular interaction with scientists putting our products to work. Many synthetic challenges land on our help desk, not as complaints, but as requests for advice or support. The feedback from end users holds more value than specifications written on paper. Specific examples include researchers encountering selectivity issues or solubility problems—sometimes the origin points right back to crystal morphology, storage, or even solvent trace levels left over from isolation. Repeated rounds of troubleshooting sharpen our attention to detail and reinforce the ties between upstream manufacturing and practical, real-world chemistry.

    Responding to Shifts in Global Logistics

    Raw materials and finished goods shipments move through complex supply chains. Recent years haven’t made things any easier, with transportation bottlenecks, customs delays, and shifting regulatory requirements. Each new challenge—be it port congestion or regional lockdowns—pushes us to refine workflows and inventory management. By holding safety stock and working closely with logistics partners, we help customers avoid project delays caused by short supply or unplanned interruptions. Strengthening local partnerships also reduces risk for urgent shipments, especially for essential pharma intermediates.

    Building Trust in a Technical Partnership

    Trading chemical intermediates is only one side of a deeper technical partnership. Customers returning year after year depend on the knowledge, technical data, transparent support, and problem-solving capacity our staff provides. Whether identifying an unexpected retention time, troubleshooting a reaction that runs slowly, or supporting a scale-up, we commit to open dialogue. Years of shared experience with compounds like 3-Bromo-2,5-dichloropyridine make clear that the right knowledge, applied diligently, underpins safe, efficient, and successful downstream chemistry.

    Summary: Real Value Rooted in Experience

    3-Bromo-2,5-dichloropyridine’s place in our product line results from years of direct involvement—careful selection of raw materials, disciplined processing, active customer support, and regular attention to process improvement. Its unique structure and reactivity offer repeatable benefits that show up not just in yield or purity, but in ease of handling, practical storage, and downstream adaptability. Both researchers and manufacturers keep relying on it across evolving markets and rising technical requirements. From firsthand accounts on the manufacturing floor to technical assistance in customer labs, the usefulness of this compound stands less as abstract promise and more as lived experience, shaped by the demands and successes of real-world chemistry.