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4-Bromomethyl-2,6-Dichloropyridine

    • Product Name 4-Bromomethyl-2,6-Dichloropyridine
    • Alias 4-Bromomethyl-2,6-dichloropyridine
    • Einecs 629-844-3
    • 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
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    Specifications

    HS Code

    994714

    Chemical Name 4-Bromomethyl-2,6-Dichloropyridine
    Cas Number 86604-75-3
    Molecular Formula C6H4BrCl2N
    Molecular Weight 240.92
    Appearance White to off-white crystalline powder
    Melting Point 58-62°C
    Purity Typically >98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Storage Conditions Store in a cool, dry, and well-ventilated place
    Synonyms 4-(Bromomethyl)-2,6-dichloropyridine

    As an accredited 4-Bromomethyl-2,6-Dichloropyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

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    Application of 4-Bromomethyl-2,6-Dichloropyridine

    Applications of 4-Bromomethyl-2,6-Dichloropyridine in Industrial Manufacturing

    As the origin manufacturer of 4-Bromomethyl-2,6-dichloropyridine, we provide this specialty intermediate for targeted sectors where it delivers dependable performance in complex synthesis pathways. Below, we outline real industrial scenarios of its use, focusing on differentiated details of regulatory compliance, process integration, dosage rationale, and expected final outputs within established downstream domains.

    1. Agrochemical Active Ingredient Synthesis

    This pyridine derivative serves as a critical building block in the synthesis of selective herbicide actives—mainly as a halogenated intermediate in the multi-step production route of chlorinated pyridine-based weed control agents. Its bromomethyl group enables high-yield coupling and ring derivatization stages essential in producing molecules with crop-specific bioactivity and environmental persistence aligned with today’s regulation boundaries. Formulators adjust input load by target molecule structure and batch scale, balancing conversion and waste minimization per process design.

    Industry compliance standards

    • EU REACH Regulation (EC) No 1907/2006 Chemical Safety Reports
    • U.S. EPA FIFRA Registration Requirements for Technical Ingredients
    • ISO 9001:2015 Quality Management (site and process)
    • Chinese GB2763 Maximum Residue Limits in Food

    Typical usage ratio

    • Ranges between 0.8–1.6 molar equivalents per final active herbicide molecule, scaled based on the targeted yield and synthetic step yield in multi-ton reactions.

    Downstream process integration

    • Charged during halogen exchange or Grignard cross-coupling as the primary functionalized ring carrier; specifically, introduced after catalyst charge and solvent addition in closed-system batch reactors.

    Final product types

    • Technical-grade selective herbicide actives (e.g., dichloropyridinyl herbicides)
    • Synthesized intermediates for pesticide formulation

    2. Pharmaceutical Intermediate for Antiviral API Synthesis

    Leading pharmaceutical manufacturers integrate this compound as a key intermediate within the controlled synthesis of certain small-molecule antiviral candidates, particularly in the preparation of pyridine-based molecular scaffolds for clinical-stage active pharmaceutical ingredient pipelines. Purity and residual halide content undergo rigorous QC, driven by regulatory and QC audit requirements in GMP-certified facilities, with batch addition calculated from the API’s targeted molar composition and solubilization protocol in API plants.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF and European Pharmacopoeia monograph standards for intermediates
    • FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • EDQM CEP/COA documentation

    Typical usage ratio

    • 0.5–1.3 equivalents relative to target pyridine core in heterocycle assembly, determined by reaction stoichiometry and API batch run scale (up to 1:1 molar for high-purity requirements).

    Downstream process integration

    • Added at the controlled nucleophilic substitution stage preceding API cyclization; handled in jacketed reactors with in-process monitoring for bromide elimination and purity control during intermediate isolation.

    Final product types

    • Clinical and commercial batch pyridine-based antiviral APIs
    • Pharmaceutical-grade intermediates for CDMO use

    3. Fine Chemical Synthesis for Specialty Coatings Additives

    Downstream specialty chemical manufacturers deploy this halogenated pyridine in the preparation of high-performance anticorrosion additives for industrial coatings. Its dichloropyridine ring enables robust reactivity in the modification of amine reactivity and weather-stabilizer precursors, with strict conformance to coating industry standards. Tighter control of usage ratio minimizes off-target functionalization and ensures compatibility with base resin matrices, especially for OEM automotive or marine application standards.

    Industry compliance standards

    • ISO 12944-6:2018 (Protective Paint Systems, Laboratory Performance)
    • ASTM D520-20 (Zinc Dust Pigment in Paints)
    • EU RoHS Directive 2011/65/EU (restriction on hazardous substances)
    • Automotive OEM Technical Approvals (e.g., Volkswagen TL226)

    Typical usage ratio

    • Generally 0.2–0.7% by weight relative to total additive blend; adjusted for final coating viscosity, zinc reactivity, and targeted salt spray resistance according to lab test protocol.

    Downstream process integration

    • Charged during additive precursor synthesis prior to blending with primary anticorrosion resin; typically fed to sealed blending vessels under inert atmosphere, followed by purification and integration into masterbatch.

    Final product types

    • Pyridine-modified coating additives
    • Industrial-grade anti-corrosive paint formulations
    • Composite epoxy systems for harsh environment applications

    4. Crop Protection Intermediates for Insecticide Synthesis

    Producers of pyridine-based insecticidal agents utilize this raw material in multistep flow chemistry for building potent active structures. Its halogen substitution pattern offers selective reactivity in site-specific methylation and allows downstream control of mode-of-action fine-tuning, serving major agricultural chemical companies. Risk controls include compliance with agricultural regulatory screening, as well as validated cleaning validation to prevent cross-contamination in campaign manufacturing setups.

    Industry compliance standards

    • FAO/WHO Specification for Plant Protection Products
    • BPR (EU Biocidal Products Regulation) for Precursors
    • ISO 17025:2017 (Testing and Calibration Laboratories)
    • EPA PRIA (Pesticide Registration Improvement Act) workflow for technical ingredients

    Typical usage ratio

    • 0.9–1.8 molar equivalents, based on insecticidal mode of action pathway and degree of substitution required in the finished active agent molecule.

    Downstream process integration

    • Fed at the nucleophilic aromatic substitution stage or during halide-exchange step in continuous-flow or batchwise agrochemical synthesis; maintained under temperature and agitation specified in validated process documents.

    Final product types

    • Technical-grade insecticide active compounds (e.g., pyridine-derived neonicotinoids)
    • Granular, emulsifiable concentrate, or suspension concentrate insecticide formulations

    5. Electronic Chemical Intermediate for Photoresist Raw Materials

    In advanced microelectronics manufacturing, particularly photoresist production for semiconductor wafer processing, this dichlorinated pyridine acts as a functionalized intermediate for designing halogenated monomers. The strict absence of trace metals and defined halide stability support process repeatability in scale-up. Semiconductor chemical plants employ this input with exact dosage tied to photochemical performance, purity thresholds, and fit within supply chain traceability for device fabrication.

    Industry compliance standards

    • SEMI C1-0705 (Requirements for Photoresist Raw Material Purity in IC Manufacturing)
    • ISO 14644-1:2015 (Cleanroom Classes)
    • JEITA Green Procurement Standards
    • RoHS Directive compliance for electronic chemicals

    Typical usage ratio

    • Typically 0.5–1.2 equivalents relative to polymer monomer backbone, adjusted for final resist sensitivity and line width control in photolithographic patterning.

    Downstream process integration

    • Introduced during the initial synthesis of halogenated pyridine monomers before polymerization; handled in contamination-controlled environments and purified by sub-ppm residuals for semiconductor standard qualification.

    Final product types

    • Halogenated monomer intermediates for advanced photoresists
    • Polymerizable resins for semiconductor photolithography applications
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    More Introduction

    4-Bromomethyl-2,6-Dichloropyridine: Bringing Precision and Consistency to Chemical Synthesis

    Some compounds grab your attention because of their specificity and reliability. 4-Bromomethyl-2,6-Dichloropyridine stands out among specialty chemicals. As folks who’ve worked with both broad-range intermediates and niche pyridine derivatives know, finding a chemical with stable reactivity and easy dosage in multi-step syntheses saves time and money. There are countless intermediates, but not all show the same balance of selectivity and stability in real lab conditions. This compound delivers that balance, which explains why more chemists and process engineers keep it in regular rotation.

    Model Features and Chemical Highlights

    This compound comes as a crystalline solid. That alone changes the workflow for anyone tired of chasing volatile, sensitive liquids that break down before they get used. Its melting point helps keep it stable on the shelf, and the crystalline form lets you weigh it with confidence instead of eyeing sticky oils and hoping the last batch held up. As a bromo-methylpyridine with two chlorines at the 2 and 6 positions, it brings a unique kind of reactivity—electrophilic, but not wild; selective, but not too sluggish.

    4-Bromomethyl-2,6-Dichloropyridine’s structure gives it more than just a catchy name. You get targeted bromination at the methyl position, while the dichloro pattern limits unwanted side reactions along the pyridine ring. I’ve seen labs switch from mono-chloro or unchlorinated bromo-methyl pyridines and immediately notice fewer purification headaches and better yields. This comes from real-world use in both pharma pilot plants and research settings, not just theory or catalog copy. A solid product lets teams focus on new chemistry instead of reworking old routes.

    Applications that Demand Precision

    In pharmaceutical R&D, one missed bond can send a whole program back to the drawing board. This is where 4-Bromomethyl-2,6-Dichloropyridine has made a name for itself. As a coupling partner, it enables the construction of more complex heterocycles with fewer side products. Medicinal chemists value it for alkylation steps in the synthesis of drug-like molecules, especially those with stringent purity targets. The dichloro-substitution pattern shields the pyridine core, directing reactions where you want them instead of where you don’t.

    Crop science and specialty materials science also put this molecule to use. One example: introducing it into custom pesticides, where the right intermediate blocks degradation in the field. Researchers in agricultural chemistry use it to make analogs that resist breakdown from UV, heat, and other field stresses. In electronic materials, that same limited reactivity finds a place in specialty polymers and photoresists. Each sector values consistent reactivity over theoretical maximum reactivity—cleaner intermediates mean smoother scale-ups and more robust final products.

    What Sets It Apart from Other Synthetic Building Blocks

    A lot of synthetic intermediates can start a reaction, but not every one finishes cleanly. Compared to mono-substituted bromomethyl pyridines or those without chlorine, 4-Bromomethyl-2,6-Dichloropyridine narrows the window of reactivity. Fewer chlorines mean more side reactions at the desired position; too many, and you lose solubility or get unexpected byproducts. The 2,6-dichloro configuration gives a sweet spot: you retain solubility in common solvents and keep byproducts low. This isn’t academic—reaction tanks are filled with grams and kilos, not micromoles, so avoiding sticky residues and off-color impurities saves real money in post-reaction work.

    Switching from similar compounds with a bare pyridine ring, folks often complain about over-alkylation or polymerization issues. I’ve worked with processes that swapped to this compound and finally put aside complicated washes and labor-intensive chromatographies. The ability to scale up with less fuss matters just as much as cost per kilo.

    Handling and Lab Experience

    If you’ve ever spent a morning fighting with a moisture-sensitive intermediate, you know it’s not fun. This product’s solid state and low volatility cut down on special handling cabinets or protective gear, streamlining prep work and storage. Disposal becomes simpler and safer—always a plus in shared lab spaces. Others I’ve worked with appreciated not having to second-guess whether the material in the bottle is still fit for use after sitting for a few weeks. Little efficiencies like this add up in environments where time and attention are precious.

    One aspect chemists from all backgrounds notice: improved batch-to-batch reproducibility. Small-batch syntheses in R&D can glide into kilo-lab and production without redesigning the entire process. This trait resonates with both younger researchers and veteran process engineers, especially as more companies push projects from bench to pilot scale in tighter timeframes. In the hands of a skilled team, the consistency built into 4-Bromomethyl-2,6-Dichloropyridine reduces troubleshooting and lets innovation lead.

    Quality Considerations and Purity

    Let’s face it: purity isn’t just about hitting a number on a certificate. It’s about trust in what you’re putting into the next step. Small impurities grow into bigger ones, so a clean starting point carries right through to the end. Suppliers with rigorous quality control produce this compound in a form that holds up to close scrutiny—both under the NMR and by those doing critical analyses. Any seasoned chemist understands that missing or misidentified contamination in an intermediate can invalidate weeks of work, burn through budgets, and frustrate everyone involved.

    Beyond product quality, documentation and transparency from the source really matter—traceable batch data, independent verification, reliable packaging. These features build trust and help lower the chance of mishaps, whether you’re at the formulation stage or running a regulated synthesis for a pharmaceutical client. Once you’ve been burned by poor documentation or off-spec intermediates, switching to a reliable version of 4-Bromomethyl-2,6-Dichloropyridine feels like a breath of fresh air.

    Solutions for Common Pain Points

    Plenty of folks working in synthetic chemistry hit the same snags: inconsistent material, unexpected byproducts, poor scalability. Over the years, I’ve seen intermediate suppliers come and go, promising pure compounds at bargain prices, only for those savings to evaporate during troubleshooting. 4-Bromomethyl-2,6-Dichloropyridine doesn’t attack from every direction—its selective reactivity streamlines reactions and eliminates much of the post-reaction tinkering. This makes project management smoother, letting teams spend energy on tuning final product features, not fixing preventable messes.

    For those worried about moving new molecules up the scale, the predictability built into this compound shrinks pilot-plant risk. Batches act the way bench reactions did; you don’t get unpredictable exotherms or mystery residue. That cuts down on wasted raw materials and lost time. In faster innovation cycles, nobody can afford repeated troubleshooting. A solid intermediate turns risk into reliability.

    Working with Regulatory Expectations

    Audits and regulatory reviews become less burdensome when the basic building blocks come from consistent, well-documented sources. 4-Bromomethyl-2,6-Dichloropyridine isn’t some experimental curiosity; it aligns with modern expectations in pharma, agri, and specialty materials sectors. Detailed characterization data saves headaches later, especially where client or regulator questions dive into supply chain or traceability. Materials that match specifications time after time simplify compliance and reporting. That’s not hypothetical—it matters during investigations, recalls, or when public health is on the line.

    Reducing Environmental Footprint

    Teams concerned about waste streams and environmental sustainability weigh intermediate choices. Consistent, selective reactivity means less solvent, less purification media, fewer secondary treatments. Every unnecessary crystallization or column turns into more solvent waste and higher disposal costs. Across years of handling everything from standard amines to fluorinated heterocycles, I’ve seen how a single smart intermediate can drop a process’s E-factor and cut disposal headaches. People in green chemistry agree: selection of reliable, well-behaved intermediates provides a lever for sustainability, not just price or speed.

    Life in the Lab: User Insights

    Real-world stories speak louder than any spec sheet. I remember early trials switching to 4-Bromomethyl-2,6-Dichloropyridine in a time-pressured project. The product curve showed less trailing impurity, and the downstream crystallization yielded twice as much purified material, using the same equipment and protocols. Researchers who test various intermediates often report the same thing: reactions become less finicky, documentation matches what’s physically in the bottle, and colleagues down the workflow suffer fewer interruptions. It matches up with the push for data-driven decisions in R&D—every hour recouped, every batch finishing smoothly, matters.

    Staying Ahead of the Curve

    Staying competitive in chemistry often depends on small, incremental process improvements. Using 4-Bromomethyl-2,6-Dichloropyridine doesn’t overhaul the workflow, but it brings a level of control and reliability rare in the world of heterocyclic intermediates. R&D departments benefit when each step in a sequence performs the same way, every time. This product makes each reaction step feel less like a gamble. Experienced teams who switch to this intermediate find themselves able to repeat their successes, building cumulative improvements into future processes.

    Most projects outgrow their development labs and move to new scales or applications. The intermediates that performed well in milligram or gram lots don’t always shine on the kilo or ton scale. Here, the advantages of pure, crystalline, and selective compounds become more obvious. Process engineers test small adjustments; control managers look for consistency across lots; and safety officers like knowing exactly how a batch will behave. 4-Bromomethyl-2,6-Dichloropyridine earns its place as a go-to synthetic step precisely because it doesn’t throw surprises into the mix.

    Factors Driving Greater Adoption

    Chemistry only gets more complex over time. Projects demand more from their reagents, not just in reactivity, but in documentation, traceability, and safety. Standards keep rising, shaped by regulatory needs, client demands, and internal goals. The recent wave of digital transformation—better tracking, more automated monitoring—highlights weak links in supply chains. Poorly characterized intermediates cost more than money; they cost trust and future business. 4-Bromomethyl-2,6-Dichloropyridine adapts to that world because it mixes sharp selectivity with well-understood, transparent supply chains.

    As more automation and digital monitoring become the norm, the value of reliable intermediates grows. Automated synthesis demands reproducible results; batch records must tie back seamlessly to input materials. No one wants to waste machine time (and capital) on questionable lots. In this modern environment, intermediates with known, repeatable properties unlock real progress in both discovery and commercialization.

    Broadening Horizons: Next Steps for Industry

    The chemical industry keeps pushing for faster, safer, and greener solutions. Every time process chemistry delivers a new shortcut or cleaner route, it reshapes what teams expect from their starting materials. 4-Bromomethyl-2,6-Dichloropyridine rides this trend by proving itself in the trenches—where successful innovation depends on real performance, not just theoretical reactivity. As regulated industries like pharmaceuticals tighten controls, and others like electronics demand more precision with fewer trade-offs, this compound shows how smart synthesis can offer both.

    Experienced chemists and engineers look for materials that work across the lifecycle of a project. That includes ease of ordering, deep documentation, and confidence that next quarter’s order will perform just like the last. Simple, predictable chemistry frees up time for higher-value thinking—not worrying about the basics. Growth-minded teams choose intermediates that can scale smoothly, adapt to changing requirements, and slot into evolving quality systems.

    Collaboration and Knowledge-Sharing Drive Progress

    Connecting with peers, sharing batch results, and comparing stories about scale-up or batch failings provides the industry with direction. Intermediates like 4-Bromomethyl-2,6-Dichloropyridine become case studies in what works and what doesn’t. As collaborative tools become more common, folks see the same answers: reliable, transparent products lead to more collective wins. This drives adoption among both early-career researchers and veteran chemists seeking to cut routine headaches.

    Over a career, you learn which products deserve a spot in the regular rotation. Some intermediates are remembered for causing pain, and some for smoothing out bumps. 4-Bromomethyl-2,6-Dichloropyridine consistently falls in the latter group. Not everything in chemical development is under your control, but the right choice of intermediate tips the scale toward success.