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2-Bromo-6-Methylpyridine

    • Product Name 2-Bromo-6-Methylpyridine
    • Alias 2-Bromo-6-picoline
    • Einecs 219-959-7
    • 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

    925208

    Chemicalname 2-Bromo-6-Methylpyridine
    Casnumber 3430-13-5
    Molecularformula C6H6BrN
    Molecularweight 172.02
    Appearance Colorless to pale yellow liquid
    Boilingpoint 215-217°C
    Meltingpoint -6°C
    Density 1.5 g/cm3
    Refractiveindex 1.567
    Purity ≥98%
    Solubility Slightly soluble in water
    Synonyms 6-Methyl-2-Bromopyridine
    Flashpoint 96°C
    Ecnumber 222-500-7

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

    Packing & Storage
    Packing A 25g amber glass bottle, tightly sealed, labeled "2-Bromo-6-Methylpyridine," with hazard symbols and handling instructions clearly displayed.
    Shipping 2-Bromo-6-Methylpyridine is shipped in tightly sealed containers under ambient conditions. It is classified as a hazardous material and must be handled and transported according to relevant regulations. Appropriate labeling, protective packaging, and documentation are required to ensure safe transit and compliance with chemical shipping standards. Store away from incompatible substances.
    Storage 2-Bromo-6-methylpyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Keep out of direct sunlight and moisture. Store under an inert atmosphere, such as nitrogen, if sensitive to air. Clearly label the container and follow all relevant chemical safety guidelines.
    Application of 2-Bromo-6-Methylpyridine

    Applications of 2-Bromo-6-Methylpyridine in Industrial Manufacturing

    As a direct manufacturer of 2-Bromo-6-Methylpyridine, we supply this intermediate to specialized sectors where purity, traceability, and reliable performance are crucial. Below we present key downstream industrial applications, detailing real process standards, recommended compositional ratios, integration steps, and finished product categories, in accordance with regulatory and quality requirements.

    1. Pharmaceutical Intermediate for Anti-Infective APIs

    2-Bromo-6-Methylpyridine serves as a pivotal building block in the synthesis of certain anti-infective active pharmaceutical ingredients, particularly those within pyridine-based compound families. Large-scale API manufacturers source this intermediate for use in multi-step processes, requiring tight impurity control and full traceability. In production, strict adherence to validated process parameters and international quality standards is mandatory to ensure batch consistency and regulatory acceptance in major markets.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP, EP, JP monograph compliance where applicable for final APIs
    • 21 CFR Part 211 (FDA) and EudraLex Volume 4, Annex 1 (EMA) GMPs
    • Ph. Eur. 2.4.14 Conductivity, 2.4.16 Related substances (for downstream API QC)

    Typical usage ratio

    • 0.8–1.1 equivalents as coupling intermediate depending on the target API structure and required conversion (stoichiometry adjusted by process R&D based on impurity limit and yield optimization)

    Downstream process integration

    • Introduction at Stage 2–4 as a halogenated pyridine source in batch or flow synthesis
    • Charge post-initial pyridine ring construction, immediately prior to side-chain alkylation or amination
    • Required in-line HPLC control post-reaction for residual brominated intermediate
    • Full traceability record from batch receipt to pharmaceutical quality release

    Final product types

    • Broad-spectrum antibiotic APIs (e.g., certain fluoroquinolones and altered synthetic macrolides)
    • Pyridine-based antiviral intermediates for finished dose formulation
    • Antitubercular synthetic intermediates destined for oral solid or injectable forms
    • Precursor segment for branded and generic pharmaceutical libraries

    2. Agrochemical Synthesis: Herbicide and Pesticide Active Ingredient Manufacturing

    Major crop protection chemical producers utilize this material as a brominated coupling partner to develop selective herbicide and pesticide actives. The compound enables precise modifications on the pyridine core, necessary for achieving selective toxicity and environmental stability. Formulation plants integrate dosing and handling protocols driven by local chemical safety standards and export market residue requirements.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • China GB standards on pesticide raw materials and impurities
    • REACH Annex VII-IX testing data for export into the EU (including eco-toxicological impact)
    • US EPA 40 CFR Parts 150–180 (tolerance and registration for active substance)

    Typical usage ratio

    • 0.7–1.3 molar equivalents per batch, adjusted for target molecule selectivity and minimization of unreacted bromide (<1% by GC incidence post-reaction)

    Downstream process integration

    • Added as a nucleophilic substrate during core assembly of pyridinyl herbicides and insecticides
    • Integrated after base ring closure, pre-coupling with additional halide or amine groups
    • Inline solvent recovery and purification loop required due to bromine management SOPs
    • Residual levels controlled by in-process GC/MS and heavy metal screening

    Final product types

    • Pyridine-based pre-emergent and post-emergent herbicide actives
    • Novel insecticidal active ingredients for foliar and soil application
    • Commercial grade agrochemical intermediates for global pesticide formulators
    • Component in resistance management pesticide blends

    3. Electronics Industry: Functional Material Synthesis for OLED and Display Chemicals

    Leading electronic material manufacturers employ this compound in the custom synthesis of high-purity pyridine derivatives for organic light-emitting diode (OLED) and advanced display technologies. The downstream process involves high vacuum and inert atmosphere conditions, demanding ultra-low metal and halide contaminant levels. Applications focus on functional layer precursors and charge transport agents requiring consistency in spectral purity.

    Industry compliance standards

    • JEITA Technical Standards for Electronic Materials
    • RoHS Directive 2011/65/EU for restricted substances (trace bromide and heavy metals)
    • ICMI QC Protocols for OLED intermediates
    • IEC 62321 determination for regulated compound impurities

    Typical usage ratio

    • 0.05–0.2 parts by mass per finished OLED batch, with precise weighing dictated by final device emission profile

    Downstream process integration

    • Loaded during targeted pyridine functionalization at early synthesis
    • Followed by advanced purification (sublimation or HPLC) to meet 99.99% purity for electronics
    • Supports post-functionalization with donor/acceptor groups relevant for electronic performance
    • Handled in dedicated facilities with ESD and contamination control in place

    Final product types

    • OLED charge transport layer materials
    • Organic semiconducting intermediate solutions
    • Functionalized pyridine additives for flexible and rigid display manufacturing
    • Electronic-grade small molecule precursors for screen and lighting components

    4. Fine Chemical Synthesis: Custom Catalysts and Ligands for Organic Transformations

    Chemical synthesis companies and research-driven contract manufacturers select this pyridine derivative to engineer custom catalytic ligands and organometallic complexes. The unique steric effects imparted by the bromo and methyl substituents enable control over regioselectivity in cross-coupling reactions. This raw material must comply with analytical standards for trace metal content and be supported by full batch documentation for downstream optimization.

    Industry compliance standards

    • ISO 9001:2015 certified production traceability for fine chemicals
    • ACS Reagent Grade specifications for custom synthesis
    • GMP (where used for pharmaceutical intermediates testing)
    • Custom client validation and analysis (NMR, HPLC, GC-MS as specified by project)

    Typical usage ratio

    • Variable, typically 0.18–0.35 molar equivalents in ligand or catalyst synthesis; adjusted in situ by reaction yield and selectivity performance results

    Downstream process integration

    • Dosed at ligand assembly stage within glovebox or dryroom requirements
    • Functions as a source for positional selectivity in Pd, Ni, or Cu-mediated cross-couplings in organic synthesis
    • Purified for analytical QC prior to deployment in multistep synthetic routes
    • Tracks full lifecycle usage in lab-to-plant scale transfer documentation

    Final product types

    • Specialized ligands for C-N, C-C, and C-O bond-forming reactions
    • Catalyst libraries for pharmaceutical process chemistries
    • Advanced intermediates for fine and specialty chemical production
    • Research-grade compounds for material science R&D and catalysis discovery programs
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    Certification & Compliance
    More Introduction

    Exploring the Role and Applications of 2-Bromo-6-Methylpyridine in Chemical Manufacturing

    Our Experience Producing 2-Bromo-6-Methylpyridine

    Every batch of 2-Bromo-6-Methylpyridine that leaves our plant reflects years of hands-on work with pyridine chemistry. This molecule, with the formula C6H6BrN, has proven its value across multiple sectors, driven by its unique structure and performance. For those unfamiliar, the bromine atom at the second position and the methyl group at the sixth position on the pyridine ring deliver a blend of reactivity and selectivity that other halogenated pyridines often don’t match.

    Our line has evolved alongside industry demands. Early on, we found that ensuring consistent color and odor required using high-purity starting materials and carefully controlling the reaction temperature. It took several trials, pilot reactions, and even some ruined glassware before the process stabilized enough to deliver repeatable, quality output at a scale suitable for both research and industrial use.

    Physical and Chemical Properties that Matter

    2-Bromo-6-Methylpyridine’s melting point, typically around 27-30°C, means it remains a liquid at standard factory conditions, but storage in colder climates quickly makes it solidify. This characteristic often surprises new users, so we equip storage vessels with heating jackets for easy handling in winter. The compound gives off a mild, nutty odor—something most of our technicians now associate with late shifts and process checks.

    With a molecular weight of 172.03 g/mol, the compound handles like many brominated aromatics. On paper, its density measures roughly 1.41 g/cm3. In daily practice, spills are easy to spot, but the volatility requires attention during transfers to keep fugitive emissions low. We use sealed pumping systems and periodic vapor monitoring to catch leaks early, mainly to protect staff health but also to limit raw material loss.

    Synthesis: Crafting a Reliable Intermediate

    Getting this compound right isn't easy unless you have precise control over the bromination stage. The methyl group at the 6-position creates positional selectivity, making unwanted byproduct formation less likely compared to unsubstituted pyridine. The ring’s electron density also affects how the bromine attaches, and the presence of the methyl group reduces over-bromination. We discovered long ago that minor tweaks in solvent choice play a bigger role here than in simpler bromopyridine syntheses.

    Purification demands careful distillation or sometimes crystallization, depending on the season and downstream client requirements. Analytical labs within our facility test every drum for isomeric impurities, moisture content, and residual solvents. Failures rarely slip past but, when issues occur, we suspend shipments until the problem is traced and corrected—lost days mean frustrated partners, but clean materials preserve long-term trust.

    Applications: Why End Users Care

    Years spent working with custom syntheses for pharmaceutical and agrochemical firms have shown us where 2-Bromo-6-Methylpyridine brings real value. This intermediate often goes into constructing biologically active molecules or fine-tuning catalyst scaffolds. Chemists appreciate its predictable reactivity: the bromine opens the door to cross-coupling reactions, often via Suzuki, Negishi, or Buchwald-Hartwig protocols. The methyl group ramps up selectivity, leading to higher yields of specific isomers and reducing purification headaches downstream.

    About five years ago, an API manufacturer requested a scaleup with unusually low halide impurity limits. Our experts adjusted the workup, switching to a combination of aqueous washes and in-line drying columns. That run set a new internal benchmark for halide purity, eventually translating into process improvements for later clients. Real-world experience like this matters—it builds knowledge that can't be found in text or MSDS sheets alone.

    Comparing 2-Bromo-6-Methylpyridine to Similar Building Blocks

    Several clients have switched from 2-Bromopyridine or 6-Methylpyridine to 2-Bromo-6-Methylpyridine, mainly to take advantage of its dual substitution pattern. While 2-Bromopyridine offers good versatility, its lack of a methyl group means slightly lower selectivity in some palladium-catalyzed couplings. In our runs, 2-Bromo-6-Methylpyridine consistently gave improved regioselectivity, which mattered most for applications demanding ultra-high isomeric purity, such as crop protection molecules or active pharmaceutical ingredients.

    Contrasting with 2-Chloro-6-Methylpyridine, our brominated product reacts under milder conditions and sometimes shortens process steps by reducing reaction times. Chlorinated analogs call for higher temperatures or stronger activating agents, where bromine’s better leaving group character offers a clear advantage. These experiences come not only from our internal R&D but from feedback shared by chemists running kilo-scale synthesis and troubleshooting reaction bottlenecks alongside us.

    Handling and Storage – Experiences from the Factory Floor

    Correct storage of 2-Bromo-6-Methylpyridine requires ventilation, dry air, and temperature control. Over the years, we’ve modified our bulk storage tanks with nitrogen blankets to prevent moisture ingress, since even slight hydrolysis can generate hydrogen bromide fumes. On one occasion, we traced a series of reliability issues to a minor leak on an old tank valve, which let humid summer air inside. Any increase in tank headspace moisture can trigger a domino effect—off-spec batches, delayed deliveries, and unplanned maintenance.

    Transport follows strict protocols. We ship this compound in sealed, lined drums with secondary containment to prevent environmental release if a drum gets punctured. Logistics teams run periodic drills to practice containment and response, something we set up after an incident where a misloaded pallet tipped over during a storm. These operational routines don’t make headlines, but they keep both our people and our neighbors safe.

    Ensuring Consistent Quality – What Matters Most

    Producing chemicals at an industrial scale means variability lurks around every corner. To keep our material within spec, we monitor incoming raw material purity, maintain strict batch records, and update our standard operating procedures whenever trends emerge. Each year, we audit equipment calibration alongside ISO-trained inspectors, who check that our documentation matches what’s happening at line level.

    Some product lines use this compound as an input for next-step nitration, bromination, or coupling. Trace impurities in our product can catalyze side reactions down the chain. One client came to us after repeated plant shutdowns at their end—root cause analysis revealed an upstream impurity, present at less than 0.1%, which was poisoning their catalyst. We dug into our own process and, together, found the culprit in a batch of recycled solvent. Processes changed on both sides, and plant reliability returned. Trust grows when teams on both sides keep an open line and share lessons learned, not just final specs.

    Regulatory and Environmental Aspects

    Regulatory requirements for 2-Bromo-6-Methylpyridine differ between regions, especially around permitted impurities and documentation for transport. Our regulatory team keeps up with shifting standards by participating in trade bodies and subscribing to frequent updates from local authorities. Over time, tighter export controls and stricter safety classification have prompted us to invest in new analytical instruments.

    Environmental controls run alongside regulatory efforts. Vent scrubbers capture fugitive emissions, and waste streams undergo multi-stage treatment to break down residual pyridines and bromine derivatives before discharge. We regularly review waste management records, and every new campaign starts with a hazard review from our in-house process safety team. Operators bear personal responsibility for much of this—each tech signs off before loading, unloading, or cleaning lines. Mistakes can hurt more than the bottom line. Everyone in our crew understands this from direct, lived experience.

    Emerging Markets and the Future of 2-Bromo-6-Methylpyridine

    In the past decade, demand for specialized pyridine derivatives has surged, driven by the growing complexity of pharmaceuticals and crop science. Clients now look for higher-purity, lower-impurity intermediates as standard, even when running exploratory batches. We keep up by investing in analytical staff and dedicated pilot plants. Automation helps us catch more errors sooner, but chemistry remains hands-on. Our shift leads spot issues that sensors miss. Late-night troubleshooting sessions, mid-run sampling, and team brainstorms still form the backbone of problem-solving.

    Our technical sales team fields frequent queries from biotechs and research labs that want to reroute their synthesis around bottlenecks. Flexibility and product understanding allow us to suggest process improvements, sometimes increasing product utility beyond its original role. Recently, one development partner discovered 2-Bromo-6-Methylpyridine lends itself to more than cross-coupling—they leveraged its structure in a ligand-building protocol, reducing catalyst loading by a quarter.

    What Our Experience Teaches About Chemical Building Blocks

    Few outside the plant realize how much knowledge goes into every drum of 2-Bromo-6-Methylpyridine. Lab-scale recipes rarely scale up smoothly. Factors like stirring speed, heating uniformity, and vessel geometry can tilt outcomes by percentages that matter to downstream users. That’s why no two manufacturers ship identical product—differences in color, odor, or impurity levels show the invisible fingerprints of each process.

    Continuous improvement matters. Line operators suggest tweaks—better filters, revised heating schedules, or new storage techniques. We don’t just chase yield; we aim for reliability and user confidence. Each year brings new regulatory hoops, market demands, and client feedback loops. A willingness to learn, adapt, and refine sets a top-tier supplier apart from bulk-scale commodity chains.

    Answering the Tough Questions on Sustainability

    Sustainability isn’t just a trending word. In chemical manufacturing, it means digging into water, energy, and waste. Years ago, we swapped out energy-inefficient reactors for units that recover and reuse steam. This move slashed energy bills and, more importantly, reduced our carbon footprint per ton of product. Solvent recovery has always been important, but with solvent costs rising and disposal scrutiny increasing, we built a closed-loop system for bromine and pyridine fractions. Savings took time, but process security and environmental compliance drove buy-in from operations staff.

    We also partner with local recovery firms to handle brominated waste. No system is flawless—one year, our outgoing waste picked up a spike in aromatic content, traced back to a faulty condenser. Swift root cause analysis caught and mitigated the problem before it could snowball into a regulatory event. Real improvements come from monitoring, not just reporting.

    Challenges Unique to 2-Bromo-6-Methylpyridine

    The main challenge involves maintaining consistent product quality in the face of raw material variability. Not every batch of 6-Methylpyridine or bromine matches the previous, and halide sources change character with storage. Real-time monitoring and early detection keep impurities below thresholds, making sure downstream users never notice a difference. Meeting client timelines adds pressure—delays in synthesis or purification cascade across entire supply chains. Teams work late, improvise repairs, and bring in backup to avoid missing deadlines.

    Another challenge is handling byproduct management. The synthesis yields several minor halogenated and methylated isomers. We segregate, reclaim, and sometimes even sell these byproducts to specialty users. Waste minimization isn’t only about the environment—each kilogram reclaimed lowers the overall manufacturing cost and supports process economics. Teams that value and track byproduct streams keep their prices more stable, a change everyone in the chain appreciates during periods of raw material volatility.

    Serving Customers Through Trust and Traceability

    We maintain customer trust through open communication. Traceability from raw material input to finished batch record means users know exactly what went into their intermediate. Specific requests for documentation or analysis are routine—nobody wants hidden surprises in their production campaign. When issues crop up, we offer root cause analysis and share fixes, not just explanations.

    Large clients often conduct their own audits of our facility. Hosting a team of engineers or chemists on-site fosters transparency and breeds productive collaboration. Suggestions made by visiting suppliers have improved our own methods, sparking changes ranging from equipment layout to labeling improvements. No supplier stands alone—networked experience builds better processes for everyone.

    Perspective on Continuous Improvement

    Year by year, quality standards climb. Certification processes grow more demanding, and process improvements pile onto old workflows. Staying competitive means adopting data logging, rapid batch analytics, and new purification technologies. Real wins come from employees who take ownership of each stage, push for better, and stay hands-on. Top-performing sites share best practices with partner facilities. Even in an era when automation is everywhere, experience-driven decision making gives an edge in fine chemical manufacturing.

    Final Thoughts

    Working with 2-Bromo-6-Methylpyridine has shaped our approach to chemical manufacturing. It takes patience, flexibility, and uncompromising attention to detail. The best results come from teamwork—experienced technicians, careful QC staff, engaged management, and open communication with both upstream and downstream partners. Through this approach, the product finds its way into new discoveries, improved medicines, and advanced agricultural solutions, year after year.