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2-Methoxy-5-Pyridineboronic Acid

    • Product Name 2-Methoxy-5-Pyridineboronic Acid
    • Alias (2-Methoxypyridin-5-yl)boronic acid
    • Einecs 824-267-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    110047

    Productname 2-Methoxy-5-Pyridineboronic Acid
    Casnumber 2905-48-6
    Molecularformula C6H8BNO3
    Molecularweight 152.95
    Appearance White to off-white solid
    Purity Typically >97%
    Meltingpoint 160-165°C
    Solubility Soluble in DMSO, methanol
    Storagetemperature 2-8°C
    Smiles COc1ccc(B(O)O)nc1
    Inchi InChI=1S/C6H8BNO3/c1-10-5-3-2-4-7(6(5)8)9/h2-4,8-9H,1H3
    Synonyms 2-Methoxy-pyridine-5-boronic acid

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

    Packing & Storage
    Packing The chemical `2-Methoxy-5-Pyridineboronic Acid` is packaged in a 5-gram amber glass bottle, sealed and labeled for laboratory use.
    Shipping 2-Methoxy-5-Pyridineboronic Acid is shipped in tightly sealed containers under ambient conditions. The packaging ensures product integrity and prevents moisture exposure. It is classified as non-hazardous for transport but should be handled with care. Shipping complies with relevant safety and regulatory guidelines for laboratory chemicals. Expedited and standard delivery options are available.
    Storage 2-Methoxy-5-pyridineboronic acid should be stored in a tightly sealed container, protected from moisture and air. Store in a cool, dry, and well-ventilated area away from incompatible materials such as strong oxidizers. Keep at room temperature or as directed by the manufacturer. Avoid exposure to direct sunlight or sources of ignition to maintain chemical stability.
    Application of 2-Methoxy-5-Pyridineboronic Acid

    Applications of 2-Methoxy-5-Pyridineboronic Acid in Industrial Manufacturing

    2-Methoxy-5-Pyridineboronic Acid serves as a precision building block in multiple advanced manufacturing workflows. Its high purity and boronic acid functionality enable essential bond formations and customized molecule structures in critical industries. Below we outline each segment’s specialized adoption, operational details, compliance focus, and the kinds of products that integrate our raw material at scale.

    1. Pharmaceutical API Synthesis: Heteroaryl Coupling Reactions

    This compound is widely adopted in the synthesis of heteroaryl-based active pharmaceutical ingredients where Suzuki–Miyaura cross-coupling establishes sophisticated pyridine motifs critical for small molecule drug pipelines. Chemists rely on its reliable reactivity for efficient introduction of methoxypyridyl units during API step synthesis, particularly for kinase inhibitors and neurological disorder drugs under GMP controls.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for APIs)
    • EU GMP Part II (Active Substances)
    • USP & EP Monographs (if applicable to intermediate)
    • FDA 21 CFR Parts 210–211 (Pharmaceutical Manufacturing)

    Typical usage ratio

    • Usage typically ranges from 0.8 to 1.2 equivalents per coupling reaction, depending on the mole ratio relative to aryl halide substrates; excess can be fine-tuned based on target API purity requirements.

    Downstream process integration

    • Material is charged during the Suzuki–Miyaura coupling step, following halogenated precursor preparation and prior to aqueous workups and crystallization.

    Final product types

    • Selective kinase inhibitors (API intermediates and completed actives)
    • Antipsychotic scaffolds
    • Pyridine-based central nervous system (CNS) drugs
    • Standards for reference compounds in medicinal chemistry labs

    2. Agrochemical Intermediate Production for Herbicide Synthesis

    2-Methoxy-5-Pyridineboronic Acid finds strategic use among agrochemical manufacturers for crafting heterocyclic intermediates employed in next-generation herbicide molecules. Boronic acid coupling enables the integration of oxygenated pyridine rings which improve binding specificity for selective weed control agents.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • FAO/WHO Guidelines for Pesticide Specifications
    • ISO 9001:2015 (Quality Management Systems in Agrochemicals)
    • REACH Regulation (EC 1907/2006 - for European distribution)

    Typical usage ratio

    • Added at 1.0–1.5 equivalents per halogenated partner in batch synthesis; precise dosing determined by targeted substitution pattern and yield optimization in laboratory pilots.

    Downstream process integration

    • Material enters at the core aryl–aryl coupling phase, after initial esterification and halogenation of precursor molecules, and before final purification or derivatization to form technical concentrates.

    Final product types

    • Pyridine-containing herbicide intermediates
    • Multi-ring precursor blocks for crop protection actives
    • Analytical standards for agrochemical R&D
    • Registered technical-grade herbicides (via later processing)

    3. Electronic Chemical Synthesis: OLED and Display Material Development

    Leading research and production facilities in the OLED and electronic materials sector employ this boronic acid for constructing nitrogen-rich ligands and electron transport layers with tailored band gaps. Incorporation of the methoxypyridine unit through cross-coupling enables custom-tuned electronic properties in thin-film displays and organic semiconductors.

    Industry compliance standards

    • IEC 62321 (Material Characterization in Electronics)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • Semi E49-0707 (Electronic Chemicals Purity Guidelines)
    • ISO 14001 (Environmental Management in Electronics Manufacturing)

    Typical usage ratio

    • Generally dosed at 0.9–1.1 equivalents in Pd-catalyzed C–C coupling reactions, adjusted relative to functional group density of the complementary aryl halide.

    Downstream process integration

    • Charged during the multistep synthesis of functional monomers for electron-transporting layers, prior to film deposition, coating, or device assembly.

    Final product types

    • OLED emitter and transport materials
    • Organic semiconductors for display panels
    • Small-molecule intermediates for custom display prototypes
    • Test compounds for circuit integration studies

    4. Advanced Material Research: Heterocyclic Ligand Synthesis

    Top-tier chemical research institutes and specialty material innovators utilize this compound in the precision assembly of heterocyclic ligands, enabling tuned metal binding in coordination complexes. These ligands support the development of new catalysts and sensor platforms, where strict composition control and reproducibility are mandatory for repeatable function.

    Industry compliance standards

    • ISO/IEC 17025 (Testing and Calibration Laboratories)
    • ACS Analytical Reagents Grade Standards
    • Institutional QA/QC Procedures for Research Materials
    • GLP (Good Laboratory Practice) for academic and private R&D

    Typical usage ratio

    • Applied at 1.0–1.2 equivalents in ligand-forming cross-coupling reactions; ratio optimized according to ligand backbone requirements and metal stoichiometry for target design.

    Downstream process integration

    • Employed in the crucial ligand construction steps, typically directly after protection/deprotection cycles and before complexation with transition metals.

    Final product types

    • Pyridine-based ligands for catalysis research
    • Sensor prototypes for environmental monitoring
    • Coordination compounds for laboratory scale-up trials
    • Reference materials for structure-function studies

    5. Custom Fine Chemical Synthesis Services

    Custom synthesis service providers integrate this boronic acid into high-complexity projects where clients require tailored methoxypyridine fragments as part of larger molecular constructs. Service labs use its stable, consistent profile to maintain synthetic throughput under strict client and regulatory oversight, especially for advanced intermediates in confidential research or patent-driven projects.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems for Custom Synthesis)
    • Client-mandated documentation & audit trails
    • GMP or non-GMP production tracks as specified by client
    • SHE (Safety, Health and Environmental) management per client contracts

    Typical usage ratio

    • Ranges broadly from 0.7 up to 2.0 equivalents per step per order scope; selection driven by molecular complexity, fragment length, and customer required specification.

    Downstream process integration

    • Utilized in multi-step sequences for fragment coupling, after initial building-block assembly and prior to any proprietary downstream converting stages dictated by client protocols.

    Final product types

    • Exclusive pharmaceutical intermediates
    • Molecule libraries for drug screening campaigns
    • Confidential specialty materials
    • Protected intermediates for R&D supply chains
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    Certification & Compliance
    More Introduction

    2-Methoxy-5-Pyridineboronic Acid: A Chemist’s View From the Workshop Floor

    Bringing Lab Reality to the Factory Bench

    Manufacturing boronic acids brings its own challenges and rewards. Some years back, after listening to researchers in medicinal chemistry wish for less hassle during Suzuki-Miyaura coupling, we spent time tuning our processes for making 2-Methoxy-5-Pyridineboronic Acid. There is comfort in consistency, especially when a batch goes straight from our workshop to a customer’s reactor in the exact purity and physical state that works in their own hands, not just ours. This compound, which has found favor with both pharmaceutical researchers and materials specialists, stands out partly because of how its methoxy group and heteroaromatic ring influence downstream chemistry. We talk with our customers often about this – what makes one boronic acid distinct from another and what those differences mean in real synthesis, not only on a spec sheet.

    The Model We Put on the Scale

    Each barrel, each glass jar, each polyethylene-lined carton carries material we have checked in-house using our own HPLC and NMR. Typical specification for our 2-Methoxy-5-Pyridineboronic Acid, identified internally as model 2M5PB-99, looks like this: purity 98% or better by HPLC area normalization, off-white to pale beige powder, melting point around 168–174°C, typically with a trace moisture content well below 1%. Fine details – loose or compact cake, tendency to pick up ambient moisture during transfers, or even the subtle aromatic undertone released during handling – can mean as much as the numbers. These are not marketing flourishes. We test for what matters to real-world users: will it dissolve cleanly in the chosen solvent, will it tolerate a bit more base in couplings, will it change character after a week on a shelf in a non-climate-controlled cabinet?

    Over the years, we’ve tuned particle size during drying so that portions dispense cleanly, avoiding the fluffy static-prone mess that some boronic acids can bring. Showing up on time and in the form you expect: this still counts as innovation, if the results lower your cost of control. In our experience, lower density and friable texture in this compound mean it is easier to blend or dissolve fast, which saves time at bench scale and in pilot runs. Handling differences matter: anyone who’s cursed at a clumping, glassy boronic acid will appreciate this.

    Usage: The Chemistry Behind the Choice

    The role of 2-Methoxy-5-Pyridineboronic Acid in drug development and advanced materials is direct. The methoxy group on the pyridine ring gives it a reactivity profile that can be a blessing or a curse. We’ve sat through enough feedback loops – sometimes a delight, sometimes a list of new headaches – to recognize how this group fine-tunes cross-coupling reactions. Some groups use it as a core for kinase inhibitor libraries; others want it for modified conductive polymers. The electron-donating methoxy substituent changes the coupling rate, sometimes driving yields higher, sometimes protecting against overreaction. The nitrogen in the pyridine ring shifts pKa, impacting solubility and the kind of side products that can appear during scale-up. Practical chemistry always forces a choice: modify your process for the building block, or pick a building block that fits your process. The best feedback we get often comes from researchers who ran parallel couplings: one with the simple phenylboronic acid, one with our 2-methoxy-5-pyridine analog. They report real-world results – cleaner mass recovery, or unexpected selectivity that didn’t show up on paper.

    In a Suzuki reaction, sometimes this compound helps overcome problems with byproduct formation or stubbornly low yields seen with other boronic acids. Some users mention less boronic acid homocoupling under air; others like the predictable solubility in DMF or dioxane. It’s not always about the highest purity number, but whether the product keeps reactivity consistent week in and week out. This reliability helps keep screening libraries and pilot plant runs on schedule. For material scientists, integration into frameworks or polymers is rarely straightforward. The methoxy-pyridine structure brings less aggregation or streaking in casting and thin film formation. We didn’t set out aiming only for the highest HPLC purity; our aim remains making a product a synthetic chemist trusts to behave across various processes, with minimum troubleshooting.

    What Makes It Different: Structure Meets Reality

    Comparing 2-Methoxy-5-Pyridineboronic Acid to cousins like 4-pyridineboronic acid or 2-methoxyphenylboronic acid, the distinctions matter less in abstract structure catalogs and more in how they mix, react, and store. The ortho methoxy group’s position ramps up electron density in the ring, impacting boronic acid stability in the presence of bases and oxidants. Standard phenylboronic acid, that classic white crystalline powder, often suffers from rapid self-condensation or diminished reactivity when trace water creeps in. Substituted pyridines, by contrast, sometimes last longer open to air but can be volatile in large jars or at warm room temperature. Our 2-methoxy-5-pyridine version stays shelf-stable and keeps free-flowing powder character through months in typical production settings. We pack and seal using methods tested across lots spanning years, not just lab-scale single trials.

    Another difference: our customers report that other pyridineboronic acids give variable yields depending on coupling partner or solvent mix. In our hands, the methoxy group tunes behavior enough that boronic acid self-decomposition drops. We see less tendency to form tan crusts or insoluble gums in product jars, which keeps both material handling and automated dispensing trouble-free. The difference gets clearer in automated or high-throughput labs, where sticky or clumping powders can jam dispensers or force extra cleaning steps. Practical benefits like these do not make it onto glossy flyers but matter in any lab trying to run more than a handful of reactions a month.

    Listening to Real Chemists: Improvements and Problems

    Our manufacturing decisions focus on where real-world problems slow downstream work. Several years ago, on-site trials showed labs using alternative boronic acids spent more time filtering out solids or purifying reaction mixtures. After shifting to consistent batches of 2-Methoxy-5-Pyridineboronic Acid, washing and filtration steps sped up by about 20%, mass recovery crept up, and users noted clearer TLCs. This doesn’t derive from a single magic trick but steady effort: tightening drying protocols, controlling for trace metal residues, ensuring each lot tested for particle flowability, not just chemical purity. One of our strengths comes from repeat feedback loops with customers: a missed delivery, or powder that starts clumping by the third weigh-out, prompts a root-cause dig, not an excuse. Synthetic chemistry always throws up surprises, but diligence on the manufacturer’s end shrinks their number.

    Some users run scale-up reactions with automatic powder feeders; others do regular small-batch hand weighing. We check for both types of handling during stability and flow tests. We also hear from researchers trying to layer new boronic acids into legacy processes, where solvent tolerance or reactivity profile can upend old protocols. Not every lot or customer comes with glowing reviews, but the direct line between process headaches and product tweaks keeps our chemists tied to the real problems. Our improvements since 2018 – better moisture exclusion, tighter sieving, more robust packaging – trace back to practical feedback, not theoretical purity numbers. More than once, a purchase manager reports the same weight shipped month after month, yet on a process visit, you’ll find our shipping staff chatting with the people opening the drums, understanding not just what left our gate but how it arrives and behaves across shifts and seasons.

    Purity and Safety: Facts Over Promises

    We make our purity claims stick with daily in-house and third-party third-lab checks on HPLC retention times, water content by Karl Fischer titration, and periodic cross-checking by NMR and GC-MS. Trouble doesn’t appear on neat spec sheets but in chromatograms riddled with late-eluting humps, or failures to crystallize after hours stirring. Every process batch gets routine metal screening by ICP-MS, focusing on labels that worry today’s medicinal chemists: Pd, Ni, Fe, Pt, Ru. Boronic acids love to pick up these hitchhikers from glassware, spatulas, or the reactors themselves. Keeping our content well under ppm thresholds gives our customers more confidence their own analytics can skip tedious trace metal panels, or at least avoid the biggest headaches in final clean-up. We store all long-term retains at -20°C in dry argon, ensuring we can back-check any product against original batch records if a customer flags inconsistencies months after receipt.

    On safety, valley reveals itself in the details. 2-Methoxy-5-Pyridineboronic Acid behaves as a low dust, low volatility powder at standard ambient conditions, with no acutely hazardous off-gassing under neutral storage. As a manufacturer, our facility staff handle it daily in standard chemical-resistant gloves and safety glasses, with vacuum transfer in place for kilo-scale drumming. User complaints about odor, skin irritation, or allergic response are rare; when those do crop up, we cross-reference processes for possible contamination or mislabeling. Fire risk remains negligible in our experience: boronic acids don’t readily support combustion like some ethers or lower molecular weight aromatics. In-process, the most frequent question involves boronic acid’s reliability in the face of repeated drying and reslurrying for different coupling partners or post-synthesis purification. We’ve run multi-month bench stability and repeat dissolution tests for exactly that reason: feedstock must endure multiple handling cycles before yielding its full value. At our site, warehouse runners and plant chemists alike prefer compounds they do not have to babysit. 2-Methoxy-5-Pyridineboronic Acid has earned some trust through years of careful observation, not just one-off checks.

    From Factory Drum to Research Breakthrough: A Manufacturer’s Perspective

    The real test of any chemical stands outside the four walls of its origin. From a manufacturing point of view, we watch our product flow from factory drum to pilot plant or medicinal chemistry hood and listen for where the process inflects from smooth to sticky. Consistent particle size, shelf stability, and reliable reactivity mean fewer stoppages. Like most working manufacturers, we’ve learned there’s no substitute for visiting a customer site, seeing problems unfold, and sharing a cup of coffee over a chromatography trace. Raw numbers and purity grades matter, but the habits and complaints of process chemists – this drum caked after four weeks, this batch stopped dissolving in THF – shape our next improvements. Hearing from someone who ordered our compound on autopilot for years, only to comment on a subtle change in appearance or ease of weighing, tells us to check for unnoticed tweaks in drying or grinding. Batches that behave identically in analytic checks but reveal subtle differences in flow or reactivity get set aside for closer internal review, not shipped out on hope alone.

    No chemical, not even one with a routine synthetic pathway, creates value unless it solves actual lab and factory needs. 2-Methoxy-5-Pyridineboronic Acid stands out within our catalogue not simply based on purity or cost but on this match: it removes pain points in downstream coupling, blends consistently with everyday solvents, and stores without drama. Any batch that avoids trouble from raw goods to late-stage API synthesis or polymer casting becomes invisible in the best sense – no emergency purchases, no panicked troubleshooting sessions, everyone goes home a touch earlier. Stubborn process managers will always pester for cheaper, faster, and higher purity; the field experience that comes from decades of real-world complaint logs and customer visits highlights what truly matters. Our product came into shape by wading through this real-world feedback, batch after batch, year after year.

    Going Forward: Continuous Improvement In the Real World

    As new synthetic challenges come from the lab bench or the process scale control room, our feedback file on 2-Methoxy-5-Pyridineboronic Acid grows thicker. Emerging applications in high-throughput automated screening or niche optoelectronic component fabrication push for still finer control of moisture content, better flowability, and lower trace metal content. We respond not just with incremental upgrades but by opening lines of real conversation: discussing problems, swapping stories on failed couplings, or digging through shared NMR spectra to root out rogue impurities. It’s a cliché to say the customer is always right, but in chemical manufacturing, the customer’s actual problem – not some abstract “requirement” – is the truest voice for improvement. Each new production run measures itself against those expectations: easy to weigh out in a busy lab, resistant to clumping in a bustling factory storeroom, a powder that keeps pace with the unpredictable tempo of research and scale-up.

    The key difference between 2-Methoxy-5-Pyridineboronic Acid and other building blocks isn’t only structure or cost, but the balance of all those day-to-day factors that define a successful material. For us, real E-E-A-T principles run through these daily habits: actually checking what we ship, listening to what went wrong, and honoring the shared knowledge between our process experts and our customers’ chemists. Over time, those habits make for better, more predictable materials and a more honest conversation about what can go right, and what needs more work, in making the best product possible.