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Pyridine-2-Boronic Acid Dimethyl Ester

    • Product Name Pyridine-2-Boronic Acid Dimethyl Ester
    • Alias 2-(Dimethoxyboranyl)pyridine
    • Einecs 624-155-6
    • 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

    330344

    Product Name Pyridine-2-Boronic Acid Dimethyl Ester
    Cas Number 132250-81-8
    Molecular Formula C7H10BNO2
    Molecular Weight 150.97
    Appearance Colorless to pale yellow liquid
    Purity Typically >98%
    Boiling Point 75-77°C at 2 mmHg
    Density 1.10 g/cm3 (approximate)
    Solubility Soluble in organic solvents (e.g., dichloromethane, THF)
    Smiles B(OC)(OC)c1ccccn1
    Inchi InChI=1S/C7H10BNO2/c1-10-8(11-2)7-5-3-4-6-9-7/h3-6H,1-2H3
    Refractive Index 1.518 (approximate)
    Flash Point 80°C (closed cup)
    Storage Conditions Store at 2-8°C, under inert atmosphere

    As an accredited Pyridine-2-Boronic Acid Dimethyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Pyridine-2-Boronic Acid Dimethyl Ester, 5g, is packaged in a sealed amber glass vial with a tamper-evident screw cap.
    Shipping Pyridine-2-Boronic Acid Dimethyl Ester is typically shipped in sealed, airtight containers to prevent moisture and air exposure. The packaging complies with chemical safety regulations, and the material is handled as a flammable, potentially harmful organic compound. Transport is conducted under controlled temperatures, and appropriate hazard labeling is provided for safe handling.
    Storage Pyridine-2-Boronic Acid Dimethyl Ester should be stored in a tightly sealed container, protected from moisture and air. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Store at room temperature or as specified by the manufacturer, and keep away from direct sunlight and ignition sources to maintain stability.
    Application of Pyridine-2-Boronic Acid Dimethyl Ester

    Applications of Pyridine-2-Boronic Acid Dimethyl Ester in Industrial Manufacturing

    Pyridine-2-Boronic Acid Dimethyl Ester serves as a high-performance intermediate in several advanced chemical synthesis routes. As the original manufacturer, we supply this material directly to controlled production environments across pharmaceutical, agrochemical, and specialty material sectors. The following sections detail its precise implementation in key downstream industries, focusing on compliance, formulation, process integration, and resulting finished products.

    1. Pharmaceutical API Synthesis (Heterocyclic Compound Construction)

    This intermediate enters multi-step pharmaceutical synthesis, especially in Suzuki-Miyaura cross-coupling reactions to build pyridine-containing active moieties. API manufacturers use it to introduce boronic acid functionality onto heterocyclic backbones—common in kinase inhibitors and anti-inflammatory drugs. Regulatory compliance remains critical, requiring validation from raw materials through to final stages and traceability in GMP records for highly regulated markets. Quality control tracks boron impurity carryover and reaction completion in each batch, meeting the batch-to-batch consistency required for scale-up.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP/NF monographs on intermediates, where applicable
    • 21 CFR Part 211 (cGMP for finished pharmaceuticals, USA)
    • EDQM CEP route documentation (Europe, where performed)

    Typical usage ratio

    • 0.80–1.10 molar equivalents relative to aryl halide coupling partners; ratio optimized for target API yield and minimum side reactions

    Downstream process integration

    • Integrates in the coupling stage of the multi-step synthesis route, post-formation of aryl halide precursors and before final purification and isolation of active substance

    Final product types

    • Kinase inhibitor APIs (e.g., in oncology drugs)
    • Non-steroidal anti-inflammatory drug scaffolds
    • Pyridine-based CNS drug intermediates

    2. Agrochemical Active Ingredient Production (Herbicide Intermediates)

    Agrochemical manufacturers employ this intermediate for boronic ester coupling reactions to construct pyridine-based herbicide and fungicide actives. The compound enables selective C–C bond formation under controlled, inert conditions, minimizing waste byproducts and meeting trace contaminant limits. Batch documentation and raw material release test certificates support regulatory filings and market access in key agricultural regions with strict residue and impurity requirements.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • Regulation (EC) No 1107/2009 (EU plant protection product approval)
    • EPA PRN 2011-3 (US Environmental Protection Agency product chemistry requirements)
    • ISO 17025-accredited laboratory release testing

    Typical usage ratio

    • 1.00–1.25 molar equivalents; adjusted by target yield and reaction selectivity for boronic coupling with halogenated heterocyclic partners

    Downstream process integration

    • Used in the final core-building step before protective group removal and formulation, inserted downstream of halide precursor generation in seed batch processes

    Final product types

    • Pyridine-based herbicides (selective and non-selective)
    • Systemic fungicide actives
    • Pre-emergent weed control agents

    3. OLED & Organic Electronic Material Synthesis

    This intermediate supports electronic manufacturers creating advanced organic light-emitting diode (OLED) emitters and electron transport materials. In Suzuki coupling stages, boronic esters facilitate formation of conjugated pyridinyl units for high-purity optoelectronic layers. Consistent purity and controlled boron content allow for defect-free deposition and reproducible device performance. All batches undergo trace impurity analysis and are documented for critical material certification programs demanded by display device suppliers.

    Industry compliance standards

    • IEC 62321 for hazardous substance assessment in electronics
    • JEDEC J-STD-033C (Moisture/reflow sensitivity control)
    • RoHS Directive 2011/65/EU (heavy metals, organoboron restrictions)
    • OEM-specific incoming chemical specifications (for display panel fabrication)

    Typical usage ratio

    • 0.95–1.05 molar equivalents relative to bifunctional halogenated partners; fine-tuned based on optical purity and film property requirements

    Downstream process integration

    • Introduced during the construction of extended conjugated ligands, right before purification via chromatography or recrystallization and downstream device layer fabrication

    Final product types

    • OLED emission layer polymers
    • Electron transport and injection materials
    • Organic solar cell donor-acceptor frameworks

    4. Advanced Fine Chemical Synthesis (Custom Specialty Chemicals)

    Specialty chemical producers use this boronic ester for targeted biaryl or heterocyclic syntheses in R&D and low-volume, high-value custom chemicals. Its reactivity profile fits applications requiring precise boron incorporation, especially in medicinal and supramolecular chemistry. Documentation and sample retention support custom QA protocols demanded in custom synthesis contracts and technology transfer agreements. Analytical method validation includes precise boron and pyridine content checks post-reaction.

    Industry compliance standards

    • ISO 9001:2015 (Quality management for chemical manufacturing)
    • REACH (EC 1907/2006) registration where manufactured or imported into the EU above 1 tonne per annum
    • Chemical safety assessment under GHS/CLP system
    • Custom accreditations per client technical agreements

    Typical usage ratio

    • 0.50–1.50 molar equivalents, flexibly tuned in process development batches to maximize selective cross-coupling and minimize unreacted boron content

    Downstream process integration

    • Stepwise integration in coupling or derivatization reactions, typically following halide introduction and prior to downstream purification for specialty end use

    Final product types

    • Reference compounds for analytical chemistry
    • Functionalized small molecule building blocks
    • Photoactive or chiral ligands for advanced research
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    Certification & Compliance
    More Introduction

    Pyridine-2-Boronic Acid Dimethyl Ester: Precision for Modern Synthesis

    The Heart of Synthesis: Our Perspective as a Manufacturer

    At our manufacturing facilities, we've watched the evolution of fine chemical synthesis from the inside out. Pyridine-2-Boronic Acid Dimethyl Ester, model 2-PDE, stands out to us on the production line for the simple reason that it keeps pace with the demands of medicinal chemistry and material science. Recipes today call for accuracy, speed, and a certain predictability which not every boronic ester can deliver. After years invested in scale-up, purification, and real-world testing alongside research teams, we see clearly where this compound shines and where its differences matter most.

    Model 2-PDE: Consistency That Saves Steps

    We manufacture the 2-PDE variant for a reason: through direct observation, this blend handles Suzuki-Miyaura couplings and oxidation reactions with fewer interruptions. The purity profile we’ve dialed in is one we can achieve batch after batch. In our operations, variability means waste. Unwanted impurities in the boronic ester slow down the cross-coupling and produce hard-to-remove byproducts. It’s become routine at our site to see chemists lose afternoons fine-tuning reaction conditions when the building block isn’t as clean or predictable as advertised. By keeping water levels low and controlling residual solvents with active moisture exclusion, our teams cut down on these adjustments. The days of guesswork recede, replaced by the simple trust that the product in the drum matches the data sheet in performance, not just on paper.

    Specifications Rooted in Real Use

    Over years supplying grams to metric tons, the practical needs of our customers have shaped the specifications we target. Pyridine-2-Boronic Acid Dimethyl Ester (C7H10BNO2, CAS 248484-57-1) comes off our line with purity usually greater than 98% by HPLC. Through full QC, we maintain water content below 0.5% (Karl Fischer titration) and residual solvents below 0.1%. We’ve seen time and again how microbatches behave differently from scale production, so our approach adjusts process parameters not once, but continuously. Our technical teams evaluate not only for purity and water content, but also monitor for common side-products unique to this boronic ester – like pyridyl isomers and dimethyl borates. These don’t always register on a basic NMR or TLC screen, yet we’ve found them a hidden source of trouble when undetected. Addressing them from the outset prevents headaches three steps downstream.

    Why Pyridine-2-Boronic Acid Dimethyl Ester?

    The decision to use this ester instead of the boronic acid or pinacol ester comes from years of direct engagement with scale-up challenges and yield maximization. During our own process R&D, we identified that the dimethyl ester form offers greater hydrolytic stability than the acid—especially in labs that see fluctuating humidity. Over the past decade, customers reported fewer batch failures tied to moisture exposure when switching to the dimethyl ester. If you’ve ever unsealed a container of boronic acid and found a lumpy, partially hydrolyzed mass, you can guess why our clients stick with the dimethyl ester. The pinacol ester can sometimes offer even greater stability, but it brings extra steric hindrance and, in several coupling scenarios, slower reaction rates compared to the dimethyl ester. Customers looking to avoid side reactions from boronate formation or to shorten reaction times turn repeatedly to our 2-PDE product.

    Observations from Production: Handling and Packaging

    Inside our plant, the real-time decisions about sensitivity and storage prove critical. Some assume all boronic esters perform alike. Experience tells us this isn’t so. The dimethyl ester variant handles brief air exposure better than pure acids but still demands tight sealing after sampling. We moved from basic polyethylene to laminated foil packaging when feedback showed minor moisture ingress even during short-term bench storage. These small changes, implemented after live production runs and customer trials, keep our product within specification from door to door. We test each lot for atmospheric pickup over simulated transport cycles; it’s a point of pride that our final product reaches both domestic and international clients still matching exit-range purity.

    Problems Clients Find—and How We Adapt

    Some of the most meaningful feedback we receive as a manufacturer doesn’t come from formal regulatory filings or generic surveys. It’s the call late in the afternoon from a process chemist who’s troubleshooting an unexpected drop in yield. The questions nearly always cut to the specific quirks of pyridine boronic esters. Water content might look acceptable in an unopened container, but once open, even two days on a humid bench can shift the landscape for a coupling reaction. The ester offers a cushion, staying homogeneous and liquid at room temperature but starts to degrade above sixty degrees Celsius if left unsecured. These front-line truths prompted our packaging upgrades and batch-by-batch water testing workflow.

    We see labs worldwide—those that order from us directly—aren’t always able to pair our ester with the same palladium precatalyst from project to project. In such cases, they ask for application notes from our analytics division, detailing which ligand and base combinations worked best with our current lot. This feedback loop, specific to our molecule and production conditions, shapes not only our technical bulletins but our own quality evaluations. Other manufacturers sometimes report a product suitable for all “standard coupling protocols,” but from hundreds of pilot reactions, we’ll offer up the truth: reaction temperatures, ligand loading, and even solvent polarity need slight tweaking depending on lot-to-lot characteristics—not due to impurities, but due to the subtle interplay of pyridine’s electron density and boron reactivity with each production scale.

    Usage in Medicinal and Agrochemical Synthesis

    Most of the 2-PDE we deliver finds its way into pharmaceutical discovery or agrochemical building blocks. At the manufacturing scale, differences in batch quality mean far more than a few percent shift in yield – they decide whether a project hits a deadline or goes back to process development. The ester group allows for direct cross-coupling, supporting iterative parallel synthesis. In the case of pyridine derivatives, each substitution pattern can affect solubility, reactivity, and the profile of side products. Our long-term partnerships with drug discovery groups exist because our material translates predictably from flask to reactor, allowing teams to swap conditions in the search for optimal routes. The compound’s manageable boiling point and liquid state at ambient conditions further streamline handling in automated systems compared to solid boronic acids.

    Large-acreage crop protection synthesis has moved in the same direction, with scale runs requiring a boronic ester that survives multiday logistics without loss of integrity. Our years in tank-to-tank transfer, combined with rigorous stability studies, turned up a small but crucial finding: the dimethyl ester, compared to other protected boronic acids, links well into both aryl-halide and alkene partners without drawing unwanted moisture, so logistics headaches shrink considerably.

    Differences From Other Boronic Derivatives

    We field regular questions about the advantages of the dimethyl ester over the free acid, the pinacol ester, and the ethylene glycol ester. Each variant brings tangible benefits and pitfalls.

    Boronic acids, including 2-pyridine boronic acid, see rapid hydrolysis with ambient moisture, particularly in subtropical storage environments. Lumps, variable feedstock, and decomposition byproducts pose significant cleanup costs. From our own supply chain, we saw return rates plummet when most pharmaceutical partners swapped to dimethyl esters.

    Pinacol esters, widely cited for high stability, suit long-haul storage and resist decomposition better than the dimethyl form. The practical tradeoff stems from steric bulk at the reaction site. In our hands, and from what clients report back, reactions with pinacol esters often call for higher catalyst loadings or extended heating to reach comparable conversions. Dimethyl esters, conversely, strike a midpoint: less sensitive than acids, faster than pinacol, and still cost-effective to produce. For iterative drug building and exploratory runs, this profile fits most workflows.

    Ethylene glycol esters occasionally substitute where downstream hydrolysis is critical, but our side-by-side pilot runs confirm that reactions with dimethyl esters generally finish in less time and with fewer purification steps. Customers in regulated industries value not only speed but traceability; our QC records and stability studies provide a thorough audit trail that helps meet these expectations.

    What Matters Most to Us—and to Our Users

    Production is only half the story in chemical manufacturing. Product consistency, clear communication with end users, and a willingness to adapt define long-term value. The nuances of pyridine boronic ester chemistry, as seen in real-time through our customer network, keep raising the standard. Each lot we ship carries a hidden record of decisions made on the production line: the quality of reagents sourced, the degree of vacuum during distillation, even the vigilance of the QC analyst checking for isomers detectable only by LC/MS.

    Feedback has shaped incremental improvements. We reduced packaging transfer losses by switching to liner-sealed drums. Weekly spot checks for hydrolyzed residues let us identify and isolate rare instability events before they reached customers. In one cycle, a surge in humidity during monsoon season forced us to halt a batch midway, then rerun it using the latest desiccant and blanket headspace controls. This sort of active problem-solving isn’t listed on any standard product bulletin, but those who have chased a failing reaction at three in the morning know that even tiny variations can determine project success. By staying in close touch with researchers, we convert individual challenges into site-wide improvements.

    Solutions to Recurring Issues: Lessons for the Future

    Recurring issues sometimes reach beyond the scope of a single product. Humidity sensitivity remains a watch point for boronic compounds generally. We tackled this by investing in automated filling lines with controlled atmosphere modules and reinforced, moisture-impermeable packaging. Each improvement creates stress tests and operational hiccups during rollout, but the net gain over time means fewer complaints, higher retained purity, and steadier downstream performance.

    Waste reduction ties directly to quality control. By tightening acceptance criteria for precursor reagents and monitoring drift in GC retention times, the number of out-of-specification batches dropped by nearly a third over three years. For contract manufacturing partners insisting on zero-defect deliveries, these hard-won gains build trust—and save both sides significant remediation costs.

    In the broader context of the chemical industry, regulatory complexity continues to grow. Rather than treat this as a bureaucratic burden, we fuse compliance with operational gain. Trace metal analysis, residual solvent profiling, and long-term stability studies, all part of our workflow, allow for early interventions and streamlined regulatory submissions—not just for our company, but for customers whose final products depend on our attention to detail.

    Quality and Trust: Real Value Beyond the Spec Sheet

    No matter how established the chemistry, it’s the daily routines at our facilities that prompt incremental gains in product value. Technical data speaks volumes, but firsthand accounts and troubleshooting logs are what guide next-generation improvements. The feedback flowing between our process engineers, customer-facing chemists, and end users informs every tweak and upgrade.

    Trust grows over time. Researchers using our Pyridine-2-Boronic Acid Dimethyl Ester often call to discuss their own project requirements—temperature sensitivity, scale transitions, and solvent compatibility. These conversations reveal gaps between theoretical performance and real-world outcomes. We count these conversations as the basis for sustained quality; every new use case brings lessons that drive manufacturing decisions.

    We’ve watched this compound’s application landscape shift: where once only specialist labs handled boronic esters, now automated synthesis and even undergraduate labs build on the 2-PDE backbone. This wider base brings new challenges. We address these by thorough documentation, hands-on advice, and technical assistance available well beyond the point of sale. By explaining the unique behaviors and storage needs of this compound, our technical support helps teams avoid common missteps and streamline workflow.

    Looking Ahead: Reliability and Innovation

    Manufacturing Pyridine-2-Boronic Acid Dimethyl Ester involves more than repeating yesterday’s recipe. Teamwork across production, packaging, logistics, and technical support ensures that the end result—our 2-PDE—remains a tool researchers can depend on. New trends in green chemistry, automation, and stricter international regulations set the direction for investment in our facility and shaping upgrades. By staying curious, responsive, and connected to where and how our products are used, we push performance forward, batch by batch.

    Feedback from hundreds of applications has colored our understanding of both the strengths and limits of this compound. Each call or message spurs new questions—on stability, compatibility, even waste minimization during handling. We build on this practical foundation, not resting on old wins, but seeking better ways to deliver quality and reliability. With every shipment of Pyridine-2-Boronic Acid Dimethyl Ester, the goal is unchanged: supply a material customers can trust, not just by our word, but by their repeatable, trouble-free results.