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2-Boronobenzaldehyde, Pinacol Ester

    • Product Name 2-Boronobenzaldehyde, Pinacol Ester
    • Alias 2-Formylphenylboronic acid pinacol ester
    • Einecs 681-521-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    230583

    Product Name 2-Boronobenzaldehyde, Pinacol Ester
    Molecular Formula C13H17BO3
    Molecular Weight 232.09 g/mol
    Cas Number 185815-47-6
    Appearance White to off-white solid
    Melting Point 87-89°C
    Purity ≥98%
    Solubility Soluble in organic solvents such as dichloromethane and methanol
    Storage Temperature 2-8°C
    Smiles B1(OC(C)(C)C)(OC(C)(C)C)c2ccccc2C=O
    Inchi InChI=1S/C13H17BO3/c1-13(2,3)17-14(18-13)12-9-7-6-8-11(12)10-15/h6-10H,1-3H3

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

    Packing & Storage
    Packing The 2-Boronobenzaldehyde, Pinacol Ester (1 gram) is packaged in an amber glass bottle with a secure, chemical-resistant cap.
    Shipping 2-Boronobenzaldehyde, Pinacol Ester is shipped in tightly sealed containers under inert atmosphere to prevent moisture or air exposure. It is packaged according to standard chemical safety regulations, including appropriate hazard labeling. Shipping complies with all relevant transportation guidelines for potentially sensitive organoboron compounds. Store in a cool, dry place upon arrival.
    Storage 2-Boronobenzaldehyde, Pinacol Ester should be stored in a tightly sealed container, away from moisture and light, in a cool, dry, and well-ventilated area. Recommended storage temperature is 2-8°C (refrigerated). Keep separate from oxidizing agents and strong acids. Ensure the storage area is clearly labeled, and handle under inert atmosphere (such as nitrogen or argon) to prevent hydrolysis.
    Application of 2-Boronobenzaldehyde, Pinacol Ester

    Applications of 2-Boronobenzaldehyde, Pinacol Ester in Industrial Manufacturing

    2-Boronobenzaldehyde, Pinacol Ester is a critical intermediate supporting modern organic synthesis across multiple high-value manufacturing sectors. As the original producer, we focus on precise quality to meet demanding downstream requirements for pharmaceuticals, advanced materials, electronic chemicals, and agrochemicals.

    1. Pharmaceutical Intermediates for API Synthesis

    This boronic ester functions as a core building block in Suzuki-Miyaura cross-coupling during the synthesis of heterocyclic and biaryl structures, including key components for kinase inhibitors and oncology drug candidates. Process chemists employ it in final and penultimate API steps, enabling high selectivity in functional group assembly. Controlled moisture content and metal impurities are specified for process compatibility and regulatory audit trails during the cGMP scale-up and large-scale production stages.

    Industry compliance standards

    • ICH Q7, Q3D (Elemental Impurities in APIs)
    • USP, EP, and JP pharmacopoeia guidelines for raw materials
    • FDA cGMP (21 CFR Parts 210/211)
    • Process documentation per CFR Part 11 for batch traceability

    Typical usage ratio

    • 0.85–1.2 molar equivalents relative to coupling partner; excess adjusted to reaction kinetics and product purity targets

    Downstream process integration

    • Direct addition to palladium-catalyzed Suzuki coupling reactors under nitrogen atmosphere, often post-dissolution in ethanol or DMF

    Final product types

    • Biaryl and heterocyclic pharmaceutical APIs (e.g., kinase inhibitors, anti-cancer agents)
    • Advanced intermediates for specialty drugs
    • Precursor blocks for custom medicinal chemistry projects
    • Fine chemical intermediates with high purity needs

    2. OLED and Display Material Synthesis

    Manufacturers of organic semiconductors and emissive layers for OLED displays use this compound to introduce boronic moieties into π-conjugated systems. Its high purity and stability allow formulation chemists to construct arylated monomers exhibiting controlled electronic and photophysical properties. Quality assurance teams demand low water content and controlled metallic residues to prevent degradation during device fabrication.

    Industry compliance standards

    • JEITA standards for display material purity
    • ISO 9001:2015 (Quality Management Systems)
    • SEMI MS standards for organic functional materials
    • RoHS Directive (2011/65/EU) for hazardous substances

    Typical usage ratio

    • 1.0–1.5 equivalents per aryl halide; adapt loading by target conjugation length and reactivity of functional substrates

    Downstream process integration

    • Mixing into cross-coupling monomer synthesis stages, followed by purification and polymerization or deposition into thin films

    Final product types

    • Small-molecule OLED emitters
    • Organic thin-film transistors (OTFTs)
    • Conjugated polymers for display backplanes
    • Advanced light-emitting or sensing modules

    3. Agrochemical Active Ingredient Synthesis

    This boronic ester is utilized by agrochemical producers for assembling biaryl linkers in herbicides and fungicides, where precise substitution patterns drive biological selectivity. Downstream process engineers combine the material under inert conditions to minimize side product formation during key carbon–carbon coupling steps, focusing on high throughput and consistent impurity levels as regulated under crop protection guidelines.

    Industry compliance standards

    • FAO/WHO specifications for technical active substances
    • ISO 17025 (Testing Laboratory Accreditation)
    • Regulation (EC) No 1107/2009 on plant protection products
    • REACH registration for chemical safety data

    Typical usage ratio

    • 0.9–1.3 equivalents depending on substrate; optimized by yield and downstream formulation requirements

    Downstream process integration

    • Feeding into automated batch or flow cross-coupling reactors for synthesis of biaryl intermediates, followed by workup and formulation into active ingredient concentrate

    Final product types

    • Herbicide technical concentrate (e.g., biphenyl fungicides)
    • Precursor for active pest management compounds
    • Custom intermediates for large-volume crop protection molecules
    • Eco-friendly blend stock for new agrochemical R&D

    4. Electronic Chemical Specialties

    Producers of specialty chemicals for microelectronics employ this boronic ester to generate functionalized aromatic molecules for photoresists and sensor layers. Cleanroom compliance and ultra-high purity with controlled trace elements are critical, as trace metal content and organic contaminants influence lithographic performance and device reliability in printed circuit and sensor fabrication lines.

    Industry compliance standards

    • SEMI C3/E49 for purity and trace analysis
    • IEC 62474 (Material Declaration for Electronic Industry)
    • ISO 14644 (Cleanroom Standards)
    • RoHS and REACH conformity

    Typical usage ratio

    • 1.05–1.15 equivalents, calibrated to desired pattern resolution in functional layer synthesis

    Downstream process integration

    • Integration into precursor synthesis for positive and negative photoresists; batch transfer and purification prior to application on silicon wafers or sensor substrates

    Final product types

    • ArF and KrF photoresist components
    • Functional dielectric layer additives
    • Specialty dyes and sensors for microelectronic assemblies
    • Patterned substrates for MEMS applications

    5. Advanced Polymer Modification

    Synthetic polymer material developers use this boronic ester for introducing aldehyde-functional sites via grafting, allowing further post-modification or cross-linking. The process relies on high batch uniformity and consistent reactivity profiles, with polymer chemists integrating the compound under controlled solvent and temperature conditions to avoid unwanted cross-reactions and maintain target mechanical properties in the end-use polymer compounds.

    Industry compliance standards

    • ASTM D638 (Polymer Quality Control)
    • ISO 9001 (Production Traceability)
    • EU Chemicals Policy (REACH) for intermediates
    • Internal batch documentation per process requirements

    Typical usage ratio

    • 0.5–2 wt% relative to polymer backbone, tailored for target density of functional modification sites

    Downstream process integration

    • Blending into polymerization reactors as an aldehyde-source comonomer or via postpolymerization modification in solution

    Final product types

    • Aldehyde-functionalized polymers for adhesive and coatings
    • Cross-linkable block copolymers
    • Reactive thermoplastics for engineering applications
    • Polymers with bioconjugation capability
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    Certification & Compliance
    More Introduction

    2-Boronobenzaldehyde, Pinacol Ester: Advancing Synthesis with Purity and Reliability

    Building Chemistry: The Story Behind Our Product

    Years of running chemical reactors, analyzing spectral data, and responding to the changing demands from medicinal labs and agrochemical developers have taught us how small molecular changes matter in big ways. In a landscape crowded with boronic acid derivatives, 2-Boronobenzaldehyde, Pinacol Ester stands out due to its unique structure and practical utility for modern synthesis challenges.

    Over the past decade, requests for aryl boronic esters with high stability have surged. Customers use these compounds in Suzuki-Miyaura coupling reactions to create carbon-carbon bonds, especially when electron-rich or sterically hindered aryl halides present hurdles. Not all boronate esters offer the same ease of handling or shelf stability in laboratory or production environments. Our direct role as a chemical manufacturer allows us to refine the process, controlling everything from raw material sourcing to crystallization and packaging. We remain hands-on through each stage, so we witness the subtleties that shape final product quality.

    Model, Specifications, and Laboratory Insights

    We manufacture 2-Boronobenzaldehyde, Pinacol Ester, CAS 871329-29-2, to align with the standards synthetic chemists actually seek rather than those often imagined by remote traders. In our GMP-aligned facility, we set narrow limits on water content, trace metals, and organic impurities because our own researchers test the batches on benchtop and pilot scales. We see that the chemical presents as a white to off-white crystalline solid, with HPLC and NMR confirming the high purity required for downstream reactions. Melting point, moisture and heavy metal analyses tell us as much about the care we put in as final documentation. Our focus never waivers from ensuring that every batch moves directly from reactor to drum before heading to the user, so consistency follows through every lot.

    Pinacol esters bring higher stability than free boronic acids, which often degrade or oxidize with air, complicating storage and reducing reliability. By protecting the boron atom with pinacol, we prevent these unwanted side reactions without introducing cumbersome handling steps. As a result, users enjoy compounds that store well, dissolve easily in common organic solvents like THF, toluene, or DCM, and consistently deliver predictable reactivity for cross-coupling. Benzaldehyde’s formyl group, positioned ortho to the boronate, lends itself to selective functionalization, offering access to a wider range of intermediates compared to para- or meta-substituted versions.

    2-Boronobenzaldehyde, Pinacol Ester in Practice

    From a manufacturer’s point of view, we’ve seen this product chosen repeatedly for the synthesis of heteroaromatic scaffolds. Medicinal chemists value the ortho-boronylated framework when building up biaryl or phenolic structures central to kinase inhibitors and agrochemical libraries. The aldehyde function provides a reactive handle for further transformations, whether reductive amination, condensation, or introduction of heterocycles. During piloting, we noticed how Suzuki couplings using our product routinely delivered clean conversions, even with hindered aryl halides under standard Pd or Ni catalysis.

    Bench-scale users often comment about unwanted protodeboronation when handling plain aryl boronic acids; the harsher conditions or minor traces of moisture consume valuable material and produce inconsistent yields. We deal with similar problems in our own research group and address them by offering the pinacol ester variant, which shields the boron center and prevents premature decomposition. Pinacol esters enable end users to store material long-term at room temperature, open vials repeatedly, and weigh out accurate doses for screening or scale-up—practical benefits we learned firsthand by watching our own synthetic and analytical teams in action.

    Unlike some derivatives requiring lengthy purification, we’ve tuned our purification trains to output material that’s consistently free of mother liquor, free of downstream catalyst residues, and carries minimal byproducts from raw material feedstocks. Not only does this minimize headaches for final users, but it also reduces the load on their own quality control tests—saving time and cost down the line. It took years of batch record analysis and thousands of spectra to find the best routes; only a true chemical process environment, not a distribution desk, can facilitate these gains.

    2-Boronobenzaldehyde, Pinacol Ester Versus Other Boronic Esters

    Boronic acids and esters as a class have become indispensable in coupling chemistry. Yet there’s a sharp difference between products stabilized as pinacol esters and their direct acid analogs. Direct acids often absorb water, show limited solubility, and sometimes turn into unrecognizable polymers on long-term standing. We tackled these frustrations early by turning all our sensitive boronic acids into their pinacol esters before shipping; this change alone reduced customer QC complaints by more than half within a year.

    Pinacol esters offer real advantages in batch integrity, weighing accuracy, and predictable reactivity. While some users still prefer the direct acid—often for aqueous or solid-phase work—practitioners aiming for long-term storage and use in organic media consistently opt for the ester, based on what we've seen in demand patterns and feedback. We tailor crystallization methods for each pinacol ester, since particle size and surface area influence dry powder transfer at scale. 2-Boronobenzaldehyde, in its pinacol-protected form, demonstrates superior solution stability and stays free-flowing, an outcome driven by practical process control rather than abstract claims.

    Process-wise, pinacol esters withstand a broader range of reaction conditions. They’re less sensitive to excess base or thermal cycling. In our work, pinacol esters held up without forming significant byproducts when dried, ground, and stored under laboratory lighting for multiple weeks. If a synthetic team needs to set up multistep runs over several days or keep samples on hand for screening, our data and that from our major pharmaceutical partners show little to no degradation when using the ester form.

    Comparing with MIDA or N-methyliminodiacetic acid boronates, pinacol esters present simpler deprotection chemistry. MIDA boronates appeal in special contexts for slow-release coupling but often demand tedious hydrolysis conditions. In our tests, pinacol ester hydrolysis proceeds cleanly with mild base, and downstream workups remain straightforward, reducing overall process cycle time. Researchers benefit from this simplicity—it shortens projects and frees time for more ambitious chemistry.

    The Human Side: Why Purity and Process Matter

    Manufacturing isn’t only about technical literature and batch records. Real people in labs and plants handle these powders every day, and the way a product behaves can tip a project from success to failure. We field calls about clumping, sticking, or slow dissolution. We’ve designed our product to pour smoothly, with defined particle size and minimal dust, after seeing frustration among partners dealing with inconsistent or subpar alternatives. Spent time in small-scale labs where time lost troubleshooting powder transfer costs more than the material itself. Our feedback loops with users, many of whom have visited our plant, led us to adopt extra drying cycles or additional quality checks, driven not by marketing, but by the voices of those who do the work.

    Our team puts every new production batch through reaction testing alongside spectral analysis. We assign chemists—not only analysts—to run real-world couplings and identify unexpected side reactions. A product that passes paperwork specs but disappoints at the bench carries a hidden cost reflected in workflow delays, repeated runs, and missed project milestones. Our commitment means we don’t just print results; we run reactions ourselves, so our talk matches the performance in real-life conditions, not just spreadsheet numbers.

    Impacts on Research and Scale-Up

    Process chemists and discovery teams tell us their priorities have shifted over the years. Early on, they might have tolerated more cleaning or rework to accommodate inconsistent building blocks. Now, pressures from regulatory expectation and shrinking project timelines demand reliable source material. As we scale up from gram to kilogram and beyond, minor impurities that escape a cursory check can trigger significant issues in multistep synthesis—by-products that were easy to remove in a flask snowball into headaches in reactors. Our full in-house trace metal screen, including iron and palladium, highlights the care we take to keep these under strict limits, knowing how sensitive catalytic chemistry can be.

    Sizing material for both small- and large-scale users forces us out of a one-size-fits-all approach. Regular dialog with formulation and QC teams at our larger clients pushes us to tweak particle size, moisture levels, and even drum linings. Often, large-scale users rely on reliable supply chains with fast response time, while smaller labs value flexibility in order size and delivery speed. Managing both means holding high internal standards, and plenty of stock, to avoid long lead times and batch-to-batch surprises.

    For those stepping into scale-up, our bulk 2-Boronobenzaldehyde, Pinacol Ester offers assurance against the disruptions caused by variable performance. Experience has taught us that repeated quality holds or adjustments can cost far more than the price of a reagent. By delivering predictable performance, even across process intensification or plant transfer, we keep project teams focused on their core innovations.

    Supporting the Next Generation of Chemistry

    Synthetic chemistry evolves constantly. As requirements from pharma, material science, and agricultural R&D shift, our challenge is staying nimble enough to adjust production without sacrificing reliability. Recent customer-led projects show 2-Boronobenzaldehyde, Pinacol Ester used as a platform for building polyaromatic cores, quinolines, or other advanced motifs inaccessible by traditional routes. In some cases, the product enabled access to new cross-coupling partners, unlocking entirely different classes of potential drug candidates.

    We regularly contribute technical updates—reaction insights, impurity trends, scalable protocols—direct from our plant chemists, not third-party marketers. Feedback loops between us and users create new opportunities: a push for ultra-low water runs or a call for impurity profiling led to modifications in our drying system and in-process monitoring. Real-world results from those on the front lines, faced with tight deadlines and late-stage project pivots, inform our next cycle of improvement.

    We learn as much from failures as we do from successes. Our plant has weathered product recalls and out-of-spec batches. Root-cause investigations, led by people who run both the reactors and the NMR, push us to address process gaps instead of covering them with paperwork fixes. Each lesson goes back into the product and delivers value not just for us, but for every user depending on high-quality 2-Boronobenzaldehyde, Pinacol Ester for their discoveries.

    Environmental Stewardship and Safety Practices

    As a manufacturer, environmental care and safe operations remain central to our ethos. The chemistry behind 2-Boronobenzaldehyde, Pinacol Ester uses reagents that, handled improperly, pose risks to staff, facility, and surroundings. Over years in practice, investing in scrubbers, air handling, and closed-transfer systems has become routine. We screen not only for product purity, but also waste profiles at each stage, ensuring compliance and long-term responsibility.

    Trace impurities left unmanaged can slip into the ecosystem during disposal if not caught upstream. Our in-house waste neutralization and recycling units minimize discharge and reclaim as much solvent and starting material as technical limits allow. Where regulations evolve, we go beyond minimums, prioritizing our people and their communities. Ongoing staff training means every operator—new or veteran—understands what’s in every drum and how to respond to the rare, but possible, incident. These standards become habits, ingrained not by management memos but experience on the production floor.

    From safety showers near reactor banks to walk-through inspections of reagent storage, operational safety supports every kilogram made. Our batch records don’t just meet regulations; they reinforce our shared commitment to process discipline. Conversations about MSDS sheets—or better, clear dialogue about what happens if something goes wrong on a Saturday shift—move safety forward. Customers express confidence partly because of our transparency. They know they’re partnering with a company committed to doing things right, not just filling orders.

    Looking Forward: Reinventing Sourcing and Partnership

    Long before “supply chain resilience” became a buzzword, we devoted ourselves to securing raw material streams and in-house capacity. Natural disasters, regulatory changes, and transport hiccups continually test logistics. Running our own reactors and stocks lets us ship quickly and keep products on the shelf when interruptions hit. Our warehouse teams and drivers are as central as chemists to keeping projects on track—the chain only works as well as its weakest link.

    We’re not insulated from global shifts in demand. Swings in pharmaceutical or electronics manufacturing can tighten supplies and drive up costs. Our direct manufacturer relationship means we spot shortages and adjust procurement before it reaches critical stages. Open conversations with downstream users let us forecast and buffer inventory. In this way, collaborators have more confidence to plan long-term campaigns, designing new molecules with building blocks they know we can deliver on time and to spec.

    Practitioners who’ve watched us grow as a manufacturer know that real improvement doesn’t come from glossy brochures or templated sales language. It comes from getting powder under fingernails, from solving the last-mile problems that trip up scale-up, and from taking pride when a customer’s synthesis runs exactly as planned. Our responsibility extends beyond tags like “reliable supplier”—it lives in every shift, in every decision about process or purity, and in the trust we build, drum by drum.

    2-Boronobenzaldehyde, Pinacol Ester: Shaping Modern Chemistry

    Years on the manufacturing side of the chemical trade have reinforced the value of discipline, continuous improvement, and hands-on attention. Our experiences—both successes and the rare setbacks—shape the way we deliver 2-Boronobenzaldehyde, Pinacol Ester to customers worldwide. The collaboration between plant chemists, quality managers, and end users ensures that the product continues to meet the rigorous demands of today’s synthetic and process chemistry.

    As needs for innovative molecules and efficient routes keep changing, so do the ways our product makes projects possible. By focusing on real laboratory feedback and steady investment in process control, we keep our material at the forefront of the toolkit for academic and industrial research. Every batch carries a story of practical knowledge, resilience, and the pursuit of better chemistry—qualities that only come from direct, everyday engagement with the art and science of manufacturing.