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Pyrimidine-5-Boronic Acid Pinacol Ester

    • Product Name Pyrimidine-5-Boronic Acid Pinacol Ester
    • Alias Pyrimidine-5-B(pin)
    • Einecs 834-522-4
    • 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
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    Specifications

    HS Code

    757475

    Product Name Pyrimidine-5-Boronic Acid Pinacol Ester
    Cas Number 1056035-46-9
    Molecular Formula C10H15BN2O2
    Molecular Weight 206.06
    Appearance White to off-white solid
    Purity Typically ≥ 97%
    Melting Point 119-123°C
    Solubility Soluble in DMSO, methanol, and ethanol
    Storage Temperature 2-8°C (refrigerated)
    Smiles B1OC(C)(C)C(C)(C)O1c2cncnc2
    Inchi Key YMJCMWDNMSEQIF-UHFFFAOYSA-N
    Synonyms 5-(Pinacol boronate)pyrimidine

    As an accredited Pyrimidine-5-Boronic Acid Pinacol Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass vial containing 5 grams of Pyrimidine-5-Boronic Acid Pinacol Ester, sealed with a PTFE-lined cap and safety labeling.
    Shipping Pyrimidine-5-Boronic Acid Pinacol Ester is shipped in tightly sealed containers, protected from moisture and light. It is classified as a chemical reagent and is transported according to applicable hazardous material regulations, typically via air or ground in temperature-controlled, padded packaging to ensure stability and prevent contamination during transit.
    Storage Pyrimidine-5-Boronic Acid Pinacol Ester should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of moisture. Keep the container tightly closed when not in use. Store under an inert atmosphere such as nitrogen or argon if possible, and avoid exposure to air to prevent hydrolysis or degradation. Handle following standard chemical storage guidelines.
    Application of Pyrimidine-5-Boronic Acid Pinacol Ester

    Applications of Pyrimidine-5-Boronic Acid Pinacol Ester in Industrial Manufacturing

    Pyrimidine-5-Boronic Acid Pinacol Ester plays a pivotal role as a building block in multiple chemical sectors, supporting efficient, reproducible production across advanced pharmaceutical synthesis, agrochemical formulation, and specialty materials manufacturing. As the direct manufacturer of this intermediate, we supply clients who demand reliable batch-to-batch performance, adherence to international safety guidelines, and proven compatibility with process-scale synthetic routes.

    1. Pharmaceutical Intermediates for Small Molecule API Development

    This boronic ester serves critical functions in the preparation of pyrimidine-containing APIs, particularly in cross-coupling reactions to construct heteroaryl motifs, which are prevalent in kinase inhibitors and antiviral drugs. Major pharmaceutical clients integrate the material into Suzuki-Miyaura coupling steps during late-stage synthesis, ensuring precise placement of pyrimidine units while maintaining trace impurity limits set by the industry. Sophisticated QC processes require predictable reactivity and minimal residual metals post-coupling, streamlining downstream purification.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP, EP, JP relevant sections for API intermediates
    • FDA 21 CFR Part 211
    • REACH registration for nonclinical-scale material handling

    Typical usage ratio

    • Used at 1.0–1.5 molar equivalents relative to halogenated aryl/heteroaryl partners in cross-coupling; actual quantity tuned based on desired conversion and pathway yield

    Downstream process integration

    • Introduced during the Suzuki-Miyaura coupling step following halogenation of the core scaffold; protocol includes in situ base addition and Pd-catalyzed batch or continuous processing under controlled temperature and inert conditions

    Final product types

    • Pharmaceutical APIs such as kinase inhibitors, pyrimidine-derived antivirals, and oncology drugs
    • Advanced pharmaceutical intermediates for further derivatization
    • Pilot-scale investigational new drugs (INDs) for clinical trials

    2. Custom Agrochemical Synthesis for Herbicides & Fungicides

    Pyrimidine-5-Boronic Acid Pinacol Ester supports agrochemical manufacturers aiming to create innovative pyrimidine-functionalized herbicides and fungicides. It participates in selective arylation to extend molecular diversity, contributing to target-specific crop protection compounds featuring improved biological activity and degradation profiles. Industrial adoption depends on its ability to deliver high coupling efficiency in large-scale reactors, minimizing byproduct formation and optimizing throughput.

    Industry compliance standards

    • FAO/WHO specification for technical-grade pesticide production
    • OECD Principles of Good Laboratory Practice (GLP) for toxicology and efficacy assessment
    • ISO 9001:2015 for agrochemical synthesis
    • REACH compliance for supplied intermediates

    Typical usage ratio

    • Applied at 1.1–1.3 equivalents relative to partner halide in the main coupling step; excess adjusted according to pilot results and desired batch throughput

    Downstream process integration

    • Added post-chlorination or bromination of aromatic precursors, followed by metal-catalyzed coupling and subsequent downstream functionalization, often in a semi-continuous stirred tank reactor setup

    Final product types

    • Heterocyclic herbicides targeting resistant weed species
    • Systemic fungicidal agents for orchard and field crops
    • Agrochemical technical concentrates for formulation

    3. Electronic Chemical Synthesis for OLED Materials

    This boronic ester supports the construction of pyrimidine-functionalized organic semiconductors, commonly used in high-brightness OLED display materials. Downstream electronics manufacturers use it for the synthesis of emissive and electron-transporting layers, leveraging its behavior in palladium-catalyzed C–C coupling to build molecular frameworks essential for device stability and color purity. Stringent QC rests on minimized trace-metal content and reliable molecular weight distribution in final organic layers.

    Industry compliance standards

    • IEC 61249-2-21 for halogen-free electronic materials
    • IPC-4101 for base materials for printed boards
    • RoHS Directive 2011/65/EU for electronic component safety
    • ISO 9001:2015 for specialty chemicals

    Typical usage ratio

    • Usually 1.05–1.2 equivalents to bromo-/iodo-electron-deficient partners; amount refined during process qualification based on photophysical yield requirements

    Downstream process integration

    • Charged into cross-coupling reactors at the formation stage of small-molecule intermediates or polymers; post-processing includes recrystallization and purification before deposition onto device substrates

    Final product types

    • OLED emissive layer materials
    • Electron-transport and injection materials for display panels
    • Precursor materials for next-generation organic semiconductors

    4. Fine Chemical Manufacturing for Specialty Dye Synthesis

    This compound finds application in the production of advanced pyrimidine-based dyes and pigments, where its reactivity in coupling chemistry enables extended conjugation and chromophore customization. Fine chemical producers rely on its predictable performance to synthesize high-purity, lightfast dyes for specialty textiles and imaging media, satisfying industry quality expectations regarding shade repeatability and low trace contamination.

    Industry compliance standards

    • OEKO-TEX Standard 100 for chemical input in textile dyes
    • ISO 9001:2015 and ISO 14001:2015 for chemical manufacturing
    • REACH Annex XVII and Annex XIV authorization for dye substances
    • ZDHC MRSL guidelines for restricted chemicals in textile supply chains

    Typical usage ratio

    • Employed at 1.0–1.2 equivalents in coupling reactions with halogenated aryl cores; variance depends on desired chromophore yield and batch scale-up performance

    Downstream process integration

    • Fed to batch or continuous stirred reactors at chromophore assembly stage; followed by acid-base workup and solvent switching to isolate dye intermediates for further functionalization

    Final product types

    • Pyrimidine-derived fluorescent and color-fast dyes for textiles
    • Formulated colorants for inkjet and specialty printing applications
    • Light-stable technical pigments for plastics and fibers
    Free Quote

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    Certification & Compliance
    More Introduction

    Pyrimidine-5-Boronic Acid Pinacol Ester: Trusted Choice for Consistent Coupling

    Experience and Reliability Rooted in Modern Chemical Manufacturing

    Day after day in our production facility, we see exactly what goes into making Pyrimidine-5-Boronic Acid Pinacol Ester stand out from the usual run of heterocyclic boron reagents. We have worked with this material for years, fine-tuning every batch to keep up with research-grade and industrial needs. Its chemical formula, C10H15BN2O2, means those in organic synthesis circles know it as a building block that answers demands for coupling reliability and functional group tolerance. Our plant operators and chemists have faced every odd impurity or reaction variable head-on—ensuring the batches you use clear our in-house HPLC and NMR checks for content and profile.

    Our Approach to Purity and Consistency

    Some may believe that all pinacol boronic esters perform alike, but not every product delivers on batch-to-batch repeatability. From the early days processing gram-scale orders to today’s multi-kilogram runs, we have watched how even small shifts in water content or changes in crystallization rate can reshape selectivity or reactivity. Moisture control proves especially important, so we avoid atmospheric exposure throughout drying and packaging. Consistent handling ensures the white to off-white solid stays powdery, reducing clumping and contaminants that lead to failure in Suzuki-Miyaura coupling reactions. Rigorous shelf-life studies tell us how storage and transport interact with boronic acid functionality, giving us clear data to share with users who work in demanding labs.

    Structural Insight: Why Pyrimidine-5-Boronic Acid Pinacol Ester Matters

    Every chemist working with complex molecules knows how crucial borylated heterocycles are for cross-coupling. The pyrimidine ring, electron-deficient by nature, delivers reactivity to a sweet spot for medicinal chemistry and advanced material projects. Adding the pinacol ester to the fifth position gives an optimal balance: stability for shipping and handling, good solubility in common organic solvents, and reliable transmetallation with palladium or nickel catalysts.

    In the early days, researchers often turned to the free boronic acid forms. We saw how easily they decomposed under moisture or air. That lesson fueled our move to scale up the pinacol ester option—retaining all the synthetic flexibility but sidestepping the instability that vexes product storage and multi-step sequences. Over thousands of samples and reactions, this choice for the pinacol ester form continues to reduce procedural hiccups and minimises loss even after weeks in the warehouse.

    Practical Use in Synthesis: Fewer Failures, Better Scalability

    Talk to any synthetic chemist on a deadline, and they’ll mention the “Black Goo Problem” that comes up with boronic acids exposed to air or water. We have pulled countless samples from reactors mid-step; the pinacol ester rarely puts you through that kind of stress. Its powdery texture dissolves without residue, easing preparation whether you’re working through one flask or loading a few reactors in sequence.

    Researchers in our quality lab regularly run test couplings to check for unexpected byproducts. The result? Less formation of boroxines and decomposition byproducts. With less time spent on column purification or redosing, project managers talk about real gains in throughput and yield. These are not abstract metrics—they show up every quarter when customers track efficiency improvements and cost savings.

    Tech Advancements: Why It Differentiates from Others

    There’s a reason our long-term partners prefer our Pyrimidine-5-Boronic Acid Pinacol Ester over cheaper imitations or the free acid analogues. Pinacol esters from unnamed sources often introduce small but critical contaminants: leftover pinacol, unprotected boronic acids, or unstable solvent residues. Years of cooperative troubleshooting with material scientists and discovery chemists have revealed how important it is to keep those below detection limits. Even a half-percent impurity can poison catalytic cycles or introduce signals that muddy downstream analytics.

    Our synthesis routes include multistage purification and drying, removing organics and keeping crystallites in their ideal morphology. Even subtle differences—such as the degree of crystallinity or slight changes in melting range—alter how these solids dissolve or react. Through feedback from our pilot and production reactors, we designed a filtration protocol that ensures the finished product is not just technically “pure” by assay, but performs identically whether you’re drawing from a fifty-gram drum or a multi-tonne shipment.

    Versatile Applications Beyond Pharmaceuticals

    Our partners in pharma synthesis first pointed out how Pyrimidine-5-Boronic Acid Pinacol Ester fits new blockbuster scaffolds. By anchoring a boronic group on the pyrimidine ring, researchers build kinase inhibitors, anti-infectives, and anti-viral leads that evade legacy resistance profiles. It’s not just the patent office that takes notice—our after-sales teams hear from university researchers and CROs who push beyond pharmaceuticals. These esters now find uses in OLED materials, agrochemical intermediates, and specialty polymers.

    Our experience shows the ester survives higher temperature protocols and scales with fewer thermal or hydrolytic surprises compared to loosely protected boronic acids. A steady record of supply to electronics groups tells the same story. Formulators value solid-state stability and low color—qualities lost if boronic acids degrade to colored impurities from trace oxygen or moisture.

    No Shortcuts in Process: Lessons from Large and Small Scale Runs

    We have handled requests that range from tens of milligrams for late-stage discovery to hundreds of kilograms for production campaigns. Our process teams remark how little tolerance the market has for inconsistency. Discovery chemists want data on precise melting ranges and spectral signatures, while process engineers focus on how the solid flows through hoppers and resists caking. Through years of scale-up work, our production lines use strict process analytics: real-timing monitoring, moisture meters at fluid bed driers, and full traceability on every lot.

    Early on, one client sent feedback on color shifts in a stored batch. That kicked off a full root-cause analysis and a change in our final step workup. Lessons like that result in better products for everyone—flatter melting curves, less odor, more consistent weights per scoop. We know from direct feedback that the work pays off: chemists report cleaner mass balances and fewer aborted batches.

    Continuous Improvement Driven by Customer Collaboration

    Direct feedback loops guide our upgrades. After a few clients reported extra filtration steps due to fine particulates, our process engineers adjusted filtration mesh and final drying parameters. The new workflow cut down on visible fines and improved automatic dispensing—saving downstream labor in automated reaction setups. We built these changes into our supply records and update specifications as performance improves, not just to create data points but to keep customers updated on what they should expect from each new drum or vial.

    Supporting Big Ideas: From Early Discovery to Manufacturing

    The world of discovery moves fast, and no one waits on paperwork or problem batches. We’ve supplied Pyrimidine-5-Boronic Acid Pinacol Ester to research teams testing wide SAR ranges, process chemists scaling pilot trials, and advanced materials engineers blending lots for proprietary electronic materials. Researchers count on this ester because it slips into both small-parallel library runs and demanding multi-step campaigns without shifting physical form or dissolving profile.

    We know that late-stage pharmaceutical projects expose weaknesses in reagents that looked fine on paper. That’s why we test our ester across a spread of solvents—THF, DME, toluene, and MeCN all show predictable reaction rates. Its fine, free-flowing nature boosts metering accuracy, reducing weighing errors, and nearly eliminating issues with transfer losses between vessels. Process chemists who scale reactions hundreds of times expect this predictability, or risk losing material in costly waste.

    Safety by Design: Practical Steps from Synthesis to Shipping

    No responsible chemical manufacturer ignores safety. At every stage of our own use, we monitor for dusting and reactivity—parameters that worry everyone down the chain. Preparing the ester with clean, repeatable crystallization minimizes airborne powder and keeps reactions manageable in both manual and automated settings. We design packages for minimal headspace, oxygen scavengers for longer shelf life, and tamper-evident closures for quality assurance.

    Internally, our product stewardship groups track solvent profiles, impurity levels, and batch histories. Each movement from reactor to warehouse to final packaging passes through weight and imaging checks. Our logistics team reports back on transit conditions and handling issues, closing the loop with all stakeholders so that losses or mishaps, which happen in chemical supply chains, stay rare and fully documented.

    Clear Differences from Non-Pinacol and Non-Boronic Counterparts

    Some ask about the tradeoff between boronic acids in free versus pinacol ester form. Real-world reaction planning reveals the details. Pinacol esters, like our Pyrimidine-5-Boronic Acid Pinacol Ester, sacrifice some direct aqueous solubility but bring robust shelf-stability and reactivity in organic solvents. Comparisons show that the free acid form breaks down with moisture, while our pinacol ester endures months in ambient storage with no notable hydrolysis. Coupling yields hold up across changing solvent grades, inconsistent stirring rates, and various catalyst systems.

    We also use clean, high-purity pinacol to avoid unwanted cross-reactivity or off-odors. Lower grade boronic esters, often paired with methyl or ethyl substituents, run a greater risk of rearrangement and decomposition in heated conditions. Our clients in discovery and process chemistry keep returning for material that withstands both trial runs and GMP-scale synthesis.

    Authentic Feedback: Real Stories from Chemists and Engineers

    We hear from researchers who run high-throughput screens, noting a marked drop in failed couplings and cleaner NMRs with our material. Process chemists regularly comment on how quickly our powder dissolves and how stable it remains on the bench during set-up and transfer.

    A few years back, one formulator at a leading specialty materials supplier dialed us in about a challenge: scaling up a key monomer required a boronic ester that didn’t darken or clump after weeks of storage. Repeated trial runs with other suppliers led to bottle after bottle of off-color, damp powders. After switching to our Pyrimidine-5-Boronic Acid Pinacol Ester and implementing a moisture-meter guided protocol, the client noted not just better yields, but less effort spent rehabilitating transfer lines and cleaning reactors. These are the gritty details—not on a chart, but lived on the bench and in the plant.

    Focused on What Matters: Performance in Critical, Sensitive Applications

    Every kilogram we ship has passed hands that know what a failed batch means to a time-crunched laboratory—a lesson best not learned by accident. We don’t cut corners on input material checks, solvent drying, or analytical confirmations. The rigorous HPLC purity standards, routine moisture testing, and batch archive sampling aren’t just formalities—they answer to customers who run tight programs with tight deadlines.

    We’ve watched the subtle interplay of structure and reactivity shape new chemical entities, materials, and routes at the vanguard of technology. Observing each iteration from gram scales in pharma startups to multi-ton requests for advanced electronics, one fact stands clear: only a boronic ester made with a steady hand and deep process knowledge delivers the right balance of reactivity and shelf life.

    Always a Work in Progress—Responding to Science and Industry

    No successful reagent or intermediate stays static. The demands of researchers change as synthetic targets get more ambitious and regulation gets tighter. We listen and refine—whether that means adjusting crystalline size distribution for automated bulk dispensing, switching to greener solvents in our synthesis trains, or tracking trace metals down to the ppb range for sensitive applications.

    Even beyond optimization, we communicate with every new order and request, making sure expectations match reality. Quality, consistency, and performance are not slogans—they guide the hands and eyes of the staff on our shop floor.

    In Summary: Pyrimidine-5-Boronic Acid Pinacol Ester as a Reliable Partner in Synthesis

    The story of our Pyrimidine-5-Boronic Acid Pinacol Ester is not just about the compound itself, but about meeting challenges head-on in practical, real-world chemistry. Our work is visible in the cleaner spectra, higher yields, fewer troubleshooting calls, and successful late-stage scale-ups noted by our clients across industries.

    In our view, the steady, measurable advantages of this product—backed by years of analytics, feedback, and technical refinement—make it a cornerstone for any research and manufacturing program aiming for repeatable success. Anyone serious about scale, safety, and reliability can trust what comes from a manufacturer that works as closely with Pyrimidine-5-Boronic Acid Pinacol Ester as we do.