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1-Methyl-4-Pyrazole Boronic Acid Pinacol Ester

    • Product Name 1-Methyl-4-Pyrazole Boronic Acid Pinacol Ester
    • Alias 1-Methyl-4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole
    • Einecs 886463-94-1
    • 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
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    Specifications

    HS Code

    604125

    Product Name 1-Methyl-4-Pyrazole Boronic Acid Pinacol Ester
    Molecular Formula C10H17BN2O2
    Molecular Weight 208.07 g/mol
    Cas Number 936329-06-5
    Appearance White to off-white solid
    Purity Typically ≥97%
    Melting Point Approximately 90-94°C
    Solubility Soluble in common organic solvents such as DMSO and dichloromethane
    Storage Conditions Store at 2-8°C, protected from moisture
    Smiles Cn1cc(C2(O)OC(C)(C)C(C)(C)O2)cn1
    Inchi InChI=1S/C10H17BN2O2/c1-8-6-7-12-10(8)11-9(14)13-15-9/h6-7H,1-5H3

    As an accredited 1-Methyl-4-Pyrazole 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 A 5-gram amber glass bottle with a secure screw cap, labeled "1-Methyl-4-Pyrazole Boronic Acid Pinacol Ester, 98% purity."
    Shipping 1-Methyl-4-Pyrazole Boronic Acid Pinacol Ester is shipped in tightly sealed containers under dry, cool conditions to prevent decomposition. The package is clearly labeled and protected from moisture, light, and physical damage. Shipping complies with all relevant chemical transport regulations, including MSDS documentation and hazard labeling, ensuring safe handling and delivery.
    Storage **1-Methyl-4-Pyrazole Boronic Acid Pinacol Ester** should be stored in a tightly sealed container, under an inert atmosphere (nitrogen or argon) to prevent hydrolysis and oxidation. Keep it in a cool, dry place, away from light and moisture. Store at 2–8°C (refrigerator) for optimal stability. Avoid sources of ignition, acids, and oxidizing agents.
    Application of 1-Methyl-4-Pyrazole Boronic Acid Pinacol Ester

    Applications of 1-Methyl-4-Pyrazole Boronic Acid Pinacol Ester in Industrial Manufacturing

    As a direct manufacturer of 1-Methyl-4-Pyrazole Boronic Acid Pinacol Ester, we focus on partnering with downstream enterprises in high-precision chemical synthesis and advanced material sectors. Below we outline verified, real-world industrial application scenarios for this boronic ester, providing critical formulation, regulatory, and process data for each field.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Leading pharmaceutical companies increasingly adopt this boronic ester in Suzuki-Miyaura cross-coupling for the synthesis of novel heterocyclic drug intermediates, especially in the development of kinase inhibitors and CNS agents. It serves as a coupling partner in late-stage functionalization under GMP-controlled conditions, enabling access to highly substituted drug precursors with minimized side reactions. Batch and flow chemistry operators integrate it for improved scalability and reproducibility across multi-step small molecule API processes.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • USP, Ph. Eur. monographs where applicable
    • FDA 21 CFR Part 210/211 (for facilities under FDA oversight)
    • EMA guidelines for impurity and residual control

    Typical usage ratio

    • 0.8–1.2 equivalents relative to the aryl halide; fine-tuned based on substrate reactivity and process optimization

    Downstream process integration

    • Used during the palladium-catalyzed cross-coupling step; added after initial solvent charging and base activation, followed by precision-controlled heating and staged purification

    Final product types

    • Novel heteroaryl intermediates for small-molecule APIs
    • Preclinical kinase inhibitor scaffolds
    • Pyrazole-based antihypertensives in development
    • CNS active pharmaceutical substance candidates

    2. Agrochemical Active Ingredient Development

    Crop science research divisions utilize this boronic ester for constructing pyrazole-containing structures in the synthesis of fungicides and insecticides via Suzuki coupling methodologies. The compound enables specific substitution patterns desirable for activity optimization and resistance management, enhancing molecular diversity in new agrochemical registration dossiers.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical materials
    • REACH regulation (EC) No 1907/2006 for chemical safety
    • ISO 17025 (for analytical testing laboratories)
    • OECD Principles of Good Laboratory Practice (GLP) for development batches

    Typical usage ratio

    • 1.0 equivalent relative to the halide partner; adjustment between 0.95–1.15 equivalents according to targeted crop formulation complexity

    Downstream process integration

    • Introduced in the coupling stage of multi-step active ingredient synthesis, followed by extraction, crystallization, and technical material formulation for regulatory testing

    Final product types

    • Pyrazole-derived fungicide actives
    • Novel insecticidal intermediates
    • Technical-grade pesticides for advanced field trials
    • Herbicide lead structures with heteroaryl motifs

    3. OLED and Functional Electronic Material Synthesis

    Manufacturers of next-generation organic light-emitting diodes and related display components select this boronic ester for constructing electron-transporting and hole-blocking pyrazole units. Its favorable stability under cross-coupling conditions supports scalable fabrication of high-purity intermediates for blue and green emitters, and its compatibility with anhydrous, oxygen-free conditions results in high yields necessary for optoelectronic material integrity.

    Industry compliance standards

    • ISO 9001:2015 for quality assurance in chemical manufacturing
    • IEC 61249-2-21 for halogen-free electronic materials
    • RoHS Directive (2011/65/EU) restricting hazardous substances
    • IPC-4101 (specification for base materials used in printed boards)

    Typical usage ratio

    • 0.95–1.05 equivalents in relation to the aryl or heteroaryl halide, optimized to minimize waste and maximize selectivity in vacuum and inert-atmosphere process setups

    Downstream process integration

    • Combined in the coupling stage for custom organic semiconductors, immediately followed by chromatographic purification and sublimation prior to vacuum deposition on substrates

    Final product types

    • Pyrazole-based electron transport materials
    • Blue and green OLED emitter precursors
    • Functionalized organic semiconductors for flexible displays
    • Sensors and lightweight, high-efficiency organic circuits

    4. Research Chemical Supply for Structure-Activity Relationship (SAR) Libraries

    Contract research organizations and medicinal chemistry labs source this high-purity boronic ester to rapidly expand SAR libraries by assembling diverse pyrazole analogues via palladium- or nickel-catalyzed cross-couplings. Its high reactivity and predictable performance under various base and ligand systems facilitate hit-to-lead and lead optimization projects, where unique substitution motifs provide critical differentiation for patent filings and biological profiling.

    Industry compliance standards

    • ISO 9001 and ISO 17034 for reference material production
    • OECD GLP for compound library generation supporting regulatory studies
    • REACH registration (if supplied into the EU) for laboratory chemical precursors
    • NIH and global funding agency guidelines for chemical traceability

    Typical usage ratio

    • 0.8–1.1 equivalents, adjusted according to the coupling partner’s electronic and steric requirements, with excess minimized to promote efficient parallel synthesis and downstream purification

    Downstream process integration

    • Reacted as one of 100–200 building blocks in automated or manual parallel synthesis modules for high-throughput preparation; post-reaction workup typically uses solid-phase extraction and LC-MS guided pooling

    Final product types

    • Micro-scale heterocyclic compound libraries
    • Pyrazole probe molecules for biological screening
    • Structural motifs supporting patent claim breadth
    • Intermediates supplied for in vitro and in vivo pharmacology

    5. Custom Heterocyclic Ligand Synthesis for Catalysis and Material Science

    Advanced laboratories in organometallic chemistry and material science apply this boronic ester to introduce 1-methyl-4-pyrazole moieties during ligand and polymer backbone production. The ability to form stable C–C bonds via cross-coupling processes expands access to structurally defined ligands critical in homogeneous catalysis, coordination chemistry, and designer materials for gas storage or separation.

    Industry compliance standards

    • ISO 9001 quality management for speciality chemical production
    • ACS reagent chemical purity specifications
    • REACH compliance and safe handling for laboratory use
    • OECD guidelines for custom chemical synthesis (applicable to academic-industry collaborations)

    Typical usage ratio

    • 1.0 equivalent to the brominated or iodinated co-monomer or ligand precursor; slight excess (1.05 equiv) may be used to ensure completion in sensitive catalyst or polymer syntheses

    Downstream process integration

    • Added at the coupling or polymerization stage, typically under argon with specialized bases and transition metal catalysts, followed by extraction and multi-stage purification to achieve ligand or polymer grade specifications

    Final product types

    • Pyrazole-containing N,N- and N,P-type ligand scaffolds
    • Heteroaryl-functionalized polymers and membranes
    • Complexation agents for transition metals in catalysis
    • Porous organic frameworks for material science applications
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    Certification & Compliance
    More Introduction

    1-Methyl-4-Pyrazole Boronic Acid Pinacol Ester: Practical Thoughts from Our Production Line

    Focusing on Real Output: Why 1-Methyl-4-Pyrazole Boronic Acid Pinacol Ester Matters

    Our daily work on the manufacturing floor puts us in direct contact with raw materials, round-the-clock synthesis, and the end-users who stake their research or manufacturing output on reliable specialty chemicals. Among the many fine chemicals we batch, 1-Methyl-4-Pyrazole Boronic Acid Pinacol Ester—model 193551-21-2 in many registries—stands out by consistently proving its worth across different synthesis projects.

    Our clients often face bottlenecks finding consistent, well-behaved boronic esters for Suzuki-Miyaura coupling and related cross-coupling chemistry. As suppliers who rely on our own reactors, solvents, and QA methods, we appreciate how much hassle can be avoided when a compound meets both reproducibility and purity needs. Plenty of researchers and chemists working far from downtown offices depend on materials shipped out of our warehouse. When they request 1-Methyl-4-Pyrazole Boronic Acid Pinacol Ester, the expectation is always high—especially on its ease of handling and its record of clean coupling transformations.

    Manufacturing Insights: Handling and Specifications

    We synthesize this ester in batch reactors using a process designed to minimize water ingress, as boronic compounds can be sensitive and degrade if exposed to the wrong environments before bottling. Most batches feature a specification with purity 98% or above by HPLC; honestly, we wouldn't send out a lot that tests below this unless a specific use case calls for it and the requester accepts that risk. Each batch lands as an off-white to pale yellow solid, sometimes with minor clumping if it's been sitting in the package for too long—readily rectified by gentle shaking or sifting. For researchers scaling up protocols or pushing multi-step processes, consistent melting point and moisture content stay crucial, so we check those in every lot.

    The pinacol ester form brings a good balance: it's stable, easy to store, and soluble in most of the solvents commonly used for catalytic couplings. We manufacture it in containers ranging from a few hundred grams up to multi-kilogram orders, and the packaging tries to keep the air out. As the hands actually filling those bottles, we see how little things—sealing liners, fast capping, the right moisture indicators—make all the difference for safe storage and transport. We learned by watching how condensation on a cold day, or box-packing in humid seasons, could affect appearance and purity if not managed at each step.

    Application and Performance in Synthetic Chemistry

    Chemists who rely on 1-Methyl-4-Pyrazole Boronic Acid Pinacol Ester generally focus on introducing the pyrazole ring onto more complex molecules, often for medicinal, agrochemical, or advanced material applications. What makes this ester appealing lies in the methyl-pyrazole structure: it couples reliably to aromatic and heteroaromatic halides. We've seen labs use it for building blocks on kinase inhibitor scaffolds, flavor intermediates, and, in some cases, introducing pyrazole motifs into OLED precursors. The pinacol ester survives storage without the decomposition seen in some free boronic acids, especially when exposed to a bit too much humidity or left open on a busy bench.

    From our in-house testing, this boronic ester dissolves quickly in dioxane, tetrahydrofuran, ethyl acetate, and can tolerate mild basic or slightly acidic conditions used during many cross-coupling runs. Its behavior in Suzuki couplings, tested over several hundred real reactions in our pilot facility, shows low side-product formation and good conversion even at mild temperatures. Researchers told us powders that clump or show visible discoloration tend to perform worse—something we've cut back on by changing our post-drying steps and by switching liners a few years back. Minimizing polymeric byproducts has become an obsession for us. That's how we keep the material to a high standard: no customer wants a slow reaction or clogged filters because of variable quality.

    What Sets This Ester Apart from the Crowd

    Working side by side with many chemists in the field, we've noticed that not all boronic esters behave the same after weeks or months on a shelf. Free 1-methyl-4-pyrazole boronic acid often suffers from self-condensation or estolide formation, especially after a few open-and-close cycles. The pinacol ester, on the other hand, keeps showing better stability and less degradation, especially under normal lab conditions. This doesn't just matter for material cost—no one enjoys repeating purifications due to byproducts.

    The ester form travels further without degrading compared to the acid—an important difference when shipping batches to different continents or storing them through the slow months. We regularly run shelf-life tests, keeping the product at various temperatures and humidity levels. Across these real-world stressors, the esterized form resists breakdown longer. Whether the shipment comes from our main reactor room or a satellite facility, the compound holds up.

    Other manufacturers may sometimes slip in analogues or alternate ester groups, which we learned over time just don't perform as well in repeated cross-coupling settings. Pinacol's bulk, paired with the methyl and pyrazole motif, make for a sweet spot of stability and reactivity. These aren't armchair theories—we've run side-by-side tests with neopentyl glycol, ethylene glycol esters, and free acids over hundreds of couplings. Pinacol remains the safest bet for consistent performance.

    Scaling, Batch History, and Lessons from the Floor

    Producing reliable 1-Methyl-4-Pyrazole Boronic Acid Pinacol Ester isn't always repeatable with just the click of a button. Batch size affects crystal shape and ease of drying—the scale impacts everything from stir time to filtration steps. Large runs can sometimes invite slight color changes or sticky residues not present in small flasks. Over time, we built up a library of process history, logging which variables—temperature, pressure, solvent choice—impact physical traits.

    A few years back, we dealt with a run that formed fine, dusty particles instead of our usual coarse powder. That unusual lot clumped badly and required more manual breaking apart before packaging. Product performance in customer hands flagged the problem: filters clogged, and measured LC-MS purity varied slightly from bottle to bottle. Learning from that experience, we adjusted our crystallization procedure and adopted slower cooling protocols, resulting in a powder that pours out of bottles cleanly and resists caking even after many days on a shipment pallet.

    Quality management requires more than paper trails or external audits. Each team member weighs in when we troubleshoot batches. The smallest hands-on steps—from filter pore size to the choice of PTFE liner versus foamed PE—directly affect the final user experience. We always test a handful of vials from each production run in our own in-house reactions, mimicking the real-world challenges researchers face. We learned early that printed specs can't catch subtle differences between lots: only direct application in a coupling reaction tells the full story.

    Supporting the Flow of Modern Synthesis

    Researchers often ask about solvent tolerance, and we've learned the compound fits into most modern cross-coupling methods. Toluene, dioxane, and DMF work well. We've run dozens of internal screens with different palladium sources and ligands. Under each condition, conversion remains high, and side reactions, such as protodeboronation, stay minimal. By contrast, free acids or non-pinacol esters showed far more variable results in internal splits, especially after slight air exposure.

    Direct feedback from synthetic chemists shapes our decisions. We heard from teams in pharma R&D that they sometimes tried cheaper or off-brand alternatives to save on budget but faced headaches from partially decomposed material, clumped powders, or sluggish coupling rates. That sidetracks projects and stretches timelines. Since adopting a stricter final inspection routine—sampling each pallet at multiple depths and sending them through actual coupling reactions—we trimmed user complaints and shipping returns dramatically.

    Product purity also translates to fewer clean-up worries downstream. Most labs appreciate knowing their final coupling mixture will contain minimal residual byproducts from the starting boronic ester. That means less time on the rotary evaporator and fewer silica gel columns to process. The knock-on effect is less solvent waste, cost savings, and a lighter environmental footprint for everyone in the pipeline.

    Spotlighting Potential Challenges and Our Own Solutions

    No process is ever perfect. We've faced issues such as minor hydrolysis during hot, humid months, or occasional foaming during solvent removal. Early on, we ran a few batches without enough air displacement during bottling; some suffered airborne moisture picking up during shipping, showing slightly higher impurity peaks on HPLC. That taught us the value of packing in a nitrogen-purged glovebox for larger production lots to keep the product fresh.

    Clumping used to pose a recurring problem, especially over extended shipping routes subject to vibration and temperature swings. We teamed up with packing suppliers, researched anti-static and moisture-resistant liner materials, and field-tested several combinations. Eventually, we settled on tight-seal wide-mouth bottles with both inner and outer seals, cutting down on both accidental ingress and static buildup.

    Cross-contamination risk surfaces when plants handle multiple boronic esters or free acids on the same shift. Our routine requires running equipment washes validated by actual analytics rather than visual checks. We run GC-MS and HPLC on rinse water, tightening acceptance to below detection for cross-contamination. This added work isn't popular with everyone, but every time we've traced a user complaint or a returned batch, the underlying issue often involved microgram traces from a prior run. Data-guided discipline, not guesswork, keeps customer trust strong.

    Transparency and Consistency: What We’ve Learned from Decades on the Line

    Over the years, repeat customers taught us to take nothing for granted in QC. Batch-to-batch variation—once shrugged off as “normal”—now triggers a trace-back and cross-verification. Every time a researcher finds an outlier result, our team dives into the paperwork, aperture logs, and, if needed, brings samples straight into the test lab for parallel chemistry runs. Such diligence isn't glamorous but proves essential. Without it, small shifts in procedure quietly magnify in customer hands, especially in multistep processes.

    Our experience shows that working close to the process, from reactor charge to the final boxed vials, builds the knowledge needed for a reliable supply chain. Customers value not just the number on a specification sheet but the guarantee that, whenever possible, one bottle will behave as the next—across seasons, shipping distances, and storage times.

    Outlook: Supporting R&D and Moving Chemical Synthesis Forward

    The team who makes 1-Methyl-4-Pyrazole Boronic Acid Pinacol Ester doesn't sit in a silo. We read scientific literature, track regulatory changes, and pay attention to where the needs of pharma, agri-science, and advanced materials are heading. Modern synthetic targets grow ever more complex, and time on the bench is precious. Reliable intermediates keep chemists focused on real discovery, not cleaning up after problematic inputs.

    We work with a broad set of labs and R&D teams. Many push for greater control of trace impurities, lower metal content, and tighter physical consistency. We've learned to document every tweak and publish transparently on what works—or doesn't—in our own plant runs. Suggestions from customer labs prompted us to improve drying cycles and explore more recyclable packaging, reducing waste once chemicals reach their destination.

    We continue to look for ways to upgrade our process, minimize energy and solvent use, and lower risks downstream. For every innovation, we cycle it through real-world testing, side by side with existing approaches. Detailed in-process controls, stronger worker training, and ongoing dialog with users shape every improvement—ensuring that each bottle supports the discoveries and buildouts happening across chemical industries.

    Choosing the Right Building Block for Progress

    Every day on the production line, our team sees firsthand the impact that a single chemical intermediate can make on the pace and outcome of research. The trust built between a manufacturer and a front-line chemist runs deeper than paperwork or product codes; it's forged in shared experience, ongoing dialogue, and the discipline to learn from every misstep. 1-Methyl-4-Pyrazole Boronic Acid Pinacol Ester has earned its place as a go-to compound by proving itself, run after run, in real working labs.

    We count the eyes and hands of every operator, technician, and analyst as part of a continuous feedback loop. Chemistry isn’t just about raw numbers or regulatory compliance—it’s about the interplay of process, adaptation, and a genuine commitment to supporting those who push science forward. We take that responsibility seriously, and it informs every bottle we send out the door.