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1-Benzyl-1H-Pyrazole-4-Boronic Acid Pinacol Ester

    • Product Name 1-Benzyl-1H-Pyrazole-4-Boronic Acid Pinacol Ester
    • Alias Pyrazole 4
    • 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

    792140

    Chemical Name 1-Benzyl-1H-Pyrazole-4-Boronic Acid Pinacol Ester
    Molecular Formula C16H21BN2O2
    Molecular Weight 280.17 g/mol
    Cas Number 1375064-77-7
    Appearance White to off-white solid
    Purity Typically ≥95%
    Smiles B1(c2cnn(c2)Cc3ccccc3)OC(C)(C)C1
    Solubility Soluble in organic solvents such as DMSO and dichloromethane
    Storage Conditions Store at 2-8°C, protected from moisture and light

    As an accredited 1-Benzyl-1H-Pyrazole-4-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 bottle labeled "1-Benzyl-1H-Pyrazole-4-Boronic Acid Pinacol Ester, 1g." Tamper-proof cap, chemical hazard symbols, and batch information included.
    Shipping 1-Benzyl-1H-Pyrazole-4-Boronic Acid Pinacol Ester is shipped in a tightly sealed container, protected from light and moisture. The chemical is packed according to standard regulations for hazardous or sensitive materials, ensuring safe transport. Temperature control may be applied if required, typically shipped at ambient or refrigerated conditions depending on stability data.
    Storage 1-Benzyl-1H-pyrazole-4-boronic acid pinacol ester should be stored in a cool, dry, well-ventilated area, away from heat, moisture, and direct sunlight. Keep the container tightly closed under inert atmosphere (e.g., nitrogen or argon) to prevent hydrolysis or degradation. Store separately from strong oxidizers and acids. Handle using appropriate personal protective equipment in accordance with chemical safety protocols.
    Application of 1-Benzyl-1H-Pyrazole-4-Boronic Acid Pinacol Ester

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

    As a direct manufacturer, we supply 1-Benzyl-1H-Pyrazole-4-Boronic Acid Pinacol Ester to downstream industries that demand precise performance and high reliability. Our material enters advanced synthesis workflows for active pharmaceutical ingredients, specialty agrochemicals, research dye intermediates, and advanced materials, where strict standards, consistent ratios, and effective process integration are required for end-product development.

    1. Pharmaceutical Intermediate Synthesis

    Our boronic ester is widely used in the creation of highly functionalized heterocyclic building blocks. Major pharmaceutical plants employ it during Suzuki-Miyaura cross-coupling reactions to assemble pyrazole-containing drug motifs. Production managers monitor tight controls on impurity profiles as this intermediate impacts final API purity benchmarks. In large-scale operations, it serves as a pivotal reagent during late-stage functionalization under cGMP environments.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP <787>: Analytical procedures for boronic esters
    • EU GMP Guidelines Part II

    Typical usage ratio

    • 0.9–1.2 molar equivalents in Suzuki reactions, adjusted per target molecule yield and functional group tolerance

    Downstream process integration

    • Charged into reaction vessel post-halide activation
    • Reacted with aryl or heteroaryl halides under catalysis
    • Inline purification by crystallization or preparative HPLC

    Final product types

    • Pyrazole-based anti-inflammatory agent intermediates
    • Kinase inhibitor precursors
    • Antiviral pharmaceutical actives
    • Central nervous system drug candidates

    2. Specialty Agrochemical Synthesis

    Agrochemical formulators introduce this boronic ester during crop protection agent production, especially for pyrazole-derived herbicides and fungicides. Process engineers select it for controlled coupling to maintain substituent integrity on highly sensitive substrates. It upholds downstream technical grade standards and supports multi-ton scale production, especially when feeding continuous synthesis modules.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001 Quality Management System
    • REACH Registration for industrial use

    Typical usage ratio

    • 0.95–1.1 equivalency relative to halide reactant

    Downstream process integration

    • Fed into batch or flow reactors during coupling stage
    • In-line filtration before further functionalization
    • Purified via solvent extraction or chromatography

    Final product types

    • Pyrazole-based herbicide intermediates
    • Selective fungicide raw stock
    • Intermediate for insecticidal agents
    • Custom molecules for field trial evaluation

    3. Organic Electronics and Specialty Polymers

    R&D groups select this compound when manufacturing electron-rich polymer backbones used in organic LEDs and field-effect transistors. Operators rely on its consistent coupling efficiency for incorporation into conductive and functionalized copolymer chains. Purity and controlled reactivity preserve optoelectronic properties across pilot and production lots, particularly where device-grade quality is critical for commercial applications.

    Industry compliance standards

    • RoHS Directive (for device raw materials)
    • ISO 14001 Environmental Management System
    • IEC 62474 Material Declaration Standard

    Typical usage ratio

    • 0.8–1.15 equivalents versus dibromo- or diiodo-monomer units, based on targeted polymer chain length and branching

    Downstream process integration

    • Dosed with transition-metal catalyst in monomer feed streams
    • Directly polymerized using C–C coupling methodology
    • Isolated by precipitation and cleaned for end-use device fabrication

    Final product types

    • OLED light-emitting substrates
    • Organic transistor materials
    • Specialty sensor films
    • Functional coatings for flexible electronics

    4. Dyes, Pigments, and Analytical Reagent Manufacturing

    Producers of specialty dyes and fluorescent labels use our boronic ester for rigid heterocycle introduction during chromophore construction. The material supports high-yield cross-couplings in dye and pigment synthesis, enabling reliable attachment of pyrazole groups in analytical reagents used for research and testing. Its defined reactivity simplifies purification steps and produces materials with stable spectral properties.

    Industry compliance standards

    • EN 71-3: Chemical Safety for Textile Dyes
    • ISO 17025 Analytical Laboratory Certification
    • REACH Compliance for specialty colorants

    Typical usage ratio

    • 0.9–1.3 mole equivalents relative to activating group, adjusted for fluorescence intensity or pigment density

    Downstream process integration

    • Introduced during main coupling or branching stage
    • Purified via silica gel column chromatography
    • Dried and milled for blend uniformity

    Final product types

    • Fluorescent dye standards for molecular assays
    • Laboratory analytical reference dyes
    • Custom pigments for specialty inks
    • Colorimetric sensor reagents
    Free Quote

    Competitive 1-Benzyl-1H-Pyrazole-4-Boronic Acid Pinacol Ester prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

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    Certification & Compliance
    More Introduction

    1-Benzyl-1H-Pyrazole-4-Boronic Acid Pinacol Ester: Reliable Building Block for Research and Manufacturing

    Practical Experience Brings Real Progress

    Every day on the production floor, we run into challenges tied to precision, consistency, and efficiency. For research teams or downstream synthesis lines, a single impurity or batch-to-batch deviation can kick off days of troubleshooting. Our operations started out supplying intermediates to local fine chemistry outfits who struggled with raw materials that couldn’t hold up to repeated transformations or tight analytic specs. That learning curve set our focus on providing robust products ready for challenging cross-coupling reactions and scale-up contexts.

    1-Benzyl-1H-Pyrazole-4-Boronic Acid Pinacol Ester sits right at that intersection of reliability and manufacturability. We’ve seen it drive key reactions for pharmaceutical research, especially in medicinal chemistry groups developing new heterocyclic scaffolds. Medicinal chemists often need to move quickly from idea to candidate, and failed coupling cycles can knock out precious work time. By controlling crystallization, handling, and final purification in-house, our teams avoid the typical bottlenecks faced when using less pure or less ‘clean’ boronic esters.

    Model Details: Consistency Is Earned, Not Assumed

    Over the years, requests for 1-Benzyl-1H-Pyrazole-4-Boronic Acid Pinacol Ester have revealed a need for models that can withstand demanding Suzuki-Miyaura or Chan–Lam coupling protocols. Not all boronic esters will deliver comparable yields, and minute differences in solubility or hydrolytic stability often throw off a synthetic route, especially during scale-up.

    We use rigorous lot-release testing for every batch. This isn’t just about a certificate stating a number; it’s about backing each shipment with data from HPLC, NMR, and titrations run directly in the same labs that produce the material. Trace water, for example, is always a concern—slight increases in water content can alter coupling efficiency or, worse, hydrolyze the ester, producing hard-to-separate byproducts. Because we handle all drying and storage in humidity-controlled rooms, the ester keeps its high purity and reliable reactivity for months, not weeks.

    Knowing What Sets It Apart

    Anyone familiar with boronic acid chemistry has run into two main stumbling blocks: hydrolysis and unpredictable behavior around amine and heteroaromatic systems. Many commercially available boronic acids fall apart when exposed to room air, let alone water or ethanol. Pinacol esters offer a working solution, but even these vary a lot with the substituents present. We have spent years actualizing protocols that deliver the 1-benzyl-1H-pyrazole scaffold intact after multiple recrystallization and isolation steps.

    Comparisons to other benzylic boronic esters show the difference in decomposition temperature and isolation yield, especially in real-world lab settings. Standard benzylic pyrazoles often bring along N-oxide side-products or incomplete reactions due to over-oxidation. Our in-house synthesis gives cleaner, easier-to-handle material without ghost peaks on analytical runs—this means chemists can focus on the actual coupling, not endless cleanup.

    Feedback from research partners shows the benefit: yields stay consistent across different batch sizes. In one case, a partner running a multi-gram pilot campaign for a drug candidate reported process reproducibility within three percentage points from 100 mg to 25 grams. This isn’t luck: it’s linked to how we avoid process shortcuts and control both milling and filtration on-site, with experienced chemists who troubleshoot right at the bench.

    Specifications Matter Because Scale Matters

    Documentation from years of real-use cases matters most when your workflow depends on predictable intermediates. A good example is the challenge of single-digit impurity spikes in Suzuki coupling. Many off-the-shelf boronates suffer from hidden instability. We guarantee a minimum assay of 98%, often exceeding this due to ongoing in-process monitoring. Purity reporting extends to all synthetic ‘neighbors’ such as unreacted pinacol, related benzylpyrazoles, and elemental contaminants.

    Solubility issues arise fast with poorly characterized esters. Subtle differences in physical form—like clumping during weighing or static buildup during transfer—can force operators to alter solvent ratios or even switch entire reaction protocols. We provide solid, free-flowing powder, fractionated for optimal particle size to enable swift, repeatable weighing and addition. This matters for both a single run in a discovery lab and a routine multikilogram production cycle.

    Some chemists chase after ‘universal’ boronic esters but end up finding each system asks for its own tailored starting materials. 1-Benzyl-1H-Pyrazole-4-Boronic Acid Pinacol Ester works smoothly with both electron-rich and electron-poor coupling partners. Its behavior in typical polar aprotic solvents also allows a bit more leeway with process optimization—saving costs on surfactants or additives meant only to compensate for poor substrate characteristics found in less refined lots.

    Supporting Innovation Through Real-World Use

    We have supplied this boronic ester for pharmaceutical projects going well beyond small molecule exploration—its structure enables formation of advanced heterocycle-linked fragments, biaryl backbones, and more. Synthetic teams handle dozens of coupling cycles a week. Sluggish reactions or incomplete conversion in late-stage runs create expensive bottlenecks, and low-quality esters make things even harder. For us, the commitment starts long before packing and labeling—during precursor selection all the way to post-synthetic QA.

    One area of growth we’ve witnessed involves the rapid development of PROTACs and related bifunctional molecules. These rely on robust cross-coupling reactions linking complex partner fragments. The consistent performance of our 1-Benzyl-1H-Pyrazole-4-Boronic Acid Pinacol Ester in such protocols leads to fewer failed runs, less material loss, and more straightforward reaction troubleshooting when surprises surface.

    Not every synthetic team wants to deal with batch-variability headaches. So we have built an internal knowledge base, recording each anomalous result and updating production specs to catch root causes. This isn’t just paperwork—it’s regular feedback loops with academic collaborators, process chemists, and advanced analytics specialists.

    Key Points Learned from Field Experience

    Paying attention to storage and shelf-life separates theory from workable practice. Left exposed to ambient air, sensitive boronic esters can degrade quickly, creating confusion in analytic testing and hungry for purification resources. Packaging the product under inert atmosphere, and loading it in custom moisture-barrier containers, extends its usable life past the average. Real users rarely have time for repurification; we keep this material ready-to-use straight from the jar.

    Having an open door for technical discussions with our partners means we often troubleshoot tricky coupling or hydrolysis cases together. Some users need stringent heavy metal controls for trace catalysis. Others require compatibility with high-throughput screening setups, where any sticky, oily, or inconsistent intermediates will block liquid handlers or ruin multi-well plates. Our feedback loop lets us adapt the product line, identifying new technical needs early and scaling tweaks across the whole workflow.

    Waste streams from process chemistry often carry implications for both cost and environmental compliance. By overseeing every upstream and downstream step, we limit unexpected byproducts that might require specialized disposal. Cleaner chemistry doesn’t just mean higher yields; it minimizes headaches outside the chemistry department, too.

    Real Value in Transparent Supply Chains

    We have seen buyers burned by lots sourced from multiple, untraceable producers and then relabeled by resellers. These lots may not follow the same synthetic pathway, or skip critical purification steps, offering inconsistent reactivity and even batch-to-batch variance within a single delivery. By synthesizing, isolating, and testing all material in-house, our facility gives industry and academic researchers confidence that each bottle will perform like the last.

    Traceability is particularly vital for GMP applications or critical research where reproducibility and audit trails are essential. No data is omitted: from synthesis date to shipping temperature logs, we maintain full records that bolster compliance efforts and provide peace of mind. This approach helps during troubleshooting: if an outlier arises, our chemists can refer directly to source-path and processing batch rather than wasting hours guessing at causes outside their control.

    Some partners, especially in regulated manufacturing environments, struggled to pin down rogue side-products traced back to unknown intermediates in commercially sourced boronic esters. The result? Delays, compliance headaches, and, sometimes, scrapped batches. Our transparent supply chain sidesteps these disruptions.

    Technical Support Drawn from Hands-On Knowledge

    A product is only as good as the support team backing it. Our technical support staff come from the same labs as our production teams. Many have run the same reactions our customers do, using the same scale and time pressures, so they bring a practical viewpoint. When users face unexpected drop-offs in reaction conversion, or inconsistent analytics from coupling processes, our specialists pull directly from internal knowledgebase and years of hands-on laboratory troubleshooting.

    No company avoids every challenge, but we approach problems directly. Collaborative troubleshooting, whether by phone or remote support, helps users work through protocol tweaks, drying regimens, or alternative solvents to get the most yield out of every batch. Our field teams maintain regular contact with long-term partners, gathering insights that help update our production protocols, ensuring continual improvement.

    Commitment to Clean Sourcing and Environmental Responsibility

    The chemistry sector increasingly faces scrutiny over raw material origins and environmental impact. We made a deliberate shift to source all precursors for 1-Benzyl-1H-Pyrazole-4-Boronic Acid Pinacol Ester from suppliers with established compliance credentials. Each lot can be traced from original precursor shipments, offering comfort both to green chemistry advocates and corporate sustainability auditors.

    Process optimization doesn’t stop with purity: we recapture and recycle solvents wherever feasible. Cutting down on process waste doesn’t just lower production emissions; it feeds into real cost savings for users—and fewer environmental headaches downstream. By managing the synthetic pathway in-house, we avoid the unknowns tied to offsite contract manufacturing or quick-fix quality checks, which can disguise underlying risks. Clean production is more than a slogan. Chemists depending on final product consistency for their own environmental filings appreciate such rigor.

    Building Trust Through Proven Outcomes

    Over the last decade, our 1-Benzyl-1H-Pyrazole-4-Boronic Acid Pinacol Ester has powered hundreds of successful synthetic campaigns. Drug discovery consortia, scale-up teams, and research faculty depend on the kind of repeatable, reproducible outcomes our operational discipline delivers. Seeing our product featured in peer-reviewed literature and registration filings comes from this steadfast emphasis on scientific integrity and user-focused support.

    In every new molecule or scale-up challenge, the right quality boronic ester pays back manyfold compared to downtimes or failed experiments. We continue investing in people and facilities so that users get more than just a raw chemical; they gain a reliable part of their innovation journey.

    Looking Ahead: Responsive Supply and Co-Development

    Science changes fast. As combinatorial chemistry and advanced medicinal discovery push for greater molecular diversity, users need flexible suppliers who remember the human side of the work. Our team fields new requests for different analogs, packaging styles, or even custom scales. Because we own our process top-to-bottom, we can respond with custom solutions—real changes, not just repackaging or rebranding. For labs running exploratory research or industry looking to ramp up new projects, our quick response saves precious time.

    We take pride in partnering with scientists who value robust, predictable materials—and who seek deeper know-how to solve not only today’s problems, but tomorrow’s unknowns. As requests for tailored derivatives and process-friendly intermediates grow, our experience with products like 1-Benzyl-1H-Pyrazole-4-Boronic Acid Pinacol Ester forms the backbone of progress.

    Summary

    Years spent in real production, with hands-on chemistry and honest troubleshooting, have shaped our product philosophy. The difference between success and struggle in chemical synthesis often hangs on subtle differences in intermediate quality, documentation, and support. Our approach—drawing on real experience with this and related boronic esters—helps our users push new boundaries in research and manufacturing with confidence.