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2-Chloro-4-Methylphenylboronic Acid Pinacol Ester

    • Product Name 2-Chloro-4-Methylphenylboronic Acid Pinacol Ester
    • Alias (2-Chloro-4-methylphenyl)boronic acid pinacol ester
    • Einecs 849-562-1
    • 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

    269938

    Chemical Name 2-Chloro-4-Methylphenylboronic Acid Pinacol Ester
    Molecular Formula C13H18BClO2
    Molecular Weight 252.54 g/mol
    Cas Number 1212192-57-8
    Appearance White to off-white solid
    Melting Point 71-75 °C
    Solubility Soluble in organic solvents such as dichloromethane and ethyl acetate
    Purity Typically ≥97%
    Storage Conditions Store in a cool, dry place, protected from light and moisture

    As an accredited 2-Chloro-4-Methylphenylboronic Acid Pinacol Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 5g chemical is packaged in a sealed amber glass bottle with a tamper-evident cap, labeled for 2-Chloro-4-Methylphenylboronic Acid Pinacol Ester.
    Shipping 2-Chloro-4-Methylphenylboronic Acid Pinacol Ester is shipped in tightly sealed, chemically resistant containers to prevent moisture and contamination. Packages are clearly labeled and comply with all relevant chemical transport regulations. During transit, the product is protected from extreme temperatures, physical damage, and light, ensuring safe and stable delivery to the destination.
    Storage 2-Chloro-4-Methylphenylboronic Acid Pinacol Ester should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep it in a cool, dry, and well-ventilated area, ideally under an inert atmosphere such as nitrogen or argon. Store separately from strong oxidizing agents and acids to prevent adverse reactions. Avoid prolonged exposure to air to preserve compound stability.
    Application of 2-Chloro-4-Methylphenylboronic Acid Pinacol Ester

    Applications of 2-Chloro-4-Methylphenylboronic Acid Pinacol Ester in Industrial Manufacturing

    Our 2-Chloro-4-Methylphenylboronic Acid Pinacol Ester serves as a highly specialized coupling reagent for advanced organic synthesis, delivering precision and efficiency to industrial operations across the pharmaceuticals, agrochemicals, specialty polymers, and OLED materials segments. Each application leverages the molecular structure and reactivity of this compound within clearly defined manufacturing processes, ensuring compliance with industry-specific quality benchmarks.

    1. Pharmaceutical Intermediate Synthesis for Targeted API Development

    Pharmaceutical manufacturers utilize our boronic ester as a key building block in Suzuki-Miyaura cross-coupling reactions for the selective synthesis of advanced intermediates, particularly for APIs featuring halogenated aromatic motifs. Its performance holds strong in elaborating complex molecular frameworks, directly influencing drug purity and overall batch yield.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • EU EudraLex Volume 4
    • Japanese Pharmacopoeia (JP), if locally marketed

    Typical usage ratio

    • 0.9 – 1.1 molar equivalents relative to the halogenated aryl halide, adjusted based on ligand and base system efficiency

    Downstream process integration

    • Charged post-halogenation stage into automated or batchwise Suzuki coupling vessels, followed by continuous extraction and purification

    Final product types

    • Halogenated benzene API precursors
    • Small-molecule kinase inhibitor intermediates
    • Pharmaceutical research reference compounds
    • Advanced intermediates for CNS and oncology drug development

    2. Crop Protection Active Ingredient Manufacturing

    In agrochemical synthesis plants, formulators choose our material for its selective reactivity in cross-coupling reactions that construct substituted biaryl scaffolds essential for next-generation herbicides and fungicides. Its stability minimizes byproduct formation, helping maintain final actives within strict identity and purity limits required for regulatory submission.

    Industry compliance standards

    • FAO/WHO Specification for Pesticides
    • ISO 9001:2015 Quality Management System
    • REACH (EC 1907/2006) for substance registration
    • China GB/T 1605 for pesticide raw materials

    Typical usage ratio

    • 1.0 – 1.2 stoichiometric ratio per aryl halide reactant, adjusted for catalyst loading and substrate reactivity

    Downstream process integration

    • Introduced in the core-coupling step after base aromatic skeleton derivatization, with subsequent catalytic filtration and product isolation

    Final product types

    • Substituted biaryl herbicide actives
    • Fungicidal intermediate building blocks
    • Pre-emergent pesticide formulation inputs
    • Custom agrochemical discovery samples

    3. OLED and Organic Electronic Materials Production

    Manufacturers in the optoelectronic sector integrate this pinacol ester in the preparation of aryl-substituted compounds used for light-emitting and charge-transport layers. Reliable batch purity and minimal metal contaminants are essential for downstream optoelectronic device fabrication, where any residue affects product lifespan and color intensity.

    Industry compliance standards

    • IEC 62321-7-1:2015 for detection of halogens and boron in electronic materials
    • RoHS Directive (2011/65/EU) for hazardous substances
    • ISO 9001:2015 for QMS in electronics industry
    • CUSTOMER-SPECIFIC MATERIAL QA protocols (major display panel OEMs)

    Typical usage ratio

    • 0.95 – 1.05 equivalents per di- or tri-halogenated aromatic substrate, calculated by target polymer growth or oligomer design

    Downstream process integration

    • Charged into anhydrous Suzuki coupling reactors under inert atmosphere, with real-time HPLC monitoring during monomer and polymer chain extension stages

    Final product types

    • OLED emitter layer monomers
    • Charge-transport intermediate materials
    • Light-emitting dendritic compounds
    • Specialty polymers for advanced display backplanes

    4. Specialty Polymer Additive Synthesis

    Specialty polymer producers use our compound to introduce chloro-methyl-phenyl functionalities into polymer side-chains, tailoring thermal and mechanical properties in engineering resins. Its precision chemistry provides control during polymer modification stages, resulting in reproducible grade performance for client-specific specifications.

    Industry compliance standards

    • ISO 9001:2015 for quality systems in polymer compounding
    • ASTM D256 and D638 for downstream polymer mechanical and thermal testing
    • EU REACH limiting hazardous residuals
    • Customer technical approval for additive safety and function

    Typical usage ratio

    • 0.5 – 3.0% by weight relative to total monomer charge, adjusted for desired functionalization density and target material property

    Downstream process integration

    • Added post-polymerization to side-chain modification reactors, with isolation by precipitation or solvent extraction; final adjustment based on FTIR/NMR analysis

    Final product types

    • Modified polyarylenes and copolymers
    • Thermally stabilized engineering plastics
    • Specialty resin modifiers for automotive or aerospace
    • Functional polymer masterbatches
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    Certification & Compliance
    More Introduction

    2-Chloro-4-Methylphenylboronic Acid Pinacol Ester: A Reliable Intermediate for Fine Chemical Synthesis

    Crafting Reliable Building Blocks at the Source

    Years spent working close to the reactors and purification lines has taught me that quality in chemical synthesis depends on the materials we put in. A well-made intermediate saves time, money, and headaches down the chain. 2-Chloro-4-Methylphenylboronic Acid Pinacol Ester represents the kind of specialized reagent that supports diverse routes in pharmaceuticals, agrochemicals, and material science. At our facility, careful attention to every batch puts real consistency into the hands of chemists working on demanding research and scale-up projects.

    Understanding the Chemical

    This boronic ester features a phenyl ring substituted with a chlorine and a methyl group, with the boronic acid end masked by pinacol. Each of those decisions in the chemical’s structure arises from years of direct feedback from organic chemists tackling Suzuki-Miyaura coupling and similar transformations. The pinacol ester form resists hydrolysis better than the free boronic acid, lasting through rigorous handling and storage. Controlling impurity levels, particle size, and water content is not just a box to tick—it means smoother reactions and more predictable yields at the user’s bench.

    Model and Purity: What Matters Most

    Our model for this product is built around multikilo synthesis, refined crystallization, and filtration so that lots remain uniform month after month. We typically target purity by HPLC of greater than 98%, and by experience, the extra effort in purification pays off in lower side-product formation at the next synthetic step. Beyond core purity, residual solvents, trace metals, and related compounds have to stay under tight internal limits because even ppm levels can poison a palladium catalyst or shift selectivity. Every shipment includes a full analysis for peace of mind.

    Physical Profile and Packing: Details that Matter

    Many users remember opening jars to discover lumpy, aggregate-laden powders that refused to weigh or dissolve evenly. We work constantly with packaging—glass or lined containers, inert atmosphere, and careful sealing—to keep the pinacol ester clean and free-flowing. Temperature and humidity controls throughout the warehouse prevent clumping, and desiccation steps at the end avoid the slow creep of hydrolysis some boronates can suffer. It’s routine for us, but more than once a customer comment has highlighted how much smoother a synthesis runs when starting materials pour cleanly from the jar.

    Why This Pinacol Ester Over the Acid?

    Chemists choose between free boronic acids and their pinacol esters based on both chemical and practical considerations. Esters usually provide greater thermal and hydrolytic stability, important for anyone who might store the reagent for months, ship it by air, or run reactions above ambient temperatures. Hydrolysis to the boronic acid under aqueous workup conditions is direct and clean, usually right at the time of coupling. Our experience aligns with published literature—pinacol esters tend to give higher coupling yields and reduce side reactions like protodeboronation compared to free acids, especially with electron-deficient systems or halogenated aromatics like this chloro-substituted ring.

    Handling Experience: Avoiding Common Pitfalls

    We have seen what happens when chemical lots carry hidden moisture, traces of solvents, or oxidative byproducts. Reactivity shifts, purification becomes a battle, and analytical data begins to look unreliable. Over the years, we tightened controls on how our product leaves the dryer, how it is transferred, and even how samples move between quality control and packing so that no contamination creeps in. Customers experimenting with gram-scale coupling see reproducible TLC plates and reliable isolation of their products. These are the small wins only possible by minding every link in the production chain.

    Applications: Cutting-Edge and Everyday

    The key value of 2-Chloro-4-Methylphenylboronic Acid Pinacol Ester lies in Suzuki cross-coupling to access complex biaryl structures. Many pharmaceutical research programs rely on these transformations for building novel kinase inhibitors, serotonin receptor ligands, and agrochemical scaffolds. Materials science labs draw on the chloro-and-methyl-substituted core for rigid linkers in OLED emitters, sensors, and advanced polymers. Our reliability as a manufacturer turns planning for scale-up into something users can approach with confidence instead of uncertainty over future sourcing.

    Distinguishing Features Compared to Other Boronates

    Other manufacturers may emphasize throughput or price, but shortcuts appear in crystalline quality, solvent residues, or batch reproducibility. Production at our site avoids batch-to-batch drift by relying on high-purity starting materials, thoroughly washing and drying all reactor components, and rigorously training operators on every unit operation. In the world of boronates, not all esters handle alkali or tolerate chromatographic purification equally, and differences show up most clearly after extended storage or in the hands of a careful analytical chemist. By running accelerated aging trials and repeated process controls, we have learned how to catch and address subtle degradation well before a product ever reaches end users.

    Environmental and Safety Principles in Action

    Attention to detail extends beyond the walls of the plant. Modern boronic esters demand handling protocols that balance chemical efficiency and responsible stewardship. Our team minimizes waste streams by reusing pinacol and optimizing aqueous workup to avoid boron-rich effluent. Operators wear sealed gloves and goggles during transfers, and air-handling units prevent vapor release from the reactor hall. Staff training covers the specific risks of boron chemistry, from eye irritancy to avoiding heat sources near stored material. This culture means the product that leaves our plant meets both quality and safety requirements while keeping worker well-being at the top of the list.

    Enabling Downstream Success

    Every year, researchers in pharma discovery or process scale-up push their reactions harder—less solvent, larger scale, higher throughput. Materials from our line maintain tight limits on water and trace metals, so each batch fits directly into automated synthesis platforms and high-throughput screening workflows. Failures at this stage are costly and trace back to poor starting materials as often as to procedural missteps. Our repeat customers know their most prized reactions rely on trust in the upstream supply chain, and this trust comes from a record of real-world performance.

    Supporting Documentation and Traceability

    Reliable supply depends not only on the material but on the documentation that rides with it. We run full HPLC, NMR, and GC-MS profiles on every lot and keep archived spectra for years to resolve any future questions. Certificate of Analysis sheets provide detailed breakdowns, not generic or templated figures. Questions raised by clients about a minor impurity, a change in melting point, or chromatographic behavior get answered by a team that remembers exactly how the product moved from raw material to purified crystalline solid.

    Customer-Driven Improvements

    Feedback from academic and industrial teams has reshaped our workflow more than once. We started offering smaller pack sizes after one research group kept losing product to moisture with larger jars open on the bench. Analytical methods expanded as synthetic chemists requested details on stereochemical purity and byproduct profiles, even when those compounds remain undetectable by routine QC. By working two directions—delivering what the market expects, and anticipating needs based on honest communication—each iteration has improved our final product.

    Scaling and Flexibility

    Scaling up the synthesis of specialty boronates reveals where production shortcuts backfire. Heat transfer and crystalline growth change character on hundred-gram to kilo scales. Our team invested in reactors with better mixing and temperature control, so even the largest lots show consistent morphology and not the broad size distribution that frustrates filtration. Additional isolation and washing steps prevent mother liquor inclusion, with batch-to-batch reproducibility proven in pilot studies. By holding firm to these principles, we have enabled our partners to move from milligram discovery right through to kilogram campaigns without costly reoptimization.

    Supply Chain Stability

    The market for key boronate intermediates has seen disruptions, especially for those with halogen or methyl substituents where upstream feedstocks can swing in purity or availability. As direct manufacturers, we forge long-term agreements with suppliers of both pinacol and aryl halides. Onsite storage and validated backup supply chains guarantee that even during market shocks, we can keep standard delivery schedules. Our inventory controls track in real time, preventing sudden shortages or quality lapses when urgent orders appear.

    Industry Standards and Regulatory Considerations

    Customers in regulated industries expect documentation and lot control suitable for both GMP and non-GMP environments. We have built out our analytical labs to offer not only the basic purity screens, but impurity profiling and toxicology support as regulations on pinacol boronates grow stricter. Data on trace elements or solvent residues are now tracked with every lot, easing the registration process for pharma or agrochemical applications. We respond to external audits, delivering not just compliance reports, but practical advice drawn from years working within evolving industry rules.

    Challenges and Ongoing Solutions

    Handling sensitive boronates means tackling oxidation—both from environmental oxygen and during workup. Years ago, complaints about occasional color changes or off-odors prompted process improvements: inert transfers, anti-oxidant treatments, and advanced testing for minor byproducts. Monitoring oxygen exposure right down to final packing has dropped incidence of discoloration and allowed longer shelf life. Oxidative stability measures taken today stem directly from lessons learned on earlier campaigns. When issues arise, rapid response and direct investigation ensure that root causes get fixed, not covered up.

    Comparisons with Other Pinacol Boronic Esters

    Some applications demand tight selectivity in couplings—minor changes in ring substitution or ester composition shift the outcome. Pinacol ester offers a practical sweet spot between stability and reactivity. We have run comparative studies against other esters—such as neopentyl glycol, ethylene glycol, and methylboronic acid derivatives—and found the pinacol group better resists hydrolysis during aqueous workup, without requiring excessive force to deprotect. Pinacol esters handle air better in bench or automated set-ups, and their crystalline nature gives reproducible handling on both small and large scale.

    Real-World Performance

    The easiest way to measure the value of our product lies in the performance data customers share. Process chemists document minimal losses during storage, while bench researchers observe the absence of problematic byproducts in paragraph-to-paragraph batch runs. A few have confirmed higher conversion at gram-scale Suzuki coupling, matching the theoretical yield found in literature with little post-reaction cleanup. Others note that our physical product outlasts typical literature shelf lifespans, with little change in quality after months in warehouse storage.

    A Commitment to Continuous Improvement

    Markets evolve, regulatory landscapes shift, and downstream innovation keeps raising the bar for starting material performance. Our organization adapts through ongoing feedback cycles—pilot production campaigns, rapid small-batch R&D, and incorporation of new analytical controls when trace byproducts or degradation routes pop up. Open lines with customers ensure every reported anomaly gets traced, tested, and used as fuel for refining the manufacturing process. Instead of viewing batch variation as a tolerable norm, we tighten processes around every lesson, closing the loop so that all future supply arrives cleaner and more consistent.

    Why Direct Manufacture Means More Than Source Control

    Chemical synthesis is collaborative. By keeping every step of production, purification, analysis, and logistics inside our facility, we maintain a level of transparency and technical accountability that lets users ask hard questions and get direct answers. Chemists on our team have spent years developing the synthesis of this pinacol ester, understanding not just the steps but also the subtle quirks of hydrolysis, crystallization, and purification unique to this structure. Only this depth of experience supports true process optimization—not just batch-to-batch uniformity, but the small improvements that compound over thousands of kilograms produced and shipped worldwide.

    Connecting Quality with End-Use Success

    Reliable laboratory and industrial production runs start with confidence in raw materials. We work daily to provide a high-purity, stable, and consistent 2-Chloro-4-Methylphenylboronic Acid Pinacol Ester that meets the rising requirements of medicinal, agrochemical, and material research. Drawing on years of technical problem solving and a deep commitment to continuous improvement, our plant delivers material trusted by leading chemists. Open communication, process transparency, and attention to every production detail create value far beyond a single order, supporting innovations at every step of the value chain.