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3-Tolylboronic Acid

    • Product Name 3-Tolylboronic Acid
    • Alias 3-Methylphenylboronic Acid
    • Einecs 275-100-8
    • 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

    713161

    Name 3-Tolylboronic Acid
    Synonyms m-Tolylboronic acid
    Cas Number 5910-44-5
    Molecular Formula C7H9BO2
    Molecular Weight 135.96 g/mol
    Appearance White to off-white solid
    Melting Point 176-180 °C
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents like ethanol and ether
    Storage Temperature Store at room temperature
    Smiles B(C1=CC(=CC=C1)C)(O)O
    Inchi InChI=1S/C7H9BO2/c1-6-3-2-4-7(5-6)8(9)10/h2-5,9-10H,1H3

    As an accredited 3-Tolylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for 3-Tolylboronic Acid (25g) is an amber glass bottle with a secure screw cap and clear hazard labeling.
    Shipping 3-Tolylboronic Acid is shipped in tightly sealed, chemical-resistant containers under ambient conditions. Packaging complies with international transport regulations for chemicals. Protective measures are taken to prevent moisture ingress and physical damage. Each shipment includes proper labeling and a Material Safety Data Sheet (MSDS) for safe handling and regulatory compliance.
    Storage 3-Tolylboronic Acid should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Keep the container tightly closed and protected from incompatible substances such as strong oxidizing agents. Store at room temperature, and ensure the storage area is equipped to handle chemicals to prevent contamination and degradation of the product.
    Application of 3-Tolylboronic Acid

    Applications of 3-Tolylboronic Acid in Industrial Manufacturing

    3-Tolylboronic Acid serves as a highly efficient intermediate in several industrial sectors, enabling the synthesis of complex molecules and value-added chemicals. The following application segments detail practical uses across established downstream industries, including the related compliance norms, integration methods, formulation ratios, and common finished goods.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers frequently use this raw material in Suzuki-Miyaura cross-coupling reactions to build biaryl structures integral to many small-molecule APIs, including oncology and anti-inflammatory compounds. Consistency in molar equivalency during scale-up and adherence to GMP guidelines are essential for successful registration and regulatory audits. Stringent traceability throughout the process assures quality and safety for finished drug substances.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • US FDA cGMP regulations (21 CFR Part 210/211)
    • European Pharmacopoeia (Ph. Eur.) and United States Pharmacopeia (USP) applicable to APIs
    • REACH substance registration (EU)

    Typical usage ratio

    • Typically 1.0–1.2 molar equivalents relative to aryl halide starting materials; adjusted based on substrate reactivity and desired purity level.

    Downstream process integration

    • Introduced during the Suzuki coupling step in API multi-step synthesis routes; process includes controlled addition under inert atmosphere followed by palladium-catalyzed reaction and purification.

    Final product types

    • Oncology drug intermediates
    • Anti-inflammatory drug APIs
    • Neuropsychiatric medication intermediates
    • Non-steroidal anti-inflammatory drugs (NSAIDs)

    2. Advanced Agrochemical Intermediate Manufacture

    Chemical production facilities apply this compound to generate biaryl-based herbicide and fungicide scaffolds through palladium-catalyzed cross-coupling operations. Control of stoichiometry and purity remains critical, particularly with agrochemicals subject to residue and environmental impact regulations. The downstream integration usually occurs in the early to mid-stage of new molecule development pipelines.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Products
    • OECD Guidelines for the Testing of Chemicals
    • EU Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market
    • ISO 9001 Quality Management System in manufacturing plants

    Typical usage ratio

    • Commonly 1.05–1.3 molar equivalents versus halogenated intermediates; increased in cases where byproduct formation is pronounced.

    Downstream process integration

    • Charged into the batch or continuous flow reactors immediately prior to base and catalyst addition; employed in intermediate or penultimate agrochemical synthesis prior to formulation into emulsion or granule forms.

    Final product types

    • Biaryl-based fungicides
    • Selective pre-emergence herbicides
    • Pesticide active intermediates
    • Seed treatment chemical bases

    3. Specialty Electronic Material Synthesis

    Producers of organic semiconductors and high-value OLED materials incorporate this building block into conjugated aromatic systems. The purity of input and the prevention of boronic acid anhydride formation are prioritized, requiring dry handling and controlled crystallization. Process validation ensures that electronic properties remain consistent for end-use in display and sensor applications.

    Industry compliance standards

    • IPC-6012 Qualification and Performance Specification for Rigid Printed Boards (for downstream use)
    • ISO 14001 Environmental Management System
    • RoHS Directive (2011/65/EU) compliance for hazardous substances
    • Internal electronic materials quality validation protocols

    Typical usage ratio

    • Ranges from 0.9–1.2 equivalents versus aryl halide monomers; fine-tuned based on molecular weight targets and purity requirements of the final polymeric material.

    Downstream process integration

    • Dosed into Suzuki coupling stages for building oligomeric or polymeric chains; followed by rigorous workup and purification before thin-film casting or device fabrication.

    Final product types

    • Organic light-emitting diode (OLED) emission layer materials
    • Semiconducting polymers for printed electronics
    • Organic photovoltaic precursors
    • Hole-transport and electron-transport materials for displays

    4. Fine Chemical R&D and Custom Synthesis

    Contract research and development laboratories employ this intermediate for rapid structure-activity relationship studies and custom libraries. These applications demand lot-to-lot consistency, high purity, and detailed COA documentation. Dosage levels adapt quickly according to each unique synthetic sequence, and trace metal content or residual solvents often undergo enhanced scrutiny, especially for downstream analytical or clinical trial applications.

    Industry compliance standards

    • ISO 17025 Laboratory Quality Management
    • GLP (Good Laboratory Practice) OECD Principles for R&D work
    • Custom project-specific QC protocols for regulated contract synthesis
    • REACH (as applicable to research and innovation scale up)

    Typical usage ratio

    • Flexibly adapted; typically 0.95–1.25 equivalents based on target compound and scale; can be optimized further according to cost or purity objective in each project.

    Downstream process integration

    • Added as a boron source during palladium-catalyzed cross-coupling; compound is purified before further functionalization or scale-up to pilot plant testing.

    Final product types

    • Custom biaryl building blocks for lead generation
    • Reference standards for pharmaceutical analysis
    • Intermediates for proprietary new chemical entities (NCEs)
    • Analytical standards for impurity profiling

    5. Dye and Pigment Intermediate Production

    Industrial pigment and dye manufacturers use this compound to introduce specific aromatic moieties into chromophore frameworks. Controlling input purity and minimizing metal catalyst residue are essential, especially for products destined for plastics, inks, or textile applications. The boronic acid mainly enters during colorant synthesis through transition metal-catalyzed arylation steps, impacting hue and lightfastness in finished dyes.

    Industry compliance standards

    • EN 71-3 Safety of Toys – migration of certain elements (for pigment use in toys)
    • REACH Annex XVII – restrictions on azo colorants
    • ISO 9001 Quality Assurance for pigment and dye manufacturing
    • Restricted Substances List (RSL) compliance for apparel and packaging markets

    Typical usage ratio

    • Usually 1.0–1.1 equivalents compared to halogenated aryl or diazonium partners; can be elevated slightly for deeper color or higher coupling efficiency.

    Downstream process integration

    • Fed into aryl-aryl coupling reactors during chromophore modification; followed by isolation, purification, and blending stages before milling and formulation into disperse or vat dyes.

    Final product types

    • Colorants for plastic masterbatches
    • Disperse dyes for polyester textiles
    • Pigments for industrial inks
    • High-performance dyes for coatings
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    Certification & Compliance
    More Introduction

    3-Tolylboronic Acid: Experience from a Chemical Manufacturer’s Perspective

    Real Production, Reliable Value

    Our team has spent years on the synthesis and purification of 3-tolylboronic acid. The product's model number is CAS 6165-68-0, simple on paper, yet the chemistry behind it requires precision and oversight, especially during the oxidative coupling and crystallization steps. In manufacturing, the smallest change in raw material or process conditions shifts purity and yield. Customers turn to us not because we sell a name, but because our product delivers repeatable results batch after batch. We know this through feedback from pharmaceutical and agrochemical partners who measure product value by its performance in real reactions.

    The Functionality That Matters

    3-Tolylboronic acid stands out for Suzuki-Miyaura cross-couplings, a staple reaction in organic synthesis. Medicinal chemists use it to install functionalized aryl groups on complex molecules. The para and ortho variants of tolylboronic acid each have their place, but in our experience, the 3-tolyl form balances reactivity and steric profile, making it a favorite for fragment elaboration. In the lab, customers stress the need for clear, fine crystals that dissolve consistently—so we maintain strict protocols on particle size and moisture content. Small details make a big difference, because poor crystallinity can stall a reaction or create headaches in downstream purification.

    What Sets 3-Tolylboronic Acid Apart

    We have seen projects stall when alternative boronic acids failed to deliver clean couplings and poor filterability. Our 3-tolylboronic acid avoids the problem because we work upstream, screening raw materials and watching out for byproduct build-up. In my experience, even a trace of boroxine impurity can affect catalyst lifetime and overall yield. To prevent this, we collect material at low temperatures and conduct real-time purity checks by HPLC and NMR. If any batch tips below 98% purity, we rerun crystallization, rather than pushing inferior product to market.

    Making a Better Building Block

    Serving medicinal chemistry teams means helping them meet tough deadlines. For a process chemist, a boronic acid that forms cakes or absorbs moisture adds risk to the workflow. Our product flows freely and keeps its form in long-term storage. Those details lower the chances of operational delays from clumping or unexpected side-products. In one instance, our client switched from a bulk broker’s lot to our 3-tolylboronic acid and reported a 12% increase in cross-coupling yields, simply due to a tighter specification on residual solvents and boroxine content.

    Consistency in Scale

    Scaling up 3-tolylboronic acid from lab grams to pilot kilos reveals real challenges. Lab recipes don’t always translate to stainless steel reactors. Heating and cooling rates need fine control. Even seemingly small details—like stirrer blade design—can impact batch outcome. We have refined our crystallization protocol across hundreds of runs, solving issues such as over-crystallization clogging the lines or solvent inclusions. It takes hands-on experience to achieve the same material quality from pilot runs all the way to ton-scale manufacturing. Our clients count on this consistency for process validation, particularly in regulated environments, where an off-batch can halt an entire project.

    Applications in Real Projects

    Every few months we receive feedback from research groups pushing 3-tolylboronic acid into the hot seat of a new project. One pharmaceutical company recently used our material to synthesize a new kinase inhibitor. They found that yields depended not just on catalyst choice, but also on the boronic acid’s water content and trace metal profile. Supporting a project like this means regular communication, batch traceability, and frequent analytical updates.

    In crop protection chemistry, several major actives begin from the 3-tolyl fragment. Our agricultural customers rely on us for timely shipments, knowing any downtime in pilot production can cost real dollars. We provide COAs based on each batch, not generic data, because in regulated markets, compliance means more than checking a box; it ensures the safety and reliability of downstream products that ultimately reach global customers.

    Purity Is More Than a Number

    Some buyers compare boronic acids by catalog specs alone. True value comes from supplier reliability over time. Repeated experience has shown us that even a few tenths of a percent off in purity, or higher moisture, can create persistent byproduct issues—especially with sensitive palladium catalysts. For every batch of our 3-tolylboronic acid, moisture is checked by Karl Fischer titration and not just once, but at different sample points. Throughout the warehouse, temperature and humidity controls keep the material dry, so it arrives at customer labs in the same condition as when it left the reactor.

    Practical Handling and Storage

    I still remember a customer complaint about a sticky, caked lot. We traced the problem to a winter shipping route with wildly fluctuating temperatures. Since then, we’ve redesigned packaging with triple-layer barriers, moisture scavengers, and tamper-evident seals. Product quality is as much about physical integrity as it is about composition. 3-Tolylboronic acid’s gentle, earthy color and crystalline form make it easy to handle in gloveboxes and open air, but maintaining that appearance through storage and transit remains a priority. Each drum is batch-labeled and traceable to the blend date—a detail that chemical engineers and QA teams value when setting up automated dosing or weighing equipment.

    Where It Fits Best—And Where It Does Not

    Not every project calls for 3-tolylboronic acid. We advise against forcing its use purely for convenience. Some aryl halides, richer in electron density, prefer more activated boronic acids, and we guide customers toward the best fit. The 3-tolyl group offers moderate reactivity and tolerates a broad range of functional groups, but certain heterocycle couplings still favor alternative partners. We make recommendations based on real-world outcomes, not theoretical reactivity charts. After fielding hundreds of inquiries, we have learned to distinguish between a request for “the strongest coupling agent” and a need for batch-to-batch consistency that saves time and rework.

    Safety Considerations Without The Hype

    In manufacturing, operator safety takes top priority. 3-Tolylboronic acid, compared to some more reactive organoboron compounds, is stable and has a favorable safety profile, but attention to dust control and spill management remains important. Our operations follow stringent protocols—fixed vacuum points, local extraction, and personnel training—the precise routines that make for a safe and sustainable manufacturing environment. Customers see these effects not just on a COA, but embedded in the reliability and cleanliness of each shipment.

    Environmental Commitment We Stand Behind

    Rising environmental scrutiny affects every step of chemical production. At our facility, we’ve worked to minimize solvent use and recover as much as possible through closed-loop distillation. The residual filtrates are evaluated for proper disposal, and clean water discharge is monitored for trace boron under strict limits. Our commitment manifests in slow, steady investment—high-efficiency condensers, low-temperature crystallizers, and solvent handling upgrades that squeeze each drum of waste for reusable material. These improvements translate to measurable reductions in waste output over the past five years.

    Supporting New Technology and Discovery

    Over the past decade, we have watched flow chemistry and continuous processing take center stage in specialty chemicals. 3-Tolylboronic acid remains a regular in these processes, and our teams provide detailed material compatibility reports in support of customer pilots and commercial rollouts. One client’s automated Suzuki-Miyaura process showed fouling and inconsistent yields with low-grade tolylboronic acid from generic sources. Bringing in our material made good on their promise of fully automated, hands-off coupling modules. Our technical liaisons now work closely with process engineers to optimize form, pack size, and delivery logistics based on the specific needs of flow reactors and automated dosing.

    Understanding Supply Chain Challenges

    Global logistics in the chemical industry grew tougher in recent years—supply chain disruptions, customs delays, and new regulatory requirements can all interrupt downstream projects. We get calls at all hours asking about restock timelines or delayed shipments. Our solution is to maintain multiple regional warehouses with on-the-ground inventory and real-time shipment tracking. Our customers value timely status updates and, on occasion, emergency resupply for critical production runs. Experience teaches us to keep a rolling buffer and strong relationships with reliable logistics partners, reducing exposure to sudden delays from weather, strikes, or geopolitical events.

    Drawing the Line on Quality Versus Cost

    Our long-term partners come to us with hard-nosed negotiations, looking for fair pricing but never at the expense of reliability. While sourcing cheaper alternatives, we have seen entire campaigns go astray due to subtle, batch-to-batch inconsistencies in product quality. We keep the bar high for our own material because we believe every dollar saved on lower quality translates into higher costs through failed lots, lower conversion, and lost project time. For clients operating under GMP or advanced research protocols, the stakes are even higher. We make the choice simple: quality holds value that cuts deeper than line-item price.

    Honest Comparisons to Similar Products

    There is plenty of discussion comparing 3-tolylboronic acid with its 2- and 4- isomers, as well as methyl-substituted phenylboronic acids. Looking closely at hundreds of customer campaigns, the 3-isomer emerges as a reliable “workhorse”—not always the flashiest, but valued for its robust coupling profile and balanced electronic characteristics. Technicians and chemists recognize subtle performance advantages; the meta-position methyl group introduces just enough steric and electronic modification for selective couplings. Some synthesis journals advocate for related compounds in niche reactions, but a wider survey among our regular customers turns up the same name again and again for mainstream aryl coupling.

    On the market, various grades circulate—lab, technical, and high-purity. We see researchers frustrated when switching between sources, finding discoloration or odd odors from polymerization gone unchecked. Purity alone doesn’t decide performance, but a lack of intentional manufacturing oversight almost always guarantees a headache. We stick to tight in-process controls, and no two batches ever get blended without supporting full analytical review—to us, it’s the only way to build trust and maintain reputation.

    The Experience of Reliable Partnership

    Chemists and engineers call us directly, not just for product, but for practical advice—what solvent systems best match with our retail batch, what storage period keeps impurities lowest, how to troubleshoot a cloudy filtration. These relationships make a difference for both sides. We are committed to providing not just a product, but the supporting data and know-how gathered through firsthand manufacture and collaborative problem solving over many years. Our lab regularly prepares custom analytical packages for customers onboarding new reactors, and we make site visits to help tailor our product for high-volume or automated systems.

    Raising the Bar Year after Year

    Technology doesn’t stand still. Each month brings new patents, regulations, and process innovations we need to adapt to. We invest in better analytical equipment, expand QC lab hours, and facilitate training for operators to maintain skills. The difference shows up where it counts—in fewer customer complaints, richer yields for process chemists, and confidence for procurement managers sourcing kilo or ton-scale materials. Data transparency runs through every shipment: batch numbers, test certificates, impurity profiles, crystallization dates—all details shared openly.

    From the Factory Floor to the Customer Bench

    Our main concern has always been how 3-tolylboronic acid behaves in real chemistry, not just on paper. Every drum, every container reflects work done by line operators, QC analysts, and technical managers. Our product earns its keep in hundreds of diverse projects: active pharmaceutical ingredient synthesis, agricultural intermediates, and new material development. We stay in close touch with researchers and raw material handlers alike, always learning ways to improve the process and product. The lessons learned from countless batches guide our manufacturing choices today and shape meaningful partnerships in the future.

    Building for the Future of Advanced Synthesis

    3-Tolylboronic acid will likely see even wider adoption as the field of organic synthesis evolves. We watch the rise of more sustainable Suzuki chemistry with broad functional group tolerance and the growth of continuous production modules. Product reliability—rooted in careful, hands-on manufacturing—remains the benchmark. Our team’s experience shows that each improvement to process, packaging, and customer support pays off in stronger outcomes for all stakeholders in the value chain, from discovery research to scaled manufacture.