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Methylboronic Acid

    • Product Name Methylboronic Acid
    • Alias methylboronic-acid
    • Einecs 'EINECS: 232-964-6'
    • 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

    136037

    Cas Number 1190-43-2
    Molecular Formula CH5BO2
    Molecular Weight 59.86 g/mol
    Appearance White to off-white solid
    Melting Point 90-92°C
    Density 0.94 g/cm³ (at 25°C)
    Solubility In Water Soluble
    Purity Typically ≥ 97%
    Synonyms Boronic acid, methyl-
    Smiles B(C)(O)O
    Inchi InChI=1S/CH5BO2/c1-2(3)4/h3-4H,1H3
    Ec Number 214-739-4

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

    Packing & Storage
    Packing Methylboronic Acid is packaged in a 25-gram amber glass bottle with a secure screw cap and hazard labeling for safety.
    Shipping Methylboronic acid is shipped in tightly sealed containers, typically polyethylene or glass bottles, to prevent moisture absorption and air exposure. The containers are labeled as hazardous, accompanying appropriate safety documents. During shipping, they are protected from physical damage, heat, and incompatible substances, complying with all applicable chemical transportation regulations.
    Storage Methylboronic acid should be stored in a tightly sealed container, away from moisture and incompatible substances such as oxidizing agents. Keep it in a cool, dry, well-ventilated area, ideally under inert atmosphere like nitrogen if possible. Protect the chemical from light and humidity to prevent hydrolysis and decomposition. Always label containers clearly and follow local regulations for storage of organic acids.
    Application of Methylboronic Acid

    Applications of Methylboronic Acid in Industrial Manufacturing

    Methylboronic Acid serves as a specialized reagent across several advanced industrial manufacturing sectors. As an essential organoboron compound, its distinct reactivity and compatibility support demanding synthetic routes, especially where tight control over purity and process validation is mandated. Below, we outline core downstream application scenarios, technical integration approaches, and compliance requirements for business customers across specialized domains.

    1. Pharmaceutical API Synthesis

    Pharmaceutical manufacturers utilize methylboronic acid in Suzuki–Miyaura cross-coupling reactions during active pharmaceutical ingredient (API) synthesis, especially in the assembly of complex molecular scaffolds. Process chemists select this raw material for its high selectivity in introducing methylboron groups and precise carbon–carbon bond formation, which is critical for the production of kinase inhibitors and advanced oncology compounds. GMP protocols require rigorous analytical verification at each batch, and full traceability of reactivity and impurity profiles for regulatory filing.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) – ICH Q7, US FDA 21 CFR Part 210/211
    • European Pharmacopoeia (EP) and United States Pharmacopeia (USP) monographs for APIs
    • ICH Q3A/B guidelines on impurity limits
    • ICH Q11 for API starting materials

    Typical usage ratio

    • Stoichiometric levels: 1.0–1.5 equivalents relative to halide intermediate, with minor adjustment based on the group reactivity and scale-up efficiency

    Downstream process integration

    • Charged during catalyst-initiated coupling step, post solvent charge and pre-base addition; quality assessment via in-process HPLC

    Final product types

    • Targeted small-molecule cancer drugs
    • Intermediate blocks for kinase inhibitors
    • Advanced pharmaceutical intermediates and building blocks

    2. Agrochemical Synthesis

    Agrochemical producers use methylboronic acid as a coupling partner for the synthesis of highly specific herbicide, insecticide, and fungicide active compounds. Demand focuses on efficient methyl group incorporation and controlled reaction kinetics during the late-stage assembly of crop protection molecules. Regulatory frameworks predicate full documentation of reagent purity and validated removal of boron traces from finished agrochemical formulations.

    Industry compliance standards

    • FAO/WHO Food and Agriculture Organization pesticide specifications
    • European Union REACH Regulation (EC) No 1907/2006
    • EPA Toxic Substances Control Act (TSCA) inventory and SIEF protocols
    • ISO 9001 for manufacturing quality management

    Typical usage ratio

    • 0.9–1.2 molar equivalents per reaction, depending on crop protection structure and batch size

    Downstream process integration

    • Added to agitated reaction stage after catalyst and ligand charge; post-reaction boron removal via aqueous extraction and phase separation

    Final product types

    • Methyl-substituted herbicide actives
    • Niche insecticides for integrated pest management
    • Triazole fungicides where controlled methylation defines activity

    3. Electronic Materials Manufacturing

    The electronics industry incorporates methylboronic acid during the preparation of organic semiconductors and specialty polymers for high-end display technologies. The compound promotes formation of high-purity, custom-tailored organic building blocks essential to OLED emitters and functionalized substrates, supporting particle-free environments and trace-metal purity required for device performance. Materials teams monitor feed purity and conversion to ensure compliance with semiconductor-grade standards.

    Industry compliance standards

    • SEMI C94 – Specifications for electronic chemical purity
    • IATF 16949 for automotive-grade electronic components
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • IEC 61249-2-21 for halogen-free electronic materials

    Typical usage ratio

    • Equimolar to 1.3 equivalents, based on target polymerization or coupling reaction; adjusted following real-time spectrometric monitoring

    Downstream process integration

    • Dosed in glovebox or inerted reactor stage, upstream of final polymer workup and purification; rigorous in-line removal of boron residues prior to device integration

    Final product types

    • OLED display emitter materials
    • Conductive organic polymer precursors
    • Advanced microelectronic sensor coatings

    4. Fine Chemical and Flavors Intermediate Production

    In the flavors and fine chemicals sector, methylboronic acid acts as a specialized coupling agent for the regioselective methylenation of aromatic compounds, supporting synthesis of custom intermediates for fragrances and flavorings. Downstream manufacturers demand precise control over residual boron content and full traceability from raw material batch to final flavor base, with auditing according to food additive regulations and purity benchmarks.

    Industry compliance standards

    • FEMA GRAS (Flavor and Extract Manufacturers Association) listing
    • EU Regulation 1334/2008 on flavorings and certain food ingredients
    • US FDA 21 CFR 172, synthetic flavoring substances and adjuvants
    • ISO 22000 food safety management system

    Typical usage ratio

    • 1.05–1.25 equivalents per aromatic starting unit; adjusted to minimize byproducts and maximize yield of flavor intermediate

    Downstream process integration

    • Introduced at the palladium-mediated coupling stage; followed by sequential treatments to remove organoboron residues before food-grade purification

    Final product types

    • Key intermediates for synthetic vanilla, anisole, or phenolic flavor ingredients
    • Building blocks for complex fragrance molecule assembly
    • Specialty aldehydes and acetals for food and beverage flavor systems

    5. Specialty Polymer and Resin Additive Synthesis

    Specialty chemical producers leverage methylboronic acid as a reagent in the design of crosslinkable and functionalized prepolymers for advanced resin systems. The introduction of boron-functional groups via controlled transesterification or cross-coupling enables enhanced resin network flexibility, tailored solvent resistance, and tunable curing characteristics. Manufacturing processes require ongoing verification of batch reactivity and physical property endpoints through in-process QC.

    Industry compliance standards

    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) compliance
    • ISO 14001 for environmental management systems in chemical synthesis
    • ASTM D638 for tensile properties of resins
    • ISO 10993-5 for polymer biocompatibility in medical or laboratory surfaces

    Typical usage ratio

    • 0.5–1.8% by weight in resin prepolymer formulations; tuned based on target crosslink density and mechanical strength profiles

    Downstream process integration

    • Added during prepolymer mixing stage prior to final curing; monitored by real-time viscosity and gelation analytics

    Final product types

    • Boron-functional specialty epoxy resins
    • Electronic encapsulants for high-value devices
    • Chemically resistant coatings and adhesives
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    Certification & Compliance
    More Introduction

    Introducing Our Methylboronic Acid – A Chemist’s Commentary from the Plant Floor

    Inside Our Process and Product: What Sets Our Methylboronic Acid Apart

    Methylboronic acid stands out in our daily work as a reagent that always delivers reliable performance. On the production floor, each batch comes out with the clean white to off-white crystalline appearance that every synthetic chemist expects. Formula-wise, we work with CH5BO2, with a molecular weight of roughly 59.86 g/mol—nothing fancy, but its chemical backbone is what matters in practice. Whether for pharmaceutical synthesis or fine chemistry, we see our customers rely on predictable melting points and unclouded purity. Quality assurance runs side-by-side with every batch—our boron content always checks out, and trace impurities stay below tight limits for all application categories.

    We run multiple reactors tailored for organoboron chemistry. Closed handling and pure water washdowns at every cleaning cycle minimize contamination, which isn’t just a production boast; contamination shows up right away in your chromatography or downstream reaction yields. We stick to rigorous protocols, from raw methylboronate esters through hydrolysis and purification, to make sure each kilogram acts as expected in Suzuki-Miyaura couplings or other C-C bond-forming reactions. Our methylboronic acid doesn’t leave you guessing about reactivity or stability: it’s got a dependable, moderate solubility in water and polar organics, easily dissolving for routine laboratories or multistep syntheses.

    Why Methylboronic Acid Earns Its Place in the Laboratory

    Our clients keep methylboronic acid in their inventory because it unlocks coupling chemistry, especially for building aryl and vinyl compounds. On our tour through process scale-ups, the single-carbon methyl boron group proves invaluable. It plugs directly into modern palladium-catalyzed protocols, handling a broader substrate range than bulkier organoboron analogs. Once you run several Suzuki couplings, you notice how our methylboronic acid gives high conversions with aryl halides and select heterocyclic compounds.

    Every scale—from a hundred grams in kilo labs to multi-ton pharma orders—uses the same backbone process. Clean methylboronic acid reacts fast and doesn’t introduce background side reactions, thanks to daily purity checks and trace-metal analysis. Water handling and pH control ensure it won’t introduce base-sensitive side products. Since plenty of boronic acids suffer from instability or insidious traces of volatile esters, we test both free acid and any residual boronate, using both NMR and GC for cross-verification. The practical effect: customers report fewer purification headaches.

    Folks who’ve tried commercial samples from less controlled sources often talk about sticky, yellowed solids or inconsistent melting points. The offbeat batches over time ruin chromatography columns or slow down scale-up. We pay full attention to dryness and storage in inert atmosphere, so the acid stays free-flowing and doesn’t absorb moisture or degrade under the plastic liner. Experience on the manufacturing line shows that even one uncontrolled variable spikes background impurities, so our cleanroom packaging pays off during both shipping and laboratory weighing.

    Comparing Our Acid to Other Boronic Derivatives and Analogues

    You might think all boronic acids act the same way, but the fact is, the subtle differences change outcomes in both bench chemistry and production. Methylboronic acid delivers unique advantages over, say, phenylboronic acid or bulkier alkyl boronic acids. It’s fundamentally less sterically hindered, giving it a sharp edge in cross-coupling with tough aryl halides. A bulkier group can block Pd-catalyzed transmetalation, but a methyl slides quickly into the reaction cycle, especially when working with electron-poor partners that sometimes resist larger boronates.

    We’ve supported dozens of customers swapping phenyl or isopropylboronic acids for our methyl analog. They report not just improved yields but also cleaner products, less homocoupling, and easier purification. The small methyl group also limits solubility problems: while some boronic acids either cake or cause phase separation, the methyl group sits right at the sweet spot for solid handling and rapid redissolution. Users working with pinacol boronate esters sometimes notice incomplete hydrolysis or lower reactivity compared to the free acid. Our acid sidesteps those extra hydrolysis steps—no need to introduce pinacol, no waiting for transesterification, and less to track in QC.

    In terms of tolerance, methylboronic acid forgives more. Customers scale up aryl methyl couplings without the nagging worry about sensitive functional groups getting swept up in side reactions. With bulkier acids, hydrophobicity or insolubility becomes a sticking point, especially in aqueous media. We’ve seen methylboronic acid outperform competitors in green chemistry protocols: water-based Suzuki couplings, for example, rely on fine solubility and rapid turnover, which this molecule provides out-of-the-bottle. No sticky residues, no delayed crystallization, just reliable results across multiple reaction types.

    Tailoring for Industry Use: What Drives Our Specifications

    Rather than ticking boxes on a data sheet, we match our production specs to years of customer feedback and hands-on troubleshooting. Our standard purity runs upwards of 98%, with most lots coming in higher by NMR and HPLC. We monitor water content, keeping it typically below 0.5%—lower for custom orders—since trace moisture shifts equilibrium toward boroxine formation and can reduce coupling efficiency. We tweak particle size on request, although the default crystalline material pours readily and weighs out easily.

    Shipping and storage get as much care as synthesis. Even minor atmospheric exposure will let some boronic acids degrade or hydrate, so we invest in foil-lined drum packaging and nitrogen blanks. From loading dock to final destination, your methylboronic acid stays stable, not clumping or reacting during transit. We’ve run accelerated stability studies across seasons, and shelf-life simply stays consistent for sealed containers. That’s the difference from plant-produced to repackaged—your material doesn’t pick up contamination or degrade en route.

    Lessons Learned from Scaling Up and Supporting User Applications

    In chemical manufacturing, we get a daily education in real-world scale-up. Early on, we saw that aggressive hydrolysis or careless filtration allowed in trace silicones or adventitious iron, which popped up later in failed coupling reactions. Now, high-purity reactors and nonmetallic filtration safeguard each lot. We’ve dialed in points on the process to minimize side-formation of boroxines, which show up as stubborn high-melting impurities if the water content or pH drifts even modestly. Apprentices on our line catch these issues with fast in-process checks, not just finished-goods inspection.

    Extensive collaboration with medicinal chemists and process engineers fine-tuned our workflow. Synthetic pharmaceutical clients demanded zero tolerance for nitrogen-based impurities, so we run batch-wise nitrogen-free, meeting strict industry demands for API building blocks. Our track record traces back to several multi-ton campaigns, where missed purity specs would have spelled trial and error in downstream runs—costing both time and raw materials.

    Because methylboronic acid often lands in preclinical and process optimization projects, traceability ranks high. Each batch carries a documented synthesis record, spectral assays, and chromatographic traces. If there’s ever a question, you can reach an actual chemist from the plant, so you aren’t left in the dark seeking answers from a sales desk. As a volume producer, our lab and production teams put feedback before slogans: if your protocol throws a curveball, our support comes based on what actually worked on the floor, not just what’s in a technical brochure.

    Quality and Safety on the Production Line: Our Viewpoint

    By making methylboronic acid ourselves, every step from raw boron input to final sealed drum stays visible and controlled. Our commitment goes beyond the minimum certifications—a simple certificate doesn’t guarantee an acid that stays stable under real-world warehouse conditions. We run regular in-house stability programs, monitoring not only decomposition but also the formation of minor by-products in real time. Each drum is sampled at fill and then stored to periodic retest, so any deviation from the norm gets flagged early.

    On our line, we maintain surgical standards in process hygiene because small molecules like methylboronic acid pick up traces from line reuse or shared agitation. Operators log every cleaning and line switch. Personal safety sits shoulder to shoulder with product purity: our protocols cover not just PPE and ventilation, but also closed transfer for all boronic acid solids. We provide written documentation tailored by application and regulatory need, matching customer requirements from advanced materials to pharma synthesis. No customer batch leaves before we’re satisfied the full origin story is accounted for, including purity, handling, and shipping timelines.

    How Our Direct Manufacturing Supports Innovation and R&D

    Sometimes an innovation springs from a supplier who listens and has a flexible process. Years of working directly with research teams pay off especially in methylboronic acid sourcing. Whether formulation chemists are trialing new polymer-bound boronic architectures or bench scientists are testing potent new bioisosteres, small differences in acidity, salt content, or residual metals make or break a research project. We run short campaign syntheses for R&D clients; if a customer needs isotopically labeled methylboronic acid or special particle size fractions, we're set up to deliver in useful quantities and on laboratory timescales.

    Open feedback loops matter: if your pilot run detects a chromatographic ghost peak, our process team investigates and, if warranted, adapts the cleanup or final drying conditions on your future lots. We see ourselves not simply as a pipeline but as a project partner, focused on outcomes and repeatability. That collaborative approach pays off in academic spin-outs and rapidly evolving biotech programs, where agility beats static supply channels every time. By controlling our own manufacturing, we can shift quickly from R&D to larger-scale campaigns, giving startups and major firms the flexibility to move without resourcing delays.

    Regulatory, Environmental Stewardship, and Our Commitment

    Boronic acids, with their role in advanced electronics, biotech, and medicine, occasionally draw regulatory scrutiny. Our team works out compliance benchmarks for both safety and environmental standards, applying best practices on solvent recovery and effluent management. We chose reaction conditions that generate minimal hazardous waste, because both safety and environmental impact affect our community and neighbors. Our containment and recycling systems remove boron from process wash water via ion exchange and precipitation, reducing the environmental footprint for every kilogram produced.

    Our operations run on quarterly site inspections not just for ISO or external audit, but for ongoing performance improvement. Keeping a close relationship with local regulators and first responders, we maintain clear hazardous materials logs, drill every quarter, and actively seek customer feedback on safety and compliance documentation. When regulatory requirements shift, such as new directives from chemical authorities or pharma guidelines, we update protocols proactively. That way our methylboronic acid stays compliant whether you’re shipping it globally or using it in regulated pharmaceutical manufacture.

    Being a Direct Producer: The Value We Give to Your Supply Chain

    As the hands-on manufacturer, we know what goes into each drum of methylboronic acid. No lengthy supply lines, no repackaged containers, and no surprises. Direct communication between our plant engineers and your purchasing or technical teams takes the guesswork out. Instead of a broker reaching for answers from a distant source, your questions about lead times, custom lot requirements, and special QC standards reach our chemists and process supervisors directly.

    We schedule production slots tailored to both short-notice orders and forward forecasts. This means we reduce the lead-time pressures typical with intermediary-sourced specialty chemicals, which often suffer from uncertain delivery schedules or quality mismatches. We understand that running out of a key reagent, or dealing with batch-to-batch drift, stops research programs in their tracks. That’s why our inventory and production cycles are structured to support not only just-in-time users but also clients booking recurring high-volume shipments.

    Open channel feedback loops give us early warnings if a user needs a custom purity, extra documentation, or special packaging. We put our own name and reputation behind every lot. That investment in consistency and openness is how we’ve built long-term trust with clients in pharmaceuticals, specialty polymers, and electronics, from gram-scale to multi-ton campaigns.

    On the Frontline with You: A Reflection

    After all these years producing methylboronic acid, from small batches up through industrial runs, we know every lot carries with it the sweat and skill of the chemists on the floor. This isn’t just a box-ticking exercise or a commodity to be traded; it’s a partnership with every customer who depends on our consistency and technical support. Our plant routines reflect not only the lessons of process chemistry but also the lived experience solving problems one vessel and one kilogram at a time.

    Providing reliable methylboronic acid means understanding its nuanced chemical behavior, responding to changing regulatory demands, and making sure every container reaches you ready for your most sensitive or high-stakes applications. Drawing from our years of hands-on experience, we back up every claim with fact—not just with numbers, but with the transparent support you expect from those who manufacture and stand by what they produce. In the lab and at scale, our methylboronic acid fulfills its promise: tried, tested, and directly delivered.