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4-Methoxy-2-Methylphenylboronic Acid

    • Product Name 4-Methoxy-2-Methylphenylboronic Acid
    • Alias 4-Methoxy-o-tolylboronic acid
    • Einecs 619-467-1
    • 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

    546857

    Name 4-Methoxy-2-Methylphenylboronic Acid
    Synonyms 2-Methyl-4-methoxyphenylboronic acid
    Cas Number 1034030-05-1
    Molecular Formula C8H11BO3
    Molecular Weight 165.98 g/mol
    Appearance White to off-white solid
    Melting Point 120-124°C
    Purity Typically ≥ 97%
    Solubility Soluble in DMSO, methanol, and slightly soluble in water
    Smiles COC1=CC(=C(C=C1)B(O)O)C
    Inchi InChI=1S/C8H11BO3/c1-6-4-7(10-2)3-5-8(6)9(11)12/h3-5,11-12H,1-2H3
    Storage Conditions Store at 2-8°C, protected from moisture

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

    Packing & Storage
    Packing The 25g 4-Methoxy-2-Methylphenylboronic Acid is packaged in a sealed amber glass bottle with a tamper-evident cap and label.
    Shipping **Shipping Description:** 4-Methoxy-2-Methylphenylboronic Acid is shipped in tightly sealed containers to prevent moisture ingress and contamination. It should be stored and transported at room temperature, away from sources of ignition and incompatible materials. Appropriate labels and documentation are provided according to relevant chemical and safety regulations.
    Storage 4-Methoxy-2-Methylphenylboronic Acid should be stored in a tightly sealed container at room temperature, away from moisture and incompatible substances such as strong oxidizers. Store it in a cool, dry, and well-ventilated area, protected from light. Avoid exposure to air and humidity to prevent degradation. Refrigeration is recommended for long-term storage to maintain chemical stability.
    Application of 4-Methoxy-2-Methylphenylboronic Acid

    Applications of 4-Methoxy-2-Methylphenylboronic Acid in Industrial Manufacturing

    4-Methoxy-2-Methylphenylboronic Acid is a boronic acid derivative widely used in fine chemical, pharmaceutical, and electronic materials manufacturing. Below we detail distinct downstream applications and how industry leaders integrate this raw material to create high-value products.

    1. Pharmaceutical Active Intermediate Synthesis

    API manufacturers frequently utilize this compound in Suzuki-Miyaura coupling reactions to construct complex aromatic and heteroaromatic scaffolds for oncology and anti-inflammatory drugs. It ensures high selectivity and reduced by-product formation, supporting stringent regulatory requirements for pharmaceutical synthesis. Operations typically source this material for integration at the late-stage arylation step, where strict metal and impurity content control is required. By enabling precise introduction of a methoxy group at a defined position, it allows scalable synthesis of specific kinase inhibitor molecules and other targeted therapies.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP, EP, JP Pharmacopoeia requirements for raw material controls
    • FDA 21 CFR Part 211 for finished pharmaceutical production
    • GMP guideline for cross-contamination reduction (ISPE baseline)

    Typical usage ratio

    • 0.8–1.2 molar equivalents per aryl halide in Suzuki coupling
    • Adjusted according to substrate reactivity and required yield
    • Final process specification often set by target API lot analysis
    • Proportion optimized based on palladium catalyst concentration

    Downstream process integration

    • Introduced during the coupling stage in multi-step synthesis flow
    • Handled within automated reactor trains for batch or fed-batch production
    • Purification via crystallization or chromatography post-coupling
    • QC controls include HPLC purity, residual palladium, and boronic acid trace analysis

    Final product types

    • Small molecule APIs for oncology
    • Anti-inflammatory therapeutic ingredients
    • Chiral intermediates for pharmaceutical R&D
    • Preclinical and clinical compound candidates

    2. Advanced OLED Material Synthesis

    Producers of organic electronic materials apply this boronic acid derivative in the synthesis of high-performance emitting and charge-transport materials for OLED display and lighting technology. Its defined substitution pattern allows fine-tuning of photophysical and solubility properties, crucial for vapor-deposition and inkjet printing applications. Material incorporation typically occurs during the last coupling step when building the central aromatic core in OLED molecules, supporting the production of highly pure electronic-grade materials.

    Industry compliance standards

    • IEC 62341 (OLED display safety and performance requirements)
    • RoHS and REACH compliance for industrial electronic polymers
    • ISO 9001:2015 for electronic material supply chain
    • JIS C 62341 for OLED device and material conformity

    Typical usage ratio

    • 0.95–1.1 molar equivalents with halide partners in cross-coupling
    • Ratio determined via luminophore optimization studies
    • Final dosage based on device efficiency targets
    • Adjusted for impurities below 50 ppm for EL-grade products

    Downstream process integration

    • Integrated in the final aromatic coupling during molecular backbone construction
    • Processed under inert atmosphere to prevent oxidation
    • Purification by gradient sublimation and recrystallization for trace metal removal
    • Characterization by UV-Vis, fluorescence, and GPC before device assembly

    Final product types

    • Electroluminescent emitter molecules
    • Hole-transport layer compounds
    • Electron-transport layer intermediates
    • Custom host/dopant mixtures for OLED displays and panels

    3. Agrochemical Ingredient Synthesis

    Manufacturers in the agrochemical sector deploy this boronic acid to form highly substituted biaryl and heterobiaryl scaffolds in modern crop protection products. These include leading insecticide and herbicide active ingredients where precise positional control of the methoxy and methyl groups defines biological selectivity and substrate range. The raw material enters key aryl-aryl coupling steps, enabling efficient scale-up of patent-protected chemistries required in new-generation agro formulations.

    Industry compliance standards

    • FAO/WHO specifications for pesticide active ingredient manufacturing
    • ISO 9001:2015 Quality Management System for agro intermediates
    • REACH registration for plant protection chemical substances
    • OECD Guidelines for Testing of Chemicals

    Typical usage ratio

    • 1.0–1.5 equivalents per aryl halide substrate for diversified substitution
    • Adjusted based on kinetic studies to maximize crop protection activity
    • Controlled to limit unreacted boronic acid in technical grade products
    • Dosing refined to meet impurity thresholds stipulated by downstream formulators

    Downstream process integration

    • Used in the core coupling unit operation within pilot and commercial synthesis pathways
    • Monitored for thermal stability and compatibility with catalyst system
    • Purified actives isolated by solvent-switching and solid-phase extraction
    • Quality tested for residual metals and by-products prior to formulation

    Final product types

    • Selective Insecticide active intermediates
    • Post-emergence herbicide components
    • Fungicide R&D candidates
    • Specialty chemical additives for seed treatments

    4. Specialty Liquid Crystal Monomer Production

    Producers of advanced liquid crystal materials utilize this boronic acid in synthesis routes for monomers and oligomers designed for high-resolution display technologies. Its methyl and methoxy substitutions support narrow nematic phase range control and optimize birefringence, critical for the next generation of LCD panels and photonic devices. Manufacturers employ it as a key reactant in the final coupling step, ensuring high-purity liquid crystal products with strict control of trace ionic and boron impurities, essential for long-term device reliability.

    Industry compliance standards

    • ISO 9001:2015 for material production and documentation
    • IEC 61290-1 for photonic and display materials
    • RoHS Directive for restriction of hazardous substances
    • JEITA ECR standards for LCD materials

    Typical usage ratio

    • 0.9–1.1 molar equivalents in the cross-coupling stage
    • Adjusted according to the required phase transition properties
    • Refined for monomer chain length uniformity
    • Minimized excess to reduce post-synthetic scrubbing steps

    Downstream process integration

    • Incorporated in the terminal coupling reaction during monomer synthesis
    • Purification involves multi-stage vacuum distillation and ion-exchange filtration
    • Quality assurance conducted via polarizing microscopy and NMR spectroscopy
    • Material transferred in inert packaging to downstream panel manufacturers

    Final product types

    • Twisted nematic LCD monomers
    • Advanced chiral dopants for displays
    • Photonic device base materials
    • High-resolution display substrate chemicals
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    Certification & Compliance
    More Introduction

    Introducing 4-Methoxy-2-Methylphenylboronic Acid: Quality from Direct Production

    Reliable Output Starts with Meticulous Synthesis

    At our facility, we’ve synthesized 4-Methoxy-2-Methylphenylboronic Acid for years, watching demand rise as research teams and process chemists recognize its value. Produced with strict attention to purity and consistency, this compound shows up in our lines as white to off-white solid, bench-tested for every parameter that affects reactivity and shelf life. Careful control over the arylation process and work-up gives a product with minimal impurities—a difference easy to spot for anyone who’s wrestled with unknowns during coupling reactions. Batch after batch, the melting point checks out between 80 and 84°C, and HPLC routinely puts purity at over 98%. Experience tells us labs can detect the difference just by the way crystals respond in simple solution prep.

    Why 4-Methoxy-2-Methylphenylboronic Acid Matters for Synthesis

    Every year, more teams push Suzuki-Miyaura cross-coupling to new heights, turning arylboronic acids into key intermediates for everything from agrochemical agents to promising new pharmaceuticals. We’ve fielded questions about substitution effects for years, and chemists tell us that the methoxy and methyl groups here offer a meaningful balance between electronic tuning and steric fit. 4-Methoxy-2-Methylphenylboronic Acid reacts efficiently with various halides, notably powering through palladium-catalyzed couplings where less finely tuned boronic acids slow down. Even at scale, our direct customers report less need for re-optimization thanks to the consistency and lower catalyst loading these batches allow.

    Application Insights from Customers in Discovery and Process Chemistry

    We’ve shipped this boronic acid to labs working from early medicinal chemistry through to scale-up. One feedback thread stands out: projects stalled by sluggish oxidative insertions found new traction using this grade. A team building methoxylated biaryl scaffolds for CNS-targeted candidates commented on improved conversions vs. unsubstituted phenylboronic acid, owing to this compound’s electron-rich profile. Our long partnerships with several multinational pharma companies let us collect use cases; in all, boronic acids form a foundation for SAR exploration, and the methoxy-methyl combination remains one of the most requested for iterative analog design.

    Process chemists in pilot plants rely on scale consistency, so they appreciate that the product’s controlled moisture content reduces batch-to-batch unpredictability during storage and use. No extra steps to dry out the acid, no check-weighing before charging. Our warehouse team maintains ambient storage thanks to the compound’s stable profile, and it ships well across a range of climates. We’ve learned that robust packaging keeps samples free-flowing, saving time for everyone down the line.

    Comparison with Other Phenylboronic Acids: What Sets This One Apart

    Many boronic acids struggle with poor solubility, erratic reactivity, or fussiness about water content. Early in our production run, we noticed that the 4-methoxy-2-methyl variant handles more like a bench-stable solid, easy to weigh out and dissolve in standard coupling solvents such as dioxane, THF, or mixtures with water. Colleagues repeating Suzuki reactions side-by-side with plain phenylboronic acid saw reaction rates speed up noticeably under standard conditions.

    Unsubstituted phenylboronic acid is the old standby, but it often brings solubility headaches and offers little advantage in tuning molecular electronics. The 4-methoxy-2-methyl structure pushes more electron density into the ring, which translates to higher reactivity with aryl halides, especially electron-poor ones. Meta or ortho methyl or methoxy substitutions can lead to lower yields due to increased sterics or unpredictable coupling outcomes. We’ve run those side-by-side, and our lab notes log higher isolated yields and cleaner product formation using the 4-methoxy-2-methyl isomer, especially on challenging substrates like ortho-bromo halides or electron-deficient chlorides.

    Customers switching from 4-methoxyphenylboronic acid to the 2-methyl-4-methoxy substituted variant often remark on the change in melting characteristics. It’s easy to handle at room temperature and doesn’t clump during storage. Whether someone is making small combi-library arrays in screening vessels or scaling up for pilot plant runs, the physical form supports both activities without extra grinding or blending.

    Addressing Supply Chain and Quality Challenges

    Relying on a direct manufacturer brings peace of mind about what’s actually going into the reaction flask. Our quality lab tracks each lot using NMR, HPLC, and water content by Karl Fischer titration. Each new batch receives a complete COA and documentation ready for any regulatory or process audit. Because our team controls raw material sourcing and all process variables, trace metals and catalyst carryover stay below relevant thresholds. Partner companies send back feedback on critical impurities, especially those that affect LCMS outcomes during early lead assessment, which allows us to incrementally fine-tune our workflow.

    Multi-step upstream synthesis calls for reliability over lengthy projects. We maintain transparent records of storage conditions and keep a retention sample from every production lot for post-market questions. This helps support claim substantiation needed for compiled regulatory filings. Project managers from APIs and fine chemical sectors have let us know this shortens tech transfer and avoids duplicate qualification work.

    Environmental Responsibility in Every Batch

    Our team takes environmental and safety compliance seriously—most new customers ask about it right away. We operate our reactor blocks at controlled temperatures with closed-loop solvent recycling, which reduces waste streams and solvent loss. Every product that leaves our warehouse follows local and international shipping guidelines for classification and packaging integrity.

    On the safety front, trained staff review MSDS data with current hazard labels, and final packaging includes clear handling guidance. We support customers during audits or incident reporting. If someone requires recyclable packaging or has specific requests regarding shipment configuration for EHS requirements, we can discuss options to fit those project goals. This all factors into making our 4-methoxy-2-methylphenylboronic acid a sustainable choice for both routine and large-scale chemistry.

    Everyday Experience in Handling and Storage

    Chemists setting up coupling reactions at the bench appreciate quick dispensing and straightforward cleaning. Our staff has refined the particle size and flow to minimize dusting and cross-contamination risk. Spill management is rarely needed given the solid form and robust containment, and any cleanup dissolves with standard organic solvents. Internal feedback from our own R&D staff informs how we package the material—easy-open bottles, tamper-evident films, and moisture-control pouches keep it fresh on the shelf. For special projects requiring inert atmosphere packaging or batch reservation, we prepare custom fills on request.

    Longevity under ambient conditions means our customers can inventory material for weeks without concern for hydrolysis, as long as the cap stays on and storage avoids high humidity. Several years back, we fielded a request from a major pharma to monitor stability under higher-than-usual temperature swings. These studies showed minimal degradation, confirming that the product holds up both in Mediterranean heat and Northern winters.

    Supporting Innovation and Faster Project Timelines

    The push for faster hit-to-lead timelines in drug discovery and materials science continually drives innovation in synthetic routes. 4-Methoxy-2-methylphenylboronic acid helps here by offering reliable and reproducible reactivity, which translates into fewer failed runs and shorter troubleshooting cycles. When every day counts, the cost of a single unexpected impurity or solubility issue compounds across parallel syntheses. We provide extra support in the form of application notes, and can run pilot samples alongside a customer’s internal methods to validate the workflow.

    Recently, a biotechnology team working in peptide modification turned to this compound to effect late-stage functionalization at an aromatic anchor point. Speed and simplicity of the coupling step cut days from standard peptide array construction. Likewise, advanced materials companies utilizing this boronic acid in developing OLED intermediates sent positive feedback after iterative screening, reporting more robust fluorescence outcomes compared to unmodified phenylboronic acid.

    Across dozens of collaborative projects, we’ve hosted remote troubleshooting sessions to address coupling efficiency and reproducibility in complicated systems. These partnerships help us refine our own process and support broader research progress.

    Differentiation Rooted in Direct Manufacturing Experience

    As the producer, not a reseller, we control every step—from raw material vetting to shipment. This control allows us to respond rapidly to customer inquiries about batch traceability, new regulatory requirements, or technical challenges arising during process scale-up. It also builds trust when forecasting stock levels and managing priority projects that can’t face backorder delays. Unlike distributors shopping around for bulk pricing, we know the precise history and handling of each batch, and adjust processes based on real-world feedback.

    Direct engagement with users gives insights no catalog listing can provide. Fine chemical synthesis is an evolving field, full of nuanced requirements that don’t seem obvious in a stock photo or a checkbox on a distributor’s portal. Our ongoing R&D program means we’re constantly evaluating upstream reagents and improving in-line analytics, giving partners a transparent view into final batch analytics and supporting compliance-driven supply chains.

    Reliable Scale for Industry, Research, and Startups

    Long-term relationships with pharmaceutical majors, university research groups, and agile start-up platforms reflect the broad appeal of robust arylboronic acids. We understand that project scale can change overnight—what starts as a handful of grams for exploratory SAR work can become multi-kilo orders for preclinical manufacturing in a matter of weeks. We’ve ramped up production capacities over time, investing in new reactor blocks and semi-automated solid handling, so that we can maintain lead times even through seasonal demand spikes.

    Startups shifting between hit expansion and candidate scale-up appreciate this flexibility; we manage inventory to accommodate their shifting needs. Contract organizations often benefit from consolidated shipments and custom labeling that lines up with multi-client projects, leveraging our experience in batch reservation and contingency planning. The result: teams can focus on science without wrestling with last-minute availability issues.

    Putting Performance Data in Customers’ Hands

    We’ve learned that real performance data matter more than glossy brochures or generic assurances. Every shipment leaves our facility with lot-specific analytics—detailed chromatograms, impurity profiles, and moisture levels—not generalizations. Synthetic chemists told us early on that missing data or incomplete traceability can derail regulatory submission or process validation. Over time, we built a streamlined documentation protocol and respond quickly to custom requests for batch history, process trace elements, or cross-referenced analysis.

    Customers facing regulatory filings or patent audits receive supplementary documentation. Whether it’s for an IND filing or internal process quality reviews, our analytical packages hold up under scrutiny, creating confidence with end users and compliance departments. We support requests for additional test material, large sample runs, and one-off project needs, collaborating to smooth the regulatory journey from hit identification through to clinical or pre-commercial production.

    Collaborative Outlook: Looking Forward in Chemical Innovation

    We see the field of aryl coupling partners changing constantly, driven by both regulatory shifts and downstream innovation. Our investment in quality, sustainability, and technical support grows out of thousands of routine shipments and as many customer conversations. With every packed bottle of 4-methoxy-2-methylphenylboronic acid, we aim to support the relentless pace of scientific discovery.

    Teams in medicinal chemistry, fine chemical process development, or materials design shape the next wave of useful molecules. Our role: deliver the precise reagents needed, on time, every time. The goals remain clear—improved reactivity, reliable physical properties, lot-to-lot purity, and robust technical backup. With knowledgeable staff, a track record of consistent quality, and the openness to discuss each project’s technical details, we help move ideas from bench to industry.