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3,4-Methylenedioxyphenylboronic Acid

    • Product Name 3,4-Methylenedioxyphenylboronic Acid
    • Alias MDPBA
    • Einecs 606-037-8
    • 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
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    Specifications

    HS Code

    353256

    Chemical Name 3,4-Methylenedioxyphenylboronic Acid
    Cas Number 299182-55-1
    Molecular Formula C7H7BO4
    Molecular Weight 165.94 g/mol
    Appearance White to off-white solid
    Melting Point 184-188°C
    Purity Typically ≥ 97%
    Solubility Soluble in DMSO, methanol, and ethanol
    Storage Conditions Store at 2-8°C, protected from moisture
    Smiles B(C1=CC2=C(C=C1)OCO2)(O)O
    Inchi InChI=1S/C7H7BO4/c9-8(10)5-1-2-6-7(3-5)12-4-11-6/h1-3,9-10H,4H2

    As an accredited 3,4-Methylenedioxyphenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g package includes a sealed amber glass bottle of 3,4-Methylenedioxyphenylboronic Acid with a tamper-evident cap and labeling.
    Shipping 3,4-Methylenedioxyphenylboronic Acid is shipped in tightly sealed containers under dry, cool conditions to prevent moisture absorption and degradation. The packaging ensures chemical stability and safety, following relevant regulatory guidelines. Proper labeling and documentation accompany the shipment to comply with chemical transportation regulations and facilitate safe handling upon arrival.
    Storage 3,4-Methylenedioxyphenylboronic acid should be stored in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong oxidizing agents. Keep the container tightly closed and protected from light. Recommended storage temperature is 2–8°C (refrigerated). Avoid exposure to heat and direct sunlight to ensure chemical stability and prevent decomposition.
    Application of 3,4-Methylenedioxyphenylboronic Acid

    Applications of 3,4-Methylenedioxyphenylboronic Acid in Industrial Manufacturing

    3,4-Methylenedioxyphenylboronic Acid serves as a critical intermediate in high-value chemical syntheses within the specialized sectors of pharmaceuticals, agrochemical actives, advanced materials, and functional electronic components. As a direct manufacturer, our expertise in production and technical support enables downstream processors to integrate this compound into demanding processes requiring high purity, strict regulatory compliance, and precise formulation. The following sections outline proven, industrial-scale applications across four focused downstream domains.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Oncology Drugs

    This compound functions as a boronic acid coupling partner in Suzuki-Miyaura cross-coupling reactions during the development of kinase inhibitor drug scaffolds and advanced intermediate building blocks. Leading pharmaceutical manufacturers utilize it due to the stability of the methylenedioxy moiety in medicinal chemistry routes, particularly during late-stage diversification of aromatic structures targeting anti-tumor efficacy. The use must adhere to stringent regulatory and traceability systems, integrating with full batch and impurity profiles.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211
    • European Pharmacopoeia (Ph. Eur.) monograph references
    • Chinese Pharmacopeia (ChP) requirements for starting materials

    Typical usage ratio

    • 0.5–1.2 molar equivalents per aryl halide substrate; exact ratio tailored to synthetic efficiency and byproduct minimization during cross-coupling stages

    Downstream process integration

    • Charged to the reactor at the transition-metal catalyzed cross-coupling step, followed by direct downstream processing to advanced intermediates or crude APIs, with subsequent purification and quality control checks

    Final product types

    • Antineoplastic API intermediates (e.g., kinase inhibitors, boronate-conjugated molecules)
    • Small-molecule targeted therapy agents
    • Patented pharmaceutical bulk intermediates

    2. Agrochemical Active Compound Manufacturing

    Downstream agrochemical producers utilize this phenylboronic acid derivative for constructing oxygenated aromatic motifs found in selected herbicides and fungicides. Its utility arises in forming biaryl linkages that offer improved resistance to metabolic degradation and enhanced field stability. It must meet the approval and renewal standards established by international agricultural chemical regulations, including limits on residual boron compounds and related synthesis byproducts.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) guidelines
    • REACH Annex II requirements for intermediates
    • ISO 9001:2015 certified traceability systems
    • OECD Good Laboratory Practices (GLP) for quality control

    Typical usage ratio

    • 0.8–1.0 molar equivalents per aryl halide or vinyl coupling partner, with adjustments based on impurity load and downstream isolation yield optimization

    Downstream process integration

    • Introduced directly into batch or flow reactors during C–C cross-coupling stages, followed by downstream phase separation, isolation, and crystallization steps specific to target molecule classes

    Final product types

    • Herbicidal actives containing 3,4-methylenedioxyaryl motifs
    • Fungicidal intermediates with enhanced physicochemical properties
    • Precursor molecules for regulated crop protection agents

    3. Design and Production of OLED and Organic Electronic Materials

    Manufacturers engaged in organic optoelectronic device fabrication rely on this compound to introduce methylenedioxy-aryl structures through palladium-catalyzed cross-coupling, tuning the electronic and optical features of hole- and electron-transport materials. The purity and precise boronate reactivity are vital for consistent batch-to-batch performance in film-forming precursor solutions, requiring conformity with electronics industry standards for material quality, residual metal testing, and supply chain integrity.

    Industry compliance standards

    • IEC 60068 electronics material reliability assessment
    • JEITA/JPCA standards for organic semiconductors (e.g., JPCA-SES-01-2019)
    • RoHS Directive 2011/65/EU (for hazardous substances)
    • ISO 14001:2015 for environmental management in materials sourcing

    Typical usage ratio

    • 0.9–1.1 equivalents per halogenated aromatic monomer; higher purity grades used for direct device application formulations

    Downstream process integration

    • Loaded into precision glassware or microreactors for monomer coupling, followed by strict purification and quality testing before blending into formulation inks or spin-coating solutions

    Final product types

    • OLED emitter and transport layer precursors
    • Organic photovoltaic active layers
    • Intermediate monomers for light-emitting or conducting polymers

    4. Fine Fragrance and Flavors Intermediate Synthesis

    Within the flavor and fragrance sector, chemists source this boronic acid to create oxygenated aromatic intermediates used in high-stability scent compositions. Its structure allows for tailored modification of aromatic ethers and aldehydes critical to the formulation of long-lasting perfumery ingredients and specific food flavoring preparations. The material must fulfill food-contact and fragrance ingredient legislation while supporting efficient conversion in multi-step synthesis operations.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards for ingredient safety
    • EU Regulation (EC) No 1334/2008 for flavoring substances
    • US FDA 21 CFR 172 Subpart F (Synthetic Flavoring Substances and Adjuvants)
    • ISO 9001:2015 for traceability in flavor processing plants

    Typical usage ratio

    • 0.7–1.0 equivalents relative to aldehyde or halide components in the key fragrance or flavor intermediates’ coupling step; optimization considers sensory impact and residuals

    Downstream process integration

    • Dosed into controlled synthesis reactors during the construction of complex multi-ring fragrance intermediates, followed by downstream purification (distillation/chromatography) and blending into finished compositions

    Final product types

    • Stabilized aromatic aldehydes for fine fragrance blends
    • Methylenedioxy-functionalized ethers used in fruit or spice flavor formulations
    • Specialty perfumery intermediates for use in premium scented consumer packaged goods
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    Certification & Compliance
    More Introduction

    3,4-Methylenedioxyphenylboronic Acid: Practical Insights from the Manufacturer’s Floor

    Introduction to a Trusted Intermediate

    Making chemical products that can consistently deliver both performance and reliability takes more than just standardized procedures. After years of running our synthesis lines, we’ve come to appreciate the nuances of 3,4-Methylenedioxyphenylboronic Acid. This compound, known in our plants as one of the workhorse building blocks for Suzuki-Miyaura cross-couplings, stands out in the catalog for several reasons: purity, reliable crystallization, and its broad compatibility with a range of downstream transformations.

    Model, Specifications, and Evaluation Criteria

    Our experience with large-batch and kilogram-scale production taught us to focus on a handful of performance indicators: assay (which typically reaches 98% or higher), moisture content, and the control of residual palladium and other potential contaminants. Laboratories rely on high-purity boronic acids, and contamination or off-spec material can shut down an entire sequence of synthetic steps. To prevent that, we manage the full synthesis and purification loop in-house, using HPLC for quantitative analysis and NMR to confirm structure.

    The standard appearance is a white to off-white solid, with finely tuned particle size that’s easy to weigh and transfer. Packing is tailored for both bench-top and pilot-scale users, so material arrives free-flowing and easy to handle. Because we’ve seen how moisture can degrade boronic acids over time, the packaging is triple-layered with desiccants integrated during fill, not just as an afterthought. We monitor shelf stability, running real-time checks, so the product remains stable from our warehouse to your bench.

    Why We Chose This Compound for Broad Synthesis

    Our research chemists chose 3,4-Methylenedioxyphenylboronic Acid after comparing yields and downstream reactivity with multiple candidates. The compound offers a clean route for constructing biaryl and heteroaryl frameworks, especially where sensitive functional groups limit the choices for coupling partners. The methylenedioxy motif doesn’t just decorate the molecule; it opens doors for medicinal chemistry and agrochemical exploration, forming the backbone of hundreds of lead optimization studies.

    Handling this compound in production highlights subtle details that researchers don’t see on paper. Isomeric impurities, which crop up easily in related phenylboronic acids, are rare—we monitor for these, especially after receiving feedback from process development teams who experienced side-product headaches from other suppliers’ stocks. Over time, our technical teams identified ways to optimize the reaction work-up and crystallization to leave less room for error or batch-to-batch drift. That’s why returning customers often cite our lot-to-lot consistency as the reason they specify our product during scale-up.

    Comparisons and Distinctions from Other Boronic Acids

    The boronic acid family covers a vast landscape, from simple unsubstituted phenylboronic acid to fluorinated, nitro-substituted, or polycyclic types. Each has its quirks. With 3,4-Methylenedioxyphenylboronic Acid, the key distinction lies in its electron-rich aromatic core, courtesy of the dual oxygen bridge. Unlike plain phenylboronic acid, reactivity in Suzuki couplings frequently proves higher, thanks to stabilization of reactive intermediates. Chemists working with electron-deficient coupling partners find this compound gives more consistent conversion, which matters when margins are tight and time is precious.

    Many clients ask about alternatives or “equivalents.” Some look at 3,4-dimethoxyphenylboronic acid or 3,5-substituted versions. From production data and collaboration with client development teams, we’ve seen that switching substituents can introduce hidden variables—lower melting points, higher hygroscopicity, even different rates of protodeboronation. Our product holds up better than its analogs under a typical aqueous work-up or when left on the bench. That keeps the process predictable. With other boronic acids, batch failures can creep in from minor formulation changes or missed moisture controls.

    Another vital difference comes from by-product profile and ease of purification. In our QC lab, monitoring every run, we see cleaner baseline readings and fewer trace side-products than with many ortho- or para-substituted boronic acids. Chemists on a tight timeline value not having to set up multiple column purifications just to remove trace contaminants.

    Applications and Use Cases: From Bench to Commercial Scale

    Medchem teams often turn to boronic acids for rapid library synthesis. Our product routinely finds its way into combinatorial arrays at CROs and in biotech discovery labs worldwide. We’ve observed that as library sizes scale up, small inconsistencies can multiply into big hurdles. We ship in both multi-gram lab vials and larger, process-ready drums. Clients report not only solid engagement at the library stage, but also smooth translation into process development, where solvent compatibility and speed of dissolution matter.

    In process chemistry, pilot and commercial-scale teams need to avoid bottlenecks. Designed with production priorities in mind, our 3,4-Methylenedioxyphenylboronic Acid streamlines catalyst choices and base compatibility. Over months of pilot runs, we recorded reproducible volume recovery and minimal fouling in reactors. Switching to this material from alternative boronates has, in several cases, reduced cycle times and improved total yields. These are results that only become clear after direct scale-up experience, not just by reading the catalog.

    API manufacturers lean on this compound for its reliability in late-stage functionalization. Our partnerships with pharma teams—governed by confidentiality—sometimes lead to new process tweaks, further refining particle consistency and residual metal content. It pays to maintain an open channel with clients working on tight regulatory timelines; process interruptions from material inconsistencies are unacceptable in these settings.

    Process Reliability and Batch Management

    From an operator’s viewpoint, reproducibility starts with a careful charge of reagent and solvent. Over hundreds of runs, we noticed that careful control of exotherms during borylation led to tighter particle distributions and easier downstream filtration. Rollouts of process changes are always supported by real-lot analytical data. Working directly with end users, not through a distributor, we incorporate suggestions into our SOPs: tweaks in water content control, shifts in drying curves, or changes in packaging style.

    We check everything with real analytical methods, not just spot-testing or relying on a single method. Each lot passes through NMR, HPLC, and GC, then the data get compared to a running historical file—this helps us catch trends early. For customers who need trace metal control, we test for palladium, copper, and iron, using ICP-MS where required. Our teams treat every data point as a tool for better process management, not just a compliance checkbox.

    Quality Commitment Rooted in Shop-Floor Realities

    Laboratory-grade boronic acids have to be clean, dry, and uniform, but shop-floor reality means upsets can strike anywhere from raw material procurement to crystallization. We keep strategic oversupply on critical reagents, source only from vetted partners, and trace every raw material to its origin. When a shipment of a key precursor once came in with an off-spec impurity profile, we were able to divert it before it reached downstream processing—and that saved a week’s worth of work. Learning to expect supply chain headaches has led us to prioritize relationship-based sourcing and constant QC oversight.

    Fielding customer requests for special particle size or custom assays is part of our day-to-day. Working with dedicated purification hardware, we can tweak the final drying cycle or reprocess lots to improve performance for specialized users. Our technical support team responds directly from the production site, so feedback goes straight to the relevant department, not through a call center. These details matter for time-sensitive programs in pharma and specialty manufacturing alike.

    Stability, Storage, and Real-World Handling

    Boronic acids sometimes draw complaints about instability during storage. This class of organics reacts with water and oxygen, risking degradation and performance loss. We learned this through more than one frustrated request for a replacement shipment. To address that risk, we run real-time as well as accelerated aging studies. The latest storage protocols recommend sealed containers under inert gas, but we also monitor user feedback on field performance, because lab chaos rarely matches the tidy shelf stability outlined in textbooks. Adjustments to packaging, drying schedules, and inventory control allow us to provide consistent product for both short-term usage and longer-term storage.

    It’s not unusual for a chemist to call after months, asking if the “old sample” remains viable. We base answers on actual shelf-life data, not guesswork, drawing from both stability studies and batch records going back several years. Chemists juggling multiple boronic acids in parallel projects often line up our material against analogs from other suppliers, measuring weight loss or moisture pickup after repeated handling. Reports show our product resisting clumping or color change better than close relatives with similar structures.

    Troubleshooting and Technical Support

    Practical work with boronic acids often reveals issues the literature glosses over. During multi-step syntheses, side reactions or decomposition can creep in, derailing timelines. We hear from project teams who’ve faced unexpected setbacks when trying to swap in cheaper alternatives. Having context built on production and post-market feedback, our technical advisors rely on bench data to suggest realistic workarounds—whether adjusting base loadings in Suzuki couplings, or running test reactions to validate catalyst compatibilities.

    Customers often consult us about problems ranging from solubility quirks to variable reactivity. Since we track and document complaints across batch histories, we’ve built a knowledge base informing tweaks for entire process lines, not just one-off fixes. Our ability to re-synthesize or re-process customized material draws from this depth of field experience, ensuring reliable solutions grounded in operational reality.

    Environmental and Regulatory Considerations

    Sustainability and compliance shape many choices in chemistry today. We monitor waste generation closely, aiming for minimal releases during both synthesis and purification. Our boronic acid line, including this compound, ships with supporting analytical documentation, easing the path for audit or regulatory filing. Overhauls in solvent use, upgrades in filter technology, and reduction in heavy metal drag-through are ongoing—in part because real gains come from constant shop-floor vigilance, not policy statements.

    Engaging directly with customers working on regulated APIs, we answer technical queries about extractables, leachables, and trace impurities with actual technical reports rather than templated customer service replies. Over the last review period, our customers passed dozens of audits using our documentation.

    We believe everyone wins if process chemistry gets more transparent, from batch genealogy to full traceability. Companies on a regulatory deadline want quick, honest answers—so we aim to keep all supporting data immediately accessible.

    Practical Upgrades and Innovations

    Improvements don’t always come from the top down. Floor staff regularly propose tweaks to workflow or purification, sometimes catching easier fixes than any top-down review. We empower operators and QC analysts to log process observations and recurring issues, leading to incremental, real-world enhancements. Last year, small cycle modifications cut drying time 18% and reduced clumping—a benefit confirmed through both handling feedback and real-world shipping stress tests.

    We log any process deviation, interrogate every batch turnaround, and use the data to trigger investigations or process upgrades. This cycle of continuous review means that when customers push our compound into new territory—whether it’s late-stage GMP pharmaceutical intermediates, fine-chemistry niches, or research-scale screenings—we’ve got the experience and flexibility to match.

    Looking Ahead: Supporting Innovation at Every Scale

    Chemistry isn’t static, and neither are the demands of our customers. From rapid library development to scale-up for commercial launches, our approach to 3,4-Methylenedioxyphenylboronic Acid reflects years of synthesis, testing, customer feedback, and hard-learned lessons from real-world complications. Reliability comes not from a single “gold standard” process, but from hundreds of incremental improvements and a readiness to adapt.

    Direct connection with users in pharma, fine chemicals, and biotech synthesis lets us stay tuned to tomorrow’s challenges. Our technical teams are always ready to support new project directions—should a client need extra-pure material for a crucial coupling, or new packaging to better protect long-term stocks, we welcome those requests and act on them quickly. That’s the value of staying close to the manufacturing process, and to the people who rely on it.

    Summary of Key Advantages

    Reflecting on daily work at the plant, advantages consistently recognized by our clients include: batch-to-batch consistency, control over particle size, rapid response to technical queries, and reliable, transparent QC records. These strengths didn’t come from theory—they come from the challenge and satisfaction of solving real process problems, together with customers who share our commitment to quality and innovation.

    Every shipment of 3,4-Methylenedioxyphenylboronic Acid carries forward this accumulated experience; each lot is more than “just” a chemical—it’s a tested, trusted intermediate that builds success in labs around the world. For every project manager, operator, and chemist counting on timely, reproducible results, we keep that promise at the core of our work.