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4-(Bromomethyl)Phenylboronic Acid

    • Product Name 4-(Bromomethyl)Phenylboronic Acid
    • Alias 4-(Bromomethyl)benzene-1-boronic acid
    • Einecs EINECS 695-963-9
    • 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

    440623

    Productname 4-(Bromomethyl)Phenylboronic Acid
    Casnumber 851414-76-3
    Molecularformula C7H8BBrO2
    Molecularweight 214.86
    Appearance White to off-white powder
    Meltingpoint 170-174°C
    Purity Typically ≥ 97%
    Solubility Slightly soluble in water, soluble in organic solvents
    Storageconditions Store at 2-8°C, protect from moisture
    Synonyms 4-Bromomethylphenylboronic acid
    Smiles B(C1=CC=C(C=C1)CBr)(O)O
    Inchi InChI=1S/C7H8BBrO2/c9-5-6-1-3-7(4-2-6)8(10)11/h1-4,10-11H,5H2

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

    Packing & Storage
    Packing Amber glass bottle, tightly sealed, labeled "4-(Bromomethyl)Phenylboronic Acid, 5 grams," with hazard warnings and lot number clearly printed.
    Shipping 4-(Bromomethyl)Phenylboronic Acid is shipped in tightly sealed, chemical-resistant containers under ambient conditions. The packaging ensures protection from moisture, light, and physical damage. All shipments comply with relevant hazardous material regulations and include labels and documentation. Handle with appropriate safety precautions upon receipt to ensure safe storage and usage.
    Storage **4-(Bromomethyl)phenylboronic acid** should be stored in a cool, dry, well-ventilated area, tightly sealed in a moisture-proof container, and protected from light. Avoid exposure to heat and incompatible substances such as strong oxidizers. Refrigeration (2–8 °C) is recommended for long-term stability. Ensure proper labeling and keep away from sources of ignition and direct sunlight.
    Application of 4-(Bromomethyl)Phenylboronic Acid

    Applications of 4-(Bromomethyl)Phenylboronic Acid in Industrial Manufacturing

    As the original manufacturer, we supply 4-(Bromomethyl)phenylboronic acid to support specialized and high-value synthesis across select downstream industrial sectors. Our product consistently meets advanced purity and quality benchmarks demanded by our direct B2B partners. Below, we provide a structured overview of the principal real-world application routes, focusing on the full context of compliance, formulation, production integration, and final product types.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) Synthesis

    Our material serves as a crucial coupling partner in Suzuki-Miyaura cross-coupling processes for the construction of biaryl scaffolds used in targeted anticancer, antiviral, and metabolic disorder drugs. Process chemists in the pharmaceutical sector leverage the compound’s dual functional groups to efficiently construct intermediates while minimizing byproduct formation. This application requires rigorous traceability from raw material to release testing in bulk API manufacturing.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II
    • USP–NF and Ph. Eur. monographs for relevant intermediates and APIs
    • 21 CFR Part 211: cGMP for Finished Pharmaceuticals (where integrated with final steps)

    Typical usage ratio

    • 0.8–1.2 molar equivalents relative to aryl halide or boronic acid partner, optimized per API target and reaction scale

    Downstream process integration

    • Direct addition to catalyst-charged reactors in medicinal chemistry labs and multi-ton industrial reactors during key C-C bond-forming steps

    Final product types

    • Pharmaceutical intermediates for kinase inhibitors
    • Hepatitis compound APIs
    • Aromatic building blocks for next-generation API development

    2. Agrochemical Intermediate for Herbicide and Fungicide Synthesis

    Major agrochemical manufacturers apply this boronic acid as an essential intermediate for synthesizing aryl-substituted active ingredients with improved potency and crop selectivity. Its bromomethyl and boronic functionalities enable precise stepwise construction of new compounds for broad-spectrum herbicides and systemic fungicides, meeting both regulatory and field-performance criteria.

    Industry compliance standards

    • FAO/WHO Pesticide Specifications
    • REACH (EC) No 1907/2006 registration for chemical intermediates
    • ISO 9001:2015 Quality Management Standards for manufacturing
    • EPA guidelines for toxicological screening (40 CFR Parts 150-189 for U.S. registration)

    Typical usage ratio

    • Selected 0.5–1.5 molar equivalents based on stoichiometry per target synthesized molecule, with adjustment depending on product scalability and impurity profile control

    Downstream process integration

    • Fed-batch and continuous flow reactors during formation of aryl-fused ring systems or after halogen-metal exchange steps in agrochemical synthesis lines

    Final product types

    • Active ingredient intermediates for post-emergence herbicides
    • Precursors for azole fungicide analogs
    • Key aromatic units for proprietary agrochemical formulations

    3. Development of OLED and Organic Electronic Materials

    R&D and production teams within the specialty electronic materials sector employ this boronic acid for Suzuki coupling in the construction of electron-transport and emissive-layer polymers for organic light-emitting diode (OLED) displays and solid-state lighting. The compound’s high purity profile directly affects the electronic and photophysical properties required by next-generation display and lighting devices.

    Industry compliance standards

    • RoHS 2011/65/EU (Restriction of Hazardous Substances in Electronics)
    • ISO 14001: Environmental Management Systems (for supply chain transparency)
    • Customer-specific QA/QC protocols for metal and halide content

    Typical usage ratio

    • 1.0 molar equivalent per aryl halide monomer; final ratios depend on molecular weight targets and polymer chain length distributions

    Downstream process integration

    • Direct charge in inert-atmosphere polymerization reactors at pilot and production scales, typically during the fabrication of emitter or matrix polymer precursors

    Final product types

    • Organic electroluminescent emitter materials for high-brightness OLED panels
    • Hole or electron-transport layers in organic semiconductors
    • Intermediate monomers for flexible display manufacturing

    4. Specialty Fine Chemicals for Advanced Material Synthesis

    Producers of specialty fine chemicals utilize this compound to access functionalized aromatic systems necessary for advanced polymer additives, responsive sensor materials, and molecular probes. The unique boronic acid and bromomethyl combination allows targeted derivatization for high-value materials with precise reactivity and selectivity specifications.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management in Fine Chemical Manufacturing)
    • Applicable local/regional chemical registration (TSCA in U.S., REACH in EU)
    • Customer-driven purity and trace impurity specifications (often <100 ppm for key trace metals and halides)

    Typical usage ratio

    • Varies from 0.2 to 1.5 molar equivalents, determined by end-product functionalization level, with lab optimization frequently required for novel compounds

    Downstream process integration

    • Charged in batch or microfluidic reactors, typically following pre-activation or protection steps to allow selective conversion to high-purity fine chemical derivatives

    Final product types

    • Functionalized specialty monomers for high-performance polymers
    • Site-specific sensor probe precursors
    • Building blocks for smart material R&D
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    Certification & Compliance
    More Introduction

    4-(Bromomethyl)Phenylboronic Acid: Proven Reliability from the Manufacturer’s Floor

    What Sets Our 4-(Bromomethyl)Phenylboronic Acid Apart

    Years of hands-on production experience have shaped the way our team approaches 4-(Bromomethyl)Phenylboronic Acid. This compound, with a molecular structure distinguished by its bromomethyl functional group linked to a phenylboronic acid core, sees real demand from synthetic chemists looking to create more complex molecules. We have observed that demand spike over time, especially in pharmaceutical and material science labs where adding structural diversity is a must for new project lines or improving property profiles in active molecules.

    Our 4-(Bromomethyl)Phenylboronic Acid comes with strict identity confirmation not as a matter of marketing, but because our reactors, purification columns, and analysis equipment have been tested under real use conditions. Our purity consistently hits or exceeds 98%, which is measured batch by batch. If you cut corners here, with lower-grade inputs or without in-process controls, side reactions start taking over, and final yields drop or impurities show up late in development. We keep contamination, moisture content, and trace metal levels in check because uncontrolled traces spoil Suzuki coupling, cross-coupling, and follow-up functionalization.

    Model and Specifications from Our Own Operation

    The material comes in a powder form with a white to off-white appearance. Those who handle real chemistry projects know that even a faint yellow tint signals breakdown or impurity. We make sure storage conditions are documented, but more importantly, our operators observe actual shelf stability. The material behaves in a reasonably air-stable way due to conscientious packing and regular batch checks—there’s less caking and less risk of hydrolysis compared to less carefully manufactured alternatives.

    Key physical constants, such as the melting point, matter to downstream users. Our melting point ranges typically reflect product consistency, hovering predictably between 165 and 172°C. That consistency signals a reliable process, not luck or chance. It comes from controlling air, water, solvents, and handling at every scale, from grams to kilos. LC-MS and NMR spectra data are generated internally, so there’s no mismatch in specs or ambiguity for researchers and formulation teams.

    Direct Insights: Real-World Usage and Application

    Boronate chemistry stands out for Suzuki–Miyaura reactions, and the bromomethyl handle of this compound often serves for follow-on chemistry. We receive regular feedback from medicinal chemists at upstream pharmaceutical innovators and intermediate manufacturers. They confirm that our material enables straightforward coupling with aryl and alkyl halides. The ortho-para relationship between the boronic acid and bromomethyl groups pushes high selectivity—yielding the expected cross-coupled products with little undesired substitution.

    Unlike basic phenylboronic acids, the bromomethyl substituent opens up series possibilities: N-alkylation, nucleophilic displacement, or further functionalization for molecular scaffolding. Some clients mention downstream difficulty if the starting acid harbors impurities like dibrominated compounds; we solve that with in-line purification and post-crystallization analytics. We’ve had customers return after struggling with jagged chromatograms and reactivity problems from other sources. These hurdles disappear when consistency takes priority at the manufacturing stage.

    Custom-run synthesis for R&D batches always stays close to scale-up prototypes for commercial batch manufacture, so bench-to-pilot data match up. The result is shorter verification cycles for clients, fewer surprises converting lab findings into plant-scale success, and better fit when regulatory documentation is needed. Practically, this saves months during the critical moments of patent races or IND filings in drug discovery settings.

    Comparisons with Other Phenylboronic Acid Products

    Some believe all boronic acids perform as interchangeable building blocks, but several real-world cases refute this. Standard phenylboronic acids (no substituents or those with less reactive side groups) hit a wall for iterative chemistry, with bulky or electronically neutral groups stalling reactivity. The 4-(Bromomethyl) group punches above its weight: chemists use the activated bromide not only for Suzuki coupling but for tethering new fragments, ring closures, and alkyl chain extensions—applications that regular phenylboronic acid cannot address efficiently.

    Manufacture of halogenated boronic acids brings additional risk of side reactions. Unlike the more forgiving plain phenylboronic acid, which tolerates broader water and heat exposure, our experience shows that 4-(Bromomethyl)Phenylboronic Acid demands careful low-temperature and dry-environment protocols. The bromomethyl group reacts more vigorously, and purity loss tracks very quickly with lax physical controls. We structure our batch operations, solvent recovery, and post-processing with these needs in mind. Where others let solvent residues slide, we have learned from failed scale-ups that stability drops fast when residual methanol or DMF persists after crystallization.

    Contamination from dibromo- or non-symmetrical substitution leads to batch rejections—an unacceptable outcome for us and for anyone working in preclinical or clinical chemistry. By pushing each batch through NMR and HPLC checks under full scan conditions and offering trace impurity documentation, we give researchers peace of mind when they’re assembling highly regulated or property-sensitive molecules. This direct link from factory practice to end-user value sets our material apart.

    Our Manufacturing Principles Meet Today’s Quality and Transparency Standards

    Questions about origin, authenticity, and traceability never slow down orders here. Each production run comes with an audit trail, keeping quality managers and regulatory affairs officers content. Customers count on reliability and openness, and we don’t dodge the need for technical documentation: we provide real batch data, not generic marketing summaries.

    Genuine manufacturing experience brings an understanding of risk management. From our perspective, mitigating batch-to-batch variation isn’t optional—no researcher wants to chase false positives because of careless input chemicals. Years of refining our process mean in-process controls, moisture checks, and impurity tracking actually happen, improving both operational yields and reliability for downstream users.

    We frequently supply to clinical candidates, scale-up programs, and academic researchers. Their care in selecting reagents tells us that transparency matters—knowing the source and integrity of intermediates can decide the success or failure of a project. We proactively monitor and update process protocols according to any changes in global standards or best practices popular in the field, keeping internal documentation accessible for external review when relevant.

    Safety, Handling, and Regulatory Considerations Shaped by First-Hand Knowledge

    Handling a halogenated aromatic boronic acid requires practical safety protocols and environmental awareness. Real process safety comes from being close to the ground—our operators and QC laboratories have encountered the common failure points, from exotherms during batch charging to dust control issues at the packaging stage. To avoid runaway reactions in the plant, we keep temperature and agitation profiles under stringent control, never losing sight of the hazards hidden in energetic intermediates and reactive byproducts.

    Proper PPE, local exhaust, and handling protocols translate to safer downstream operations. There’s no substitute for real process experience—practically, this means tight bottling controls, robust leak prevention during transfer, and rigorous waste tracking for residues. Customers building their own safety dossiers for regulatory submissions in pharma, agrochemicals, or electronics appreciate receiving clear GHS labeling and hazard classification information, so integration with their own safety management becomes seamless.

    Solving Common Challenges in Cross-Coupling Chemistry with Consistent Input Materials

    Chemists at the bench rely on robust boronic acids for their coupling chemistry, but problems often stem from inconsistent input material. We’ve seen conversions drop and byproducts rise when suppliers ignore tiny shifts in impurity or water content. That risk disappears with real manufacturing discipline. When evaporation, distillation, and inert gas protection are enforced at scale, our product keeps its shelf life and lets researchers repeat critical reactions without setbacks.

    Our technical teams support process scale-up and troubleshooting. They have witnessed cast-offs producing unpredictable behavior in test runs—which get solved when users switch to a controlled, consistent source. Bridging the gap from small-scale bench synthesis to commercial or kilo lab production brings unique hurdles, but by holding process variables steady, our product helps chemists reduce work-up and purification steps, saving on both cost and timeline.

    Some researchers face sluggish coupling rates or incomplete conversion because of cheap, under-purified starting material. Real improvements show up when they switch to our high-spec boronic acid—reaction times drop, side products shrink, and reproducibility goes up. That isn’t theoretical: customer feedback and our own internal R&D confirms the value of using a material made by process experts who’ve optimized not just the chemistry, but also the operational workflow behind it.

    Environmental and Supply Chain Accountability

    Responsibility comes with large-scale manufacturing. We implement business practices that track solvent use, waste production, and emissions. Regular audits drive improvements and transparency for partners who want documented environmental impact; requests for origin and traceability are met with actual process history instead of standard templates. This builds trust, not only with regulatory inspectors but also with procurement teams working for multinational customers.

    Managing sourcing from raw materials on up means we anticipate possible shortages and monitor geopolitical events. By developing multiple supply lines for our own upstream inputs, we shield our production and customer orders from disruptions. Our warehouse, batch planning, and volume forecasting use live updates from the factory floor, never simply reacting to seasonal swings in logistics or price shocks.

    Continuous Improvement Based on Direct Industry Feedback

    The manufacturing world moves fast—tools, standards, and requirements never sit still. Our teams don’t rest on checked boxes: feedback loops with downstream users and a steady flow of information from chemists and engineers help us spot weak points or improvement areas. If a customer points out a handling issue or requests an analytical parameter not found in standard literature, we run verification in our labs and update our protocols, keeping the communication clear and the improvements ongoing.

    Collaborating closely with academic labs, biotechs, and global pharmaceutical developers keeps our approach grounded in how chemistry actually happens. This lets us share firsthand advice about material compatibility, handling quirks, or scale-up solutions. Instead of chasing trends or overstating capabilities, we share the reality that process optimization, quality, and transparency require open dialogue. That’s built into our approach, not bolted on afterwards.

    A Manufacturer’s Perspective on the Real Value of 4-(Bromomethyl)Phenylboronic Acid

    Some see specialty boronic acids as just another entry in a catalog, but real manufacturing experience makes clear that not all sources deliver what advanced chemistry needs. Our teams see firsthand the difference between bulk intermediates processed casually and those built for demanding environments. For new drug candidates, OLED precursors, and fine-chemistry toolkits, every step—from raw material vetting to packing controls—affects your ability to innovate and scale.

    We don’t bypass thorough training or quality investment just to cut corners on price. The value of 4-(Bromomethyl)Phenylboronic Acid built on careful source control pays off in faster R&D cycles, real reproducibility, and the peace of mind engineers and chemists count on. Our direct manufacturing expertise means we stand behind every shipment with a track record proven in the lab and at scale. When quality, purity, and reliability shape the future of your discoveries, a controlled, experienced source becomes more than a vendor—it becomes part of your process.