Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

4-Bromophenylboronic Acid

    • Product Name 4-Bromophenylboronic Acid
    • Alias AKOS BBS-00003443
    • Einecs 613-292-1
    • 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

    111135

    Name 4-Bromophenylboronic Acid
    Synonyms 4-Bromobenzeneboronic acid
    Cas Number 5118-13-8
    Molecular Formula C6H6BBrO2
    Molecular Weight 200.83 g/mol
    Appearance White to off-white powder
    Melting Point 285-289°C (dec.)
    Solubility Slightly soluble in water
    Purity Typically ≥ 97%
    Smiles B(C1=CC=C(Br)C=C1)(O)O
    Inchi InChI=1S/C6H6BBrO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4,9-10H
    Storage Conditions Store at room temperature, keep container tightly closed

    As an accredited 4-Bromophenylboronic 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-Bromophenylboronic Acid comes in a sealed amber glass bottle with a screw cap and safety labeling for laboratory use.
    Shipping 4-Bromophenylboronic Acid is shipped in tightly sealed containers, typically under inert atmosphere to prevent moisture exposure. Packaging complies with relevant chemical transport regulations. It is handled as a hazardous material, ensuring safety with appropriate labeling and documentation, and is generally shipped by ground or air according to international chemical shipping standards.
    Storage 4-Bromophenylboronic acid should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong oxidizers. Keep it out of direct sunlight and at room temperature or as recommended by the manufacturer. Avoid exposure to air and humidity to prevent degradation and ensure product stability.
    Application of 4-Bromophenylboronic Acid

    Applications of 4-Bromophenylboronic Acid in Industrial Manufacturing

    4-Bromophenylboronic acid serves as a crucial intermediate in advanced organic synthesis. Its unique boronic acid structure enables cross-coupling technologies, facilitating the production of high-value chemicals across several industrial sectors. Below we present verified downstream application paths, each with compliance, usage, process, and end-product specifics drawn from real manufacturing practice.

    1. Pharmaceutical Active Ingredient Synthesis

    Manufacturers of small-molecule drugs use this compound as an essential building block in Suzuki-Miyaura coupling reactions to form biaryl and aryl-heteroaryl bonds. It plays a vital role in synthesizing kinase inhibitors, anti-tumor agents, and cardiovascular pharmaceuticals—often as a core component for introducing a brominated aromatic ring. Production lines incorporate it at early or intermediate steps, ensuring consistency in batch integrity and allowing precise structural modifications. Strict material traceability and validation govern the integration process, supporting cGMP manufacturing protocols for regulated drug molecules.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (Finished Pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) and United States Pharmacopeia–National Formulary (USP–NF) requirements for raw materials
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • Applied at 1.0–1.5 molar equivalents relative to halogenated coupling partners; actual ratio depends on target molecule and process route
    • Reaction scales often 0.1–10 kg batch depending on clinical or commercial supply requirements

    Downstream process integration

    • Direct input in Suzuki cross-coupling during intermediate or final synthetic steps
    • Heated under inert atmosphere using Pd-catalysts and suitable base in aqueous-organic mixtures
    • Subsequent deprotection, purification, and QC at each stage

    Final product types

    • Small molecule kinase and protease inhibitors
    • Novel anti-cancer compounds
    • Pharmaceutical reference standards
    • Specialty intermediates for clinical trial material

    2. Electronic Material Precursors (OLED and Display)

    Display panel producers and OLED material formulators employ 4-bromophenylboronic acid as a source for developing rigid biphenyl or heteroaryl frameworks used in emissive layers and charge transport materials. Precision use enhances photoluminescent efficiency in devices by enabling well-defined molecular architectures. Electronic grade material is utilized under strictly controlled cleanroom conditions, ensuring low ionogenic impurities, which are critical for thin-film device stability. This compound enables scalability in synthesis for downstream vapor deposition or ink formulations.

    Industry compliance standards

    • JEITA Standard EM-3601B for organic materials in electronic components
    • RoHS Directive (EU) 2015/863 on hazardous substances restrictions
    • ISO 14644 Cleanroom Standards for contamination control
    • IEC 61249 series for base materials in printed wiring assemblies

    Typical usage ratio

    • 0.8–1.2 equivalents compared to co-coupling aryl halide reagents; adjusted per emission spectrum requirements
    • Batch inputs measured in gram to multi-kg scale for pilot or commercial runs

    Downstream process integration

    • Key ingredient for cross-coupling assembly of small molecules and polymers used in active display layers
    • Feeds directly into vacuum deposition, spin coating, or inkjet printing formulations after synthesis
    • After coupling, further purified by recrystallization or chromatography for minimal trace contamination

    Final product types

    • OLED device emissive and transport layer compounds
    • Organic semiconducting polymers for thin-film transistors
    • Photoresist sensors and display coatings
    • Active layers for flexible electronic displays

    3. Agrochemical Intermediate Manufacturing

    Pesticide and herbicide industrial plants use this boronic acid component to construct advanced agricultural actives through palladium-catalyzed couplings. Manufacturers select it for introducing bromo-substituted biaryl units, which are prevalent in new-generation crop protection chemicals. The compound ensures reproducible yields and contributes to chemical selectivity, reducing unwanted by-product formation. Material management under Responsible Care and REACH protocols safeguards environmental and occupational safety throughout the process chain.

    Industry compliance standards

    • European REACH Regulation (EC) No. 1907/2006
    • ISO 14001 Environmental Management Systems
    • FAO/WHO specifications for pesticide manufacturers (JMPS)
    • Responsible Care Global Charter for chemical facilities

    Typical usage ratio

    • 0.95–1.1 molar equivalents based on reaction efficiency and target molecule complexity
    • Process batches typically 10–500 kg, adjusted for campaign production scale

    Downstream process integration

    • Reacted in key C–C coupling steps to install substituted phenyl rings during intermediate or penultimate stages
    • Feeds directly into step-growth synthesis for complex apiary or crop actives
    • Material passes through purification, formulation, and quality controls prior to authorized market release

    Final product types

    • Biphenyl herbicide active compounds
    • Systemic fungicide intermediates
    • Selective insecticide raw materials
    • Registered plant growth regulator bases

    4. Specialty Polymer Monomer Synthesis

    Advanced engineering polymer and resin manufacturers utilize this compound to prepare functionalized aromatic monomers for use in high-performance thermoplastics and specialty copolymers. The regulated introduction of bromoaryl units modifies mechanical and thermal properties, facilitating new materials for electronics encapsulation, separation membranes, and chemical-resistant coatings. Application typically involves solution or melt-phase polymerizations, where purity influences polymer chain uniformity and performance predictability in demanding end uses.

    Industry compliance standards

    • ISO 9001 Quality Management for specialty polymer production
    • UL 94 Flammability Standards for plastics
    • ASTM D638 for polymer mechanical properties testing
    • REACH and TSCA inventory verification for monomer inputs

    Typical usage ratio

    • 0.5–1.2:1 molar ratio relative to secondary monomer or comonomer; actual dose set by target polymer structure
    • Added in pilot (1–10 kg) or industrial (10–500 kg) quantities based on batch scale

    Downstream process integration

    • Incorporated during pre-polymerization monomer charging or as a functional end-cap in solution/melt reactors
    • Mixed directly with other aromatic and non-aromatic monomers to establish block or random copolymer architectures
    • Post-polymerization purification by precipitation or extraction before compounding and processing

    Final product types

    • High-performance aromatic polyesters and polyamides
    • Membrane separation films with enhanced selectivity
    • Electronics encapsulation resins
    • Chemically resistant industrial coatings
    Free Quote

    Competitive 4-Bromophenylboronic Acid prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    4-Bromophenylboronic Acid: A Closer Look from the Manufacturing Floor

    Understanding the Backbone of Cross-Coupling Chemistry

    Walk into our batch reactor hall on any given morning and you’ll likely spot the telltale barrels set aside for today’s run of 4-Bromophenylboronic Acid, or 4-BPBA as we call it on the floor. Chemists who work daily with Suzuki-Miyaura and other palladium-catalyzed couplings know the value of a clean, consistently pure boronic acid. Our job as manufacturers isn’t just to deliver another flask of powder or crystalline compound—it’s to provide a robust, reliable reagent that does not leave you second-guessing yield, purity, or batch reproducibility.

    What specifics separate a competent supplier from one worthy of your trust? Every kilo of 4-Bromophenylboronic Acid that leaves our plant is the product of several decades of scaled organic synthesis and hands-on troubleshooting. Our approach is grounded in details, frankly, overlooked by the catalogs and intermediaries that fill the market with generic offerings and broad technical bulletins.

    A Practical Perspective on Specifications

    4-Bromophenylboronic Acid boils down chemically to C6H6BBrO2. It manifests as a pale solid, distinguishable by a faint pink tinge if handled incorrectly, which flags oxidative degradation. In-house, each reactor is flushed with nitrogen before charging solvents, and we keep oxygen levels as low as possible throughout synthesis. Over the years, we learned this isn’t an academic exercise. Even trace oxygen can shift a batch out of specification, impacting your chromatography results downstream. Our standard runs meet a minimum purity of 99.5% HPLC—verified in-house with both HPLC and GC analysis, not least because certain impurities elude one technique but not the other.

    Water content sits beneath 0.5% (Karl Fischer, daily calibration checked). Some suppliers gloss over residual moisture, assuming end-users will dry samples before use. Through dozens of custom projects—especially contract manufacturing for pharma intermediates—we witnessed what happens when assumptions fail: variable stoichiometry, failed reactions, wasted palladium, lost time. We address water at every stage. After isolation, vacuum ovens with regulated temperature ramps ensure crystals never melt or decompose. We don’t ship anything without logging residual solvent screening, either. The most diligent user deserves transparency, not excuses.

    Sourcing and Raw Material Traceability

    The bromobenzene feedstock forms the backbone for multiple downstream products here. Our procurement team sources the starting materials from regularly audited partners. Contractual samples get pulled every quarter and sent for full impurity profiling. Many forget that the quality of a single barrel of bromobenzene can set the tone for months of manufacturing. Bad feedstock doesn’t just waste a day on the line; it can derail R&D and cost you credibility with your own customers. We’ve found an open relationship with raw-material suppliers pays off tenfold in finished product reliability.

    Synthetic grade solvents in our process cycle back through triple distillation trains. For larger-scale production, solvent recovery isn’t just about sustainability. Residual methyl ethyl ketone or tetrahydrofuran left in your 4-BPBA can interfere with binding sites in catalyst systems or result in NMR peaks that muddy structure elucidation. As a manufacturer, we control our solvent grades and maintain careful separation between production trains, because mixing “just once” to save costs always snowballs into greater problems.

    Why Do Small Differences in 4-BPBA Matter?

    Some colleagues in academia tell us that if a boronic acid passes melting point and TLC, it’s “pure enough.” Anyone who’s run late-stage Suzuki couplings under time pressure will tell you otherwise. Small nuances in the crystal lattice—caused by subtle isomer contamination or inadequate washing—lead to erratic dissolving behavior. For automated reactions, unexpected insolubility results in failed screens or needlessly repeated runs. We fine-tuned our crystallization and filtration protocols so that what you pull from our drum on day one will match the aliquot you save for day thirty, every time.

    Another difference rests in how we package the finished acid. Boronic acids readily suck up moisture from air, sometimes deteriorating within hours. We spent several seasons testing polyethylene versus laminated foil liners, discovering that a properly sealed, desiccated atmosphere protects the powder months after opening. QC checks every drum for seal integrity rather than cutting corners with off-the-shelf containers. We want you to be as confident in the first weigh sample as the last.

    Common Uses and Real-World Impact

    4-Bromophenylboronic Acid features most heavily in pharmaceutical, agrochemical, and advanced materials synthesis. It plugs into Suzuki couplings with halogenated aryls and various vinyl groups, yielding biaryls and styrenic building blocks. Contract clients designing kinase inhibitors or new OLED frameworks rely on consistent 4-BPBA quality for series scale-up. In the past, fluctuations in melting point or excess chloride had brought some clients batches of poor results—not because the chemistry failed, but because underlying feedstock problems tainted the run. Consistent material sidesteps all that guesswork.

    We’ve worked with catalytic groups needing hundreds of kilos per month, as well as academic labs purchasing just a few grams. High-throughput screening setups highlight batch differences right away; an impurity as slight as 0.2% can throw off reaction yields. Larger industrial campaigns experience the same problem, magnified by scale, and an evening of lost reactor time or hang-ups in a kilo-scale continuous flow step can cost thousands in wasted downstream processing.

    From a manufacturing perspective, we take interest in how our customers use 4-Bromophenylboronic Acid. We periodically run joint process optimizations with client teams, sharing tweaks that have improved solubility in green solvents, or tips on staging addition to avoid oxidative coupling. We recognize that robust product is only half the story; collaborating on usage and applications extends value all the way to the chemist at the bench.

    Comparisons and Key Differences to Related Boronic Acids

    4-Bromophenylboronic Acid isn’t just an interchangeable stand-in for other aryl boronic acids. The para-bromo substituent enhances both reactivity and selectivity in many transition-metal catalyzed couplings. Our material’s consistent crystalline structure and low isomeric impurity also distinguish it from 2- or 3-bromophenylboronic acid analogs, where ortho or meta substitution creates steric and electronic variance that influences both the rate and outcome of the reaction.

    We routinely produce other boronic acids, including phenylboronic acid and substituted variants. Consistently, the challenges around 4-BPBA focus on the electron-withdrawing, activated nature of the para-bromo group. It can elevate reactivity or, if handled poorly, encourage side reactions like deboronation or bromine exchange. Our process adjustments—like strict temperature mapping during quench—come directly from years spent fixing those very issues at scale in our reactors.

    Another meaningful distinction lies in handling: while many aryl boronic acids pose storage headaches due to self-condensation or decomposition, our purification and packaging protocols stem from hands-on experience with long-term stability. Minimizing boroxine formation and controlling transient oxidation products add to the overall reliability for end users.

    Challenges in Large-Scale Manufacturing and What We Learned

    Ask our shift leaders and production chemists about the toughest batch of 4-BPBA, and stories will follow. Small batch runs might seem straightforward, yet scale invariably brings complexity. Stirrer speeds that suit a 5-liter lab kettle create dead zones in a 1,000-liter reactor, and a three-minute exotherm control delay can throw off crystallization for the entire lot. Over time, we learned to run each scale as its own process: different cooling rates, different antisolvent addition timing, and more rigorous impurity monitoring.

    Contamination sometimes sneaks in from unexpected places—plastic tubing, subcontracted truck tankers, or changes in raw water hardness. A single missed cleaning step in the process reveals itself not on day one, but when a downstream partner calls weeks later over a chromatogram spike. We invest heavily in batch documentation, scaling up not only procedures but also personnel training cycles. Even small tweaks—like batchwise nitrogen backblowing or in-house formulated washing solvents—keep each production consistent and reproducible.

    Managing Risk Throughout the Supply Chain

    Modern chemical supply chains span borders and time zones, leaving room for error at many points. By managing synthesis in-house, we keep tight control over scheduling, traceability, and compliance with environmental, health, and safety regulations. Each delivery batch can be traced back through both process and raw-material records, allowing us to provide transparent documentation when customers request it—no stonewalling, no vague references.

    Packaging and logistics require just as much attention as wet chemistry steps. One incident with broken containers or misapplied UN hazard labeling can stall an entire supply, particularly with tightened border controls or stricter end-user certifications in recent years. Our logistics coordinators train directly with our QC and production teams; feedback from shipping incidents filters directly back to procurement and plant operations for continuous improvement. Good chemistry extends right to the point where you open that package in your lab.

    Responding to Regulatory Pressures and Industry Standards

    Increasing scrutiny from regulatory agencies—especially in pharmaceutical and agrochemical applications—has raised the bar for documentation. We routinely review and revise our internal standards, driven not simply by regulation but by the real consequences downstream when something slips through the cracks. Counterfeit or poorly manufactured 4-Bromophenylboronic Acid from unverified sources continues to circulate globally. Common issues include mislabeling, unknown contaminants, sub-par purity, and cross-contamination by banned substances, which create immediate risk for clients with strict compliance requirements.

    Our plant withstands regular audits, both internal and external, and commits resources to stability studies spanning months. We actively document shelf-life and offer real feedback to customers when requested. If a standard batch shows signs of aging, we reprocess or replace it—even at a cost to us—because damaged trust impacts far more than a single shipment. Our philosophy is simple: protect your process so you can create without reservation.

    Ongoing Research and Product Development

    Not a year goes by without customer requests for tweaks and tailored applications. This R&D collaboration spurred us to explore greener solvents, pressure profile mapping, and downstream compatibility adjustments for 4-BPBA. Our team revisits process parameters regularly, often inspired by customer data that highlights where bottlenecks or variabilities show up in novel catalytic systems.

    We partner directly with select clients conducting advanced materials development, especially in electronics and light-emitting devices. These projects demand exceptional batch-to-batch consistency and zero tolerance for transition-metal contamination. Responding directly to end-user challenges, our team developed in-house polish filtration and advanced spectroscopic monitoring to ensure that even trace metals remain below detection thresholds.

    New process ideas often originate from the very “pain points” customers report. Sometimes, adjusting crystallization temperature troubleshooting prevents stubborn needle-shaped crystals and enhances solubility in green solvents. Other times, we work on stabilizing the boronic functionality against accidental thermal exposure—particularly important for continuous flow settings. Routine engagement with end users pushes us to evolve practices, rather than stagnate.

    A Manufacturer’s Perspective: What Matters Most

    Stepping beyond specifications, packaging, and paperwork, the ultimate marker of quality resides in how easily our customers can translate 4-Bromophenylboronic Acid into useful chemistry. No bench chemist or scale-up engineer wants headaches from doubt in starting materials. We share your frustration every time a bad batch derails hours of effort; having walked those floors and watched what happens both in the plant and at the customer site, we never lose sight of these details.

    Our job is to get the details right today, tomorrow, and every batch thereafter. Emphasizing traceability, continuous improvement, and practical transparency, we foster trust across every link in the chain. We stay accountable, not only through analytics but by maintaining a direct line to how our products perform on your side of the bench.

    Concluding Thoughts from the Production Line

    By keeping tight control over our 4-Bromophenylboronic Acid—from sourcing to production, purification, packaging, and shipping—we commit to more than just supplying another building block. This product reflects the challenges, learning, and shared pursuit of better scientific results built on grounded experience and rigorous practice. We welcome feedback, learn from every hurdle, and aim always to deliver material ready to meet your needs, whether that’s for a few grams or several metric tons.

    In manufacturing, no detail is too small. Every stage, every precaution, every tweak to lift product quality makes a tangible impact—one that translates to results you see on paper, in spectra, and in the success of your chemistry.