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3-Acetylphenylboronic Acid

    • Product Name 3-Acetylphenylboronic Acid
    • Alias 3-Acetylbenzeneboronic acid
    • Einecs 625-551-4
    • 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

    827738

    Product Name 3-Acetylphenylboronic Acid
    Cas Number 87199-23-5
    Molecular Formula C8H9BO3
    Molecular Weight 163.97 g/mol
    Appearance White to off-white powder
    Melting Point 171-174 °C
    Purity Typically ≥98%
    Smiles CC(=O)C1=CC(=CC=C1)B(O)O
    Solubility Soluble in DMSO, slightly soluble in water
    Storage Conditions Store at 2-8°C, tightly sealed
    Synonyms 3-Acetylbenzeneboronic acid

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

    Packing & Storage
    Packing The 3-Acetylphenylboronic Acid is packaged in a 25g amber glass bottle, clearly labeled with safety information and chemical details.
    Shipping 3-Acetylphenylboronic Acid is shipped in tightly sealed containers to prevent moisture absorption and contamination. The packaging complies with chemical safety standards and includes appropriate labeling indicating its chemical nature. It is transported under ambient conditions, but care is taken to avoid extreme temperatures and direct sunlight. Safety documentation accompanies each shipment.
    Storage 3-Acetylphenylboronic Acid should be stored in a tightly sealed container, protected from moisture and air. Keep it in a cool, dry place, away from direct sunlight and incompatible substances, such as strong oxidizing agents. Store at room temperature or as specified on the label. Ensure proper labeling and restrict access to trained personnel, observing appropriate chemical hygiene practices.
    Application of 3-Acetylphenylboronic Acid

    Applications of 3-Acetylphenylboronic Acid in Industrial Manufacturing

    As a direct manufacturer, we supply 3-Acetylphenylboronic Acid to multiple industries where it functions as an advanced boronic acid derivative in downstream synthesis. Below, we detail verified industrial applications across key segments, with compliance, formulation ratios, integration points, and end-use product types specified according to current market and regulatory requirements.

    1. Pharmaceutical API Intermediate Synthesis

    Pharmaceutical manufacturers employ 3-Acetylphenylboronic Acid as a building block in the synthesis of active pharmaceutical ingredient (API) intermediates, particularly for small molecule drugs that incorporate heterocyclic or biaryl motifs. It serves in Suzuki-Miyaura coupling reactions to introduce acetylphenyl groups into complex molecules. Facilities use this compound under controlled conditions, typically in multi-step batch synthesis prior to final API generation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 211 (US GMP for Finished Pharmaceuticals)
    • EU GMP Volume 4 (European Medicines Agency guidelines)
    • Chinese Pharmacopoeia—API & raw material requirements (Current Edition)

    Typical usage ratio

    • Used in 0.8–1.2 mole equivalents relative to the halogenated aryl coupling partner; actual proportion depends on process scale, desired yield and coupling efficiency.

    Downstream process integration

    • Added during the key cross-coupling step, generally after the initial halogenated precursor and prior to palladium catalyst addition. Reacted in organic solvents such as toluene or DMF under inert atmosphere to avoid moisture sensitivity, followed by downstream purification of synthesized intermediate.

    Final product types

    • Branded and generic oncology APIs
    • Selective kinase inhibitors
    • Anti-diabetic small molecule drugs
    • Specialty pharmaceutical intermediates for CNS treatments

    2. Agrochemical Active Ingredient Production

    Major agrochemical manufacturers use 3-Acetylphenylboronic Acid to construct biaryl and aromatic ketone frameworks in plant protection compounds, especially for herbicides and insecticides. This compound participates in palladium-catalyzed bond formations, introducing controlled aromatic moieties critical for biological efficacy and environmental stability.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius—Pesticide Formulation Guidelines
    • ISO 9001:2015 for chemical process quality management
    • ECHA REACH Regulation (EC) No 1907/2006
    • SDS compliance per GHS/CLP (EU, US, China)

    Typical usage ratio

    • Applied at 1.0–1.1 mole equivalents in Suzuki coupling reactions for aromatic active group installation. Process chemists adjust ratio depending on residual impurity control and cost optimization.

    Downstream process integration

    • Introduced in the core active ingredient assembly step directly after halide activation and prior to formulation with adjuvants, housed in jacketed reactors with real-time HPLC monitoring for residual boronate.

    Final product types

    • Seed treatment concentrates
    • Post-emergent herbicides
    • Systemic insecticides
    • Growth regulator intermediates

    3. Electronic and Specialty Material Synthesis

    Material science companies harness the reactivity of 3-Acetylphenylboronic Acid during the production of advanced organic electronic components and functionalized polymers. It is essential for the preparation of monomers with acetyl-functionalized aryl groups, enabling subsequent polymerization for OLEDs, advanced sensors, and specialty coatings.

    Industry compliance standards

    • RoHS Directive 2011/65/EU for electronic material restrictions
    • IPC-4101D for high-performance composite materials
    • ISO 14001:2015 Environmental Management Systems
    • REACH Registration for monomer safety

    Typical usage ratio

    • Utilized at 0.9–1.05 mole equivalents during coupling with halogenated monomers; adjusted for minimizing residual boronic acid and side polymers in the final batch.

    Downstream process integration

    • Fed into monomer coupling systems, generally under nitrogen purge at controlled temperatures, before subsequent polycondensation or cross-linking. QC departments carry out FT-IR and GC-MS analysis to ensure target acetyl moiety incorporation.

    Final product types

    • OLED display components
    • Electroluminescent films
    • Photoresist resins
    • Organic conductive coatings

    4. Fine Chemical Synthesis for Fragrance and Specialty Intermediate Suppliers

    Producers of fine chemicals use this material to construct key aromatic ketones and custom intermediates for perfumery and specialty chemical applications. It allows for tailored acetylation in advanced organic synthesis, satisfying demand for rare, structure-specific phenyl derivatives in bulk and custom orders.

    Industry compliance standards

    • IFRA Code of Practice for fragrance raw materials
    • ISO 9001:2015 for batch traceability and QC
    • REACH compliance for European market supply
    • FDA 21 CFR (as applicable to indirect food contact)

    Typical usage ratio

    • Selected at 1.0 mole equivalent for high-conversion coupling with brominated or iodinated aromatics. Scaled processes may lower the ratio to minimize post-synthesis purification requirements where tolerance allows.

    Downstream process integration

    • Added into coupling reactors after melting-point controlled feeding and pre-dissolving in polar aprotic solvents. Purification utilizes crystallization or column chromatography, with GC/IR confirmation of aromatic integrity.

    Final product types

    • Specialty fragrance intermediates (e.g., phenyl acetones, complex musks)
    • Synthetic flavor precursor chemicals
    • Intermediate ketones for custom fine chemical synthesis
    • Aromatic raw materials for dye production
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    Certification & Compliance
    More Introduction

    3-Acetylphenylboronic Acid: Direct from the Manufacturer’s Laboratory Bench

    Understanding 3-Acetylphenylboronic Acid Up Close

    Every batch of 3-Acetylphenylboronic Acid we produce comes from hands-on experience with aryl boronic chemistry and an eye for practical use. Not every chemist will say this, but working at the source of manufacture for boronic acids means the process isn’t simply about technical specifications—it is about keeping a sharp awareness of how each tweak in synthesis directly influences a thousand downstream outcomes. Our 3-Acetylphenylboronic Acid has shaped countless research projects, and our team knows it not just by name or CAS but by the actual color, grain, and even the way it feels in lab glassware.

    This compound, known structurally as 3-acetylphenylboronic acid and typically referenced in our catalog under the model APBA03, traces its reputation to its balanced reactivity and dependable purity profile. Unlike basic phenylboronic acid, its 3-acetyl functional group brings depth to Suzuki-Miyaura couplings, providing a reliable path for forming biaryl structures that push boundaries in both medicinal and materials chemistry. We have watched academic teams successfully create inhibitors for specific kinases, and we've seen industrial clients integrate this molecule into pilot-scale custom syntheses for optoelectronics.

    Manufacturing 3-Acetylphenylboronic Acid: Lessons from Hard Practice

    Every kilogram of our product comes out of a continuous effort to keep impurities—especially regioisomeric boronates or hydrolysis-sensitive tars—below the tight thresholds set by industry or journal reviewers. In practice, off-the-shelf variants sometimes carry over leftover starting materials that can trip up a clean cross-coupling, especially when scaling experiments beyond milligram quantities. We have invested in refining the crystalline isolation to make sure the product stores safely, flows well when pouring, and does not cake in the bottle. These hands-on improvements have come directly from watching researchers struggle with commercial samples that clump or turn tan after a few months on the shelf.

    The workflow in our plant relies as much on human oversight as it does on tightly regulated reactors. You can’t spot a sluggish hydrolysis rate from a datasheet, so our staff tests beyond HPLC numbers: we rely on routine checks with proton NMR and LC-MS for trace organics and keep batch logs that backtrack every deviation to the starting phenyltriflate or boronic ester. The extra effort pays dividends, especially for customers who require consistent kinetics in their coupling reactions.

    Specifications Born From the Lab, Not a Marketing Sheet

    We have watched procurement specialists gloss over assay figures, not always realizing that quality within a certain band can save days on the bench. Our 3-Acetylphenylboronic Acid clocks consistently above 98% HPLC purity with a water content below 0.5%. Each batch’s melting point sits comfortably within the expected 174-178°C window, a range we have dialed in by iterating through solvent systems and drying protocols.

    Some manufacturers blend batches or accept borderline material to fluff reported assay figures. We do not. With requests from customers who run high-sensitivity reactions, we often provide extended chromatograms on request. We’ve seen how a 1-2% impurity—undetectable until you find a stalled coupling—can push a project into unexpected troubleshooting. On several occasions, chemists have shared LC spectra showing only our material passes their internal standards without any “ghost peaks.”

    What Makes 3-Acetylphenylboronic Acid Stand Out

    There is a reason researchers—especially those designing kinase inhibitors, heterocycles, or OLED materials—prefer the 3-acetyl substituent over standard phenylboronic acid or its methylated cousins. The meta-acetyl group tempers the boronic acid’s reactivity, often leading to a sweet spot: high conversion rates with fewer oily byproducts post-coupling. Connecting aryl units with steric or electronic modulation improves overall yields and product isolation, especially in multi-step synthesis histories where each gram matters.

    Some end-users opt for basic phenylboronic acids, chasing lower cost. We see where that decision leads: sometimes you save a little on the input but pay in time, cleanup, and extra column chromatography. Our team maintains that investing in a correctly substituted boronic acid, such as 3-acetyl, pays off especially when scaling beyond the small flask. Our industrial clients report fewer labor hours lost to rework, especially when producing final-active pharmaceutical ingredients or scale-up intermediates.

    Product Consistency and Its Impact on Downstream Synthesis

    Reactors in real-world plants don’t always mirror idealized lab-scale conditions. A small increase in residual acetate or sodium from the synthesis can affect crystallization and isolation in a hundred-liter vessel. We monitor these parameters directly, using periodic ICP-MS and titration for boron quantification, techniques we settled on after learning how minor deviations affected client runs. Our records show multiple instances where a careful tweak—a lower temperature in the carbonylation step, a longer quench, or finer filtration—produced a product batch with markedly better clarity and filterability, translating to easier downstream handling.

    We’ve collaborated with both pharma and R&D partners who provided feedback not just on chemical purity, but on properties like solubility in DMSO, methanol, and toluene. Sometimes a minor impurity shifts solubility curves just enough to cause issues in automated synthesis platforms. Through trial and error, supported by customer dialogue, our manufacturing adjustments align with reality in the lab, not just theory in a test report.

    Direct Manufacturer Support—Not Just a Sales Channel

    A chemical’s certificate of analysis only scratches the surface when projects depend on reliability. Customers have brought us real questions: "What’s your sodium content per batch?" or "Does this batch show any ortho-acetyl isomer?" Our technical team answers from lived experience—not from detached documents, but from the synthesis bench where we refine processes and witness failures.

    Several years back, a customer in the OLED sector reported an unexpected byproduct in a pilot run. They shared NMR data and we ran side-by-side analyses with our own infrastructure, finally narrowing down the issue to a subtle variation in solvent hygiene. Working together, we modified a step in the synthesis protocol—switching to a different solvent lot, extending the vacuum drying cycle, and running cross-checks on the byproduct signature. The client’s next pilot run passed all specifications and moved forward without hitch. These adjustments, born from experience rather than conjecture, would have been impossible without tight integration between manufacturing expertise and user feedback.

    Applications: Real-World Accounts and Not Just Theoretical Potentials

    Over the years, we have watched 3-Acetylphenylboronic Acid secure its place in medicinal chemistry. The meta-acetyl group gives medicinal chemists flexibility in designing molecules that disrupt protein-ligand binding, especially in kinase inhibitor exploration. We’ve supported several university teams and start-ups as they moved quickly from early SAR sets to viable preclinical candidates. In one series of collaborations, our product helped generate robust yields of boron-containing inhibitors that advanced to animal studies, with feedback highlighting clean mass spec profiles and minimal side-reactions in the Suzuki stage.

    Our 3-Acetylphenylboronic Acid travels far: it has built up molecular libraries for drug discovery, served as a linchpin in constructing arylated polymers for advanced materials, and helped fine-tune photophysical properties in optoelectronic devices. We track successes not just in sales numbers but through publications and patents referencing our lot numbers, which confirms our product’s performance under both academic and commercial scrutiny.

    The difference isn’t theoretical. One electronics firm scaled up to production of new blue-light emitters and found their previous supplier’s material left trace metal contamination that destabilized final devices. By switching to our carefully monitored batches, their yields improved and rejects decreased. Not every manufacturer tests for traces of activating metals or solvents, but over years, we have learned that even ppm-level residues can make or break success for end-users in sensitive applications.

    Addressing Challenges in Aryl Boronic Acid Sourcing

    Anyone who regularly sources boronic acids knows that global supply tightens, prices fluctuate, and quality can waver. We have steered through times when key starting materials grew scarce, when logistics delayed deliveries, and when global events upended normal inventory flow. Recent years have underscored the value in fostering direct relationships and holding strategic stocks of both starting triflates and critical reagents. Overcommitting or diluting quality to fill orders only creates setbacks down the line, so our approach is to scale production deliberately and monitor every deviation.

    Counterfeit and mislabeled chemicals occasionally find their way to unwary customers. We have assisted more than one customer in diagnosing products from unverified vendors that caused mysterious reaction failures. A few grams of poorly characterized boronic acid can derail weeks of effort—sometimes only a distinct NMR signature or melting point flags off-spec product, but we have run more involved analyses with clients who brought us batches from questionable sources. In some cases, we diagnosed decomposition from poor storage and shared real guides on how to keep boronic acids dry, away from heat and light. These troubleshooting sessions benefit not just our own production cycles but raise the standard for the whole supply chain.

    What Sets an Original Manufacturer Apart from Resellers and Distributors

    Nobody can speak about the challenges of scaling boronic acid synthesis without living through a few process upsets. We have seen resellers market chemicals with little true knowledge about their origins, handling, or seasonal batch differences. Problems only come to light later: a failed library build, mystery peaks in analytics, or outright project delays. As an original manufacturer, there’s no hiding behind paperwork. Each batch we ship has passed through our hands, our reactors, and our quality systems. Every inquiry finds an honest answer because we have nothing to hide—if an out-of-spec or off-color batch ever occurs, we address it at root cause, not just by pulling from a distant warehouse.

    Our customers value the difference. New clients quickly realize they gain not just a chemical, but a relationship with a team who understands their workflows down to the solvent and glassware level. Procurement that connects directly with true manufacturing builds confidence and shortens the supply chain—issues get addressed quickly, and technical challenges can be discussed in depth. In the long run, this fosters not only better chemistry but real partnerships.

    Ongoing Commitment: Continuous Improvement and Feedback Loops

    Perfection in chemistry rarely comes from a single iteration. Our continuous focus on refining every element of the 3-Acetylphenylboronic Acid workflow is a direct response to end-user experience. Through regular feedback channels, batch retrospectives, and hands-on follow-up, we always look for new marginal improvements: whether that means reducing trace sodium, refining the dry-box process, or implementing new analytics as our customers’ requirements evolve.

    Our staff maintains an open-door policy with process engineers, synthetic chemists, and analysts—sharing both successes and lessons from near-misses in the plant. This knowledge becomes part of training for every technician and color every decision on manufacturing improvements. Several times, we have modified protocols after receiving just a single offhand comment from a customer who encountered problems we hadn’t seen at scale. This culture rewards candor and expertise, not just efficiency.

    The Bottom Line: Why Direct Manufacturer Quality Matters for 3-Acetylphenylboronic Acid

    This compound is not just a line item in a catalog for us—it forms part of a body of work born from practical synthesis, real-world applications, and feedback-driven improvement. Those who purchase or specify 3-Acetylphenylboronic Acid for cross-coupling, library design, or advanced material synthesis will recognize immediately the value in starting with a product grounded in true manufacturing oversight. Our product reflects lessons learned batch after batch, collaboration after collaboration, and countless conversations with researchers working at the cutting edge.

    Choosing a dependable, direct-from-source manufacturer creates advantages: not only consistent purity, but honest guidance, access to batch records, and a direct line to the team that can answer the most technical questions based on hands-on experience. Many of our most loyal customers came to us after losing weeks to poorly characterized material from third parties. We meet their trust with diligence, from the starting benzene ring to the final bottle they open in the lab.

    Our commitment as a dedicated manufacturer runs deeper than simple supply: it extends to every product shipped and every researcher supported through their most challenging synthetic steps. In a field where materials quality can decide both daily results and long-term innovations, we stand by our process, our hands-on knowledge, and our product.