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4-Acetamidophenylboronic Acid

    • Product Name 4-Acetamidophenylboronic Acid
    • Alias 4-Acetamidophenylboronic acid; 4-(Acetylamino)phenylboronic acid; N-(4-Boronophenyl)acetamide
    • Einecs 690-082-5
    • 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

    560762

    Chemical Name 4-Acetamidophenylboronic Acid
    Cas Number 869926-29-6
    Molecular Formula C8H10BNO3
    Molecular Weight 178.98 g/mol
    Appearance White to off-white powder
    Melting Point 210-214°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in DMSO and methanol
    Storage Temperature 2-8°C (Refrigerated)
    Smiles CC(=O)Nc1ccc(B(O)O)cc1
    Synonyms 4-(Acetylamino)phenylboronic acid

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

    Packing & Storage
    Packing 4-Acetamidophenylboronic Acid, 5 grams, is packaged in a sealed amber glass bottle with safety labeling and tamper-evident cap.
    Shipping 4-Acetamidophenylboronic Acid is shipped in sealed, airtight containers to ensure product stability and prevent contamination. It is typically transported as a solid powder, protected from moisture and light. Shipping follows all applicable regulations for chemical materials, with labeling for handling, storage, and safety instructions clearly provided.
    Storage 4-Acetamidophenylboronic acid should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Keep the container tightly closed when not in use. Store separately from incompatible substances such as strong oxidizing agents and acids. Proper labeling and containment are essential to prevent contamination and ensure safe handling. Use in accordance with standard laboratory chemical storage guidelines.
    Application of 4-Acetamidophenylboronic Acid

    Applications of 4-Acetamidophenylboronic Acid in Industrial Manufacturing

    4-Acetamidophenylboronic Acid serves as a critical intermediate across multiple industrial production environments, especially in the development of advanced pharmaceuticals, specialty polymers, diagnostic tools, and organic electronic materials. As an established manufacturer, we have aligned formulation and supply capabilities with the strict quality and process requirements demanded by these sectors. See representative application segments below:

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Manufacturers in the pharmaceutical sector use 4-Acetamidophenylboronic Acid primarily in Suzuki coupling reactions to construct biaryl moieties for next-generation small molecule drugs, including kinase inhibitors and selective receptor modulators. Our process-grade batches support both R&D and cGMP manufacturing, providing high assay material that integrates efficiently into automated HPLC-monitored reaction trains. Reactant proportioning depends on targeted molecular frameworks, but tight batch-to-batch reagent quality ensures reproducibility from lab to plant scale.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP Pharmaceutical Excipients Monograph (where applicable)
    • EDQM Certification of Suitability (CEP) for EMA submissions
    • 21 CFR Parts 210-211 (FDA Drug GMP)

    Typical usage ratio

    • Mol ratio 1.05–1.20 equivalents per aryl halide, adjusted based on substrate reactivity
    • Concentration 0.02–0.10 mol/L in batch or flow reactors
    • Adjusted according to process scale and desired yield optimization

    Downstream process integration

    • Reactant introduced after substrate aryl halide addition during palladium-catalyzed cross-coupling
    • Upstream: Solubilization in polar aprotic solvent (e.g., DME, DMF)
    • Downstream: Purification by preparative HPLC, crystallization, or flash chromatography
    • Stepwise release testing for in-process control (IPC) of intermediates

    Final product types

    • Oncological pharmaceuticals (small molecule kinase inhibitors)
    • Antidiabetic agents
    • CNS active compounds for neurology therapeutics
    • API reference standards for quality control labs

    2. Diagnostic Reagent Manufacturing

    Diagnostic reagent producers employ this compound as a building block in the synthesis of boronic acid-derived probes and affinity ligands for biomedical assays. Chemical bioconjugation requires strict input chemical purity, as trace contaminants impact downstream assay fidelity. The boronic acid moiety binds diol-containing biomolecules, so process formulation includes defined stoichiometry and mild temperature control to preserve functional group integrity during ligand assembly.

    Industry compliance standards

    • ISO 13485:2016 Medical Devices QMS for IVD reagent production
    • EU IVDR (Regulation (EU) 2017/746) for diagnostic reagents
    • REACH Registration for laboratory chemical use
    • CLIA compliance (for US-manufactured diagnostic kits)

    Typical usage ratio

    • Batch assembly: 1.00–1.10 equivalents per linker/biomolecule activated group
    • Working concentration: 20–50 mmol/L in aqueous or mixed organic buffer systems
    • Modifier feed varies by probe type and sensitivity requirements

    Downstream process integration

    • Direct coupling to peptides, enzymes, or magnetic bead surface groups during bioconjugation step
    • Post-conjugation, excess is removed by dialysis or filtration
    • Quality checked by HPLC and functional assay prior to kit assembly
    • Stability monitored via QC sampling of stored conjugates

    Final product types

    • Fluorescent or chromogenic biosensors
    • Immunoassay kits (ELISA, lateral flow)
    • Affinity chromatography media
    • Clinical chemistry calibrators and controls

    3. Specialty Polymer Synthesis

    4-Acetamidophenylboronic Acid supports production of functionalized high-performance polymers through incorporation into backbone or side-chain motifs for advanced engineering applications. Applied in free radical or step-growth polymerizations, it introduces boron-acetamido groups that grant unique surface and binding properties to the final resin. Polymer chemists control monomer feed ratios tightly to achieve designated mechanical strength and chemical resistance profiles, while also observing strict process controls to meet industrial safety expectations.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Polymer Manufacturing
    • RoHS Directive (2011/65/EU) for electrical/electronic polymer components
    • ASTM D638 (mechanical testing of plastics)
    • REACH Annex XVII restricted substances compliance

    Typical usage ratio

    • 5–15 mol% in copolymer formulations depending on application (e.g., membrane, adhesive, biosensor substrate)
    • Up to 25 mol% for surface modification resins
    • Adjusted according to polymer backbone structure and property targets

    Downstream process integration

    • Dispersed or pre-reacted with co-monomers prior to polymerization
    • Integrated in in-situ or post-polymerization grafting processes
    • End-use testing performed on cured or molded materials for target parameters
    • QC sampling at multiple points in polymer line for impurity content analysis

    Final product types

    • Ion-exchange resins for chemical process industries
    • Membranes for biomedical device housings
    • Adhesives with specialty bonding capability
    • Custom surface-treated plastics for analytical applications

    4. Organic Electronic Material Development

    Material science labs and scale-up producers apply 4-Acetamidophenylboronic Acid in the synthesis of conjugated molecular building blocks, vital for manufacturing organic semiconductors, OLED emitters, and hole transport layers. Carefully controlled coupling reaction conditions, including base and catalyst selection, guarantee reproducible electronic property profiles. Downstream, the finished molecules become components in layered device architectures, where input purity and homogeneity directly impact device yield and lifetime.

    Industry compliance standards

    • RoHS and REACH substance restrictions for electronic materials
    • ISO 14001 Environmental Management Systems
    • IEC 61249-2-21 halogen-free requirements (where applicable)
    • Internal specifications for trace metal and impurities content

    Typical usage ratio

    • 0.5–1.5 equivalents per electronic aryl halide substrate in cross-coupling
    • Feed concentration: 0.05–0.20 mol/L in reaction mixture
    • Ratio adjusted according to desired molecular weight and device application

    Downstream process integration

    • Introduced as a coupling partner during precursor synthesis for organic semiconductors
    • Recrystallized or chromatographed before device deposition
    • Film-forming precursors processed into thin layers by spin-coating or vapor deposition
    • Final testing includes electronic mobility and photoluminescence analysis

    Final product types

    • OLED emitting layer materials
    • Organic thin film transistor (OTFT) functional coatings
    • Light-harvesting layers for OPV solar cells
    • Custom tuning components for printed electronics
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    Certification & Compliance
    More Introduction

    4-Acetamidophenylboronic Acid: Our Experience from Synthesis to Application

    Introduction to 4-Acetamidophenylboronic Acid

    Producing 4-acetamidophenylboronic acid goes well beyond transferring a formula from paper to plant floor. Every batch leaves our reactors with plenty of learning attached, much of it reflecting years of thriving among the constant cycle of research discovery and customer-driven feedback. Chemists know this compound as a key partner in Suzuki-Miyaura cross-coupling, but what often gets overlooked is how manufacturing practices, starting material selection, and strict process discipline set the tone for reliability down the chain. The model our factory produces has a CAS number of 869353-01-9, with purity levels commonly exceeding 98%, and particles that hold tight to defined granulometry for better handling in the lab or plant.

    Our Focus on Quality

    Every drum or bottle of 4-acetamidophenylboronic acid we ship rides on months of work developing robust crystallization steps and a comfortable margin of storage stability. Unlike some commodity boronic acids that attract water like thirsty sponges, our batches emerge with consistent moisture profiles, thanks to vigilant drying regimes and ongoing investment in cleanroom methods. The process itself leans heavily on high-grade acetanilide and boronic acid precursors to minimize color bodies and tricky side products. We keep the focus on minimizing meta isomer and other common organic contaminants, which often escape notice until they trigger problematic signals in downstream LC-MS or HPLC analysis—issues we first spotted in our own QC labs after customer complaints many years ago.

    The customer gets to experience an easy-to-weigh, free-flowing powder instead of the clumped, yellowing granules that show up elsewhere. Differentiation doesn’t come just from marketing claims; it follows an unrelenting loop of in-process checks—loss on drying, purity by HPLC, trace inorganic testing by ICP-MS. Our field salespeople push back if they see even the smallest deviation during site audits, ensuring lot-to-lot reproducibility. Longevity on the shelf matters just as much as sharp NMR signals; we have products sitting in customer fridges two years after delivery, measuring up to original specs.

    What Sets Our Process Apart

    The boronic acid market isn’t kind to shortcuts. Sourcing matters. We built out supplier agreements with partners who meet tight specifications on acetanilide and phenylboronic acid bases. This prevents the trace halogens, residual solvents, and particulates that derail downstream use—an issue that hit us early on when a single lot of subpar precursor made its way into a pharma pilot plant. The learning stuck. To lock in a tight melting point and stick to our color index targets, every fermenter run sees close monitoring of pH, temperature, and reagent feeds, logged and trended over thousands of cycles. It’s no secret recipe—long days spent focusing on minor tweaks make a difference in how the powder behaves and how it scales into research or process settings.

    Storage and packaging matter. Moisture-proof liners, inert gas headspace, and double-sealed drums prevent boronic acid degradation—features that grew out of real-world feedback, not a design committee. While some producers source bulk from contract partners who may lack insight into stability, our integrated batch records help us track performance and recall every parameter when troubleshooting is called for. There’s pride in opening a fresh pack, catching that clean, neutral aroma, and seeing crystalline powder, not a block of fused material.

    Working with Customers and Technical Support

    Feedback teaches lessons no textbook can. Pharmaceutical researchers using 4-acetamidophenylboronic acid as a Suzuki partner are the fastest to spot deviations; even low-level impurities can destroy the outcome of a scale-up run. Once, a customer flagged a shadow peak in LC traces. We tracked it to a new drying cycle, adjusted our times, and invited them back for another audit. This practical loop of dialogue with our downstream partners lets us adapt in real time. Our technical team sees themselves as problem solvers rather than ticket closers, supporting customers who use this compound in everything from batch medicine synthesis to functionalized material fabrication.

    Collaboration goes deeper than sample testing. Over the past decade, we built a back-and-forth with contract chemists and development scientists that goes beyond shipping certificates of analysis. We review results under NDA, tweak batches, and often send out splits from pilot runs. Getting in front of issues—whether crystal habit, filterability, or solubility in key solvents like NMP or DMF—means we avoid last-minute surprises that cost everyone time and money. Laboratories using older versions of our product have reached out about updated regulatory needs for elemental impurities, and our in-house batch records and archived samples let us answer quickly and with confidence.

    Technical Properties and Handling Experience

    Our staff spend countless hours exploring physical and chemical traits of 4-acetamidophenylboronic acid. The core product is an off-white crystalline solid, usually clocking in above 98% purity on HPLC. Each batch aligns with a melting point range of approximately 255–260°C, which we check against archived reference material to ensure authenticity and stability. Loss on drying tests returns results below 0.5%—figures we only hit after multiple internal projects focused precisely on eliminating atmospheric moisture pickup in our packaging line.

    Handling in the plant means regularly transferring finished material from cold storage to weighing hoods, where powder flow properties come to the fore. Early production runs produced powder that caked after a week in the warehouse. Sore backs from prying open bricks inspired tweaks to drying and milling that eventually gave us a product with natural pourability. This attention to daily detail leads to easier, safer dosing in the customer’s lab. As for solvent compatibility, 4-acetamidophenylboronic acid dissolves reliably in DMSO, DMF, and other polar aprotic solvents, allowing flexibility for reaction engineers developing new Suzuki protocols. Our technical support regularly fields questions about material compatibility, always referring back to decades of factory and customer reports.

    Typical Uses and Emerging Demands

    Most requests for this compound come from pharmaceutical and agrochemical research teams focused on aryl or heteroaryl coupling. The utility in Suzuki cross-coupling stands out for generating complex biaryl scaffolds, which then become intermediate points for kinase inhibitors, anti-inflammatory drugs, or crop protection agents. We see our compound supporting everything from medicinal chemistry campaigns in global pharma to agrochemical projects in specialty crop development. The ability to generate clean, high-yielding cross-couplings with low by-product formation is where our lot-to-lot consistency shows up.

    Newer applications keep appearing. Material scientists order 4-acetamidophenylboronic acid for functionalizing surfaces in sensor arrays, medical diagnostics, and even early-stage organic electronic components. Our R&D group collaborates with cross-disciplinary teams exploring polymer-bound boronic acids and clickable handles for advanced ligation chemistry in bioorthogonal settings. The diversity of usage drives us to keep investing in purification, supply chain resilience, and process analytics.

    Regulatory landscapes shift, especially for customers filing new chemical entities or supporting dossiers for agrochemical registrations. Our product development team reviews impurity profiles and residual solvents to match ICH Q3A/B and relevant global guidelines, adapting to evolving requirements of major regulatory bodies. Routine method development led to a set of in-house protocols for detecting and quantifying common boron by-products, letting customers file solid CMC documentation with confidence.

    Supply Chain Transparency and Traceability

    In recent years, expectations on supply chain traceability have intensified. The industry as a whole faces tighter calls to track raw material origin, qualification audits, and documentation. Early on, we struggled with fragmented data, making root cause analysis slow and frustrating. Overhauling our ERP and batch reporting systems let us catch and eliminate at-risk suppliers, reinvesting in quality and proactive compliance. Now, every lot of 4-acetamidophenylboronic acid we make links directly to a digital batch record connecting analytical test results, raw material documentation, and customer shipment histories.

    Quality alone is not enough; reliability underpins every customer relationship. Disruptions during the pandemic put this belief through severe tests. Where others slowed down, we doubled up on buffer inventory, staggered production schedules, and prequalified alternate routes for crucial intermediates. Customer projects didn’t halt because of our supply: performance in tough times builds loyalty faster than glossy brochures. Inventory cycling and real-world stress tests gave us data-driven justification for choosing packaging materials and limiting rework or extended storage windows.

    Comparing with Commodity and Competing Products

    Differences between our 4-acetamidophenylboronic acid and less controlled offerings start at the raw materials. We use material with documented impurity profiles to avoid trace halides and polycyclic aromatics, both of which can skew reaction yields. Over time, customers report lower baseline levels of boron-related side products—a direct outcome of focused process development.

    Many third-party traders and brokers flood catalogs with variable-quality product, sourced from turn-key facilities with little hands-on process understanding. Scientists seeking to scale a gram of material to kilogram lots often find out too late that inconsistency in crystalline habit or a persistent yellow tint arises from corner-cutting on purification—not from unavoidable process artifacts. Some batches in the global market ship with visible fines or oversized granules, increasing both dust risk and reactivity problems. Our strict particle size distributions in the final drum mean less filtering and cleanup, smoothing transfer from lab discovery to pilot-scale reactors.

    We test extended stability and compatibility for sensitive Suzuki protocols, as well as side-product generation in complex multi-step synthesis scenarios. Feedback from these real-world challenges lets us refine batches, pushing product design based on chemists’ demanding requirements, not just QC spot checks or minimum regulatory acceptances seen elsewhere. Our investment in analytical infrastructure—ranging from benchtop NMR to high-resolution mass spectrometry—lets us offer both improved baseline purity and application-tailored data sets that others can’t match.

    Environmental Responsibility and Waste Reduction

    Boronic acid processes are not always easy on the environment. Early on, we grappled with waste issues—aqueous boron streams, solvent emissions, and residual spillage. Fixing these or designing controls into the process felt like a heavy lift. Yet, investments in closed-loop scrubbing, on-site solvent recovery, and boron reclamation paid off. Not only did our disposal costs shrink, but we also received measurable boosts in process yield and community standing.

    Our local water treatment partnership—born from honest conversations with municipal authorities—helped us validate effluent levels, tweak wastewater protocols, and publish improvements with transparent third-party verification. Today, our records show a steady reduction in both solid and aqueous waste per kilo of product shipped, proof that operational discipline can deliver environmental and operational wins. Recent addition of heat exchangers and improved vacuum control further drove down the plant’s energy intensity per product ton.

    Constant Improvement: What We Learned from Setbacks

    Every production setback pushes us to understand root causes and invest in upgrades. A few years ago, persistent caking forced us to revisit our drying process; we found that microclimate patterns within storerooms were enough to rehydrate marginal product. The response included better air circulation, new packaging films, and rotating stock more frequently. Turbidity in filtrate from older filter cloths drove us to overhaul equipment maintenance guidelines. Minor issues, if left unchecked, have a way of snowballing into costly recalls or customer dissatisfaction.

    Open communication lines with customers make the biggest difference. A chemist in Europe pointed out that our earlier batches threw off HPLC baselines, likely from a barely-there impurity missed by our standards. Digging deeper, our analytical team cross-referenced spectral signatures and implemented a new, more sensitive reference standard that tightened our release criteria. The improvement wasn’t huge in QC terms, but for that customer’s oncology pipeline, it meant a product that could comfortably pass all regulatory checks.

    Looking Forward: Responding to Future Market Needs

    Our teams pay close attention to new trends: rising expectations for documentation, digital batch records, and granular trace element reporting. We observe regulatory updates, adapt protocols, and proactively inform our customers of major process or compliance improvements. Collaboration with academic partners has deepened our understanding of emerging cross-coupling methods, including photoredox and nickel-catalyzed chemistry. These trends influence how our product behaves in new settings and prompt us to preemptively strengthen analytics and batch characterization routines.

    Transparency drives both innovation and trust. We’re working toward expanded process automation and plan to offer even more detailed release data—boron isotope ratios, microcontaminant scanning, and supply chain documentation. Commitment to sharing lessons learned, rather than glossing over rough patches, grounds our relationships with chemists who rely on 4-acetamidophenylboronic acid for critical research, new drug launches, or advanced material development.

    We welcome inquiries from laboratories interested in learning more about technical performance, supply models, and the direct experience that comes from years of making and improving this versatile building block. While the chemistry enables scientists to reach new frontiers, our daily work ensures they have what they need—batch after batch.