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4-Carboxyphenylboronic Acid

    • Product Name 4-Carboxyphenylboronic Acid
    • Alias 4-Boronobenzoic acid
    • Einecs 619-365-1
    • 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

    915369

    Chemical Name 4-Carboxyphenylboronic Acid
    Cas Number 14047-29-1
    Molecular Formula C7H7BO4
    Molecular Weight 165.94 g/mol
    Appearance White to off-white powder
    Melting Point 283-287°C (dec.)
    Purity Typically ≥ 97%
    Solubility Insoluble in water, soluble in DMSO and methanol
    Density 1.43 g/cm³
    Pka 8.6 (carboxyl group)
    Smiles B(C1=CC=C(C=C1)C(=O)O)(O)O

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

    Packing & Storage
    Packing A 25-gram amber glass bottle with a white screw cap, labeled “4-Carboxyphenylboronic Acid,” includes hazard warnings and purity details.
    Shipping 4-Carboxyphenylboronic Acid is shipped in tightly sealed containers to protect from moisture and contamination. Packaging complies with chemical safety regulations, and the product is labeled with appropriate hazard information. Shipping is handled by authorized carriers with documentation, ensuring safe transit under ambient or specified temperature conditions as required by chemical safety guidelines.
    Storage 4-Carboxyphenylboronic acid should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from moisture, heat, and incompatible substances such as strong oxidizing agents. Protect it from direct sunlight. Store at room temperature and avoid exposure to air to prevent degradation. Follow all applicable safety regulations and procedures when handling and storing this chemical.
    Application of 4-Carboxyphenylboronic Acid

    Applications of 4-Carboxyphenylboronic Acid in Industrial Manufacturing

    4-Carboxyphenylboronic acid finds specialized use across several advanced industrial domains, supporting end-users in the synthesis of high-purity intermediates, specialty polymers, innovative electronic materials, and critical bioactive compounds. The following applications reflect real downstream scenarios, divided by processing approach, industry standards, and actual usage parameters guided by both our technical experience and verified customer case studies.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical manufacturing frequently utilizes this compound in Suzuki coupling protocols to produce biaryl-based API cores, particularly in oncology research and antidiabetic drug classes. The controlled introduction of the carboxyphenylboronic functional group ensures high selectivity during aromatic bond formation, supporting scalable GMP operations in small-molecule drug factories.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF and European Pharmacopoeia monographs relevant to specific APIs
    • FDA 21 CFR Part 210/211 for finished pharmaceuticals

    Typical usage ratio

    • 0.8–1.2 mol equivalent per aryl halide substrate in batch or continuous reactor protocols—adjusted depending on electronic properties of the coupling partner

    Downstream process integration

    • Added during the cross-coupling stage after substrate activation and prior to purification; inclusion is often in the presence of base (e.g., K2CO3) and Pd catalyst, followed by aqueous workup and chromatographic separation

    Final product types

    • Synthesized pharmaceutical intermediates for anticancer, antidiabetic, and anti-inflammatory drugs
    • Custom biaryl fragments for contract research organizations (CROs) and pilot-scale pharma facilities

    2. Specialty Polymer Modification for Hydrogels

    Polymer engineering companies incorporate 4-carboxyphenylboronic acid into hydrogel networks to modify swelling properties, adhesion, and glucose-responsive behaviors. The material’s boronic acid group interacts covalently with diol-containing monomers, creating dynamic networks suitable for biomedical and sensor applications.

    Industry compliance standards

    • ISO 10993 Biological Evaluation of Medical Devices – Part 5: Tests for Cytotoxicity
    • USP Class VI plastics testing (where hydrogels interface with biological tissues)
    • ISO 13485:2016 Medical Devices Quality Management Systems

    Typical usage ratio

    • 2–6 wt% relative to total monomer mass; the amount adapts to required cross-linking density and target mechanical properties

    Downstream process integration

    • Dissolved or dispersed into the aqueous monomer mix prior to radical polymerization; functionalization occurs during network formation, with attention to pH control to maximize boronic ester formation

    Final product types

    • Smart hydrogel discs and sheets for glucose-sensing platforms
    • Biomedical patch materials for wound management
    • Microfluidic device absorbers and portable diagnostic cartridges

    3. Organic Electronic Materials: OLED and OTFT Fabrication

    Finely tuned organic electronics rely on boronic acids as key building blocks for synthesizing precision biaryl and polyaryl motifs, critical for organic light-emitting diode (OLED) emitters and organic thin-film transistor (OTFT) active layers. This compound supports the controlled creation of conjugated structures, affecting charge mobility and stability within display and flexible electronics manufacturing.

    Industry compliance standards

    • IEC 62341 for OLED display safety and performance
    • RoHS Directive 2011/65/EU on restriction of hazardous substances in electrical and electronic equipment
    • JEITA standards for organic electronics materials

    Typical usage ratio

    • 0.6–1.5 equivalents per aryl-halide functionalized electronic intermediate, depending on chain length and electronic requirements of the target oligomer

    Downstream process integration

    • Employed during solution-phase Suzuki coupling to assemble biaryl linkages; product is purified by recrystallization or chromatography before downstream device fabrication, ensuring defect minimization and reproducibility

    Final product types

    • Organic semiconducting polymers for OLED backplanes
    • Active layers in OTFT displays and sensors
    • Emissive materials for solid-state lighting prototypes

    4. Chemical Sensor Reagent Formulation

    Analytical device manufacturers use this boronic acid as a reactive component in colorimetric and fluorometric sensors designed to detect carbohydrates, catechols, and peroxides. Conjugation to signaling dyes produces selective binding sites, particularly in biosensor strips and solution-based glucose detectors, allowing differentiation based on molecular recognition.

    Industry compliance standards

    • ISO 13485:2016 for medical device reagent components
    • CE marking standards for in vitro diagnostic (IVD) devices
    • Sigma Aldrich confirmed methods for calibrating laboratory analytical reagents

    Typical usage ratio

    • 0.2–2.0 wt% of the total sensing matrix; adjusted according to required analytical sensitivity and background interference levels

    Downstream process integration

    • Conjugated to reporter molecules during sensor matrix formulation; added prior to film casting or immobilization onto detection substrates during batch or continuous processing

    Final product types

    • Disposable glucose test strips
    • Sensing films for laboratory analyzers
    • Pre-coated diagnostic cartridges for point-of-care biomarker detection

    5. Fine Chemical Synthesis for Agrochemical Intermediates

    Manufacturers of agrochemical actives utilize this material to build biaryl motifs employed in advanced herbicide and fungicide scaffolds. Its specificity in Suzuki–Miyaura reactions offers high yield of desired coupling products, reducing side reactions and simplifying post-reaction purification in downstream synthesis campaigns.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 9001:2015 Quality Management for agrochemical production
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EC 1907/2006)

    Typical usage ratio

    • 1.0–1.3 equivalents per brominated or chlorinated aromatic intermediate—tailored based on the substrate’s reactivity and required yield for scale-up

    Downstream process integration

    • Fed into catalytic cross-coupling reactors alongside halogenated co-reactants; product is typically separated via liquid–liquid extraction, then crystallized before formulation into the final agrochemical

    Final product types

    • High-purity biaryl intermediates for fungicides
    • Advanced herbicide precursors
    • Key building blocks for select insecticide research pipelines
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    Certification & Compliance
    More Introduction

    4-Carboxyphenylboronic Acid: Experience from Manufacture to End-Use

    Decades on the Production Floor: Understanding the Realities of 4-Carboxyphenylboronic Acid

    In all the years spent inside chemical plants, laboring over syntheses, watching pressure gauges, and troubleshooting crystallization tanks, a few specialties stand out for their versatility and challenge. 4-Carboxyphenylboronic Acid belongs to this category. Chemists rarely see this molecule outside of a technical journal, but for manufacturers, each batch tells its own story, both during production and long after it’s shipped to clients who depend on reliability.

    Although raw boronic acids share some reactivity, the 4-carboxy substitution gives this acid a distinct place on the workbench and in downstream chemistry. From the first steps—starting as basic aromatic substrates, working up through controlled reactions, and ending with careful purification—experience has shaped both safety expectations and process choices. Every time a new customer comes to us, curiosity often meets a mix of experience, warnings, and optimism, especially when their application demands something just beyond the standard.

    Model and Specifications: The Working Details

    We’ve run the 4-Carboxyphenylboronic Acid line up to commercial scale multiple times. The product crystallizes to a white to pale off-white powder, with consistent particle size thanks to our filtration and drying protocols. Typical purity, as regularly tested by HPLC, reaches 98% or above. Water content, controlled by vacuum drying, keeps below 0.5% to avoid hydrolysis during sensitive transformations. Molecular formula, C7H7BO4, with a mass of about 165 grams per mole, shows up clearly in our QC reports. Every operator knows the smell, the feel under the spatula, and the way the powder settles on the trays after oven drying.

    Some users care about the fine details: bulk density, batch-to-batch reproducibility, and the absence of residual solvents, especially for API intermediates. We tighten our controls based on this feedback. At scale, even minor tweaks—adjusting crystallization temperature or switching solvent ratios—bring noticeable improvements in handling or downstream performance. Over time, we’ve adopted such small improvements after direct requests from medicinal chemists and polymer researchers, who notice these subtleties right away in their own results.

    Unique Features from the Manufacturing Perspective

    Handling boronic acids brings certain quirks. 4-Carboxyphenylboronic Acid draws some moisture from the air, so our team seals every drum while still warm from drying. Older methods left faint clumping, difficult for small vials and automated feeders. Now we vacuum seal the stock in nitrogen to guarantee flow properties, even during humid shipping seasons.

    Stability has been reliable across many batches, though it took some years to arrive at this point. We saw how some unchecked microparticles tended to yellow on storage. The solution came from upgrading the filtration and minimizing exposure to strong light in the final drying area. Anyone running kilo-scale production knows these headaches can multiply down the road, and these hard-learned lessons reflect in today’s clean, odorless powder. There’s a careful balance between efficiency and quality metrics, since adding extra purification can drive up costs and reduce yield, but long-term repeatability carries more weight for the applications our partners pursue.

    End Uses: Success Stories from the Field

    Chemists order 4-Carboxyphenylboronic Acid for Suzuki-Miyaura cross-coupling. The extra carboxy group at the para position opens new doors for creating advanced biaryl structures, linking complex pharmaceuticals, and preparing organic electronic materials. We’ve watched this compound become a starting point for medical imaging agents, fluorescent probes, and smart drug delivery vehicles. Teams in universities and startup labs both share feedback on yields, purification struggles, and the subtle differences between production lots.

    One biopharma client reported higher yields in their conjugation reactions, attributing success to the consistent purity and particle size of our 4-Carboxyphenylboronic Acid. In another situation, a polymer scientist highlighted the product’s ability to anchor boronate esters, leading to materials with improved hydrophilic balance. Our production team incorporates this direct feedback into daily process checks, rather than waiting for customer complaints. Updates in our documentation systems ensure that each change, even the smallest, is logged and reflected in regular audits.

    Differences Compared to Other Boronic Acids

    Among boronic acids, the 4-carboxy derivative stands apart for two main reasons: water solubility and functionalization flexibility. Most arylboronic acids dissolve poorly in water, complicating large-scale reactions for anyone aiming to avoid chlorinated or aromatic solvents. The para carboxy group improves solubility, and gives a reactive handle for further chemical transformations—forming esters, amides, or direct metal chelation.

    On our production line, we treat 4-Carboxyphenylboronic Acid differently from species like phenylboronic acid or 3-pyridylboronic acid. The carboxylic group requires extra attention in pH adjustment and crystallization. Yield optimization comes not from theoretical calculations but from repeated batches, subtle tweaks, and months of monitoring analytical results. Our operators quickly learned how to distinguish a well-formed batch by appearance and drying time.

    As for safety, our records show fewer incidents with this material than with more volatile boronic acids. Lower dustiness reduces respiratory risks, especially with our current sealing system. Every new batch still gets analyzed for potential trace metals and organic impurities—some sourced from the raw materials, others from reactor walls or cleaning solvents. We share all test results with clients, building trust through transparency rather than slogans.

    Keeping Pace with Evolving Industry Demands

    Years ago, only a handful of pharmaceutical projects mentioned 4-Carboxyphenylboronic Acid. Now, requests come in from diverse sectors, including agricultural chemistry, diagnostic startups, and energy materials. Most inquiries start with fundamental questions about batch safety, consistency, and impurity profiles. Over time, we’ve learned that responding openly to these needs keeps our product relevant and trusted. One memorable case involved a university requesting deeper insights into our process route so they could replicate small-scale runs for their own research. By providing insight into our approach—careful temperature profiles, rapid isolation, and extensive post-crystallization drying—they solved their own bottlenecks. We benefited, too, adapting their improvements back into our process.

    Another important evolution involved sustainability questions, which now form a regular part of supplier audits. Our team streamlined waste reduction and improved filter media recycling, steps which slashed process water use and reduced regulatory headaches. Every batch now includes a process summary with environmental data for clients focused on Green Chemistry initiatives. Some clients choose vendors based not just on pricing but on objective environmental performance, so we take this reporting as seriously as purity metrics.

    Concrete Problem Solving: Lessons from Practical Experience

    Real-world process failures teach more than any textbook. Years ago, one failed reaction traced back to minute contamination—just a minor residue left in a storage vessel. Trained eyes on the final filtration step solved the mystery. We updated the vessel cleaning protocol, and introduced spot-checking on random drums.

    Powder compaction during international shipping used to create lumps that frustrated users. Initial ideas leaned on mechanical mixers, but dedicated repackaging under inert atmosphere made the difference. This upgrade eliminated user complaints about irregular dosing, especially for robotic synthesis platforms.

    Customers researching scale-up for gram-to-kilogram synthesis expressed concerns about purity drift and impurity buildup during larger runs. Our answer came by setting up in-line purity monitoring at key steps—not a process required by spec, but justified by time saved tracking down deviations before they reached finished stock. This measure improved reproducibility for both internal use and customer reactions.

    Transport regulations for boronic acids drove us to invest in improved package labeling and moisture-resistant drums, lowering costs from rejected shipments at customs checks. Each of these changes began as a headache, but they now form part of our standard operating protocols.

    Supporting Research, Scale-Up and New Application Development

    Clients across research and industrial sectors count on predictable, detailed delivery documents, allowing their compliance teams to clear hurdles for regulated work. Each shipment leaves with chromatograms, spectral data, and recent batch impurity lists, reducing guesswork required for quality assurance.

    Our team fields questions about custom modifications—alternate salt forms, micronization for specialty dispersions, or impurity-tailored synthesis for scale-up feasibility studies. While large customizations can complicate scheduling, incremental process changes in consultation with users often deliver tangible rewards. Recent examples include shifting filtration to exclude a persistent 4-carboxy-phenol impurity and optimizing the drying step, which helped bring batch performance in line with customer feedback for a high-purity pharmaceutical intermediate.

    We keep close contact with scientists using 4-Carboxyphenylboronic Acid in rapid prototyping and high-throughput screening. These fast-moving projects depend on every batch maintaining analytical fingerprints, batch after batch. By aligning upstream process controls to customer schedules, the lab floor and the production line work together.

    Technical Support and Communication: An Ongoing Partnership

    Fielding technical support means more than sending product sheets—it means walking through real applications, troubleshooting failures, or recommending best practice handling and storage. End users frequently ask how to dissolve or process bulk 4-Carboxyphenylboronic Acid when embarking on large-scale development. We learn from their approaches, tweaking particle size or drying procedures to support unique workflows.

    Supporting documentation includes real analytical runs, not generic templates, and onsite technical teams answer downstream process challenges, sometimes even traveling to customer sites to help implement critical steps. This hands-on support keeps us in tune with the realities of ever-changing research requirements. Feedback—whether a phone call from a bench chemist or detailed summary from a QC team—directs our own internal adjustments far more directly than top-down management decisions.

    We address intellectual property and confidentiality issues in compliance with local laws and customer agreements. Documentation stays with the product, not just registered in a computer, giving shop-floor workers and researchers shared, accessible knowledge.

    Balancing Performance and Practicality: Why Experience Matters

    Manufacturing specialty organoboron compounds demands constant awareness, since regulatory compliance, supply chain hiccups, and research innovation can collide unexpectedly. 4-Carboxyphenylboronic Acid, with its combination of practical chemical features, stability, and user feedback-driven production, forms a core reference point for anyone in the field. Its successful adoption traces back to people who spend time on the factory floor, log the data, talk to their customers, and aren’t shy about changing protocols to adapt to new science.

    Our collective experience proves that sustainable success can’t rely only on chemical theory. Hands-on process improvement, responding directly to market shifts, and keeping quality standards front and center remain the only way to earn customer loyalty. Every container leaving our warehouse tells a story—not only about molecules, but about the people and choices behind every lot of 4-Carboxyphenylboronic Acid.