Anhui Liwei Chemical Co., Limited
Products

4-Boronophenol


    • Product Name 4-Boronophenol
    • Alias 4-Hydroxyphenylboronic acid
    • Einecs 240-898-3
    • Mininmum Order 1 g
    • Factory Site Lingwu, Yinchuan, Ningxia, China
    • Price Inquiry sales2@liwei-chem.com
    • Manufacturer Anhui Liwei Chemical Co., Limited
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    176666

    Cas Number 25629-18-1
    Molecular Formula C6H7BO2
    Molar Mass 121.93 g/mol
    Appearance White to off-white solid
    Melting Point 120-125°C
    Solubility In Water Slightly soluble
    Synonyms p-Hydroxyphenylboronic acid
    Smiles B(C1=CC=C(C=C1)O)O
    Inchi InChI=1S/C6H7BO2/c8-6-3-1-5(2-4-6)7(9)10/h1-4,8-10H
    Ec Number 695-539-1

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

    Packing & Storage
    Packing 4-Boronophenol, 25g, is supplied in a sealed amber glass bottle with a tamper-evident cap and clear hazard labeling.
    Shipping 4-Boronophenol is shipped in tightly sealed containers to prevent moisture and air exposure, typically under inert gas. Packaging complies with relevant chemical safety and transport regulations. Handle with care—store at controlled room temperature, away from incompatible substances. Label containers clearly, and include safety data sheets with each shipment to ensure safe handling.
    Storage 4-Boronophenol should be stored in a cool, dry, well-ventilated area, away from sources of moisture and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light. Store in a chemical-resistant, labeled container on a secure shelf. Use appropriate secondary containment to prevent spills, and follow all relevant safety and regulatory guidelines during storage.
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    Tel: +8615380400285

    Email: sales2@liwei-chem.com

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    Certification & Compliance
    More Introduction

    4-Boronophenol: A Practical Look at Its Role and Value in Chemical Synthesis

    Introduction to 4-Boronophenol

    From the manufacturing floor to applied research and industrial production, 4-Boronophenol stands out as a versatile and highly functional compound. We produce 4-Boronophenol at the source, not only as a raw material but also as a key building block supporting many downstream syntheses. Behind every batch, careful control over purity, consistency, and trace impurity levels builds reliability into each shipment. This isn't just another commodity—4-Boronophenol sits right at the crossroads of scalable production and high-end application.

    Product Model and Specifications—What Sets Ours Apart

    Among phenylboronic acids, 4-Boronophenol (CAS 5122-94-1) offers a unique substitution pattern. Carrying a boronic acid group directly opposite a hydroxyl group on the benzene ring, the para-orientation confers distinct reactivity compared to ortho or meta isomers. Here, boronic acids are prone to forming reversible covalent bonds with diols, amines, and various nucleophiles, while the phenolic group adds another layer of chemical utility.

    Our process prioritizes fine-tuned crystallization to achieve a purity consistently above 98%. A rigorous approach to solvent removal and particle sizing pushes us ahead of bulked-up imports that rely on surface-level quality control. Spectroscopic and chromatographic checks back every drum and jar, reducing the risk of batch-to-batch variability—a common headache in lab development or scale-up.

    We focus on producing a solid that dissolves readily in polar organics and suitable aqueous buffers—vital for those seeking reaction efficiency or easy handling on bench or plant scale. By optimizing filtration and drying, trace moisture stays well below less scrupulous competitors. Customers have noticed the difference: reproducibility, lack of yellowing, and no fouling in synthetic runs.

    Where 4-Boronophenol Makes the Difference

    In organic synthesis, 4-Boronophenol shows its worth wherever controlled cross-coupling comes into play, especially in Suzuki-Miyaura reactions. The predictable reactivity of the boronic acid group enables straightforward formation of biaryl and aryl-heteroaryl bonds without excessive byproducts or tarring. Through years of collaboration with academic and industrial groups, we've seen this compound accelerate the route to advanced intermediates in pharmaceuticals, agrochemicals, and even specialty polymers.

    Our experience has taught us how boronic acids, including 4-Boronophenol, offer a particular advantage over organostannanes or organozincs: lower toxicity, ease of handling, and less environmental impact downstream. Instead of spending valuable time and resources on strict containment, waste treatment, or exhaustive purification that comes with certain alternatives, users can move directly from reaction to work-up using established protocols.

    In our own pilot plant, switching to 4-Boronophenol for cross-coupling steps has reduced downtime during purification, improved yields by shaving off side reactions, and lowered solvent consumption. Clients in medicinal chemistry appreciate that the para-hydroxy group can act both as a protective handle and a subsequent derivatization point. We've worked with teams searching for kinase inhibitors, fluorescent probes, and diagnostic agents, all capitalizing on the functional flexibility of this molecule.

    4-Boronophenol in Diagnostics and Materials Science

    4-Boronophenol doesn't stop at classical synthesis. The boronic acid motif readily forms boronate esters with sugars, diols, and certain nucleic acid residues. This tendency proves crucial in the design of glucose sensors, as well as in the assembly of supramolecular materials. Our technical team has partnered with groups building sensing devices, where the accuracy and responsiveness of the boronate-diol interaction can define commercial viability. Consistency across batches, which we maintain with strict process monitoring, helps device makers avoid costly recalibration or failed validation in clinical trials.

    Material scientists look for molecules that promote directed assembly, durable linkages, and modular chemistry. The dual functionality in 4-Boronophenol, both electron-donating and electron-accepting tendencies, helps construct frameworks and coatings tailored for specific electronic or optical properties. The ease of further derivatization from the phenolic end is an added benefit: it provides a springboard for custom ligands or surface modifications. Our output supports projects ranging from smart hydrogels to molecularly imprinted polymers, responding to real needs traced back to clear feedback from our partners.

    Comparing 4-Boronophenol with Related Compounds

    Much of the practical value in 4-Boronophenol can be appreciated by contrasting it with close relatives. Meta- or ortho-boronophenols, for instance, display different solubility and reactivity properties, often complicating downstream synthesis. Some researchers may turn to 4-aminophenylboronic acid or unfunctionalized phenylboronic acid, but these lack the same directionality and electronic influences exerted by the para-hydroxyl group.

    Through internal assessment, we’ve seen that 4-Boronophenol generally provides sharper, more predictable transitions in HPLC and LC-MS analysis, which eases in-process control and accelerates both development and QC cycles. Other boronic acids may appear interchangeable on paper, yet those who've worked through real-world scale-up know how seemingly small substitutional changes can swing reaction outcomes. Our product’s consistent morphology and solid-state characteristics mean fewer headaches caused by clumping, flow issues, or hot spots in reactors—details that move from a lab notebook into the margins of process economy.

    Another issue arises with phenol itself, or with dihydroxybenzenes: though abundant and cheap, they can't participate in the same palladium-catalyzed coupling reactions because they lack the boron group. On the flip side, unprotected phenylboronic acid can lose reactivity or degrade too rapidly under moist conditions—something we monitor closely in our packaging and storage lineup.

    Quality as the Outcome of Hands-on Experience

    Synthesizing 4-Boronophenol isn’t without its challenges. Phenol starting materials must be carefully handled to avoid side reactions. Boronation relies on precise control of temperature and reagent stoichiometry to avoid ring over-substitution or catalyst deactivation. Over the years, we've refined our process to limit the need for excessive purification steps, which cut both time and waste. Our operators log minor fluctuations during every run, building a feedback loop that has improved both yield and purity.

    By working close to the source of demand, quality control moves beyond batch certificates. Daily use of spectral analysis—NMR, HPLC, GC-MS—gets hands-on. This gives us early warning if a process drift might lead to trace contaminants, tinting, or even subtle issues like inconsistent particle size that could show up later as filtration problems during formulation. We don’t leave this to chance or just paperwork.

    In one instance, a customer flagged minor discoloration in a finished compound after scale-up. Investigation showed that a slight change in our oven drying schedule altered the microcrystalline habit, trapping tiny bits of moisture that later oxidized in storage. Adjusting granulation and final drying temperatures restored the bright white product everyone expects—testimony to the value of knowledge passed along shop floor to analytical lab, and back again.

    Shipping, Storage, and Application: Lessons from the Field

    Anyone sourcing 4-Boronophenol directly from a manufacturing line knows how environmental exposure impacts quality. Moisture and air rapidly change the color and, over extended storage, may reduce usable product life. We've adapted by moving to double-layer, moisture-barrier packaging as the standard, with desiccant packs included in every drum. On our floor, fresh lots go from reactor to final container with minimal exposure, cutting opportunities for contamination that can plague materials shipped long distances or stored in poor conditions.

    End users across pharma and materials science have adapted our packaging specifications based on direct feedback—switching from bulk hoppers to single-use packs when sensitive compounds must avoid even minor water pick-up. We supply just-in-time schedules for those running lean, high-throughput facilities. Our flexibility comes from understanding what matters: losing a day chasing down quality deviations impacts downstream production more than marginal differences in price or logistics.

    Environmental and Safety Considerations

    Handling boronic acids presents minimal hazard compared to more volatile or toxic organometallic inputs. Traditional Grignard or organotin reagents call for reactors purged of moisture and oxygen, plus heavy PPE and containment. In contrast, 4-Boronophenol allows for efficient coupling reactions under much milder conditions. In our facility, trained staff work with open reactors using well-ventilated hoods and standard containment. Storage compatibility gains an advantage as well: less chance of unwanted side reactions, pressure buildup, or hazardous byproducts during long-term storage.

    Landfill and water toxicity ratings for boronic acids trend lower, and disposal through standard chemical waste partners proceeds smoothly. We maintain compliance with evolving environmental regulations—something our environmental health and safety team tracks continuously. Customers enjoy reduced paperwork for end-of-life disposal compared to outdated coupling agents. It’s not just a box-ticking exercise: over the years, safer alternatives in routine chemistry drive ongoing improvements in both workplace safety and public perception of our industry.

    Scaling Up: Repeatability from Gram to Tonne

    Researchers building a new synthesis route need to know performance transfers from small vial to plant reactor—our reputation rides on it. In the pilot lab, our chemists have patience and process awareness: batch-by-batch comparisons, volumetric titrations, and control of pH and heat load make all the difference across scales. When we supply a new lot for scale-up, we hand over detailed analytical profiles and trackable production batch histories. The direct transferability has saved time and avoided wasted materials for customers pushing toward submission of regulatory data or embarking on preclinical evaluation.

    This experience isn’t theoretical. In one scale-up for a specialty pharmaceutical, we supplied 4-Boronophenol for a Suzuki step late in a synthetic sequence. Weak spots in an earlier, third-party sourced lot blocked consistent conversion. Once our material came in, consistent conversion rates were restored and product isolation improved. By monitoring specific conductivity and byproduct formation in real time, our operators closed the data loop with both the client's R&D and our own teams—ensuring every subsequent batch met or exceeded the original pilot run.

    That in-house feedback shapes ongoing optimization. Adjustment of solvents, tweaks in filtration routines, and even minor shifts in drying conditions reflect real data, not legacy assumptions. Users who need kilogram-scale lots—whether for a standard coupling or for exploration in new functional materials—see measurable improvements both in delivery timelines and in usable yields.

    Challenges and Solutions: What Industry Faces and How We Tackle It

    Scaling production or maintaining purity as demand grows has proven a challenge for the sector. Impurities and variability in particle form can waste resources or spark off specification rejections in process development. Shortcuts in drying, handling, or packaging compromise consistency—leading to costly batch failures further along the chemical value chain.

    Within our operations, we respond to these issues with continual monitoring and practical troubleshooting. We reject over-automation for the sake of it and preserve hands-on oversight by skilled technicians throughout every synthesis, filtration, and packing step. QC technicians are enabled to stop the line and investigate anomalies rather than just pass on problems. Audits by our clients couldn’t be passed without this culture of vigilance and accountability, shaped from decades of feedback and evolving practice.

    Another industry-wide issue is the sourcing of high-grade intermediates against a backdrop of spot shortages, shipping delays, or sudden regulatory shifts. By retaining core manufacturing in-house—rather than sourcing blended intermediates from third parties—we don't get sidetracked by supply surprises or non-traceable contaminants. Inventory management means steady product for existing clients, with the flexibility to take on additional requests for R&D or novel synthesis paths.

    Operational feedback pushes process improvement constantly. Process bottlenecks, such as build-up during precipitation or filter cake hardening, have been met with physical adjustment of agitators or introduction of anti-caking agents only after confirming chemical compatibility. Feedback loops like these, from plant to desk and back to plant, distinguish the direct producer from re-baggers or pass-through brokers.

    4-Boronophenol: Real-world Impact and Customer Stories

    A product is more than its purity statement; its true merit shows up under commercial and research pressures. Pharmaceutical customers, for example, share how reliable 4-Boronophenol deliveries have kept projects on track when schedule slips on a late-stage compound can sink clinical timelines. Having spent time on both procurement and lab sides ourselves, we understand the frustration when trace lot contamination or paperwork delays drag projects behind target. A steady hand at the production end brings confidence that goes beyond the data sheet.

    In another case, a materials science client developed a new diagnostic device leveraging boronic acid-sugar recognition. They prioritized batch consistency to pass rigorous validation steps—gaining both regulatory approval and customer trust for their deployed product. Our role didn’t stop at supply: tech support shared data, addressed queries on impurity profiles, and adjusted shipping to fit rapid prototyping schedules, all drawn from direct experience with what matters in a manufacturing environment.

    Even smaller users—independent contract research groups and university labs—comment on the professional difference they notice compared to buying generic grade intermediates. It comes down to more than chemical composition: reproducibility, transparency, and a willingness to communicate hard truths about product limitations or compatibility with challenging reagents build lasting trust. Over the years, collaboration on new applications or troubleshooting of challenging syntheses has generated improvements that feed directly into how we design, test, and support 4-Boronophenol.

    Continued Innovation and Looking Ahead

    Chemistry is never static. The types of molecules needed by industry and research change as product lifecycles accelerate. Feedback from users, changing environmental requirements, and fresh regulatory landscapes drive us to refine and adapt our manufacturing pipelines. Continuous investment in analytics, from spectral libraries to particle size determination, keeps our 4-Boronophenol on par with evolving expectations. Formalizing these strategies at plant level makes success sustainable, and delivers a product that reflects lessons learned and a willingness to innovate.

    We are always ready to adapt specifications for unique downstream requirements, be it for new coupling partners, alternative solvent systems, or creative applications in next-generation materials or biosensors. Our job is to supply both consistency and flexibility—reflections of longstanding technical know-how shaped by day-to-day operational realities.

    The Value of Direct Supply and Experience

    4-Boronophenol, produced at the factory floor level, offers more than a line on a catalog. Every lot shipped reflects insight, improvement, and a commitment to quality inherited from years of chemical manufacturing experience. Researchers and industrial users gain resilience, reliability, and collaboration—all from dealing with producers who know their material inside and out. The difference shows in each final product—from advanced therapies to precision materials—helping shape future innovation in chemistry and industry alike.