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HS Code |
929340 |
| Chemical Name | 4-Propoxycarbonylphenylboronic Acid |
| Molecular Formula | C10H13BO4 |
| Molecular Weight | 208.02 g/mol |
| Cas Number | 104350-07-2 |
| Appearance | White to off-white solid |
| Melting Point | 170-175°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C, in a dry place |
| Synonyms | 4-(Propoxycarbonyl)phenylboronic acid |
| Smiles | B(C1=CC=C(C=C1)C(=O)OCCCN)(O)O |
| Application | Used as an intermediate in organic synthesis and Suzuki coupling reactions |
As an accredited 4-Propoxycarbonylphenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle containing 25 grams of 4-Propoxycarbonylphenylboronic Acid, labeled with chemical name, purity, and hazard symbols. |
| Shipping | 4-Propoxycarbonylphenylboronic acid is shipped in secure, chemical-resistant containers to prevent contamination and moisture exposure. Packaging complies with all relevant safety and regulatory guidelines. The product is labeled with hazard information and shipped via approved carriers, ensuring safe handling during transit. Temperature control is maintained as required for chemical stability. |
| Storage | 4-Propoxycarbonylphenylboronic Acid should be stored in a tightly sealed container, away from moisture and incompatible substances. Keep it in a cool, dry, and well-ventilated area, ideally at 2-8°C (refrigerator). Protect from light and sources of ignition. Proper labeling and adherence to safety data sheet (SDS) recommendations are essential for safe handling and storage. |
Applications of 4-Propoxycarbonylphenylboronic Acid in Industrial Manufacturing4-Propoxycarbonylphenylboronic acid serves as a specialized intermediate in advanced industrial sectors. Its structure provides unique reactivity for carbon–carbon bond formation and ester group transformations, supporting innovation in targeted downstream processes. Below we detail its practical roles in key application fields. 1. Active Pharmaceutical Ingredient (API) Synthesis—Aryl Boronic Acid Cross-CouplingPharmaceutical manufacturers rely on this compound as a functional boronic acid for Suzuki-Miyaura cross-coupling, introducing a protected aromatic group while maintaining high purity. It allows medicinal chemists to construct biaryl structures found in kinase inhibitors, anti-cancer drugs, and investigational small molecules. Quality management dedicates batch controls to ensure trace metals and impurity profiles remain within strict specification ranges throughout multi-step synthesis campaigns. Industry compliance standards
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2. Agrochemical Intermediate for Herbicide and Fungicide SynthesisAgrochemical producers employ 4-propoxycarbonylphenylboronic acid as a coupling building block, especially for synthesizing biaryl derivatives that exhibit herbicidal and fungicidal properties. Its ester moiety facilitates selective hydrolysis or further transformation after the coupling step, ensuring precise substitution patterns without side reactions common to other reactive groups. Plant-scale facilities optimize batch input based on targeted product structure and process yield data. Industry compliance standards
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3. Electronic & OLED Chemical PrecursorElectronics industry manufacturers select this functionalized boronic acid for preparing advanced organic semiconductors. It serves as a linker in the synthesis of conjugated polymers and arylated fluorene derivatives, contributing to controlled molecular weight distribution in organic LED (OLED) and TFT applications. Production environments perform rigorous metal residue and particle filtration to meet electronic industry purity requirements. Industry compliance standards
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4. Advanced Materials for Specialty Polymers and CoatingsSpecialty polymer formulators use this compound to introduce aryl boronic acid motifs, which allow for further modifications such as cross-linking or pendant functionalization. Its protected ester group can undergo transesterification or selective hydrolysis, enabling block copolymer synthesis for coatings requiring high chemical resistance or tailored adhesion. Thorough in-process validation and cleanliness checks remain crucial to avoid introducing trace organometallic residues into polymer matrices. Industry compliance standards
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5. Chemical Reference Standards and Analytical SynthesisAnalytical laboratories and custom synthesis providers utilize this compound as a reference material and for targeted derivatization reactions where a propoxycarbonyl protected aryl boronic group is required. It ensures traceable results in method validation, purity reference calibration, or in the preparation of analytical intermediates for chromatographic applications. Batches are certified for traceability, solvent residuals, and stability for analytical use cases. Industry compliance standards
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Every step in the creation of 4-Propoxycarbonylphenylboronic Acid reflects years of hands-on experience with organoboron technology. As a direct manufacturer, we've learned that consistency begins with raw material purity and continues through to the care in our finishing procedures. Our model, designated 4-Propoxycarb-Ph-B(OH)2, has built a reputation with chemists working in pharmaceutical research, agrochemical synthesis, and advanced materials discovery. The formula encapsulates more than a string of atoms—it carries the signature of our meticulous processes and the commitment of every technician involved in its crafting.
Specifications are more than numbers—they are checkpoints honed by daily practice. The product has a well-defined melting range, tight purity parameters by HPLC, and routinely low moisture content thanks to controlled drying protocols. We monitor for trace metallics in every batch, using equipment tuned over countless calibration cycles. Each sample tells its own story in the lab, and batches that don’t meet expectations never leave. Our entire workflow stays geared toward producing a product that synthetic chemists can rely on without doubting the next reaction’s outcome.
Over years of meeting with clients and fielding questions, we've noticed how the real value of 4-Propoxycarbonylphenylboronic Acid shines during Suzuki-Miyaura couplings. Its para-positioned propoxycarbonyl group provides electronic effects that make palladium-catalyzed cross-couplings more straightforward, often leading to improved conversions in arylated and heterocycle products. Research teams in drug discovery pipelines gravitate toward this molecule because it unlocks access to complex active pharmaceutical ingredient intermediates. Factory-scale batch syntheses feature it for key acylation sequences—our process supports kilogram-level production runs for clients scaling up preclinical work. The story comes full circle when clients report higher yields or cleaner isolation steps, reducing waste and trimming downstream purification costs.
Having produced a broad range of arylboronic acids, we’ve seen subtle changes in structure profoundly affect outcome. 4-Propoxycarbonylphenylboronic Acid stands apart from its methyl or ethyl ester cousins, as the longer propoxy chain influences both solubility and reactivity during coupling reactions. This isn’t just academic—the para-propoxycarbonyl substitution helps temper hydrolytic instability that can frustrate work-ups using similar boronic acids. Chemists tell us this difference saves time in column chromatography and sidesteps formation of boroxine byproducts often seen with more volatile analogs. The resulting crude tends to filter better, cutting down on total solvent use and exposure in the lab. Every manufacturing lot carries a fingerprint—those working with the methyl analog quickly spot the slower reaction rates or observe extra foaming in aqueous systems. Our product’s profile reduces those headaches, making it a preferred choice for demanding industrial-scale or sensitive laboratory settings.
On our shop floor, the work doesn't end when a reactor stops churning. Cell leader reviews, cross-training, and over-the-shoulder mentoring ensure that even as outputs climb, standards don’t slip. Technicians handle crystallizations by hand, recording viscosity and color changes to catch deviations early. Recrystallization solvents and temperature ramps have been fine-tuned over dozens of production cycles—this hands-on routine narrows the spread in particle size and boosts flow during packaging. Unlike what reaches the market from intermediaries, nothing gets relabeled between us and the customer. Our brand tags reflect real inspection data and direct experience, and every sample request triggers a new review by our QC chemists. This continual dialogue pushes the process to keep up with evolving industry needs—it’s not just about what the certificate says, it’s about what people see on the bench every day.
We engage with leading academic and commercial labs to keep our product tuned to real-world goals. This feedback shapes minor modifications, such as adjusting particle size distribution for better suspension in automated continuous-flow systems or optimizing container materials for longer shelf-life at ambient storage. As direct producers, we have the agility to react to a client’s scale-up trial—if a university team inverts the usual solvent system, we take those learnings back to the plant for the next run. Our notepads fill with insights from these collaborations, and every improvement helps move the needle for the community at large. This spirit of open communication empowers us to support development projects where technical flexibility matters more than bulk pricing.
From the warehouse to the workbench, handling 4-Propoxycarbonylphenylboronic Acid requires attention to detail that only working with the chemistry teaches. Moisture content must stay low—our drying ovens run slow cycles calibrated against seasonal humidity swings, since boronic acids pick up water quickly if left uncapped. Freshly filled drums receive tamper-evident seals, and we include desiccants in every shipment. Technicians avoid open scoops; instead, we provide easy-flow pour tops and recommend single-use spatulas, which our own staff prefer on the filling line. Extended storage never gives rise to problematic solidification, a result of controlling particle aggregation at the micron level during synthesis. Labs working on long-term projects mention the convenience of retrieving consistent, free-flowing powder from start to finish, streamlining multi-month research without worrying about caking or degradation.
Manufacturing boronic acids safely and responsibly isn’t just about compliance. Over a decade ago, we began to redesign solvent selection and minimize heavy metal waste. Today, we recover and purify organic solvents with proprietary in-house distillation setups, and non-recoverable fractions get separated for high-temperature incineration, ensuring hazardous residues never cross into the water table. Plant operators collect statistical data on water and energy consumption daily, tracking improvements from seemingly minor tweaks—like adjusting cooling water cycles—into tangible carbon footprint cuts. We replaced labor-intensive manual pH neutralizations with closed-loop titration systems to cut down on operator exposure and make exothermic reactions easier to control. Even off-spec waste receives careful processing; boron slurries remain isolated, never mixed with other waste streams, to limit cross-contamination.
Fielding calls from chemists frustrated by unreliable supply or inconsistent purity, our technical support team draws on their direct shop floor experience. We’ve assisted troubleshooting on multi-step syntheses where a minor shift in boronic acid quality made or broke a patent submission. Process chemists noted our product’s higher solubility in DMF and tested reaction times; production campaigns reported lower filtration loss using our batches. We gather these insights, log them, and pass them to our staff for immediate response—every issue triggers a root-cause investigation. Instead of distributing blame, we invite researchers for process visits, getting firsthand feedback for the next iteration. Directly hearing what works and what doesn’t reverses the usual customer relationship—our internal teams see firsthand the difference that seamless product performance delivers.
The skill behind our product’s performance reflects ongoing training. Every new hire cycles through both the pilot and commercial plants before leading production themselves. Our older technicians mentor the new hands, teaching how a genuine batch of 4-Propoxycarbonylphenylboronic Acid should smell, how its crystals scatter in the tray, and what purity ‘feels’ like under an IR lamp. Our bulk weighing stations feature double checks—every sample receives both automated and manual mass verification. Career chemists draw from a continuous education fund, taking part in webinars on new cross-coupling technologies and quality advancements. Our group shares discoveries internally, keeping everyone challenged and engaged, from night shift operators to R&D staff. The result is not just stable production—it is a culture where every unit meets a shared bar for excellence.
Regulatory tides can shift quickly, especially with upcoming restrictions on specific solvents, or new classifications for intermediate compounds. We keep a close eye on documentation standards—audit-readiness shapes more than just file cabinets. Tracking raw material origins and rigorous chain-of-custody records, we make sure our documentation responds as fast as legal changes emerge. Chemists working at the bench don’t feel these pressures, but shop floor managers and documentation teams often coordinate days in advance to ensure unchanged lead times for our clients. Market volatility—driven by global events or by the emergence of newly published couplings—means we prepare buffer inventory to bridge temporary supplier gaps. Our direct relationships with glassware and filter manufacturers let us adjust supply without lag, smoothing variations for our partners developing new compounds or scaling up established syntheses.
Every successful campaign in the lab reflects process discipline upstream. Our team meets weekly to go through production records not just for compliance, but to find marginal gains—solvent recapture rates, reaction temperature profiles, or post-reaction pH control. Client feedback becomes actionable targets, such as developing a denser powder version for automated weighing stations in high-throughput screening labs. Sometimes innovation begins with a single operator’s suggestion—a batch record annotated with a near-miss or a shortcut that worked—collated and shared so small changes stack up over time. We aim for flexibility: tooling up new packaging for customers who request single-use sachets or adjusting particle fineness based on performance reports. Our production supports client process improvement efforts, keeping their operations competitive and reliable.
We invest in equipment that enables scalability without compromising the product’s properties. Our multi-purpose reactors permit both small-batch custom development and multi-tonne commercial campaigns, allowing us to serve exploratory researchers and major manufacturers alike. Automated monitoring and closed-transfer lines keep time, temperature, and addition rates within strict tolerances—crucial for hitting the same purity every run. By minimizing manual handling, we cut both risk and operator fatigue, letting teams focus on confirming that every lot performs as promised. This flexibility allows us to rapidly shift between different boronic acid derivatives if new structure-activity relationship studies demand it, leveraging our supply chain relationships to maintain speed and reliability.
Our position as a manufacturer puts transparency and accountability at the core of each transaction. Our order fulfillment happens alongside real-time status updates, and any shipping anomaly triggers a direct response from our logistics coordinator. Clients gain access not only to lots and batch documentation, but also to technical staff prepared to explain any deviation or unexpected observation. In conversations with regular buyers, we learn how production schedules impact research milestones or funding cycles—in some cases, we have expedited custom syntheses to help a partner’s clinical batch materialize on time. This commitment grows stronger through ongoing dialogue, whether adjusting shipping dates around holidays or developing alternate pack sizes for easier solvent addition.
Behind every kilogram of 4-Propoxycarbonylphenylboronic Acid exits a production line guided by thousands of hours’ experience, real-world feedback, and a continuous drive for betterment. Synthesizing this compound demands more than recipe-following; it calls for a deep familiarity with nuances of structure, reactivity, and customer demand. As manufacturers, we don’t simply fill orders—we engage in a hands-on partnership, working with the entire supply chain to keep research and industry moving forward. Each batch reflects what’s possible when expertise, observation, and action converge at scale.