|
HS Code |
318464 |
| Product Name | 3-Ethoxycarbonylphenylboronic Acid |
| Cas Number | 869353-23-7 |
| Molecular Formula | C9H11BO4 |
| Molecular Weight | 193.99 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 92-95°C |
| Purity | ≥98% |
| Solubility | Soluble in organic solvents such as DMSO, DMF, and methanol |
| Smiles | B(C1=CC=CC(=C1)C(=O)OCC)(O)O |
| Boiling Point | Decomposes before boiling |
| Density | 1.26 g/cm³ (estimated) |
| Storage Condition | Store at 2-8°C, protected from moisture |
As an accredited 3-Ethoxycarbonylphenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 5-gram amber glass bottle, sealed with a screw cap, and labeled with hazard, CAS, and supplier information. |
| Shipping | 3-Ethoxycarbonylphenylboronic Acid is shipped in tightly sealed containers under ambient conditions. Packaging complies with chemical safety regulations to prevent moisture and contamination. It is labeled with proper hazard information and handled as a laboratory chemical. Shipping may be subject to local regulations and restrictions depending on destination and quantity. |
| Storage | 3-Ethoxycarbonylphenylboronic acid should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature (15–25 °C). Avoid exposure to incompatible materials such as strong oxidizing agents. Store away from sources of ignition and always follow standard laboratory safety protocols when handling this chemical. |
Applications of 3-Ethoxycarbonylphenylboronic Acid in Industrial Manufacturing3-Ethoxycarbonylphenylboronic Acid serves as a specialized intermediate in advanced organic synthesis, supporting high-value manufacturing for pharmaceuticals, agrochemicals, OLED materials, and fine specialty polymers. Our production focuses on strict process control, traceability, and regulatory compliance to enable precise large-scale formulation and end-use performance. Below are key industrial application segments supported by our raw material. 1. Pharmaceutical Intermediates for Targeted Oncology APIsLeading pharmaceutical manufacturers use this compound to construct biaryl scaffolds for kinase inhibitor APIs, utilizing Suzuki-Miyaura cross-coupling reactions. The material enables selective functionalization and downstream purification in multi-step API synthesis, especially for anticancer agents with carboxylate groups. Batch records often link the purity grade to final molecule conformational integrity and regulatory filings. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. High-Purity Electronic Materials for OLED EmittersOLED material manufacturers incorporate this compound for the construction of luminescent aryl building blocks, crucial for emitter layer synthesis in display panels. The boronic acid group supports efficient C–C bond formation, controlling purity and defect levels in electronic-grade organic semiconductors. Quality control emphasizes trace metal removal to reduce device pixel failure rates. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Fine Agrochemical Synthesis for Novel Herbicide CompoundsAgrochemical producers utilize this intermediate during the aromatic substitution stage for new-generation herbicide actives. The compound fits aryl-coupling reaction parameters used in scalable plant protection formulations, ensuring traceability and batch-to-batch consistency for regulated field application registration. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Specialty Polymer Synthesis for Advanced Material PerformanceSpecialty polymer manufacturers use this raw material to introduce functional phenyl units in high-performance polymer chains. The inclusion process optimizes polymer solubility and glass transition temperature enhancements, suitable for high-strength coatings and engineering plastics with defined optical or thermal properties. Batch documentation links each raw material lot to final polymer QC data. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 3-Ethoxycarbonylphenylboronic Acid prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Many years in the chemical manufacturing sector have taught us how important it is to get small details right—especially with advanced reagents. 3-Ethoxycarbonylphenylboronic Acid, CAS number 871127-26-3, comes up repeatedly in conversations with colleagues and customers who need reliable performance in their synthesis work. While the formal name might sound intimidating, this compound sits at the core of cross-coupling reactions for agrochemicals, pharmaceuticals, and advanced materials. The way we approach its production is shaped by our experience and commitment to rigorous quality.
Gallons of solvent, kilograms of boron reagents, and careful hands in every shift all play a part in getting product consistency. As a manufacturer, we know how much researchers rely on a repeatable melting point and a predictable HPLC purity—often above 98%. Impurities from the raw materials or side reactions in catalytic steps can pose real problems. Impurities rarely just slow things down; a single unknown interfering substance can throw off a pharmaceutical intermediate and cause weeks of setbacks. We battle that in our reactors using careful temperature controls, tight vacuum filtration, and follow-up analysis with NMR and chromatographic checks for each lot.
Working with 3-Ethoxycarbonylphenylboronic Acid has also revealed a lot about packaging. It might puzzle outsiders, but the right packaging stops hydrolysis and guards against accidental exposure. Many compounds with boronic acid functionality react slowly with moisture, but once enough water enters the container, batch integrity falls apart. Glass bottles with PTFE-lined caps end up being more than a delivery vehicle—they’re the difference between a shelf-stable product and one you need to remake. Every year, we review feedback from buyers and partners to refine our storage approach, always aiming to ship out powder with the crisp, off-white appearance researchers expect.
We have watched demand for 3-Ethoxycarbonylphenylboronic Acid grow alongside the surge in Suzuki-Miyaura cross-coupling research. With its ethoxycarbonyl group, this compound provides a unique entry point as a masked carboxylic acid. The ethyl ester function stays intact through many reaction conditions, only to be unmasked after the key aryl-aryl or aryl-heteroaryl bond formation. This kind of selective reactivity matters to chemists. It opens up possibilities for making substituted aromatics that would not survive harsher routes.
Some of our customers compare this product to standard phenylboronic acid or pinacol boronate derivatives. What they find is a balance between ease of handling, stability under Suzuki conditions, and simple deprotection to the carboxylic acid after coupling. Pinacol boronates often bring extra steps with their stability, but they do not always offer the clean hydrolysis that the ethoxycarbonyl group releases. For anybody running medicinal chemistry campaigns, fine-tuning late-stage functionalization has a direct impact on speed and resource use. The flexibility our product gives proves most effective during rapid library synthesis.
You will see specification sheets all over the internet, but making these standards mean something in daily work is another challenge. For us, the starting point is always a solid assay result. The people on our production floor do more than just check paperwork; every new batch runs through an in-house HPLC system, often with method development tailored to spot the tiniest breakdown products. Not every manufacturer will go to this length. Our regular process for 3-Ethoxycarbonylphenylboronic Acid maintains purity above 98%, recorded by both HPLC and NMR integration. Minor residual solvents stem from crystallization processes but always get trimmed by progressive drying rather than shortcuts.
On the solid-state front, the crystalline form drives filterability and downstream reaction efficiency. Granule size matters less than flowability and dust control—losing material to the air during flask charging means time wasted recapturing or cleaning up. We owe it to our clients to package and ship product in a way that supports the best outcome in every lab, from gram-scale academic work to hundreds of kilograms for commercial campaigns.
Over the years, we have learned how pricing pressure shapes how factories operate. Sometimes new entrants take shortcuts: less rigorous impurity control, recycled solvents not fully stripped, "mixed-batch" philosophy to keep stock moving. These choices might seem trivial when the compound first arrives. Trouble builds up down the line, with fouled reactor loads, inconsistent result reproducibility, and unexplained side products. Years of troubleshooting reactions alongside our customers consistently show us that the quiet, persistent investment in production discipline pays off. No headline-grabbing innovation—just careful cleaning, skilled hands, and validation at every stage.
Unlike some alternatives circulating from traders and brokers, our 3-Ethoxycarbonylphenylboronic Acid comes directly out of our own reactors. We take responsibility for every variable: where the boric acid starts, how we dry and grind it, the way our staff rinse vessels between runs. This kind of traceability is impossible to guarantee on the open market when anonymized intermediaries introduce risk at every handoff. In the field, most buyers do not see that difference up front, but they call us when residues and off-odors creep in, or when results do not match literature procedures. That is one reason why our engineers double-check every unexpected outcome, even from samples returned after long storage. Knowledge about failure informs stronger procedures, batch after batch.
Producing boronic acids and their derivatives used to mean high levels of boron waste. As regulations tightened and customers pursued more sustainable operations, we changed our catalyst protocols, waste acid neutralization, and extraction steps. 3-Ethoxycarbonylphenylboronic Acid presents some specific challenges; trace boron residues tend to remain in aqueous effluents, where local regulators set strict limits. We work closely with our effluent treatment team to monitor outflows and adapt ion-exchange resins to capture boron before discharge, ensuring compliance and a lower environmental footprint. Every kilogram of contained boron not only cuts costs on waste disposal, but also prevents regulatory headaches—something only long-term manufacturers come to respect.
Solvent selection matters as much as waste water control. Typical syntheses start with halobenzenes and boronic ester intermediates, which call for a suite of polar and non-polar solvents for phase separations. For 3-Ethoxycarbonylphenylboronic Acid, optimizing for minimal solvent loading reduces exposure risk and transportation bulk. Years back, we moved away from chlorinated solvents entirely on these lines, substituting with safer alternatives and tweaking reaction times. These changes came slowly, through trial, error, and listening to the stories from process chemists doing real work in noisy, cramped pilot plants.
Walk into our quality lab and you will see battle-worn analytical instruments running validation standards, not just new paperwork. For this boronic acid, every lot must match a strict IR fingerprint, align with reference NMR, and confirm peak integrity on calibrated chromatography systems. We learned not to rely on a one-size-fits-all HPLC method—impurities in this product often shift under acidic or basic mobile phase, so we switch columns and detectors regularly. Some competitors might skip these steps, trusting older data. Our approach values ongoing calibration over legacy results, catching seasonal or supplier-based raw material shifts before they cause major problems.
Packing samples into inert-atmosphere vials, especially during high summer humidity, keeps moisture pickup low. We took this lesson from a string of failures many years ago; today, real-world QA means dryrooms, tight resins, and the patience to regrade finished goods if any storage sampling shows drift. By investing in resilience instead of marketing hype, we maintain product integrity and deliver what our partners actually use, not just what they expect on a website.
For customers, the real test does not happen in our factory but in their lab notebooks. Our partners use 3-Ethoxycarbonylphenylboronic Acid to build biphenyl carboxylates, heteroaryl-coupled libraries, and key pharmaceutical intermediates—often scaling the same set of coupling conditions from a single well plate to reactors large enough to fill a pallet. Having a direct line of communication with users gave our team feedback about which product characteristics matter most: clean dissolution in reaction solvent, low foaming on addition, and a quick, single-step hydrolysis after coupling. Each time a synthetic route stalls, we check the final structure, scan for sidebursts, and offer advice based on both our test data and the anecdotes customers share around the world.
Some smaller labs struggle with clogging and filtration during workup; we have taken these experiences back into our own process design, shifting particle size and adding filtration steps upstream to save time downstream. In scale-up settings, minor impurities that seemed harmless at gram-scale suddenly create colored residues or downstream separation headaches. By tracking these trends over the years, our plant team reduced non-volatile residues that hinder distillation and purification, lowering waste and total costs for buyers attempting first-time kilogram campaigns.
Supply chain fragility increased after major global disruptions, and specialty reagents like 3-Ethoxycarbonylphenylboronic Acid saw dramatic swings in lead times. As a manufacturer, we buffered common raw materials and developed local supplier relationships to shield against scarcity. Stockpiling brings its own risks—over-aged stock can drift in purity or lose physical integrity. We resolved these challenges by rotating inventory quickly, tying release schedules to real demand, and storing all raw materials under climate control rooms.
Delivering just-in-time means more than resource juggling. By taking full responsibility for every link—from raw boric acid reception to vacuum-packing the end product—we limit mid-stream bottlenecks and avoid the unknowns that come from third-party handling. During periods of tight shipping windows, open communication with port authorities prevented months-long delays. Other buyers told us about losing time and money on untraceable or mislabelled reagents; our solution orients around transparent paperwork and real-time tracking.
Controlling packaging and shipping from a single site produced another unexpected benefit: a strictly controlled chain of custody. Our customers understand who to contact, and how batches relate from shipment to shipment. In an era of increasing compliance and security requirements, this kind of consistency and traceability proved to be more valuable than promises or marketing brochures.
Inside pharmaceutical research, 3-Ethoxycarbonylphenylboronic Acid acts as a versatile partner for building carboxy-functionalized aromatics—essential for molecule libraries aiming at kinase inhibitors, anti-infectives, or chemical probes. Process chemists report less time spent debugging couplings when working with pure, well-characterized batches. In our own labs, we ran multiple validation syntheses to verify robust conversion rates and consistent yields. Across different aryl bromides and heterocycles, we tracked catalyst efficiency, baseline stability, and workup compatibility under varying conditions.
This field testing guides our manufacturing improvements. Customers share results, both good and bad. Every reaction failure gets a full review, from starting material sourcing to workup solvent choices. Regularly, a subtle contaminant or humidity-induced transformation identified in these exchanges leads to a tweak in our production setup. These collaborations force us to keep our standards higher than industry minimums, always targeting performance that stands up to the pace of modern pharmaceutical development.
Confidence in specialty reagents does not grow out of aggressive sales tactics or glossy brochures. For us, every start-up or established firm buying 3-Ethoxycarbonylphenylboronic Acid wants not just “yet another” boronic acid, but a reliable partner with predictable, clean, and reproducible results. We structure our feedback loops for swift response: direct lines to process chemists, quick sample shipments for troubleshooting, and data-driven adjustments to batch records.
Many users now choose to audit our operations directly, walking through synthesis bays, quality labs, and warehouse spaces. We always welcome these visits; nothing replaces the reassurance of clean floors, visible SOPs, and practical answers to tough questions. Years of investment in staff training and technical upgrades make these audits easy rather than stressful. Open collaboration teaches us as much as it helps our partners; often, a customer’s question will trigger process improvements none of us anticipated before.
Manufacturing specialty chemicals well means more than making molecules; it means listening to daily problems and working with users to solve them. For 3-Ethoxycarbonylphenylboronic Acid, process knowledge, feedback cycles, and direct accountability form the basis for product integrity and trust. Our whole team—from production to analytics, packaging to shipping—focuses on delivering a compound that makes your research and production run smoothly, reliably, and confidently.
Every year brings new challenges: technical tweaks to achieve higher purity, regulatory changes tightening environmental standards, and customer demands for quicker, more detailed support. We accept these challenges, knowing the lasting value of steady discipline in working with complex boronic acids. Through steady improvement, honest communication, and transparent oversight, we deliver more than a bottle of reagent—we offer the shared benefit of experience, accountability, and a commitment to scientific progress.