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HS Code |
326813 |
| Product Name | 4-Ethoxycarbonylphenylboronic Acid |
| Cas Number | 128843-06-5 |
| Molecular Formula | C9H11BO4 |
| Molecular Weight | 193.00 |
| Appearance | White to off-white powder |
| Melting Point | 165-170°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Structure | Para-substituted phenylboronic acid with ethoxycarbonyl group |
| Boiling Point | Decomposes before boiling |
| Synonyms | 4-(Ethoxycarbonyl)phenylboronic acid |
| Storage Conditions | Store at 2-8°C, protected from moisture |
| Smiles | B(C1=CC=C(C=C1)C(=O)OCC)(O)O |
| Inchi | InChI=1S/C9H11BO4/c1-2-14-9(11)7-3-5-8(6-4-7)10(12)13/h3-6,12-13H,2H2,1H3 |
As an accredited 4-Ethoxycarbonylphenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 4-Ethoxycarbonylphenylboronic Acid (1g) is a sealed amber glass vial with a screw cap and clear labeling. |
| Shipping | 4-Ethoxycarbonylphenylboronic Acid is shipped in secure, chemical-resistant containers to prevent contamination and moisture exposure. Packaging complies with relevant hazardous material regulations. The product is typically dispatched via ground or air transport, with appropriate labeling and documentation, and should be stored in a cool, dry place upon arrival to ensure product integrity. |
| Storage | 4-Ethoxycarbonylphenylboronic acid should be stored in a cool, dry, well-ventilated area, away from moisture and incompatible substances such as strong oxidizers and acids. Keep the container tightly closed when not in use, and store at room temperature or as recommended by the supplier. Protect from direct sunlight and sources of ignition. Properly label storage containers to ensure safe handling. |
Applications of 4-Ethoxycarbonylphenylboronic Acid in Industrial ManufacturingAs a direct manufacturer with full production traceability, we supply 4-Ethoxycarbonylphenylboronic Acid into critical synthesis routes for downstream B2B sectors. All application information here reflects actual usage validated by customer formulations, process audits, and compliance requirements. The following sections outline specific industrial scenarios where this compound supports regulated finished goods manufacture. 1. Pharmaceutical Intermediate Synthesis (API Manufacturing)Throughout advanced pharmaceutical manufacturing, 4-Ethoxycarbonylphenylboronic Acid acts as a key coupling partner in Suzuki-Miyaura cross-coupling reactions to construct complex biaryl motifs central to modern active pharmaceutical ingredient (API) scaffolds. Our clients integrate this raw material early in their synthesis modules where controlled boronic acid chemistry ensures the precise introduction of ethoxycarbonyl-substituted phenyl rings. Downstream purification steps require full solubility testing and trace impurity analysis, aligning with regulated markets’ pharmacopoeial standards. Industry compliance standards
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2. Agrochemical Active Ingredient ProductionMajor crop protection formulators employ 4-Ethoxycarbonylphenylboronic Acid as a boron-containing building block to synthesize selective herbicides and high-value fungicidal actives. The compound’s well-characterized substitution pattern yields increased molecular stability and helps establish a favorable environmental fate profile in downstream field applications, which clients validate through GLP field and residue studies. Industry compliance standards
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3. Electronic Materials & OLED Intermediate ManufacturingSpecialty electronics and OLED component suppliers utilize this compound for precise aryl-aryl bond construction in organic semiconductor precursors and emissive layer intermediates. The ethoxycarbonyl group introduces defined electronic effects, influencing carrier mobility and color tuning in final device layers, which is verified through device fabrication trials and layer purity control. Industry compliance standards
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4. Fine Chemical Synthesis for Specialty Polymer AdditivesIn the specialty polymer sector, 4-Ethoxycarbonylphenylboronic Acid finds use as a functionalized aryl donor in branched or crosslinked polymer architectures, enabling downstream polymer modification with controlled polarity and mechanical property enhancements. Customers validate structure–function correlations by spectroscopic and mechanical testing of resultant polymer blends. Industry compliance standards
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5. Chemical Research and Analytical Reference StandardsContract research organizations and analytical reference producers source this material to prepare reference compounds for method validation, trace impurity benchmarking, and scale-up process development. Its purity and lot-to-lot consistency allow for certified preparation of assay markers used in regulatory filing and customer documentation, meeting established audit trail and documentation protocols. Industry compliance standards
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We have been developing, refining, and manufacturing 4-Ethoxycarbonylphenylboronic Acid for years, fine-tuning our process across batches large and small. This compound, sometimes recognized by its CAS number 87199-17-5, emerges from careful organoboron chemistry and lends itself steadily to contemporary pharmaceutical and fine chemical syntheses. Our facilities handle this intermediate with careful environmental controls to maintain each lot's integrity and purity. This isn’t a byproduct of outsourcing or contract blending. It is the result of dedicated synthesis, monitored step by step on our production floor.
Chemists in our plant start with strict selection of starting materials. We employ consistent Suzuki-Miyaura cross-coupling conditions and have designed a work-up system that drives reproducibility for each run. Our team routinely reviews yields, impurity profiles, and moisture content—not as a checklist, but to chase down anomalies and deliver stable quality from kilo lab to tonne scale. Early on, we realized that tight control over water and trace metals makes a genuine difference for crystallinity and bench behavior. This material ships as a fine solid, typically white to off-white, staying free-flowing with appropriate storage and packing. These seemingly simple facets grew out of years fighting caking and decomposition, vigorously troubleshooting every step from filtration to drying.
The unique value of this boronic acid comes from its role in modern coupling reactions. Medicinal chemists use it to build complex carbon frameworks, install ethoxycarbonyl-protected aromatic units, and develop analogs for bioactive molecules. Early on, we noticed demand jump whenever a major pharmaceutical patent referenced aryl boronic acids in intermediate steps. Over time, synthetic strategies have increasingly favored organoboron chemistry, given its mild conditions and compatibility with sensitive functional groups. As a direct manufacturer, we pay close attention to these shifts—noting sudden upticks for SAR studies, API development, or customized ligands.
Boron-containing reagents like ours stand apart from traditional halogenated intermediates. Unlike halides, phenylboronic acids allow for cross-coupling reactions under palladium catalysis with fewer byproduct challenges and softer environmental footprints. We see direct feedback from research clients: they prefer this approach over classical Friedel-Crafts or nitration for making biphenyl motifs and other core pharmacophores. By offering a boronic acid with an ethoxycarbonyl substituent at the para-position, our product delivers critical versatility—allowing further derivatization and robust protection under synthetic conditions.
From the first few hundred grams out of the glass reactor, we aimed for more than acceptable purity ranges. Our QA team approaches each lot with high-performance liquid chromatography (HPLC), nuclear magnetic resonance (NMR), and Karl Fischer titration, verifying that moisture, residual solvents, and trace metal content fall well below workable thresholds. We’ve invested in catalyst recovery and mother liquor recycling systems that minimize downstream contaminants. Years of hands-on batch analysis taught us that even small changes in synthesis temperature, order of addition, or crystallization time shape the outcome—the texture of the solid, its shelf life, and its reactivity.
We tune our process parameters using past production records and hands-on troubleshooting—not by theoretical optimization alone. After several scale-ups, we learned how partial pressure and choice of base during the boronation step influence both product yield and byproduct spectrum. Bulk customers rely on us for consistency; small variations in particle size or solubility can ripple all the way to milligram-scale discovery chemistry. Long-term partnerships hinge on our track record: no unexplained color changes, no residue, no hidden compromises. Several customers have sent back observations that our batches dissolve quickly in organic solvents and show cleaner baselines on TLC compared with other sources.
Most research and production chemists know that handling boronic acids sometimes brings headaches: clumping, hydrolysis, sticky residues in glassware. Through iterative process improvements, we’ve reduced water content and ensured residual catalysts stay tightly bounded or removed altogether. 4-Ethoxycarbonylphenylboronic Acid from our lines typically stores well under desiccation and resists hydrolytic degradation longer than unrefined grades on the market. Our staff has sampled competitors' offerings and often found higher levels of pinacol esters, trace halides, or colored fines — inconvenient detours for those seeking clean NMRs or preparative chromatography.
On the benchtop, users report smooth dosing by spatula, dust-free transfer, and easy weighing in open air. Over months, our development team monitored stability under various light and humidity conditions. By purposely storing retained samples in challenging settings, we mapped out the boundary between safe handling and avoidable decomposition, advising our bulk customers on best-practice storage from experience, not guesswork.
After over a decade manufacturing boronic acids and their derivatives, we notice clients turning to 4-Ethoxycarbonylphenylboronic Acid for several key transformations. One major application remains in Suzuki-Miyaura cross-coupling, where this compound enables assembly of substituted biaryl scaffolds, pharmaceuticals, and agrochemical leads. The ethoxycarbonyl group, as a protected carboxyl, offers additional functionalization points post-coupling and allows sequential synthetic operations without deprotection headaches.
Process development teams especially value the robust scale-up we achieve. Our reactors range from pilot glassware through stainless steel fermenters—offering precise temperature and atmosphere control. Scale-up data guides each parameter change, so routine lots echo the qualities seen at the R&D level. This isn’t an exercise in theoretical chemistry; onsite engineers, maintenance crews, and operators track process drift in real time, recalibrating for batch variability. Neither excess sodium salts, skipped solvent distillation, nor slack QA sampling passes muster. By focusing on real process knowledge instead of off-the-shelf parameters, we keep quality producers coming back.
Across the landscape of boronic acids, subtle differences matter. Direct comparison with phenylboronic acid, pinacol boronate esters, or related para-substituted aryl boronic acids reveals distinctions that shape project outcomes. Phenylboronic acid itself lacks the ethoxycarbonyl group, removing a useful point for post-coupling modifications. Pinacol boronate esters show better stability against air and moisture but can introduce more cumbersome deprotection steps and residual esters during work-up and purification.
For chemists aiming to introduce carboxyl or ester handles in their products, our 4-Ethoxycarbonylphenylboronic Acid eliminates extra steps. It slots into common synthetic schemes in place of less functionalized boronic acids, giving process chemists and medicinal teams more flexibility when planning downstream routes. We’ve seen this difference bear out in pilot projects and full-scale campaigns—for example, in the streamlined preparation of phenylacetic acid derivatives or protected amino acid analogs, which otherwise demand additional strategic maneuvers.
We track emerging demand from the pharmaceutical sector. As new patent filings reference boronic intermediates, requests spike for precise isomers and functional groups. Environmental directives and process safety add new pressure: regulators in several markets demand detailed impurity profiles for all intermediates, not just finished actives. Our company responded early by establishing robust traceability and full spectra archives for each batch.
Market trends show that researchers move away from hazardous tin, mercury, or halogenated reagents. Boronic acids, like our 4-Ethoxycarbonylphenylboronic Acid, answer this call with milder, more sustainable chemistry. They support green chemistry initiatives and simplify post-reaction purification, as residual boron byproducts remove easily with aqueous work-ups or solid-phase scavenging. Clients in Japan, Europe, and North America now request strict documentation for the trace elements, water content, and extractables—a challenge that rewards direct manufacturers who maintain strict batch analytics and process discipline.
We didn't settle on our protocol overnight. Early process iterations looked good on paper, yet scale-up revealed new challenges—uncontrolled foaming, oily residues clogging filters, or batches that refused to dry evenly. Rather than shuffling these concerns to a distributor, our technical staff addressed each issue hands-on: adjusting stirring speeds, reagents' addition order, and washing sequences to ensure everything from yield to appearance met customer needs.
One lesson: crystallization temperature profiles matter enormously. Too fast, and form changes or amorphous layers develop, reducing ease of handling and batch-to-batch consistency. Too slow, and impurities cling to product crystals, disrupting color and purity. Our plant supervisors built a decision log, refining the crystallization window through dozens of cycles, sharing findings with everyone from QA chemists to scale-up engineers. The end result: 4-Ethoxycarbonylphenylboronic Acid excludes fine impurities and retains a reliable shelf life, traced every step of the way from raw inputs to finished drums.
Researchers and process engineers notice real differences between materials from direct manufacturers and those sourced through brokers or trading firms. In our experience, extra handling, repacking, and warehousing add small but cumulative impurities, elevate water content, and erode reactivity. Our shipping teams routinely field questions on recent lots: typical analyses, batch specs, moisture profile, and any updates on stability testing. By producing at a single, integrated site, we reduce uncertainty for each recipient, minimizing the unknowns often associated with third-party resellers.
Meetings with research customers reveal preferences for technical support rooted in actual manufacturing know-how. Lab chemists want guidance beyond "store dry," seeking troubleshooting tips that only come from years spent seeing how this boronic acid behaves in different solvents and reactions. We actively pass along real insights — stripping solvents under vacuum, dissolving in polar and nonpolar systems, or recognizing signs of latent decomposition. This comes not from manuals, but from repeated practice and close observation during every batch run.
We take pride in our record of responsible production and quality control. The production line features closed handling systems, waste management protocols, and real-time analytics to prevent contamination and emissions. Solvent recovery systems, vent scrubbing, and in-process monitoring keep operations in tight compliance with evolving global guidelines. The adoption of recyclable packaging and careful tracking of carbon output aligns with the sustainability commitments of our customers—especially in industries increasingly scrutinized for environmental impact.
Quality assurance is not a paper trail. Each batch receives a full set of analyses—moisture, purity by HPLC, residual metal screening, and structural confirmation by NMR. By holding to these standards, we’ve built durable trust with partners requiring both documentation and consistent hands-on performance. The field feedback we receive helps us direct investment in improved drying, packaging, and process automation.
Supply chain stability and reliable logistics continue to test every chemical manufacturer. We invest in raw material stockpiles, qualified alternate sources, and proactive shipment planning. As demand for 4-Ethoxycarbonylphenylboronic Acid rises, driven by both established and emerging markets, we maintain production flexibility—quickly shifting from smaller R&D batches to large-scale campaigns without skipping quality steps. Our internal teams review contingency plans, cross-train on critical operations, and audit key suppliers under a continuous improvement ethos.
Technical teams watch regulatory developments and proactively update procedures—anticipating new guidelines for purity, traceability, and environmental compliance. We share updates and best practices directly with clients, reducing the friction for researchers and procurement officers facing tighter regulatory environments.
Bringing 4-Ethoxycarbonylphenylboronic Acid from kilogram lots to commercial supply takes more than academic know-how and a spec sheet. Setting up the right reactor design, running consistent purifications, troubleshooting off-spec batches, and delivering direct-to-user shipments hinge on real-world experience. Continuous improvement, customer feedback, and in-house innovation keep us grounded in the tangible needs of chemists using this essential intermediate every day.
We continue building technical knowledge batch by batch and remain committed to meeting the needs of researchers and production chemists with a material that bridges reproducibility, safety, and next-generation application potential. As organoboron chemistry continues to grow, we see new uses for this compound at the intersection of medicinal chemistry, materials science, and advanced synthesis. Every lot leaving our site reflects the efforts of teams in the lab, plant, and shipping department—a testament to direct manufacturer expertise and responsibility.