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4-Formylphenylboronic Acid

    • Product Name 4-Formylphenylboronic Acid
    • Alias 4-FPBA
    • Einecs 630-447-2
    • 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
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    Specifications

    HS Code

    314705

    Productname 4-Formylphenylboronic Acid
    Casnumber 87199-18-6
    Molecularformula C7H7BO3
    Molecularweight 149.94
    Appearance White to off-white powder
    Meltingpoint 218-222°C
    Solubility Slightly soluble in water; soluble in DMSO and methanol
    Purity Typically ≥98%
    Synonyms 4-Formylbenzeneboronic acid, p-Formylphenylboronic acid
    Storagetemperature Store at 2-8°C
    Smiles B(C1=CC=C(C=C1)C=O)(O)O
    Inchikey DEIWJFWQBJTOQN-UHFFFAOYSA-N
    Ec Number 617-181-7

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

    Packing & Storage
    Packing The 4-Formylphenylboronic Acid is packaged in a sealed amber glass bottle, containing 25 grams, with hazard and identity labeling.
    Shipping 4-Formylphenylboronic Acid is shipped in tightly sealed containers to prevent moisture absorption and contamination. The product is packaged according to safety regulations, typically inside protective secondary packaging. Shipping is conducted under ambient conditions, with appropriate labeling for chemical safety, and conforms to relevant transport guidelines for hazardous materials.
    Storage 4-Formylphenylboronic 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 2–8 °C (refrigerated). Avoid exposure to incompatible substances such as strong oxidizing agents. Proper labeling and secure storage will help prevent degradation and ensure laboratory safety.
    Application of 4-Formylphenylboronic Acid

    Applications of 4-Formylphenylboronic Acid in Industrial Manufacturing

    4-Formylphenylboronic Acid offers critical functionalities across diverse chemical transformation workflows. Its organoboron structure supports carbon-carbon coupling and fine chemical synthesis under controlled industrial settings. Below, we outline its specialized use cases in real-world manufacturing sectors by process, compliance, formulation, and final output.

    1. Pharmaceutical Intermediate Synthesis (API Construction)

    This compound serves as a key building block in the multi-step synthesis of pharmaceutical active ingredients. Process chemists incorporate it for Suzuki-Miyaura cross-coupling to append aromatic aldehyde motifs, enabling structure–activity optimization in drug discovery and scale-up campaigns. Its reactivity profile is favorable for constructing bioactive derivatives in oncology, metabolic, and CNS product pipelines, where trace impurity control and selective transformation are business-critical.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA for finished pharmaceuticals)
    • EDQM CEP for European API registration
    • Chinese Pharmacopoeia (ChP), European Pharmacopoeia (Ph. Eur.) references for starting materials

    Typical usage ratio

    • 0.7 – 1.3 molar equivalents relative to partner halide in cross-coupling; ratio fine-tuned based on target API yield and downstream purification constraints.

    Downstream process integration

    • Charged at the first Suzuki reaction step after halide activation. Reaction temperature, time, and solvent are adapted to minimize byproducts. In-process controls used for aldehyde recovery and residual boron levels.

    Final product types

    • Small molecule APIs with aromatic aldehyde moieties (oncology drugs, CNS actives, antivirals)
    • Regulatory drug substance intermediates
    • Specialty research chemicals for medicinal chemistry

    2. OLED & Electronic Materials Synthesis

    Materials manufacturers adopt 4-Formylphenylboronic Acid for constructing conjugated organic frameworks used in high-performance electronics. It functions in precision cross-coupling reactions to incorporate functional formyl groups onto phenyl rings, which are essential for molecular tuning in emitter and host materials. Quality and consistency are monitored tightly due to downstream requirements for purity, stability, and electro-optical characteristics in display technology substrates.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • JEITA Standards for Organic Electronics (Japan)
    • RoHS Directive 2011/65/EU for hazardous substances in electronics
    • REACH Annex XVII for substance registration

    Typical usage ratio

    • 1.0 – 1.4 equivalents per aryl halide, depending on target luminescent polymer structure and solvent uptake. Ratios optimized for chain length and end-group fidelity.

    Downstream process integration

    • Fed into polymerization or post-functionalization steps via Suzuki coupling. Integrated at stages where incorporation of formyl functionality is crucial for emission properties. End-product QC includes color purity, charge mobility, and residual boronic content.

    Final product types

    • Organic light-emitting diodes (OLEDs) emitters and hosts
    • Conjugated polymers for display backplanes
    • Small molecule semiconductors for thin-film transistors

    3. Agrochemical and Crop Protection Intermediate Manufacturing

    In agrochemical synthesis, this raw material participates in the creation of advanced intermediates for fungicides, herbicides, and plant growth regulators. The aldehyde-boronate dual functionality provides process chemists with efficient routes to varied functionalized phenyl derivatives. Process development includes careful consideration of reaction conditions to meet environmental, occupational, and residue-level standards for global crop protection markets.

    Industry compliance standards

    • FAO/WHO Good Laboratory Practice (GLP) for pesticide ingredient production
    • ISO 9001:2015 with ISO 14001:2015 for environmental controls
    • EU Regulation (EC) No 1107/2009 for plant protection product approval
    • US EPA Inert Ingredient Review for pesticidal formulations

    Typical usage ratio

    • 1.0 – 1.2 equivalents per active intermediate, tuned according to targeted conversion and byproduct elimination in the final downstream coupling step.

    Downstream process integration

    • Charged during the late-stage intermediate functionalization, often in batch reactors under inert atmosphere with catalytic systems. Post-coupling, purification includes multi-solvent washes and crystallization based on residue specifications for pesticide registration.

    Final product types

    • Key intermediates for herbicide and fungicide actives
    • Precursors for phenyl-based plant growth regulators
    • Specialty agrochemical fine chemicals for seed treatment agents

    4. Active Matrix Resin and Specialty Polymer Production

    Resin and specialty polymer manufacturers select 4-Formylphenylboronic Acid for precision aromatic substitution and functional polymer end-capping. It is used in high-value resin classes requiring tailored reactivity, thermal resistance, and cross-linking capacity. Downstream production demands tight control of functional group distribution to achieve high performance in specialty coatings, binder systems, and engineered plastics.

    Industry compliance standards

    • ASTM D256, D1238 for polymer property evaluation
    • ISO 14001:2015 for environmental management in polymer manufacturing
    • UL 94 flame rating for plastics
    • REACH registration for downstream polymer ingredients

    Typical usage ratio

    • 0.4 – 1.0 functional equivalents per oligomer or pre-polymer chain, adjusted according to target molecular weight and cross-linking degree for specific resin properties.

    Downstream process integration

    • Incorporated into the chain extension or end-capping stage of resin synthesis. Used under controlled temperature and pH to promote uniform functionalization and prevent side reactions impacting polymer integrity.

    Final product types

    • Thermosetting phenolic and epoxy resins with aromatic aldehyde groups
    • Functionalized specialty plastics for electronics encapsulation
    • Cross-linkable binders for composite materials

    5. Laboratory Chemical Building Block Supply

    Research institutions and chemical manufacturers utilize this compound as a precision building block for small-scale synthesis, reference standards, and new molecule prototyping. Its controlled boronic acid and aldehyde functionalities suit parallel synthesis, structure–reactivity studies, and analytical standard production where batch traceability and analytical purity are required to support advanced scientific research and product verification.

    Industry compliance standards

    • ISO 17025:2017 for chemical analysis laboratories
    • GLP standards for analytical reference material production
    • GHS/CLP compliance for labeling and packaging
    • National Institute of Standards and Technology (NIST) traceability for reference materials

    Typical usage ratio

    • Varies from 0.1 – 2.0 mmol in academic or pilot-scale reactions; amounts adjusted for experiment scale, substrate excess, and analytical needs.

    Downstream process integration

    • Measured directly into round-bottom reactors or vials for controlled synthesis. QC performed via HPLC/GC after each synthetic run. Material handling flowsheet includes full batch documentation for reproducibility.

    Final product types

    • Synthesized organic compounds for chemical libraries
    • Analytical reference standards for method validation
    • Intermediates for custom reaction development
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    Certification & Compliance
    More Introduction

    4-Formylphenylboronic Acid: A Closer Look at Its Role and Value in Fine Chemical Synthesis

    Real Experience with Manufacturing 4-Formylphenylboronic Acid

    Years spent in chemical manufacturing don’t just hone technical skills. They build a sense for what makes a truly useful compound. 4-Formylphenylboronic Acid, with the model identifier 87199-15-3, has earned its spot in the portfolio for a good reason. Its chemical structure tells a story: a boronic acid group paired with a formyl-functionalized phenyl ring. This arrangement gives the material a unique reactivity, making it a go-to building block for modern synthesis, especially in pharmaceutical and material science laboratories.

    In the plant, we control the synthesis from raw benzoic acid derivatives, carefully regulating temperature, pressure, and pH to coax out a high-purity, pale powder. Every batch runs through exhaustive quality checks, because anything less than 99% purity risks throwbacks during downstream reactions. We test for moisture, elemental content, and residual solvents, holding the bar high because even minuscule impurities tangle up catalytic work and pharmaceutical product reliability. High resolution NMR and HPLC analyses confirm structure and purity well above the industry norm, with certificate data shared directly with our clients’ R&D teams. Form, function, and traceability intertwine; each batch number records its journey from start to finish, building trust with the scientists who stake million-dollar projects on reagent quality.

    The Role of 4-Formylphenylboronic Acid in Modern Synthesis

    Almost every week, we get questions about how our 4-Formylphenylboronic Acid compares to standard boronic acids or to similar derivatives. Real-world applications drive these questions. In Suzuki coupling, for example, the ortho positioning of the formyl group allows for selectivity that standard phenylboronic acids can’t match. Medicinal chemists value that extra handle for construct design, so our product shows up in both small-scale screening and kilo-lab trials. Some customers purchase it specifically to access formyl-directed transformations, or to introduce a boronic acid group onto aromatic aldehydes where step efficiency matters.

    Compared to more common boronic acids, the formyl group provides a dual reactivity window. In one route, it participates readily in cross-coupling under palladium catalysis, delivering high yields and cleaner products for both library and process-scale chemistry. In another, the aldehyde readily undergoes condensation or reduction, offering customers a way to pivot from aromatic acids to alcohols or imines without reconstructing their synthetic routes. This multi-use flexibility shortens project timelines and sidesteps several classical protection-deprotection cycles. It’s a tangible advantage borne out by feedback from research chemists, not just theoretical promise.

    Practical Standards Set by Manufacturing Experience

    Reproducibility sits at the center of modern chemical manufacturing. For 4-Formylphenylboronic Acid, the challenge isn’t just making the product once—it’s producing it reliably from batch to batch. We have invested in dedicated glass-lined reactors to prevent cross-contamination and to protect sensitive boron-based reagents from trace metals or organics that sneak into stainless steel systems. Each production line includes in-line sampling and validated cleaning protocols. Any deviation in color or analytical fingerprint sends the material back for rework or disposal. Batch-to-batch consistency saves downstream waste and troubleshooting for every user, which reflects back in the steadily rising reorder rates from global pharma, biotech, and specialty chemical sectors.

    Our logistics team handles the packaging with equal care. Moisture remains a constant threat to boronic acid shelf life, so we ship under argon in sealed high-density polyethylene containers. Desiccant packs and double-walled liners reinforce stability during transport and storage. These steps make a difference, as even minor hydrolysis during shipping can degrade yields in reactions and lead to costly failures in screening programs. Customers working in different climates recognize the stability advantage, leading to partnerships grounded in real-world reliability—not just price competitiveness.

    What Sets 4-Formylphenylboronic Acid Apart from the Crowd

    Product differentiation goes beyond specifications on a technical sheet. In the case of 4-Formylphenylboronic Acid, the presence of both the boronic acid and formyl groups on a single aromatic ring creates a synergistic advantage that doesn’t exist in simple analogs. Other boronic acids, such as phenylboronic acid or 4-methoxyphenylboronic acid, usually serve as single-function units in cross-coupling or as starting points in sensor development. 4-Formylphenylboronic Acid manages twice the workload.

    Customers engaged in medicinal chemistry notice this difference early. The flexible reactivity of the formyl group allows them to pivot synthetic plans mid-route. Instead of synthesizing additional intermediates or isolating new building blocks, researchers exploit the dual reactivity in a single compound, lowering costs and minimizing waste. Libraries of candidate molecules, especially for kinase or protease inhibitors, benefit from the reduced synthetic burden.

    Material scientists, on the other hand, value the product for designing advanced polymers and sensor systems. The boronic acid moiety interacts with diol-containing or saccharide-rich environments, giving rise to functional polymers with tailored response profiles. Adding a formyl group on the same ring expands the design palette, allowing straightforward introductions of backbone cross-linkers or fluorescent tags by reductive amination or hydrazone formation. This speeds up the creation of custom materials for diagnostics and sensing, an aspect that’s increasingly in demand from academic labs and industrial research teams alike.

    Addressing Customer Pain Points from the Manufacturing Side

    We keep fielding inquiries from researchers struggling with batch variability from less experienced suppliers. Inconsistent color, off-spec melting point, and trace heavy metal contamination have been reported in products sourced elsewhere. Even minor defects impact catalyst performance and contaminate high-sensitivity applications. Our team tracks each step of the synthesis, dehydration, and purification, integrating both human oversight and in-line analytics. A documented chain of custody from raw material warehousing to final QA ensures that our 4-Formylphenylboronic Acid outperforms on reliability, not just on cost or availability.

    Storage and shelf life remain areas where practical experience counts. We train downstream users to store the product below 25°C, ideally under inert gas, away from direct sunlight and atmospheric moisture. Some clients have improvised with repackaging or secondary containment, but we emphasize the importance of maintaining original packaging integrity. Our technical support staff often works side by side with customer process teams to troubleshoot unexpected reactivity or storage issues, drawing on years of hands-on problem-solving.

    Observations from Day-to-Day Manufacturing and Distribution

    Supply chain reliability has shifted from a background concern to a top priority throughout the chemical industry. Every world event, every trade dispute, echoes through availability and pricing. Our strategy focuses on building robust relationships with both raw material vendors and logistics partners, securing multi-source routes, and investing in local inventory buffers from North America to Europe to Asia. The payoff has been clear during periods of supply crunch—instead of backorders, we keep product rolling to our customers, preserving timelines on drug discovery, material testing, and pilot plant scale-ups.

    Packaging, labeling, and documentation also receive scrutiny from our side. Each container ships with batch-specific certificates of analysis, providing both the expected technical data and the details upstream customers use to clear regulatory reviews. Custom labeling reflects the criticality of proper inventory tracking in regulated environments, where a misplaced decimal or incorrect unit can disrupt entire research programs. Years of experience have taught us to address these operational details before they create bottlenecks for our partners.

    Practical Application Case Studies from the Field

    One major pharmaceutical client used our 4-Formylphenylboronic Acid as a linchpin in a development program for kinase inhibitors. Early iterations with third-party materials failed screening due to trace palladium and inconsistent product purity. After switching, their synthesis delivered target compounds reproducibly, with final HPLC purities exceeding 98% across the board. Project managers reported that eliminating rework and resynthesis saved weeks of precious development time, highlighting how steady quality translates into direct R&D cost savings.

    In material science, research groups exploring glucose sensors leveraged the boronic acid’s specific diol binding paired with aldehyde-directed linkage chemistry. Their advanced polymer formulations delivered sharper signal response and reproducibility over previous designs, thanks to the combined structure in our product. A university team published results citing the reliability of the feedstock as a key enabler. We take pride in supporting discoveries that couldn’t have advanced so efficiently without this specific reagent.

    Smaller contract research organizations remind us daily that service matters as much as chemistry. Rush orders often arise as project scopes shift. Our ability to flex production slots and expedite air freight shipments has convinced several partners to make our 4-Formylphenylboronic Acid their default input, not just for one project, but as a platform chemical for ongoing library expansion and scale-up.

    Continuous Improvement through Customer Collaboration

    In a fast-moving field, nobody holds all the answers. We listen carefully to feedback from formulators and process chemists. Some prefer tighter particle sizing, while others request isolated product fractions for specific transformations. Our R&D and production teams make incremental adjustments based on real user demands, rather than theoretical surveys. Every adjustment—whether in crystallization, drying times, or secondary purification stages—grows from partnership, not one-way instruction.

    Factory staff regularly hosts visiting scientists, both from direct clients and academic consortia. These open-house tours deepen the exchange, revealing operating details and shared solutions—like improving moisture handling or fine-tuning purity profiles. Cross-learning ensures that the final product reflects joint expertise, not just supply-chain performance. Post-project reviews highlight where we succeeded or fell short, and these honest appraisals shape both our technical roadmap and everyday plant operations. Growth comes from shared experience, not just from isolated process tweaks.

    The Value of Direct Manufacturing in Product Integrity

    Ownership of the entire manufacturing process gives us a hands-on view that traders or third-party distributors lack. We catch issues at the earliest points, like subtle color shifts signifying trace contaminant presence. Investing in plant upgrades, introducing automated filter presses, and building in-process checks—all come from our direct investment in making a better product. Clients who visit our plant gain confidence from witnessing in-house analytics and production transparency, fostering relationships built on observable fact, not marketing or intermediary promises.

    Direct manufacturing also means full accountability for every bottle that leaves our facility. There’s no ambiguity when an issue arises; our technical team traces difficulties to a specific process step, whether raw material inconsistency, process drift, or packaging misstep. A feedback loop from user lab to technician’s bench keeps us sharp and constantly improving. No request goes unheard; we work with scale-up partners to validate new process windows and production systems before full commercial rollout. This approach sets us apart in reliability, integrity, and customer confidence.

    Looking to the Future: Innovation, Sustainability, and Responsiveness

    Sustainability forms an ever-larger part of chemical manufacturing responsibility. We source solvents and inputs from audited suppliers, reducing hazardous byproduct generation wherever possible. Waste streams pass through continuous monitoring and reclamation, not just periodic checks. Our operations meet stringent local and international standards, from emissions controls to hazardous material handling protocols. By keeping production under one roof, we maintain direct oversight and learn from each incident to minimize environmental footprint.

    Innovation stems from this ground-level perspective. Scaling 4-Formylphenylboronic Acid from kilogram to multi-ton volumes tests every system, from reactor design to safe packaging solutions. Our technical staff relishes the challenge of adapting production lines and logistics chains for high-volume, high-purity delivery. Responsive supply chains, transparent communication, and relentless product benchmarking keep us ahead in a market where cheap substitutes falter under the realities of pharmaceutical or high-tech infrastructure.

    Real Benefits for Users Across Sectors

    Customers using our 4-Formylphenylboronic Acid don’t just receive a reagent—they secure a competitive edge. Pharma companies value quality control and batch repeatability, which keep candidate pipelines moving and regulatory filings airtight. Academic teams get stable, reproducible material for their high-stakes grant research, avoiding the project delays and wasted funding that follow unexpected reagent inconsistencies. Material scientists leverage the dual-reactivity for new sensors, functional polymers, and diagnostic materials that set trends in emerging fields like point-of-care medical devices.

    Industry partnerships deepen with every delivery, long after the initial sale. Our technical specialists support troubleshooting, guide users in optimal reaction design, and flag emerging supply issues before they disrupt downstream planning. Mutual trust has brought us into collaborative product development on next-generation boronic-acid compounds, targeting additional functional groups and synthetic handles custom fit to unique client projects. We see this as the future of specialty chemical manufacturing: seamless collaboration, rapid response, transparent process, and robust, reliable product lines.

    Why 4-Formylphenylboronic Acid Remains a Must-Have Reagent

    The feedback we get underscores the compound’s role as a practical, efficient, and versatile platform in modern organic synthesis. The balance of formyl and boronic acid moieties continues to open doors for method developers, library builders, and innovators in molecular design. Manufacturing it is more than a technical challenge—it’s an opportunity to support discovery, enable new science, and foster relationships grounded in integrity and experience.

    Our team stands behind every shipment, inviting clients to benefit from decades of know-how and a longstanding commitment to quality, transparency, and innovation. Through ongoing conversation and technical partnership, we aim to keep 4-Formylphenylboronic Acid at the cutting edge of chemistry, building a legacy that rests as much on trust and performance as it does on chemistry itself.