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HS Code |
122618 |
| Product Name | 4-Nonylphenylboronic Acid |
| Cas Number | 851728-86-2 |
| Molecular Formula | C15H25BO2 |
| Molecular Weight | 248.17 g/mol |
| Appearance | White to off-white powder |
| Melting Point | 95-99°C |
| Purity | Typically ≥97% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Synonyms | 4-Nonylphenylboronic acid; p-Nonylphenylboronic acid |
As an accredited 4-Nonylphenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 4-Nonylphenylboronic Acid, securely sealed with a screw cap for chemical stability and protection. |
| Shipping | 4-Nonylphenylboronic Acid is shipped in tightly sealed containers to prevent moisture and contamination. It is packed according to regulatory standards, often cushioned with inert materials. Transport is typically via ground or air service, labeled as a chemical product. Handling requires chemical-resistant gloves and safety protocols during receipt and unpacking. |
| Storage | 4-Nonylphenylboronic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat, moisture, and incompatible substances such as strong oxidizing agents. Protect it from direct sunlight and sources of ignition. Ensure proper labeling and keep it out of reach of unauthorized personnel. Store according to all relevant safety and regulatory guidelines. |
Applications of 4-Nonylphenylboronic Acid in Industrial ManufacturingAs a reliable direct manufacturer, we supply 4-Nonylphenylboronic Acid to specialized downstream partners engaged in advanced material synthesis and fine chemical production. This compound contributes unique properties in highly regulated sectors where selectivity and chemical stability are critical to downstream product performance. The following detailed scenarios demonstrate authentic industrial adoption grounded in real-world process requirements, formulation protocols, and end-use specifications. 1. Pharmaceutical Intermediates SynthesisMajor pharmaceutical producers use 4-Nonylphenylboronic Acid as a coupling partner in Suzuki-Miyaura cross-coupling reactions, targeting the construction of biaryl motifs fundamental to patented small-molecule APIs. Its hydrophobic tail enhances solubility in organic-phase media, supporting higher product yields and reduced purification load. Our technical team collaborates with pharma formulators to determine the ideal input ratio based on substrate reactivity and subsequent synthetic steps which follow stringent regulatory documentation and cleaning validation requirements. Industry compliance standards
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2. Electronic Specialty Chemicals – OLED Material ManufacturingManufacturers of organic electronic devices, especially OLED display component suppliers, adopt 4-Nonylphenylboronic Acid for selective aryl-aryl bond construction in the core of high-purity emitter and charge-transport molecules. The branched nonyl group mitigates aggregation, assisting manufacturers in controlling crystallinity and device operational life, and meets strict trace metal limitations. Input proportions are determined by efficiency targets and material qualification runs for blue and green emission profiles. Industry compliance standards
Typical usage ratio
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3. Agrochemical Active Ingredient DevelopmentLeading crop protection formulators employ 4-Nonylphenylboronic Acid in the synthesis of biaryl-containing herbicide and fungicide scaffolds. The material’s compatibility with heteroaromatic halides is leveraged in multi-step synthetic flows, supporting scalable introduction of bulky groups that affect agrochemical selectivity and field persistence. Usage levels are determined by target molecule yields, environmental fate data, and the need for minimal unreacted boronic residue prior to formulation registration. Industry compliance standards
Typical usage ratio
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4. Polymer Functionalization Additive4-Nonylphenylboronic Acid is applied as a functional monomer for surface modification or chain-end functionalization within specialty polymer manufacturing. Producers of advanced engineering polymers and responsive hydrogels use the unique boronic acid group to impart reactive sites for biosensor attachment or to tune surface wettability for membrane applications. The nonyl side chain modulates compatibility with hydrophobic matrices. Input rates depend on desired functionalization density and downstream monomer co-feed ratios. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Each batch of 4-Nonylphenylboronic acid emerges from real effort, measured precision, and consistent attention to what researchers and manufacturers actually request. We work at the level of grams and kilograms, meeting tight purity specs and keeping variability from batch to batch minimal. Our teams don’t focus just on outputs—we pay just as much attention to what comes in. Raw materials need careful sourcing and documentation, not just for compliance but because even a slight impurity in nonylphenol or boronic acid changes the downstream application profile. Over the years, teams in our plants have gotten used to handling the waxy, sometimes hard-to-manage intermediates required for this type of boronic acid. This isn’t a routine item for the chemical industry, and for years, much of our process development has focused on scaling the reaction safely and repeating the product’s performance, batch after batch.
Chemists designing Suzuki-Miyaura cross-couplings, those pursuing custom ligands, or scientists searching for unique hydrophobic handles for biosensors all pull from experience—the very reasons our product lineup includes nonyl-substituted aryl boronic acids. The nonyl group’s linear, nine-carbon tail introduces solubility and bulk distinct from phenylboronic acid or shorter-chain analogs. Researchers who’ve worked with standard phenylboronic acid sometimes don’t anticipate how much the nonyl chain will affect reactivity and compatibility. Over the years, customers have reported stability in organic phase and less aggregation in certain solvents. Our best-performing nonylphenylboronic acid shows a melting point range that resists clumping during storage, leading to easier weighing, measuring, and incorporation into multi-step processes.
We’ve seen first-hand in our process labs how these characteristics impact not just research efficiency, but real-world cost and operability. Some of our academic partners use this compound as a tailored building block in advanced materials, while others report benefits when developing ligand systems for transition metal catalysis. This isn’t just theory—every few months, we handle inquiries about how custom variants perform with different halides or metals. As the manufacturer, we keep technical back-and-forth open, interpreting data in-house and collaborating with those pushing the limits of the chemistry.
Our regular production batches deliver 4-Nonylphenylboronic acid at purities of 97 percent or higher, based on HPLC and NMR testing. Because impurities affect reactions, we invest in repeated method validation and continuous improvement. Over years of real feedback, we improved crystallization and filtration, ensuring a stable, off-white to light yellow powder ready for immediate use. Scalability matters. One-time orders, recurring contracts, and custom quantity requests all come through the same system. Our protocols tighten up specs instead of relaxing when volumes scale up. That’s because we meet not just R&D needs, but the requirements of pilot and manufacturing-scale users who have much less tolerance for inconsistency.
Where typical off-the-shelf boronic acids can suffer from hydration issues or inconsistent reactivity, our 4-Nonylphenylboronic acid exhibits good handling and shelf stability in sealed containers, provided basic dry storage conditions are met. Our documentation travels with the product; researchers can reference full QC data and audit trails for each lot.
For over a decade, we’ve watched the customer base diversify. Pharmaceutical synthesis, electronic material developers, specialty coatings scientists, and academic innovators—they all look for something a bit different from 4-Nonylphenylboronic acid. Among all boronic acids, the nonyl chain offers a rare blend of hydrophobicity and reactivity. Some clients exploit the nonpolar tail to control phase behavior in aqueous-organic systems. Others leverage the electron-donating effect of the nonyl chain to tune oxidative addition steps in metal-catalyzed couplings.
We stay in conversation with those who formulate sensor surfaces and diagnostic reagents. Their teams emphasize how subtle differences in chain length and substitution point alter signal response and background noise. As a manufacturer deeply embedded in these cycles, we measure feedback against our analytical standards and find small process tweaks can translate into better site selectivity or more predictable immobilization for biochemical platforms. It’s not always dramatic—the difference often comes out in overall reproducibility, especially when transitioning from bench-scale to pilot quantities.
Coping with scale-up poses real-world challenges. Adapting bench protocols to 100-gram, 500-gram, or batch-kilogram scales doesn’t only involve multiplying reagents. Heat management, agitation, filtration rates, and waste handling all take on a new cadence. Each time a new customer requests a custom scale, our team brings previous run data, practical workarounds, and a healthy skepticism toward over-optimistic timelines. We learn with every order, sometimes dialing back scale or adding cleaning cycles between synthesis steps to keep quality high and contamination near zero.
Experienced chemists notice the contrast between this molecule and simpler aryl or alkyl boronic acids. The nonylphenyl group shapes the electronic character and solubility, giving advantages in systems where polarity and phase separation play roles. For instance, 4-Nonylphenylboronic acid acts differently from 4-Butylphenyl or 4-Octylphenyl analogs in palladium-catalyzed cross-coupling—users often see smoother phase transitions or lower foaming. That can matter enormously when scaling up or working with strictly anhydrous protocols.
Industrial users in the polymer and advanced materials field explain that residual volatility and hydrophobicity both influence performance in the final matrix. Our experience shows the nonyl chain gives more persistence, less leaching, and often cleaner end-stage conversion profiles. These practical outcomes build on real batch histories, not just claims in catalogs. We judge our own product against documented side-product occurrence, ease of filtration, and time-to-completion in key applications. This isn’t just competitive talk—it takes hundreds of production runs to develop comfort with any specialty boronic acid, especially one that opens up as many options as the nonylphenyl variant.
One recurring theme in customer feedback involves purification. Some boronic acid intermediates retain problematic pinacol or glycol residues; our process addresses this up front, minimizing extraction steps for downstream chemists. Where users previously reported time lost to column clean-up, they now transfer dry solid with confidence or, in some pilot lines, charge the reactor directly from the supplied bottle.
People who actually use this material—whether in micromole or kilo quantities—tend to trade practical advice. In feedback, researchers recommend tight containers, simple desiccants, and a habit of closing jars after each use. In our plants, storage stability follows from low moisture pick-up and a powder form that flows well in standard glassware or reactors. We keep packaging practical, balancing the needs of glove-box chemists with those of plant operators scaling new runs.
One concern with boronic acids is the slow hydrolysis some experience in humid air. Earlier iterations of our own product had more caking, but incremental upgrades in drying and final milling solved most of that—customers now report less clumping, less time spent breaking up chunks, and easier dosing for automated systems. What seems like a packaging or flow issue actually shapes yield and cost in busy labs. We’ve tested multiple packaging options, moving from simple glass vials for R&D to lined HDPE and composite cans for operational users, all based on real incidents and user input. We don’t insulate ourselves from customer feedback or pretend that a lab-standard vial always works for every scale.
Colleagues in the field sometimes ask how to extend shelf life or identify purity decline. The rule of thumb we use internally is straightforward: dry, room temperature storage, out of light, and tightly sealed. We supply bulk product with clear labeling and full certificates. Analytical snapshots travel with each lot, so that later quality checks have a real data baseline. Sometimes users share returned samples or images of aging product—anything unusual gets run through our own lab, ensuring all feedback cycles reinforce habit and not just theory.
Over the years, the chemistry community’s needs and regulatory expectations have both changed how we work. Safety, traceability, and sustainability now anchor our process development, including how we handle waste and recover solvents. A decade ago, waste minimization was seen mainly as an operational gain; now, customers—especially in pharmaceuticals and advanced materials—push us for lifecycle data and sustainable sourcing. We invest in greener boron sources and regularly evaluate safer solvents and energy-saving reactor designs.
Every year, the pressure to improve increases. We regularly upgrade the parts of synthesis where boronic acid formation overlaps with environmental impact. Currently, solvent selection and improved solid isolation protocols account for most of our year-to-year process investment. Our engineering teams avoid shortcuts that could impact end-user performance, and any improvement involves multiple scale-up and validation rounds. There’s no margin for error. Clients, in particular those scaling molecule libraries or custom ligands, require precise documentation of changes and side-by-side comparisons on their own platforms. We keep those lines open—not just through monthly reports, but through technical calls and regular visits when required.
We also maintain an open-door policy for collaborative troubleshooting. Practical chemistry rarely moves in a straight line, and unexpected issues come up. Whether it’s a question of incompatibility with a new palladium source or an observation about an anomalous TLC spot, end-users reach out. We respond, sharing our own results or reproducing reported issues. This transparency repays itself in trust—many of our long-term clients first came to us with a problem or disappointment with a competitor’s batch. We value these opportunities, using detailed post-mortem analysis to tune our process, packaging, or even communication style for future orders.
There’s no single profile for those who come to us for 4-Nonylphenylboronic acid. The pharmaceutical sector continues to drive the largest volume, seeking custom aryl boronic acids for ligand synthesis, API intermediates, and methods development. Across the globe, academic labs innovate with new sensor designs and electronic interfaces. Over the past few years, more material scientists and applied research groups request this compound for tailored polymer architectures, advanced coatings, and surface modifications challenging to achieve with shorter or branched alkyl substituents.
With each wave of inquiry, new uses emerge. We work with researchers exploring boronate-based sensors, immobilization chemistry, and alternative cross-coupling protocols beyond palladium catalysis. Engineers from electronics and coatings industries experiment with controlling charge transfer or hydrophobic layering in thin films. This constant flow shapes our product roadmap and R&D agenda. Investment in analytical depth—NMR, GC-MS, LC Methods—ensures we stay responsive to new purity targets or custom grade requirements. Our in-house R&D keeps us flexible; any significant lot deviation gets immediate evaluation, with clear communication to our users and adjustments to maintain the highest standards.
We notice, too, a trend toward pre-mixed solutions and custom blends. Operational teams with scaled-up needs request ready-to-use solutions in specific solvents or blends prepared under inert conditions. Our plant infrastructure accommodates these requests, delivering finished solutions that skip repeated handling and minimize operator risk. Every shift in demand brings plant-floor adjustments, from blending tank setups to revised cleaning validation. These aren’t theoretical pivots—they’re grounded in feedback, real production performance, and continual staff training.
Behind every bottle or drum shipped out, there’s a manufacturing story and a cycle of feedback between us and our partners. Product quality, adaptability, and responsive problem-solving drive our long-term relationships in the field. By engaging deeply with those who actually apply 4-Nonylphenylboronic acid, we’re able to shape not just the chemistry, but the real-world outcomes in all those labs, pilot plants, and production floors worldwide. Our commitment to transparency, rigorous analytical checks, and continual innovation gives us—along with our customers—the confidence to keep pushing boundaries and discovering what this molecule can achieve.