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HS Code |
872115 |
| Product Name | 4-Isopropylbenzeneboronic Acid |
| Cas Number | 5122-95-2 |
| Molecular Formula | C9H13BO2 |
| Molecular Weight | 164.01 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 185-190 °C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically ≥97% |
| Density | 1.15 g/cm³ (approximate) |
| Smiles | CC(C)c1ccc(B(O)O)cc1 |
| Inchi | InChI=1S/C9H13BO2/c1-7(2)8-3-5-9(6-4-8)10(11)12/h3-7,11-12H,1-2H3 |
As an accredited 4-Isopropylbenzeneboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 4-Isopropylbenzeneboronic Acid is packaged in a sealed amber glass bottle with a tamper-evident screw cap. |
| Shipping | 4-Isopropylbenzeneboronic acid ships in tightly sealed containers to prevent moisture exposure. Transported as a solid, it is typically packed in polyethylene bottles or amber glass vials. Standard shipping uses ground or air delivery, depending on the destination, and follows all chemical safety and hazardous material regulations. Temperature control may be applied if required. |
| Storage | 4-Isopropylbenzeneboronic acid should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong oxidizers. Protect the chemical from direct sunlight and store it at room temperature or as specified on the manufacturer’s label. Ensure proper labeling and prevent exposure to air to maintain product stability. |
Applications of 4-Isopropylbenzeneboronic Acid in Industrial Manufacturing4-Isopropylbenzeneboronic Acid plays an important role as a boron-containing building block in multiple sectors. The sections below highlight real downstream applications based on market demand, industry-specific requirements, and our direct supply relationships with leading manufacturing clients. 1. Pharmaceutical API Synthesis (Suzuki Coupling)Producers of small-molecule pharmaceuticals regularly select 4-Isopropylbenzeneboronic Acid as a reactant in Suzuki–Miyaura cross-coupling reactions. This material supports the introduction of isopropylphenyl motifs within advanced drug intermediates and final active pharmaceutical ingredients. Manufacturing chemists use this compound to achieve precise aryl substitution on complex scaffolds required for next-generation kinase inhibitors, non-steroidal anti-inflammatory drugs, and oncology targets. Industry compliance standards
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2. Agrochemical Intermediate ProductionAgricultural chemistry manufacturers incorporate 4-Isopropylbenzeneboronic Acid to introduce substituted phenyl groups when synthesizing new-generation crop protection agents. The boronic acid group ensures high selectivity and yield during biaryl assembly—especially for compounds targeting broad-spectrum herbicides and insecticides. Consistent batch quality supports safe large-scale use and downstream regulatory registrations. Industry compliance standards
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3. Electronic Chemicals: OLED Material Synthesis4-Isopropylbenzeneboronic Acid has established value for electronics manufacturers in the development of high-purity OLED materials. Precision-bonded boronic acids contribute to functional layer construction in organic light-emitting diode technologies. The chemical supports low-metal impurity standards in aryl-aryl linkages needed for efficient conductive polymers and pixelation compounds, addressing strict device reliability criteria. Industry compliance standards
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4. Specialty Fine Chemical Research & DevelopmentCustom synthesis labs and specialty chemical R&D centers utilize 4-Isopropylbenzeneboronic Acid in discovery workflows where controlled aryl group transfer is needed. The molecule enters new molecule construction, including ligands for catalysis, photoinitiators, and non-clinical bioactive probes. Researchers rely on batch-certified, impurity-profiled lots to meet project-specific exploration and regulatory assessment needs. Industry compliance standards
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There’s a journey behind every fine chemical that goes beyond material safety data sheets and catalog numbers. Having worked with 4-isopropylbenzeneboronic acid for many years, the process reflects more than a simple production run. We pay close attention from reagent selection to final checks. This compound—recognizable by its CAS number 163430-81-1—draws interest from synthetic chemists for solid reasons. Our familiarity with its quirks began when requests from pharma researchers came in, hunting for functionalized boronic acids that offered consistent results batch after batch.
Each run starts with freshly distilled isopropylbenzene and a careful analysis of boron content in raw reagents. Skipping any step here only invites headaches further down the line. The reaction goes by the Suzuki route, and there’s no shortcut on purification. Even a 0.5% impurity in this chemical can ruin downstream cross-coupling reactions. We use a proprietary combination of extraction and crystallization, designed with actual chemist feedback, to keep color and dissolution within narrow limits. End users, especially those in complex molecule synthesis, rely on this predictability.
4-Isopropylbenzeneboronic acid looks simple on paper, but handling requires attention to detail. At room temperature, the product forms a white to off-white powder—free-flowing, never clumpy, if the moisture is below 0.5%. Boronic acids take up water from the air fast, which can be trouble for coupling reactions needing dry conditions. Our controlled areas measure humidity around the clock. For packaging, we double-layer the inner bags and always fill under inert gas. That practice (learned from a few ruined shipments years ago) cuts complaints about degradation or unexpected color changes to zero.
Chemists sometimes ask us what sets 4-isopropylbenzeneboronic acid apart from classic phenylboronic acid or substitutes like 4-methoxyphenylboronic acid. Small changes in structure bring enormous differences in downstream chemistry. That is clear every time we discuss product behavior with medicinal chemistry teams or material science researchers. The isopropyl group sitting on the benzene ring brings increased hydrophobicity. This alters solubility in organic solvents and helps tweak reaction conditions for Suzuki-Miyaura couplings.
Consider the selectivity. Where unsubstituted phenylboronic acid sometimes lacks stability, 4-isopropylbenzeneboronic acid stands up to slightly more challenging conditions. The group at the para position redistributes electron density on the ring, which in practice means this compound survives side reactions that destroy more reactive analogues. This effect isn’t just theory—it shows up in HPLC and NMR analyses every time someone brings us a reaction mixture for troubleshooting. In practice, that can mean the difference between overnight yields and days spent cleaning up side products.
We have supplied the isopropyl derivative for custom polymer runs that needed tailored hydrophobicity, and pharmaceutical groups have flagged it as an enabler for synthesizing bioactive biphenyls. The robust physical profile means fewer solubility headaches in toluene or dioxane. Those who swap from other boronic acids often comment most on the difference in powder handling—ours stays loose and pours easily, with no stickiness or caking even after months on the shelf, thanks to our moisture protection.
There’s pressure in the market to chase higher assay numbers and ever-lower metals content. We listen because researchers want product with real, measurable quality, not just fancy paper certificates. Our 4-isopropylbenzeneboronic acid consistently assays above 98% (HPLC), with boron content checked by titration, and heavy metals scrutinized for even trace contamination. Most cycles, the melting point lines up in the 156–160°C range. Stability studies over several years confirm retention of both appearance and reactivity, so long as the air and moisture exposure stay low.
Some manufacturers chase larger batch sizes at the expense of batch-to-batch consistency. We stand by smaller runs with in-process controls. We test each batch in-house using NMR, IR, and GC-MS. Only those that pass get released. It helps partners run their reactions with confidence—no late-night panic because an impurity crept in, skewing conversion rates. On more than one occasion, we’ve received panicked calls from research teams who picked up material elsewhere only to find surprise impurities derailing their synthesis.
One challenge with boronic acids comes from their sensitivity to oxygen, water, and high temperatures. Our staff train thoroughly in the best practices for handling these sensitive intermediates. We shifted from simple drums to custom-HDPE containers, adding moisture indicators and vacuum-purging systems—lessons drawn from too many ruined deliveries in the early days. Feedback looped straight into container redesigns that now support smoother supply to research parks and bulk users alike.
The journey from lab notebook to scaled chemistry runs isn’t smooth without robust intermediates. 4-Isopropylbenzeneboronic acid sees use on both sides of the research fence. In academic labs, students use it to explore coupling reactions and to test catalyst systems. Some of the earliest orders came from university teams designing new solid-state materials—projects looking to control packing in aromatic frameworks for advanced electronics.
Scale-up tells a different story. Process chemists demand high repeatability and minimal clean-up. On the pilot line, 4-isopropylbenzeneboronic acid’s behavior stays steady across scales, maintaining reactivity and purity. Our field teams have watched it stand out in multi-kilo runs, when comparable products from other outfits struggled with clumping, slow dissolution, or mysterious off-odors. Extra care in final drying, free from oven hotspots, makes the product more manageable. Purity checks on the pilot batches often mirror those of the original research scale because we refuse shortcuts at either step.
Plants producing advanced intermediates need certainty in boronic acid quality. Downtime caused by impurities or failed reactions impacts multi-million-dollar development programs. By keeping the synthesis tight and the packaging foolproof, we enable partners to focus on their chemistry. The product moves from coupling to isolation without building up colored residues or stubborn emulsions in extraction—an advantage noted by process engineers who have seen lesser grades slow down entire production campaigns.
Years back, some shipments came back with complaints about crystalline grit or powder agglomeration—a sign of subtle moisture uptake. We reached out to users, analyzed the failed samples in detail, and redesigned our logistics chain. Storage facilities now monitor temperature and humidity with alert systems. Product moves from driers to packaging rooms in less than thirty minutes, and we reject any batch that shows early signs of clumping. Shipping times dropped as well, with new partnerships formed with carriers who could guarantee temperature stability for the entire route.
Quality doesn’t stop with leaving the loading dock. We solicit post-shipment lab analysis from experienced partners. Every few months, our team gathers to review impurity profiles and trace elements from both our own tests and those run independently by bulk customers. This discipline pinpoints sources of variation and keeps us honest—no margin for wishful thinking. When research labs or pharma clients mention even subtle deviations in melting point, solubility, or color, we respond with a full root-cause investigation. Open data lets partners trust that reported specifications match the contents in the bottle every time.
There’s a crowded field in fine chemicals, and the difference between an actual manufacturer and resellers shows in product consistency and technical support. We run our own reactors, know our own people, and track raw materials to their source. This control matters. Inquiries come in from teams who have suffered through inconsistent shipments—some batches fine, others slowing down work, all from third-party traders with little stake in outcomes. We stand behind our product with unfiltered transparency. If something goes wrong, users get direct answers, not runarounds.
Partners in medicinal chemistry and electronic materials expect not just reliable chemicals but also real answers to technical queries. With every kilogram we ship, practical experience comes along for the ride. We help troubleshoot reactions, adjust solvent strategies, and flag real-world limits in process chemistry. This feedback loop gives us a window into how our product functions in the real world, not just on paper, and keeps our own R&D moving forward. Lines of trust often start with a single batch but build with consistent, transparent service.
Interest in greener chemistry grows each year. We have seen stronger push for boronic acids that function in milder, less hazardous media. 4-Isopropylbenzeneboronic acid holds up under a variety of coupling conditions that minimize the need for excess base or phase transfer additives. Most users report low byproduct formation, which translates to less solvent waste during work-up and less strain on downstream purification. This not only reduces cost but also lessens the environmental footprint of larger scale processes.
Our own team experiments regularly with emerging catalysts and greener reaction systems, logging data on yields, recoveries, and ease of work-up. Sharing this with users accelerates knowledge. In practice, some have gone from classical biphasic reactions to nearly solvent-free coupling with little need to adjust the boronic acid input. Each tweak gets logged and, if useful, integrated into our process notes for future updates in manufacturing. Our willingness to adapt and share tested operational changes benefits everyone in the chain.
Stories circulate of counterfeit or adulterated intermediates making their way into research labs and, worse, into regulated synthesis runs. We counter this with full traceability on every batch—each synthesis is coded and recorded along with a complete assay, from identity to residues. Shipments come with lot-specific documentation, and we retain retain samples that can be drawn on if any anomaly appears in the field.
Teams using our product rarely face hurdles when validating supply for GMP or regulatory needs. The relationship stretches beyond sales—our technical liaisons know the history of every run and stay ready to answer questions about supply chain, synthesis, and characterization. Decades in the lab, not just in an office, anchor every answer we give. The ongoing relationship centers on mutual respect and the knowledge that shortcuts today invite trouble tomorrow.
Each year brings fresh challenges in fine chemical manufacturing. Increased scrutiny around solvent usage and energy demand in boronic acid synthesis drove us to revisit legacy steps. New drying techniques, smarter solvent recovery, and real-time compositional analytics bring our operation in line with rising expectations. Investments in analytical equipment—LC-MS, ICP-OES, automated powder handling—spring from actual problems encountered in past campaigns.
Researchers’ needs evolve quickly, and we do too. Incoming requests for custom purities or specific particle size distributions merit close attention. In one project, a partner’s new ligand system needed a tighter fraction of particle sizes to reduce dusting losses. We responded by modifying our crystallization and screening parameters, yielding higher usable product per batch. Problems like these shape our factory floor, calibrate our equipment, and inform our training.
By focusing on what users actually ask for—not what looks good on generic spec sheets—we keep output relevant and trusted by those pushing the boundaries of modern chemistry. We carry these lessons forward on each new scale-up and every shipment.
The world rarely sees what goes into getting a single boronic acid right, but every successful reaction or development project that relies on our 4-isopropylbenzeneboronic acid brings our efforts full circle. By owning the process from raw material to warehouse door, we make refinements based on sweat, feedback, and honest mistakes. Our customers reap the benefits in consistency, reliability, and technical clarity.
Making this compound is more than about meeting specs. It is about delivering the performance researchers expect every single time. In our view, strong relationships, open data, and constant learning will continue to drive improvements in 4-isopropylbenzeneboronic acid and its family of analogs.