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HS Code |
513079 |
| Product Name | 3-Isopropoxyphenylboronic Acid |
| Cas Number | 1173139-59-7 |
| Molecular Formula | C9H13BO3 |
| Molecular Weight | 180.01 g/mol |
| Appearance | White to off-white powder |
| Melting Point | 124-128°C |
| Solubility | Soluble in DMSO and methanol |
| Purity | Typically ≥ 97% |
| Smiles | CC(C)OC1=CC(=CC=C1)B(O)O |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Synonyms | 3-(Propan-2-yloxy)phenylboronic acid |
As an accredited 3-Isopropoxyphenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 25g of 3-Isopropoxyphenylboronic Acid is supplied in a sealed amber glass bottle with a secure screw cap for protection. |
| Shipping | 3-Isopropoxyphenylboronic Acid is shipped in tightly sealed containers to prevent moisture absorption and contamination. It is packaged according to standard chemical handling regulations, with appropriate labeling for safe transport. The shipping process ensures protection from extreme temperatures and direct sunlight, and complies with all relevant safety and environmental guidelines. |
| Storage | 3-Isopropoxyphenylboronic acid should be stored in a cool, dry, and well-ventilated area, away from heat and direct sunlight. Keep the container tightly closed and protected from moisture, as boronic acids can hydrolyze. Store separately from strong oxidizing agents, acids, and bases. Use proper chemical storage practices and safety precautions, including clearly labeling the chemical container. |
Applications of 3-Isopropoxyphenylboronic Acid in Industrial ManufacturingAs the direct manufacturer, we supply 3-Isopropoxyphenylboronic Acid for advanced organic synthesis across several specialized industrial sectors. Its unique boronic acid structure supports high-value transformations in pharmaceuticals, agrochemicals, electronics, and specialty polymers. Below we detail distinct real-world downstream applications, compliance requirements, usage ratios, process integration points, and finished goods resulting from its industrial use. 1. Pharmaceutical API Intermediate Synthesis3-Isopropoxyphenylboronic Acid serves as a key coupling partner in the Suzuki-Miyaura cross-coupling to construct biphenyl motifs in drug intermediates. Major pharmaceutical plants utilize this reagent to prepare highly substituted aromatic rings, essential for targeted kinase inhibitors and central nervous system drug candidates. Its high purity reduces byproduct formation and simplifies downstream purification in multi-step syntheses under cGMP production. The ability to introduce the isopropoxy substituent expands the physicochemical property space for novel API structures, enabling diverse synthetic strategies in the drug pipeline. Industry compliance standards
Typical usage ratio
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2. Agrochemical Active Ingredient SynthesisAgrochemical manufacturers employ 3-Isopropoxyphenylboronic Acid as a core building block in the production of novel herbicide and fungicide scaffolds. The isopropoxy group modulates target binding and improves crop safety profiles in several proprietary compound series. It reacts in metal-catalyzed cross-coupling sequences to deliver substituted phenyl rings critical for agrochemical efficacy, forming robust intermediates for downstream protection chemistry and formulation. Stringent impurity control and lot-to-lot reproducibility are mandatory throughout these processes to meet market and regulatory expectations in crop protection products. Industry compliance standards
Typical usage ratio
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3. OLED and Advanced Electronic Material SynthesisSpecialty chemical and electronic materials manufacturers utilize 3-Isopropoxyphenylboronic Acid to engineer precision-substituted aromatic units for OLED ligands, semiconducting polymers, and advanced display matrices. The isopropoxyphenyl moiety enhances electron mobility and charge-transport in complex architectures, introduced via Suzuki cross-coupling on aryl halides with strict moisture and particulate requirements. High monomer purity supports device lifetime and efficiency, with all handling in ultra-clean environments to align with electronics industry yield targets. Industry compliance standards
Typical usage ratio
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4. Specialty Polymer Modifier ManufacturingIn performance plastics and specialty polymer sectors, formulators introduce 3-Isopropoxyphenylboronic Acid as a functional comonomer or as a cross-linking agent precursor. Incorporation of the isopropoxyphenyl structure imparts chemical resistance and modifies the thermal profile of engineered resins, especially in high-performance coatings and advanced composites. It reacts in Suzuki and C–C coupling schedules before upscaling to extrusion or polymerization, with real-time monitoring for degree of functionalization and molecular weight distribution. Stringent supplier qualification is required to maintain consistent downstream production. Industry compliance standards
Typical usage ratio
Downstream process integration
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Hands-on experience with 3-Isopropoxyphenylboronic Acid (IPPBA) stretches well beyond the technical details found on a label. Every batch begins with an eye for real-life laboratory demands and ends up being weighed on scales by chemists who value consistent handling. Model number 698397-82-5 has become a familiar sight in our facilities over the years, both by drum and by flask, chosen by chemists who know their way around boronic chemistry.
From our point of view as the primary manufacturer, the greatest benefit of offering 3-Isopropoxyphenylboronic Acid comes from responding directly to what working laboratories ask for. Our chemists see how even small changes can affect a Suzuki-Miyaura coupling— water content, particle size, color, melting point. This molecule’s structure ranks it among the more versatile arylboronic acids, maintaining high solubility in common organic solvents and steady reactivity for complex coupling schemes. We manufacture every lot ourselves and follow strict quality controls. The attention begins with reagent-grade solvents and continues through to filtration and final drying.
Boronic acids share broad utility, but subtle differences in structure influence their real output at the bench. 3-Isopropoxyphenylboronic Acid doesn’t just fill a gap in a catalog— its isopropoxy substitution gives distinct electronic properties that make a difference in cross-coupling selectivity and response to bases in a reaction. In our hands, the compound’s aromatic core with the isopropoxy group at the meta position reliably boosts yields in specific Suzuki reactions that have stubborn side-reactions with unsubstituted phenylboronic acid. For medicinal chemistry labs, this translates into higher confidence scaling from milligrams up to kilogram orders.
By offering this specific arylboronic acid, we contribute to fields working with heterocycle synthesis or the modification of complex pharma intermediates. Experience on production lines helps us see how this IPPBA fits as a step up from more common boronic acids, especially in projects that need a balance between electron-donating groups and minimal steric hindrance. Our own staff chemists have relied on this precise variant for site-directed installations of functional moieties and to keep sensitive ligands intact throughout multistep syntheses.
From our perspective, nothing matches the sum of many years correcting imperfections on the production floor. Magnetically stirred vessels show right away how a slight moisture uptick can affect aggregation. For arylboronic acids, clumping and color shifts often point to handling or shipping errors, so we always finish each lot with in-house moisture testing. We use Karl Fischer titration to keep water content below 0.5%, since higher numbers quickly spoil coupling efficiency. Our designated drying protocols—vacuum oven and gentle nitrogen stream—aren’t arbitrary: They are based on direct observations of product performance and cost per batch.
Chemists often mention how certain boronic acid derivatives arrive as lumpy, discolored powders or, worse, as cakes that resist transfer from bottle to flask. Through hands-on refinement, we have optimized for a free-flowing white to off-white powder averaging a particle size below 150 microns. We package material on the same day as drying, and direct fulfillment eliminates unnecessary journeys that can expose the product to air and light. Unlike many distributors or brokers, our oversight never leaves the shop floor from starting materials to packed bottles. This reduces customer complaints about degraded batches or paperwork discrepancies.
Supplying research institutes and pharmaceutical companies with gram to multi-kilogram quantities places unique demands on the manufacturer. We’ve learned the real bottleneck isn’t usually the core chemistry—most competent synthetic shops can assemble an arylboronic acid—but rather the follow-through: batch-to-batch reproducibility, precise analytical documentation, and flexibility on order size. Our experience with 3-Isopropoxyphenylboronic Acid has come from responding to feedback that insisted on stricter purity—commonly ≥98% by HPLC, but, when possible, we match even tighter specifications for teams doing scale-up validation or regulatory submissions.
Our packaging practices reflect priorities other than just “shipping fast.” Those working with these compounds know how boronic acids react to oxygen and moisture, especially at high humidity. From loading lines to sealed bottles under inert gas, a seamless process aims to prevent off-odors, hydrolysis, or the slow formation of boroxines. Our direct involvement at each stage comes from our understanding that each lot might form the basis for a new lead compound or a pilot run destined for clinical research.
Working with this compound shows the importance of tuning synthesis and work-up steps beyond textbook protocols. Acid-sensitive APIs, for example, demand mild purification that won’t introduce unwanted breakdown or byproducts. As a manufacturer, we control temperatures and timepoints during extraction and crystallization. These adjustments have come from seeing failed industry attempts—customers sharing stories of “off” batches that produced byproducts they couldn’t trace. As a result, we employ double recrystallization where the target molecule profile matters, and we keep all syntheses under tight inert atmosphere, right from Grignard steps to boronic acid formation, minimizing air exposure and side reactions.
By keeping every variable under supervision, we help chemists avoid surprises in both research and production pipelines. Side products like phenols and oligomers get screened out early, thanks to batch GC and NMR checks before bottling. Our QC team runs routine physical inspections, watching for subtle signs that bulk material might pack poorly or clump after storage. Rather than simply moving product based on COA paperwork, our shipments reflect what the shop floor would use for its own projects.
Arylboronic acids come in dozens of variations, but direct comparison of working traits highlights where 3-Isopropoxyphenylboronic Acid stands out. Both chemoselectivity and solubility in standard solvents—THF, ether, dioxane, or dichloromethane—improve with the isopropoxy group at the 3-position. Those handling solid-liquid mixing for high-concentration reactions see this first-hand: slurries maintain flow and do not require protracted sonication or forced agitation.
From our testing, IPPBA resists hydrolytic degradation better than some ortho-substituted analogs. In downstream coupling, we observe that mixtures with Pd(PPh3)4 exhibit less stalling and cleaner isolation of products than with similarly sized, but less electron-rich, boronic acids. This means that research teams investing in series libraries see more hits and relief from common clean-up headaches. Compared to more popular but unsubstituted phenylboronic acids, ours gives subtly higher room-temperature reactivity, avoiding the need for higher catalyst loadings. For those in kinetic optimization, this translates into smoother scale-ups with more predictable exotherms.
Supplying larger volumes tests every system we’ve put in place, from raw material sourcing to packaging. Over time, scaling up 3-Isopropoxyphenylboronic Acid to the multi-kilogram range taught us to watch for mixing behavior not obvious at small scale. Certain anti-caking agents favored by bulk traders sometimes led to trace contamination. By avoiding these shortcuts and favoring mechanical sieving paired with well-controlled humidity, our bulk customers receive the same lot-to-lot performance as those buying research amounts.
Shipping in airline-safe, moisture-proof cartons—each with tamper indicators and lot-specific analytics—ensures clients worldwide open bottles that are ready to use. Each shipment reflects refinements made after years of feedback. International customers sometimes have unique import criteria; working on the production side makes it easier to respond with the exact documentation that customs officials request. We keep a record of every certificate, spectral scan, and manufacturing test for follow-up, a process that feels more like stewarding inventory for a demanding lab than moving commodity goods.
Our interaction with innovation comes in real time. Synthesizing this compound in-house gives us a close-up view of what researchers in universities and drug discovery labs pursue. Those developing new coupling reactions or designing high-throughput screening platforms need precise, interference-free boronic acids. Our development team has collaborated with academic groups running isotope labeling or library synthesis, offering alternate batches with deuterium labels or minor process tweaks. Being the producer, we can act on a request for a different particle size, alternate salt forms, or the tightest purity standard, answering questions within a working week rather than passing messages between brokers.
Feedback from research chemists lets us adjust our own handling tips—suggesting dissolution procedures, storage at −20°C after opening, or sample vials for method qualification. We notice trends: an upsurge in use with continuous-flow systems prompted us to evaluate how IPPBA behaves in packed-bed reactors and shared those data with frequent buyers. We have experimented with stabilizing agents and packaging overlays, always testing for any impact on reaction outcomes or storage life. Discussions with users challenge us to keep reducing trace metal content and halide residue, knowing they will push 3-Isopropoxyphenylboronic Acid into ever more critical syntheses.
As a hands-on producer responsible for large batches, we see the practical impact of green chemistry considerations. The synthesis of IPPBA presents opportunities to minimize solvent waste and energy use. Over several process revisions, we replaced halogenated extraction solvents with greener alternatives and installed closed-loop filtration, reducing environmental footprint. The lab-to-large-scale journey of this compound tracks our commitment to both product safety and regulatory compliance. Quality remains grounded in daily routines—routine emission checks, solvent recycling audits, yearly reviews of raw material traceability. Our paperwork never leaves safety as an afterthought, from production records to globally recognized transport documents.
Clients expect transparency, so we provide up-to-date safety and purity disclosures. Safety Data Sheets come with each shipment, listing every significant hazard and correct handling practices—direct knowledge from working all day with the same chemical in-house. Keeping poison control numbers and reference information at the ready improves our own lab safety as much as it does for end users. Many projects depend on full regulatory compliance, whether for preclinical research, pilot scale, or cross-border transit. The real-world value of this compound connects as much to the people handling it as to those performing reactions, and we remain available to troubleshoot short lead times, rare specification requests, or new regulatory filings.
Relationship with our customers extends beyond a sales cycle. Routine calls and feedback forms shape our internal processes, leading to gradual but constant improvement of 3-Isopropoxyphenylboronic Acid. Those using SDS and analytical reports to plan scale-ups often flag minor documentation gaps, which helps polished future certificates for clarity. We actively encourage questions about trace impurity profiles, long-term storage, and performance in non-traditional reaction media such as ionic liquids or mechanochemical reactors. Insights from the bench matter: Real-time feedback reveals when one shipment performed better in high-throughput settings or withstands storage over multiple freeze-thaw cycles.
We collect data on returned lots, identify sources of caking or off-color change, and pass those details through process improvement meetings. Our delivery methods have changed based on feedback — where glass became impractical for larger orders, we engineered a multilayer polymer system tested for compatibility and permeability. Ensuring lot integrity right up to opening spurs trust and cuts down on time lost to repeat analysis. Open communication about stability tips, dissolution rates, and batch history form the backbone of our manufacturing reputation.
Direct manufacturing control keeps 3-Isopropoxyphenylboronic Acid available, reproducible, and reliable for every user, from R&D bench to scale-up production. Over years in the business, we’ve found that success with this compound tracks most closely with careful, daily attention to the real-world needs of chemists—accuracy, cleanliness, and full transparency from order to lab flask. Hands-on refinement, strict packaging, and willingness to adapt processes have made this product a mainstay in our catalog and a problem-solver for thousands of users. That knowledge forms the foundation of every batch, and it shapes how researchers trust and select our product for their own innovations.