|
HS Code |
795875 |
| Chemical Name | 3-Methoxyphenylboronic Acid |
| Synonyms | Meta-Anisylboronic Acid |
| Molecular Formula | C7H9BO3 |
| Molecular Weight | 151.96 g/mol |
| Cas Number | 10240-89-0 |
| Appearance | White to off-white powder |
| Melting Point | 124-128 °C |
| Solubility | Soluble in ethanol, DMSO, and slightly soluble in water |
| Boiling Point | Decomposes before boiling |
| Storage Temperature | 2-8 °C |
| Purity | Typically ≥97% |
| Functional Groups | Boronic acid, Methoxy, Phenyl |
| Related Impurities | Contains varying amounts of anhydride |
| Application | Used in Suzuki-Miyaura cross-coupling reactions |
| Inchi Key | NQEYQQXLJXJATC-UHFFFAOYSA-N |
As an accredited 3-Methoxyphenylboronic Acid (contains varying amounts of Anhydride) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g white solid, sealed in a screw-cap amber glass bottle, labeled with hazard information, Sigma Aldrich branding, and product details. |
| Shipping | **Shipping Description:** 3-Methoxyphenylboronic Acid (contains varying amounts of anhydride) is shipped in tightly sealed containers to prevent moisture uptake and degradation. The chemical is typically packaged in inert atmosphere (e.g., under nitrogen) and shipped at ambient temperature. It is classified as non-hazardous; standard chemical transport regulations apply. |
| Storage | **3-Methoxyphenylboronic Acid (contains varying amounts of anhydride) should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong oxidizers. Store the chemical at room temperature and protect it from light. Recommended chemical storage cabinets and desiccators are ideal for maintaining its stability.** |
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We manufacture 3-Methoxyphenylboronic Acid under controlled conditions, and every batch starts with pure intent and a small team of seasoned operators who know their way around a boronic acid reactor. The full name, 3-Methoxyphenylboronic Acid, spells out its structure: a phenyl ring with a methoxy at the third position, all balanced by a reactive boronic acid group. The model we specialize in features varying amounts of anhydride, a choice that takes root in years of direct client interaction, understanding what drives organic synthesis in labs large and small. The variant offered here goes beyond a standard specification. Through hands-on process checks and repeated drying, our team stabilizes both the acid and its anhydride forms, allowing customers who value consistency and predictable yields to sidestep some common headaches in Suzuki-Miyaura couplings and related applications.
Anyone who’s made or handled boronic acids knows their quirks: moisture sensitivity, tendency to polymerize, variable shelf life. Working closely with bench chemists and process engineers who use our product, we saw how some batches might tilt toward the acid, while others contain more anhydride, depending on drying conditions and storage. Instead of fighting these transitions or masking them behind neutral claims, we address them head-on. There is an interplay between the acid and anhydride forms—sometimes, the anhydride actually improves solubility for palladium-catalyzed couplings, especially where rigorous water exclusion matters. Our process harnesses this feature and tunes the preparation to optimize recovery and reactivity for cross-coupling reactions.
Chemists chasing high yields and low byproducts don’t always want a strictly pure acid or a strictly neat anhydride. Reaction partners, catalyst selection, and even solvent choice shape what’s best on any given day. A rigid single-form product often demands wider process adjustments. Our model, which accepts the natural coexistence between acid and anhydride, saves researchers from having to precondition their materials every run. Years ago, we noticed some customers attempted in-house rehydration or drying of boronic acids, introducing variability and sometimes dangerous side reactions. Our direct experience with these risks pushed us to supply a material ready to use as-is, with composition tailored by process cues rather than an inflexible purity number on a label.
Reaction performance rarely comes down to purity alone. Some competitors might ship 3-Methoxyphenylboronic Acid in strictly anhydrous or hydrate-rich forms, but our hands-on work with research groups across pharmaceutical, agrochemical, and electronic material sectors revealed that many operators actually prefer a product with a slight edge in anhydride. The batch is easier to handle, less likely to clump during weighing, and disperses more efficiently in organic solvents. While other products may tout narrow composition ranges, our longtime customers report that our open approach—clearly stating that varying amounts of anhydride are present—gives them the confidence to skip time-consuming pre-conditioning and proceed directly to their synthesis, knowing batch-to-batch variance won’t undercut their results.
Nothing teaches like a failed scale-up. Years back, we had pharmaceutical clients run side-by-side trials with ultra-pure acid versus our blended composition. What happened surprised a few seasoned chemists: the ultra-pure acid stalled under particular coupling conditions, while the variant containing anhydride smoothly delivered target yields. The difference hinged on water content management and the subtle effects trace anhydride can have on catalysis. Seeing this outcome, we took steps to fix not just the composition, but also the moisture balance, packaging, and the speed with which batches reach our clients’ benches.
People tend to underestimate boronic acids until a batch sits too long in a humid storeroom or gets repackaged under harsh light. Over the decades, we’ve watched how careless storage transforms even the best batch into an unreliable starting material. It’s not just about chemical purity, but about keeping the balance between acid and anhydride in check. In our factory, we calibrate drying ovens, monitor packaging humidity, and regularly review shelf-life studies. We use containers engineered to keep contents dry, avoiding the unnecessary use of vacuum desiccators at the user’s site. This angle matters most for customers in climates with high ambient moisture—our packaging choices cut down on clumping, free-flowing issues, and unwanted hydrolysis, reducing last-minute surprises when a chemist opens a jar on a big synthesis day.
Many customers compare our 3-Methoxyphenylboronic Acid to other common boronic acids like 4-methoxy or 2-methoxy analogs. In our own workshops, we’ve run direct tests to see differences play out in catalyst compatibility and reactivity. The meta-positioned methoxy group offers just the right set of electronic properties for certain cross-couplings, often improving selectivity and yield compared to ortho or para substitution. Our production line is set up to ensure this selectivity is carried through from kilo batches to ton scales. While other manufacturers sometimes focus only on dry powder flow, we go deeper and look for crystalline purity, color, odor, and batch reactivity based on feedback loops from our largest clients.
Over the last decade, we watched the industry swing from a focus on brute-force commodity boronic acids toward fine-tuned inputs for active pharmaceutical ingredient synthesis. As regulatory standards tightened and reaction pathways diversified, demand shifted for consistent, application-driven materials that could go straight into automated reactors and high-throughput screens. It’s easy to make a one-size-fits-all product, but customers running parallel syntheses want logging and tracking—records that our process can provide. The understanding that every specification tweak impacts the soul of a reaction came from repeated collaborations with chemical engineers troubleshooting unexpected drop-offs in purity or yield. We learned that transparency about components and proactive sharing of test results leads to longer partnerships and fewer interrupted development timelines.
Our plant’s control room keeps the lines open with chemists from big labs and boutique development floors alike. Instead of hiding behind generic marketing terms, we talk shop: solvent compatibility, bath stability, filtration tips. Years ago, a contract manufacturer flagged inconsistent results with a competitor’s anhydride-free batch, clogging their columns due to rapid hydrate formation. Swapping in our model fixed the problem and kicked off a multi-year relationship. By maintaining clear dialogue, we provide a backstop for chemists encountering real-world scenarios, building trust not through claims, but repeatable results.
Safe shipping and storage of 3-Methoxyphenylboronic Acid is about as practical as it gets. We’ve had the whole spectrum on our loading docks: drums bound for large intermediates makers, glass jars prepared for bench chemists in university settings, and the odd rush order juggled through international logistics. The technical team runs regular risk assessments, constantly checking regulations and threat models. By creating packaging protocols that keep product stable and safe through varying climates, we bypass the need for urgent customer calls when humidity spikes or supply chain glitches delay delivery. In tough times, this flexibility saves projects from derailing due to physicochemical surprises nobody wants.
The surge in automated synthesis and digital chemistry means customers lean on manufacturers for materials that play nicely with robots, cameras, and batch readers. Our variant—delivering both acid and anhydride species—has turned out to be a good fit for these setups, balancing reactivity and physical handling in a way a pure acid sometimes can’t. With direct lines to customers developing new pharmaceuticals and advanced materials, we collect on-the-ground feedback and modify operation parameters accordingly: grind time, moisture content, and sieve size. Every process tweak reflects real troubleshooting stories from working chemists with equipment that doesn’t forgive mistakes. These close partnerships teach us to focus on the hands and eyes of actual operators, not just regulatory paperwork.
Quality assurance springs up from tactical work—not checklists, but direct batch testing, real-time analytics, and factory walk-throughs. Audits in our facility always include the people who run reactors and packers who spot subtle color changes before testing instruments do. On occasion, human senses find batch outliers faster than any strip or chromatogram, and we document these edge cases into process improvements. Past regulatory snafus in the industry taught us that surprise findings and communication delays cost real money and damage hard-earned trust. Our ongoing investments in staff training, test equipment, and documentation all pay dividends when a customer asks, “What’s different about this batch, and why?”
Each setpoint on our process chart ties to a feedback loop with end users. We don’t adopt arbitrary purity or anhydride fractions— lab experience and real project outcomes shape every tweak. If departments in charge of process scale-ups need tighter controls or specs drift toward ranges that don’t serve the widest group of customers, we adjust. Our process flow sheets have grown thick from these iterations, capturing decades of empirical success and lessons from mistakes not just in the factory, but in customer pilot plants and kilo labs. If the next wave of research demands a new balance between acid and anhydride, our setup allows for nimble change with full traceability, satisfying even the most detail-oriented procurement team.
Though we originally focused on pharma and fine-chem markets, the ingredient has found unexpected homes: organic electronics, specialty polymers, bioconjugation experiments. Our technical team encourages direct customer requests for tunable forms or bulk customizations. Customers involved in pharmaceutical synthesis sometimes need large volumes with batch-specific moisture limits. Others in specialty chemistry tweak their own methods mid-project, and ask us to coordinate drying, milling, and delivery according to just-in-time schedules. Each industry pushes the product into new spaces, building competence in applications we’d never anticipated. Open feedback cycles keep us honest and flexible, adapting not only specs, but entire service and delivery approaches to new research frontiers.
As a manufacturer—not a trader or passive packager—our edge rests on direct interplay with the chemistry. We see every batch under actual factory lighting, manage every shipment, and track every post-delivery comment, satisfied or otherwise. By refusing to abstract the product behind paperwork, managers stay close to the controls. Old-school batch records and new-school digital inventories come together, ensuring that experience, not only regulations, shapes product performance. This on-the-floor vantage lets us adapt to new market needs without sacrificing knowledge or stringency that make the difference during scale-up, troubleshooting, and high-pressure development cycles.
For those who view every boronic acid as interchangeable, it’s easy to miss subtle yet critical differences. Our making of 3-Methoxyphenylboronic Acid, incorporating carefully managed levels of anhydride, comes from listening and watching—reacting to what customers and chemists taught us over the years. Our approach blends predictable process with responsive service. Those lessons, whether won from accidental batch failures, market swings, or direct bench collaborations, all culminate in the stable, reliable material that leaves our plant and reaches innovators worldwide.