|
HS Code |
319470 |
| Chemical Name | 4-Methoxy-3,5-dimethylphenylboronic Acid |
| Synonyms | 4-Methoxy-3,5-xylylboronic acid |
| Molecular Formula | C9H13BO3 |
| Molecular Weight | 180.01 g/mol |
| Cas Number | 89081-51-0 |
| Appearance | White to off-white solid |
| Purity | Typically ≥97% |
| Melting Point | 129-132°C |
| Solubility | Soluble in DMSO, methanol, ethanol, slightly soluble in water |
| Storage Conditions | Store at 2-8°C, protected from moisture |
| Smiles | COc1cc(C)c(B(O)O)c(C)c1 |
| Contains Anhydride | Yes, contains varying amounts |
As an accredited 4-Methoxy-3,5-dimethylphenylboronic 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 | White plastic bottle with a screw cap, Sigma-Aldrich label, 10g net weight, hazard symbols, CAS and product number displayed. |
| Shipping | **Shipping Description:** 4-Methoxy-3,5-dimethylphenylboronic acid (contains varying amounts of anhydride) is shipped from Sigma Aldrich/Merck/TCI in tightly sealed containers, protected from moisture and heat. Package labeling complies with chemical safety regulations. Standard ground or air shipping methods are used, ensuring safe, regulated, and compliant transport of laboratory reagents. |
| Storage | 4-Methoxy-3,5-dimethylphenylboronic acid (contains varying amounts of anhydride) should be stored in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from moisture. Store at room temperature or as specified on the manufacturer's label (Sigma-Aldrich/Merck/TCI). Avoid excessive heat and direct sunlight to maintain chemical stability. |
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Among organoboron compounds, 4-Methoxy-3,5-dimethylphenylboronic Acid stands out for its role in modern organic synthesis. In our facility, each batch carries a consistent profile, though this material often contains varying amounts of anhydride—a characteristic reflecting the real-world demands of chemical manufacturing over pure lab conditions. Our process works from the ground up: starting from fresh precursors, we use tightly controlled reaction conditions to generate a finished product that meets high-purity benchmarks commonly required in cross-coupling chemistry and related fields.
The standard product range offers a white to off-white crystalline appearance, traceable lots with detailed analytical records, and purity levels typically above 97% by HPLC. We provide the product both in its monomeric form and as a variable-content mixture with the corresponding anhydride, addressing both academic and industrial requests. Customers working at scale need to understand the implications of this variability. Integration of the anhydride does not hinder typical reactions, but it offers certain handling efficiencies, especially during long-distance shipping or storage in humid environments.
Solubility remains strong in common organic solvents. Water content, measured by Karl Fischer titration, is documented for every lot, which helps users adjust reaction conditions with precision. Bulk orders include a Certificate of Analysis with NMR, IR, and GC traces, so chemists can evaluate performance before use. It’s no secret—lots with a slightly higher anhydride fraction sometimes perform with greater consistency in Suzuki-Miyaura coupling, especially under low-polarity or slightly basic conditions. We’ve supported customers in adjusting loadings or modifying solvent regimes to achieve the best results with our product.
Direct manufacturing experience tells a unique story that can get lost when descriptions are polished too much by intermediary sellers. As the producer, we understand how the interplay between moisture level during boronation, batch size, and drying technique (whether by vacuum oven, fluidized bed, or atmospheric air-dry) all impact the final blend of acid and anhydride. Removing every last trace of anhydride would require harsh drying that’s both energy intensive and, for most application scenarios, unnecessary. Instead, we validate usability across a range of industries—pharmaceuticals, agrochemicals, specialty polymers—by showing consistent reactivity and purity, even as the physical form varies.
By manufacturing in-house, we have the flexibility to shift between product grades depending on seasonal needs or customer project requirements. For long-term customers, we can offer tailored lots—either closer to purely the boronic acid, or selected for slightly higher anhydride—even mid-year, without waiting for third-party approval. The market benefits: faster turnaround, less waste, and a real feedback loop between chemists and production teams.
From practical knowledge, this boronic acid earns its keep in carbon-carbon bond-forming reactions, particularly as a coupling partner in Suzuki, Chan-Lam, and Miyaura protocols. Organic chemists, whether in industry or at the bench, value reliability and clean conversions. Over years, those who use our product in direct arylation or heterocycle synthesis share repeat success stories with us—good yields and predictable purification, often using standard silica columns or precipitation methods. This compound stands up to a range of bases, from potassium phosphate to sodium carbonate, and rarely throws surprises whether in dioxane, toluene, or mixed aqueous-organic systems.
With the presence of anhydride, some users initially reported concern about side reactions or inconsistency. In practice, feedback guided our improvements in packaging moisture barriers and guidance documents. Once chemists adjust minor parameters—such as making sure to calibrate for the neat boronic acid content—the compound slides naturally into multistep syntheses. Its two methyl groups at the 3 and 5 positions buffer reactivity, and the methoxy at the 4 position allows for selectivity in electrophilic aromatic substitution downstream. Real-world users—people designing molecules for trial runs or for kilogram-scale pharmaceutical intermediates—appreciate the absence of problematic impurities, thanks to our dedicated post-synthesis purifications and active in-line monitoring.
As demand shifted toward greener processes, users have asked about product stability under atmospheric conditions or during extended storage. Our experience points to the mix of acid and anhydride improving shelf-life compared to the monomer alone, largely due to reduced hygroscopicity and clumping. Customers report pulling material from bags opened weeks earlier with no loss in efficacy. Such practical outcomes beat theoretical claims or supplier leaflets that ignore day-to-day handling.
Many users ask how our 4-Methoxy-3,5-dimethylphenylboronic Acid stacks up against similar compounds. Compared to simpler phenylboronic acids, this molecule’s electron-rich structure improves compatibility with electron-deficient aryl halides. Those working with ortho-substituted partners notice fewer problems with protodeboronation during elevated-temperature reactions. Chemists seeking alternatives to classic para-methoxy boronic acids often find the extra methyl substituents provide improved product stability, especially in air and under basic aqueous conditions.
Competing products from larger multinational suppliers sometimes advertise "ultrapure" form with minimal declared anhydride presence. In truth, barring extensive and costly drying, most boronic acids revert to a similar balance. We accept this physical reality, focusing on practical purity and lot-to-lot reliability. We have watched as some customers, swayed by premium pricing for “anhydride-free” lots, get the same results with our batches—sometimes even with smoother workups thanks to our post-synthetic washing steps that reduce residual byproducts.
Users sometimes prefer other functionalized boronic acids for solubility or unique reactivity. For those working in medicinal chemistry, the methoxy-dimethyl substitution frequently fits SAR studies, offering electronic effects and steric bulk that drive specificity in bioconjugation or late-stage diversification projects. Over years of supplying both academic and pharma firms, we've learned that what matters is not just nominal percent purity, but how the product performs—direct from the factory, under real process conditions, with support for troubleshooting from those who actually make the compound.
Direct manufacturing lets us see—on a nearly daily basis—what operators, pharmacists, and chemists actually prefer. We don’t choose the lowest-cost bags or drums; instead, we use lined PE vessels or vacuum-sealed pouches, based on what experience tells us survives both lab and warehouse. Each lot moves from production hall to analytic lab, then to climate-monitored staging before shipment, limiting exposure that would change the acid/anhydride balance. Batch documentation comes from hands-on analysts who’ve run hundreds of samples, not from software templates or generic paperwork. Customers get a clear quantitative breakdown and—most important—a real person’s name on the approval slip.
We’ve learned over years of production runs and process feedback that chemists value transparency about anhydride content. Rather than claiming an illusory “anhydride-free” purity, we spell out actual batch analysis and past performance profiles. This helps researchers predict reactivity and control impurity profiles in their target molecules. Consistent documentation—and responsive dialogue about what that means for specific synthetic goals—sets direct producers apart in a segment crowded by intermediaries who only repeat what comes on the data sheet.
The most common issues faced during synthesis arise from moisture effects. Bulk handlers want to avoid caking and mechanical bridging. Inconsistent anhydride content can throw off stoichiometry for those using automatic weighing or dosing equipment. Over time, we streamlined packing: choosing materials with proven moisture vapor transmission rates and working in climate-controlled environments. We also developed batch-specific recommendations for slurrying or dissolving, saving end-users from trial-and-error.
For research users needing tightest specification, we produce “custom batch” lots that go through staged drying and multiple closed transfers. For industrial clients scaling up, we advise on parameters—solvent selection, temperature regime, agitation—based on the form and anhydride content of the material at hand. Unlike middlemen, our advice comes directly from the plant floor. Routine feedback—both positive and critical—drives our continuous improvement, and we publish updates for operational best practices in our in-house bulletins.
The story of this product is one of constant adaptation. Direct access to each production stage lets us implement minor changes—an extra water wash, a slower crystallization ramp, a tweak in solvent concentration—based on actual customer usage data. As a direct producer, we don’t have the option to blame upstream suppliers. All responsibility stops here, in our plant, where customer feedback translates immediately into action. From the drum loading dock to the chemist’s flask, our product’s journey is one continuous loop of attention, learning, and honest communication.
If a batch prompts concerns—maybe due to unexpectedly high anhydride content, color change, or HPLC irregularity—we investigate root causes using data not just from this particular lot, but from years of archived runs. Anomalies rarely escape experienced eyes. We retrain or retool processes where needed. This gives customers a sense of real partnership, not just transactional exchange. The trust we’ve built, shipment after shipment, validates our approach: focus on reproducibility, be candid about what’s in the drum, and anticipate customer needs based on real-world synthesis, not marketing plans.
4-Methoxy-3,5-dimethylphenylboronic Acid remains a versatile building block for evolving chemistry challenges. From first kilograms produced in cramped lab space to current volumes supporting multistep scale-up, every stage brought lessons. Keeping open lines of communication with users—getting updates on what works, what frustrates, and what new applications arise—lets us stay ahead. Newer regulations, push for green chemistry, and ever-changing demands from pharmaceutical synthesis remain steady drivers for process improvement.
People seek more than a specification sheet; they need evidence that the supplier understands what actually happens once a bottle is opened. Reliably supporting the bench chemist and the plant manager means sharing our own data, owning up to variability, and providing guidance that doesn’t start and end at the transaction. As the direct manufacturer, we stand behind every lot, every drum, every tweak in process, so customers absorb more value, limit waste, and trust that real people—not algorithms or brokers—stand at the other end of the supply chain. This connection, grown through years of taking calls and fixing problems, shapes a product that not only meets technical needs, but fits into the living, changing world of modern chemistry.