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HS Code |
203006 |
| Product Name | 4-Methoxy-3-Nitrophenylboronic Acid |
| Cas Number | 139301-42-7 |
| Molecular Formula | C7H8BNO5 |
| Molecular Weight | 196.96 |
| Appearance | Light yellow to yellow powder |
| Purity | Typically ≥98% |
| Melting Point | 155-160°C |
| Solubility | Slightly soluble in water, soluble in DMSO and methanol |
| Synonyms | 3-Nitro-4-methoxyphenylboronic acid |
| Inchi Key | NLTORZXPIDHYHZ-UHFFFAOYSA-N |
| Smiles | COC1=CC(=C(C=C1)[N+](=O)[O-])B(O)O |
| Storage Conditions | Store at 2-8°C, protect from moisture |
| Chemical Class | Aromatic boronic acid |
As an accredited 4-Methoxy-3-Nitrophenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 1-gram package features a sealed amber glass vial, labeled with “4-Methoxy-3-Nitrophenylboronic Acid,” batch number, and hazard symbols. |
| Shipping | 4-Methoxy-3-Nitrophenylboronic Acid is shipped in tightly sealed containers to protect it from moisture, light, and air. The packaging complies with chemical safety regulations, clearly labeled with hazard information. It is transported under ambient conditions, following protocols for handling and storage of organic chemical reagents. Appropriate documentation accompanies all shipments. |
| Storage | 4-Methoxy-3-Nitrophenylboronic Acid should be stored in a cool, dry, and well-ventilated area, away from moisture, heat sources, and direct sunlight. Keep the container tightly closed and protect from air and incompatible substances such as strong oxidizing agents. Store under an inert atmosphere, such as nitrogen or argon, if necessary, and ensure proper chemical labeling and segregation. |
Applications of 4-Methoxy-3-Nitrophenylboronic Acid in Industrial Manufacturing4-Methoxy-3-Nitrophenylboronic Acid is a specialized boronic acid derivative that serves as a key intermediate in fine chemical synthesis and advanced materials production. As a manufacturer, we support high-value application scenarios where this raw material provides functional advantages for pharmaceutical, agrochemical, and materials industry processes. The following sections present authentic industrial use cases, highlighting real compliance frameworks, formulation guidance, integration points, and end product types for each downstream field. 1. Pharmaceutical API Synthesis – Suzuki-Miyaura Coupling IntermediatesThis boronic acid plays a crucial role as an electrophilic partner in Suzuki-Miyaura cross-coupling reactions. Pharmaceutical manufacturers utilize this intermediate for constructing complex aromatic API precursors, enabling the assembly of molecules used in next-generation oncology and central nervous system (CNS) therapies. The compound’s ortho-nitro and para-methoxy functionalization facilitates selective coupling under mild conditions, supporting scalable GMP manufacturing of late-stage medicinal entities. Industry compliance standards
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2. Agrochemical Intermediate ManufacturingIn the agrochemical sector, downstream formulators employ this boronic acid as a modular building block for synthesizing substituted aromatic herbicides, fungicides, and insecticides. Its electron-donating and -withdrawing group combination enables precise tuning of bioactivity profiles during SAR optimization in early and late-stage R&D, preceding scale-up to pilot and commercial plant production. Industry compliance standards
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3. OLED and Advanced Material SynthesisManufacturers of organic optoelectronic materials integrate this compound into elaborated synthesis chains for high-brightness OLED emitters and small molecule semiconductors. The presence of both nitro and methoxy substituents permits precise bandgap tuning and improved charge-transfer properties, essential for high purity, high performance organic layers in electronic displays and lighting devices. Industry compliance standards
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4. Specialty Dye and Pigment Intermediate ProductionThe fine chemicals industry uses this boronic acid to construct substituted nitroaromatic frameworks as part of the synthesis pathways for specialty dyes such as azo, anthraquinone, and triarylmethane derivatives. Its specific substitution pattern improves dye fixation on functional textiles and provides enhanced photostability required for industrial pigment producers serving the coatings and ink industries. Industry compliance standards
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5. Medicinal Chemistry Research Reagent SupplyAcademic and industrial medicinal chemists procure this compound as a privileged boronic acid for rapid access to analog libraries in structure-activity studies. Its dual electron effects enable broad substrate scope, making it a standard component in automated synthesizer and parallel synthesis setups, supporting hit-to-lead optimization and patent-protected scaffold generation. Industry compliance standards
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Behind every successful cross-coupling reaction, you’ll find building blocks that earn their keep, not just in yield but in work-up and purity. 4-Methoxy-3-Nitrophenylboronic Acid stands out as one of those. As chemical manufacturers, we get to see how backbone reagents like this keep chemical synthesis moving efficiently from gram-scale research all the way to pilot runs. At our facility, we work with this boronic acid as both a customer-demanded product and a step in our own fine chemicals portfolio. Our close attention to process consistency means you get the same high assay, batch after batch, with the kind of granular traceability only a manufacturer sees up close.
Every bottle of 4-Methoxy-3-Nitrophenylboronic Acid that leaves our pipelines has a targeted appearance—off-white to pale yellow solid, stable when kept in cool, dry conditions, and free-flowing rather than clumpy. That matches the lot monitoring we run through for each batch, taking the operation beyond checkboxes. Our usual purity readings, by HPLC and NMR, push upwards of 97%, because we understand that end users fight unexpected impurities in coupling reactions. In practice, trace inorganic residues run very low, since downstream customers in pharma and materials need interference-free performance.
On the production floor, consistency proves more than a slogan—it’s built into our own QA process, with spot chromatography and moisture checks, since even small blips can throw a synthesis off track. For air and moisture sensitivity, our team takes care of proper packaging with nitrogen-flushed containers, so opened bottles don’t lose performance. Having watched a wide variety of customers work with this boronic acid, we’ve seen how a poorly managed batch can clog dissolving stations, delay scale-up, or erode analytical benchmarks.
Few intermediates match the unique utility of substituted phenylboronic acids when developing arylated molecules. 4-Methoxy-3-Nitrophenylboronic Acid brings two distinct functional groups—methoxy and nitro—into the Suzuki-Miyaura and Chan-Lam coupling playbook. It’s most common in assembling biaryl frameworks, specialty pharmaceuticals, and custom electronic materials. Our team has helped process engineers in both large and boutique firms capitalize on its dual reactivity. The electron-donating methoxy and the electron-withdrawing nitro both shape reactivity in ways no unsubstituted boronic acid can.
During method development, these two groups let chemists fine-tune the electron density along the arene, impacting both the rate and selectivity of coupling. Our technical support teams share lessons across dozens of real cases: researchers have used this acid to build kinase inhibitors, specialty dyes, and a host of advanced polyanilines. In academic labs, its versatility helps as a teaching tool for exploring both steric and electronic effects within catalytic cycles.
The compound’s solubility profile fits most standard organic solvents—usually acetonitrile, DMF, dioxane, and toluene—though precise solubility depends on ambient temperature and concentration. Since the solid dissolves quickly with heat and stirring, reaction setup wastes little time. And as most customers tell us, well-made batches cut down on pre-dissolution problems, a step that sometimes gets overlooked until it’s too late.
Within our own product lineup, we compare 4-Methoxy-3-Nitrophenylboronic Acid directly against close cousins: simple phenylboronic acid, 4-methoxyphenylboronic acid, and 4-nitrophenylboronic acid. These variants might swap out the methoxy or nitro group, but such tweaks have huge effects on synthetic strategy. Working on the floor, we’ve followed first-hand how loss of the nitro swing changes oxidative stability, while absence of methoxy pulls down reactivity in certain cross-couplings.
When clients run head-to-head trials, this compound outperforms unsubstituted analogues in terms of both conversion rates and the fine-tuning needed for regioselectivity. For some applications, especially where electronic balance along the aromatic core controls reactivity, 4-Methoxy-3-Nitrophenylboronic Acid brings an ideal midpoint between push-and-pull effects. More simply, it’s the answer when you want balance—fuelling faster couplings, smoother purifications, and higher purity targets. Over the years, synthetic routes using this boronic acid have delivered distinctly better isolated yields in challenging step-ups than lighter or over-modified variants.
Users sometimes ask about trialing just the methoxy or just the nitro version. In our experience, that can make sense for certain stacks where single-modification is desired. But in medicinal and agrochemical discovery, where SAR optimization runs hot, the dual-group compound stays king. We routinely see medicinal chemists pair this with halogenated aryl partners to unlock new compound libraries at pace—something unattainable with simpler boronic acids.
One thing people don’t always see from the customer side is the day-to-day struggle for batch-to-batch consistency. Manufacturing 4-Methoxy-3-Nitrophenylboronic Acid involves several critical reaction and isolation points. Small changes—temperature slip, wrong solvent grade, barely degraded starting material—shift the outcome. We have invested in batch reactors with precise control systems, allowing for stepwise addition and consistent agitation. Every output gets run through in-house analytical, with spectra archived by batch for long-term reference. From conversations with partners and internal R&D practitioners, these records become essential when an unusual result pops up somewhere downstream. Fast troubleshooting beats finger-pointing every time.
Solvent removal, washing routines, and careful drying stages keep our moisture readings tight and color consistent. Boronic acids attract water easily, a fact often missed by non-specialists. Moisture-laden acid can brown during storage or muddie downstream chemistry. Over the years, we’ve improved our final drying to below 0.5% moisture, compared to higher market averages—this translates to cleaner reaction starts and simpler filtration for our users. Our onsite team knows if that golden-yellow tinge appears, something slipped between isolation and package. These visual checkpoints do more than look good; they reinforce the right process every time.
Production scale varies: kilo-lots for routine supply, up to multi-kilo runs for CDMO projects. We commit to maintaining specification, even when custom synthesis demands a process tweak. Clients working under cGMP constraints trust that we run validated clean-outs and record keeping, so every gram ships traceable and compliant, no matter the order size.
As original producers, not just intermediaries, we gain feedback direct from bench chemists and process engineers. Many clients update us about both wins and bottlenecks—speed, grindability, and unexpected side-reactions. We use this input to tighten up our own upstream steps. Last year, several pharma teams flagged that cuts in drying time led to powder caking in moist climates. We adjusted both the drying cycle and packaging. As a result, customers across tropical markets now report smoother material handling, and reactant losses dropped during recovery.
For clients running custom routes, subtle impurities—like trace chlorides or oxidized byproducts—once triggered chromatic spots in thin-layer analytics. Chemists flagged abnormal side-spots; we tracked them back to a minor solvent impurity in a precursor. Correcting that raw material source resulted in visibly cleaner boronic acid, confirmed both by in-house NMR and external validation. This kind of closed-feedback loop is how in-house manufacturing tightens reliability over time, something resellers can’t usually guarantee.
The real value comes through flexibility. Need a batch with non-standard mesh size for automated reactors? We can run a custom grind. Looking for bespoke packaging to suit a glovebox transfer? Our in-house team packs and seals under argon. As regulations shift or research targets move to new scaffold classes, we keep pace with documentation upgrades and in-line process tweaks, responding much faster than outfits sourcing from third parties.
Running reactions with specialty boronic acids, even as classic as Suzuki couplings, means minimizing variables. Every synthetic chemist faces pressure on both time and margin. We watch as bench chemists rely on predictable melting point, homogeneity, and pourability—traits usually overlooked until crunch time. A batch that survives winter shipping, keeps consistent color, and preserves the boronic function leads to reproducible results, not lucky outcomes.
Our process team holds years of detail-driven troubleshooting. Decoding anomalous melting points or inconsistent solubility often traces back to overlooked drying conditions, solvent residues, or trace metal contamination. Each source error knocks downstream reactions off balance, wasting materials and time. By controlling every step internally, we cut these issues before they hit your bench. Every improvement builds on customer trials, industry quality standards, and our own direct experience running synthetic campaigns.
For bulk projects, consistency means more than analytical data—it means every drum or kilogram holds up when split across multiple runs and shifts. In the past, a missed impurity in a kilo batch led to a delayed campaign. That story still drives our commitment to full-lot analytics and real-time batch communication. Clients who’ve run through three or four vendors often notice the difference immediately: material flow, analytical reliability, and the absence of "surprises" during scale-up or downstream product QC.
The market’s requirements don’t stand still—new catalysts emerge, green chemistry pushes toward water or non-traditional solvents, and detection limits tighten. As a manufacturer, we gear up for these changes early. Our process chemists keep tabs on literature developments and collaborate with academic partners to develop next-generation handling and purification protocols. That experience turns into smoother scale-up for new pharmaceutical intermediates, specialty polymers, and targeted library compounds.
Sustainability sits at the front of new projects. Our team now runs solvent recovery units inline and recycles wash streams, minimizing both cost and environmental impact. Periodic process revalidation ensures that yield improvements do not sacrifice purity, thanks to upgrades in process monitoring and final analytics. Our experience shows that long-term trust grows, not with a flashy product launch or sales pitch, but with an unbroken supply of quality material and transparent communication—especially when you get a batch that just works, every time, in your method.
For more challenging custom projects, we work through pilot-scale runs on fresh compounds with unique substitution patterns. The lessons learned there feed directly back into how we handle core products like 4-Methoxy-3-Nitrophenylboronic Acid. New analytical methods, ramped-up purification flows, and creative packaging all build from our own practical research, greatly accelerating response time for those who need non-standard solutions.
Everything we know about this compound comes from direct practice. It’s easy to write up technical data sheets, but working side-by-side with real operators and R&D teams sharpens our picture of what truly matters. Moisture tolerance, smooth handling, reliable reactivity—all mean more with actual laboratory feedback guiding future tweaks. We ship with confidence because we know each drum’s full quality trace, not because we read it from a stock list or data card.
The key factor driving customer loyalty for our 4-Methoxy-3-Nitrophenylboronic Acid isn’t just analytical numbers. It’s the everyday performance in synthetic campaigns, the assurance during project crunch times, and the constant, transparent dialogue with the scientists using it at the cutting edge. As a primary manufacturer, we don’t cut corners handing you someone else’s risks; we stand behind every package from the first fill to your final filter. That mindset, built through daily challenge and improvement, keeps our customers coming back—and keeps innovation moving forward in every field where this reagent counts.