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HS Code |
629591 |
| Productname | Dibenzofuran-4-Boronic Acid |
| Casnumber | 1072951-37-7 |
| Molecularformula | C12H9BO3 |
| Molecularweight | 212.01 g/mol |
| Appearance | White to off-white powder |
| Meltingpoint | 221-224 °C |
| Purity | Typically ≥ 97% |
| Solubility | Slightly soluble in water |
| Storagetemperature | 2-8°C |
| Smiles | B(C1=CC2=C(C=CC=C2)OC1)(O)O |
| Inchi | InChI=1S/C12H9BO3/c14-13(15)10-6-7-12-9(5-4-8-3-1-2-8)11(10)16-12/h1-7,14-15H |
As an accredited Dibenzofuran-4-Boronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Dibenzofuran-4-Boronic Acid is packaged in a sealed 1-gram amber glass vial with a screw cap and tamper-evident seal. |
| Shipping | **Shipping Description for Dibenzofuran-4-Boronic Acid:** Dibenzofuran-4-Boronic Acid is shipped in tightly sealed containers, protected from moisture and light. The package complies with chemical safety regulations, and is labeled as a laboratory reagent. Shipping is typically via ground or air, depending on destination, with all relevant documentation included for safe and compliant transport. |
| Storage | Dibenzofuran-4-boronic acid should be stored in a cool, dry, and well-ventilated area, away from heat, moisture, and sources of ignition. Keep the container tightly closed and protected from light. Store separately from strong oxidizing agents, acids, and bases. Ensure proper chemical labeling and secure storage to prevent unauthorized access or accidental exposure. |
Applications of Dibenzofuran-4-Boronic Acid in Industrial ManufacturingDibenzofuran-4-boronic acid serves as a key intermediate in the advanced synthesis of fine chemical materials. Our production is dedicated to supporting B2B clients in sectors that demand high-purity building blocks for specialty compounds. On this page, we outline four verified downstream applications, providing critical integration, compliance, and formulation details based on real manufacturing practices. 1. OLED Material Synthesis for Electronic DisplaysDibenzofuran-4-boronic acid is widely used in the manufacturing of organic light-emitting diode (OLED) materials, specifically as a boronic acid coupling component in Suzuki–Miyaura cross-coupling reactions. Downstream producers integrate this raw material to introduce dibenzofuran motifs into emissive or transport layers. It supports precise tuning of emission wavelengths and improves hole-transport properties for device manufacturers producing high-performance display panels in consumer electronics, automotive dashboards, and professional monitors. Industry compliance standards
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2. Pharmaceutical API Intermediate ProductionDibenzofuran-4-boronic acid acts as a critical intermediate for synthesizing advanced active pharmaceutical ingredient (API) scaffolds, especially where dibenzofuran cores provide metabolic stability or biological activity. Medicinal chemistry groups and contract manufacturing organizations use it in multi-step syntheses to build heteroaromatic structures designed for anti-cancer, anti-viral, or central nervous system (CNS) pharmaceutical candidates. Industry compliance standards
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3. Agrochemical Advanced Intermediate ManufacturingThis boronic acid serves as a feedstock in the synthesis of certain crop protection agents which require extended aromatic ring systems for biological activity. Downstream agrochemical producers value the molecule for its ability to introduce dibenzofuran-linked moieties that enhance target binding or degradation profiles of new herbicide and fungicide actives. Industry compliance standards
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4. Specialty Polymer Precursors for Advanced MaterialsIn advanced polymer synthesis, dibenzofuran-4-boronic acid provides a route for designing rigid, planar aromatic units within the polymer main chain. Downstream manufacturers utilize it for producing poly(arylene)s and related high-performance polymers employed in demanding electronic, optoelectronic, or membrane separation applications. The material allows precise molecular weight control and backbone engineering, resulting in enhanced thermal and chemical stability for specialty films and coatings. Industry compliance standards
Typical usage ratio
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Years of hands-on work in boron-based chemistry have shaped how we view our catalog, and dibenzofuran-4-boronic acid stands out. We approach every lot with careful attention to detail. The industry relies on the purity and consistency of intermediates, and nobody feels that demand more directly than the people who spend every day working with actual raw materials and reactors, not just spreadsheets or catalogs. For many chemists targeting C–C bond formation by Suzuki coupling, the position of the boronic group on the aromatic system affects every downstream outcome—yield, selectivity, and sometimes even the physical stability of the finished product. A genuine advantage comes from working with a manufacturer who not only knows the CAS number but who has watched these reactions occur—in kilogram and sometimes multi-ton scale—day after day.
Dibenzofuran-4-boronic acid appears in our workflow because of a blend of performance and reliability. We produce and check each batch using equipment chosen for day-to-day dependability, not just theoretical sensitivity. Every lot undergoes NMR, HPLC, and elemental analysis, and the importance of rigorous QA stems from running processes ourselves, not outsourcing with fingers crossed. Our typical batch offers a purity of 98.5% or higher by HPLC, because we’ve seen sub-par starting materials choke reactions at kilo scale, resulting in hours lost and solvent waste—not just a failed small vial on a bench in a test lab. Moisture and breakdown products get tracked closely. There’s a noticeable difference between a redissolved powder and fresh isolated material, especially for cross-coupling work. From personal observation, customers who source this building block from producers like us see their palladium loads drop, their workups stay cleaner, and they can rely on downstream transformation—because we check for pinacol ester contamination, unreacted dibenzofuran, and trace level transition metal impurities before sending it out.
We package and store dibenzofuran-4-boronic acid in airtight containers and under dry argon, because over the years, we’ve faced every excuse for batch-to-batch inconsistency—humidity in warehouses, careless transfers, and transit roughness. Neat powders turn to sticky messes or degrade into non-traceable byproducts, erasing hours of planning. Our background in handling, not just selling, means we use desiccant-lined bottles and select packaging to minimize degradation. We still hand-check every shipment. Having to re-do purification or manage a failed order on a Friday night is the kind of pain we refuse to pass on to customers.
Lab data rarely reflects full-scale process issues, so our take on dibenzofuran-4-boronic acid comes from actual production experience, not just literature searches or industry whitepapers. Our chemists reached for this intermediate during scale-ups of pharmaceutical targets, OLED coatings, and specialty polymer monomers. Among Suzuki–Miyaura couplings, the 4-position boronic acid on dibenzofuran offers more than just a unique substitution pattern—it often brings electronic advantages, both activating the aromatic and sometimes providing extra solubility, thanks to the local environment of oxygen and boron on the heterocycle. These points crop up in real reactor logs and yield tables, not just synthetic schemes. Clients in materials science have told us about differences in thermal stability during their device fabrication.
We see requests spike from drug discovery groups who want late-stage diversification at the 4-position. Our colleagues in organometallics notice improved selectivity in sp^2–sp^2 couplings versus 2-substituted analogs, probably due to less steric congestion at that location on the heterocycle. With years on production lines, we’ve noticed the final product crystals developed from 4-boronic acid intermediates often exhibit greater uniformity and packing, aiding purification and further derivatization. Process chemists care about that because it means fewer headaches during filtration or lyophilization. End customers like electronics manufacturers have told us consistent input from a direct manufacturer has saved time and costs at the device assembly stage.
Plenty of boronic acids populate the market, but the experience changes drastically depending on source, purity, and isomer. Having handled different dibenzofuran isomers, even the small difference between 2- and 4-boronic acid shows up strongly in actual production runs. In the 4-position, the boronic acid sits farther from the ring oxygen, meaning less intramolecular hydrogen bonding—so it typically dissolves faster in polar aprotic solvents and often resists hydrolysis better during standard workups. In our plant’s hands, this means higher mass recovery and a more predictable reaction fate, whether the protocol runs at atmospheric or pressurized conditions.
Our actual users—ranging from medicinal chemists to material scientists—comment on the difference in impurity profiles and ease of workup. Synthetic steps involving 2-boronic acid frequently stall or encourage side products that consume time and require extensive purification. That’s not a problem we’re seeing in our 4-boronic acid batches. Seasoned users call out the crystallization behavior; the 4-isomer favors larger, more filterable crystals, easing both mechanical separation and washing. In process chemistry, that counts for more than theoretical literature yields.
Direct procurement from traders or aggregators sometimes delivers unstable or mixed material, causing delays. Our own production keeps both the yield and quality lock-tight, which matters enormously for large scale runs or high-stakes projects. We measure each lot’s melting point—typically between 175 and 178°C—and routinely see less batch-dependent drift in the end performance. Our batch records confirm virtually all lots stay within a tight impurity range; by knowing exactly which solvents and conditions create pitfalls, we can steer around them. It is not something a pure distributor sees; this comes from monitoring our own reactors and step-by-step crystallizations.
Several advanced materials projects have relied on dibenzofuran-4-boronic acid as a cornerstone for new conjugated polymer backbones. At scale, even small differences in byproduct profile can spell the difference between a seamless chromatography step or hours spent trouble-shooting. We’ve responded to requests adjusting particle size for specific reactors, and soliciting feedback to optimize how our material disperses. For one production customer synthesizing a series of bis-aryl compounds, shifting from a generic supplier to our direct batch meant a 15% bump in yield, a one-step cut in purification, and savings in rejected material.
We take pride in having trained our technical support team to field questions from the floor—these are people who have spent years doing the chemistry before answering phones. Where other suppliers can only repeat catalog information, we can discuss how subtle process changes (like palladium or base choice) interact with the specific impurity profile present in our material. On several occasions, this has resolved bottlenecks in downstream hydrogenation or cyclization steps, making a product possible that had stalled with other suppliers' inputs. Actually making the chemistry work, not just listing a compound, is the approach we favor.
Experienced chemists have run into troubles with boronic acid instability—especially hydrolysis, deboronation, and oxidative decomposition. Early in our manufacturing journey, we encountered entire reactors rendered useless by the slow breakdown of marginal materials. The lesson learned: always start with fresh, uncontaminated stock, and use moisture- and oxygen-free transfer whenever possible. For dibenzofuran-4-boronic acid, we’ve invested in improved isolation from water during synthesis and packaging, and built a workflow where every kilogram is double-checked at dispatch. Our long-term approach brought observable progress: less powdery, amorphous waste, and more reliable crystalline input, leading to better reaction control for downstream users.
Scale-up exercises revealed another common challenge: boronic acid self-condensation. During our own scale transitions, batch homogeneity suffered until we refined drying protocols and bottle purging routines. Once that element of the process improved, off-color and gummy residues nearly disappeared, solvent usage dropped, and we no longer faced delays caused by unknown oligomers appearing at purification. Professional chemists on tight timelines appreciate that kind of dependability, especially with high-value projects.
Our experience providing dibenzofuran-4-boronic acid to both R&D labs and pilot plants shaped every element of our workflow. In the early days, scale-up experiments exposed weak points in handling and transport. Uncontrolled exposure to air, poor bottling, or inconsistent particle sizing translated directly to user frustration. We answered by reworking our own SOPs—now powders get packed as soon as the last traces of solvent evaporate, never left exposed on the bench overnight. Even at scale, each drum is checked for caking, and staff pull random samples for retesting before any shipment leaves our site.
On custom request, we’ve produced lots tested for extended low-metal content, fuel-grade, and batch-specific particle morphology. If a project needs a certain kinetic profile, we’re open about what we know: sometimes grinding finer helps, but occasionally that exposes more surface to hydrolysis. We offer tailored advice, learned from real mishaps and victories. Sometimes, the best route comes from talking to the bench staff using it, rather than sticking to stock answers.
Producers must pay attention to environmental impact more than anyone else along the supply chain. Our facility maintains exhaust gas monitoring because accidental fluorobenzene or boric acid byproducts, even in trace levels, compound the regulatory headaches for everyone. After years of managing waste during boronic acid manufacture, we invested in recovery systems that reduce runoff and recycle solvents, eliminating the buildup of troublesome residues. Modern compliance calls for more than just passing audits; a direct investment in cleaner chemistry always pays off, both in cost savings and in long-term sustainability. Feedback from clients in Europe, North America, and East Asia shows growing demand for full traceability—not just COAs, but process transparency, documented at each stage.
A number of our partners—especially in pharma—ask for full documentation of starting materials and process routes, so they can support filings with transparency. Because we own our own reactors, we supply both batch records and enough material for pilot trials without resorting to stopgap vendors. Our direct link back to the synthesis line means easier compliance with REACH, TSCA, and other regional rules—not just a paper trail, but proof that the actual process adheres to regulatory limits. We have built-in monitoring of trace metals, halogen content, and residual solvents, because we know what happens at the factory floor impacts the final user, not just the regulator.
We learn the most when our partners push the product into new applications—novel ligands, advanced polymers, untested reaction sequences. With each project or pilot campaign, we see how batch features like polymorph form, residual solvent, and fines content shift reaction yields or equipment wear. Every kilogram that leaves our facility stretches our team’s perspective, and we respond in real time to trends and issues. Recently, demand for more physically robust batches—less powder, more granulate—saw us overhaul our isolation process, resulting in easier handling and improved shelf stability. In the rare event of a setback, such as a shipment delayed in transit, we step up to replace or rework material rather than deflecting blame.
Maintaining open channels with customers means we don’t get comfortable or generic in our supply approach. Instead, we keep a running dialogue, from the initial quotation to post-delivery feedback. In the last two years, this has led to meaningful upgrades in our QA methods, logistics strategies, and the technical documentation we provide. What doesn’t change is the belief that direct, hands-on production brings a product closer to both the chemistry and the chemist. Dibenzofuran-4-boronic acid is more than just a catalog reagent—it moves from idea to product, not as an abstract commodity, but as a managed, supported tool in the hands of professionals who rely on it every day.
People often ask about the real benefits of sourcing directly from the actual maker instead of middlemen. The difference shows up in service, reliability, and technical understanding. We believe in direct lines of communication: you’re not stuck chasing third-party reps or automated ticketing systems. When feedback about solubility, particle morphology, or stability comes in, our head chemist walks down to the production floor and watches the next batch run. If a batch falls even slightly outside spec, we put it aside and troubleshoot, rather than sending it out hoping no one notices. This approach draws on decades of manufacturing tradition—involvement, not detachment. If a modification to our process would serve your needs better, it lands on our R&D schedule.
Everything we do with dibenzofuran-4-boronic acid connects directly to the needs of real people running real chemistry. Delays, downtime, and off-spec shipments mean losses on both ends. As manufacturers, we want every product to uphold confidence—not through marketing slogans, but by repeatedly delivering chemistries that work where and how you need them. That attitude guides the skills, investment, and day-to-day labor in our factory, shaping a better experience not just for us but for every partner, customer, and end-user who relies on our reliability.