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HS Code |
323116 |
| Name | 1,4-Phenylenebisboronic Acid |
| Chemical Formula | C6H8B2O4 |
| Molecular Weight | 163.76 g/mol |
| Cas Number | 13666-96-9 |
| Appearance | White to off-white powder |
| Melting Point | 290-292 °C (dec.) |
| Solubility | Slightly soluble in water; soluble in DMSO, methanol |
| Purity | Typically ≥98% |
| Density | 1.32 g/cm³ |
| Storage Conditions | Store in a cool, dry place; keep container tightly closed |
| Synonyms | p-Phenylenediboronic acid, 1,4-Benzenediboronic acid |
| Inchi | InChI=1S/C6H8B2O4/c9-7(10)5-1-2-6(4-3-5)8(11)12/h1-4,9-12H |
| Smiles | B(O)(O)c1ccc(cc1)B(O)O |
As an accredited 1,4-Phenylenebisboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1,4-Phenylenebisboronic Acid, 25g, packaged in a sealed amber glass bottle with a screw cap, labeled with safety and identification details. |
| Shipping | 1,4-Phenylenebisboronic Acid is shipped in tightly sealed containers to prevent moisture absorption and contamination. It is packed with cushioning material and labeled according to hazardous material regulations. The shipment follows all safety guidelines for chemicals, including documentation of contents and proper storage conditions, typically at room temperature and away from strong oxidizers. |
| Storage | 1,4-Phenylenebisboronic Acid 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 oxidizing agents. Protect from light and air exposure to prevent degradation. Ideally, store at room temperature or below. Always follow safety guidelines and refer to the material safety data sheet (MSDS) for specific instructions. |
Applications of 1,4-Phenylenebisboronic Acid in Industrial Manufacturing1,4-Phenylenebisboronic acid acts as a key raw material in specialized chemical synthesis, enabling diverse downstream manufacturing processes in advanced polymers, pharmaceutical intermediates, OLED materials, specialty adhesives, and advanced diagnostic reagents. As an experienced manufacturer, we maintain compliance with up-to-date industry standards at every production and QC step. 1. Electronic Materials – Organic Light Emitting Diodes (OLEDs)Many OLED producers use 1,4-Phenylenebisboronic acid as an essential cross-coupling partner for the synthesis of conjugated linker units in emissive layer molecules, particularly for blue and green emitting materials. The raw material participates in Suzuki-Miyaura coupling reactions with aryl halides, forming rigid frameworks in final display polymers. Tight control over metal contamination, reproducibility, and fluorescence properties is required during this process. Industry compliance standards
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2. Pharmaceutical Synthesis – API Intermediate ProductionMany pharmaceutical manufacturers utilize 1,4-Phenylenebisboronic acid as a bifunctional building block for the construction of API molecular frameworks, especially in Suzuki coupling reactions for oncology, anti-viral, and CNS drug intermediates. Stringent control of residuals and trace impurities is essential to comply with GMP and global pharmacopoeia specifications during multi-stage synthesis and scale-up. Industry compliance standards
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3. Specialty Polymer Production – Conjugated Polymers and Conductive MaterialsProducers in the advanced polymer sector use 1,4-Phenylenebisboronic acid to introduce boron-terminated units into pi-conjugated polymer chains, essential for electronics and solar cell backplanes. The material supports repeatable polymer backbone growth and incorporation of electron-transporting units, facilitating tuning of film thickness and electronic performance. Quality focus lies in maintaining polymer solubility and molecular weight control through precise stoichiometric balance. Industry compliance standards
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4. Diagnostic and Bioanalytical Reagents ManufacturingProducers of advanced diagnostic kits employ 1,4-Phenylenebisboronic acid to synthesize glucose-sensing polymers and capture agents, utilizing its diol-binding capacity to anchor sensing ligands for selective analyte recognition. The material supports high affinity interaction with saccharides, and robust batch-to-batch purity and trace metal control are mandatory for compatibility in sensitive in vitro diagnostic systems. Industry compliance standards
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5. High-Performance Adhesives and Crosslinking SystemsSome advanced adhesive producers leverage 1,4-Phenylenebisboronic acid as a dual-functional crosslinker for specialty thermoset and structural adhesives, especially for electronics and transportation applications. It forms boronate bonds with polyol and catechol groups within adhesive resins, enhancing cohesive strength, temperature resistance, and chemical durability. Precise metering and formulation testing enable optimization for each curing protocol and substrate compatibility challenge. Industry compliance standards
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Every batch of 1,4-Phenylenebisboronic Acid that leaves our facility reflects decades of experience in boron chemistry. The molecular structure, C6H4(B(OH)2)2, lends the compound versatility across organic synthesis, pharmaceutical intermediate production, and material science research. As we handle the full synthesis process in-house, we maintain control over purity, particle size, and water content from initial raw materials to final packaging. In our observation, very few boronic acids stack up to the straightforward reactivity and stability profile of the 1,4-phenylenebis variant, especially where double boronic functionality enables more efficient cross-coupling reactions.
Customers typically reach out to us looking for boronic acids able to deliver consistent performance batch after batch. The 1,4-Phenylenebisboronic Acid shines here. Careful handling during synthesis and purification matters—a lesson we learned through several production scale-ups where minor moisture ingress or insufficient crystallization history yielded product inconsistencies. Our ongoing investments in drying technology and inert atmosphere handling directly address these everyday manufacturing challenges. By sticking to rigorous impurity monitoring (especially pinacol and residual organics), we now supply a product that chemists can trust for Suzuki coupling or sensor applications, with predictable melting points and solubility profiles.
Through years of feedback from academic and industrial users, it became clear that purity, specific surface area, and homogeneity affect reaction yield as much as theoretical reactivity. Raw boronic acids sometimes carry occluded solvents; residual toluene or dioxane can throw off measured results in sensitive syntheses. As a manufacturer, we deploy proprietary solvent removal methods, then confirm key specs using both NMR and KF titration. Our QC teams track trace metals (Fe, Cu, Ni), understanding that even parts-per-million shifts can poison catalytic cycles in cross-coupling. The resulting powder flows smoothly and disperses reliably—a point appreciated by production teams scaling up from milligram to kilogram.
In the early days, most requests landed in the range of 98–99% purity, and few customers expected exact lot-to-lot consistency. Over the last decade, increased demand for error-free pharma intermediates and reproducible scientific results led us to develop variants with lower trace water and tighter particle distribution. Direct conversations with formulators revealed problems where the product picked up environmental moisture despite sealed packaging—now, we ship 1,4-Phenylenebisboronic Acid in double-layered containers, using desiccant packs. Engineers at several electronics companies reported difficulties with unwanted adduct formation during storage; by tightening our drying protocols, we helped ensure cleaner downstream reactions. These tweaks have stuck because the people using the chemical set the standard, not the catalog.
A chemist working with simple arylboronic acids like phenylboronic acid will notice crucial differences with 1,4-Phenylenebisboronic Acid. The symmetrical para orientation of the boronic groups opens up routes in the assembly of rigid, extended frameworks for molecular electronics. Dual reactivity enables higher functional density per molecule, working especially well in tedious Suzuki-Miyaura coupling steps where other bisboronic configurations (like ortho- or meta-) might struggle with steric hindrance. We saw this first-hand during an exploratory project with a materials science group, where only the para variant produced the targeted conjugated polymer at workable conversion.
Compared to derivatives such as 1,3-phenylenebisboronic acid or cyclohexylbisboronic acid, 1,4-Phenylenebisboronic Acid brings reliably high yields with aromatic ring rigidity, promoting more linear polymeric assemblies or frameworks. Feedback highlights cleaner reaction profiles in both laboratory and pilot-plant scales, avoidance of side reactions typical for ortho derivatives, and increased shelf life under typical storage conditions. Some teams appreciate the environmental stability: although all boronic acids show some hydrolytic vulnerability, this particular structure resists rapid degradation in dry, cool storage.
Every week, we field questions from research and production chemists needing to clone literature syntheses or create new functional scaffolds for drugs or sensors. Over the years, we’ve watched 1,4-Phenylenebisboronic Acid become a go-to substrate in Suzuki-Miyaura couplings, driven by both research curiosity and manufacturing need. Chasing high-purity oligomers of biaryls, one group relied on our product to cut steps out of their old route, reducing time in batch reactors while boosting overall recovery. Another industrial user running pilot polymer synthesis scaled up from tens of grams to tens of kilograms, citing crystalline uniformity and stable purity across shipments as the primary factor allowing seamless process transfer from bench to plant floor.
We take part in these dialogues, learning where bottlenecks appear, how the powder performs across multiple grams, or where adjustments in crystal form speed up downstream isolation. It’s never just about moving finished goods; it’s about plugging real chemistry into working, efficient manufacturing.
Boronates present headaches in moist environments. We’ve dealt with returns and process stoppages when customers found products clumped or partially hydrolyzed. The root cause often came back to packaging—years ago we used simple high-density polyethylene bottles, which let tiny amounts of water vapor through during transit. Since switching to multi-layer foil-lined jars with integral seals, clumping and off-spec moisture content have dropped significantly. Several teams running automated powder feeders now report consistent dosing, zero line stoppages, and lower material loss.
The chemistry behind this need for dryness reflects straightforward reality: both positions in 1,4-Phenylenebisboronic Acid can form boronate esters or be susceptible to slow hydrolysis, throwing off yields and increasing impurities in subsequent steps. Few things frustrate bench chemists more than a compound that degrades on the shelf, so our focus on packaging and post-production drying comes directly from their experience. We built moisture analysis and packaging checks into our standard workflow, not as a box-checking exercise, but as a necessary extension of product reliability.
Projects from OLED research to small-molecule drug discovery put 1,4-Phenylenebisboronic Acid to work in wholly different environments. In any setting, reproducibility matters. Users in the materials field focus on assembly of two- or three-dimensional frameworks, counting on each batch's defined boronic content to deliver clean cross-linking and robust electronic properties. In pharma and agrochemical research, accurate titration of boronic acid function means fewer process surprises and easier QA/QC sign-off.
Through repeated, wide-ranging feedback, we learned that customers facing tighter documentation and regulatory review especially prize a transparent supply chain for building blocks like 1,4-Phenylenebisboronic Acid. We retain full traceability and release data for each lot, not just as a sales tactic but to enable reliable regulatory filings. The result: fewer production holdups and less requalification work, speeding customers’ timelines and keeping scale-ups on track.
Iteration is core to the way we manufacture specialty boronic acids. Several years ago, a few minor off-odors in one lot signaled upstream solvent residues missed during drying. Internal review and customer discussion led to new process controls. These included additional GC/MS screening, which now eliminates even trace residues of halogenated solvents, commonly a sticking point for high-spec applications.
Another case involved particle size distribution—early powder forms contained large aggregates dragging down flowability in automatic pill presses. After sharing sieve analysis data with a long-term customer, we switched to a micronization finishing step better tuned for their equipment. From that point forward, shipped material passed through feeders without bridging or sticking issues. Each production cycle now uses customer-driven input; our largest volume users have a direct line to manufacturing for spot adjustments.
Sometimes, incremental changes solve problems that new equipment or new processing can’t. We noticed that even slight inconsistencies between batches—such as residual chloride content from acidic wash-downs—could trigger variable yields in Suzuki couplings. In-house tests pinpointed where rinse cycles needed adjustment, right down to final drying atmospheres. After tightening these controls, customer complaints about variable reactivity all but vanished.
Lab managers stressed that opaque, ambiguous specification sheets kill time in regulated environments. In response, our documentation now includes concrete data backed by batch records, not just general claims. This shift resulted from years of two-way communication—an advantage that trading houses and resellers rarely bring.
Direct production experience shapes how we approach safety and environmental impact. We recover nearly all process solvents, recycling high-value streams in a closed system to limit chemical waste. As demand scaled up, solvent selection changed: instead of chlorinated options, we now stick to greener choices whenever possible, benefiting both our workers and downstream users. This impacts not only compliance and reporting but also lowers chances for trace impurities common with less controlled sources.
We also address waste from byproducts; arylboronic acid synthesis produces organoborates and minor borates, yet through improved stepwise purification they rarely end up in final product. This continuous review, sparked in part by customer audits and regulatory change, keeps both policy makers and industrial labs confident in the quality and environmental safety of our material.
New application areas always carry their own surprises, and we’ve learned to expect learning curves. Recently, a customer in the field of molecular sensing requested a custom crystalline habit, aiming for higher surface areas and ease of packing into test cell devices. Experience told us that tweaking our crystallization rates shifts crystal morphology without needing extraneous surfactants. Through a few pilot batches—guided more by test data than theory—we dialed in a form that passed their loading and reactivity requirements, all while keeping impurity levels low.
ESG criteria now inform purchasing for major R&D programs. Chemists and project managers seek partners who guarantee not just high-purity material but also transparent, sustainable operations. Our in-house production, tracked from earliest borate precursor to finished acid, supports these priorities—never leaving supply chain doubt for users facing outside audit. Direct manufacturer-to-user relationships create faster response times and genuine accountability for grade or preparation adjustments.
Shipping and handling seem mundane, but real results depend on product quality at the moment it hits the lab bench or plant reactor. Many advanced users have told us that even great materials, chemically, let them down if bottling, shipment, or storage wreck the powder’s flow or promote hardening. So, we made careful improvements to packaging lines and trained shipping teams to flag temperature spikes, helping counteract summer heat during transit. Customers in tropical and coastal climates now receive product that performs the same in June as it does in December.
Some customers struggled with measurement issues connected to static; carefully grounding drums, introducing anti-static liners, and using polyethylene spatulas in high-humidity packaging spaces prevented electrostatic clumping and sticking. Small operational tweaks on our end keep end-users focused on research, not fixing powder handling issues.
Our in-house R&D centers around customer-initiated feedback. While other boronic acids, especially monofunctional types, claim ease of use, 1,4-Phenylenebisboronic Acid distinguishes itself through dual reactivity and predictable assembly in borylation and coupling environments. Researchers appreciate the minimized byproduct profile—proven by several direct comparisons to commercial competitors, where our proprietary purification and solvent-removal steps resulted in higher isolated yields in downstream chemistry.
We remain directly responsible for the process from raw supply to labeled product. This single-source manufacturing enables swift fixes to the rare off-spec batch, without finger-pointing between vendors or supply chain delays. As other producers come and go, our track record builds confidence not only for established clients but also for new users aiming for reliable results.
Real understanding comes not from chasing trends but from daily attention to performance, application feedback, and hands-on care in production. The challenges of handling, packaging, and custom spec adjustment for customers pushing the limits inspire new solutions every season. Stronger packaging, frequent testing, data-driven QC, and a readiness to adapt set direct, domestic production apart from third-party trade. The reputation of our 1,4-Phenylenebisboronic Acid wasn’t built overnight—it evolved through project-by-project improvement, guided as much by customer pain points as by textbook chemistry.
Product reliability does not come from broad claims or theoretical descriptions. Quality performance at the bench and plant level draws on the granular decisions made every day in the factory—choices about solvents, operational timing, analytical methods, and collaborative responsiveness when something goes wrong. Our 1,4-Phenylenebisboronic Acid stands as a case study in transparent supply, backed by hard-won expertise and ongoing dialogue with those who rely on specialty boronic chemicals to keep their work moving forward.