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HS Code |
709968 |
| Chemical Name | 1-Pyrenylboronic Acid |
| Cas Number | 2381-77-7 |
| Molecular Formula | C16H11BO2 |
| Molecular Weight | 246.08 |
| Appearance | Yellow to light brown powder |
| Melting Point | 270-274°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Boiling Point | Decomposes before boiling |
| Storage Conditions | Store at 2-8°C, keep dry |
| Smiles | B(C1=CC2=CC=CC=C2C3=CC=CC=C13)(O)O |
| Inchi | InChI=1S/C16H11BO2/c18-17(19)16-10-12-5-1-3-7-14(12)15-9-4-2-6-13(15)11-16/h1-11,18-19H |
As an accredited 1-Pyrenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 1-Pyrenylboronic Acid contains 1 gram in a sealed amber glass vial, labeled with chemical details and safety warnings. |
| Shipping | 1-Pyrenylboronic Acid is shipped in sealed, inert containers to prevent moisture and air exposure. It is handled as a non-hazardous solid but requires precautions to avoid prolonged contact. Shipping complies with chemical transport regulations, ensuring the package is labeled and accompanied by appropriate documentation for safe handling and delivery. |
| Storage | 1-Pyrenylboronic 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 oxidizers. Protect it from direct sunlight and sources of ignition. Store under inert atmosphere (e.g., nitrogen or argon) if possible, to prevent degradation and hydrolysis. Always follow standard laboratory chemical storage guidelines. |
Applications of 1-Pyrenylboronic Acid in Industrial Manufacturing1-Pyrenylboronic acid finds specialized application in advanced material synthesis and organic electronics, supporting industrial innovation through its unique structural and electronic properties. Our manufacturing expertise ensures consistent supply of high-purity product for critical downstream processes across sectors that demand tight specification control and established compliance practices. 1. Organic Light-Emitting Diode (OLED) Material SynthesisLeading OLED panel producers incorporate this boronic acid in the fabrication of polycyclic aromatic compounds, especially during cross-coupling reactions to build conjugated emitter cores for blue and near-UV emission layers. The boronic acid moiety enables Suzuki-Miyaura coupling for the precise assembly of pyrene-containing building blocks, resulting in highly efficient, stable, and color-pure emissive molecules. Manufacturers optimize addition rates based on targeted device performance and substrate compatibility, always maintaining batch traceability as required for consumer electronics use. Industry compliance standards
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2. Fluorescence Probe Reagent Production for BioanalysisBioanalytical reagent manufacturers use the compound to synthesize high-sensitivity, pyrene-based fluorescent probes for nucleic acid detection and protein-ligand studies. Its boronic acid group enables covalent linkage to oligonucleotide backbones and polysaccharide chains, harnessing pyrene’s intense fluorescence for enhanced assay sensitivity. Production facilities scale addition to balance probe brightness and minimize background signals in bioassay kits tailored for regulated diagnostic markets. Industry compliance standards
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3. Advanced Conjugated Polymer Production for Electronic DevicesProducers of high-performance organic polymers for electronic circuitry integrate this boronic acid for controlled construction of alternating copolymers, especially in applications demanding charge mobility and photophysical durability, such as organic thin-film transistors (OTFTs). The material’s regular insertion in Suzuki or Stille coupling stages yields consistent electronic band structures, supporting quality requirements for printable electronics and anti-counterfeit features. Industry compliance standards
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4. Photoactive Surface Modification in Sensor ManufacturingDevelopers of optical and electrochemical sensors exploit the photoactivity and boronic reactivity of our material to tailor sensor substrate surfaces for selective recognition of saccharides, catechols, and environmental contaminants. Chemical engineers employ surface grafting or covalent immobilization on glass, gold, or silicon wafers, using pyrene fluorescence to monitor interaction events in situ. The ratio and introduction method are determined by target analyte sensitivity and sensor lifetime under regulatory test protocols. Industry compliance standards
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From years behind pilot reactors to scaling new boronic acid derivatives for demanding research programs, the path to reliable 1-Pyrenylboronic Acid production never plays out without a few stories. As a specialty chemicals manufacturer, we see more than white powders and catalog numbers—we witness firsthand the challenges researchers face sourcing pure, well-characterized pyrene derivatives. Since our earliest boronic acid campaigns, consistent performance has guided our process design. Each lot’s purity, solubility, and reproducibility comes from a hands-on understanding of organic synthesis, not guesswork, not handoffs, and not reselling. Close feedback from customers—whether they work in molecular electronics or medicinal chemistry—shapes the way we tackle every batch.
1-Pyrenylboronic Acid brings a unique set of chemical properties thanks to its pyrene core fused with a boronic acid group at the 1-position. Pyrene itself rings familiar to researchers for its strong π-π stacking, fluorescence, and ability to serve as a probe in biophysical studies. Adding a boronic acid group enables Suzuki-Miyaura cross-coupling, opening the door to conjugated polymers, advanced sensing materials, and novel bio-conjugates. In our shop, technicians treat this material with the same care as a high-purity reference standard. Our model most commonly supplied corresponds to the compound with CAS 769076-69-3, with single-digit ppm impurity levels and a physical form that simplifies handling. Don’t confuse this with generic aromatic boronic acids or lesser pyrene derivatives—substitution at the pyrene 1-position shows much greater reactivity in cross-coupling and delivers superb optical properties without the background noise seen from multi-substituted analogs.
Preparation of 1-Pyrenylboronic Acid rarely plays by textbook rules. In practice, controlling regioselectivity and minimizing oxidation during synthesis calls for both tailored protocols and reliable in-process analytics. We learned early on that oxygen exclusion and careful pH adjustment determine product quality. Even small shifts in temperature or moisture level during workup greatly influence yield and crystal habit. Investing in specialized glassware and monitoring each step helps keep contaminants away. Our senior chemists recall running dozens of iterative reactions, only to see fluorescence profiles off by a fraction. Today, we use high-resolution chromatography and in-line NMR to make sure each batch hits target purity and meets all optical specs laid down by our R&D partners.
Nearly every conversation with synthetic researchers comes down to more than simple purity numbers. While many third-party suppliers focus on batch size or one-time price points, we look at the physical and chemical behavior under real-use conditions. 1-Pyrenylboronic Acid can crystalize in different forms depending on moisture exposure or post-processing. We began offering both crystalline and amorphous forms based on customer insight—polymer labs often want fine powder for ease of metering, while materials scientists sometimes request larger crystals. Our main grade targets a well-defined particle range suitable for accurate weighing and reproducible solubility, reducing hassle during scale-ups or multi-step projects.
Pyrene derivatives are finicky. In scaling output from lab bench to pilot reactors, our teams discovered that doubling a batch never means doubling success. Subtle reactor hydrodynamics, stir efficiency, and heat transfer can all influence byproduct formation. We once watched a promising technical route deliver 99% NMR purity on a 5-gram scale, only for the signal-to-noise to plummet at 250 grams. Re-examining each stage, we tuned agitation speed, loading sequence, and solvent degassing protocols. That hard-won control translates into stable supply chains today—customers running medicinal arrays or working with organic semiconductors count on batch-to-batch reproducibility. One-off samples might pass muster in screening, but only tightly controlled manufacturing keeps those traces of pyrene carbocation impurities at bay.
Many labs see boronic acids as almost interchangeable, but practice quickly proves otherwise. Our support teams often field questions about why 1-Pyrenylboronic Acid outperforms its simple phenyl or naphthyl analogs in cross-coupling. Structurally, the extended aromaticity of pyrene increases the electron density on the ring, impacting the transmetalation step in Suzuki-type reactions. In side-by-side studies, we’ve watched our material deliver higher conversions and cleaner product isolation, thanks in part to tighter control over aggregation and solubility. Where triphenylboronic acid products may struggle to overlap fluorescence spectra or blend into certain conjugated polymers, the 1-pyrenyl group lends distinct electronic and emission features. Years of analytical work confirm our lots show low trace-metal and halide content, lowering side reaction risk for critical coupling runs.
Pyrene chemistry rewards a close look at the placement of functional groups. We see recurring demand for 1-substituted over other regioisomers because of greater chemical stability and coupling efficiency. Some customers once tried moving to 2- or 4-pyrenylboronic acid, only to discover lackluster reactivity and more difficult purification. We’re regularly asked to compare the two, and our direct synthesis data always comes back supporting the sharper performance and versatility of the 1-position. Even minor differences in fluorescence lifetimes and quantum yields change how a conjugated pyrene function acts in a finished device or analytic sensor. That’s why our product development always focuses on precise regioisomer control right from starting materials.
Data sheets and certificates of analysis can only tell so much. Years in chemical manufacturing teach that any lot can carry invisible baggage: residual solvents, off-ratio isomers, trace heavy metals, or micron-scale impurities. We don’t let a batch move to inventory without deep-dive analytics—high-performance liquid chromatography, mass spectrometry, and microtrace metal assessment. For several of our bigger pharma customers, 1-Pyrenylboronic Acid’s ultimate value rests on purification and long-term stability. We’ve built custom storage solutions and cold-chain supply for sensitive boronic acid esters, minimizing hydrolysis that plagues some parallel synthetic work. This groundwork delivers the confidence our partners need to commit resources to scale and commit to multi-year research.
Academic and industrial researchers often call on us in early project stages to walk through practical aspects of using 1-Pyrenylboronic Acid for material synthesis. Pyrene’s robust optical absorption and emission means this boronic acid helps build organic semiconductors, solar-cell precursors, and photovoltaic devices that outperform simple aromatic alternatives. In several spin-coating polymer projects, our customers needed ultra-high-purity samples to avoid device shorts. We've learned that high moisture—even low ppm—decreases device performance dramatically. Our labs developed specialized inert packing and shipped early-morning couriers to preserve product from air and light. Meeting these standards brings real-world results: more repeatable film formation, improved process yields, and lower device failure rates.
Pyrene units lend excellent photophysical properties, which find roles in advanced biosensors, fluorescent switches, and live-cell studies. Researchers working with peptide conjugates or DNA labeling kits keep returning for our 1-Pyrenylboronic Acid due to the high purity and tight control over boron isotopic ratio. We recall supporting a group investigating glucose sensors that depended on reversible boronate-diol binding—small shifts in impurity content made or broke their sensor selectivity. By maintaining tight tolerances in both stoichiometry and trace profiles, we’ve helped move new diagnostic approaches out of concept and onto the benchtop. These stories reinforce our focus on quality assurance—knowing someone’s research depends on trace-level performance, we keep pushing for higher analytical resolution in every batch.
There’s no shortcut to practical experience handling boronic acids. In our facilities, every operator receives training on low-humidity manipulation and specialty glassware for air-sensitive stocks. We suggest keeping 1-Pyrenylboronic Acid in hermetic packages inside a desiccator, using PTFE tools to avoid metal ion contamination during weighing. From a decade of storage-log tracking, we've seen that batches packed under argon show markedly better shelf stability and process performance. For downstream derivatives, we recommend direct transfer via powder funnels, avoiding prolonged exposure to ambient air. Such small steps keep downstream processes reproducible and minimize batch-to-batch headaches for our manufacturing partners.
Manufacturing doesn’t end at the shipping dock. We commit to staying involved with each shipment, supporting technical troubleshooting and protocol development. We’ve worked side by side with polymer chemists unraveling substrate compatibility issues or advising medicinal chemistry teams assembling complex bioconjugates. Early-stage researchers have sometimes struggled with dissolution rates for 1-Pyrenylboronic Acid in high-performance liquid chromatography mobile phases; our practical suggestions—like pre-sonication or deoxygenation—have prevented wasted time and materials. Providing this depth of support comes from real process experience, not a script. Relationships built on listening and honest data build real trust.
We see the pace of innovation in pyrene-based chemistry accelerating fast. Research into organic light-emitting diodes, flexible electronics, and artificial photosynthesis now relies on more than commodity-grade boronic acids. Our development teams follow the expanding toolbox of post-Suzuki functionalizations, such as click chemistry and palladium-free coupling. Drawing on ongoing feedback, we keep refining our production lines, exploring greener reaction media and recyclable catalysts to keep ahead of regulatory and environmental demands. These process changes don’t just tick boxes—they yield purer, more reproducible products for next-generation applications.
Scaling up production holds environmental and safety concerns. Boronic acids like this one require specialized wastewater handling and careful end-of-process filtration. Our experience with closed-loop solvent recovery and on-site effluent treatment means we manage both costs and sustainability targets. Introducing high-efficiency filtration removes particulate byproducts that can compromise final compound stability. We also continually audit our supplier chain for high-quality pyrene cores and minimally contaminated reagents, which raises up both our performance and the longevity of every batch we ship.
Academic publications and intellectual property filings steadily confirm what developers in our community have noticed: using high-grade 1-Pyrenylboronic Acid pays off in lower device failure and greater reproducibility. Organic field-effect transistors, light-harvesting arrays, and next-gen sensors rely on surface and trace purity that only manufacturers with a hands-on approach can secure. Across our partners in OLED and solar research, prototypes built with our refined lots push higher conversion efficiencies and longer device life, translating initial purity investments into practical performance gains.
Growing alongside our customers’ research highlights another key aspect: transparent, prompt, and knowledgeable support. Our technical specialists routinely assist buyers not just in logistics but with on-the-ground troubleshooting—whether it’s a failed coupling run, an unexpected fluorescence shift, or a need for a custom batch specification. Our commitment never stops with a shipped kilo or gram; it stretches through every project iteration. Regular feedback loops shape not just current production but the next rounds of quality control updates and process refinements. In our view, this wraps up what it means to be a true manufacturer—generating solutions, adapting quickly, and passing on practical knowledge with each lot.
New questions and possibilities keep appearing as researchers stake out new territories in carbon-based electronics, diagnostics, and advanced analytics. We see our role not as distant suppliers but as partners invested in success, always working to deliver well-characterized, reliable, and technically supported 1-Pyrenylboronic Acid. Each batch captures a decade of trial, error, analytics, and improvement, all aimed at helping the next innovation emerge faster, cleaner, and more reliable than the last.