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Propylboronic Acid

    • Product Name Propylboronic Acid
    • Alias PBA
    • Einecs 241-815-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    730476

    Cas Number 4956-35-0
    Molecular Formula C3H9BO2
    Molecular Weight 87.92
    Iupac Name propylboronic acid
    Appearance colorless to light yellow liquid
    Density 0.89 g/cm3
    Boiling Point 184-186 °C
    Melting Point -21 °C
    Solubility In Water reacts
    Purity typically ≥ 97%
    Synonyms 1-propylboronic acid
    Smiles B(CCC)(O)O
    Inchi InChI=1S/C3H9BO2/c1-2-3-4(5)6/h5-6H,2-3H2,1H3
    Refractive Index 1.430

    As an accredited Propylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Propylboronic Acid is supplied in a 25g amber glass bottle with a tight-sealed cap, labeled for laboratory use only.
    Shipping Propylboronic acid should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It must be labeled as a chemical substance and handled according to standard chemical transport regulations. Store and transport at room temperature in a dry, well-ventilated area, avoiding exposure to heat, sparks, and strong oxidizers.
    Storage Propylboronic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture, heat, and sources of ignition. It should be kept away from strong oxidizing agents and acids. Store under inert atmosphere, such as nitrogen or argon, if possible. Properly label the container, and handle with appropriate personal protective equipment to avoid contact.
    Application of Propylboronic Acid

    Applications of Propylboronic Acid in Industrial Manufacturing

    Propylboronic acid serves as a specialized building block in fine chemical synthesis, offering targeted reactivity for downstream industries with demanding quality, safety, and regulatory profiles. Our proprietary synthesis guarantees high-purity grades supporting critical production processes in pharmaceuticals, agrochemicals, advanced materials, and specialty intermediates. Below we outline specific industrial application scenarios where this compound delivers unique functional advantages and compliance performance.

    1. Pharmaceutical Intermediate Synthesis

    Our material plays an essential role as a coupling partner for creating biaryl structures and other complex architectures via Suzuki-Miyaura cross-coupling reactions in pharmaceutical manufacturing. Process chemists rely on its selectivity and controlled reactivity, supporting the synthesis of active pharmaceutical ingredients (APIs) and high-value drug intermediates requiring strict traceability and impurity control. Formulators adjust dosage based on molecular equivalence and reactivity with halide substrates.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 cGMP for Finished Pharmaceuticals (FDA)
    • EU Guidelines for GMP (EudraLex Vol 4)
    • USP / EP / JP monographs on raw material purity (where applicable to intermediates)

    Typical usage ratio

    • 0.8–1.2 molar equivalents relative to aryl or vinyl halide substrates; adjustment based on conversion rates and catalyst loading

    Downstream process integration

    • Charged during the key cross-coupling step, following halide activation and prior to catalyst introduction, under inert atmosphere with temperature-controlled reaction vessels

    Final product types

    • Pharmaceutical grade biaryl intermediates
    • Structure-active arylated API scaffolds
    • Regulatory-submitted bulk intermediates

    2. Agrochemical Active Ingredient Manufacturing

    Crop protection producers utilize propylboronic acid as a core reagent to construct specialized biaryl or alkyl-aryl motifs within fungicides and herbicides by facilitating transition-metal-catalyzed couplings. Regulatory dossiers require evidence of batch-to-batch consistency and residual boron removal, necessitating reliable sourcing and process visibility. Formulation chemists optimize charge ratios to manage both cost and conversion.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Technical Grade Material
    • OECD Guidelines for the Testing of Chemicals
    • ISO 9001:2015 Quality Management Systems (applied to agrochemical manufacturing)
    • REACH Registration, Evaluation, Authorisation of Chemicals (EC No 1907/2006)

    Typical usage ratio

    • 1.0–1.5 molar equivalents compared to halogenated precursor; ratio selected according to target conversion efficiency and required impurity profile for downstream technical concentrate

    Downstream process integration

    • Introduced at the Suzuki reaction stage for C–C bond formation, followed by phase-separation, solvent washing, and downstream formulation to technical concentrate or EC/SC formulations

    Final product types

    • Aryl-based herbicide intermediates
    • Biaryl fungicide technical materials
    • Key synthesis modules for selective insecticides

    3. Electronic Materials and OLED Intermediates

    Manufacturers of advanced electronic materials and organic light-emitting diode (OLED) intermediates employ this boronic acid in constructing high-purity aryl cores, directly impacting emission wavelength control and device stability. Stringent specifications for trace metal and boron residue compliance necessitate precise feedstock handling under controlled atmospheres, and batch record traceability for color purity and performance validation. Usage quantities scale with molecular design and target functional group placement.

    Industry compliance standards

    • IPC-1752 Materials Declaration Management Standard
    • RoHS Directive (2011/65/EU) compliance for materials used in electronic components
    • ISO 14644 Cleanroom Standards (for critical assembly and synthesis lines)
    • Corporate customer specifications for OLED intermediate quality and trace metal limits

    Typical usage ratio

    • 1.0–1.1 molar equivalents for cross-coupling; occasionally up to 1.3 depending on side reactions and desired yields

    Downstream process integration

    • Dosed at the organometallic coupling step before purification; post-reaction, the crude intermediate advances to chromatographic refinement to ensure photoactive purity

    Final product types

    • OLED emission layer precursors
    • Organic semiconductor coupling units
    • Specialty aryl core materials for flexible electronics

    4. Specialty Fine Chemical Synthesis

    Custom synthesis suppliers and advanced intermediates developers incorporate our propylboronic acid to build tailored biaryl, diaryl, or arylalkyl patterns for dyes, catalysts, and small molecule performance materials. Customers demand certified low-metal and low-residual profiles for scale-up feasibility and application in regulated or performance-critical systems. Operators modulate input ratios for cost management and reaction selectivity, responding to the complexity of the synthetic target.

    Industry compliance standards

    • Chemical Facility Anti-Terrorism Standards (CFATS) for specialty chemical facilities (if applicable)
    • ISO 9001 Quality Management Systems
    • Customer-specific material specification agreements and product purity certificates
    • Transport and storage compliance per UN Recommendations and GHS

    Typical usage ratio

    • 1.0–1.3 molar equivalents depending on the electronic demand of the aryl halide and risk of homocoupling side-products

    Downstream process integration

    • Integrated at the solution-phase or solid-supported coupling reaction stage, with post-reaction purification via re-crystallization, distillation, or chromatographic separation

    Final product types

    • Dye intermediates for optical materials
    • Ligands for homogeneous catalysis
    • Modified aryl additives for specialty polymers
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    Certification & Compliance
    More Introduction

    Introducing Propylboronic Acid: From Our Factory Floor

    A Closer Look at Propylboronic Acid Production

    Making chemicals with clear provenance and consistent quality means understanding every step of the process, and few compounds illustrate that like Propylboronic Acid. Over years of mixing, measuring, and testing, we've found that focusing on purity and performance pays off both in the lab and in industrial applications. Propylboronic Acid brings together propyl and boronic functional groups in a formula many research teams now call essential for organic synthesis, especially for cross-coupling reactions. The batch work in our factory lines up with strict control points, real-time tracking of pH, moisture, and temperature, plus in-house GC and NMR confirmation for identity and purity. No two runs look exactly the same in detail, but every batch completes the same journey from raw boric acid and propyl bromide to isolated product, purified and ready to ship.

    Why Propylboronic Acid Earns Its Place in Select Chemistry

    Through the years, we watched the demand for boronic acids rise across pharmaceutical and agrochemical sectors. One reason stands out: the Suzuki-Miyaura coupling. In the bench-scale days, chemists made do with small samples and variable sources, but scaling up uncovered the obstacles. Water sensitivity, by-product removal, and shelf life all came into sharp focus. Propylboronic Acid handles these challenges with a balance of reactivity and manageable storage compared to its methyl or phenyl analogs. Its carbon chain length makes it less volatile than methylboronic acid but less hydrophobic than higher-order alkylboronic acids—useful for solution handling and formulation tasks.

    We've tested its behavior firsthand with aryl halides and palladium catalysts, seeing clean conversion and minimal side-reaction problems. The boronic acid we ship carries careful documentation on residual water content, and we keep moisture to a tight spec, as even a small excess starts to undermine coupling yields and reproducibility. Many of our partners share their reaction recipes, comparing results across batches; this feedback loop plays a direct role in our own process refinements.

    Transparency in Sourcing and Specifications

    Every bottle starts with the choice of raw input. We source boronic and propyl compounds from trusted upstream producers, checked by our own in-house QC before entering the line. Specifications for Propylboronic Acid have settled around a purity of at least 98 percent by HPLC, with a colorless crystalline appearance and a melting range checked on every lot. Unlike more moisture-volatile alkylboronic acids, propylboronic acid grants some flexibility in storage but does best sealed against ambient air; we've seen first-hand the clumping and color drift that comes from open-air exposure.

    We don't rely solely on third-party certificates. Our on-site analytical lab pulls samples from every batch and runs NMR and FTIR scans—tools familiar to every chemist but handled with a factory discipline. Each data point tells us not just about that day's output, but about subtle shifts in our upstream feeds or shifts in process conditions. For example, slight rise in residual propyl impurities signals a drift in column separation, flagged for immediate tune-up.

    Practical Experience: How Propylboronic Acid Makes a Difference

    The story of propylboronic acid's popularity stems from its manageable reactivity. Comparing it to methylboronic acid, we've tracked two key benefits in daily factory life: longer shelf stability and fewer incidents of spontaneous polymerization. We caught early issues with glassware etching from more volatile boronic acids and adjusted our storage labs accordingly. Another common choke point with boronic acids lies in handling during scale-up. Methyl and ethylboronic acids often bring headaches with high vapor pressure, leading to losses and stricter storage demands. Propylboronic acid strikes a balance—low enough volatility for bench work, high enough reactivity for efficient coupling.

    Our warehouse crew notes that containers holding propylboronic acid survive longer on shelves without degradation than their ethyl analogs, based on regular content checks. From an industrial standpoint, less waste means less cost, and more predictable supplies. Many researchers try a few rounds of product before choosing a regular vendor; the steady feedback on batch consistency influences our production tuning more than any marketing push ever could.

    Handling and Usage Tips: What We’ve Learned

    Having watched hundreds of customer orders filled and tens of thousands of grams pass inspection, a simple lesson emerges: no two chemistry setups are quite alike. Users often have different approaches for using propylboronic acid, but two themes repeat. First, keep it dry—desiccators pay for themselves when dealing with boronic acids. We have tracked reaction yields with and without this step, and the difference can be striking. Even slight water exposure translates to by-product formation and drops in yield during coupling reactions. Second, pay close attention to temperature control during storage and use. Warmer temperatures above room temperature nudge some boronic acids towards impurity formation.

    To reach target yields in Suzuki couplings or similar processes, our clients rely on solvent choice and catalyst load as much as starting material purity. We collaborate with several academic labs to optimize loading and scale-up approaches. Through these partnerships, we uncovered that propylboronic acid reacts more cleanly with electron-poor aryl halides than some branched alkylboronic acids, and works well with both traditional and newer ligands. In pharma R&D, its moderate hydrophobicity allows for fast extraction steps and ease of removal at work-up.

    Comparisons with Related Boronic Acids

    There are plenty of options for C3-C5 alkylboronic acids, but over time patterns stand out. Methyl and ethylboronic acids evaporate more quickly, leading to flash loss and more hazards in open transfer. Butylboronic acid and higher analogs bring stronger hydrophobicity and more waxy textures, often complicating solution dosing and mixing. Propylboronic acid drop-casts in the lab as a near-solid at room temperature, manageable by spoon or spatula, and dissolves nicely in many polar organic solvents.

    Compared to phenylboronic acid, the propyl analog resists slow crystallization in sealed jars, even after weeks of storage. Practically, this shortens the prep time for large-scale batches, saving both labor and resources. The reactivity profile maintains the delicate balance needed for selective coupling: neither too sluggish for electron-poor aryl halides, nor so aggressive as to spark side-chain reactions with sensitive partners.

    It’s also worth noting that propylboronic acid’s lower toxicity profile compared to, say, organostannanes makes it a safer option for routine lab work. Many of our clients in scale-up ventures mention environmental and safety compliance as top considerations during raw material selection. Because the propyl group’s length fits most carbon chain extension needs in pharmaceuticals, propylboronic acid picks up many synthesis jobs that either require sharp selectivity or mild reaction partners.

    Production Challenges: How We Deal With Them

    No extended production run goes by without a dental look at bottlenecks. Boronic acid syntheses often face hydrolysis, by-product formation, and purification challenges. In the early days, yield losses stemmed from humidity sneaking into reactors and storage vessels. After some ruined batches and midnight trouble-shooting, proactive moisture monitoring and sealed process loops now form the backbone of quality control. Investing in glass-lined reactors helped reduce metal contamination and upholds the integrity needed for downstream pharmaceutical applications.

    Handling propylboronic acid means more than chemistry. On the factory floor, attention to ergonomics and cross-contamination makes a real difference. Regular cleaning minimizes cross-batch interference, and glove policy has evolved to include dual-layer systems in sensitive production zones. Not all manufacturers keep these standards, but we've seen direct improvements in both product quality and worker satisfaction. These measures add cost but cut down on recalls and customer complaints.

    We pay similar attention to waste handling. The by-products from propylboronic acid synthesis may pack some residual boron, so we use controlled collection and neutralization steps. This strategy not only reduces environmental burden but tightens compliance for hazard classification and transport. Factory routines include regular training, so new staff stay alert to safe handling, especially with spill risk during large-batch transfer.

    Listening to Labs: How Users Drive Our Process

    Our best feedback rarely comes from a spreadsheet or market survey; it arrives by phone, email, or a note scribbled in a batch test report. Academic groups, pharma labs, and R&D outfits have shared countless suggestions, from asking for different grade packaging to reporting reaction anomalies. Some groups requested extra-dry lots, pushing our water content specs to new lows. Others wanted re-sealable packaging to prevent repeated air exposure. These requests led us to invest in both improved sealing technologies and upgraded desiccator facilities. Real-world usage reveals what the best SOPs miss, so we keep open lines with all our partners.

    We also adapted packaging as needs changed. Small research groups often prefer gram-scale vials, while larger industry customers favor sealed bags or jugs of up to 25 kilograms. Each size brings its set of packaging and handling details to manage, like double-bagging for larger quantities or vacuum-sealing for sensitive formulations. Every tweak comes from cumulative experience, and each improvement in supply chain robustness gets reflected in the feedback we see from downstream labs and industries.

    Shipping accuracy takes priority, especially for overseas partners. Even a one-day delay can disrupt production or bring whole lines to a standstill. Because propylboronic acid remains sensitive to temperature and moisture, we invest in climate-controlled shipping options for longer distances or high-temperature regions. The extra care may add to shipping cost, but it pays off in steady supply and consistent product quality at destination.

    Regulatory and Sustainability Considerations

    As chemistry regulations get stricter worldwide, compliance shapes every stage of production. Boronic acids face scrutiny for both safety and environmental impact, so we keep up to date on shipping requirements, labeling protocols, and safety documentation for every region where our product travels. Our team invests in annual training, keeping current on evolving standards in the EU and US, as well as shipping rules for East Asia and South America.

    Sustainability stretches deeper than just compliance paperwork. Minimizing waste output and tightening solvent recycling directly reduces both cost and footprint. With boronic acid syntheses, solvent volumes can climb quickly, so we install distillation units to reclaim and purify the bulk of organics used in process. Packing greener solvents into process design has yielded surprising improvements in both product purity and downstream handling. As the industry leans toward more sustainable synthesis, our own factory shifts more resources into R&D for bio-based and low-impact chemical routes.

    How Propylboronic Acid Fits Into the Larger Market

    Over the past decade, changing trends in chemical R&D have expanded the role of boronic acids. Propylboronic acid now features in many patent filings for active pharmaceutical ingredients, crop protection compounds, and battery materials. Each field comes with its quirks, and we adjust our production to match. For the pharma sector, the focus remains on ultra-high purity and minimal metals—no shortcuts accepted. For electronics and polymer customers, batch-to-batch consistency wins the day. In other fields, flexibility in supply quantities and timelines takes top priority.

    Our on-the-ground experience shows that one-size-fits-all approaches rarely work, especially with a compound like propylboronic acid that has niche uses. We remain hands-on with production, tailoring process steps and QC parameters to match the real-world scenarios our clients report back. It means more work per batch, but the results speak for themselves in lower reject rates, higher customer repeat rates, and direct word-of-mouth referrals.

    The Future of Propylboronic Acid Production

    Today's chemical manufacturing runs on both tradition and new tech. Automated control systems, remote QC sampling, and web-connected instruments now sit next to flask-and-stirrer setups. Even so, every new instrument or updated protocol comes under real-world testing before it gets the final stamp of approval. Over years of batches and countless shipments, we've learned that attention to detail carries through from raw material loading to final product release.

    We’re preparing for shifts as next-gen coupling techniques and greener chemistry gain traction. Several customer partners now pursue biocatalytic boronic acid syntheses, hoping to cut out harsher reagents and shrink energy footprints. Our R&D team works side by side with these groups, sharing insights and redirecting production lessons back to our own shop floor. Every new breakthrough builds on the foundation of safe, reliable chemical supply—and the lessons learned from decades with compounds like propylboronic acid.

    Conclusion: Pride in Crafting a Reliable Building Block

    Some products come and go with the latest trends; propylboronic acid remains a workhorse of modern synthesis. From Suzuki couplings in pharma plants to early-stage research tools in academic labs, this compound sees daily use not by chance but because of its down-to-earth performance and reliable results. We take pride in every lot that leaves our factory, having seen firsthand the difference careful, steady hands make in chemical manufacturing. Propylboronic acid may not be the flashiest compound, but it shows its value by how often it's chosen, how well it fits into established synthetic routes, and how many projects succeed because they trusted a stable, well-made supply.

    As technology and chemistry shift, we’ll continue tuning, improving, and sharing what we learn on the path from raw material to finished propylboronic acid—one batch at a time.