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3-Propoxyphenylboronic Acid

    • Product Name 3-Propoxyphenylboronic Acid
    • Alias 3-Propoxybenzeneboronic acid
    • Einecs 842-630-0
    • 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
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    Specifications

    HS Code

    963355

    Chemical Name 3-Propoxyphenylboronic Acid
    Cas Number 1072954-65-2
    Molecular Formula C9H13BO3
    Molecular Weight 180.01 g/mol
    Appearance White to off-white powder
    Melting Point 110-114°C
    Purity ≥98%
    Solubility Soluble in DMSO, methanol, and ethanol
    Density 1.18 g/cm3 (estimated)
    Smiles B(C1=CC(=CC=C1)OCCC)(O)O
    Storage Temperature 2-8°C
    Synonyms 3-Propoxybenzeneboronic acid

    As an accredited 3-Propoxyphenylboronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 10g 3-Propoxyphenylboronic Acid is supplied in a tightly sealed amber glass bottle with a printed chemical-resistant label.
    Shipping 3-Propoxyphenylboronic Acid is shipped in tightly sealed containers to prevent moisture and contamination. It is packed according to chemical safety regulations, with clear labeling and appropriate hazard documentation. The package is handled with care, stored at room temperature, and shipped via ground or air transport, depending on customer requirements and shipping guidelines.
    Storage 3-Propoxyphenylboronic acid should be stored in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizers and acids. Store at room temperature or according to the manufacturer’s recommendations. Proper labeling and secure placement are essential to avoid accidental exposure or contamination.
    Application of 3-Propoxyphenylboronic Acid

    Applications of 3-Propoxyphenylboronic Acid in Industrial Manufacturing

    3-Propoxyphenylboronic Acid serves as a strategic intermediate in organoboron chemistry. Our factory supplies this compound for advanced downstream synthesis in high-precision industries. The following key applications illustrate actual industrial use cases, integration methods, manufacturing compliance, and formulation specifications.

    1. Pharmaceutical API Synthesis

    This compound functions as a boronic acid building block for proprietary drug molecules, especially in targeted oncology small-molecule synthesis. It is utilized in Suzuki-Miyaura coupling processes to construct biaryl skeletons of several kinase inhibitors. The compound supports efficient C–C bond formation under mild conditions, reducing degradation of sensitive functional groups, which is vital during post-modification or late-stage appendage of pharmacophores in cGMP synthesis lines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 210/211
    • Japan Pharmacopoeia (when exported to Japan)
    • EMA EudraLex Volume 4

    Typical usage ratio

    • Used at 1.2–2.5 molar equivalents relative to halogenated partner; exact ratio adjusted depending on reactivity of the coupling substrate and catalyst system (Pd/C or Pd(PPh3)4)

    Downstream process integration

    • Feeds into Grignard or Suzuki cross-coupling step in process reactors with inert atmosphere
    • Enters at intermediate preparation stage after primary structure assembly
    • Purified using preparative HPLC for subsequent reactions

    Final product types

    • Oncology drug intermediates
    • Kinase inhibitor APIs
    • Immunomodulating agent precursors

    2. Electronic Materials: OLED Intermediate Synthesis

    In advanced materials manufacturing, this boronic acid plays a key role as a coupling agent in the synthesis of high-performance OLED emitter molecules. It supports the assembly of rigid, planar aromatic frameworks, which enhance charge mobility and stability of next-generation organic electronic components. This material’s controlled reactivity and solubility facilitate streamlined post-synthesis purification, which is critical for defect-free optoelectronic layer production.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • IEC 62321 for electronic substance restriction (ensuring low impurities such as heavy metals)
    • RoHS (2011/65/EU) for material input to electronic devices

    Typical usage ratio

    • Employed at 0.8–1.5 equivalents relative to aryl halide, adjusted to minimize byproduct formation in microreactor setups

    Downstream process integration

    • Dosed in automated batch or flow reactors for polymeric and small molecule coupling
    • Introduced at precursor assembly stage preceding device-grade purification

    Final product types

    • OLED emitter molecules
    • Small-molecule organic semiconductors
    • Active layers for display panels

    3. Agrochemical Intermediate Development

    This boronic acid finds significant use in the synthesis of complex herbicide and fungicide active compounds, particularly those requiring biaryl ether or biphenyl linkage. Its chemical structure enables efficient formation of C–C bonds under aqueous and mild temperature conditions, which reduces decompositional losses in sensitive downstream chemistries. Crop protection manufacturers specify this input for syntheses where residue profiles and traceability are regulated under global agrochemical control statutes.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • US EPA 40 CFR Part 180 (Tolerances for Pesticide Residues)
    • REACH (EC 1907/2006) for registration and supply chain disclosure

    Typical usage ratio

    • Ranges from 1.0–2.0 equivalents per mole of halogen substrate; adjusted according to desired product purity and downstream yield optimization

    Downstream process integration

    • Added in intermediate coupling steps before esterification or amidation
    • Integrated into multi-stage flow or batch synthesis
    • Subjected to inline GC-MS for monitoring residuals before formulation

    Final product types

    • Biaryl herbicides
    • Fungicide intermediates
    • Custom agrochemical scaffolds

    4. Specialty Polymer Synthesis for Advanced Coatings

    Manufacturers of advanced coatings use this boronic acid derivative to build functionalized monomers for specialty polymers, imparting tailored surface properties to coatings used in electronics, automotive, and aerospace sectors. Its integration enables the formation of polymers containing boron-rich side chains, resulting in improved adhesion, electrical properties, and chemical resistance. Batch process control is critical to ensure downstream product robustness and conformance with electronic and automotive material standards.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management
    • TSCA Inventory Listing for US chemical management
    • ASTM D4060 (Wear Resistance) where applicable

    Typical usage ratio

    • Monomer charge of 2–5 wt% in copolymerization batch, adjusted to achieve specified surface property targets

    Downstream process integration

    • Dosed in monomer preparation step prior to radical or condensation polymerization
    • Purified intermediates further processed under vacuum stripping units
    • Final resin integrated into coating formulation blending lines

    Final product types

    • Conductive and anti-static coatings
    • Scratch-resistant polymer films
    • Optically functionalized varnishes
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    Certification & Compliance
    More Introduction

    Introducing 3-Propoxyphenylboronic Acid: Consistent Quality from Our Experienced Manufacturing Facility

    Over the last decade, we have focused intensively on producing a reliable supply of specialty boronic acids, including 3-Propoxyphenylboronic Acid (commonly referred to by researchers as 3-propoxyphenylboronic acid, CAS Number 5122-95-2). Over the years, customer feedback and the shifting needs of R&D departments pushed us to refine our production techniques, from the earliest kilo-scale batches to multi-ton outputs for pharmaceutical partners. Every step of our process reflects a hands-on understanding of why chemists and procurement managers seek out this molecule—as well as what sets a consistent lot apart from an inconsistent one.

    What is 3-Propoxyphenylboronic Acid?

    This compound carries a molecular structure built around the phenylboronic acid skeleton, with a propoxy group occupying the meta position. The formula C9H13BO3 gives you a starting point, but practical users notice more than the theoretical chemistry—for most synthetic steps, reactivity and purity matter most. Developed primarily for Suzuki-Miyaura cross-coupling reactions, it finds its way into routes for biaryl derivatives, leveraged by pharmaceutical and fine chemical companies alike.

    What stands out with 3-Propoxyphenylboronic Acid is its unique balance between hydrophobicity and manageable solubility. The propoxy chain shields parts of the molecule during coupling, changing how it interacts with catalysts or solvent systems. From our experience running dozens of pilot reactions with customers’ ligands and palladium sources, small differences in side-chain length or position can make or break yields.

    Our Manufacturing Process: Facts from the Line

    We rely on well-established organometallic approaches to assemble high-purity 3-Propoxyphenylboronic Acid. The boronation step tends to be demanding—side products can appear during oxidative work-up if the oxygen content isn’t tightly controlled, so our approach uses oxygen-scavenging protocols and real-time reaction monitoring. In our early days, inconsistent color and melting points led to unnecessary purification steps. We learned that controlling the grain size of the raw propoxybenzene dramatically reduced impurity formation, improving filtration at scale and giving more reproducible spectral data.

    Current lots produced at our facility reach assay values above 98.5%. Moisture content stays below 0.5%—once customers flagged sticky batches that clumped in storage, we overhauled drying equipment and beefed up our nitrogen blanket procedures. Users expect a white to off-white powder, sometimes with faint tinting due to minor oligomerization, and IR/HPLC traces confirm the material matches the reference standard every cycle. We run full trace metal analyses, since palladium-catalyzed cross-couplings can suffer even from residual levels, and keep these below 10 ppm for key metals. The cost to us is extra analytics and staff hours; the benefit for partners shows up in smoother scale-ups.

    Addressing Needs in Synthesis and Scale-Up

    Across the global market, demand for 3-Propoxyphenylboronic Acid keeps pace with growth in heterocycle and biphenyl building blocks—especially where solubility tweaks can improve synthetic efficiency. The propoxy substituent acts as more than just a blocking group. From a chemist’s standpoint, it gives better performance in certain solvent and base conditions than shorter alkoxy analogs like methoxy or ethoxy options. We have tracked orders from labs working on kinase inhibitors and other bioactive scaffolds where tuning the electronics of the ring mattered.

    Our technical team engages directly with customers planning pilot manufacturing runs. More than once, we have worked with development chemists to check compatibility with their preferred coupling partners—some use phosphine ligands renowned for stubborn impurities, others want reassurance that the side-chain doesn’t introduce unforeseen side reactions during deprotection. Our QC records give them confidence: low water content, tight melting point ranges, and traceability from raw materials to packing. Nobody in production wants downtime due to clogging or undetected fines, so we guarantee free-flowing powder and implement batch-wise sieve testing throughout the year.

    Comparison to Other Phenylboronic Acid Derivatives

    There’s a reason customers ask about the propoxy version even when ethoxy or tert-butyl groups look appealing on paper. In several in-house tests run side-by-side, the propoxy group delivers a more predictable response in cross-coupling reactions requiring mid-polar solvents, especially methyl-tetrahydrofuran or DMF mixes. While smaller alkoxy groups can yield volatile impurities and product losses during work-up, the propoxy length increases thermal stability without locking the molecule into water-insoluble clumps.

    Some competitors offer mixed positional isomers, blurring meta and para- forms; our chromatographic controls ensure that only the meta-propoxy derivative leaves our plant. Researchers with time-pressured projects count on matching spectral data from batch to batch, especially during scale-up for toxicology or GMP intermediates. With patents and regulatory filings increasingly dependent on fine details, we keep robust archived samples and retain documentation stretching back for five years per lot. We’ve fielded more than one regulatory inquiry from customers in North America and Europe seeking proof of process control—and our records always close those questions without extra tail-chasing.

    Reliability and Trust in a Crowd of Suppliers

    Regularly, questions crop up about consistency—what keeps our material from batch drift, how we back up claims about purity, or what sort of shelf-life real customers can expect. A decade of repeat orders from top companies reflects more than marketing; it’s about knowing that time spent doubting raw material sources saps energy from real innovation. In the early years, issues like inconsistent hydroxide scavenging or temperature swings produced awkward conversations with our first big customers. Every one of those failures taught us to put experienced eyes on each step, not to delegate oversight to automation alone.

    Return purchases and multi-ton annual offtakes from project managers building CRAMS relationships or pharmaceutical intermediates give us a fine-resolved sense for what people really value. Several years of survey responses show storage and stability questions rank just as high as price or delivery. Customers expected a dry, shelf-stable powder that remains easy to weigh or dissolve, even after months warehoused in humidity or heat. Resolving sporadic caking with upgraded packaging and desiccant systems grew from those requests, not from theoretical shelf-life studies.

    Supporting Innovation: Collaboration from Discovery to Kilo-Scale

    The most valuable partnerships often involve joint troubleshooting, not just shipped parcels. Synthetic chemists working on new analogs frequently ask about in-process color changes, solubility issues, or possible contaminants detectable by HPLC. Our technical staff, most with hands-on bench time, communicate directly with end-users. In one recent example, a partner scaling up a functional intermediate noticed minor yield drops and color shifts. We jointly discovered that subtle pH variances in the work-up step influenced the recovery of 3-Propoxyphenylboronic Acid. Tuning our production’s final filtration accordingly kept the product within spec and avoided their costly repeat reactions.

    We constantly run application labs, collaborating on real solutions—how best to dissolve material in varied reaction solvents, how to minimize residue during transfer, or which cross-coupling conditions maximize yields for specific scaffold classes. These case-by-case adjustments provide practical benefits missing from off-the-shelf data sheets. Researchers developing medicinal chemistry pipelines get access to analytical methods, impurity fingerprints, and shipment samples ahead of full runs. We know firsthand that small tweaks translate into smoother timelines and less wasted material.

    Quality You Can Trace, from Raw Materials to Shipment

    We source each incoming batch of propoxybenzene and boronic acid reagents from qualified suppliers who meet stringent audit protocols. In practice, this means full spectral libraries for each shipment, periodic on-site audits, and a willingness to halt production if a lot falls outside agreed specs. Years ago, a single out-of-spec raw shipment forced us to halt manufacturing for a full production cycle, but it saved downstream partners from serious process headaches. We track batch numbers, maintain a sample archive of each lot, and keep a tight feedback loop with our logistics team—shipping only once full analytical clearance lands from our QC department.

    Throughout production, each lot goes through GC and HPLC analysis for purity and side-product profiling, moisture determination by Karl Fischer, and visual inspection for any color drift. Finished product leaves our facility in sealed, airtight containers under dry nitrogen or desiccant; this guards against moisture-based hydrolysis, which can ramp up acid content and reduce cross-coupling efficiency. Our team records and verifies each certificate of analysis sent with final shipments, offering customers a full technical package on request.

    Environment, Safety, and Responsible Production

    Responsible manufacturing means more than just regulatory box-checking. Our facility meets or exceeds local and international benchmarks for emissions and process safety. Waste streams generated during 3-Propoxyphenylboronic Acid synthesis go through neutralization and solvent recovery before disposal. We select process solvents with proven recycling routes and invest steadily in equipment that tightens controls on fugitive losses. Regular safety drills and ongoing staff training give everyone on the floor ownership of production integrity and accident prevention.

    Process changes are reviewed not just for technical soundness but also for downstream impact—on waste burden, solvent usage, and worker exposure. For example, periodic audits led us to swap out older batch reactors for scrubbed, jacketed designs that enhance both product quality and emissions capture. Our customers depend on us to keep their supply risk-low and avoid costly interruptions due to non-compliance, process upsets, or supply chain disruptions.

    Supporting Sustainability While Meeting High Standards

    As a manufacturer, we face growing scrutiny about the full lifecycle footprint of our products. For 3-Propoxyphenylboronic Acid, this means tracking not just the key yield and process metrics, but also our energy efficiency, solvent usage, and waste minimization. We have invested in energy audits, optimized reaction times, and run solvent swaps aimed at pushing both costs and emissions down. These incremental changes give partners a lower-carbon choice and streamline documentation for those targeting green chemistry practices or life-cycle analyses.

    Shipping procedures favor light, recyclable secondary packaging and, where possible, we coordinate deliveries to maximize container fill. End-of-life planning for unused stock remains a topic with our enterprise clients, who appreciate both regulatory compliance and access to technical support if disposal questions arise. It’s not only about keeping current customers confident, but also about meeting the expectations of new regulatory environments and increasingly ESG-aware buyers.

    Continuous Improvement and Market Feedback

    The market for boronic acids, especially those with custom alkoxy modifications like 3-Propoxyphenylboronic Acid, grows more sophisticated year by year. As scaling requirements change, from kilo-labs to full manufacturing campaigns, manufacturers cannot succeed by standing still. We lead regular reviews of our production methods, incorporating findings from customer pilot runs, feedback from analytical partners, and our own QC records. In one recent example, adaptations in drying and sieving protocols improved not just powder flow, but also shortened batch release times and reduced fine-content variability.

    We keep a constant line open with technical managers at customer sites, understanding the pulses and pivots of changing research needs. When regulations or project plans alter course, our production chemists adapt quickly—modifying packing, shifting delivery formats, or realigning analytical targets when the demand for clean-room supplies jumped in the wake of new drug development guidelines. We believe a direct, informed conversation with every customer beats rigid specs that struggle to accommodate evolving workflows.

    Meeting Global Challenges with Reliable Local Solutions

    We have seen a surge in global sourcing challenges, from freight interruptions to raw material bottlenecks. A stable domestic supply becomes critical for partners who require responsive order fulfillment or backup delivery plans. During the pandemic, many teams experienced multi-month lags for key building blocks. Our investment in domestic storage, redundant supply chains for critical reagents, and trained in-house staff allowed us to keep shipments on schedule—securing production timelines for partners with zero-tolerance policies for supply interruptions.

    Multi-site warehousing and flexible lot sizes give customers options: large-volume offtakes for upcoming manufacturing campaigns, or tailored splits for phased R&D campaigns and multi-site validations. Our logistics records show that rapid, accurate shipments cut development stalls, shortened method transfer times, and reduced cost overruns for product launches relying on solid, available starting materials.

    Practical Solutions for Research and Industry

    3-Propoxyphenylboronic Acid will continue to play a niche but vital role for chemists exploring new routes for advanced intermediates, specialty pharma targets, or polymers. Our journey in manufacturing this compound reflects the importance of listening, adapting, and keeping a technical hand in every batch. It's easy to look at catalog listings and see only part of the picture—but by maintaining real traceability, regular process audits, and a tight customer feedback loop, we deliver a product that reflects not just chemical performance, but a knowledge-driven, collaborative approach.

    Questions about batch-to-batch variation, field performance, or compatibility with emerging cross-coupling catalysts get real answers from our technical teams—not just template responses from a call center. We support our partners across every stage from sample submission to kilo-scale manufacturing, fielding technical questions, collaborative optimization, and ongoing post-sale support.

    In the hands of skilled chemists, 3-Propoxyphenylboronic Acid delivers more than just functional groups—it becomes part of the unseen infrastructure powering new discoveries and product launches. Our commitment to its quality reflects a decade’s worth of direct, measurable experience, and we look forward to supporting the next generation of innovation with the same hands-on expertise.