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(4-Formyl-1-Naphthalene)Boronic Acid

    • Product Name (4-Formyl-1-Naphthalene)Boronic Acid
    • Alias 4-Formyl-1-naphthaleneboronic acid
    • Einecs 832-415-0
    • 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

    665863

    Productname (4-Formyl-1-Naphthalene)Boronic Acid
    Casnumber 1036567-69-5
    Molecularformula C11H9BO3
    Molecularweight 200.00 g/mol
    Appearance White to off-white solid
    Meltingpoint 226-230°C
    Purity Typically ≥98%
    Solubility Insoluble in water; soluble in DMSO and methanol
    Storagetemperature 2-8°C
    Synonyms 4-formylnaphthalene-1-boronic acid
    Smiles B(C1=CC=CC2=C1C=CC=C2C=O)(O)O
    Inchi InChI=1S/C11H9BO3/c13-7-9-6-8-2-1-3-10(12(14)15)11(8)5-4-9/h1-7,14-15H

    As an accredited (4-Formyl-1-Naphthalene)Boronic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging contains 5 grams of (4-Formyl-1-Naphthalene)Boronic Acid in a sealed amber glass vial, labeled with chemical details.
    Shipping (4-Formyl-1-Naphthalene)boronic acid is shipped in secure, airtight containers to protect against moisture and light. Packaging follows all relevant safety and regulatory guidelines for chemical transport. Standard shipping is via ground or air, with appropriate labeling, and includes documentation such as SDS for safe handling and compliance.
    Storage (4-Formyl-1-naphthalene)boronic acid should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Store at room temperature or lower, in a cool, dry, and well-ventilated area, ideally under an inert atmosphere such as nitrogen or argon. Avoid contact with strong oxidizing agents and acids to ensure chemical stability and prevent degradation.
    Application of (4-Formyl-1-Naphthalene)Boronic Acid

    Applications of (4-Formyl-1-Naphthalene)Boronic Acid in Industrial Manufacturing

    As the direct manufacturer specializing in (4-Formyl-1-Naphthalene)Boronic Acid, we support advanced synthesis processes across sectors with rigorous quality control and tailored support for your downstream formulation needs. Our production capabilities align with strict standards required by specialty chemicals, ensuring reliable supply for high-value applications. Below we outline key industrial scenarios where this raw material functions as a core intermediate or building block, including critical details relevant to your use case.

    1. Pharmaceutical Active Ingredient Synthesis

    Pharmaceutical companies employ (4-Formyl-1-Naphthalene)Boronic Acid as a pivotal intermediate in the Suzuki-Miyaura cross-coupling to introduce naphthalene frameworks into small molecule APIs—commonly targeting kinase inhibitors and antifungal agents. Its formyl group supports advanced heteroaromatic coupling for next-generation drugs requiring precise molecular configuration, entering multi-step processes where boronic acids enable controlled aromatic substitutions under GMP constraints.

    Industry compliance standards

    • ICH Q7 Certificate of GMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) API general monograph standards
    • 21 CFR Part 211 – US FDA cGMP for Finished Pharmaceuticals
    • USP General Chapters <800>, <1078> for quality and solvent controls

    Typical usage ratio

    • 0.2–0.6 mole equivalents relative to the halide coupling partner, adjusted per batch yield targets and molar efficiency in the API synthesis pathway

    Downstream process integration

    • Charged during Suzuki coupling stage under argon; utilized before reduction/oxidation functionalization sequences in active moiety construction

    Final product types

    • Oncology small molecule APIs (e.g. kinase inhibitors)
    • Antifungal compounds featuring naphthalene substructures
    • Intermediates for CNS therapeutics requiring planar aromatic scaffolds

    2. OLED and Organic Semiconductor Material Development

    R&D and industrial-scale manufacturers of organic optoelectronics utilize this boronic acid derivative to construct extended π-conjugated systems during OLED emitter and hole-transport material production. The formyl-naphthalene moiety is critical for fine-tuning electronic properties in the Suzuki coupling polymerization steps, driving high mobility in organic semiconductors and color purity for display applications.

    Industry compliance standards

    • RoHS 2 (Directive 2011/65/EU) compliance for electronic chemical raw materials
    • IEC 62474: Material declaration for electronic industry supply chains
    • REACH Regulation (EC) No 1907/2006 for import and downstream use
    • ISO 9001:2015 for optical material production processes

    Typical usage ratio

    • 5-20% by weight in the monomer charge for polymeric emitter or transport layer synthesis, varied according to target layer thickness and emission wavelength

    Downstream process integration

    • Fed into batch polymerization reactors via Suzuki cross-coupling with aryl halides; purified intermediates introduced to thin-film deposition units via spin coating or vapor deposition

    Final product types

    • OLED display emissive layers for consumer electronics
    • Organic thin-film transistors (OTFTs) used in flexible sensor arrays
    • Photovoltaic organic semiconductors for specialty solar modules

    3. Agrochemical Intermediate Manufacturing

    Agrochemical formulators leverage (4-Formyl-1-Naphthalene)Boronic Acid in the synthesis of active fungicide and insecticide molecules with fused aromatic backbones, optimizing pest resistance and bioactive duration. The reagent underpins Suzuki coupling and downstream derivatization steps, supporting pathways towards high-value crop protection molecules under international quality frameworks.

    Industry compliance standards

    • FAO/WHO JMPR guidelines for pesticide active ingredient synthesis
    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 17025-certified QC for agrochemical intermediates
    • Directive 91/414/EEC on market authorization of plant protection products in the EU

    Typical usage ratio

    • 10–25% of core aromatic reactant feed by molecular weight, precise charge established by process optimization to maximize intermediate output

    Downstream process integration

    • Introduced after halide activation steps in Suzuki coupling reactors, followed by hydrolysis or alkylation to generate target crop protection compounds

    Final product types

    • Broad-spectrum triazole fungicides
    • Naphthalene-derived botanical insecticides
    • Pre-formulated technical grade intermediates for contract tolling

    4. Specialty Dye and Pigment Intermediate Production

    Manufacturers in the high-performance dye sector integrate (4-Formyl-1-Naphthalene)Boronic Acid to synthesize colorants with enhanced chromatic intensity and lightfastness, particularly for disperse dyes and anthraquinone pigment classes. Its formyl function enables late-stage condensation or cyclization, while boronic acid cross-coupling expands color possibilities and supports stable dye frameworks for demanding textiles and plastics.

    Industry compliance standards

    • OEKO-TEX® Standard 100 Annex 6 for textile chemicals
    • DIN EN 12852 for pigment coloration in food contact materials
    • ZDHC chemcheck certification audit for responsible chemical management
    • ISO 105-B02: Color fastness testing in textiles

    Typical usage ratio

    • 8–15% by weight in the dye or pigment synthesis blend, modulated based on color depth and desired degree of aromatic extension

    Downstream process integration

    • Added after initial azo or aldehyde activation; processed by batchwise cross-coupling, followed by purification and particle-size adjustment for end-use compatibility

    Final product types

    • Disperse dyes for synthetic fiber textiles
    • High-performance organic pigments for plastics and automotive coatings
    • Color-fast anthraquinone dye intermediates for specialty textile applications

    5. Advanced Liquid Crystal Material Synthesis

    Liquid crystal material developers harness this compound for synthesizing naphthalene-based mesogenic cores required for high birefringence and rapid-switching liquid crystal displays (LCDs). Its chemical structure enhances anisotropic properties crucial in advanced display technologies. The boronic acid enables high-yield Suzuki coupling with tailored halides, supporting production of high-purity LC tailspheres for both display and photonic devices.

    Industry compliance standards

    • IEC 61249-2-51: Materials for printed boards and other interconnections for LC applications
    • ISO 9001:2015 for optoelectronic material production
    • REACH Annex XVII on restricted substances for electronic devices
    • Industry LCD QC standards for residual solvent and phase purity

    Typical usage ratio

    • 3–10 mol% as core builder in mesogen synthesis, modulated per required birefringence and twisting power of the target LC formulation

    Downstream process integration

    • Charged during core mesogen assembly by Suzuki coupling, followed by purification, then introduced to LC formulation blending and thermal cycling units

    Final product types

    • High-birefringence liquid crystal mixtures for thin-film transistor LCDs
    • Tunable photonic crystals for smart glass and display modulation
    • Specialty LCs for advanced low-voltage switching displays
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    Certification & Compliance
    More Introduction

    4-Formyl-1-Naphthalene)Boronic Acid: Precision for Modern Chemical Synthesis

    Introduction to a Key Building Block

    Chemistry demands more than just access to active reagents—it thrives on purity, reliability, and consistency. Doing business strictly as a true chemical manufacturer brings home the reality that every batch, every yield, every result matters. That’s particularly true in the world of complex boronic acids, where (4-Formyl-1-Naphthalene)Boronic Acid stands out as a proven workhorse for advanced organic synthesis. Years of hands-on manufacturing and partnerships with process developers have shown that quality control makes the difference between a promising trial and repeatable, market-ready chemistry.

    What Sets This Molecule Apart

    The nature of (4-Formyl-1-Naphthalene)Boronic Acid opens doors for a wide variety of cross-coupling strategies, excelling in Suzuki-Miyaura reactions and beyond. Chemists value its formyl functionality merged on a naphthalene backbone—two structural motifs that offer flexibility for downstream modifications. These characteristics don’t come by accident. Making this compound in our facility requires attention to solvent choice, reaction atmosphere, and work-up methods that don’t compromise the sensitive formyl group.

    Over time, we’ve invested in techniques that minimize impurities, especially isomeric or decomposition byproducts common in less controlled settings. Purification relies on recrystallization steps that ensure robust isolation of the desired product. This hands-on approach takes more effort but pays dividends when customers notice reductions in side product formation during critical transformations.

    Consistent Quality Backed by Experience

    Labs synthesizing advanced pharmaceuticals, OLED intermediates, or next-generation functional materials often write for detailed batch histories, analytical testing, and real-world validation. Production at scale demands processes that avoid batch-to-batch variability. We learned early that relying on outsourced or variable raw materials can jeopardize entire runs. Bringing key upstream steps in-house provided a lever to manage supply risks and to control trace metal and moisture levels, both of which matter in palladium-catalyzed environments.

    Throughout every step, spectroscopic and chromatographic assessments check for homogeneity and absence of contaminants like polycyclic aromatic residues or boron-related fragments. Thin layer chromatography and HPLC always confirm the correct retention factors, while NMR serves as the final fingerprint—confirmed by those of us who have worked up from flask to reactor. This isn’t a game of box-ticking, but a direct line from bench experience to delivered bottle.

    Role in Suzuki-Miyaura Reactions and Emerging Synthesis

    Researchers reach for (4-Formyl-1-Naphthalene)Boronic Acid when they seek aryl extensions that tolerate further derivatization. The naphthyl core confers stability, but the formyl group gives flexibility—allowing introduction of heterocycles, fine-tuning of electronics, or straightforward access to further aldehyde transformations. We’ve seen it drive successful syntheses of custom dyes, complex ligands, and high-value drugs.

    Conditions for coupling reactions benefit from consistent boronic acid quality. Boronic acids can degrade under humid storage, leading to boroxine formation, but careful packaging and desiccated handling keep the product fresh. In our experience, the feedback loop runs straight from manufacturing through shipment: if end users face caking or unwanted boroxine, we adjust desiccation and moisture controls immediately. That level of responsibility follows from watching hard-won reactions struggle due to small lapses.

    Specifications with Real-World Impact

    Spec sheets alone never tell the whole story. Over the years, we’ve observed how small deviations in melting point or moisture content impact sensitive reactions. That’s why melting range, HPLC purity, water content, and appearance aren’t just checked, but tracked across every production lot. Typical product appears as an off-white to pale yellow solid, free-flowing and stable under inert atmosphere. We aim for purity levels greater than 98 percent, knowing little improvements can cut downstream purification steps for our customers.

    Particle size matters, too. Incorrect granulometry leads to slow dissolutions or clogging in automated systems. Our team routinely sieves product and samples average particle size throughout shifts, knowing that end users depend on reliable dosing and transfer. Analytical data files are always available, and we encourage open communication so formulation or process engineers reach us directly.

    Comparison with Related Boronic Acids

    Many labs ask how (4-Formyl-1-Naphthalene)Boronic Acid stacks up against simpler phenylboronic acids or alternative naphthalene derivatives. The answer centers on reactivity and selectivity. Simple phenylboronic acids typically lack the electron-withdrawing impact or steric bias from the formyl-naphthalene system. This difference shapes reaction rates and the outcome of complex multi-step syntheses. Substituting a methyl or ethyl for formyl shifts both the electron density and the pathway for transformation.

    Among naphthyl boronic acids, placement of the formyl group and overall substitution pattern shift selectivity, solubility, and even color. Experience in manufacturing these analogues demonstrates that positional isomers need different purification approaches. This can introduce challenges in controlling isomeric purity, a priority whenever the application relates to pharma, agrochemicals, or electronics.

    Usage: Beyond the Standard Playbook

    The biggest innovations rarely follow a template. Over time, our customers have taught us more about surprise applications than any reference book could. Years ago, an OLED group contacted us with specific batch history questions after noticing variability in device performance from another supplier. Their work relied on consistent functionalization of the naphthyl core, and they required not only strict purity, but also documented storage and handling procedures. Their questions led us to implement batch-by-batch barcode scanning through final packaging.

    Pharmaceutical teams frequently use (4-Formyl-1-Naphthalene)Boronic Acid as an intermediate or building block for active compound libraries. Cooperative feedback from multiple pilot plants highlighted a shared challenge: formyl group instability under strongly basic conditions and sensitivity to metal contamination. Working through those observations, we refined washing and extraction routines, ultimately extending shelf life and maintaining high formyl content. Spectral libraries now include spectra showing how to spot partial hydrolysis or oxidation.

    Materials science teams often exploit the rigidity of the naphthalene core and the reactivity of both the boronic acid and formyl group. In areas such as conjugated polymers or specialty dyes, small changes in impurity profile translate into shifts in absorption or fluorescence. Several labs turned to us for further purification, because their optical performance depended on trace-level control—which industrial specs overlook. Drawing from hands-on synthesis and quality assurance, we worked alongside specialists to deliver additional recrystallization or gradient HPLC separation where standard purification failed.

    Supply Chain Realities and Traceability

    As a manufacturer, stability and transparency in the supply chain rank higher than speed. We’ve seen the risks that come with poorly documented sourcing: variable quality, ambiguous origins, and lost batches. That’s why all starting materials reach us through direct, documented supply agreements, and every process adheres to internal controls managed by those with decades of practical chemistry experience. Our facility uses dedicated reactors and glassware for boronic acid production to reduce cross-contamination risks.

    Customers increasingly request Certificate of Analysis details that capture testing methodology. We publish exact test conditions and reference spectra from our own runs—never generic or copied from the literature. Trace element analysis (ICP-OES or AAS) reports boron and trace metals at every run, because process chemists in pharma or electronics often call for tighter specs than standard brochures advertise.

    Continuous Improvement Driven by Practical Experience

    The best improvements come from closing the feedback loop between those who make chemicals and those who put them to work day after day. Years spent running pilot plants and scaling up from grams to kilos taught us that process capability can't just be bolted on at the end—it requires deliberate investment in analytical development, logistics, and hands-on training. Every kilogram of (4-Formyl-1-Naphthalene)Boronic Acid carries the fingerprints of dozens of process trials, iterative improvements, and real lessons learned on the factory floor.

    Adding robust in-process monitoring caught problems before they became failures. Early attempts at larger scale revealed that batch time, temperature control, and quenching order introduced subtle variances in impurities and formyl group longevity. By standardizing each variable, we reduced "mystery" yields and provided more reliable product for customers working on tight timelines.

    The practical realities go beyond the obvious. Bottling and packaging matter as much as upstream synthesis. Packing under inert gas, checking seals, and using controlled humidity rooms means our end users find the product as specified—no chalking, no lumping, and no boroxine-related surprises. Real transparency and reporting, not just glossy data sheets, let customers trust not just the product, but the process behind it.

    Supporting Modern R&D With Reliable Building Blocks

    A reliable stream of high-quality (4-Formyl-1-Naphthalene)Boronic Acid underpins breakthrough projects in small- and large-scale chemistry. Over time, our perspective as manufacturer keeps bringing home that repeatability underlies discovery. Commercial teams, research groups, and manufacturing plants each bring different requirements to the table. Staying close to development and formulation labs—sharing practical lessons on solubility, batch handling, and reaction monitoring—makes us partners, not just suppliers.

    We keep core production steps in-house to tighten variables that matter most—purity, particle size, and contaminant profile. With eyes on emerging markets, increased documentation requirements, and regulatory transparency, we've scaled both our batch and analytic capacity. Every run gets an audit trail with raw data and signed records. That level of oversight comes from long-term investment in people and equipment, not shortcuts.

    Key partnerships with clients led to small changes like improved bottle labeling, immediate shipment notifications, and pre-delivery batch reporting. The hands-on cycle between bench chemist and production manager ensures critical details aren’t lost in translation.

    Challenges of Manufacturing in a Changing Environment

    The chemical landscape keeps evolving, with demands for higher specs, lower environmental impact, and better lifecycle transparency. For a compound like (4-Formyl-1-Naphthalene)Boronic Acid, these shifts shaped our approach to solvent management, waste minimization, and product stewardship.

    Engagement with customers points to new requirements around solvent traces, sustainable packaging, and reduced byproducts. Drawing from decades in process chemistry, we adapted equipment and protocols, switching to greener solvents where possible and recapturing boron waste streams for reprocessing. This pivot came through collaboration with clients concerned about both compliance and long-term impact.

    Maintaining a stable price point through raw material spikes, regulatory headwinds, or logistics hiccups remains a daily test. Our direct sourcing and in-house manufacturing safeguard against many typical disruptions, but we keep a close eye on lead times and shipping vulnerabilities, sharing accurate updates with every client.

    The Real Value of Manufacturing Experience

    Years spent making (4-Formyl-1-Naphthalene)Boronic Acid sharpened our respect for chemistry as both a science and a craft. Small details—choice of drying agent, selection of glassware, real-time analytical checks—tip the scales between routine success and problem-solving on the fly. Among all the lessons, one stands out: investing in fundamental control and open dialogue with customers creates a feedback loop that outlasts any trend.

    By centering production on staff who have worked every synthesis step firsthand, we deliver both reliable product and a knowledge base our customers can draw from as their needs evolve. Every kilo sold comes with the lessons of every batch before it, checked and double-checked in the search for better chemistry.

    Meeting Tomorrow’s Innovation Needs Today

    Every innovation depends on foundational building blocks. For research teams, production sites, and developers crafting the next materials or drug candidates, those underpinnings come from manufacturers committed to continuous learning, documented quality, and direct communication. Our work with (4-Formyl-1-Naphthalene)Boronic Acid demonstrates that commitment, shaped through years of direct manufacturing, analytical rigor, and partnership with the scientists who depend on what we make.

    As performance standards and innovation targets keep rising, staying ahead means investing not just in new tools, but in knowledge—carried forward by those who work both at the bench and in the plant. With this product and every batch that follows, we stand by the belief that ground-level experience, attention to detail, and open exchange create the chemistry that moves industries forward.