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1,4-Diphenylbutadiyne

    • Product Name 1,4-Diphenylbutadiyne
    • Alias Diphenylbutadiyne
    • Einecs 211-299-0
    • 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
    VTB
    Specifications

    HS Code

    267161

    Cas Number 4236-43-1
    Molecular Formula C16H10
    Molecular Weight 202.25 g/mol
    Appearance Pale yellow solid
    Melting Point 112-114°C
    Density 1.09 g/cm³
    Purity Typically ≥98%
    Solubility In Water Insoluble
    Solubility In Organic Solvents Soluble in chloroform, benzene, and ether
    Flash Point >110°C
    Storage Conditions Store in a cool, dry place, tightly closed
    Structural Formula Ph–C≡C–C≡C–Ph
    Smiles C1=CC=C(C=C1)C#CC#CC2=CC=CC=C2

    As an accredited 1,4-Diphenylbutadiyne factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 5-gram amber glass bottle, sealed with a screw cap, labeled "1,4-Diphenylbutadiyne," includes safety and handling information.
    Shipping 1,4-Diphenylbutadiyne should be shipped in tightly sealed containers, protected from moisture and incompatible substances. Transport conditions must prevent exposure to heat, sparks, or open flames, as the compound is flammable. Compliance with relevant local and international regulations for hazardous materials ensures safe handling during transit. Proper labeling and documentation are required.
    Storage 1,4-Diphenylbutadiyne should be stored in a cool, dry, and well-ventilated area, away from heat, open flames, and sources of ignition. Keep the container tightly closed and out of direct sunlight. Store separately from oxidizing agents and strong acids. Ensure proper labeling and secure storage to prevent accidental exposure or mixing with incompatible substances.
    Application of 1,4-Diphenylbutadiyne

    Applications of 1,4-Diphenylbutadiyne in Industrial Manufacturing

    As a direct manufacturer of 1,4-Diphenylbutadiyne, we focus on supporting advanced industrial sectors where this performance intermediate drives specific value in polymer synthesis, organic electronics, and specialty chemical processes. The following sections outline prominent commercial application scenarios grounded in market-proven practice, each with distinct regulatory, formulation, and production integration requirements.

    1. Organic Light-Emitting Diode (OLED) Materials Production

    OLED and organic electronic device manufacturers employ 1,4-Diphenylbutadiyne for its structure-directing function in the synthesis of tailored conjugated polymers and low-molecular-weight emitters. Its unique triple-bond conjugation enables the formation of π-conjugated systems essential for charge transport and emission purity in high-specification displays and lighting modules. Precise dosing in batch polymerization directly affects luminance, device longevity, and spectral characteristics.

    Industry compliance standards

    • IEC 62341 (OLED display device performance)
    • RoHS Directive (2011/65/EU, hazardous substance restriction)
    • REACH Regulation (EC) No 1907/2006, registration and SVHC content limits
    • Customer QMS: ISO 9001 or IATF 16949 for electronics supply chain traceability

    Typical usage ratio

    • Monomer feed ratios: 0.5–5 mol% in copolymer backbones; adjusted for molecular weight control and desired bandgap.

    Downstream process integration

    • Introduced in monomer stage of Suzuki, Sonogashira, or direct arylation polymerizations; solvent and temperature profiles tailored for defect minimization.

    Final product types

    • OLED display active layers (smartphones, automotive clusters, monitors)
    • Organic transistor and light-emitting diode components (lighting panels, signage)

    2. Specialty Cross-Linker for High-Performance Polymers

    In advanced polymer production, compounders incorporate this diyne to achieve controlled cross-linking within aromatic and conjugated polymer networks. Its rigid backbone and terminal alkyne groups confer elevated thermal stability and mechanical strength, especially in high-temperature thermoset resins and electronic encapsulation matrices. Manufacturing settings demand scrutiny of cross-link density and monomer reactivity to ensure product reliability and performance specification adherence.

    Industry compliance standards

    • UL 94 (Flammability of plastic materials)
    • IPC-4101 (Base materials for rigid and multilayer printed boards)
    • ISO 14001 (Environmental management systems for chemical production)

    Typical usage ratio

    • Cross-linking agent: 0.2–2.0 weight % depending on resin chemistry, flow control, and final glass transition temperature target.

    Downstream process integration

    • Blended into resin formulations prior to curing or extrusion; dosing optimized through batch rheology and QC assays for reproducibility in cross-link density.

    Final product types

    • Electronic encapsulants for semiconductors and sensors
    • High-heat-resistant thermoset films and prepregs for aerospace and PCB substrates

    3. Synthesis Intermediate in Liquid Crystal Alignment Materials

    Producers of specialty alignment layers for TFT-LCD panels and next-generation displays utilize this molecule as a direct precursor in crafting rigid, rod-like compounds conferring improved liquid crystal orientation and surface uniformity. The controlled introduction of the diyne group proves fundamental for photoalignment and high-resolution display technologies, contributing to pixel response time and viewing angle characteristics.

    Industry compliance standards

    • IEC 61747 (LCD performance requirements)
    • ISO 178 (Plastics—determination of flexural properties, for film substrates)
    • Customer-specific Green procurement standards (Sony Green Partner, Samsung Eco-Partner)

    Typical usage ratio

    • Intermediate feedstock: typically 1–3 mol% in alignment agent prepolymer synthesis, adjusted per molecular design and desired optical parameters.

    Downstream process integration

    • Undergoes step-growth or addition reactions; functionalization with photoreactive side chains occurs prior to thin film deposition or coating.

    Final product types

    • Liquid crystal display alignment coatings
    • Photoalignment materials for optical films

    4. Building Block in Conjugated Molecular Sensors

    Researchers and commercial producers of chemical and biological sensors integrate this butadiyne as a skeleton-forming unit for conjugated receptor synthesis. Its electron-transport facilitators and capacity for functionalization enable customized recognition motifs in detection layers, aiming for high selectivity and rapid signal propagation in analyte-responsive field-effect transistors or colorimetric devices.

    Industry compliance standards

    • ISO 13485 (Medical device quality management, for biosensor components)
    • EMC Directive 2014/30/EU (Electromagnetic compatibility in sensor electronics)
    • Relevant FDA guidance where sensors target clinical diagnostics

    Typical usage ratio

    • Precursor component: 1–10 mol% in synthetic sequences, tuned to optimize performance for target analyte and device architecture.

    Downstream process integration

    • Incorporated in organic synthesis phases—often under palladium-catalyzed couplings—followed by functional group introduction and polymerization for sensing layer fabrication.

    Final product types

    • Electrochemical biosensors for glucose, ions, or pathogens
    • Field-effect transistor (FET) sensor chips
    • Chemical vapor sensors for environmental monitoring

    5. Template Molecule in Advanced Carbon-Rich Nanomaterials

    Manufacturers focused on carbonaceous nanostructure production—such as graphdiyne films and nanoribbons—utilize this compound as a molecular template, leveraging its linear triple-bond system to direct controlled polymerization and allow scalable synthesis of highly ordered carbon networks. These nanomaterials enable next-generation applications requiring high electron mobility, tunable bandgaps, and exceptional mechanical endurance.

    Industry compliance standards

    • ISO/TR 13014 (Nanotechnologies – Material characterization and physicochemical properties)
    • OECD Guidelines for the Testing of Chemicals, Section 4 (nanomaterial safety)
    • In-house QC based on ASTM E56 nanomaterial best practices

    Typical usage ratio

    • Monomer utilization: 5–20 mol% in graphdiyne or poly-diyne synthesis, adjusted by intended surface area and electrical property targets.

    Downstream process integration

    • Employed at the solution-phase or interfacial polymerization stage; subsequent processing includes vacuum annealing and film transfer or direct deposition onto device substrates.

    Final product types

    • Conductive graphdiyne films for flexible electronics
    • Carbon-rich composite electrodes for supercapacitors and batteries
    • Nanoribbons or porous membranes for gas separation units
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    Certification & Compliance
    More Introduction

    Introducing 1,4-Diphenylbutadiyne: Experience Rooted in Chemical Manufacturing

    Real-World Expertise in Butadiyne Synthesis

    Every batch of 1,4-Diphenylbutadiyne produced at our facility draws on decades of hands-on synthesis and purification practice. This compound is more than a molecular formula—our experience with it started on benches lined with glassware, hour after hour of column chromatography, controlling impurities at each step. We do not ship material based solely on a spec sheet. Each drum or jar represents an ongoing process of learning and adjustment. Growing demand for specialty intermediates in organic electronics and functional materials pushed us to refine our production, scale up from pilot to manufacturing, and adapt quality control tools to suit the final users’ application goals.

    The Chemistry Behind 1,4-Diphenylbutadiyne

    This is not a bulk commodity. 1,4-Diphenylbutadiyne features a conjugated diyne bridge linking two phenyl groups. That unique backbone makes it a different animal compared to simply-structured butadiynes like 1,4-butadiyne or its terminal-alkyne cousins. The compound’s extended π-system gives it electronic properties sought after in organic materials: researchers and industrial teams rely on that structure whether aiming for conductive polymers, optoelectronic layers, or nanoassemblies. At the gram or kilogram scale, purification requires more effort and monitoring compared to low-molecular-weight alkynes. We work closely with our lab and process teams to keep polycondensation by-products out of the finished product, ensuring consistency and high assay every time.

    Understanding Model and Specifications: Beyond the Numbers

    For us, “model” means the way we approach every order. Most customers request the solid form, most often a crystalline powder. Typical shipments range from a few grams for an academic or pilot-study run, up to kilogram lots for downstream manufacturing. Standard purity targets at least 98% GC, with detailed certificates of analysis provided on each lot—something we learned was critical after listening to researchers struggle with off-grade resins from generic traders. In our experience, the last percentage point in purity often affects polymer performance outcomes, especially in sensitive light-emitting or charge-transport functions.

    Melting points and spectral data—proton NMR, carbon-13 NMR, and IR—are all matched routinely with published literature values and controlled with batch retention samples. Sometimes clients running advanced spectroscopy request extra analytics: we’ve met those requests by incorporating mass spectrometry, element analysis, and polymerization tests into our reporting. Because we synthesize in-house, there is no uncertainty about the identity, and every analytical data package is matched with a retained sample for retesting or third-party validation if needed.

    1,4-Diphenylbutadiyne in Application: Reliability Underpinning Innovation

    Chemistry’s practical work takes place far from the catalog page. We see 1,4-Diphenylbutadiyne deployed by teams building photonic devices, sensors, and targeted molecular systems. Its structure supports the assembly of linear chains and crosslinkable frameworks. From coating thin films to forming host-guest inclusion complexes, clients rely on physical consistency: batch-to-batch reproducibility, real bulk density data, and absence of contaminants that could derail a week’s worth of lab work. Over the years, we’ve fielded and solved problems few sales agents would ever hear about—like a trace contaminant from an off-spec catalyst leading to colored by-products, or unexpected polymerization stalling thin-film growth in OLEDs. Those lessons feed back into our practice. Shipping a kilogram is not enough if a single chromatographic repeat shows a spike out of place; resolving those process hiccups builds trust and reliability.

    Different from Other Products, Chemically and Practically

    At first glance, diphenylated butadiynes might seem interchangeable. Yet experience tells a different story. 1,4-Diphenylbutadiyne differs from similar diynes—such as 1,4-bis(trimethylsilyl)butadiyne, 1,4-diphenylbutadiene, or basic aromatic acetylenes—by combining rigidity and conjugation with a stability profile friendlier to storage under inert gas. Some alternatives offer easier solubility or lower cost, but do not share the same backbone or polymerization properties. Certain users have tried switching to less expensive analogs, expecting comparable results in their devices, only to run into miscibility troubles, poor yield in target polymer chains, or irreversible decomposition during melt processing. The phenyl ends of this compound offer steric and electronic buffering, easing problems tied to instability of raw diynes. In practical terms, that often means fewer purification steps for end users and higher usable yields during downstream functionalization.

    The most notable difference lies in real-life polymerization and coupling performance. Colleagues in the OLED and field-effect transistor segments have returned to 1,4-Diphenylbutadiyne after rounds of unsuccessful trials on similar structures, finding that minor shifts in backbone rigidity or substituent bulk change polymer morphologies and device function. Those outcomes cannot be predicted on paper or from simulation alone. Knowledge from chemical processing, coupled with long-term feedback from device fabricators, drives us to maintain strict process discipline at every cycle.

    Production Practice: What Only a Manufacturer Sees

    Sources of off-grade product rarely show up in the literature. Early on, controlling the Glaser coupling reaction posed challenges in solvent choice, copper source, and oxygen introduction. Too much oxygen, and overcoupling causes tri- and tetraphenyl contaminants; too little, and incomplete conversion leaves reactive residues. Technical teams tuning reaction time and catalyst ratio make the difference. Once the correct parameters were set, scale-up revealed new sticking points: crystallization from solvent required tight temperature control to avoid microinclusions, and filtering of copper residues had to be tuned batch by batch. Over years, documenting trends in spectral impurities gave us the experience to spot—and address—process drifts before they resulted in off-spec lots. No distributor tells you about the deep blue color shift signaling a trace contaminant or the surface tackiness that signals partially hydrated batches. Only sleeves-rolled-up work teaches these points.

    Recycling process solvents and managing copper-containing waste made us early adopters of closed-loop environmental practice. As discharge regulation changed, our in-house separation, neutralization, and recycling units reduced environmental impact without trading away product quality. Experience told us that complexation of copper with reaction by-products would leak into the product if not addressed, especially as we scaled reaction volumes. Adjusting waste recovery in tandem with synthesis proved critical for cost, regulatory compliance, and occupational health. That history deepens our respect for the molecule, not just as a commodity but as a challenge and opportunity.

    Real-World Logistics: Shipment, Storage, and Support

    Clients often underestimate the logistics needed for special compounds. Years shipping 1,4-Diphenylbutadiyne taught our team to use airtight, inert-packed jars or drums, depending on lot size. Routine packing under nitrogen reduces risk of slow oxidation or contamination. Our warehouse team learned to check for surface discoloration or clumping that may indicate moisture ingress—practical steps born from batches at risk. Storage at ambient temperature typically suffices, yet long-term projects request cold storage for archival purity; we support both, and provide split-batch storage for compound longevity studies.

    The needs of university research groups are not identical to those at pilot plants or R&D labs of major electronics firms. We work with labs seeking only 5 or 10 grams as well as those needing multi-kilogram monthly commitments, and our production and packaging lines adjust accordingly. Questions on bulk density, dissipation during handling, and analytical standards come directly to our chemists. Direct manufacturer contact means detailed, practical answers, not catalog cut-and-paste.

    Practical Issues and Solutions Around Synthesis and Quality

    Process stability remains a constant challenge. Even minor variations in catalyst or solvent lots have sometimes introduced fractionally higher levels of persistent impurities, such as oxidized phenyl by-products or residual copper salts. These may not show up in quick tests but become visible during more sensitive polymerization runs or downstream device fabrication. We faced this problem two years ago during a spike in global demand for acetylenic intermediates, needing to switch to secondary solvent grades. Whole runs had to be recleaned and retested, resulting in extra work and some delivery delays.

    The solution did not come from adjusting paperwork but from returning to the chem lab: running fresh trials, tweaking the work-up, ramping up preparative HPLC to remove stubborn impurities, and working in parallel with customers who flagged the issue. Detailed batch tracking became the new normal—each drum tracked by unique lot and sub-batch code, all analyzable down to raw material source and synthesis date. This hands-on approach, from process adjustment to seamless sharing of test results, increases transparency for all users and feeds into continuous improvement.

    Why Experience Matters: Supporting Researchers and Developers

    Having produced and shipped 1,4-Diphenylbutadiyne across industries and continents, we have seen firsthand the shifts in research focus, from laboratory photophysical studies to robust, scaled-up manufacturing for sensors or flexible electronics. Teams working on organic light-emitting diodes or field-effect transistors highlight the need for consistent, well-characterized product. Some aim for semiconductor-grade performance; others target fundamental studies of conjugated π-systems. For both, batch purity, trace impurity avoidance, and clear communications matter more than lowest bidding or fastest shipment.

    We find that open technical discussions with users—especially those scaling up for device trial—prevent misunderstandings and failures before they begin. Many academic teams were first exposed to 1,4-Diphenylbutadiyne through our compound kits sent out in collaboration projects; over time, several developed new demonstration devices or high-impact publications citing material sourced directly through us. Commercial clients moving from bench to pilot scale depend on that continuity, requesting technical guidance on solution preparation, cross-linking, or co-polymerization options matched by reliable raw supply.

    Feedback Loop: Learning from Customers and Our Own Teams

    Direct relationships with device engineers, junior chemists, and R&D teams drive improvement in our product offering and service. We regularly integrate feedback—whether it comes as requests for new packaging formats, tighter analytical standards, or faster reporting of certificates of quality. Introducing small-batch packaging and responding to consistent feedback on transport safety brought about more robust tracking and online document delivery systems. These steps arose not from policy directives, but from repeated conversations and accumulated trust.

    Our technical support team, drawn from experienced chemists, engineers, and logistics specialists, knows how to answer specifics—how to dissolve the compound in low-boiling solvents, how to recover stray crystals from packaging, how to handle residual copper trace. Organizational experience has taught us that high-specification work is never complete. Cross-functional review of client return claims and field failures—a step some companies skip—uncovers lessons for future batches. Mistakes, solved honestly and directly, translate into a stronger overall offering.

    Ongoing Challenges and Industry Landscape

    Supply pressures in the fine and specialty chemical market continue to affect raw materials, especially in the wake of global logistics shifts and ongoing environmental scrutiny of copper-mediated processes. Navigating these changes requires steady supplier relationships and technical flexibility: qualifying multiple vendors for solvents, assessing the intermediate quality, and staying alert for small but significant changes in impurity profiles as environmental or safety regulations shift. Our track record adapting to these cycles strengthens trust among long-time partners.

    1,4-Diphenylbutadiyne’s price and availability never stand still. As demand fluctuates—especially from fast-growing areas such as next-generation flexible electronics or photonic sensors—capacity planning and inventory management need updating, not just in response to numbers, but in anticipation of technical trends. Our response incorporates both chemical manufacturing realities and deep engagement with end users. Because we manufacture, we know the pinch points of seasonal supply shortages, the headaches of last-minute order spikes, and the uncertain territory of new application development. Rather than react, we prepare, controlling not only the finished product, but also the risks and opportunities of its application downstream.

    Conclusion: Putting Experience to Work

    From laboratory synthesis to full-scale production, every step in our handling of 1,4-Diphenylbutadiyne draws on real experience: testing, listening, adapting, and refining the product and the way it reaches users. Our chemists, engineers, and technical support staff do not hide behind technical jargon. Instead, they put knowledge to practical use, addressing the daily realities of specialty chemical manufacture and supply. This compound’s future holds promise as both a building block and a technology enabler; and we remain committed to supporting every project, every development, and every technical hurdle with honest, informed effort.