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1,3-Diethynylbenzene

    • Product Name 1,3-Diethynylbenzene
    • Alias meta-diethynylbenzene
    • Einecs 207-024-1
    • 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
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    Specifications

    HS Code

    972428

    Cas Number 535-75-1
    Molecular Formula C10H6
    Molar Mass 126.16 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 223 °C
    Melting Point −25 °C
    Density 0.979 g/cm³
    Refractive Index 1.601
    Solubility In Water Insoluble
    Flash Point 82 °C
    Chemical Structure 1,3-disubstituted benzene with ethynyl groups
    Smiles C#CC1=CC=CC(=C1)C#C
    Inchi InChI=1S/C10H6/c1-3-9-5-4-6-10(7-9)2-8-9/h1-2,4-7H
    Pubchem Cid 12775
    Synonyms m-Diethynylbenzene, 1,3-Benzenediyldiethyne

    As an accredited 1,3-Diethynylbenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 1,3-Diethynylbenzene; tightly sealed, labeled with hazard symbols and product details.
    Shipping **Shipping Description for 1,3-Diethynylbenzene:** 1,3-Diethynylbenzene should be shipped in tightly sealed containers, protected from light, heat, and moisture. It is a flammable solid and must be transported in accordance with relevant hazardous materials regulations, accompanied by proper labeling and documentation. Handle with care to prevent leaks, spills, or exposure during transit.
    Storage 1,3-Diethynylbenzene should be stored in a tightly sealed container, under an inert atmosphere such as nitrogen or argon, and kept in a cool, dry, and well-ventilated area away from sources of ignition. Protect from moisture, strong oxidizers, and acids. Store away from direct sunlight and heat sources to prevent degradation or hazardous reactions.
    Application of 1,3-Diethynylbenzene

    Applications of 1,3-Diethynylbenzene in Industrial Manufacturing

    As a specialized manufacturer of 1,3-Diethynylbenzene, we supply this advanced aromatic monomer to global industries where its unique triple-bonded structure is indispensable for high-performance polymers, electronics materials, specialty resins, and aerospace-grade composites. Below, we outline principal downstream industrial applications based on direct field practice, formulation feedback, and compliance with sectorial technical requirements.

    1. Polyimide Resin Production for Electronic Films

    Producers of flexible and high-temperature-resistant electronic films incorporate 1,3-Diethynylbenzene as a reactive monomer in the polycondensation process. Its functional ethynyl groups enable superior crosslinking, producing polyimide films that retain dielectric stability and dimensional integrity under prolonged thermal and electrical stress, critical for substrate layers in flexible printed circuits, smartphones, and high-performance display panels.

    Industry compliance standards

    • IEC 61249-2-21 (Flame retardant, halogen-free electronic materials)
    • RoHS Directive 2011/65/EU & Amendments (Restriction of hazardous substances)
    • UL 94 VTM-0 (Flammability safety for flexible materials)
    • JIS C5013:2021 (Japanese industrial standard for polyimide films)

    Typical usage ratio

    • 1.0–8.0 wt%, adjusted based on desired crosslink density and end use heat resistance; standard levels for substrate films range 2.5–5.5 wt% by dry resin mass.

    Downstream process integration

    • Incorporated during monomer blending prior to polycondensation; solution-cast with solvent into continuous films; secondary thermal crosslinking step above 300°C finalizes film property enhancement.

    Final product types

    • Flexible polyimide films for PCB base material
    • Electronic insulation tapes (e.g., polyimide adhesive tape)
    • Display and sensor cover layers
    • Flexible flat cable substrates (FFC/FPC)

    2. High-Performance Thermosetting Resin Formulations for Aerospace Composites

    Composite manufacturers rely on the high thermal stability and rigidity conferred by 1,3-Diethynylbenzene when synthesizing specialty thermosetting matrix resins, such as polybenzoxazine and polycyanurate types. By participating in multi-functional network formation during curing, this monomer significantly boosts the glass transition temperature and maintains mechanical properties at elevated service temperatures, directly supporting the fabrication of advanced structural components for aircraft and spacecraft.

    Industry compliance standards

    • SAE AMS 3726 (High-temperature composite matrix systems)
    • AS 9100 (Aerospace QMS requirements)
    • NADCAP AC7122 (Composites fabrication accreditation)
    • FAA 14 CFR Part 25, Appendix F (Flame, smoke, toxicity tests for aircraft interiors)

    Typical usage ratio

    • 2.0–7.0 mol% in monomer blends for polybenzoxazine and polycyanurate thermosets, typically tuned to 3.5–6.0 mol% for aerospace-grade prepreg manufacture to meet qualification criteria.

    Downstream process integration

    • Blended with main resin precursors in a high-shear reactor; pre-impregnation of carbon or glass fibers performed before B-stage curing; full crosslinking achieved during autoclave or oven post-curing at 250–350°C.

    Final product types

    • Primary and secondary aircraft structural panels
    • Spacecraft equipment housings
    • Heat shields and fairings
    • Radome covers

    3. Specialty Crosslinker for Advanced Ceramic Matrix Composites (CMC)

    Ceramic parts processors employ 1,3-Diethynylbenzene as a heat-activated crosslinker in the precursor impregnation route for CMCs, especially silicon carbide and carbon fiber-based systems. It enables in-situ polymerization and carbonization, forming dense, thermally stable interphases that improve flexural strength and microcrack resistance, necessary for next-generation gas turbine and industrial furnace components.

    Industry compliance standards

    • ASTM C1341 (Standard test for flexural properties of CMCs)
    • ISO 14662:2020 (Composites—Prepreg acceptance criteria)
    • GE Aircraft Engine Specification E50TF218 (CMC materials)
    • NADCAP for nonmetallic materials processing

    Typical usage ratio

    • 0.8–2.2 wt% in the preceramic polymer feed, adjusted for fiber architecture and desired porosity after pyrolysis.

    Downstream process integration

    • Added to preceramic polymer solution before vacuum infiltration of fiber preforms; post-impregnation, shaped parts undergo controlled pyrolysis at 800–1100°C to convert organic phase into ceramic bonding matrix.

    Final product types

    • Turbine engine stator shrouds
    • Industrial hot zone supporting structures
    • Thermal barrier liners
    • Combustion chamber liners

    4. Molecular Precursor for Electronic-Grade Carbon Materials

    The electronic materials sector utilizes 1,3-Diethynylbenzene as a precursor for forming highly graphitic, structurally controlled carbon intermediates, which are applied in the manufacture of supercapacitor electrodes, specialized battery anode additives, and micro-patterned conductive films. Its ethynyl groups polymerize into rigid networks that, upon high-temperature treatment, yield carbon materials with superior purity and tailored microstructure, ensuring electrical conductivity and consistency needed for advanced storage devices.

    Industry compliance standards

    • IEC 62391-1 (Fixed electric double-layer capacitors)
    • GB/T 31484 (Cycle life requirements for lithium ion battery cells)
    • ISO 9001:2015 (Manufacturing quality management)
    • JEITA RC-1001 (Electronic carbon materials standard)

    Typical usage ratio

    • 5.0–15.0 wt% as carbon precursor, precise ratio customized against target specific area and graphene sheet yield; typical levels for supercapacitor electrodes cluster around 7.5–10.0 wt%.

    Downstream process integration

    • Polymerized in situ or via solution casting onto current collector foils; thermally treated under inert atmosphere at 1,000–2,700°C to achieve desired carbonization and graphitization.

    Final product types

    • Supercapacitor activated carbon electrodes
    • High-rate lithium-ion battery anodes
    • Printed carbon conductive traces for microelectronics
    • 3D microstructured carbon scaffolds

    5. Modifier in Heat-Resistant Adhesive Formulations

    Adhesive compounders add 1,3-Diethynylbenzene to modify the curing kinetics and thermal stability of high-temperature, solvent-resistant adhesives primarily used in electronics assembly and industrial bonding. Its aromatic and ethynyl functionality establishes a denser, thermally enduring network upon curing, enabling adhesives to maintain shear and peel strength under continuous exposure to elevated temperatures in demanding applications.

    Industry compliance standards

    • ASTM D1002 (Shear strength of adhesives)
    • UL 746C (Polymeric adhesives for electrical equipment)
    • EU REACH (Registration, Evaluation, Authorization and Restriction of Chemicals)
    • JIS K6804 (Adhesive performance requirements for electronics)

    Typical usage ratio

    • 0.5–3.0 wt% in total adhesive formulation; adjusted up to 3.5 wt% for flame-retardant grades or bonding applications requiring 200°C+ service temperatures.

    Downstream process integration

    • Dispersed within resin or prepolymer blend during initial mixing; full incorporation by vacuum mixing before addition of hardeners; standard thermal or UV-activated curing at 120–180°C depending on resin type.

    Final product types

    • SMD (surface-mount device) assembly adhesives
    • Heat and chemical-resistant structural adhesives
    • Sensor bonding compounds
    • Automotive underhood component adhesives
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    Certification & Compliance
    More Introduction

    Getting to Know 1,3-Diethynylbenzene: A Manufacturer’s Experience

    The Role of 1,3-Diethynylbenzene in Innovation

    Working many years with specialty aromatic compounds, you start to notice which molecules spark significant changes in advanced materials. Among them, 1,3-Diethynylbenzene (also known as m-diethynylbenzene) often gets overlooked, yet it consistently shapes the possibilities in everything from adhesives to high-performance polymers. With two ethynyl groups attached to a benzene ring, its molecular structure delivers more than laboratory intrigue; it forges new chemistry in real-world manufacturing that smaller, less capable molecules can’t handle.

    Almost daily, technical teams bring up this aromatic compound when clients ask to push the limits of thermal or chemical resistance. The molecule's backbone—the benzene ring—paired with the linear ethynyl functionalities, allows controlled reactivity and backbone rigidity. This duality equips manufacturers with a building block that doesn't just fill a need, it challenges the status quo in specialty polymers and electronic components.

    Our Model of 1,3-Diethynylbenzene: An Inside Look

    On our production line, each batch follows tightly controlled parameters. We manufacture our 1,3-Diethynylbenzene under anhydrous conditions, using premium feedstock intermediates. We’ve found this disciplined approach reduces ash and limits unwanted side products—which means customers don’t waste time troubleshooting their own syntheses. Each batch consistently passes purity targets above 98%, which gives researchers and process engineers a head start with less post-purification.

    Our team relies on gas chromatography and NMR analysis to verify product identity and purity. Material leaves our facility as off-white to light yellow crystalline solid, with melting point data included on lot sheets. Standard packaging ranges from grams for R&D to kilogram lots for pilot or commercial projects. Special requests come up frequently (hermetic sealing, custom pack sizes) and we accommodate when manufacturing schedules allow, because we know the headaches contamination or degradation can cause in downstream chemistry.

    What Makes 1,3-Diethynylbenzene Stand Out

    Some might glance through a catalog and group diethynylbenzenes together. In practice, the placement of those ethynyl groups changes everything. Placing both ethynyl groups at the 1,3-positions (meta arrangement) turns the molecule into a unique crosslinker—one that unlocks high glass transition temperatures (Tg) in thermosetting resins. By contrast, its para or ortho isomers (1,4- or 1,2-) set off different polymerization kinetics and lead to networks with alternative mechanical profiles.

    Working directly at the reactor, we sometimes run controlled studies comparing m-diethynylbenzene against its isomers. Consistently, the meta-isomer achieves a balance between processability and final polymer durability. Chemists that depend on subtle structure–property relationships, such as those in aerospace materials R&D and microelectronics, often specify the 1,3-isomer after screening alternatives.

    From Reactor to Marketplace: The Manufacturing Reality

    Those outside of manufacturing may not see the effort poured into preparing each shipment of 1,3-Diethynylbenzene. Sourcing reliable raw materials, carefully handling acetylenic intermediates, and maintaining inert atmospheres—it’s all crucial. Over years of running these reactions, we’ve identified risks at each step. Ethynyl functional groups demand low moisture and oxygen, as traces of either can lead to side reactions, lower yield, and diminished performance in final applications.

    For each lot, we document the entire workflow and log analytical data at each stage. We’ve learned that clients appreciate transparency, especially when their own performance hinges on tight batch-to-batch reproducibility. Failing to control minute impurities leads to downstream headaches for customers, particularly in electronic device assembly or specialty monomer synthesis. We have seen firsthand that even minor impurities—trace amounts of unwanted halides or oxidized byproducts—can deactivate polymerization catalysts or cause coloration in clear products.

    Instead of passively accepting marginal quality, our operations focus on risk prevention. We work with reactor coatings that resist corrosion from acetylenic compounds and invest in bulk handling that prevents static-induced sparks—small details, but critical for safety and long-term supply commitments.

    Uses and Benefits Beyond the Obvious

    On the production floor, the versatility of 1,3-Diethynylbenzene means more than just laboratory experiments. Our regular clients span industries as diverse as advanced composites, functional adhesives, optoelectronics, and specialty filtration membranes. One recurring theme: wherever engineers need high-performance thermoset polymers with excellent dimensional stability and resistance to heat, this molecule appears in their formulations.

    Polymer chemists use its reactive ethynyl ends for cyclotrimerization or click-chemistry routes. Heat or metallic catalysts trigger polymerization, leading to a rigid, aromatic network. These materials deliver mechanical strength and heat resistance well beyond traditional epoxies or phenolic resins. In aerospace prepregs, for instance, a crosslinked matrix built partly from our 1,3-Diethynylbenzene maintains shape and mechanical integrity at temperatures that cause older materials to soften or fail.

    Microelectronics is another field where the compound outperforms other crosslinkers. Thin films and coatings built from this aromatic skeleton resist solvents, radiation, and thermal cycling, supporting decades-long operation of electrical components. Battery manufacturers and membrane scientists also value the molecule’s contribution to chemical inertness.

    Learning from Real-World Projects

    Sitting down with polymer engineers who use our 1,3-Diethynylbenzene often gives insight you won’t find in academic journals. One team, developing a new generation of circuit boards, shared that minor tweaks to the ethynyl content affected the reliability of their solder masks. Others in the aerospace sector have demonstrated that a higher loading of the compound translates to longer component lifespan during repeated thermal stress cycles.

    Feedback cycles shape our own continuous improvement. Once, a batch intended for a European composites manufacturer displayed slight off-color and didn’t achieve the expected gel time. Instead of dismissing it, we ran additional GC-MS analyses and traced the cause to a reagent vendor who shifted solvent grades just before shipment. This discovery led us to tighten starting material checks and expand our analytical panel. Each of these small refinements—driven by conversations with R&D teams—pushes us closer to reliable, reproducible chemistry.

    Differentiating from Other Aromatics and Ethynyl Compounds

    Direct comparison with other aromatic crosslinkers like phthalic anhydride, bisphenol A, or common acetylene-terminated resins, makes clear the unique role of 1,3-Diethynylbenzene. Many popular alternatives offer only one reactive site per ring, or attach groups that interfere with crosslink density. The two ethynyl groups in the 1,3-positions establish a balanced reactivity: robust crosslinking without excessive brittleness, and manageable cure schedules for industrial processing.

    For example, many phenylethynyl-terminated oligomers need higher energy input or leave behind more volatile byproducts. By contrast, 1,3-Diethynylbenzene promotes cleaner reaction mechanisms, producing networks with fewer residual molecules. This difference shows up in downstream testing, where cured polymers exhibit lower extractables, higher modulus at elevated temperatures, and reduced shrinkage during cure.

    End-use partners value these distinctions. In manufacturing electronic substrates exposed to thousands of thermal cycles, superior retention of electrical and mechanical properties links directly to the molecular backbone we supply. Similarly, in specialty adhesives for optics, a clean polymer network, free from mobile side products, means minimized risk of fogging or yellowing during aging.

    Practical Realities: Shelf Life, Storage, Handling

    Handling 1,3-Diethynylbenzene in bulk can trip up even seasoned chemists if they forget the compound’s sensitivity to air and light. Ethynyl-containing aromatics benefit from being stored under inert gas, in dark, sealed containers, away from direct sunlight or high temperatures. Our team watches moisture ingress because even small water traces can degrade reactive sites, and with the acetylenic functionalities, the material will sometimes form tars or insoluble residues if mishandled.

    Over time, we’ve adopted a kit for long-term storage: vacuum-sealed glass bottles packed with calcium chloride, all tagged with production date and recommended use-by window. We’ve seen product performance drop when users keep material open to lab air, so practical handling guidelines accompany each shipment. These safeguards come not from theory but from many batches observed over years.

    What Reliability Means for Our Clients

    For many customers, nothing replaces experience with a consistent production partner. If they’re developing a new high-temperature thermoset or assembling precision sensors for harsh environments, they often stake project milestones on the regularity of each shipment received. Any variability in 1,3-Diethynylbenzene purity, particle size, or reactivity can ripple through to end-use inspection failures or product recalls.

    We keep logs on every lot, from supplier invoices through packing and shipping. Analytical records go back years, and we share major certificate-of-analysis data for every shipment. This builds confidence and helps customers plan process changes, regulatory submissions, or performance upgrades. Over many joint developments, we’ve seen robust communication prevent mistakes, reduce process lockups, and even save on regulatory re-verification.

    Solving Problems at Scale

    From a technical perspective, scale-up brings its own set of challenges. Producing 10 grams in a flask differs from preparing multi-kilogram lots in dedicated reactors. Reactor fouling, heat management during the final cyclization step, and maintaining product crystallinity all demand close monitoring. We built redundancy into our production chain, including backup solvent purification, oxygen scrubbers for nitrogen supply, and alternate crystallization tanks.

    Our technical staff runs split-batch trials at pilot scale before launching full commercial lots. We cross-check melt points, particle morphology, and analytical signatures between scales. If a pilot lot displays unusual behavior, we stop, troubleshoot, and resolve before committing to large-scale runs. This avoids supply interruptions, and it lowers risk for both us and our partners.

    By sharing process notes and data with customer engineers, we’ve helped teams transition from benchtop formulation to pilot to true production. Successful application isn’t only about shipping material; it touches every aspect of chemical control, logistics precision, and personal follow-up.

    Environmental and Regulatory Insights

    Sourcing and manufacturing specialty aromatics attracts close attention to regulatory standards and environmental responsibility. Our operations follow strict waste minimization protocols, and we work regularly with waste processors for solvent recycling and neutralization of acetylenic byproducts.

    Compliance teams regularly request documentation on synthetic pathways, impurity profiles, and safe-disposal methods. Our internal records detail the absence of heavy metals, polychlorinated biphenyls, and known restricted substances. Analytical methods verify that residual solvents remain below recognized thresholds, which helps customers build safer, more robust supply chains and meet evolving regulatory frameworks worldwide.

    Environmental impact remains a driver for research. By-product treatment and safe shipping procedures for acetylenic aromatics involve protocols tested by experience. We choose low-toxicity solvents and invest in closed-loop transfer systems. In process audits, visitors often comment on our proactive approaches—like real-time monitoring for minute process leaks, or secondary containment for every drum that leaves the plant.

    Why Direct Manufacturing Matters

    Having hands-on control over each part of the process—from raw material selection, through synthesis and finishing, to final drum filling—gives us control over purity, consistency, and on-time delivery. Any deviations show up quickly, and years of cumulative technical know-how guide corrective action in the plant rather than waiting for problems to emerge downstream. Chemical manufacturing, at its core, rewards those who build expertise batch by batch, year by year.

    We have watched industry demands shift, with customers revising formulations to reduce legacy additives, lower processing temperatures, and simplify downstream purification. Direct feedback shapes ongoing product evolution, whether for new grades with finer particle size, dust suppression, or alternative packaging. Real-world success, measured by consistent final performance, always traces back to the stability and reliability of the starting materials—the foundation we aim to deliver every day.

    Addressing Challenges and Looking Ahead

    Each day brings new requirements. Unexpected spikes in demand can push operational planning. Changing regulatory frameworks call for quicker updates in documentation and process transparency. But at the foundation, adaptation comes from production floor experience—those lessons learned guiding tomorrow’s batches.

    Collaborative problem-solving makes us better. Whether it's reducing impurity footprints through vendor qualification, investing in new filtration equipment, or developing non-traditional solvent systems to lower environmental load, we take cues from real feedback, not just theoretical models. Customer partnerships, joint research, direct conversations about failures and successes—these form the backbone of ongoing improvements, supporting a broader community of chemists, engineers, and manufacturers relying on 1,3-Diethynylbenzene for their own breakthroughs.

    A Trusted Raw Material for Advanced Chemistry

    Throughout years of manufacturing, 1,3-Diethynylbenzene shows itself as more than a chemical on a shelf. Each lot reflects technical skill, process integrity, and ongoing collaboration. Every delivered batch supports innovation in applications the original chemists might never have imagined. Whether the need is for extreme-temperature adhesives, next-generation electronics, or bespoke composites, reliable access to this specialty aromatic forms part of the foundation for progress.