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Trans-1,3-Pentadiene

    • Product Name Trans-1,3-Pentadiene
    • Alias cis-1,3-Pentadiene
    • Einecs 212-191-2
    • 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

    599729

    Cas Number 2004-70-8
    Molecular Formula C5H8
    Molecular Weight 68.12 g/mol
    Iupac Name (E)-penta-1,3-diene
    Synonyms trans-1,3-Pentadiene, (E)-1,3-Pentadiene
    Appearance Colorless liquid
    Boiling Point 39-40 °C
    Density 0.659 g/mL at 25 °C
    Melting Point -146 °C
    Refractive Index 1.412 at 20 °C

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

    Packing & Storage
    Packing Trans-1,3-Pentadiene is packaged in a 500 mL amber glass bottle with a secure cap, labeled with hazard and product information.
    Shipping Trans-1,3-Pentadiene is shipped in tightly sealed containers, typically under an inert atmosphere such as nitrogen to prevent oxidation. It should be stored and transported away from heat, sparks, and open flame, due to its flammability. Shipping must comply with relevant hazardous material regulations, including proper labeling and documentation.
    Storage Trans-1,3-Pentadiene should be stored in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep the container tightly closed and properly labeled. Store it away from oxidizing agents and acids. Use explosion-proof equipment and ensure proper grounding and bonding. Ensure compliance with local regulations regarding flammable and volatile organic compounds.
    Application of Trans-1,3-Pentadiene

    Applications of Trans-1,3-Pentadiene in Industrial Manufacturing

    Trans-1,3-Pentadiene enables the precise synthesis and efficient processing of high-performance specialty intermediates in advanced manufacturing workflows. As the original manufacturer, we cooperate closely with downstream partners and R&D teams in several distinct sectors, supporting quality compliance and consistent raw material traceability.

    1. Specialty Polymer and Elastomer Synthesis

    Leading polymer and elastomer producers use trans-1,3-pentadiene as a key diene monomer in advanced copolymerization processes. Its unique structure provides controllable reactivity during free-radical and coordination polymerizations, directly influencing the microstructure, cold resistance, and tensile behavior of high-performance elastomers found in oil-resistant seals, hoses, and vibration isolation parts. Precise dosing in proprietary feedstock blends helps balance crosslink density and processability. We support large-scale operations relying on in-line raw material purity monitoring and consistent monomer reactivity for reproducible polymer grades.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems for Chemical Manufacturing)
    • REACH Regulation (EC) No 1907/2006 for registration and control in Europe
    • ASTM D1418 (Standard Practice for Rubber and Elastomer Nomenclature)
    • GB/T 16720 (China Industrial Rubber Chemical Raw Material Standards)

    Typical usage ratio

    • Polymerization recipes: 1%–10% by weight of total monomer feed; the exact ratio depends on desired copolymer chain configuration and downstream curing requirements

    Downstream process integration

    • Continuous or batch monomer feeding before catalyst or initiator addition in suspension, emulsion, or solution polymerization units
    • Co-dosing with butadiene, isoprene, or styrene monomers based on finished polymer architecture

    Final product types

    • Specialty synthetic rubbers used in automotive, aviation, and chemical process equipment
    • Engineering elastomers for gaskets, dynamic seals, and acoustic isolators
    • Polydienes and copolymers for flexible fuel lines and hoses

    2. Agrochemical Intermediate Manufacturing

    Trans-1,3-pentadiene serves as a foundational raw material in agrochemical synthesis, permitting precise functionalization steps in the production of crop protection actives. Chemical manufacturers depend on its consistent purity when performing staged Diels-Alder reactions and selective hydrogenations. This enables high-yield conversion into intermediates for herbicides and insecticides, particularly where structural consistency determines regulatory batch acceptance. Our technical support includes traceability documentation and impurity profiling aligned with global plant protection requirements.

    Industry compliance standards

    • FAO/WHO Guidelines on Pesticide Specifications
    • ISO 9001:2015 Certification applicable to active ingredient manufacturing
    • EPA 40 CFR Part 158 (US EPA Pesticide Registration Requirements)
    • China GB 2763 (Max Residue Levels for Pesticides in Foods)

    Typical usage ratio

    • Reaction steps: 5%–30% molar basis as a dienic reactant; the actual ratio is determined by the route to target intermediate structure and multi-step impurity carry-through assessment

    Downstream process integration

    • Fed into Diels-Alder cycloaddition reactors as a diene partner for formation of cyclohexene derivatives
    • Purified prior to selective hydrogenation, functional group derivatization, or halogenation to yield agrochemical precursors

    Final product types

    • Intermediates for herbicide and insecticide actives (e.g., substituted cycloalkenes)
    • Key structural units in crop protection agents subject to national registration
    • Building blocks for plant growth regulator synthesis

    3. Fragrance and Flavor Ingredient Manufacturing

    The diene undergoes targeted cycloaddition and oxidation to produce highly valued fragrance intermediates, which downstream producers incorporate in finished fine chemicals for consumer applications. Its defined reactivity supports batch reproducibility and low-odor impurity levels in the resulting aldehydes and ketones. Cosmetic and flavor houses rely on monomer traceability and consistent organoleptic profiles to maintain compliance under IFRA and food safety regulations, especially in Europe and North America.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • EU Regulation (EC) No 1334/2008 on Flavourings
    • US FDA 21 CFR 172.515 (Synthetic Flavoring Substances and Adjuvants)
    • ISO 9235 (Aromatic Natural Raw Materials–General Guidelines)

    Typical usage ratio

    • Ingredient processing: 2%–20% by molar balance relative to other dienophiles or oxidizing agents, with adjustments per required intermediate purity and sensory standards

    Downstream process integration

    • Introduced during the synthesis of cyclic ketones, aldehydes, and lactones through Diels-Alder cyclization and controlled oxidation steps
    • Typically purified in post-reaction workup to meet IFRA and FDA flavor ingredient criteria

    Final product types

    • Cyclic and acyclic fragrance intermediates used in perfumery
    • Flavoring aldehydes and lactones for food and beverage formulations
    • Precursors for aroma chemicals in toiletries and household products

    4. Pharmaceutical Intermediate Production

    Trans-1,3-pentadiene features in pharmaceutical manufacturing as a dienic building block for active ingredient and specialty intermediate synthesis. Its molecular geometry enables highly specific cyclizations and ring-formations when paired with pharmaceutical-grade dienophiles under GMP-controlled environments. Careful control of introduction and impurity management are essential, especially where regulatory filings require impurity profile documentation to ICH Q3A/B and FDA standards. We work directly with API producers to supply consistent grades supporting reproducible synthetic yields.

    Industry compliance standards

    • ICH Q7 (GMP for Active Pharmaceutical Ingredients)
    • US FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • EU GMP Annex 1 (Manufacture of Sterile Medicinal Products)
    • Ph. Eur. and USP Monographs (where applicable to intermediates)

    Typical usage ratio

    • API synthesis: 2%–12% molar equivalent in multi-step reaction chains, with exact dosing calibrated to reactant excess and stage-specific yield optimization

    Downstream process integration

    • Added as a reactant in key ring-formation and functionalization steps for non-aromatic cyclic intermediates
    • Subjected to strict QC release on residual solvents and by-products prior to further derivatization

    Final product types

    • Pharmaceutical intermediates for antihypertensive and anti-inflammatory APIs
    • Cycloalkene-derived and unsaturated ring system precursors
    • Non-aromatic cyclic units for advanced oncology research compounds
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    Certification & Compliance
    More Introduction

    Trans-1,3-Pentadiene: Shaping Specialty Chemicals with Precision

    A Closer Look from the Manufacturer’s Bench

    Years of experience turning raw hydrocarbon feedstocks into refined monomers has given us a deep understanding of how molecules like trans-1,3-pentadiene bring real value in the lab and on the production line. Our team works with butadiene as a precursor, using targeted dehydrogenation techniques and well-tuned distillation processes. Every time we process a batch, we see firsthand how the tiniest variations can impact outcomes: a few degrees in temperature, the purity of the catalyst, or the storage atmosphere will influence not only the yield but the quality and stability of the final product. The result is trans-1,3-pentadiene that delivers on polymerization performance, processing reliability, and material consistency, not just a molecule in a drum.

    Understanding the Product

    Our trans-1,3-pentadiene consistently achieves a purity above 98%. The chemical structure, with its two conjugated double bonds, sets it apart from saturated hydrocarbons and provides the key reactivity that compound developers expect. The trans- configuration allows for better alignment during polymerization, yielding materials with improved thermal and mechanical stability compared to similar cis-isomers. By controlling the production process from hydrocarbon selection to final purification, we minimize contaminant levels that could interfere with downstream chemical reactions.

    From a physical standpoint, trans-1,3-pentadiene leaves the line as a colorless, volatile liquid with a sharp, distinctive odor. Its boiling point sits just under 43 degrees Celsius, so our storage systems rely on tightly sealed, cooled tanks that minimize pressure buildup and evaporation losses. Our logistics crews have developed a rhythm for filling, labeling, and moving shipments with a mindset attuned to both safety and the quirks that come with handling low-molecular-weight olefins.

    Direct Applications for Downstream Users

    Trans-1,3-pentadiene finds firm demand in the creation of specialty polymers, high-stress elastomers, and advanced resin technologies. Research groups reach out to our technical support desk seeking insights about achieving better molecular weight distribution in copolymerization projects. Custom adhesive developers order trans-1,3-pentadiene to lend flexibility and tack while giving up less heat resistance than alternative softening agents.

    The monomer’s double bonds – separated by a single methylene bridge – open up several reaction possibilities. Additives teams routinely use trans-1,3-pentadiene as a building block for antioxidants intended to stabilize engine lubricants. Crop protection labs transform this diene into intermediates for herbicides and insecticides, capitalizing on the reactivity of the unsaturated sites. We often ship custom drum lots to electronic materials manufacturers, who blend it into advanced photoresists and flexible circuit substrates, where the end-use demands both precise cure profiles and robust low-temperature flex.

    Comparing Trans-1,3-Pentadiene to Related Products

    Anyone working with conjugated dienes has seen the options: trans-1,3-pentadiene, cis-1,3-pentadiene, and 1,3-butadiene dominate conversations at industry conferences. Customers sometimes ask why stay with trans-1,3-pentadiene when butadiene costs less in volume. In our process operations, it is easy to spot that butadiene’s shorter chain limits the length and branching of the resulting polymers, sometimes making it difficult to tune soft segment content or achieve targeted glass transition temperatures. Trans-1,3-pentadiene’s longer carbon skeleton brings a natural increase in flexibility and allows for a broader crosslink density in finished materials.

    The decision to run with the trans– over the cis–form comes down to more than just chemical structure. Our polymer engineering colleagues report that trans-1,3-pentadiene’s geometry reduces internal strain during curing. That translates to better toughness and lower shrinkage, key needs in electronic encapsulants and automotive elastomers. Cis-1,3-pentadiene works for certain applications demanding high impact resilience, but its reactivity can complicate storage and scaling, as the molecular packing leads to more rapid aging or polymerization under less controlled conditions.

    In specialty coatings, formulators gravitate toward trans-1,3-pentadiene for its ability to form harder films after crosslinking, avoiding the rubbery, flux-prone surfaces typical of butadiene-rich blends. Paint and sealant developers often share positive feedback from testing cycles, noting improved scratch resistance and less color fade over time.

    Handling and Safety Know-How

    Anyone filling or emptying a tank of trans-1,3-pentadiene recognizes the volatile speed and low flashpoint of this diene. Years of incident reporting have demonstrated that routine vigilance pays off. Proper venting, inert nitrogen blankets over storage, and strict control of ignition sources serve operators well. Our training teams update procedure manuals regularly, including practical drills with pressurized leak scenarios. Because pentadienes are especially flammable, we designate storage areas well away from heat exchangers and smoking zones, and all transfer hoses and pumps carry grounding cables to dissipate static.

    On production lines, we see how trace contaminants such as peroxides or acidic residues can trigger premature reactions, so we run frequent analytics throughout the shift. Dedicated glassware and sealed metal reactors prevent cross-contamination with other olefins or aromatics. Any unused product goes through vented recovery before being recycled or incinerated with full VOC controls.

    Shipments to customers—whether by drum, ISO tank, or smaller packaging—include clear markings and up-to-date certificates of analysis. For research quantities, we fill smaller flasks under an argon atmosphere to guarantee shelf stability. Disposal and emergency procedures remain part of our core technical support offerings to all buyers.

    The Role in R&D and Pilot Programs

    Collaboration with R&D partners brings a steady stream of new requirements and test protocols. In recent years, several universities reached out needing small lots of isotope-labeled trans-1,3-pentadiene for reaction mechanism studies. Our ability to custom-tailor batches, whether that means ultra-low water content or a precise isotope ratio, results from close control over each stage of synthesis.

    Innovation happens fastest when a clear feedback loop connects the pilot bench to full-scale production. During scale-up, we work side-by-side with customer teams to modify feed and distillation regimes, ensuring the bulk monomer reflects the same characteristics as early test lots. We employ online gas chromatography and spectrophotometry to monitor consistency, comparing each fraction to tightly defined quality standards.

    Emerging product areas, such as photoinitiated resins for additive manufacturing and advanced composite matrices, push us to refine and tune our process. A thorough understanding of trans-1,3-pentadiene’s reactivity—especially its propensity to participate in Diels-Alder and cationic reactions—lets us supply material optimized for each novel target application.

    Addressing Industry Shifts and Regulatory Pressures

    Sustainable chemistry has moved steadily up the agenda as environmental constraints tighten. As manufacturers, our challenge is to maintain high-purity outputs while cutting energy use and waste generation. Process energy audits over the past year highlighted clear areas for savings: we recovered more heat from dehydrogenation coils, recycled inert gases within the distillation section, and replaced bulkier cooling systems with more focused temperature control loops. These improvements have lowered greenhouse emissions and earned positive marks during environmental audits.

    Chemical regulations such as REACH in Europe or the TSCA inventory in the US bring new demands for testing and traceability. We work closely with our regulatory team to document impurity profiles, track all feedstock sources, and participate in hazard update efforts with industry consortia. Updated safety data and compositional disclosures are shared with customers directly and posted through approved industry platforms, aiming for clarity rather than generic statements.

    On the product stewardship front, we have invested in research with academic partners to explore possible alternatives to mercury-based catalysts and to test less hazardous stabilizing agents. Discussions with regional authorities have driven upgrades to our waste capture systems, especially for volatile organic emissions and trace byproducts.

    Supporting Supply Chain Reliability

    End users depend on steady availability of specialty chemicals, especially in markets where material outages can halt an entire manufacturing line. We balance forward-planned production runs and flexible batch sizes to meet ongoing fluctuations in demand for trans-1,3-pentadiene. Facility upgrades, including redundant reactor trains and expanded onsite storage capacity, narrow the risk of disruption from upstream interruptions or equipment downtime.

    We keep direct lines open to both suppliers and customers, sharing information on market conditions and expected lead times. If raw material streams tighten or logistical bottlenecks arise, we work to re-balance sourcing among long-term partners rather than looking to spot markets where quality assurance can suffer.

    Periodic risk assessments verify that both physical infrastructure and digital order tracking systems match the scale and sensitivity of our operations. Our customer service staff provide shipment status updates and technical guidance in real time, focusing on clear, direct communications rather than automated scripts.

    Ongoing Technical Support and Knowledge Sharing

    The questions we receive range from best practice handling guidelines to recommendations about co-monomer selection and process troubleshooting. Our technical advisors, many with decades on production floors, field support inquiries from polymerization engineers, resin formulators, and academic researchers alike. Fielding questions about free radical inhibitors, shelf-life maximization, or compatibility with specific catalysts has become part of the daily routine.

    With each inquiry and customer collaboration, we expand the collective knowledge base. Information on new processing parameters, end-use case studies, or performance observations is shared through technical bulletins, training sessions, and site visits. These ongoing efforts reinforce user confidence, keep teams current with process refinements, and push the envelope for trans-1,3-pentadiene’s role in both established and experimental applications.

    Future Outlook for Trans-1,3-Pentadiene

    Market trends point to continued expansion in performance resins, castable elastomers, and specialty coatings where trans-1,3-pentadiene serves as a foundational building block. Increasing demand for lightweight, impact-resistant materials across the automotive, electronics, and construction sectors gives this diene even more strategic relevance. Ongoing R&D projects focus on refining the monomer’s reactivity profile to suit new polymerization technologies, such as living anionic systems and UV-curing approaches.

    Process improvement targets now include further reductions in waste, tighter raw material recycling, and options for green feedstocks. New sensor arrays in the plant provide real-time data for batch adjustment and quality review, letting us spot deviations immediately and redirect product flow as needed. We see strong interest from customers in sourcing monomers produced with a smaller carbon footprint and are channeling efforts into both new reactor designs and sustainable logistics planning.

    Conclusion: Trust Through Experience and Commitment

    Years of making, testing, packaging, and shipping trans-1,3-pentadiene have shown us how critical real-world expertise is for success in specialty chemicals. Every step, from reaction setup to final shipment, requires more than formulaic procedures—experience, attention to detail, and a willingness to adapt make the difference between average and outstanding product performance. The interplay between molecular science, plant operations, and customer collaboration carries over into every drum and every application. As the industry landscape evolves and the demands on material producers increase, we draw on hands-on knowledge and technical openness to ensure that each order of trans-1,3-pentadiene meets the high bar our partners expect.