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1,3-Hexadiene

    • Product Name 1,3-Hexadiene
    • Alias Sym-Trimetethylene
    • Einecs 203-893-7
    • 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

    615384

    Name 1,3-Hexadiene
    Cas Number 592-42-7
    Molecular Formula C6H10
    Molar Mass 82.15 g/mol
    Appearance Colorless liquid
    Density 0.675 g/cm³
    Boiling Point 68°C (154°F)
    Melting Point -119°C (-182°F)
    Flash Point -17°C (1°F)
    Solubility In Water Insoluble
    Vapor Pressure 91 mmHg at 25°C
    Chemical Structure CH2=CH−CH=CH−CH2−CH3

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

    Packing & Storage
    Packing 1,3-Hexadiene is packaged in a 500 mL amber glass bottle with a secure screw cap, clearly labeled with hazard warnings.
    Shipping 1,3-Hexadiene is shipped as a flammable liquid, typically in tightly sealed, labeled drums or containers that comply with UN 2378 regulations. It requires cool, well-ventilated storage, away from sources of ignition and incompatible substances. Appropriate hazard labeling and documentation are mandatory during transport to ensure safe handling and regulatory compliance.
    Storage 1,3-Hexadiene should be stored in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. Keep the chemical in tightly closed containers made of suitable materials, such as glass or metal, and away from oxidizing agents. Ensure proper labeling and secondary containment to prevent leaks or spills, and comply with relevant safety regulations.
    Application of 1,3-Hexadiene

    Applications of 1,3-Hexadiene in Industrial Manufacturing

    1,3-Hexadiene serves as a specialized intermediate across several high-value sectors, where its diene structure supports advanced synthesis and polymer modification. The following outlines verified downstream scenarios that utilize this material within compliance frameworks, provision requirements, and production protocols established by international industry.

    1. Specialty Elastomer Modification

    Manufacturers incorporate 1,3-hexadiene to tailor the performance properties of hydrogenated nitrile rubber (HNBR) and related copolymers, especially to enhance oil and thermal resistance. Direct introduction during the copolymerization step with acrylonitrile and butadiene enables these elastomers to meet strict automotive and oilfield sealing requirements for durability and swelling resistance under aggressive fluids and temperatures. Strategic adjustment of monomer ratios and conversion ensures both processing consistency and end-use property optimization for critical sealing solutions.

    Industry compliance standards

    • ISO 23936-2 (Elastomers for Oil and Gas Industry)
    • SAE J200 (Automotive Rubber Materials Classification)
    • ASTM D1418 (Rubber Nomenclature)
    • REACH Annex XVII (Restriction on Specific Substances)

    Typical usage ratio

    • Generally 2–10% of total monomer charge by weight in NBR or HNBR copolymerization; proportion varies based on target polymer backbone saturation and required property balance for oil resistance versus flexibility.

    Downstream process integration

    • Fed to the polymerization reactor as a co-monomer during emulsified or solution copolymerization, with dosing sequenced alongside acrylonitrile and butadiene under inert atmosphere protocols.

    Final product types

    • HNBR seals, gaskets, O-rings for automotive and drilling uses
    • Elastomeric hoses for hydraulic and oil transport
    • High-durability vibration dampening mounts

    2. Cycloalkene Synthesis for Fragrance Intermediates

    As a pure feedstock, 1,3-hexadiene participates in selective metathesis or cyclization reactions to build cyclohexene derivatives. These intermediates—particularly methylcyclohexene variants—serve fragrance and aroma chemical synthesis at scale, meeting the purity and traceability standards of the global flavor and fragrance sector. Optimization at the catalyst and reactor scale is critical for yield and impurity control to comply with both REACH registration and IFRA guidelines for fragrance safety.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards and Guidelines
    • REACH Regulation (EC No 1907/2006)
    • ISO 9235 (Aromatic Raw Materials—Vocabulary)
    • Food Chemicals Codex (for aroma ingredient production where applicable)

    Typical usage ratio

    • Stoichiometric levels determined by molar equivalence in ring-closing metathesis or cycloaddition, typically providing 1.0 equiv of diene per target cyclization step; adjustments based on catalyst throughput and downstream purification efficiency.

    Downstream process integration

    • Dosed to a batch or continuous flow reactor containing metathesis catalyst (usually Ru, Mo, or W complexes); process includes temperature-controlled reaction, subsequent purification by distillation and fractional crystallization before formulation.

    Final product types

    • Methylcyclohexene and cyclohexene intermediates for fine fragrance bases
    • Aroma chemicals for detergent and personal care blends
    • Flavor ingredient building blocks for beverage and confectionery houses

    3. Crosslinking Agent Precursor in Advanced Polymer Networks

    Producers leverage the diene moiety to generate active crosslinking agents for unsaturated polyester and polyurethane resin systems, targeting high strength and low shrinkage composites. The bifunctional structure supports controlled density of crosslink points, enabling manufacturers to fine-tune mechanical, chemical, and thermal properties of networks used in electronic encapsulation, automotive composites, or structural adhesives—particularly in regimes where avoiding overly rigid or brittle cure is essential.

    Industry compliance standards

    • UL 94 (Flammability Testing of Plastic Materials)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in Electrical/Electronic Equipment)
    • ISO 10993-5 (Biological Evaluation of Medical Devices—Cytotoxicity, for related biomedical applications)
    • ISO 9001 (Quality Management Systems)

    Typical usage ratio

    • From 0.5–3% by weight as a functional crosslinker precursor in unsaturated polyester resin or polyurethane formulation; selected according to desired cure kinetics, crosslink density, and end-use performance profile.

    Downstream process integration

    • Introduced during resin prepolymer synthesis stage or added during formulating step immediately prior to catalyst and initiator addition; disperses into main resin matrix under controlled mixing and temperature, reacting during thermal or catalytic cure cycle.

    Final product types

    • Encapsulating compounds for electronic modules
    • Composite structural panels (SMC/BMC)
    • High-performance adhesives for aerospace and automotive

    4. Chemical Intermediate for Agrochemical Synthesis

    The compound finds critical application as a microwave- or solvent-assisted coupling partner for preparation of bicyclic building blocks and specialty olefins in the synthesis routes of select herbicides and crop protection agents. Quality control and trace analysis of trace impurities and isomer composition are paramount to match agrochemical regulatory submissions globally. Manufacturers must adapt usage according to route selectivity and product registration requirements within major markets such as the US, EU, and Japan.

    Industry compliance standards

    • FAO/WHO JMPR Guidelines (Joint Meeting on Pesticide Residues)
    • EU Regulation 1107/2009 (Placing of Plant Protection Products on the Market)
    • EPA 40 CFR Part 158 (USA Pesticide Registration Data Requirements)
    • ISO 17025 (Testing and Calibration Laboratories, for product and intermediate QC)

    Typical usage ratio

    • Utilized at 1–1.2 mole equivalent for key coupling or cyclization step; proportion varies with synthesis pathway—often balanced with efficiency goals and byproduct minimization in continuous flow or multistep batch setups.

    Downstream process integration

    • Fed into synthesis reactors at the intermediate coupling or cyclization stage, frequently under controlled heating and inert conditions; product stream typically subjected to multi-step purification before further functionalization toward the target agrochemical structure.

    Final product types

    • Agrochemical intermediates for selective herbicide APIs
    • Pyridine/pyrimidine-based crop protection agents
    • Bicyclic olefinic compounds employed in the synthesis of insecticides and fungicides
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    Certification & Compliance
    More Introduction

    1,3-Hexadiene: Performance and Perspective from the Source

    Reintroducing a Classic Olefin

    Working daily with specialty olefins sharpens your eye for both subtle shifts in molecular structure and the hard demands of downstream processes. Among the family of dienes, 1,3-hexadiene sets itself apart with real utility on the floor and in the lab. Unlike longer-chain conjugated dienes and branched variants, its linear six-carbon backbone paired with alternating double bonds offers both striking reactivity and ease of purification. As direct manufacturers, we appreciate the role that purity and lot-to-lot reproducibility play for chemists and engineers building more advanced chemistries—there’s just less headache, less waste, and more predictable results when the core feedstock matches expectations every time.

    What Sets 1,3-Hexadiene Apart

    We have often seen confusion between different hexadiene isomers. 1,3-hexadiene—unlike its 1,4 or 2,4 siblings—features conjugated double bonds at the core of its structure. That conjugation unlocks a higher reactivity profile in selective cyclization, telomerization, and cross-coupling. The industry leans on these features for functionalization routes, particularly in the production of fragrances, agrochemical intermediates, and specialty polymers. The distinct pattern of double bonds in 1,3-hexadiene also changes its boiling and vapor pressure, which directly affects its behavior in closed and automated reactor systems. Consistent handling and reliable separation during distillation come from understanding these fundamental characteristics.

    Specification Consistency from Synthesis to Final Packing

    Every barrel of 1,3-hexadiene we ship started life on our own reactors, under strict quality controls. The product passes through repeated distillation to remove oligomers, water, and light hydrocarbons, and ongoing spectroscopic checks track both major impurities and trace levels. Typical purity hovers at 98 percent or better, with fewer than 500 ppm of typical byproducts like cyclohexene or lower dienes. As we see it, cutting corners at any point only comes back later as application failures or complaints. Bulk users—especially those scaling new polymerizations or designing fragrance syntheses—can’t afford drift in input quality. We keep documentation open for every lot, showing NMR and GC profiles so that process chemists downstream can adjust protocols ahead of time if needed.

    Handling in Real-World Plant Settings

    No chemist works in isolation from reality. Unreactive side streams, shelf-life limits, and routine handling losses matter. 1,3-hexadiene has a distinctive sharp odor and high flammability akin to other low molecular weight dienes. More unforgiving are the auto-polymerization risks, especially if inhibitors are absent or temperatures run hot. Most batches we dispatch contain a stabilized form—usually with trace amounts of p-tert-butylcatechol to guard against runaway self-reaction. Feedback from end-users often circles back to storage and pumping difficulties: the product requires inert atmospheres, and even small leaks or exposure to atmospheric oxygen can trigger discoloration or formation of gels. Regular training, grounded in our own incident history, keeps plant teams aware of safe practices. You won’t find such insights in a spec sheet, but from direct experience, these are the details that save material and downtime.

    Downstream Use Cases: What Customers Actually Do

    Most technical literature catalogs dozens of uses for linear dienes, but practical demand for 1,3-hexadiene centers around three main sectors. In the world of synthetic rubber, it bridges the gap between butadiene and higher molecular weight feedstocks, offering unique chain transfer properties that help design custom copolymers and fine-tune elasticity or barrier properties. Academic groups reach for high-purity material in metal-catalyzed transformations—especially for building conjugated systems, multi-component coupling reactions, and as a probe in mechanistic experiments. Flavors and fragrance houses value 1,3-hexadiene not just for direct olfactory profiles, but for the wide palette of derivatives built from its backbone. Scent molecules as diverse as musks and green notes rely on selective oxidation and cycloaddition of this diene. Supplying into these creative industries, manufacturers like us adjust impurity targets, blending protocols, and even container types to guarantee a clean slate for every new synthetic challenge.

    Comparing Alternatives: Why Not Just Use Butadiene or 1,5-Hexadiene?

    We sometimes field questions about why customers specify 1,3-hexadiene over more common feedstocks such as butadiene or its less reactive isomer, 1,5-hexadiene. Butadiene (C4H6) offers lower cost per ton and sits at the heart of bulk polymer production, but its volatility and propensity to autopolymerize limit its direct functionalization options. The difference lies in how the electron distribution in 1,3-hexadiene's string of double bonds makes it more suited for Diels-Alder reactions and transition-metal catalyzed couplings. 1,5-hexadiene’s non-conjugated structure can’t match the range or selectivity for these applications. True, the market for 1,3-hexadiene is smaller and prices reflect tighter supply, but the step up in performance per kilogram for specialty projects frequently justifies the investment.

    Environmental and Regulatory Considerations

    The chemical landscape isn’t static—environmental pressures, evolving REACH and TSCA rules, and shifting end-user requirements every year force us to sharpen our approach. 1,3-hexadiene counts as both a volatile organic compound and a potential hazardous air pollutant, so our production lines anchor on closed-loop transfer, vapor recovery, and aggressive fugitive emission tracking. Scrap handlers run either closed incineration or catalytic vapor oxidation, bypassing traditional flaring which risks higher emissions. Customers downstream are building more sophisticated life cycle assessments, and we cooperate by making batch history, stored inhibitor levels, and even production waste volumes available to partners who need the data. These transparency steps didn’t come overnight, but evolved as both regulators and downstream users demanded higher confidence in feedstock sourcing and handling.

    Insights on Shelf Life and Logistical Realities

    Shipping air- and moisture-sensitive chemicals across continents turns up dozens of headaches that only hands-on experience can teach. 1,3-hexadiene is nothing like a standard petrochemical feedstock—its shelf life depends on storage in dry, oxygen-free steel drums, preferably packed under inert gas and away from direct sunlight. Not every destination, especially remote sites or emerging markets, comes equipped for that level of care. We ship with overpacks and precise labeling, and coordinate with experienced hazmat carriers. Distributors and bulk storage facilities receive advanced training and practical guidelines from our team, based on lessons learned from product returns, contamination, or cross-reactivity with previous drum residues. Over years, these details separate reliable partners from opportunistic traders who treat every hydrocarbon as interchangeable. We favor repeat clients who invest in compatible drum cleaning and closed transfer equipment—not because of contract clauses, but because losses and hazards decrease over time.

    Research and Process Support from the Manufacturing Side

    Formulators and process chemists often present us with process bottlenecks they can’t resolve with textbook solutions. Certain metal-catalyzed reactions lose yield due to trace acid content, while polymerization pilots see unwanted branching tied back to ineffective inhibitor packages. Early on, we learned that routine feedback loops—direct calls between our technical staff and customer R&D—shorten development cycles and prevent costly reruns. Our chemists support method development and trouble-shoot side reactions that only crop up at full scale. For example, a customer scaling fragrance intermediates ran into downstream gel formation linked to trace peroxides accumulated during solvent recovery. Our in-plant team ran extra distillation passes, tracked the LOT history, and adjusted cleaning cycles, eliminating the problem after just one production run. These hands-on collaborations go far beyond standard product supply, and foster ongoing trust.

    Innovation at the Reactor Scale

    Every few years, incremental upgrades in our reactor technology seem to ripple out through customer applications. Moving from batch to continuous processing let us tighten control over impurity profiles, particularly methylpentadiene side products. The addition of online NIR spectrometry reduced human error and sped up decision-making during fractionation, while more precise dosing of inhibitors cut down on background gel formation in storage. We see downstream users gaining predictable conversions and reduced batch-to-batch variability, particularly in polymer R&D and fine chemical synthesis. Being the first plant in our region to take up self-cleaning distillation columns paid off in shorter maintenance schedules and far less cross-contamination—results that materialize directly in final customer yields and reproducibility.

    Practical Advice from the Production Floor

    Procuring the right grade of 1,3-hexadiene along with the right technical support saves time and money. Our plant managers emphasize that bulk buyers should invest in online tracking of drum storage conditions and periodic on-site audits. Small errors—drums stacked in open yards, missed inhibitor checks, absent sealing gaskets—can snowball into spoiled material and safety incidents. We urge process engineers to standardize unloading protocols and train new hires in recognizing sensory signs of product degradation. As manufacturers, we stand by our batch histories and work with users to resolve issues before downstream problems escalate. Over the years, we’ve also compiled case studies of successful troubleshooting and process improvements, helping both sides avoid repeating common mistakes.

    Looking Ahead: Building Confidence and Collaboration

    The landscape for 1,3-hexadiene will continue to evolve along with regulatory, synthetic, and market trends. Renewed demand from advanced polymer R&D, the shift toward greener solvent usage, and ever-tightening safety controls all push for further openness between suppliers and users. On our end, sustained investment in quality controls and process innovation allows us to deliver not just a molecule, but a launchpad for customers’ creativity and efficiency. We know from experience that open dialogue—sharing not just spec sheets but direct process know-how—lets both sides grow. Chemists and engineers tackling new challenges need confidence that their building blocks arrive as promised, every time. By anchoring our production to the realities of the factory floor and the feedback loop from the lab bench, we keep raising the standard for what a core feedstock can deliver.