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HS Code |
497411 |
| Iupac Name | Cyclohexa-1,4-diene |
| Molecular Formula | C6H8 |
| Molar Mass | 80.13 g/mol |
| Appearance | Colorless liquid |
| Melting Point | -100 °C |
| Boiling Point | 83 °C |
| Density | 0.867 g/cm³ |
| Solubility In Water | Insoluble |
| Refractive Index | 1.487 |
| Cas Number | 628-41-1 |
As an accredited 1,4-Cyclohexadiene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1,4-Cyclohexadiene is supplied in a 500 mL amber glass bottle with a secure screw cap and warning hazard labels. |
| Shipping | 1,4-Cyclohexadiene should be shipped in tightly sealed, approved containers, protected from heat, ignition sources, and direct sunlight. Transport under controlled temperature if possible. Ensure proper labeling and compliance with hazardous materials regulations (e.g., flammable liquid). Handle with care to prevent leaks and spills during transit. Consult relevant transport guidelines. |
| Storage | 1,4-Cyclohexadiene should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from sources of ignition and heat. Protect from direct sunlight and incompatible substances such as oxidizing agents. Storage under inert gas (e.g., nitrogen) is recommended to minimize oxidation. Handle in accordance with standard laboratory safety practices, wearing appropriate personal protective equipment. |
Applications of 1,4-Cyclohexadiene in Industrial Manufacturing1,4-Cyclohexadiene is a key feedstock used in advanced chemical synthesis, electronic materials, agrochemical intermediates, specialty polymers, and fine chemical production. As an experienced manufacturer, we provide high-purity material precisely adapted to each industrial segment below. 1. Agrochemical Intermediate SynthesisMajor agrochemical producers incorporate 1,4-cyclohexadiene as a starting material for producing selective herbicide and insecticide intermediates. The compound readily undergoes Diels-Alder and catalytic hydrogenation reactions, facilitating controlled functional group introduction for advanced active molecule synthesis. Our product supports process routes requiring low aromatic impurities and precise isomeric ratios, contributing to catalyst longevity and batch-to-batch yield consistency in regulated agrochemical manufacturing operations. Industry compliance standards
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2. Specialty Polymer and Resin ManufacturingResin producers use 1,4-cyclohexadiene as a precursor enabling unique cycloaliphatic and functionalized polymer chains. The compound acts as a monomer or comonomer with well-controlled unsaturation, allowing efficient copolymerization with maleic anhydride and vinyl monomers to achieve desired molecular weights, heat resistance, and surface properties. Our high-stability supply meets precise requirements on trace metal and peroxide levels critical for optical resins and high-durability coating applications. Industry compliance standards
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3. Electronic and Semiconductor Chemical SynthesisProducers of advanced electronic materials utilize 1,4-cyclohexadiene as a functional building block for organosilicon and high-purity aromatic intermediates. The compound participates in controlled hydrogenation and dehydrogenation reactions required in LCD panel and photoresist monomer preparation. Consistent low-particulate and ultra-low metal content material minimizes contamination risk in cleanroom-scale semiconductor syntheses. Industry compliance standards
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4. Pharmaceutical Bulk Intermediate ProductionLeading pharmaceutical manufacturers demand 1,4-cyclohexadiene as a core intermediate in complex synthesis routes, including the preparation of aromatic amines and heterocyclic scaffolds for APIs. The compound permits controlled aromatic ring introduction while facilitating halogenation, nitration, and hydrogenation steps under cGMP conditions. Strict batch traceability, residual solvent analysis, and low aromatic hydrocarbon content are maintained during multi-step synthesis to ensure quality and regulatory compliance of final intermediates. Industry compliance standards
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5. Fine Chemical and Fragrance Ingredient ManufacturingProducers of high-purity fine chemicals and fragrance intermediates select 1,4-cyclohexadiene for its controlled cycloaliphatic to aromatic conversion properties. The compound serves as a precursor for benzene derivatives via dehydrogenation, enabling targeted synthesis of musky and woody scent molecules. Our continuous process capability ensures uniform batch profile, supporting both large-scale industrial and small-batch specialty production for regulated fragrance markets. Industry compliance standards
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Competitive 1,4-Cyclohexadiene prices that fit your budget—flexible terms and customized quotes for every order.
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Ask any chemist running a plant: some chemicals rise above the list of niche agents and become true workhorses. 1,4-Cyclohexadiene is one of those classics. In our years of manufacturing this compound, we’ve watched customers in pharmaceuticals, agrochemicals, fine chemical synthesis, and research come back again and again because it does what’s asked of it, and does so cleanly and predictably.
We manufacture 1,4-Cyclohexadiene with a clear eye for quality and long-term repeatability. Our product has a typical purity above 98%, and every batch undergoes gas chromatography and spectroscopic checks before shipment. For most applications in synthesis, research, and scale-up, that level of purity supports reactions and delivers reliable yields. Over time, we’ve found that off-odors, color impurities, and trace side-products—often ignored by traders—cause headaches during scale-up, so we tighten controls and routinely invest in purification infrastructure. You’ll find our standard product in drums or steel cylinders, depending on your volume and storage protocols. Bulk customers often request bespoke packaging to match their handling and logistics systems, and we respond based on direct consultation between your engineers and our own.
Making chemicals at industrial scale means knowing which molecules bring value in multi-step syntheses. 1,4-Cyclohexadiene’s double bonds, positioned para on the six-membered ring, set it apart from saturated cyclohexane, which lacks that unsaturation, and from 1,3-cyclohexadiene, which has a different electronic distribution and chemical behavior. The conjugated system in 1,3-cyclohexadiene can sometimes bring extra reactivity, but for hydrogenation, cycloaddition, and reduction reactions, 1,4-cyclohexadiene generally offers fewer surprises during process optimization.
In a real-world synthesis, our chemical engineers prefer 1,4-Cyclohexadiene for several transformations such as selective hydrogenations or as a sacrificial donor in transition metal catalysis. Unlike aromatic benzene, which resists most addition reactions, and cyclohexene, which lacks the symmetrical double bonds for certain steps, 1,4-Cyclohexadiene fits into catalytic cycles with greater predictability. Chemists looking to introduce functionality at defined positions, or gently reduce aromatic rings, often rely on it as a safer, better-controlled option.
Pharmaceutical and agrochemical manufacturers order our 1,4-Cyclohexadiene for use as an intermediate—meaning it’s the launching point for more complex molecules. As an industrial supplier with insight into downstream specs, we’ve had cases where shifting from 1,3- to 1,4-diene opened new synthetic pathways or improved selectivity. It’s this sort of practical experience that drives us to keep producing to such tight specifications; side reactions cost time and money during scale-up, and no one wants to chase down contaminants in a kilo-batch because the input solvent had unknown traces.
The product rarely sits on the shelf for long. Many buyers use 1,4-Cyclohexadiene for preparing cyclohexene by partial hydrogenation, or as a hydrogen donor in transfer hydrogenation processes. Its lack of aromatic stabilization makes it more reactive in some reduction and addition reactions, and that gets reflected in classic organic syntheses as well as modern catalytic cycles using palladium, rhodium, or nickel complexes. More than a few research articles and patents name it specifically—not just “cyclohexadiene,” but 1,4- for its unique performance profile.
Those familiar with dienes notice quickly that not all are created equal. Cyclohexane’s all-single-bond structure makes it unhelpful for reactions needing unsaturation. 1,3-Cyclohexadiene, with double bonds at adjacent positions, behaves differently: often, its conjugation and electronic effects lead to alternative outcomes, which can really matter if your endpoint requires precise connectivity or minimal byproducts. In our history, the biggest confusion comes when buyers, often under price pressure, substitute the wrong isomer. We actively educate process teams and procurement engineers to clarify the distinctions—because the difference in outcome isn’t subtle.
Benzene, a common starting material, stays unreactive to most attempts at hydrogenation outside harsh conditions. It’s also far less useful as a hydrogen donor. By contrast, 1,4-Cyclohexadiene’s two double bonds welcome addition, reduction, and functionalization, all at milder temperatures and pressures. This difference pays off in energy savings and simpler equipment needs—something that makes a difference as energy and environmental costs climb.
Practical experience handling 1,4-Cyclohexadiene beats theoretical recommendations every time. This product can oxidize if exposed to long storage in open containers or contact with copper tubing, so our sites use stainless steel or lined storage drums, and we train operators to blanket containers with nitrogen after use. If you’ve ever received off-grade diene from an outside supplier, you know the pain: trace peroxides and degradation turn simple reactions into troubleshooting headaches. Fresh, protected supply chains deliver consistency, so our after-sales team follows up with safety and logistics calls as soon as a new customer signs on.
Temperature swings affect shelf life. We ship with real-time temperature indicators for export loads, since too much heat or sunlight can accelerate decomposition. These upgrades are not cosmetic. They keep our product within spec, especially for buyers in climates with harsh summers or winters, and the cost is minor compared to downstream rework or failed runs.
In past years, dyes and fragrances formed a steady market alongside the big pharmaceutical and agrochemical uses. Now, transfer hydrogenation, polymer chemistry, and sophisticated material synthesis have taken center stage. Flexible packaging projects, battery research, and specialty coatings also pull this ingredient off our lines. We field technical service calls for everything from ligand synthesis in enantioselective catalysis, to batch production of specialized intermediates, to fuel additive research.
What makes 1,4-Cyclohexadiene stand out is its efficient handling of hydrogen—either giving it up or accepting more, depending on the process. It creates opportunities for step economy and atom efficiency, trends that are only growing as chemists aim to downgrade waste, improve throughput, and cut energy use. If users report an outlier in process behavior, our R&D teams start from incoming raw material checks rather than guessing at randomness. That root-cause focus saves jobs, and is a key part of how we eliminate waste streams and hazardous side-products.
Environmental imperatives and regulatory demands have forced change in how we run our plants. Decades ago, lost vapor and open transfer lines were overlooked. Modern plants now collect all off-gassing and run real solvent recovery, not just for cost but to meet local air quality standards. We supply safety data and regulatory disclosure documentation with every batch. Unlike some sellers, we include upstream traceability, so when international buyers face audits, our documentation passes muster.
Our processes steer away from hazardous solvents in purification, relying on distillation and charcoal treatment to reach spec without overcomplicating downstream waste. Some users in high-regulation zones ask for full lifecycle insight on environmental impact. We built systems to track and report on waste, energy, and even transportation footprint, so real compliance can be demonstrated, and so customer brands are covered when their buyers ask tough questions.
Recurring questions hit our chemists and technical service staff. Among them: “How does your material perform in catalytic hydrogenation?” and “Will your 1,4-Cyclohexadiene match our old spec?” Our response isn’t templated—we offer to test application-specific performance in our own pilot plants, using our raw material with your catalysts and conditions. No two customers run identical operations, and differences in base purity, storage time, or the specific isomer matter to real-world outcomes.
Procurement specialists sometimes compare price per kilo as the only metric. But knock-on costs from off-grade or wrongly isomerized material overwhelm any penny saved at contract stage. Years of solving customer batch failures—wasted time, product recalls, plant downtime—have taught us that provenance and validation give better value than a number on a spreadsheet.
A solid relationship between chemical producer and end-user makes a real difference. Over the years, our team works with advanced automation and in-line monitoring, delivering lots with batch-specific analytical data. Not just the COA, but real NMR or GC traces if a customer needs—for example, those making high-value APIs or electronics intermediates. If regulatory authorities shift allowed process aids or limit certain impurities, we swing our process to match, supported by direct plant-scale experimentation rather than guesswork.
Optimizing yield and minimizing downtime means tracing any process anomaly back to the input. Sometimes, even slight peroxide content or traces of other cyclohexadienes throw off a multi-step process. By controlling these from the production line onward, we help you streamline downstream filtration, avoid troublesome color bodies, or pinpoint possible reaction stalling at the source.
Today’s chemical development landscape pushes for speed and reproducibility. Medicinal chemists developing new compounds push for chemicals that work every time and cut risk from side reactions or oxidative degradation. Our product’s low tendency for side-reactions in catalytic processes speeds up reaction times and helps teams avoid bottlenecks. In one customer collaboration, using our purified 1,4-Cyclohexadiene shaved hours off a hydrogenation step and boosted selectivity, saving on catalyst costs and cleanup cycles.
If process scale-up teams can count on input purity, their job gets easier. In-house QC at your site isn’t enough: purity and composition really must be locked down before the drum leaves our site. Otherwise, the downstream problems multiply, from unpredictable filtration load to unexpected off-odors that could spoil a pharma-grade batch.
Countless times, chemical makers new to a product will jump in based on commodity prices. But 1,4-Cyclohexadiene’s quirks in storage, tendency for peroxide formation, reactivity profile, and handling sensitivity all punish shortcuts. We’ve learned to manage these issues through infrastructure, operator training, and lots of laboratory work. Buyers who treat it like a generic solvent or simple hydrocarbon often encounter trouble; as manufacturers, we cut through the confusion and deliver a product you can build on.
As production scales up worldwide, some plants ‘stretch’ shipping times and loosen up analytical controls under pricing pressure. We’ve seen first-hand the kind of process shutdowns and regulatory flags this triggers—especially in life sciences or high-purity applications where even minor contamination isn't tolerated. Regular re-validation and communication across the supply chain solve these issues, and we partner with customers to handle them together.
Innovation in synthesis comes from feedback and close collaboration. By working hand-in-hand with customers, our R&D team implements process tweaks and tests new purification methods for 1,4-Cyclohexadiene that directly address field-identified problems. We invest in pilot-scale runs and offer free technical consultation, because every new reaction developed using this compound can open doors for both our plants and your project teams.
There’s nothing hypothetical about this approach. One partner, developing a specialty material for optoelectronics, needed ultra-high purity to avoid short circuits in their product. Our engineering team worked side-by-side, adjusting distillation cut points and running extra purification steps. The result? Fewer manufacturing rejects and more predictable product life. Experienced chemical makers know this is how products advance from laboratory curiosity to industrial staple, and it’s how new ideas make it to commercial scale.
Our focus on safety, repeatability, and end-use feedback has shaped every aspect—from feedstock qualification through final container sealing. By listening to users, not just meeting a bare minimum spec sheet, we keep 1,4-Cyclohexadiene relevant, reliable, and trusted. We don’t take shortcuts with raw material sourcing, and never dilute or blend down our product to fill a gap or hit a quota. Every decision is based on what downstream manufacturing will need, not what just fits an invoice.
Years of supplying across markets—pharma, polymers, fine chemicals—have proven that shortcuts in manufacturing or documentation cost more than any up-front saving. It’s easy to chase volume, but more rewarding to meet strict global standards and keep buyer trust. Our technical staff step in when process challenges arise, offering data-driven answers based on experience, not brochure promises.
The sector never stands still. Environmental restrictions, growing demand for green chemistry, and tougher quality requirements all push us to evolve. Regular upgrades to equipment, operator retraining, and ongoing collaboration with users across the supply chain ensure we meet changing market needs—and help those at the cutting edge of research unlock new reactions and materials.
1,4-Cyclohexadiene’s niche as a building block in synthesis, catalyst cycles, and material innovation isn't going away. Demand will likely diversify, as new applications pop up in unexpected fields and tighter regulations raise the quality bar. Through ongoing investment in process stability, quality controls, and user-focused R&D, we plan to support our customers through these shifts—just as we have for decades.