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HS Code |
225979 |
| Chemicalname | Cyclohexene |
| Molecularformula | C6H10 |
| Molarmass | 82.15 g/mol |
| Casnumber | 110-83-8 |
| Appearance | Colorless liquid |
| Odor | Mild, sweet odor |
| Boilingpoint | 83 °C |
| Meltingpoint | -103 °C |
| Density | 0.811 g/cm³ |
| Solubilityinwater | Insoluble |
| Flashpoint | -12 °C (closed cup) |
| Vaporpressure | 70 mmHg (20 °C) |
| Refractiveindex | 1.446 (20 °C) |
| Autoignitiontemperature | 244 °C |
| Pubchemcid | 8076 |
As an accredited Cyclohexene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Cyclohexene is packaged in a 500 mL amber glass bottle with a tightly sealed cap and a label displaying hazard warnings. |
| Shipping | Cyclohexene should be shipped in tightly sealed containers, protected from light, heat, and sources of ignition, since it is flammable. Containers must be clearly labeled and compliant with regulatory guidelines. During transit, it should be kept upright, in well-ventilated areas, and handled according to hazardous material shipping regulations. |
| Storage | Cyclohexene should be stored in a cool, well-ventilated area away from heat sources, open flames, and direct sunlight. Keep the container tightly closed and protect it from moisture and incompatible materials such as strong oxidizers. Use approved safety containers to prevent leakage. Clearly label storage areas and containers, and ensure they are equipped with appropriate spill containment measures. |
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Purity 99%: Cyclohexene with 99% purity is used in organic synthesis for pharmaceutical intermediates, where high purity ensures efficient reaction yields. Boiling Point 83°C: Cyclohexene with a boiling point of 83°C is used in industrial distillation processes, where its volatility allows easy separation from reaction mixtures. Stability Temperature 25°C: Cyclohexene with a stability temperature of 25°C is utilized in storage and transport applications, where it remains chemically stable and safe under ambient conditions. Molecular Weight 82.15 g/mol: Cyclohexene with molecular weight of 82.15 g/mol is used in polymerization processes, where precise molecular weight aids in accurate formulation and product consistency. Refractive Index 1.446: Cyclohexene with a refractive index of 1.446 is employed in analytical laboratories, where the specific optical property enables reliable compound identification. Density 0.811 g/cm³: Cyclohexene with density 0.811 g/cm³ is applied in solvent blending operations, where predictable density facilitates accurate mixture formulations. Impurity Content <0.1%: Cyclohexene with impurity content less than 0.1% is used in fine chemical manufacturing, where low impurities prevent unwanted side reactions and ensure product quality. Viscosity 1.02 cP: Cyclohexene with viscosity of 1.02 cP is utilized in coating formulation, where low viscosity enables smooth application and uniform film formation. Water Content <0.05%: Cyclohexene with water content below 0.05% is used in moisture-sensitive syntheses, where low water prevents hydrolysis and ensures reaction integrity. |
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Chemists and chemical engineers know cyclohexene as more than a formula in a textbook. For anyone who has ever set foot in a research lab or a chemical factory, this compound often stands right at the crossroads of practicality and creativity. Its model, C6H10, seems straightforward. Yet, behind every simple hydrocarbon ring, there’s a story of versatility and enduring relevance that shapes how industries work—whether you’re making everyday products or breaking ground on new processes in pharmaceuticals, plastics, or specialty chemicals.
The excitement about cyclohexene doesn’t just come from what it looks like on paper, but rather what it can do on the production floor and in the research sphere. I’ve worked with cyclohexene on various projects—sometimes in advanced polymer synthesis, other times in basic research. Each time, I’ve been reminded just how easily this molecule adapts. It’s not just a precursor for a single pathway. Cyclohexene stands as a key intermediate: it takes you from basic hydrocarbon sources to more sophisticated, functionalized products like nylon or high-performance coatings. But the journey doesn’t end at broad industrial use. Even in education and research, cyclohexene often provides an accessible option for studying alkene reactivity, oxidation reactions, and selective hydrogenations.
Cyclohexene features a six-membered ring with one double bond. Unlike its sibling, cyclohexane, it brings an extra layer of chemical reactivity to the table thanks to the unsaturation. I’ve always found that its distinctive sweet, somewhat sharp odor gives away its personality before you even see its clear, colorless liquid form. The physical feel of handling cyclohexene in the laboratory starts with safety first, as it shares flammability and sensitivity with other volatile hydrocarbons. That double bond, though, is the center of its practical use: through it, cyclohexene invites additions, oxidations, and polymerizations.
On spec sheets, cyclohexene commonly appears at a purity of 99 percent or higher, boiling at about 83 degrees Celsius, with a density just a bit lighter than water. What jumps out to me in day-to-day use is not just the numbers, but how tightly those specs control the outcome. Too much water in the supply, for example, can make or break a reaction. Impurities like peroxides crop up if storage isn’t airtight. And that’s not a small matter when you’re running a plant-scale process or working up sensitive analytic methods for high-purity end products.
Every chemist gets familiar with alkenes—ethylene and propylene, to name a couple—but cyclohexene sits in a sweet spot. Its ring system brings stability, yet it reacts more gently than straight-chain alkenes. Sure, if you need lightning-fast polymerization or commodity-scale feedstocks, you might reach for other alkenes. But cyclohexene offers a balance: it’s reactive enough to make complex molecules, but not so wild it causes uncontrollable byproducts unless provoked. In practical terms, this allows research labs and industrial operators alike to carry out sophisticated transformations with solid yields and manageable side reactions.
Some of the best examples come from the field. In one plant operation I observed, cyclohexene found its stride as an intermediate in the manufacture of adipic acid. This, in turn, feeds into the production of nylon-6,6—a material woven into everything from car tires to sportswear. Moving across the synthetic landscape, cyclohexene proves handy in cycloaddition reactions, especially the Diels-Alder. This often feels like chemistry’s version of creative block stacking: cyclohexene’s ring system pairs up with various dienes, enabling new, often intricate carbon-carbon bonds. Pharmacies and healthcare labs benefit, too—cyclohexene serves as a springboard for medicinal molecules, including those that become anti-inflammatory drugs or agents to tweak central nervous system activity.
So much of what makes cyclohexene valuable comes down to its straightforward double bond. This site gets targeted for epoxidation, hydration, or halogenation, allowing chemical engineers to customize its structure for whatever purpose is at hand. Even fragrance and flavor chemists find cyclohexene useful; subtle molecular tweaks on this base structure lead to new aroma compounds, giving soaps, cleaners, and food products a distinctive presence.
Those who’ve spent time in synthesis labs become acquainted with the quirks of cyclohexene, from its volatility to the tendency for peroxide formation upon storage. My early days in the lab taught me the smell of an old bottle—a little sharper, a sign that it’s time for a new supply. Anyone overseeing a stockroom quickly learns not to take stability for granted. Any production or research operation always stays one step ahead by storing cyclohexene in tightly sealed, light-resistant containers, away from sources of ignition.
In terms of environmental precautions, cyclohexene mirrors many hydrocarbons. Spills evaporate quickly, but proper containment makes a difference. Fumes can irritate, and airborne concentration needs monitoring. During years of working with similar solvents, I’ve come to appreciate well-ventilated spaces and reliable detection equipment. Even seasoned staff can overlook the risk once daily routines take over. The reality is that short-term exposure rarely causes serious harm if safety precautions stick in place, but vigilance always wins in the long run.
Like all petroleum-derived intermediates, cyclohexene links back to the journey from refinery to end-user. It typically enters the scene from cracking cyclohexane or dehydrogenating cyclohexanol. This raises a key question for the modern chemical industry: can we reduce the energy intensity and environmental impact associated with these processes?
Sustainability often feels like a buzzword, but for professionals in the field, it’s an everyday concern. Cyclohexene relies on fossil-based inputs, and every ton produced leaves a carbon footprint. Yet, innovative groups have started probing for ways to make cyclohexene from renewable resources. Some reports showcase microbial fermentation as an alternative route—a promising direction, if technology scales up in a cost-effective way. Based on my time consulting for startups, I’ve seen experimental work aiming to tweak microbial metabolism. The results are not yet factory-ready, but the direction is unmistakable: the push for green chemistry is influencing even legacy products like cyclohexene.
Stacking cyclohexene next to cyclohexane, benzene, or straight-chain olefins isn’t just a theoretical comparison. Teams in chemical plants look at stability, reactivity, and toxicity profiles. Benzene, despite its powerful aromatic characteristics, comes with heightened health risks and stricter regulatory scrutiny. Cyclohexane is more inert, less likely to react in unintended ways, and easier to store over long periods. Still, cyclohexene balances the two: reactive enough for transformations but not so dangerous or environmentally persistent as the aromatic cousins.
Chemists often favor cyclohexene when they want a controlled alkene reactivity inside a cyclic scaffold—ideal for producing epoxides, diols, or other specialty compounds. Alkenes like 1-hexene can polymerize faster, but they don’t replicate the ring-based chemistry cyclohexene enables. In the plastics industry, this means cyclohexene helps shape specialty polymers, adhesives, and modifiers for materials that need targeted properties—toughness, flexibility, resistance to solvents, and more. From my work on copolymer synthesis, cyclohexene’s contribution often shows up indirectly: materials built this way stand up better to thermal cycling and environmental exposure over time.
Old hands in the lab don’t overlook storage. I remember running into trouble early in my career after an unmarked bottle of cyclohexene sat out for weeks. Peroxide tests came back positive, rendering the sample useless and prompting an unpleasant round of cleanup and reporting. Regulations aside, best practices do more than protect the environment—they also keep product quality sharp and production workflow smooth. Industry guidelines recommend limiting exposure to heat, light, and oxygen. Tight-fitting lids, dark bottles, and frequent monitoring all form part of the regular routine when cyclohexene rotates through inventory.
Transport safety deserves attention, too. Cyclohexene’s volatility means suppliers package it with clear hazard warnings, and logistics staff treat it with the respect flammables deserve. While local regulations vary, best practice is always about the same: short transit times, well-trained personnel, and secure containers minimize risk on both the small and large scale. Over time, a pattern emerges—careful handling leads to fewer incidents, lower replacement costs, and a safer workplace culture.
Educational institutions regularly choose cyclohexene for organic chemistry demonstrations. I’ve taught undergraduates on how to recognize the telltale signs of an alkene through its bromine decolorization or its reaction with potassium permanganate. Cyclohexene’s clear, predictable reactivity makes it a staple in practical exams, letting students see and feel the transformations described in class. These experiences stick with students as they enter the workforce, providing a foundation in how to handle chemicals meticulously—a skill everyone keeps refining, long after formal education ends.
A broader shift is underway in how chemical producers and users think about hydrocarbons. Even as cyclohexene remains a workhorse, companies face mounting pressure to minimize emissions, cut hazardous waste, and switch, where possible, to renewable sourcing. This is part of a larger industry reckoning—a move away from single-minded focus on price and convenience. Having sat through industry roundtables, I’ve seen how procurement officers now question suppliers about traceability and life cycle impacts, not just purity and price. Companies are adapting, upgrading environmental reporting, and investing in cleaner production routes.
Labs and startups draw inspiration from these trends, exploring biobased routes as alternatives. Success stories remain rare, but there’s a sense of optimism that with every pilot project and incremental advance, new ways to produce cyclohexene at industrial scale using green chemistry principles could become commercially viable. For now, the industry chooses the tried-and-true petrochemical sources, but no one doubts the importance of constant evolution.
Regulatory trends play an outsize role in shaping the fate of cyclohexene. International agencies keep adjusting guidelines related to air emissions, water discharges, and storage safety. In my consulting experience, facility audits often reveal gaps between management intent and shop-floor reality. Addressing these isn’t about box-ticking for auditors—it’s about safeguarding workers, communities, and ecosystems. Up-to-date training, transparent data tracking, and effective emergency response plans all go into a program that manages cyclohexene risks without slowing down the business.
On the customer side, priorities keep shifting. Product designers in the automotive, electronics, or consumer goods spaces increasingly want assurances their suppliers use responsible sourcing and take active steps on sustainability. Cyclohexene now rides into the market alongside environmental certifications and compliance reports—these matter as much to procurement as technical parameters. We’ve seen this firsthand in R&D, where teams reevaluate legacy products and processes for compliance with new stewardship norms.
Things rarely run perfectly, especially in high-throughput chemical production. I’ve had to troubleshoot process upsets linked to off-spec cyclohexene—unexpected impurities knocking reactivity out of sync or color changes revealing contamination. Each incident typically calls for close analysis: tracking back to supplier, checking batch records, or adjusting purification steps. Field experience highlights the value of building strong relationships with reliable suppliers and investing in routine in-house quality checks. Consistency in chemistry comes from vigilance, not wishful thinking.
On the research side, using cyclohexene in combination with catalytic systems often leads to puzzles that demand hands-on problem-solving. Reaction yields vary, side products tease out unknowns, and every successful outcome feels earned. Experienced chemists share what they know: start with dry solvents, keep equipment scrupulously clean, and don’t cut corners on reagent quality. While cyclohexene generally behaves predictably, surprises underline the importance of robust experimental design.
The push to modernize chemical manufacturing has reached cyclohexene. Digital tools—remote sensors, advanced data analytics, AI-driven predictive models—are now part of an operator’s everyday toolkit. I’ve watched facilities upgrade in real time, shifting from paper records to integrated digital platforms that catch process deviations and record compliance data automatically. This doesn’t erase traditional know-how so much as amplify it—providing early warnings, tighter controls, and better transparency for regulatory bodies and investors alike.
Process improvement also targets waste reduction. Engineers apply process intensification strategies to cut raw material use and lower byproduct formation. For cyclohexene, these advances mean less energy wasted as heat, tighter control over product quality, and a smaller environmental footprint. In practical terms, every improvement in yield or purity pays dividends: less waste to manage, lower cost per ton, and a smoother ride through regulatory scrutiny.
Collaboration forms another pillar of progress. Producers, researchers, downstream users, and regulators find themselves drawn into new kinds of partnerships. Trade groups now serve as platforms for sharing best practices, updating safety protocols, and moving the entire industry toward greener, safer standards. Personal experience bears this out—informal networks often play a decisive role in catching safety gaps or technical blind spots before they grow into major incidents.
Lab managers, plant engineers, and academics share their insights not just for professional credit, but to support a culture that values safety, sustainability, and innovation. That spirit plays out across conferences, training workshops, and even public communication. As cyclohexene travels through supply chains worldwide, these collaborative efforts ensure it brings more value with less risk—a lesson that applies across the spectrum of chemical products.
Cyclohexene continues to play an outsized role in the chemical industry, not so much because it shouts for attention, but because it’s useful across so many applications. From shaping the composition of everyday plastics and textiles to enabling advances in medicine and environmental technology, its legacy grows with every experiment and production run. Behind every bottle, there’s a community of chemists, engineers, technicians, and safety professionals working to adapt, innovate, and stay ahead of changing needs and higher expectations. As new technologies emerge and sustainability climbs ever higher on the agenda, the story of cyclohexene reminds us that even familiar chemicals have the capacity to surprise and evolve if the work continues—thoughtfully, responsibly, and with eyes open to the future.