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HS Code |
590730 |
| Chemical Name | 2-(1-Cyclohexenyl)Cyclohexanone |
| Molecular Formula | C12H18O |
| Molecular Weight | 178.27 g/mol |
| Cas Number | 4439-35-8 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 303-306 °C |
| Melting Point | N/A (liquid at room temperature) |
| Density | 0.990 g/cm³ (approximate) |
| Refractive Index | 1.517 (at 20 °C) |
| Flash Point | 126 °C |
| Solubility In Water | Insoluble |
| Purity | Typically ≥ 98% |
| Storage Conditions | Store in a cool, dry, and well-ventilated place |
As an accredited 2-(1-Cyclohexenyl)Cyclohexanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100g, sealed with a screw cap; labeled with product name, chemical formula, hazard warnings, and supplier details. |
| Shipping | 2-(1-Cyclohexenyl)cyclohexanone is typically shipped in tightly sealed, chemical-resistant containers to prevent exposure to air and moisture. Transport is conducted in compliance with local regulations for non-flammable, low-toxicity chemicals. Proper labeling and documentation ensure safe handling, with precautions taken to avoid extreme temperatures, physical damage, and contamination during transit. |
| Storage | 2-(1-Cyclohexenyl)cyclohexanone should be stored in a tightly sealed container, away from moisture, direct sunlight, and sources of ignition. Keep the storage area cool, dry, and well-ventilated. Store separately from strong oxidizers and acids. Use proper chemical storage cabinets that are clearly labeled and compatible with organic chemicals to minimize the risk of accidental reactions or spills. |
Applications of 2-(1-Cyclohexenyl)Cyclohexanone in Industrial Manufacturing2-(1-Cyclohexenyl)Cyclohexanone serves as a critical intermediate in multiple downstream industrial processes due to its unique bicyclic structure and reactivity profile. As the primary manufacturer, we supply this compound in quantities optimized for large-scale chemical synthesis and formulation. Our material supports high-performance requirements across distinct chemical sectors, each with specific technical, regulatory, and quality standards. Below we outline key application scenarios with detailed information on compliance, integration, and dosage control. 1. Synthesis of Advanced Fragrance Ingredients for Fine ChemicalsThis compound finds substantial demand in the fragrance industry, particularly as a precursor in the synthesis of macrocyclic musks and polycyclic musk intermediates. Large flavor and fragrance manufacturers exploit its reactivity in Grignard-type reactions, resulting in advanced macrocyclic ketones used for creating high-stability fragrance notes in perfumes and premium consumer products. Procurement teams prioritize traceable batch quality and consistent physical profile to meet product development requirements. Industry compliance standards
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2. Agrochemical Synthesis—Key Intermediate for Cyclic Ketone HerbicidesAgrochemical producers employ the material in the production of cyclic ketone-based herbicides, where it undergoes selective functionalization to introduce activity-enhancing substituents. This route allows for the development of novel herbicidal molecules that target resistant weed species. Technical process teams focus on maintaining strict in-process analytical control to meet impurity thresholds mandated by agrochemical regulations. Industry compliance standards
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3. High-Performance Polymer Modifier for Specialty CoatingsManufacturers of advanced coating resins use this raw material as a ring-structuring monomer to impart rigidity and improved solvent resistance in specialty polymer chains. Its incorporation modifies the glass transition temperature and enhances the scratch-resistance of coatings applied to automotive plastics and electronic housings. Application technicians monitor batch mixing parameters to retain uniformity and homogeneity throughout the resin matrix. Industry compliance standards
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4. Pharmaceutical Intermediate in API Synthesis—Steroidal and Nonsteroidal StructuresIn pharmaceutical manufacturing, this compound acts as a scaffold in the synthesis of complex steroidal and nonsteroidal API structures. Medicinal chemists integrate it into multi-step reaction pathways to construct key carbon frameworks, particularly where the bicyclic skeleton confers biological compatibility and metabolic stability. Manufacturing teams refine purification steps in line with cGMP and ICH guidelines to achieve regulatory batch release. Industry compliance standards
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5. Precursor for Advanced Adiponitrile and Diamine Production in Nylon SynthesisNylon manufacturers utilize the compound as a precursor for producing specialty cyclic diamines and adiponitrile derivatives that serve as chain extenders in high-grade polyamide production. Technical teams emphasize feed purity to maximize conversion rates and achieve targeted mechanical and thermal properties in the resulting polymers. In-line QA systems verify intermediate concentrations and ensure consistent polymerization outcomes on commercial scales. Industry compliance standards
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In our production workshops, everything comes down to what happens in the reactor. On the morning shift, we often talk over coffee about the pressure settings, the temperature range, and the faint but unmistakable scent of new intermediates in the air. Compounds like 2-(1-Cyclohexenyl)Cyclohexanone matter to us, not because they boast a catchy profile for marketing, but because they represent the sort of reliable building blocks that drive complex industrial synthesis forward.
2-(1-Cyclohexenyl)Cyclohexanone falls under the family of cyclic ketones with a nuanced structure: two cyclohexane rings joined through an enone bridge. We produce it in batches that meet the demands of both pilot and industrial volumes. Each batch is analyzed with gas chromatography, and we keep a close eye on the purity—it cannot fall short, because color and yield both respond to even minor impurities. The product presents itself as a solid white material or pale yellow, depending on process variables and batch age. Melting point sits in a narrow window, bridging the requirements of manufacturers crafting high-end intermediates.
Over the years, we have invested steadily in both closed sampling and nitrogen protection. This compound benefits from handling in equipment set up to limit oxygen contact; even minor oxidation alters both reactivity and odor. The product demands stainless steel, not glass-lined kettles, for maximum yield on cyclization and minimum fouling. Transport uses drums that survived our own drop tests on the plant road. Any off-gassing or unusual pressure inside these drums gets checked before outgoing shipments leave the yard.
In our direct work with research innovators and bulk-process organizations, we’ve seen requirements for 2-(1-Cyclohexenyl)Cyclohexanone come from surprising avenues. The pharmaceutical sector leans on this compound because of its ability to build up bicyclic scaffolds, which often reappear in drug candidates targeting neural receptors. Agrochemical developers, on the other hand, appreciate the clean transformation possible from this ketone for a range of macrocyclic intermediates. Flavor and fragrance customers, fewer in number but exacting in specification, bring different knowledge to the table. They judge this chemical not just by analysis, but by how it performs under catalytic hydrogenation or further cyclization steps, which can shift subtle profiles of aroma molecules.
From our vantage point, these end uses demand a nimble production ethos. It’s not enough to only offer high purity. Consistency between lots, transparency on impurity profiles, and a willingness to support scale-up all matter equally. Real-world production does not always match textbook yields. The compound’s reactivity means no two continuous runs are exactly identical. We have seen certain downstream users request tailored particle size or even specified chiral purity, although for most applications, the racemate suffices.
Operators who have handled both monocyclic ketones—say, cyclohexanone—or fused-ring analogues, like decahydronaphthalenones, know the difference. 2-(1-Cyclohexenyl)Cyclohexanone brings physical and chemical distinctions to a synthesis line. It resists hydrolysis more than α,β-unsaturated monocyclic analogues, yet remains open to hydrogenation and functionalization. Compared to other diketones, our product offers excellent chemical selectivity for Michael additions, especially under mild base or acid conditions. Many high-throughput screens favor this substrate when other options give too many side-products or require post-purification.
On the physical side, our batch samples deliver a melting point that provides just enough flexibility for downstream operations. Too low, and the melt complicates crystallization. Too high, and you risk incomplete dissolution for reaction or transfer. Chemists in both pharma and specialty chemical companies mention this cardinal feature as easing the transition from kilogram-scale up to multi-ton campaigns.
Scaling up 2-(1-Cyclohexenyl)Cyclohexanone meant focusing on several process levers that don’t turn up in the published literature. We start with cyclohexanone feeds passed through in-line filtration, because upstream contamination leads to pronounced batch-to-batch inconsistency. Our hydrogenation catalyst formulation took months to refine; standard catalysts gave too much over-reduction, or degraded with extended runs. We kept pilot reactors online across three seasons to chart how ambient humidity and supply chain variability altered key quality indexes.
Engineers in the plant learned not to trust automation for every process control parameter. Human adjustment at critical timepoints—adding sodium hydride or adjusting rate of nitrogen sparge—often makes the difference on endpoint color and side product thresholds. The difference between a 98% and a 99.5% GC result always traces back to these “on the ground” choices. It forms the backbone of the reliability that end users note, only ever after the third or fourth resupply.
Customers do not just want a spec sheet and a shipping notice. Their chemists dial direct, and they ask questions: will the compound persist through a strong acid wash? Will minor diene side-products form in a Grignard setup? We built our answers not just by reading, but by keeping close to pilot line data and internal application testing. Samples sent out to partners return with notes and questions, and these results fold back into our process revisions.
A few years ago, a client struggled with a competitive product, reporting fouling in a continuous flow Diels-Alder process followed by slow clogging of in-line filters. We sent not only a new sample, but a technical operator who had grappled with similar filtration on a winter overnight shift. The result wound up an improvement not only for one customer’s yield, but for our own drum filling process, now equipped with new mesh grades.
Agrochemical partners cited oxygen-sensitivity concerns in extended storage. We changed our fill line from broad-head to lidded nozzles and reduced oxygen content in drums below 0.5%, using real-time headspace analysis. These fixes demanded investment and retraining, but paid off in shelf-life improvements noted by all buyers.
We keep safe handling at the center of shop floor operations. This material releases a low threshold amount of vapor if exposed to open air for more than a minute, especially at temperatures over 25°C. We do not just rely on ventilators—each loading station includes active vapor monitors and immediate access to PPE. All operators train with spill simulation kits, because we learned early that a messy transfer sets production back hours.
Waste solvent recovery receives direct attention from our process engineers. Fractional distillation units recover both process solvents and allow us to concentrate this compound for reuse or energy recovery, depending on purity after each run. Spent catalyst finds its way to certified recovery channels. Plant management measures success with monthly solvent-loss reports—each percentage point matters.
We implemented feedback loops with local environmental agencies years ago, tracking process effluents downstream of our quench tanks. Whenever we saw a jump in organic content, root-cause analysis traced back to poorly timed venting or insufficient condensation in scrubbers. This compound responds to minor operational lapses, but lessons learned at bench scale now guide our standard operating procedures.
Our product line did not expand overnight. The first time we shipped this compound, the color spec was too broad, and we overestimated its stability in standard HDPE drums during summer heatwaves. Several drums bulged or sweated at the seams, prompting a switch to coated steel and a change in storage advisories sent out with shipment documentation. Through each round of customer complaints and improved process trials, we put lessons into product design.
Smart automation now helps with dosing and maintenance on the process lines, but we lean heavily on informal check-ins among the plant staff. Standard management feedback comes after reviewing not just lab data but feedback from crew members, who spot leaks, unusual odors, or minor process hitches before tech logs even update. Our best process refinements owe everything to this hands-on tradition—an unending cycle of problem, fix, result, and new learning.
We push process innovation by adopting kinetic studies, in-line IR and NMR monitoring, and catalyst screening. Every yield increase comes from understanding not just the chemistry, but movements and decisions made by technicians on the ground. When side-product levels spiked in high-humidity months, a suggestion from a floor supervisor about pre-conditioning raw material lots ended up as a permanent change. Each iterative fix translates into a record of reliability end-users trust.
We have walked shop floors in client facilities dry-running synthesis steps, observing first-hand how this ketone blends, separates, or reacts. In pharma synthesis, the reaction to form bicyclic aminoalcohols using this compound follows a roadmap built on process patience—slow addition, careful pH control, and prompt, cold filtration. The quality of our material means operators skip extra purification, shaving days off project timelines. For specialty coatings producers using 2-(1-Cyclohexenyl)Cyclohexanone as a reactive oxygen barrier, shelf tests show strong performance even after six months, tracked with ambient and accelerated aging.
Some customers deploy our material as a reactant in photoinitiator synthesis. Here, trace impurities common to small-lot or resold product lines set off color drift or loss of photo-reactivity downstream. Our direct synthesis model, controlled logistics, and filtered storage prevent many of these quality headaches. These differences are not about cost; they cut time to project completion and unlock production economies for downstream lines.
Teams in fine chemical manufacturing noted the product’s resilience to secondary amine or thiol addition, key steps in both pharma active ingredient manufacture and electronics precursor production. These findings did not just emerge from theory—a group of process chemists worked several weekends in our pilot plant with analytical support onsite to characterize product formation and stability. Any small change in peroxide content or process water traceability found its way into both our formulations and shipment justification paperwork.
Years back, a run of inconsistent batches revealed flaws in our process mapping. We caught the problem only after a week of elevated off-color complaints from multiple buyers, each one reliant on our material for separate market sectors. The source: a shipment of under-spec raw cyclohexanone, which passed minimum checks but failed to deliver at performance levels needed for consistent hydrogenation. From that point, we tightened collaborative controls not just inside the plant, but with upstream partners, building raw material audits and data-sharing into procurement contracts.
Occasionally, end-users still push back on trace levels of non-target ketones, especially on sensitive synthesis lines. We maintain transparency and prioritize batch-specific certification, always tracing anomalies back to their process step. We also conduct on-site visits and virtual troubleshooting, which sometimes reveals factors as mundane as pump lubricant contamination or allowance of direct sunlight during storage.
We watch market demand and R&D trends closely, both through direct order flow and participation in technical think-tanks. The success of 2-(1-Cyclohexenyl)Cyclohexanone aligns with broader moves in drug discovery, agricultural yield improvement, and sustainable aromatic synthesis. This synchrony lets us allocate resources—whether to pilot new process technology, upgrade containment, or trial new stabilizer additives. Our approach grows from the ground up, with every change justified by field experience and operational data, not abstract promise.
2-(1-Cyclohexenyl)Cyclohexanone functions as a backbone for countless molecular constructs. The sort of reliability demanded by markets—whether in pharma, agro, flavor, or specialty synthesis—rests on choices made at production, not just testing. Every operator and technical lead in our plant brings real, continual learning to the table. We stay ready to adapt as end-users and global trends shift. That’s the certainty we bank on as chemical manufacturers dedicated not to flashy promises, but to performance that endures shipment, synthesis, and final formulation.