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HS Code |
907184 |
| Chemical Name | Ethyl 4-Oxocyclohexanecarboxylate |
| Cas Number | 18665-80-6 |
| Molecular Formula | C9H14O3 |
| Molecular Weight | 170.21 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 120-122°C at 10 mmHg |
| Density | 1.106 g/cm³ |
| Melting Point | -23°C |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically ≥ 98% |
| Refractive Index | 1.465-1.475 |
| Smiles | CCOC(=O)C1CCC(=O)CC1 |
| Synonyms | Ethyl 4-oxocyclohexanecarboxylate; Ethyl 4-oxocyclohexane-1-carboxylate |
| Storage Temperature | Store at 2-8°C |
| Flash Point | 97°C |
As an accredited Ethyl 4-Oxocyclohexanecarboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Ethyl 4-Oxocyclohexanecarboxylate is supplied in a 50g amber glass bottle with a secure screw cap and clear labeling. |
| Shipping | Ethyl 4-Oxocyclohexanecarboxylate is shipped in tightly sealed containers, protected from moisture and light. It should be transported according to local regulations for chemicals, using appropriate labeling. Ensure the package is upright, secure, and stored at ambient temperature. Handle with care to prevent leaks or spills during transit. |
| Storage | Store **Ethyl 4-Oxocyclohexanecarboxylate** in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition and direct sunlight. Keep away from incompatible substances such as strong oxidizers and acids. Ensure appropriate labeling and access to spill containment materials. Use in a chemical fume hood, and observe standard laboratory safety practices during handling and storage. |
Applications of Ethyl 4-Oxocyclohexanecarboxylate in Industrial ManufacturingEthyl 4-Oxocyclohexanecarboxylate offers defined functional groups suitable for precise intermediate synthesis in several specialty chemical sectors. As a direct manufacturer, we support B2B customers with tailored options for integrative process performance, regulatory needs, and reliable supply. 1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient ProductionPharmaceutical manufacturers employ Ethyl 4-Oxocyclohexanecarboxylate as a key ring-structured intermediate in the multi-stage synthesis of APIs, targeting specific corticosteroids and anti-inflammatory agents. Its ketone and ester dual functionality enables efficient subsequent transformations, such as selective hydrogenation, hydrolysis, and alkylation. Controlled use supports batch reproducibility and traceability in regulated drug manufacturing environments that require stringent documentation and impurity management across all process steps. Industry compliance standards
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2. Agrochemical Synthesis of Herbicide and Insecticide IntermediatesAgrochemical firms utilize this raw material as a core building block in heterocyclic ring systems essential for certain herbicide and insecticide molecules. Its reactivity and purity support consistent yields in industrial-scale acylation and amination processes. The compound's compatibility with green chemistry protocols enables process optimization for regulatory compliance, particularly regarding residual solvent and trace impurity control in multi-step crop protection agent synthesis. Industry compliance standards
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3. Fragrance and Flavor Synthesis for Fine ChemicalsThe compound enters advanced manufacturing lines for high-value aroma chemicals, particularly those involving cyclic ketone and ester functionalities to impart woody, musky, or camphoraceous notes. Specialty fragrance houses and flavor ingredient suppliers rely on its stability during multi-step transformations, which may include Baeyer–Villiger oxidation, reductive amination, or customized transesterification. Raw material provenance and lot traceability remain essential to downstream auditing and customer acceptance. Industry compliance standards
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4. Polymerization Precursor in High-Performance Coating ResinsProducers of high-performance coating and adhesive resins incorporate Ethyl 4-Oxocyclohexanecarboxylate as a specialty monomer or chain-modifying agent within polyester and polyacrylate resin systems. Chemical characteristics facilitate specific molecular weight distribution, cross-linking density, and flexibility tuning during bulk or solution polymerization. Strict control of raw material purity and feed stability matters for ensuring reproducible physicochemical profiles of final coatings, especially in automotive and electronics applications. Industry compliance standards
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5. Synthesis of Imaging and Diagnostic ChemicalsSpecialty producers in the diagnostic imaging industry use this compound as a cyclohexanone precursor for synthesizing functional chelating agents and labeled small molecule probes. Its defined reactivity profile serves molecular design in radio-labeled ligand preparation, MRI contrast agent precursors, and other bioactive imaging substances. Material qualification processes demand verification against rigorous analytical specifications and trace GE (Good Engineering) and documentation standards. Industry compliance standards
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Our years in chemical production have given us a front-row view of what drives demand and shapes trust in fine intermediates like Ethyl 4-Oxocyclohexanecarboxylate. Our teams don’t just operate reactors and distillation columns — we also keep a close eye on how inventive chemists in pharmaceutical, agrochemical, and fragrance sectors push the boundaries of synthetic design. Every batch of this specialty ester reflects a belief that start-to-finish stewardship brings value beyond a catalog listing.
This compound has found a clear place in several synthesis routes that require a balance of stability and reactive functionality. From our work supporting pilot to commercial-scale programs, experience has shown that reliable, reproducible crystallinity and pure output are indispensable. Customers have shared how subtle differences in impurity profiles can make or break complex heterocycle assembly, which is why every production run is closely monitored for both major and trace components.
Ethyl 4-Oxocyclohexanecarboxylate’s six-membered core and its ethoxycarbonyl and oxo substituents lend the molecule unique utility. The keto functionality, positioned on a cyclohexane ring, sets it apart from simpler esters or cyclohexanone derivatives. In our current processes, the final product emerges as a clear to pale yellow liquid, often crystallizing on standing. Typical GC purity exceeds 98% as measured by our in-house validated methods. Water content is controlled to under 0.5% by Karl Fischer titration, built on the fact that water traces can make downstream reductions sluggish or unpredictable.
One of the recurring topics in process meetings deals with byproducts unique to the material’s own synthetic pathway. The potential presence of cyclohexanecarboxylic acid or residual ethyl esters of off-target cyclohexanones can impact users. Our approach has grown from years of hands-on troubleshooting — from solvent selection that discourages transesterification, to distillation strategies tuned for the physical properties of structurally related impurities. This focus comes directly from responding to researchers who flagged that earlier supplier offerings showed drifting assay results over months in storage.
Customers often ask about storage and handling, since esters can sometimes hydrolyze or slowly degrade. Based on our ongoing stability assessments, the compound keeps its integrity for months stored sealed at room temperature, away from sunlight and moisture. Container selection matters; we avoid ultra-reactive plastics in favor of glass and select fluoropolymer liners for metal drums. There’s always an urge in plant operations to push bigger volumes through quickly, but fielding calls about minor cloudiness or unexpected color shifts has shown us that attention during packaging pays dividends for both us and our clients.
Chemists working with Ethyl 4-Oxocyclohexanecarboxylate see it as a versatile node in building targets with functional group diversity. We’ve seen the ester group harnessed for controlled hydrolyses, transesterification, or reduction to alcohols depending on the needs of the next step. The ring ketone is another anchor point: from alkylations and condensations to reductions, its reactivity profile enables smooth formation of intermediates central to antihypertensives, CNS therapeutics, and some anti-infectives.
Development scientists often ask about its performance in comparison to methyl esters, especially in ring expansion or contraction steps. Drawing on dozens of reactions run in our own pilot lab, the ethyl ester behaves with less volatility and greater resistance to accidental hydrolysis under neutral or mildly acidic conditions. That subtle difference can save time on rework, particularly for larger-scale preparations or where the length of the alkoxy side chain plays into solubility and purification downstream.
On the aromatic side, cyclohexanone derivatives with their beta-keto esters may offer other advantages, but ethyl 4-oxocyclohexanecarboxylate strikes a middle ground between stability and lability. Our site’s application chemists have fielded requests for custom analogues with methyl, propyl, or tert-butyl esters; after numerous rounds of bench testing, ethyl falls into a proven window of cost-effectiveness and synthetic flexibility.
Several partners in the pharma and agrochemical space use this intermediate as an entry point to more heavily functionalized small rings or bicyclic cores. The controlled reactivity under both basic and acidic conditions plays into cross-coupling, Michael addition, and other fragment construction approaches. Our production operators find that precise control during the oxidation and esterification stages determines how much finishing work, like flash chromatography or recrystallization, the client downstream needs to perform.
Users working at gram-to-kilogram scale appreciate batch reports that go beyond a typical COA. One long-time partner once described spending weeks chasing down the source of a persistent unknown peak, which eventually linked back to poor solvent stripping in an earlier process version. Closing that loop with direct communication saved them at least a month of analytical time.
Having our hands on the actual reactors and QA samples gives us a clear edge over trading operations. We don’t have to depend on secondhand information or hope that a middleman noticed subtle errors. Instead, we watch parameters like oxygen content, pressure profiles, and exact solvent ratios in real time, which lets us course-correct before minor deviations impact the final product.
This level of oversight also means that spec adjustments or custom requests can be handled rapidly. A client exploring asymmetric reductions once asked for extra material with a tighter-than-standard enantiomeric excess. Using our own chiral columns and reference standards, we delivered a batch to meet that challenge without the inflexibility of mass-market supply chains. As direct manufacturers, we maintain records back to the first kilogram produced. This traceability lets partners review not just the current assay and moisture, but also the batch’s elemental analysis, spectral signatures, and observations during crystallization — things distributors seldom have access to, yet matter a great deal to scientists troubleshooting synthetic sequences.
The experience built from both successes and setbacks along the production line leads to incremental improvements. If an issue cropped up because a crystallizer was run too cold, or if a particular filtration medium reduced yield, those lessons stay in-house and affect every subsequent batch. Revisiting customer feedback, we’ve altered how we neutralize and wash, which reduced odors and off-residue in the final products.
We field calls about analytical support, too. A project manager recently described an upstream impurity showing up at 0.2% by GC-MS, only to discover — with help from archived batch data — that certain column settings during in-process purification influenced the residue profile. By handling everything from extraction to final filtration in house, we offer not just material, but also deep-rooted process data and analytical confidence.
Experience with many ketonic esters makes clear that Ethyl 4-Oxocyclohexanecarboxylate sits in a class of its own for a few reasons. Its relatively non-aromatic, flexible ring core enables hydrogenation, reduction, and cross-coupling steps that aromatic or highly substituted rings tend to resist. Chemists value the direct, controllable reactivity of the mono-keto position, which allows for predictable condensation, alkylation, or reduction outcomes.
Unlike 4-oxocyclohexanecarboxylic acid or methyl analogues, the ethyl ester’s solubility profile supports a broader range of solvents. This reduces the number of extractions or work-ups needed after each transformation. Having produced both methyl and ethyl versions in parallel, our teams have seen appreciably greater batch yields and lower loss during purification of the ethyl compound, especially at pilot scale. The volatility and hydrolysis resistance also reveal themselves during routine vacuum stripping, as product loss is noticeably lower.
For those exploring structure-activity relationships, switching from ethyl to longer-chain esters offers diminishing returns — added bulk rarely compensates for reduced rate of hydrolysis or increased handling challenges. Over several campaigns, we’ve observed that customers who started with less common alkyl esters usually circle back to the ethyl variety once they weigh cost, process flexibility, and consistency.
Differences extend beyond the chemistry into regulatory and quality expectations. Project managers often request non-GMO, allergen-free, or heavy metal-tested batches. Our constant monitoring and in-house microchemical checks let us guarantee compliance to evolving regulations, with certification records on hand for audit or submission. The machinery, audits, and workflows have been built up with direct client collaboration, not aimed at warehouses, but true production lines.
Our on-site process chemists have worked elbow-to-elbow with customers during the crucial months of moving from bench to pilot plant. Reproducibility turns abstract quality claims into actual manufacturing success. In one case, a customer moving to multi-kilogram scale noticed increased byproduct formation. They shipped samples to us for cross-analysis, and our team pinpointed a heating rate discrepancy due to scale-related insulation differences. We fed that correction back in real time. Working this way, we bridge the gap between knowledge and industrial reality.
Process development in drug and crop-protection research rarely moves in a straight line. With our ground-level access to both material and data, we’ve been able to tweak several production variables at customer request. Whether it meant reformulating a solvent system, switching to an alternative drying technique, or validating stability under accelerated aging, the knowledge we’ve gathered has trimmed project timelines and cut excess analytical legwork.
Large-scale pharmaceutical clients often need parallel stability, stress, or compatibility data. Having our QC labs just steps from the plant floor, we generate real-time, actionable trend analysis that translates directly into specification refinements. Instead of weeks lost to repeated external testing, our own scientists adjust on the fly, sending updated methods or new analytical packages without red tape.
Someone new to chemical sourcing might see Ethyl 4-Oxocyclohexanecarboxylate as just another reagent. Yet, years in the field have shown how product consistency, responsiveness, and hard-won process knowledge set direct manufacturers apart. Many customers have told us how a single batch flaw, or a factory that can’t trace a spectral anomaly, can disrupt entire medicinal or process chemistry timelines. Our integrated management of production, quality, and documentation continues to raise standards far beyond what simple traders deliver.
Feedback channels keep us keenly aware of not only what goes right, but also what customers genuinely need. We tweak our specifications and packaging based on explicit usage data: clarity on viscosity, particle size, and shelf-stability doesn’t just fill a datasheet — it reduces manufacturing headaches.
Ongoing R&D invests in process intensification, green chemistry alternatives, and waste minimization, often spurred by direct client initiatives. By running in-house analytical development alongside process improvement, changes are implemented with an eye on both regulatory compliance and consistency.
Our journey manufacturing Ethyl 4-Oxocyclohexanecarboxylate reflects a commitment to detail. Every kilogram shipped owes its character to incremental changes tested and proven on the factory floor, not in abstract strategy meetings. From bespoke purification tweaks, to quick pivots for nonstandard analytical requests, delivering on time and to promise has built our reputation one batch at a time.
We keep lines of communication open with every customer. If issues with downstream performance pop up, our production and development teams are ready to collaborate, drawing from our database of method tweaks and past project records. The practical knowledge born of solving air-sensitive runs, or troubleshooting pump compatibility, helps us anticipate — and head off — the kind of problems that cost weeks or months for formulation chemists.
This product isn’t just another molecule in a supply catalog. It connects our process engineers, QC specialists, and end-user chemists in a network of problems solved and insights shared. Through every run, every analysis, and every shared customer win, the story of Ethyl 4-Oxocyclohexanecarboxylate continues to prove that what happens in actual manufacturing matters more than any generic specification or supply claim. Our goal remains unchanged: to back our partners’ ambitions with the solid, real-world support only a direct, accountable manufacturer can provide.