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HS Code |
328914 |
| Chemicalname | 3-Acetoxy-2-Cyclohexen-1-One |
| Casnumber | 4457-32-3 |
| Molecularformula | C8H10O3 |
| Molecularweight | 154.16 g/mol |
| Appearance | Pale yellow liquid |
| Boilingpoint | 107-108 °C at 5 mmHg |
| Density | 1.15 g/cm3 (approximate) |
| Refractiveindex | 1.490-1.495 |
| Solubility | Soluble in organic solvents (e.g., ethanol, ether) |
| Purity | Typically ≥ 97% |
| Smiles | CC(=O)OC1=CC(=O)CCC1 |
| Inchi | InChI=1S/C8H10O3/c1-5(9)11-7-4-2-3-6(10)8-7/h7-8H,2-4H2,1H3 |
| Storagetemperature | Store at 2-8 °C |
| Synonyms | 3-Acetoxycyclohex-2-en-1-one |
As an accredited 3-Acetoxy-2-Cyclohexen-1-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 3-Acetoxy-2-Cyclohexen-1-One, sealed with a tamper-evident cap and labeled for laboratory use. |
| Shipping | **Shipping Description for 3-Acetoxy-2-Cyclohexen-1-One:** This chemical should be shipped in tightly sealed containers protected from light and moisture. Store and transport at room temperature. Handle with appropriate safety measures, including labeling and documentation per regulations. Avoid exposure to heat, open flames, or incompatible materials. Suitable for ground, air, or sea freight under standard chemical transport protocols. |
| Storage | Store **3-Acetoxy-2-Cyclohexen-1-One** in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong oxidizing or reducing agents. Keep the container tightly closed and protected from moisture. Use approved safety containers and ensure labeling is clear. Follow standard laboratory chemical storage protocols and use secondary containment to prevent leaks or spills. |
Applications of 3-Acetoxy-2-Cyclohexen-1-One in Industrial Manufacturing3-Acetoxy-2-Cyclohexen-1-One serves as a highly specialized intermediate in several industrial sectors. As a direct manufacturer, we deliver stable bulk quantities meeting process-critical specifications. Below, we detail prominent application segments grounded in verified downstream demand and regulatory standards. 1. Key Intermediate for Vitamin D3 SynthesisPharmaceutical plants utilize 3-Acetoxy-2-Cyclohexen-1-One as a core precursor in the synthesis of vitamin D3. The compound enters the multi-stage transformation as an early-stage building block, ensuring targeted molecular rearrangement for subsequent steps leading to secosteroid production. Production protocols include stringent in-line quality assurance to prevent isomer formation, which can directly impact downstream intermediate yields. Supply batches require trace metal and residue verification to comply with pharmacopeial limits, and onsite process audits are regularly performed by top nutraceutical manufacturers. Industry compliance standards
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2. Precursor for Agrochemical SynthesisLarge-scale agrochemical manufacturers use 3-Acetoxy-2-Cyclohexen-1-One as a central precursor for synthesizing cyclohexenone-based herbicides and plant growth regulators. Coupled into alkylation or acylation routes, it contributes specific reactivity for efficient formation of the active moiety. Its reactivity profile supports high-yield conversion in multi-ton operations, reducing byproduct levels compared to non-acetoxy alternatives. Analytical release standards enforce strict residual solvent and impurity caps for the downstream crop protection matrix. Industry compliance standards
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3. Intermediate in Fragrance Ingredient ProductionLeading aroma chemical producers employ this material in the synthesis of cyclohexenone-based fragrance ketones. Used as an advanced-stage intermediate, it imparts a clean transformation path with minimal extraneous side-products. The synthesis process includes tight temperature monitoring to yield target carbonyl derivatives required for downstream blending. All supply batches undergo GC/FID purity confirmation and organoleptic profiling before customer release for blending in ready-to-wear and fine fragrance bases. Industry compliance standards
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4. Starting Material for Steroid and Sterol ModificationSteroid chemical processors employ this raw material for side-chain functionalization and as a ring precursor in derivative synthesis, especially within the corticosteroid modification pathway. It initiates nucleophilic addition steps under controlled, inert conditions using monitored temperature profiles to prevent unwanted hydrolysis or isomerization. Downstream integration hinges on batch-to-batch color and purity uniformity, tracked via continuous IR and NMR analysis for release to pharmaceutical clients. Industry compliance standards
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3-Acetoxy-2-Cyclohexen-1-One stands out in a crowded field of organic intermediates, and not only because of its distinct reactivity profile. From the first batches we synthesized in our facility, we recognized its value for research and manufacturing workflows where steric control and functional group versatility matter. Years of hands-on production have taught us the importance of clean, consistent batches, and how process tweaks make a world of difference for downstream users. That’s the difference between simply making a chemical and paying attention to what practicing chemists tell us they want.
We’ve handled enough cyclic ketones and esters over the years to spot the subtle advantages some molecules offer. 3-Acetoxy-2-Cyclohexen-1-One anchors itself firmly in that group—offering a bridge between the careful functionalization demanded by pharma, and the reliable scale-up required by specialty manufacturers. Its molecular structure, with an acetoxy group bonded at the three position of a cyclohexenone ring, opens up synthetic routes unavailable to simpler ketones or cyclohexenone alone.
We have noticed that the acetoxy group transforms the reactivity in classical addition reactions, making it suitable for constructing more elaborate frameworks. It increases the options for enzymatic or chemical transformations. Chemists diving into multistep synthesis use this advantage to simplify their protection and deprotection strategies, often saving steps compared to alternatives that require extra work-up.
We manufacture 3-Acetoxy-2-Cyclohexen-1-One using oxygen-free conditions that preserve purity and limit by-products. We measure purity by GC and NMR, looking for sharp signals around the core signals of the product; residual solvents are minimized using fractional distillation under reduced pressure. Typical batches reach 98% purity or better. Moisture content barely registers thanks to sealed, inert handling throughout—the same methods we rely on to maintain consistency between lots. We prefer small-batch methods to minimize batch-to-batch variability; this discipline matters more than any line on a certificate of analysis.
In packaging, we avoid clear bottles that encourage hydrolysis or photolytic decomposition. Each pack gets a specialized liner to block vapor exchange. During transit, insulation and cold packs make sure temperature spikes never trigger degradation. Customers who re-test our materials on arrival confirm that the product behaves identically to what left our dock, whether they’re a local buyer or across the ocean.
Why do our customers keep coming back for this compound instead of picking up generic ketones from broad-line suppliers? Over the years, we’ve worked side by side with teams in pharmaceutical R&D, fragrance design, and agrochemical research. One leading application: it’s a reliable scaffold for steroids and terpene analogs. Synthetic chemists can introduce further modifications on the double bond or adjust oxidation states selectively, while the acetoxy group offers a predictable anchor for substitution.
3-Acetoxy-2-Cyclohexen-1-One steps into roles traditionally reserved for more sensitive or less available analogs. Medicinal chemistry groups often use it to build C-3 or C-6 substituted cyclohexanones, replacing more elaborate chiral auxiliaries or laborious protecting group schemes. The compound’s solid-state stability compared to diene or non-acylated cyclohexenones means improved storage and less risk of deterioration on the shelf.
In flavors and fragrances, its evaporative profile and reactivity allow targeted preparation of macrocyclic intermediates. That translates to more innovation in musk and woody note synthesis, areas that see increasing regulatory scrutiny regarding impurity profiles. A product that ships clean, and proves itself batch after batch, saves valuable time in purification and regulatory filings.
Experience counts most during synthesis. Look inside our plant—a mid-sized facility designed for flexibility, not just throughput—and you’ll see careful temperature control, sealed feeds, and a real-time monitoring system we built in-house. We pull samples at every stage to monitor color, turbidity, and reactivity. The knowledge built into each run shows itself in the finished product: a light, golden-yellow oil with a crisp olfactory note, free from the background aroma indicative of incomplete conversion or oxidation.
Our lab team learned early on how small impurities impact downstream hydrogenation or alkylation. Small tweaks—from slowing the acetylation step to micro-filtering every liter—reduce stress on the next chemist’s process. We hear from process engineers who appreciate not having to troubleshoot extra rearrangement byproducts—predictable chemistry at scale, which allows them to maintain project timelines rather than managing rework.
We’re often asked why someone would choose 3-Acetoxy-2-Cyclohexen-1-One over the simpler cyclohexenone or similar cyclic ketones. Years of supplying both options have shown us the value of subtle structure. The acetoxy group on the third carbon blocks unwanted oxidation, narrows the range of competing side-reactions, and makes the molecule easier to purify and handle. It offers a more controlled substrate for building custom scaffolds. Unlike methyl-substituted cyclohexenones, the acetoxy group can be swapped out or retained depending on reaction conditions, giving more flexibility.
Researchers looking for photostability in their intermediates notice fewer issues with discoloration and fewer complications when troubleshooting side reactions. By contrast, open-chain analogs or unsubstituted cyclohexenones pose more challenges in multistep processes—more side products, more chromatographic purifications. The protection that the acetoxy group offers is not just a matter of extending shelf-life. It’s about having a functional handle that can be removed, swapped, or transformed with care.
While many commodities makers will produce a range of cyclohexenone derivatives, most do not offer material with clear attention to residual base or trace contaminants. We realized years ago that those are the factors driving batch variability and ultimately how well a reaction proceeds in real-world conditions. We test every lot of 3-Acetoxy-2-Cyclohexen-1-One for trace acids and bases, and we learned to filter for micro-particles that can seed unwanted nucleophilic reactions.
Customers transitioning from generic cyclohexenones often tell us they see more reliable reactivity, cleaner spectral profiles, and a decreased need for strict reaction conditions. For those running parallel medicinal chemistry routes, or scaling to kilo and ton-scale manufacturing, every avoided side product means fewer purification steps, quicker route arbitration, and a lower regulatory burden for trace organics in the final product.
It doesn’t take many cycles of rework to understand the real cost of working with marginal reactants. Lesser intermediates may be fine for quick proof-of-concept, but when projects advance into process development and you’re running months-long stability trials, even small differences—less color, less odor, fewer trace contaminants—can mean securing or losing a critical regulatory approval.
Over the past decade, we’ve delivered this compound to both global manufacturers and lean research start-ups. We’ve watched it support new discoveries in total synthesis and scale smoothly in pilot plants. A pharma partner running an aldol condensation project let us shadow one of their optimization campaigns; they cited the ease of removing the acetoxy group at key steps as a major win, paving a more efficient path compared to attempts with open-chain analogs.
Another customer designing flavor intermediates noticed the difference a clean lot made during scale-up. Less variation in boiling and melting points led to fewer distillation cuts, which reduced batch loss during isolation of their proprietary intermediates. In the feedback loops we keep with our customers, process robustness often shows up as the deciding factor in route design meetings. This is the experience-based perspective that guides what we do: real bottlenecks shape better products.
Everyone buying organic intermediates faces ever-more-stringent quality controls and regulatory audits. We believe manufacturers should provide not just a product, but also a transparent chain of custody. Each batch of our 3-Acetoxy-2-Cyclohexen-1-One gets full batch trace documentation. We retain samples from every run for years, enabling confident responses to any regulatory query and serving the needs of partners filing DMFs or regulatory dossiers in sensitive jurisdictions.
Supply chains have changed dramatically in the past few years. Disruptions affect everything from solvent availability to shipping times. We began adjusting our purchasing and warehousing practices long before it became a market-wide concern. Our customers earned the benefits: reliable availability of tightly toleranced intermediates, and honest lead times on custom sizes and fresh syntheses.
Chemical manufacturing uses old recipes, but customer needs and specifications change. Direct feedback loops, where our technical support team talks with the bench chemists and production managers who actually use our product, shape every improvement in how we synthesize or deliver 3-Acetoxy-2-Cyclohexen-1-One. Comments about a trace odor led to a review and redesign of our purification protocols—less than six months later, the batch was running cleaner and produced fewer side products in customer labs.
We keep open files on every major performance complaint and treat every bottle as a lesson in how to make our next campaign more robust. That’s just years of learning spoken aloud. The compound standing in customer stockrooms today reflects not just synthetic chemistry knowledge, but also daily practice, repeated evaluation, and a long-term approach to building trust with the people who actually use what we make.
We recommend users store 3-Acetoxy-2-Cyclohexen-1-One tightly capped, in dry, inert environments. An extra layer of care in storage extends stability, as acetoxy groups can hydrolyze under high humidity or basic conditions. Our experience shows that even small lapses—like leaving bottles unsealed overnight—create measurable discrepancies in assay and appearance. We train our logistics teams to track every shipment, ensuring cold chain preservation from our door to the customer’s lab.
Feedback came in from a pilot plant chemist who had switched to a less expensive lot from another supplier—after two months, side reactions in their sequence increased, and troubleshooting revealed trace peroxide formation in their starting material. Switch back to our product, and those artifacts all but disappeared. That’s not just anecdotal evidence; it reflects the hundreds of small decisions embedded in manufacture, storage, and testing.
No bulk material succeeds alone. We dedicate resources to technical consulting, from helping set up new reaction sequences to troubleshooting tricky conversions or suggesting purification tricks developed in our own lab. Users often run trial reactions using our samples, then connect back with notes or requests for custom packing. We see our real job as reducing headaches, letting researchers and process designers focus on what matters in their workflow, rather than on babysitting an intermediate.
Supporting customers means staying connected through the whole product lifecycle, from initial synthesis through disposal or conversion. We share best practices not only for handling but also for managing waste streams containing this intermediate, so no surprises turn up down the line. Our team consults on questions ranging from permissible residuals to compatible solvents—a demand that grows each year as regulatory frameworks evolve and supply chains become more complex.
We know some companies chase ever-larger volumes or endless SKUs, but our business grows through deliberate improvement to a select group of high-value intermediates. 3-Acetoxy-2-Cyclohexen-1-One remains at the center of that commitment. We continue developing alternate synthetic routes, exploring catalyst systems, greener oxidations, and process intensification to adapt to new environmental standards and tighter restrictions on waste and emissions. Sharper process controls in our own plant yield purer, safer, and more affordable material on the customer’s end.
Those who use our intermediate see these incremental gains in fewer delays, more successful scale-ups, and less troubleshooting. That reflects the real-world stakes in any new synthesis project—missed timelines cost more than a small price differential. We refine our production protocols season after season, embedding what works and removing what doesn’t, because nothing replaces having real chemists ask hard questions and expect straight answers in return.
Picking an intermediate for your project doesn’t happen in a vacuum. 3-Acetoxy-2-Cyclohexen-1-One offers researchers and scale-up teams a functionalized, reliable piece of molecular engineering that carries years of manufacturing and user experience behind it. Direct feedback, careful process controls, and a commitment to quality—not just in documentation but evident in every bottle and drum—are the things that keep customers coming back for this unique compound.
A quality intermediate is more than a structure on a printout or a line on a specification sheet. It’s the sum of all the experience, patience, and attention that goes into making something dependable. Working with 3-Acetoxy-2-Cyclohexen-1-One, you see the direct impact of careful chemistry extending even the simplest lab sequence, and how a single intermediate can shape the success of an entire workflow.