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HS Code |
960695 |
| Cas Number | 53916-08-0 |
| Molecular Formula | C10H16O4 |
| Molecular Weight | 200.23 g/mol |
| Iupac Name | ethyl 4-acetyl-5-oxohexanoate |
| Appearance | Colorless to pale yellow liquid |
| Solubility | Soluble in organic solvents |
| Smiles | CCOC(=O)CCC(=O)CC(=O)C |
| Inchi | InChI=1S/C10H16O4/c1-3-14-10(13)5-4-9(12)7-8(2)11/h3-5,7H2,1-2H3 |
| Pubchem Cid | 3715861 |
| Storage Temperature | Store at 2-8°C |
| Synonyms | Ethyl 4-acetyl-5-oxohexanoate; Ethyl 5-oxo-4-acetylhexanoate |
As an accredited Ethyl 4-Acetyl-5-Oxohexanoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The product is supplied in a 25g amber glass bottle, sealed with a screw cap and labeled “Ethyl 4-Acetyl-5-Oxohexanoate, 25g.” |
| Shipping | **Shipping Description:** Ethyl 4-Acetyl-5-Oxohexanoate is shipped in tightly sealed containers, protected from moisture and direct sunlight. Transport is conducted in compliance with local and international regulations for hazardous chemicals. Appropriate labeling and documentation accompany each shipment to ensure safe and secure handling during transit. Avoid exposure to heat and ignition sources. |
| Storage | **Ethyl 4-acetyl-5-oxohexanoate** should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from heat, direct sunlight, and sources of ignition. Keep it separated from incompatible substances like strong oxidizers and acids. Store under an inert atmosphere (e.g., nitrogen) if recommended, and always follow local regulations and the manufacturer's guidelines for safe chemical storage. |
Applications of Ethyl 4-Acetyl-5-Oxohexanoate in Industrial ManufacturingEthyl 4-Acetyl-5-Oxohexanoate serves as a key synthetic intermediate in multiple chemical production sectors. As an original material manufacturer, we support downstream partners with high-purity batches, analytical documentation, and technical support tailored to application-specific production requirements. 1. Pharmaceutical Intermediate for β-Keto Ester API SynthesisMajor pharmaceutical companies use Ethyl 4-Acetyl-5-Oxohexanoate as a central β-keto ester intermediate during the multi-step synthesis of certain active pharmaceutical ingredients, including those in anti-inflammatory and antidiabetic medication classes. It supports controlled enolate reactions and subsequent heterocyclic integrations within strict GMP environments. Industry compliance standards
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2. Agrochemical Synthesis for Herbicidal Active Ingredient ManufacturingLeading agrochemical producers apply this raw material in the targeted synthesis of heterocyclic and β-keto herbicidal compounds. Its stable ketone structure allows for high-yield enolate alkylation and ester condensation reactions, which are foundational steps for building modern crop protection products that must meet regional residue regulations. Industry compliance standards
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3. Fragrance Intermediate in Fine Chemical Perfumery SynthesisSpecialty aromatic chemical manufacturers utilize Ethyl 4-Acetyl-5-Oxohexanoate as an intermediate for the creation of musk-type and fruity esters. Its controlled reactivity allows for precise acetylation and chain elongation, central to synthesizing aroma compounds that conform to IFRA standards for global fragrance applications. Industry compliance standards
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4. Specialty Polymer Modifier for Resin and Coating FormulationsManufacturers of polyester and alkyd resins integrate this compound to introduce controlled ketoester branching and crosslinking points. Its structure supports precise molecular weight management and improves the flexibility and adhesion of industrial coatings and advanced polymer systems. Industry compliance standards
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5. Fine Chemical Building Block for Advanced Organic SynthesisContract chemical manufacturers and R&D centers employ this material for constructing complex β-dicarbonyl frameworks in targeted custom molecule development. The compound’s dual carbonyl positions and chain length enable synthesis pathways for research-only, non-commercial advanced intermediates and specialty molecules validated under ISO and local chemical handling regulations. Industry compliance standards
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Years of running reactors and columns have taught us a few things about what it takes to make a consistent batch of Ethyl 4-Acetyl-5-Oxohexanoate. It’s not a common topic over lunch but it’s one of those specialty esters that can sit quietly behind the scenes in fragrance intermediates, fine chemicals, and research. From our perspective as the manufacturer, we don’t see it as just another barcode in the warehouse. We think about the raw material purity, the way temperature profiles affect yields, and the equipment’s long-term wear when you crank out hundreds of kilos at a time.
In our factory, Ethyl 4-Acetyl-5-Oxohexanoate typically goes out under the model: EA5OX. We produce lots from a few kilograms per drum up to multi-ton lots, always batch stamped for full traceability. The molecular formula, C10H16O4, and a clear to slightly yellow liquid look simple at a glance. Every batch gets a GC purity profile over 98%, moisture measured by Karl Fischer, and a careful check on residual starting materials. Over the years, we tweaked catalyst loads, solvent choices, and distillation settings to get tighter specifications. A small run for lab-scale research demands different attention compared to the heavy drums that leave our loading dock for industrial customers.
As a building block, Ethyl 4-Acetyl-5-Oxohexanoate plays an important role in the toolkit of an organic chemist. For the larger clients, our product usually moves on to become a precursor in pharmaceutical synthesis, and we see it find use in agrochemical research. Some customers chase complex heterocycles, others tweak fragrance notes – all relying on purity and consistency. Fragment coupling in drug candidates benefits from the stable carbonyl and ester groups in the molecule. In many fine chemical programs, control over trace byproducts and batch-to-batch variation makes a visible difference for downstream steps. Several partners send their own analytical staff for joint QC, which works best when there’s real transparency between chemist and producer.
It’s easy to line up catalog entries for esters, but experience in actual manufacturing tells a different story. We have worked to bring down the level of aldehydic impurities, which can poison further reactions. In the beginning, lots sometimes showed yellow tints or faint side odors that complicated downstream use; feedback from early adopters pushed us to tweak finishing steps. Some buyers ask about solvent residues because even minor traces can trigger problems under catalytic hydrogenation. To address this, we made sure each batch goes through longer vacuum stripping and tighter analytical control before shipment.
Our team has seen the trade-offs between running faster or optimizing recovery. Sometimes it’s tempting to raise throughput to satisfy a rush order, but we found that pushing the process beyond certain limits invites headaches. Unreacted acetoacetic ester or unconverted starting material can show up on the GC if pressure or temperature swings too far. We’ve paid the price of learning these lessons over years and now build extra checkpoints into every release.
Customers sometimes ask why our Ethyl 4-Acetyl-5-Oxohexanoate looks or behaves differently compared to a competitor’s. Some offer a lower price, but the product might arrive with haze, higher acid number, or surprising headspace impurities. After years of troubleshooting reactions with clients, we see how minor contaminants can sabotage expensive syntheses. We focus on cutting these at the source. We deliberately avoid a one-size-fits-all approach — small-scale synthetic needs are not just a scaled-down version of industrial campaigns.
Comparing our version to other esters like ethyl acetoacetate or methyl levulinate, the unique substitution at the fourth and fifth carbons brings a distinctive value. The extra acetyl group adds flexibility in the hands of a chemist aiming to build complexity with fewer steps. Many customers have tried substituting with other chain-length esters, but experience has shown those swaps often lead to reduced yields or tricky side reactions. We’ve worked with universities and industrial labs chasing structure-activity relationships and have seen firsthand, in gram and ton batches, how reliable product identity impacts progress.
Grasping the full value of Ethyl 4-Acetyl-5-Oxohexanoate means looking past specs on a PDF. The effort starts before the first kilogram emerges from the reactor. We track temperature ramps tightly since overheating near the acetylation step accelerates side-product formation. Process operators run through a dozen checkpoints from charge to finish, understanding well that a single out-of-spec drum can ripple through downstream value chains. In scale-up, we tune mixing and agitation speeds to hit exact phase separations, which can look trivial but decide if your batch will pass QA.
Incoming raw material testing, routine calibration for in-process probes, and stubborn attention to off-odors or discoloration distinguish a well-made product from one riding on chance. It’s not unusual for a batch to pass conventional tests but show haze or mild off-notes; we have learned to trust operator instincts alongside lab numbers. Several staff can recall times when an unusual shift in GC pattern caught a near-miss before the batch went downstream. These experiences give us a different perspective than reading from a standard product sheet.
Conversations with formulation chemists tell us new ways our product fits into their workflow. Some feedback points to clean hydrolysis and alkylation steps, where byproduct control saves days of column work. Others come from flavor and fragrance developers searching for new top-note intermediates. Our relationship with users gets built from these technical back-and-forths; we don’t view feedback as just paperwork. Several teams have opened up about projects stumbling over unanticipated trace impurities, seeking out root causes together rather than quick blame. Years of this collaboration led us to review not just terminal COA specs, but subtle batch differences that can matter in exotic syntheses.
We also hear from contract manufacturing organizations about the need for files and traceability. We maintain end-to-end production records — not just for regulations but for diagnostic work. Sometimes, an unexpected retention time or color shift points back to a reagent source or equipment maintenance issue. Over time, these records prove their worth not just at audit but in proving product consistency.
Batch reproducibility stands out as one of the most demanding aspects. Pure chemical logic meets day-to-day variability: slight changes in raw material source, seasonal humidity, or tiny adjustments on the reactor can all reflect in the final product. We fix attention on incoming ethanol and diketone purity, knowing from many cycles that low-grade supplies spell more cleanup in the distillation stage. We’ve adjusted solvent exchange routines and made it standard to revalidate instruments with every campaign. Several times, we switched out vendors when slight shifts in the boiling point or color index started creeping into readings.
On occasion, customers have returned to us with unexplained results—maybe a failed crystallization or an unknown impurity showing up in NMR spectra. Instead of issuing standard paperwork, we go back into past retention samples, crosschecking batch records, and reassigning lab staff to the root cause. Most of these problems have stemmed not from catastrophic process failures but from minor lapses or unforeseen interactions. Having an internal feedback loop, and not just outsourcing investigations, has let us catch and correct gaps quickly.
Operating a plant brings safety into every step, not just for regulation, but to protect teams and clients. We’ve developed material handling protocols to minimize operator exposure to the more volatile intermediate stages. Though Ethyl 4-Acetyl-5-Oxohexanoate itself isn’t particularly volatile, process byproducts can include traces of strong-smelling or aggressive materials. Our crew gets full access to safety gear and regular drills, and we design equipment layouts to keep vapor and spill risks contained. Years ago, we underestimated the buildup of acetyl vapors in a transfer line and paid with downtime and costly cleanup. We built redundancy into venting and now monitor air quality during critical steps.
From environmental perspective, we set up secondary containment and solvent recycling projects to reduce chemical loss. Effluent streams get sampled both at the equipment and at discharge, keeping us ahead of local and export regulations. We shifted several processes to closed-loop solvent recovery, and found even moderate investment paid off in cleaner end product and reduced disposal costs. Sharing best practices with partners, we have seen how a little more caution at source reduces trouble for everyone later.
With global regulations changing, meeting compliance isn’t just a box-ticking exercise. Our experience in export markets shows that paperwork is only the final step of a more involved journey. Local authorities might request detailed impurity profiles, full process flowcharts, and batch histories before giving a green light. We spent time working with customers on registration dossiers, making sure no step gets missed. Some users ask about pending regulatory watchlists or new purity thresholds; we adapt quality checks so nothing falls through the cracks if standards change month to month.
Demand can swing rapidly based on end-user innovations, and our stock and planning teams keep routine contact with clients about likely forecast changes. We try to avoid last-minute scrambles that compromise quality by holding buffer inventory of both raw materials and finished product, even if it strains storage at times. We run simulations on batch timing and ship schedules — sometimes the chemistry feels simple compared to logistics.
Looking ahead, R&D continues to play a major role as we field more requests for modified esters or unusual purity profiles. Customers in pharmaceutical development look for microimpurity thresholds we never considered in older processes, often at parts-per-million levels. Analytical chemists in our team run ever-tightening LC/MS and GC-MS profiles and discuss results directly with client scientists. This cross-talk drives both improved synthesis yield and the selection of future process steps. On more than one occasion, close work with a customer has led us to redesign a purification stage, eliminating hard-to-remove byproducts.
Building real partnerships with downstream users means going beyond filling orders. We value practical understanding — not just seeing a waveform, but knowing what it will do at the next reaction step. Several of our staff rotate through technical support, giving them a chance to see our product in action at customer labs and bring feedback to engineering and QC. These cycles help us tune future production for improved usability and let us anticipate and address brewing problems before they become serious. This loop drives continuous improvement, keeping our standards high in a shifting market.
Manufacturing Ethyl 4-Acetyl-5-Oxohexanoate links us with every user who tries to solve a synthetic puzzle in the lab or scale up a process for commercial production. Success grows from a direct line between shop floor, technical support, and the people developing the next molecule or product in their own facility. Instead of fading into the background as another factory output, each batch reflects choices about process, raw material, feedback, and the lessons learned from missteps and improvements. We keep learning from our own experience, helping users meet both routine targets and troubleshoot the surprises that chemistry always brings. Our commitment to careful, transparent manufacturing comes from years of doing, not just promising, and we look forward to improving the journey one batch at a time.