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HS Code |
488936 |
| Product Name | Ethyl 2-Benzylacetoacetate |
| Cas Number | 4923-39-7 |
| Molecular Formula | C13H16O3 |
| Molecular Weight | 220.27 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 165-167°C at 10 mmHg |
| Density | 1.094 g/cm³ at 25°C |
| Refractive Index | 1.496-1.500 |
| Solubility | Insoluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Smiles | CCOC(=O)C(Cc1ccccc1)C(=O)C |
As an accredited Ethyl 2-Benzylacetoacetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 500g amber glass bottle securely sealed with a plastic cap, labeled "Ethyl 2-Benzylacetoacetate," including hazard and handling information. |
| Shipping | **Shipping Description:** Ethyl 2-Benzylacetoacetate should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Handle with care and comply with local and international chemical transport regulations. Typically shipped as a liquid, it is not classified as hazardous for transport but should be kept away from strong oxidizers and open flames. |
| Storage | Ethyl 2-Benzylacetoacetate should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep it away from incompatible substances such as strong oxidizers and acids. Always store at room temperature and ensure proper labeling to prevent accidental misuse. Use personal protective equipment when handling. |
Applications of Ethyl 2-Benzylacetoacetate in Industrial ManufacturingEthyl 2-Benzylacetoacetate has established technical value across several specialized downstream industries, primarily through its role as a key intermediate in the synthesis of advanced organic compounds. Our manufacturing expertise supports bulk, quality-controlled supply for customer formulations, ensuring compliance and traceability in demanding production environments. Explore practical application details below, including dosage ranges, compliance benchmarks, and integration workflow for each focused industrial sector. 1. Pharmaceutical Intermediates for Anticonvulsant Active IngredientsThis material serves as a precursor in multi-step synthesis routes for several anticonvulsant drugs. Formulators employ it to enable controlled condensation and ring-closing reactions, which form the core structures found in critical APIs such as phenobarbital derivatives. Process chemists value its reactivity for introducing benzyl moieties under consistent purity requirements. All stages must adhere to validated GMP workflows to satisfy strict regulatory and pharmacopoeial standards. Industry compliance standards
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2. Synthesis of Agrochemical Intermediates for Pyrrole and Pyridine HerbicidesDownstream agrochemical formulators use this raw material to create central building blocks in the manufacture of certain heterocyclic herbicides. It reacts in key steps forming the benzyl-substituted pyrrole or pyridine rings, which deliver targeted weed control activity. Its consistent quality and trace impurities profile directly impact reproducibility in the final agrochemical product, with attention to regulatory traceability for environmental and crop safety. Industry compliance standards
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3. Fine Fragrance and Flavor Intermediate for Aroma CompoundsManufacturers in the fragrance and flavor sector use this ingredient to synthesize key aromatic ketone derivatives, essential in composing complex notes for both perfumery and food applications. Process control is critical to achieve batch-to-batch olfactory consistency and to comply with purity specifications relevant to consumer safety. Downstream integreation involves regulated reaction steps that convert this intermediate into desirable ester or ketone aroma molecules. Industry compliance standards
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4. Specialty Chemical Synthesis for Custom Dyestuff IntermediatesChemical manufacturers rely on this material for producing advanced intermediates that participate in the synthesis of high-performance dyestuff molecules. Its structure enables controlled introduction of benzyl-acetoacetate moieties into chromophore scaffolds. This integration step is vital for spectral tuning and color fastness improvement in demanding textile and industrial dye applications, meeting specialty formulation requirements and defined quality parameters. Industry compliance standards
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We produce Ethyl 2-Benzylacetoacetate in our facility, where hands-on experience with esterification, purification, and process control runs deep. For us, every batch tells a story about persistence and attention in the lab. Chemists and engineers work in sync to refine conditions, drawing on years of accumulated trials and adjustments to hit high purity levels and consistent yields. Our focus is narrow but precise: we understand both the quirks and strengths of this molecule. It doesn’t reach the market until every drum has been checked in-house, every analysis repeated using both classical and modern assumptions for structure confirmation and impurity profiling.
Ethyl 2-Benzylacetoacetate, by formula C13H16O3, stands out among substituted acetoacetates. Sometimes, people outside the factory overlook how the attachment of a benzyl group on the 2-position changes reactivity dramatically. This single substitution is more than a name—on the bench, it shifts selectivity in condensation, alkylation, or cyclization steps. It changes solubility profiles and influences the choice of solvent systems in downstream transformations. Not every synthetic target calls for this variant, but its application in key pharmaceutical and agrochemical syntheses keeps production both challenging and rewarding.
We source high-grade benzyl halides and acetoacetic esters for controlled reactions under basic conditions. Temperature, solvent, stirring rate, addition sequence—all these play a role in the reaction outcome. On a factory scale, small differences in base strength or the presence of trace water bear out in the batch’s crystalline quality, yield, or color. Our teams sweat the anomalies, starting with analytical controls and moving through distillation and crystallization until the product matches known spectra. You can smell the difference as a fresh batch emerges from the reactor: a slight, fruity nuance, well-separated from the sharper notes of starting materials. Careful purification sets our product apart from off-grade lots often peddled by less disciplined producers.
Our model for Ethyl 2-Benzylacetoacetate production targets purity of 99% min, with GC and HPLC confirming batch repeatability. Water, residual solvents, and trace impurities all have clear limits, established from trials and feedback from users in fine chemical synthesis. We keep storage simple—sealed containers, away from heat—because we know not every customer can maintain elaborate climate controls. Moisture sensitivity doesn’t become obvious until months have passed; years back, we learned older batches lose luster and develop faint byproducts. Since then, each fill receives a nitrogen blanket right after packing. It’s one of those small details that isn’t obvious to outsiders but matters deeply to customers running multi-step syntheses.
We still remember initial frustration during scale-up, when problems crept into distillation—foaming, slow throughput, fluctuations in head temperature. Our shifts handled each hiccup one at a time, adjusting vacuum settings and condenser temperature profiles. Several cycles later, we landed on a method that balances throughput with product quality, skipping the shortcuts that can leave lingering traces of high boilers or benzyl byproducts. That’s the value of in-house manufacturing: we learn from our own mistakes, and refuse to let those lessons fade after a season.
The benzyl group on the acetoacetic acid backbone makes all the difference in certain synthesis schemes. Regular ethyl acetoacetate drops away in reactivity once you introduce specific nucleophiles or run conditions demanding more stabilization next to the carbonyl. The benzylamino or benzylalkyl backbone makes N- and C-alkylations sharper and opens the door for cyclization pathways otherwise out of reach. We talk to downstream users constantly—particularly those in heterocycle synthesis and active pharmaceutical ingredient production. Their pain points become our challenges. If another acetoacetate would work, they wouldn’t be asking for our product. They want the slight twist in selectivity that comes from the benzyl substitution.
Not all benzyl-containing esters behave the same way. Some carry impurities a regular trader might overlook, like byproducts of incomplete esterification or odd isomers creeping in through uncontrolled side reactions. Years ago, we saw a batch from an outside supplier that ran slightly yellow. The difference showed up in downstream NMR spectra—tiny, but enough to stall a six-step sequence for one of our regular pharma partners. That mistake sharpened our resolve to control every step ourselves. Now, every lot is checked by more than one chemist before it gets our okay.
There’s a saying in plant management: “Quality is not what you say, but what you do.” Every reactor charge gets monitored and logged by people with skin in the game. Ethyl 2-Benzylacetoacetate doesn’t hide problems easily, but once in a while, unexpected contamination in a raw material crops up. Our hands-on QC crew catches them—not the paperwork. We keep co-founder-level involvement on the floor, often sampling with the younger chemists, using HPLC, and cross-checking against old spectra stored in battered lab notebooks. It’s not just about certification for the sake of a stamp. We treat every kilo as if our own jobs depend on its accuracy—because, in a way, they do.
Most shipments we fulfill end up in R&D or pilot-plant settings—places where reliability matters as much as price and where a failed batch costs weeks, not just pennies. One common application is as an intermediate for pharmaceuticals targeting heterocyclic frameworks. The benzyl group gets cleaved or transformed into other functionalities, and purity at each junction dictates the ease of further reactions. We also support applications in agrochemical production. Some customers use it for making specialty colorants and flavors, but the pharma sector has always stood out in feedback and performance demands.
Bench chemists often ask what makes our Ethyl 2-Benzylacetoacetate more predictable in practice. It comes down to hands-on testing and direct answers when things don’t go as planned. Once, a client flagged a stuck condensation step. Instead of pointing to theory, our process engineers reviewed solvent choices and trace moisture from their own lab’s storage. A fresh shipment, with more meticulous moisture control, solved the issue. That exchange led us to tighten our own post-purification drying process, and the next lots shipped with even greater stability.
Generic acetoacetate esters fill a need, but they can’t match the selectivity and downstream reactivity that Ethyl 2-Benzylacetoacetate brings to the table. Beyond that, trading houses and resellers sometimes carry over residues that affect the final transformation. We’ve been burned by this ourselves in the past, relying on outside sources during supply chain crunches only to find unexpected impurities that showed up under TLC after step three of a routine coupling. That’s one benefit of keeping process control in-house. Each lot stays traceable to its source, its conditions, and the exact steps used in its making.
In side-by-side lab trials, customers routinely report cleaner intermediate isolations and higher yields in downstream steps using our product. Part of that tracks back to purity, but the rest comes from predictable, stable behavior batch after batch. If an alternative ester works for a given route, we don’t try to talk anyone into switching. Our users come from places where small differences matter—where the next three steps rest on clean conversions and batch data from real runs, not paper certificates.
We stay up-to-date with guidance from regulatory agencies for both chemical registration and downstream uses, especially in pharmaceuticals and specialty pesticides. REACH considerations, status under various national chemical inventories, and pre-registration requirements for new product development often loom large for customers. We learned the ropes by preparing our own technical dossiers—no broker in between—so if a regulatory quirk comes up, we trace the paperwork back to the source. Our plant runs internal audits, marries documentation with production records, and keeps samples archived in case any batch history needs checking.
We’ve spent years sitting across from regulators, updating SDS sheets, accounting for trace solvent use, and making certain no raw material substitution sneaks through unvetted. Sometimes, a new customer’s compliance officer requests more granular batch data. That’s never a problem for us. Records live on our own servers, and our staff knows which tank, valve, and lot number tie into each shipment. We find that makes a difference when building trust, especially for customers with demanding end-use audits looming.
Some companies talk about sustainability as an add-on. For us, the pressures to reduce waste and improve efficiency come straight from costs, employee safety, and daily risk. We break down all side streams from Ethyl 2-Benzylacetoacetate synthesis, distilling off solvents for reuse or safe disposal and handling byproducts per local environmental codes. Our team led an effort to reduce base consumption in 2018, trimming chemical use without compromising yield. These measures keep our environmental footprint controlled and our solvent bills lean.
Inside the plant, we have strict protocols for handling flammable liquids and controlling exposure to reactive chemicals. Personal protection, air handling, and fire safety are everyday priorities, not just checkpoints for auditors. Over the years, we shifted from older, single-use PPE to upgraded, reusable systems after employee suggestions, which lowered our incident frequency and improved morale. When our people flag a near miss, we investigate—not out of fear of fines, but from the knowledge that a safe plant supports a stable workforce and uninterrupted supply.
Ethyl 2-Benzylacetoacetate fits best in hands-on labs driving new compound discovery, medicinal chemistry, and specialty material design. The molecule’s structure isn’t just about theoretical appeal. Small modifications in chemical building blocks cascade into innovation for new drugs, crop protection products, and even electronics. We see promising uses with advanced heterocycles and fused ring systems—places where fine control in each intermediate step spells make-or-break for the discovery pipeline.
We keep our technical support team in close touch with users at the bench, not just purchase departments. If a synthesis project catches a bottleneck, the line to our process team stays open. Sometimes, the solution hides in an adjustment to the pH profile; other times, switching batch sizes or scale-up methods reveals efficiencies neither side spotted alone. By holding direct technical talks, we help chemists troubleshoot both routine and hairy steps, learning with them in the process.
A memory sticks from a project with a major research center, where a team couldn’t get a ring-closure reaction to stick, thinking the issue sprang from the catalyst. Our own bench chemists had faced this years before, and suggested a tweaked temperature window and longer preheating cycle. The next batch hit expectations, and the bench riders sent us a snapshot of their NMR with the “cleanest spectrum ever.” That kind of exchange keeps us learning, too.
Process improvements and increasing demand for specialized building blocks keep us busy. Users push us for purer batches, fewer byproducts, and cleaner documentation. We keep investing—adding inline analytics, tightening removal of trace benzyl impurities, and making process steps traceable in real time. With tighter market requirements and more projects migrating to large-scale synthesis, consistency across the board saves headaches before shipping.
We never duck a tough question from chemists who order our material for high-stakes synthesis. Being the manufacturer, the responsibility ends right with us when a batch underdelivers. Failures stick with us, and every challenge teaches ways to improve. Caring about that outcome, day after day, lays the groundwork for trust. We know our Ethyl 2-Benzylacetoacetate carves out a niche in the right synthesis, and our focus on process details, active troubleshooting, and staying grounded in practice—not just paperwork—has shaped how we approach the product from start to finish.
Ethyl 2-Benzylacetoacetate represents more than just another acetoacetate in our line. Its role in medicinal chemistry, especially for targets needing the benzyl motif, keeps it relevant despite continuing evolution in synthetic techniques. Our journey began with a few hundred-gram runs and now stretches to multi-ton shipments, but the heart of manufacturing stays with those runs at the boundary of the known and the uncertain. We keep listening to feedback, working at the bench, and drawing lessons from each campaign. The path forward is never routine, but the challenges we face today guide the batches that come off our line tomorrow.