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HS Code |
380838 |
| Chemicalname | Ethyl N,N-Dimethyloxamate |
| Casnumber | 2659-63-6 |
| Molecularformula | C6H13NO3 |
| Molecularweight | 147.17 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 87-89°C at 11 mmHg |
| Density | 1.00 g/cm3 |
| Solubility | Soluble in organic solvents such as ethanol and ether |
| Refractiveindex | 1.424-1.428 |
| Flashpoint | 96°C |
| Smiles | CCOC(=O)C(=O)N(C)C |
As an accredited Ethyl N,N-Dimethyloxamate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of Ethyl N,N-Dimethyloxamate is supplied in a sealed, amber glass bottle with a tamper-evident cap and hazard labeling. |
| Shipping | Ethyl N,N-Dimethyloxamate should be shipped in tightly sealed containers, protected from light and moisture. It must be handled by trained personnel and accompanied by appropriate hazard labels and documentation. During transport, it should comply with all relevant regulations for chemical substances to ensure safe and secure delivery. |
| Storage | Ethyl N,N-dimethyloxamate should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from moisture. Store in a designated chemical storage cabinet, and ensure proper labeling. Avoid prolonged exposure to heat and direct sunlight to maintain its stability and integrity. |
Applications of Ethyl N,N-Dimethyloxamate in Industrial ManufacturingEthyl N,N-Dimethyloxamate functions as a critical intermediate in high-value chemical synthesis routes across multiple downstream sectors. As the original manufacturer, we support industrial end-users with precise composition guidance, process synchronization, and adherence to international compliance for reliable scaling in key applications. 1. Pharmaceutical Intermediates ProductionEthyl N,N-Dimethyloxamate acts as a strategic building block in the multi-step synthesis of active pharmaceutical ingredients, notably in certain antihypertensive and antineoplastic APIs. Formulators integrate the material during early or mid-stage reactions, typically through ester exchange or amidation, to achieve structural motifs not accessible with other oxamate derivatives. Compliance with GMP and impurity profile controls ensures product suitability for regulated drug substance manufacturing. Industry compliance standards
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2. Agrochemical Synthesis (Herbicide and Pesticide Manufacturing)Major agrochemical producers incorporate Ethyl N,N-Dimethyloxamate as a tailored intermediate for certain selective herbicide and insecticide actives. It facilitates the introduction of specific oxamate functionalities to boost active molecule selectivity and environmental stability. The raw material fits into scaled production with in-line reaction monitoring, ensuring traceability for global agrochemical export compliance. Industry compliance standards
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3. Specialty Fine Chemical SynthesisIn advanced fine chemical operations, Ethyl N,N-Dimethyloxamate enables formation of high-purity esters and amides, supporting tailored performance products such as photoinitiators, UV-absorbers, and colorants. The material allows for precise control of functional group introduction, critical when synthesizing specialty chemicals for electronics or polymer-modifier markets. Batch documentation and full traceability ensure compatibility with international quality standards. Industry compliance standards
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4. Organic Laboratory Reagents and Research ChemicalsContract research organizations and academic laboratories utilize Ethyl N,N-Dimethyloxamate as a targeted reagent for synthetic method development and validation of catalytic processes. Its well-defined structure enables precise mechanistic studies in C-N, C-O bond formation, and asymmetric methodology. Small-scale but highly regulated supply ensures suitability for high-purity experiments requiring formal analytical validation. Industry compliance standards
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Competitive Ethyl N,N-Dimethyloxamate prices that fit your budget—flexible terms and customized quotes for every order.
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For the past two decades, our workshop has seen Ethyl N,N-Dimethyloxamate leave the reactor day after day. It starts as raw material—clear, pure, with a molecular formula C6H11NO3—that we know by look and smell. Our standard batch comes under the model ENDOX-01, reflecting not an abstract code, but a real production design that’s been refined through trial, customer feedback, and plenty of troubleshooting on the plant floor. In a world full of similar-sounding oxamates, knowing the specifics behind what you’re selling and why it’s produced this way matters—at least if you want customers to count on you year after year.
Operators here will tell you that the best Ethyl N,N-Dimethyloxamate runs as a clear, colorless liquid with a faint but distinct ester note. Every shift, we check not just purity—using our in-house HPLC and GC—but also real-world traits like pour point, viscosity, and stability once the drums leave our factory. The standard assay for us runs above 99 percent, but controlling color and eliminating water content down to below 0.2 percent makes just as much difference in downstream processes. In the labs of some clients, these “small” details mean higher yield, less fouling, fewer headaches. In our process, getting that right batch after batch means regular maintenance checks, fresh catalyst lots, and QC staff who log everything—not just numbers, but observations.
Chemists often ask: why go to the trouble of using oxamates instead of another ester or amide? Our experience says Ethyl N,N-Dimethyloxamate’s value shows up in selectivity and reactivity—especially as a building block in the synthesis of pyrroles, pyrazoles, and other key heterocyclic intermediates. Many of our pharma customers look to this material for its cleaner reaction profiles. The ethyl group offers better solubility in organic media, and the N,N-dimethyl substitution helps avoid unwanted side reactions. We see this every time we get analytical reports back showing fewer byproducts, less column time, and higher purity downstream. Unlike diethyl oxalate or methyl oxamate, which often introduce unwanted moisture or suffer from poor reactivity under mild conditions, Ethyl N,N-Dimethyloxamate handles demanding steps—especially where gentle hydrolysis or selective N-alkylation matters.
For agrochemical and specialty pigment makers, these differences add up to more reliable yields. Our partners in the colorant sector routinely find that finer dispersion and dye intensity trace back to cleaner, purer batches of oxamate starting materials. Ethyl N,N-Dimethyloxamate often sits at the head of these syntheses; switches to cheaper, less consistent sources almost always mean headaches later down the production line. The feedback loop between supplier and client grows from these direct production outcomes—not from theoretical specs on a datasheet, but from what really happens when a material meets the next reactant.
Scale matters. We support clients from small-scale R&D batches—literally hand-bottled in our analytical lab—to multi-ton orders drum-filled under nitrogen and packed within a day’s notice. Handling experience has taught us that Ethyl N,N-Dimethyloxamate needs stable, sealed storage under dry, cool conditions to hold maximum reactivity. The sharp eye of an operator who notices a color shift and flags a drum before shipment has saved more than one customer a wasted week of pilot plant trials. Logistics staff keep drums away from potential moisture ingress and even small sources of local heat, as the ester bond and oxamate framework can slowly hydrolyze or degrade under rough warehouse conditions.
Customers in pharmaceutical R&D value carefully packed 1kg or 5kg aluminum drums that arrive with batch-specific COA and complete traceability—no two batch numbers ever repeated, all linked to our full production log for auditing years after shipment. Bulk buyers pay equal attention to drum integrity and chain of custody, knowing that a single leaky seal spells trouble in high-purity, multi-stage projects. Over years, we’ve lived through every permutation—custom packaging, expedited resupply after a last-minute scale-up, coordinating exports around shifting international regulations. If Ethyl N,N-Dimethyloxamate is the last limiting reagent in a plant batch, response times and logistical cooperation build trust in a way that single lots never can.
To us, purity means more than a number on a certificate. Each batch passes FT-IR and NMR verification in-house; selected shipments get GC-MS for deeper impurity profiling. We reject anything that shows even minor ester hydrolysis or side chain oxidation, since those flaws become expensive bottlenecks or lost product further down our customers’ lines. Removing even small contaminants means constant investments in purification—new column media, better in-process monitoring, and sometimes procedural overhauls when a single lot surprises us with an off-odor or trace impurity. Our team’s understanding comes not from theory but from seeing output after output improve as controls tighten.
Comparing our product to alternatives, many clients come back after problems with off-brand supplies—issues like undetected water content, inconsistent melting points, or even container contamination. We welcome direct audits and retain reference samples from every lot, ready for side-by-side checks. In years of collaboration with leading pharmaceutical plants, our Ethyl N,N-Dimethyloxamate has helped eliminate costly chromatographic purifications, reduce waste, and support consistent process validation against regulatory standards. This is a result of practical, day-in, day-out improvements in plant routines, testing equipment upgrades, and employee training—rather than surface-level specification updates.
Our collaboration with customer technical teams goes past transactional selling. Chemists who call with process questions get direct access to our own R&D staff—the same people who run pilot reactor campaigns, troubleshoot crystallization steps, and optimize purification for every lot. Many process improvements at client facilities trace back to mapping solvent compatibility, exploring reaction temperature ranges, and eliminating steps that lead to fouling or loss of yield. We share case experiences—such as the unexpected benefit of switching from methyl to ethyl oxamate for solubility in certain polar-aprotic solvents, or the improvement in control during scale-up batches.
We see some labs focus too heavily on chase for higher concentration at the expense of purity or stability, especially in the drive to scale up. The lesson isn’t just about reaching a magic percentage; it’s about ensuring that every lot performs to expectation under real-world process stresses. Our team flags any unusual batch-to-batch shifts and tracks them—sometimes learning from the customer before our own in-plant testing even picks up changes. Years of these exchanges shape product refinement, leading to in-process adjustments that humble any assumption that “good enough” is really good enough.
Many manufacturers claim technical equivalence between different oxamates—with little practical insight into why glassware, reactor wall residues, or impurity carryover differ batch by batch. We’ve stood next to plant engineers at client sites and seen exactly how our Ethyl N,N-Dimethyloxamate beats out lower-grade competitors. Solubility testing on production-scale batches reveals real limitations in cheaper grades, which often turn cloudy or drop solids with only minor blending hiccups. Tighter purity and controlled water content translate into downstream stability—less hydrolysis, no ugly precipitates, and better shelf life even under tough conditions.
There’s a practical toughness in our approach—expecting that every user will push the material in slightly different ways, whether in synthesis, formulation, or analytical validation. Instead of banking on “meets spec” claims, we supply full batch histories, offer on-site troubleshooting, and revisit core production assumptions whenever a new customer application stretches our standard model. Our regular investment in plant upgrades—improved distillation columns, advanced analytical tech, and routine split-batch analysis—doesn’t just serve quality audits. It feeds back directly into more robust, user-friendly products that downstream chemists rely on, batch after batch.
We work with researchers exploring next-gen pharmaceutical intermediates who need reagents that won’t introduce hidden risks—a task where repeat performance matters every bit as much as technical novelty. For new discoveries, the difference between a successful route and a dead end can be as small as an impurity in Ethyl N,N-Dimethyloxamate, or an unnoticed difference in extraction behavior tied to a particular lot’s moisture content.
We keep a pipeline open to academic and industrial discovery—sharing application notes, cross-testing with collaborators, and responding to requests for custom specifications. Insight grows through hands-on trials, process scale-up runs, and close post-mortem reviews whenever a batch falls short. Every change in our process gets logged not just for regulatory reasons, but because continuous feedback from the front lines of synthesis shapes what this product can do in the real world.
Nearly every field using Ethyl N,N-Dimethyloxamate now faces regulatory scrutiny—from pharmaceutical APIs to agricultural intermediates. Customers depend on materials that conform not just to purity specs, but to the shifting rules on solvent residues, trace metals, and process contaminants. Our plant answers these demands by tightening controls, investing in data logging, and making every batch traceable through its entire lifecycle.
Environmental control starts at sourcing. We vet input materials from longstanding suppliers whose own traceability systems make surprises rare and correctable. Our waste management team tracks every effluent batch, not just for compliance, but to ensure process changes don’t tip the balance toward avoidable releases or unplanned emissions. These steps aren’t just corporate check-boxes—they support cleaner syntheses downstream, boosting customer confidence and shrinking the footprint for everyone in the value chain.
Being prepared for customer audits—down to showing the full trail of batch records, environmental releases, and corrective actions—demonstrates more than compliance. It builds real confidence that our Ethyl N,N-Dimethyloxamate shipments rise above basic “meets spec” claims, consistently supporting demanding new developments in safer, more efficient synthetic chemistry and manufacturing.
The drive to produce superior Ethyl N,N-Dimethyloxamate never stops at meeting last year’s benchmarks. Lab and plant staff review every QC trend, investigating root causes of even marginal drifts in assay or trace impurity formation. Over years, we’ve changed everything from reactor internals to filtration routines, learned from in-process hiccups, and re-tooled purification steps to boost yield and minimize side-products. Each improvement began with a problem brought by a customer and ended in a more robust product, better able to endure process stress and contribute to more effective syntheses.
Some customers push for ever-lower limits on process byproducts, especially when developing new therapies or fine chemical derivatives. Our analytical team often introduces updated validation methods directly from these challenges—then rolls them into plant protocols after months of field experience. In cases where existing standards don’t fully capture real customer requirements, we develop internal benchmarks that better reflect process needs and safety priorities. The technical know-how this generates stays inside our plant but shapes every drum that rolls onto the loading dock.
Having produced this compound across dozens of batches each year, our team sees demand trends shift with macroeconomic cycles but also with the introduction of new API routes, agricultural applications, and specialty pigment formulations. Many new inquiries spring from word-of-mouth recommendations inside industry circles—chemists telling other chemists about a supplier whose oxamate delivers reaction reliability, not just paper specs.
Competitors enter the field, but years of hands-on troubleshooting, process transparency, and real-world application support set a tough standard. We regularly supply to demanding multinational plants, small-scale innovation startups, and university labs experimenting at the boundary of what’s next in functional heterocycles, polymer additives, and specialty dyes. This broad range of end users sharpens our own insight into where Ethyl N,N-Dimethyloxamate fits best—and where added value can outpace simple pricing.
After long experience—multiple plant upgrades, learning from process failures and candid customer audits—we’ve built up a practical understanding of what real performance looks like in this field. Ethyl N,N-Dimethyloxamate, when produced with care, delivers batch-to-batch repeatability, surface cleanliness in reactors, and the low impurity profiles that demanding industries now expect. Its differences from other related compounds show up clearly throughout the process chain: better handling, sharper yields, easier downstream processing, and tighter analytical control.
It’s easy for outsiders to confuse this family of chemicals; to those inside the industry, the distinctions are measured in time saved, trouble avoided, and innovation made possible. Ongoing dialogue with end users matters more than marketing claims. If we have learned anything from decades making this product, it’s that putting in more effort at the manufacturing end saves countless hours and cost at the user’s lab bench or production plant. Documented quality, transparent process records, and willingness to answer every “why” from the customer side keep us striving for better—and ensure that every shipment of Ethyl N,N-Dimethyloxamate earns its key place in synthesis, year after year.