|
HS Code |
286669 |
| Product Name | Ethyl Trifluoropyruvate |
| Cas Number | 13081-18-0 |
| Molecular Formula | C5H5F3O3 |
| Molecular Weight | 170.09 |
| Appearance | Colorless to pale yellow liquid |
| Density | 1.352 g/cm3 |
| Boiling Point | 85-86°C at 15 mmHg |
| Refractive Index | 1.369-1.371 |
| Purity | Typically ≥98% |
| Solubility | Soluble in common organic solvents |
| Smiles | CC(=O)C(=O)C(F)(F)F |
| Synonyms | Ethyl 3,3,3-trifluoro-2-oxopropanoate |
| Storage Temperature | 2-8°C |
| Hazard Classification | Irritant |
As an accredited Ethyl Trifluoropyruvate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
|
Purity 98%: Ethyl Trifluoropyruvate with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high-yield and low-impurity active compound formation. Boiling Point 97°C: Ethyl Trifluoropyruvate with a boiling point of 97°C is used in temperature-sensitive catalytic processes, where it minimizes thermal degradation and maximizes product selectivity. Molecular Weight 164.08 g/mol: Ethyl Trifluoropyruvate with a molecular weight of 164.08 g/mol is used in fine chemical formulation, where it enables precise stoichiometric dosing for predictable reaction outcomes. Density 1.328 g/cm³: Ethyl Trifluoropyruvate at 1.328 g/cm³ density is used in organic synthesis applications, where it provides optimal mixing and dispersion in solvent systems. Water Content <0.5%: Ethyl Trifluoropyruvate with water content below 0.5% is used in anhydrous condensation reactions, where it prevents unwanted hydrolysis and increases reaction efficiency. Stability Temperature up to 35°C: Ethyl Trifluoropyruvate stable up to 35°C is used in storage and transport of reactive intermediates, where it maintains integrity and reduces decomposition risk. Enantiomeric Excess >99%: Ethyl Trifluoropyruvate with enantiomeric excess greater than 99% is used in asymmetric synthesis, where it delivers high optical purity in chiral drug development. |
| Packing | A 25g amber glass bottle, tightly sealed with a screw cap, labeled ‘Ethyl Trifluoropyruvate’, displaying hazard warnings and supplier details. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for Ethyl Trifluoropyruvate: 80–100 drums, each 200 kg, securely packed, compliant with chemical safety regulations. |
| Shipping | Ethyl Trifluoropyruvate is shipped as a liquid in airtight, chemical-resistant containers, typically under cool, dry conditions away from sources of ignition. Proper labeling and documentation are required due to its hazardous nature. Transportation follows regulations for flammable and potentially harmful chemicals, ensuring safety for handlers and the environment. |
| Storage | Ethyl Trifluoropyruvate should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent moisture and air exposure. Keep it in a cool, dry, and well-ventilated area, ideally in a refrigerator at 2–8 °C. Store away from incompatible substances like bases and oxidizing agents. Avoid direct sunlight and sources of ignition. |
| Shelf Life | Ethyl Trifluoropyruvate typically has a shelf life of 12–24 months when stored tightly sealed, protected from moisture, and in a cool place. |
Competitive Ethyl Trifluoropyruvate prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615651039172 or mail to sales9@bouling-chem.com.
We will respond to you as soon as possible.
Tel: +8615651039172
Email: sales9@bouling-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Walking through our production halls, the story of Ethyl Trifluoropyruvate begins with fluorochemicals and a sharp awareness that high-purity reagents shape almost every new development in pharmaceuticals and agrochemicals. This compound comes off our reactors through careful control, with each batch reflecting years of steady refinement of our own processes. We’ve learned that high fluorine loading in an α-ketoester changes how reactions proceed, and for research chemists hunting for new building blocks, Ethyl Trifluoropyruvate answers a set of practical questions few other reagents do.
Our Ethyl Trifluoropyruvate rolls out with batch-to-batch purity above 98 percent by GC assay, thanks to controlled distillation and experienced oversight. From my own daily oversight, I can say that even small missteps in purification let down researchers, so each liter receives the same scrutiny as ten-liter synthesis runs. Its specification as C5H5F3O3, with a strong trifluoromethyl group, translates into distinct chemical reactivity compared to more common α-ketoesters like ethyl pyruvate or ethyl benzoylformate. Working with direct feedback from those who depend on this chemistry, we keep water content well below 0.05 percent, documented by regular Karl Fischer titration, because sensitivity to hydrolysis turns into lost yield downstream.
Those back in the research lab see this solid, pale liquid for what it really delivers: the ability to introduce a trifluoromethyl group at a pivotal site in a molecule. It sees frequent use when making advanced fluorinated intermediates, where the electron-withdrawing CF3 tilts outcomes in catalytic transformations, Michael additions, and enolate chemistry. Ethyl pyruvate can take part in similar condensation reactions but leaves molecules lacking the vital fluorine that modern drugs often need. After close discussions with process chemists, the strongest contrast comes out – ethyl trifluoropyruvate can swing major selectivity differences in C–C bond-forming steps, while closely related α-ketoesters like methyl pyruvate or benzoylformate lack this push-pull behavior from the fluorines and change how the entire downstream reaction performs.
Direct bench trials show that the reactivity of ethyl trifluoropyruvate has made it a staple for constructing 3,3,3-trifluoro-derivatives of various heterocycles. Its volatility, which can frustrate less-experienced handlers, keeps us focused on careful packaging and small-quantity deliveries — a lesson learned from regular field calls. We ship this under nitrogen, sealed in fluoropolymer-lined containers, because leaks or moisture rob the product of its clean edge. The experience of shipping dozens of crates every month teaches that moisture ingress can start invisible but shows up fast in purity assays, so packaging remains a tight operation with constant inspection.
Our team tracks specification details beyond what broad catalogs mention. Typical refractive index falls in a narrow window of 1.350 to 1.354, and we keep residual acidity test results on file. We take old-fashioned pride in clear, traceable chromatography for every outgoing barcode, matching against NMR and GC-MS controls that give us hard evidence of product identity. If photo-sensitive breakdown or oxidation ever does occur in sample vials, we answer by fresh production and not by repackaging or blending old lots. Many users judge esters by smell alone — it should retain a slightly sharp, ether-like odor, not a foul or rotten trace, which reflects our commitment to quick, protected transit routes and deliberate storage at 2–8°C.
Practically, our experience shows the solubility profile sets real expectations for formulation work. Ethyl trifluoropyruvate dissolves well in dichloromethane, chloroform, and THF, without the tendency to separate or form microdroplets that can complicate weighing or mixing. Some surface suppliers repack under atmospheric conditions or send out material in standard amber glass, but we have seen such repackaged goods test at subpar acid content or with acidic impurities that signal hydrolysis already underway. Over several years, we have stepped away from such risks, working closely with contracted courier cold chains to ensure less than 48 hours between reactor and final customer wherever possible.
Most uses we support head straight into the hands of medicinal chemists, agrochemical process teams, or specialty polymer researchers. For example, it finds consistent use as a synthon in Suzuki or Heck reactions where the introduction of a trifluoromethyl group imparts crucial metabolic stability. Our discussions reveal the demand primarily stems from drug candidates targeting CNS or antiviral spaces, where trifluoromethyl groups change a molecule’s lipophilicity and metabolic fate. Large firms test small batches on the bench, then scale up reactions in their pilot plants, coming back to us for regular supplies integrated with their production calendars. We have seen it used in, among others, synthesis routes leading to trifluoromethylated pyrazoles, isoxazoles, and key intermediates for plant growth regulators — a highlight of modern reaction design.
From the shop floor up to the QC lab, our logs match feedback: Ethyl trifluoropyruvate performs predictably in nucleophilic addition, especially with amines to give rise to pyrazoles and triazoles. Our client analysts tell us about its role in Claisen and Michael condensation steps that often shape the backbone of new pesticides or functionalized monomers. As a practical note, its reactive CF3 group stays intact under a wider variety of conditions than simpler ester analogues. Running scale-ups in our pilot reactors, we find yields rarely slip below 90 percent in such applications, provided standard moisture barriers and programmed temperature slopes are observed.
In daily production, patterns become apparent. Regular esters like methyl ethyl ketone or simple pyruvates attract a certain bulk volume but behave physically and chemically in typical, less demanding ways. Where they act as basic C–C building blocks in old-school chemistry, Ethyl trifluoropyruvate unlocks a whole new toolkit for introducing CF3 functionality at key positions on the carbon chain. We have seen that while some chemists attempt to substitute with methyl or benzyl trifluoropyruvate, the difference in physical properties (boiling range, volatility, and resistance to spontaneous hydrolysis) has convinced most experienced labs to prefer the ethyl version for routine synthetic use.
Personal conversations with production chemists reveal that boiling point matters sharply here: Ethyl trifluoropyruvate holds a middle ground, allowing safe rotary evaporation but not much room for error if left on the bench for extended periods. Lab trials confirm that methyl trifluoropyruvate, by contrast, flashes off too easily in solvent removal, while bulkier alkyl or aryl esters do not dissolve as cleanly in the expected solvents. Repeated real-world tests dramatize the importance of handling Ethyl trifluoropyruvate with trained staff, meaning cold-chain storage, nitrogen headspace, and use of PTFE seals at each transfer step. We accept such measures as standard, not luxury, because product integrity traces directly to customer results — this cycle of learning keeps us in close touch with advanced synthesis groups worldwide who build with this molecule every week.
We have stood by during reactions riffing on classic literature, as customers reconstruct routes dating back to the 1990s synthesis of CF3-containing heterocycles, adapting each run to new heteroarenes or chiral centers. Through all of this, we see our Ethyl trifluoropyruvate give crisp, reproducible yields, clear TLC spots, and simple workups compared to competitors’ batches. By keeping direct technical dialogue open, our team provides not just a drum of chemicals, but pointers on pre-chilling glassware, using controlled addition funnels, and filtering through dry columns. We field regular questions: shelf life, best solvents, best bases for those tricky alkylations, and what to do if a batch turns color or forms a haze. Our answers come from shopfloor walking and direct batch handling, not just from regurgitated technical files. With each delivery, we seek feedback, and every complaint prompts a root-cause trace that often improves not just this product, but every downstream batch — a cycle we consider essential for reproducible innovation in specialty fluorochemicals.
Real experience shows that supply glitches for Ethyl trifluoropyruvate create bigger headaches than those for more generic α-ketoesters. Most research deadlines rely on fast, reliable turnaround. Over the years, we have built our own core inventory of raw trifluoroacetic acid ethyl ester and methyl glycolate, securing contracts with up-the-chain suppliers, and keeping two months of raw stock at all times. This insulates downstream users from spot shortages that can crop up as global fluorochemical demand ebbs and flows. In our warehouses, each outgoing liter carries real traceability, down to the lot’s starting day and reactor vessel — no relabels and no pooling or dilution. If a user flags a performance issue, we match it to our sample archive and can often provide backup by the day. This sort of back-and-forth only comes from long-term manufacturing, and it pays off as results line up time after time on mass spec and NMR for end users.
Production of Ethyl trifluoropyruvate, if not strictly controlled, raises risks worth taking seriously. Leaky valves, old Teflon gaskets, or even a power blip on a distillation run can degrade purity. Each operator on our floor receives annual refresher training, not just in paperwork, but in real-world scenarios — fumigation practice for accidental leak cleanup, handling moisture-contaminated batches, quick nitrogen sparge for open fills. We engineer scrubber systems to vent off residual acid gases, double-check all transfer lines for PTFE linings, and run biweekly environmental checks on solvent recovery. Over years, we have reduced waste generation per kilogram output by nearly 35 percent, recycling all non-halogenated solvents wherever practical. The goal here has always been consistency, predictability, and visible safety — because our operators’ daily exposure and local community trust matter as much as product metrics.
For those using Ethyl trifluoropyruvate in scale-up work, we always recommend splash-resistant PPE, local exhaust at transfer stations, and cold storage in desiccated environments. From a manufacturer’s experience, accidental skin or eye exposure doesn’t just demand paperwork — it means direct action, fast decontamination, and real clarity in protocols. We don’t leave it to chance, and never rely on generic MSDS sheets alone; every new employee sees practical demos and end-to-end batch follow-throughs. This hands-on approach extends to partners at pilot sites — walkthroughs, phone briefings, and, when needed, sending out a technical expert to de-risk new reactions. Such investment pays back in trust and fewer surprises, cementing industry partnerships year after year.
Market realities remind every chemical manufacturer that product quality cannot drift. While some third parties attempt to cash in on momentary demand spikes, real value for both us and our partners comes from direct, repeat relationships. We respond to regulatory audits and share our complete batch histories with major compliance inspectors. Before we let a drum leave, each passes through not just one, but multiple signoff gates — operator, quality control, and final supervisor release. Our clients around the world, from Argentina to Denmark, have come to expect this. If a miss happens — a delivery delayed, an unexpected haze, a compatibility check falls short — we resolve the complaint directly, shipping replacement or supporting troubleshooting without the runaround that can come from multi-layered traders.
Continuous improvement counts most. Regular technical exchanges with researchers at the sharp edge of medicinal chemistry keep our process sharp. If an end user innovates a more efficient condensation or snappier catalyst, we update our internal FAQ, share learnings with our other clients (with permissions, never violating IP of course) and adjust our production SOPs where justified by the data. Our culture values this open channel; we find that most new batch improvements start with a casual field observation, which, given structure and focus, delivers tangible gains in reliability and safety. Today's Ethyl trifluoropyruvate is already better and cleaner than last year's, and that evolving edge keeps us keenly invested in the hard details each new batch brings.
For all our exposure to the fast-changing world of specialty fluorochemicals, we measure success in the trust built up with each user. Our hope is that through direct and transparent collaboration, through the hard-earned lessons of good and bad batches, every new milestone in synthesis and development gets a little more predictable and robust. Ethyl trifluoropyruvate stands as a living example of how honest craft, constant vigilance, and open conversation build not only better chemicals but a smarter, safer chemical industry, batch by batch and year by year.