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HS Code |
410439 |
| Product Name | Ethyl 3-Hydroxy-4,4,4-Trifluorobutyrate |
| Cas Number | 55950-11-1 |
| Molecular Formula | C6H9F3O3 |
| Molecular Weight | 186.13 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 65-67 °C at 20 mmHg |
| Density | 1.284 g/mL at 25 °C |
| Refractive Index | 1.390-1.394 |
| Flash Point | 81.2 °C |
| Purity | Typically ≥98% |
| Smiles | CCOC(=O)CC(C(O))C(F)(F)F |
| Solubility | Soluble in organic solvents, limited in water |
As an accredited Ethyl 3-Hydroxy-4,4,4-Trifluorobutyrate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g amber glass bottle with secure cap, labeled “Ethyl 3-Hydroxy-4,4,4-Trifluorobutyrate,” hazard symbols, batch, and expiry details. |
| Shipping | Ethyl 3-Hydroxy-4,4,4-Trifluorobutyrate should be shipped in tightly sealed containers, protected from moisture and direct sunlight. Transport under cool, dry conditions is recommended. Follow all applicable regulations for handling and labeling chemicals. Ensure proper documentation and safety data accompany the shipment to comply with local and international chemical transport guidelines. |
| Storage | Ethyl 3-Hydroxy-4,4,4-Trifluorobutyrate should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizing agents. Keep the container tightly closed and protected from moisture. Store at room temperature or as specified on the manufacturer’s label, and ensure proper labeling and secondary containment to avoid accidental spills. |
Applications of Ethyl 3-Hydroxy-4,4,4-Trifluorobutyrate in Industrial ManufacturingEthyl 3-Hydroxy-4,4,4-Trifluorobutyrate supports several high-value industrial sectors with precise roles in chemical synthesis and downstream conversions. As the original manufacturer, we highlight thoroughly validated downstream application pathways where this intermediate has become integral to advanced process engineering and specialty materials output. 1. Pharmaceutical Intermediate for Trifluoromethyl-Substituted APIsPharmaceutical ingredient manufacturers employ this compound to develop trifluoromethyl-substituted building blocks required for specialty active pharmaceutical ingredients. The molecule’s reactive hydroxy group and the fluoroalkyl segment enable access to complex fluoro-organic synthons critical for advanced small-molecule drug actives. Engineering teams in high-containment GMP plants configure its introduction at the earliest stage of multi-step batch synthesis for maximum structural fidelity. Industry compliance standards
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2. Agrochemical Synthesis — Herbicide IntermediateCrop science manufacturers use this molecule as a key intermediate to construct trifluoromethyl-containing herbicides and active pesticide substances. Its introduction allows for the formation of stable C–F bonds, lending enhanced bioavailability and environmental stability to the final agrochemical molecules. Industry compliance standards
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3. Specialty Fluorinated Monomer Manufacture for Fluoropolymer AdditivesProducers of high-performance polymers and film additives rely on this raw material for its ability to introduce controlled trifluoromethyl groups, enhancing chemical and thermal resistance in the resulting specialty monomers. Used predominantly in electronic and automotive-grade fluoropolymers, its hydroxy functionality enables further cross-linking or copolymerization reactions in downstream resin plants. Industry compliance standards
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4. Fine Chemical Intermediate in Advanced Organic SynthesisFine chemical producers incorporate this material as a highly specific building block for synthesizing advanced organofluorine compounds. The unique substitution pattern supports preparation of fine chemicals with applications in molecular imaging, contrast agents, and specialty reagents, demanding strict batch traceability and analytical validation across the process chain. Industry compliance standards
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5. API Impurity Marker Synthesis for Analytical StandardsReference material producers in the pharmaceutical and chemical analysis sectors utilize controlled batches of this compound to synthesize relevant impurity markers for registration dossiers and method validation. Its stable isotope configuration and chemical purity enable precise derivation of reference compounds mirroring genuine process-related impurities in regulated drug substances. Industry compliance standards
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Ethyl 3-hydroxy-4,4,4-trifluorobutyrate carries a reputation across pharmaceutical and agrochemical labs. As a direct manufacturer, we know the ins and outs of synthesizing this compound, along with its quirks, its strengths, and where its real value shows up. Our model for this product features a purity minimum of 98% by GC, and our batches consistently meet this benchmark. For those who work with fine chemicals, small things make big differences. We don’t just ship barrels; we run every lot through a string of analytical checks, including NMR and HPLC, to confirm structural integrity and purity before sealing a drum.
We understand why every detail matters in this business. Customers might spot a molecule’s IUPAC name, or CAS number, and move on, but at the plant you live with it. Ethyl 3-hydroxy-4,4,4-trifluorobutyrate has the fluorinated character that makes it a favorite for introducing stability and metabolic robustness into API intermediates and specialty crop protection agents. Standard packages run from kilogram units up to hundreds of kilos, packed in HDPE drums under tight moisture control. This compound has a clear, colorless appearance and a boiling range between 90–94 °C at reduced pressure; proper handling of distillation and temperature control builds up the cleanest output possible.
Moisture’s an enemy for this material, so every drum leaves here dry as a bone with a moisture content under 0.2%. The flash point, usually over 85°C, matters for storage, and we advise customers on proper grounding and inert atmosphere handling. We see our output end up as an intermediate for synthesizing complex molecules; its presence helps drive the introduction of the trifluoromethyl group with fewer byproducts than some older approaches.
Our experience tells us the bulk of demand still comes from pharmaceutical research. Over the past decade, patent literature records a steady use of this building block for aryl trifluorobutyrates, florfenicol analogs, and similar structures. Many customers screen it as a starting point for asynchronous, enantioselective transformations, depending on the pathway. The hydroxy group on the 3-position plays a big part in opening up subsequent reactions: it’s reactive without being so unstable that it degrades too easily on the bench.
Some who walk through our door seek out this specific molecule for its flexibility in derivatization. It lets medicinal chemists introduce both the trifluoromethyl unit and an ester handle efficiently. This saves steps right in the early stage of a synthesis project. Downstream, a customer might transform the hydroxy group by protecting it, oxidizing it, or coupling it directly onto aromatic scaffolds.
Agrochemical researchers have leaned on this compound as a feedstock, leveraging the same functional groups to develop new herbicides, fungicides, and growth regulators, often chasing better environmental stability and bioactivity. We’ve seen projects that use it as a seed for pro-drugs, tweaking the release rate through the ester linkage.
A common question we get: how’s this product set apart from close structural cousins? In our work, small changes in the molecule—say, shifting the hydroxy position, or swapping an ethyl group for methyl—throw off the whole process. Ethyl 3-hydroxy-4,4,4-trifluorobutyrate delivers specific balance: the 4,4,4-trifluoro part acts as a strong electron-withdrawing group without over-stabilizing the molecule, which helps downstream chemistry keep moving forward.
Its closest competing products, like methyl 3-hydroxy-4,4,4-trifluorobutyrate, or ethyl 2-hydroxy-4,4,4-trifluorobutyrate, look similar on paper but show distinct reactivity during scale-up. In our reactors, we’ve pushed both and tracked yields and byproducts. We saw better control and less side reactivity with the ethyl 3-hydroxy variant. That translates into better yields and simpler purification on the customer’s end. Direct feedback from partners tells us those small wins, aggregated over hundreds of runs, add up.
Customers value this product for its reliability, but that doesn’t happen by accident. Every kilo on the scale links back to our choices at the plant: from solvent purity to how we scrub and dry our reactors. Our synthesis skips harsh reagents, favoring milder agents to keep impurity profiles down. We also refuse to rush the final estification step, which sets us apart from operations where residual acidity can hurt downstream reactions. Over the years, we have logged careful feedback from recurring clients. Whenever a batch had a trace contaminant, we worked backward, tracked every step and changed our washing protocols. That’s how quality sticks around.
It’s tempting in this market to chase cheaper costs by cutting steps, lowering purity specs, or bulking out with cheaper solvent systems. We’ve watched corners get cut and shipments get rejected. Our history shows that chemists downstream spot the difference quickly.
Tracking each batch from raw material intake to packed drum isn’t just a slogan: every lot’s analysis and engagement with formal regulatory frameworks ensures traceability. Our chemical process avoids chlorinated solvents to keep chance impurities out, and our plant management keeps strict maintenance logs, which means less risk of cross-contamination.
We know from experience this molecule brings some challenges in safe handling, mostly around its volatility and toxicity. Though acute toxicity falls within moderate levels compared to other fluorinated esters, inhalation and contact are still no joke. Our production workers always use appropriate PPE, run in well-ventilated fume hoods, and check for leaks on every drum filling.
Customers sometimes approach us with stories of product arriving elsewhere with strange odors or yellowing. That narrows down to bad packaging or moisture ingress, both of which spoil sensitive materials like ours. All our containers use thick-walled HDPE with inner liners to block vapor diffusion, plus tamper-proof seals. Over the years, we moved away from metal drums due to corrosion risk. Care in capping and double-sealing avoids the slow buildup of acidic decomposition products that can ruin entire shipments.
The market’s shifting toward greener chemistry and more sustainable production cycles. We have listened to requests for lower-waste, lower-emission synthesis steps. In 2019, we switched one step from a legacy chlorinated byproduct process to a fluorine-balanced reaction. This cut our solvent waste streams by about 40%, based on internal audits.
We stay in touch with regulatory changes too. The growing scrutiny of persistent organic pollutants puts a spotlight on all fluorinated chemicals, especially in Europe. Our track record with REACH registration and consistent compliance with local environmental laws gives customers and regulators confidence that we take stewardship seriously. Inside our labs, we continue to seek ways to make the hydroxy-ester more accessible, keep waste and off-gassing down, and audit our energy usage quarterly.
Some clients push for even higher purity or optically active versions. We can deliver these under custom projects, using chiral separation steps and advanced analytical support. It takes more time and effort, but direct engagement with researchers drives us to re-invest in new equipment and methods to meet shifting needs.
We’ve fielded countless calls about troubleshooting side reactions, purification issues, and formulation hiccups involving ethyl 3-hydroxy-4,4,4-trifluorobutyrate. Our technical team has spent weeks at customer pilot plants, helping debug process steps and test new conditions. Direct support matters—chemistry on paper rarely works out the same way in tanks and reactors. We’ve advised on optimal solvent swaps to avoid hydrolysis, and guided process engineers in fine-tuning pH and removal of trace water from storage environments.
Some customers have faced regulatory questions about residual solvents or unexpected byproducts. Our up-to-date COAs reflect actual methods in use, including NMR and LC-MS scans for low-level impurity detection. When stricter compliance hit one region, we invested in extra purification and got documentation in place fast so our customers never faced interruptions. Our approach to process validation, informed by decades in the industry, means rare batch-to-batch variation. We engage with auditors openly, backing up our word with complete traceability from raw material forward.
One unique part of making advanced intermediates is the sheer speed of feedback. Over years of close work, we’ve learned from our top R&D partners that ease of derivatization—the low-temperature reactions, the clean ester cuts, and stable trifluoromethyl group—help drive their process development. For some, tiny changes in byproduct profile can derail whole campaigns. We share full analytical packages and open our doors to lab-to-lab conversations when downstream issues crop up. This helps both sides: we get to optimize the process before anything leaves the gate, and they get a supplier who actually knows the product and its quirks, not just someone moving pallets.
Our partnership approach has led to real-world solutions: revised purification protocols, specialized packing, and joint testing of new use-cases. When a laboratory ran into unexpected hydrolysis, we adjusted our stabilization regimen and switched up packaging, eliminating the problem within three production cycles.
Long-term business in specialty chemicals relies as much on experience as on published specs. Every successful batch of ethyl 3-hydroxy-4,4,4-trifluorobutyrate owes something to the people running reactors and QA systems, not just to the equipment. Our senior process engineers have adjusted column conditions over dozens of campaigns, dialing in a routine that consistently yields above 90% and cuts post-purification down to just a single crystallization.
We’ve worked through solvent replacements, handled temperature swings in summer and winter, and dealt with unexpected power outages. All these things matter more to chemical manufacturing than the typical end-user might imagine. Every time a minor incident caused downstream trouble for a customer, we took it as an opportunity to audit and improve the process rather than brush it off as routine risk.
The difference between a reliable manufacturer and a sporadic one shows up in those quiet moments—checking the dryness of every drum, running an extra chromatogram at the end of a late shift, or catching a label typo before shipping. That direct, hands-on approach means nobody gets stuck with compromised product or a stalled synthesis campaign.
Customers sometimes ask us how to pick between different trifluorobutyrate building blocks for scale-up work. Our advice rests on what we’ve seen across a decade of campaigns. This specific compound’s mix of ester group, secondary alcohol, and trifluoromethyl tail gives just the right balance between reactivity and stability for many pharmaceutical targets. It stands up better against hydrolysis and excessive side reactions than methyl-based alternatives, and often delivers cleaner runs even as a feedstock for further functionalization.
Not every project needs the high purity or safety margins we build in by default, but for those at the leading edge of research, those extra measures mean faster progress and fewer disappointments. Chemists working at the front lines appreciate a material that holds up both in glassware and at plant scale. Our deep understanding of all stages—from raw materials and synthesis, through quality control and shipment—translates to a smoother experience and less risk for partners.
The future of fluorinated building blocks is shifting as industry demands increase around sustainability, safety, and ever-tighter regulatory controls. We track trends in advanced material applications, including specialist polymers and high-value diagnostics. Our team experiments with greener reaction schemes and investigates options for even finer impurity control. Ethyl 3-hydroxy-4,4,4-trifluorobutyrate will remain a core offering, supported by years of hands-on experience and feedback loops with the users who push innovation forward.
Our direct approach lets us learn fast, adapt processes, and guarantee a consistent supply chain from our reactors to your bench. Every shipment leaves our plant having passed the same rigorous success criteria led by operators who know the real-world impact of a single unstable molecule. Behind every drum stands a skilled team committed to safety, sustainability, and support—qualities we have earned not by chance, but through long years in the field, one batch at a time.