Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

Methyl Trifluoropyruvate

    • Product Name Methyl Trifluoropyruvate
    • Alias MTP
    • Einecs 'EINECS 242-209-3'
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    286870

    Chemical Name Methyl Trifluoropyruvate
    Cas Number 52021-82-4
    Molecular Formula C4H3F3O3
    Molecular Weight 156.06
    Appearance Colorless to pale yellow liquid
    Boiling Point 93-95 °C at 12 mmHg
    Density 1.401 g/cm³
    Purity Typically >97%
    Smiles COC(=O)C(=O)C(F)(F)F
    Inchi InChI=1S/C4H3F3O3/c1-10-3(9)2(8)4(5,6)7/h1H3
    Solubility Soluble in organic solvents
    Refractive Index n20/D 1.374

    As an accredited Methyl Trifluoropyruvate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Methyl Trifluoropyruvate is supplied in a 25g amber glass bottle, securely sealed with a PTFE-lined cap for protection against moisture.
    Shipping Methyl Trifluoropyruvate is shipped in tightly sealed containers under inert atmosphere, typically cooled with dry ice to maintain stability. It is classified as a hazardous material due to its reactivity and potential health hazards. Appropriate labeling and documentation are required, and handling by trained personnel is recommended during transit.
    Storage Methyl 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 place, ideally in a refrigerator (2–8°C) or cold room. Store away from acids, bases, and oxidizing agents, and ensure proper labeling and containment to avoid accidental release.
    Application of Methyl Trifluoropyruvate

    Applications of Methyl Trifluoropyruvate in Industrial Manufacturing

    Methyl Trifluoropyruvate serves as a key fluorinated building block in fine chemical synthesis, enabling high-value downstream manufacturing across the pharmaceutical, agrochemical, specialty chemical, and advanced materials sectors. As a direct manufacturer, we support global clients with consistent quality, full regulatory documentation, and supply chain transparency.

    1. Pharmaceutical Intermediates Manufacturing

    Methyl Trifluoropyruvate remains vital in the synthesis of pharmaceutical intermediates particularly for the creation of fluorinated amino acids, β-keto esters, and advanced peptidomimetics. It enables site-specific fluorination for active pharmaceutical ingredient (API) candidates with enhanced metabolic stability and unique pharmacological profiles. Large-scale peptide synthesis facilities integrate this raw material precisely during key condensation or alkylation steps, under strictly controlled GMP conditions. Batch-to-batch consistency, trace metal specifications, and rigorous impurity profiling define our partnership with API manufacturers. Sterile operations and solvent systems must control water content and reactive byproduct formation to maintain pathway specificity and meet stringent finished drug impurity limits.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • US FDA 21 CFR Part 210/211
    • European Pharmacopoeia monograph Ph. Eur. 5.0
    • ChP (Chinese Pharmacopoeia), if for China market supply

    Typical usage ratio

    • Varies between 0.8 – 1.5 molar equivalents based on target fluorinated intermediate
    • Adjusted according to downstream yield, target purity, and specific active functional group requirements

    Downstream process integration

    • Added at the fluorination or condensation step in multistep flow or batch synthesis
    • Solvent choice (e.g. DMF, DMSO, MeOH) tailored to nucleophilic activity and substrate compatibility
    • Careful pH and temperature control to avoid hydrolysis
    • Subsequent purification by crystallization or normal-phase HPLC

    Final product types

    • Fluorinated amino acid derivatives for peptide APIs
    • Pyrimidine and pyridine-based drug precursors
    • β-keto ester intermediates for anti-infective or central nervous system drugs
    • Advanced peptidomimetic building blocks for targeted therapies

    2. Agrochemical Synthesis

    Manufacturers of advanced agrochemical actives depend on methyl trifluoropyruvate to introduce fluorinated moieties into pesticide, herbicide, and fungicide molecules. Its unique reactivity permits the creation of active compounds with improved biostability and selective field persistence. During downstream processing, the material is dosed precisely to control product selectivity and limit unwanted byproducts, supporting regulatory compliance for environmental safety. Our facility ensures stringent QC for elemental fluorine content and confirms residual solvent profiles required for environmentally regulated crop protection manufacturing. Advanced application often requires integration with continuous flow chemistry systems to maintain reproducible conversion and control process emissions.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for agrochemicals
    • European Union Regulation (EC) No 1107/2009
    • US EPA registration standards (40 CFR Part 158)
    • ISO 9001:2015 for quality control management

    Typical usage ratio

    • Employed at 1.0 – 2.5 molar equivalents relative to pesticide precursor to maximize selectivity and conversion
    • Ratio adjusted for specific crop protection actives and regulatory limits for impurities

    Downstream process integration

    • Dosed into reaction vessel during electrophilic addition or acylation stage
    • Requires staged addition in flow reactors to prevent overfluorination
    • Product isolation via solvent extraction and preparative chromatography under reduced pressure
    • Waste stream processed according to environmental health and safety guidelines

    Final product types

    • Selective fluorinated herbicides
    • Systemic fungicides with enhanced activity window
    • Pesticide actives with reduced environmental persistence
    • Pre-emergent crop protection formulations

    3. Fluorinated Specialty Chemical Production

    Specialty chemical companies leverage this raw material in the development of high-performance fluorinated additives, surface-active agents, and fluoro-organic ligands. The trifluoromethyl unit imparts stability and special reactivity essential for heat-resistant coatings and surface modification agents used in electronics and polymer industries. Technical teams monitor the integration of this compound in pilot and commercial scale reactors, focusing on reaction completeness and solvent compatibility critical to specialty chemical performance. Downstream products often require fine-tuned purification through vacuum distillation or column chromatography to meet application-driven purity needs. Our process control and analytical design provide customers with reproducible specifications for each supplied batch to ensure reliable industrial operations.

    Industry compliance standards

    • ISO 9001:2015 for chemical quality management
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EU)
    • GHS (Globally Harmonised System) labeling for specialty fluids
    • UL 94 for polymer additives (if materials enter flame-retardant applications)

    Typical usage ratio

    • Used at 0.5 – 2 wt% in coatings and surfactant formulations
    • 1.0 – 1.2 molar equivalents in small molecule ligand synthesis
    • Tuning of dosage based on required fluorine loading in final specialty molecule

    Downstream process integration

    • Incoporated during the fluorination stage of specialty additive or surfactant synthesis
    • Post-reaction purification step includes distillation or silica-gel chromatography
    • Batch and semi-continuous processes applied for different product volumes
    • Process safety assessment conducted for scale-up

    Final product types

    • Heat-resistant fluorinated coating agents
    • Fluorochemical ligands for catalysts
    • Surface-active agents for wetting and leveling
    • Specialty intermediates for electronics fabrication

    4. Advanced Polymer Synthesis

    Polymer manufacturers value methyl trifluoropyruvate as a fluorine donor in functional monomer synthesis. This use case enables the creation of polymers with high chemical resistance, low surface energy, and unique dielectric properties. Industrial polymerization lines integrate this ingredient to introduce trifluoromethyl functionalities during key monomer formation reactions. Each batch undergoes monitoring for unreacted raw material and byproduct elimination to ensure high-grade polymer specifications. The complexity of these downstream uses demands robust material tracking and process adjustment to match polymer grade and end-use application, from wire insulation to specialty membranes.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management
    • ASTM D3159 for fluoropolymer analysis
    • UL 94/V-0 fire resistance for insulation materials
    • REACH full-registration for polymer raw materials (where required)

    Typical usage ratio

    • Employed at 0.3 – 1.2 molar equivalents in functional monomer synthesis
    • Dosage tailored according to target fluorine content and downstream polymer processing technology

    Downstream process integration

    • Added during polymer precursor monomer formation via nucleophilic addition
    • Followed by chain extension or radical polymerization
    • Additional purification of monomers before polymerization to remove side products
    • Polymer QC includes NMR and GPC validation

    Final product types

    • Fluorinated acrylic copolymers
    • Low-surface-energy coating resins
    • Specialty electrical insulation films
    • High chemical-resistance engineering plastics
    Free Quote

    Competitive Methyl Trifluoropyruvate prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Methyl Trifluoropyruvate: Our Experience, Our Standards

    Methyl Trifluoropyruvate stands out as one of the most technically rewarding products we have developed over our years in specialty fluorinated chemicals. This molecule, often designated by the formula CF3COCOOCH3, grew out of sustained collaboration between our chemists in both R&D and production. Handling this compound successfully requires both respect for its chemistry and a realistic appreciation for what demanding customers expect.

    What Sets This Material Apart

    Many compounds bear the “trifluoro” tag, but few deliver the carbonyl reactivity combined with the electron-withdrawing power that methyl trifluoropyruvate provides. This dual reactivity shows in the breadth of synthetic applications chemists report. The presence of the trifluoromethyl group, set alpha to a carbonyl, shapes the behavior of the molecule in ways that simple esters cannot match. This added group fundamentally reshapes nucleophilicity, acidity of protons, and the outcome of condensation reactions. The methyl ester at the tail end makes purification by distillation or liquid-liquid extraction predictable.

    Our ongoing work in the fluorochemicals space shows a clear demand for a methyl trifluoropyruvate with high purity, low water content, and a defined color. Most applications, especially those headed toward pharmaceutical intermediate synthesis, simply fail if the residual acidity is high or if storage stability wavers. From the earliest days, we set the bar high, rejecting batches with color above a pale yellow or with hydrolyzable fluoride content above 0.05%. These controls do not come from external regulations alone — repeated failures in complex lab syntheses drive them. Peers who set looser specifications often see higher returns or more customer complaints.

    Applications Built on Real Chemistry

    This compound does not serve as a simple solvent or carrier. Its main value emerges where chemists need potent electrophilic species, especially in asymmetric synthesis and fluorine introduction arrays. Through feedback from medicinal and agrochemical research groups, we know that many laboratories seek this pyruvate ester during the construction of β-keto esters or when seeking to introduce trifluoromethyl motifs into bioactive cores.

    We have walked through process optimizations in custom synthesis, sometimes working alongside customers on-site. Each time, the key concern involves batch-to-batch consistency and minimization of impurities that might form unwanted side-products. In catalytic asymmetric transformations, any trace of non-fluorinated pyruvate or methanol residue interferes with sensitive catalyst systems. Chemists working with chiral ligands for enantioselective transformations point to this compound’s reliable behavior when made and stored correctly.

    Some competitors propose ethyl or tert-butyl versions of trifluoropyruvate to lower volatility or adjust solubility. In our experience, the methyl variant offers a good compromise: it remains easy to purify by vacuum distillation, providing a sharp boiling profile, and integrates well into existing laboratory or pilot plant apparatus. Ethyl and bulkier derivatives sometimes linger as traces that complicate downstream separation — our technical teams regularly assist clients pursuing clean mass balances in their analytical data.

    Specifications Sourced from Real Requirements

    We define batches of our methyl trifluoropyruvate using GC, NMR, and titration methods developed after thorough failure analysis. The market contains many technical grade offerings but labs focused on research, scale-up, and regulated production rarely tolerate even minor contamination. The main requests that come from our own chemists and external clients highlight water content, color, trace metals, and acid numbers. Once, a pharmaceutical team flagged side-reactions from less than 0.1% hydrolyzed product — we adjusted our drying protocols rather than offering generic assurances.

    The product emerges transparent and colorless, and shows near-ideal behavior under common storage conditions. We use dedicated glassware and avoid exposure to metals that could trigger discoloration or side-product formation. In packing, our teams insist on freshly sealed borosilicate or fluoropolymer-lined containers for shipments above 250 grams. Inventory that stays too long in steel drums or absorbs moisture does not leave our site. Having reprocessed more than one drum for a partner with strict IR or MS targets, we recognize how even small deviations turn into batch rejections downstream.

    Handling, Storage, and Practical Recommendations

    Methyl trifluoropyruvate asks for respect in handling. We prepare every package with a focus on moisture protection and clarity about shelf stability. Our logistics department tracks customer delivery feedback. If glass bottles arrive with condensation, or if trace decomposition appears in transport, we investigate before the next order leaves the dock. Chemists who receive our product put it straight into freezer storage under nitrogen if extended work is planned. Exposure to atmospheric moisture or basic surfaces visibly reduces shelf life and purity.

    Every technical question we field about solubility, chemical compatibility, or application in specific synthetic pathways draws on experience accumulated since the product debuted in our lineup. Methanol, ethers, and non-nucleophilic polar solvents suit this compound best; strong base or nucleophilic conditions rapidly generate hydrolysis or addition byproducts. Our own process development teams follow the same recommendations.

    Comparing with Other Trifluoro Compounds

    The trifluoromethyl functional group pops up in dozens of laboratory and catalog organics — from trifluoroacetic acid to trifluoroethanol to the various acetoacetates. Yet, methyl trifluoropyruvate anchors a corner of reactivity that frees up downstream chemistry. Many fluorinated reagents push costs higher with limited shelf stability or require tricky handling. This material boasts a shelf life measured in months under correct storage. The reactivity profile offers a sweet spot: both powerful enough for Michael additions or as an acylating agent, but not so unstable as to polymerize or darken rapidly.

    Working hands-on with both methyl and ethyl variants of trifluoropyruvate, our teams have documented how the methyl group speeds up certain condensation reactions and simplifies purification. Bulkier alkyl esters can linger into the final APIs or active crop protection agents, muddying NMR spectra, and in one case causing regulatory headaches. By focusing production on the methyl ester, we streamline timelines for downstream chemical development.

    Batches of methyl trifluoropyruvate trace their origins to both proprietary processes and decades-old literature. We have re-tuned legacy synthetic routes to limit side products that once required post-reaction scrubbing. This means that end-users see lower odor, better yields in test reactions, and fewer ghost peaks during HPLC or LC-MS analysis. Technical service requests that come to us often mention challenges with earlier, less-refined products from catalog traders. Our chemists have rinsed out enough battered glassware and rebuilt enough pilot plant runs to know how small differences in reagent purity ripple into much greater costs downstream.

    Usage Stories from the Field

    Research and process chemists in synthetic fields recognize methyl trifluoropyruvate’s versatility. It steps in as a synthon for trifluoromethylated building blocks, especially for fragments destined for pharmaceuticals or high-performance electronics. One team, optimizing a new fluoroalkylated amino acid, reported that switching to our product shortened their hydrogenation and purification times by nearly a quarter. Those stories find echoes in development labs looking to maximize the output of rare and costly chiral ligands.

    Organic labs frequently challenge suppliers to provide reagents with both high reactivity and stability. Over time, customer requests led us to track and report metrics beyond standard assay and appearance — including details like peroxide content and residue after rotary evaporation. By engaging directly with users, we pinpoint what specifications make applications work or fail. This information goes into our batch control sheets, not just into sales literature.

    At multi-kilo and pilot scales, handling demands change. Solvent compatibility extends from DCM to acetonitrile, and as runs scale up, even small traces of transition metal salts or dust show up in end-user QC. Our batch records include the traceability of all metalware, and facility clean-out between campaigns, because lower-grade reagents in these syntheses routinely lead to regulatory risk or outright production failures later on.

    Market Trends and Technical Challenges

    Researchers push to integrate more fluorinated moieties into active molecules, boosting bioavailability and metabolic stability. As a fluorine-rich synthon, we see demand for this pyruvate steadily rising, despite challenging prices pushed up by HF and fluorine derivative supply constraints worldwide. Because many critical applications live in emerging synthetic pharmaceuticals and agricultural actives, every improvement in purity or in process safety gives tangible value down the road.

    Global supply chains for fluorinated reagents remain exposed to volatility. Our investment in local precursor synthesis and flexible production scheduling grew out of hard lessons in allocation and bottlenecked feedstocks. Once, an abrupt shortage in a CF3-bearing intermediate forced an entire month of unplanned downtime. No distributor or trading house resolved the bottleneck for us. Only added in-house purification steps and local supplier partnerships made output stable again.

    We learned that while many other manufacturers simply resell or repackage bulk material, meeting the standards of modern advanced chemistry means building in quality from synthesis onward. Each impurity profile draws our attention; every new substrate or synthetic target from a client pushes us to refine characterization protocols. This vigilance results in measurable success — customers return for the technical data and batch consistency that consistently simplifies their own validations and regulatory filings.

    Support and Troubleshooting Based on Direct Feedback

    Direct engagement with seasoned researchers drives most incremental improvements. If a research user flags a side product, our analytical teams schedule joint reviews. One QC manager from a European lab tracked down a puzzling baseline drift in their GC analysis to a trace byproduct in material from a generic supplier. We pulled our own archive samples, walked through both NMR and mass spectrometry comparisons, and identified gaps in their conforming specification. They now require our certificates as part of every incoming materials check.

    For all routine and non-routine questions, we assign the same technical staff who actually manage our reactors or prep our in-process samples. End users wanting application advice talk with chemists practicing hands-on fluorine chemistry, not just sales managers. Training for new users covers safe handling, options for recycling solvent streams, and troubleshooting in high-throughput settings. These conversations shape future product improvements much more than any industry trend report ever could.

    Continuous Improvement, Practical Production Realities

    Every step in bringing methyl trifluoropyruvate to a research or production setting creates a feedback loop into our plant. If shipment batches reveal new storage sensitivities, we shift packaging or review warehouse ventilation. Customer discoveries of incompatibility in a new reaction guide investment in alternative drying or purification systems. Once, a pilot partner’s complaint about delayed deliveries led to new inventory management workflows that prevent finished stock from ever sitting idle near plant exhaust lines.

    Through every improvement, care, and workaround, the core motivation springs from first-hand experience. Our top product batches represent multiple rounds of process troubleshooting, response to adverse transport conditions, and direct input from expert users. The learning curve stays steep, given the growing complexity of synthetic applications worldwide. Each knot untied in handling, purification, or shipping gets reported back and integrated as a practical solution.

    Looking Ahead: Evolving with the Needs of Science

    Demand for reliable fluorochemical intermediates stretches further every year, shaped by both audacious new targets in pharmaceutical pipelines and tightening regulatory scrutiny. As regulatory frameworks shift and technical demands rise, only flexible and technically proficient suppliers will keep up. Our investment stays focused on direct manufacturing and hands-on technical development, avoiding the distraction and inertia that burdens trading houses or arms-length resellers.

    For every batch of methyl trifluoropyruvate that leaves our site, the path between chemical innovation, robust quality, and application support remains clear. Our practical, experience-driven approach lets our team deliver what working chemists, not distant marketers, actually need to succeed. By capturing lessons from both routine production and extraordinary trouble tickets, we aim to keep technical chemistry both achievable and rewarding.