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3,3,3-Trifluoropropionic Acid

    • Product Name 3,3,3-Trifluoropropionic Acid
    • Alias TFPA
    • Einecs 206-236-9
    • 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

    711962

    Cas Number 13116-91-5
    Molecular Formula C3H3F3O2
    Molecular Weight 128.05 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 131-133°C
    Melting Point -31°C
    Density 1.389 g/cm³ at 25°C
    Refractive Index 1.340
    Acidity Pka 1.31
    Solubility In Water Miscible
    Flash Point 82°C
    Synonyms 3,3,3-Trifluoropropanoic acid
    Purity Typically ≥ 98%
    Smiles OC(=O)CC(F)(F)F
    Ec Number 236-045-7

    As an accredited 3,3,3-Trifluoropropionic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 100 mL, with a secure screw cap; features hazard labeling, product name, quantity, and supplier details.
    Shipping 3,3,3-Trifluoropropionic Acid should be shipped in tightly sealed, corrosion-resistant containers, clearly labeled, and stored upright. Transport in compliance with local, national, and international regulations for hazardous chemicals. Avoid extreme temperatures and direct sunlight. Ensure packaging prevents leaks and exposure. Use appropriate protective equipment during handling and shipment.
    Storage 3,3,3-Trifluoropropionic acid should be stored in a tightly closed container in a cool, dry, well-ventilated area away from incompatible substances such as strong bases and oxidizing agents. Protect it from moisture and direct sunlight. Store at room temperature, and keep away from sources of ignition. Proper chemical labeling and safety signage should be clearly displayed.
    Application of 3,3,3-Trifluoropropionic Acid

    Applications of 3,3,3-Trifluoropropionic Acid in Industrial Manufacturing

    As a dedicated producer of 3,3,3-Trifluoropropionic Acid, we supply this specialized fluorinated carboxylic acid to advanced manufacturers who require precise performance in their downstream formulations. The following sections detail key application fields where our product plays a critical role in fine chemical synthesis, pharmaceutical development, agrochemical intermediates, specialty polymer modification, and electronic materials, with clear operational parameters for industrial partners.

    1. Pharmaceutical Intermediate Synthesis

    3,3,3-Trifluoropropionic Acid functions as a building block in the synthesis of fluorinated pharmaceutical intermediates required for the production of cardiovascular, anti-inflammatory, or central nervous system drugs. Reactors in pharmaceutical API plants dose our acid to introduce a metabolically stable trifluoromethyl group, increasing active ingredient bioavailability and half-life. Our material enables acylation or condensation reactions under strictly controlled Good Manufacturing Practice environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. monographs for related APIs/intermediates
    • 21 CFR 211 – FDA cGMP for Finished Pharmaceuticals
    • REACH Registration for imported raw materials in the EU

    Typical usage ratio

    • 0.5–1.8 mol equivalents per target intermediate in multi-step organic synthesis; precise quantity adapts to substitution pattern and overall stoichiometry

    Downstream process integration

    • Dosed during key fluorination or alkylation steps in closed batch or semi-continuous glass-lined reactors; often isolated as a sodium salt derivative for further processing in intermediate crystallization and API coupling stages

    Final product types

    • Antiarrhythmic drug intermediates (e.g., Class III agent precursors)
    • Fluorinated statin intermediates
    • CNS-active compound intermediates with enhanced metabolic stability

    2. Agrochemical Active Ingredient Manufacturing

    Producers in the agrochemical sector utilize our trifluoropropionic acid as a precursor when synthesizing active moieties for herbicides, fungicides, and insecticides that require electron-withdrawing groups for selectivity and environmental resistance. The acid provides structural fluorination in selective acid chlorides and amides required for high-performance crop protection products.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for fine chemical manufacture
    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) guidelines
    • China GB/T 1605 general quality norms for technical materials
    • EU Regulation (EC) No 1107/2009 for Plant Protection Products

    Typical usage ratio

    • 0.8–2.5% by weight of total batch in targeted derivatization steps for triazine, pyridine, or phenoxy-substituted agrochemical active ingredient syntheses; adjusted based on final molecular design and process conversion rates

    Downstream process integration

    • Introduced at the acylation or amide formation stage using automated dosing pumps in jacketed reactors; often converted to acid chloride with thionyl chloride in-situ before coupling or cyclization

    Final product types

    • Fluorinated amide herbicide actives (e.g., for selective weed control)
    • Precursor to triazole fungicide cores
    • Building block for insecticide active intermediates

    3. High-Performance Polymer Modification

    Specialty polymer manufacturers employ this acid to introduce trifluoromethyl-functional groups onto aliphatic or aromatic backbones, thereby enhancing hydrophobicity, dielectric properties, and chemical resistance of advanced engineering plastics and fluoroelastomers. Production lines integrate the acid during copolymerization or post-polymer modification phases for use in automotive, aerospace, and high-voltage insulation applications.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 (Environmental Management Systems)
    • UL 94 Flammability Standard for safety-critical polymers
    • RoHS Directive 2011/65/EU for hazardous substances restriction
    • FDA CFR 21.177.1550 (if formulated for food contact applications)

    Typical usage ratio

    • 0.3–1.5% by weight in bulk resin mass for copolymerization, or in post-functionalization blends; ratios chosen for balance of performance, compatibility, and processing ease

    Downstream process integration

    • Added during in-reactor copolymer synthesis of fluorinated acrylics or polyamides; can also be grafted post-polymerization in a solution-phase or melt-blending process, typically under inert atmosphere to prevent decomposition

    Final product types

    • Fluorinated high-performance plastics (films, rods, sheets)
    • Modified polyimide and fluorosilicone elastomers
    • Insulating films for microelectronics and heavy-duty wire/cable

    4. Electronic Chemicals and Photoresist Formulation

    In the electronics sector, precision formulators use our product as a key intermediate for the introduction of trifluoromethyl groups into advanced photoresist chemicals, dielectric materials, or cleaning agents. The material ensures low residue, controlled volatility, and compatibility with semiconductor-grade manufacturing protocols, critical for wafer processing and precision pattern transfer.

    Industry compliance standards

    • SEMI C15.1 Specification for Liquid Photoresist
    • IPC-4101D/41 Performance Specification for High-Speed Laminates
    • ISO 14644-1 Cleanroom and Controlled Environment Standards
    • JEITA EIAJ ED-4701/300 (for material reliability testing)

    Typical usage ratio

    • 0.05–0.2% by weight in advanced photoresist formulations; ratio strictly determined by target solubility, etch resistance, and baking profile in lithography processes

    Downstream process integration

    • Incorporated in resist blending tanks during pre-polymer or resin modification phase; solvents and additives introduced sequentially by programmable dispensing lines in ISO Class 5–7 cleanrooms, downstream of monomer purification

    Final product types

    • Photolithography photoresists for IC fabrication
    • High-frequency PCB base film (polymer dielectric enhancement)
    • Wafer cleaning agents free of ionic and metal contaminants
    Free Quote

    Competitive 3,3,3-Trifluoropropionic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Insights on 3,3,3-Trifluoropropionic Acid from a Manufacturer's Bench

    Long-Term Commitment to Purity and Performance

    Nobody knows the expectations of researchers and formulators better than those of us who spend the better part of our days with raw chemicals and reaction vessels. Over the years, we have dealt with our share of challenges producing high-purity 3,3,3-Trifluoropropionic Acid (TFPA) and understand how minor impurities can disrupt entire production processes. This is not the kind of compound that allows for short-cuts; its niche applications depend on consistency batch after batch. In our facility, we blend practical experience with a rigorous approach to quality control, aiming to ensure every shipment delivers reliable results under tight specifications.

    Navigating the Chemistry: Knowing the Substance Inside Out

    Our chemists handle 3,3,3-Trifluoropropionic Acid by molecular formula C3H3F3O2, which features a three-carbon backbone and a trio of fluorine atoms at the terminal end. The trifluoromethyl group does two things—it draws electronic density and modifies the chemical behavior dramatically when compared with non-fluorinated propionic acid. We typically manufacture TFPA through selective fluorination techniques, optimizing temperature, reaction time, and catalyst choice to minimize side reactions and improve yield. We believed early on that controlling these parameters, and not treating them interchangeably from batch to batch, gave our product greater reliability not just on paper but in real-world processes.

    Broader Perspective: How This Acid Stands Apart

    Most carboxylic acids exhibit a familiar chemical reactivity: they act as proton donors and show modest polarity. 3,3,3-Trifluoropropionic Acid changes the rules. Three fluorine atoms latch tightly onto the terminal carbon, greatly boosting the acid's electronegativity and making the compound more acidic than standard propionic acid. Users quickly notice a lower pKa, which means easier deprotonation and expanded compatibility with nucleophilic reagents.

    Here in the plant, we see how this makes a real difference. Customers using TFPA as a specialty intermediate tell us that the acid’s fluorinated structure resists oxidation and many metabolic breakdown processes. The result is a raw material with both a long shelf life and specialized reactivity. Formulators in agrochemical and pharmaceutical sectors see TFPA as a way to introduce strong electron-withdrawing groups or to mimic metabolic resilience found in fluorinated drug candidates. No other simple propionic acid gives quite the same effect. Suppliers of regular propionic acid or monofluorinated analogues do not deliver this distinct trifluoromethyl-driven property set.

    The Product on Our Loading Dock: Practical Details and Lessons Learned

    We carry TFPA in both standard and high-purity grades, focusing on color, moisture, and residual by-product content. Meeting demanding purity cutoffs—often exceeding 99%—always starts on the lab bench with small test runs and extensive chromatographic profiling. One of our best investments has been in regular GC-MS and NMR monitoring, which has spared us countless hours chasing down invisible contaminants. Decades ago, we learned that storage matters. Keeping TFPA in airtight, inert-lined drums reduces the risk of hydrolysis and color change. With the right packaging, we regularly ship the product over long distances without a drop in quality.

    Several customers look for highly specific batch data and even request customized synthesis routes to match their own validation documentation. Our team handles special requests for alternative isotopic labeling and incorporation of TFPA into complex reaction pathways. We have handled everything from one-liter pilot runs to multi-ton scale-ups, working directly with process chemists at other manufacturing plants. The expertise gained from direct production, rather than from theoretical study or resale, has given us an edge. We can pin down the source of unwanted color or odor and adjust the synthesis before a problem grows into a shipment recall.

    Comparing 3,3,3-Trifluoropropionic Acid to Other Fluorinated Building Blocks

    A few years back, a major customer wanted advice on replacing trifluoroacetic acid, which is volatile and strongly corrosive, with something easier to handle for certain syntheses. The obvious step up was to try TFPA, which boasts less volatility and offers a longer carbon chain, opening up new coupling opportunities on the alpha-carbon. Unlike trifluoroacetic acid, TFPA’s three carbon atoms give it a flexibility for building block design—whether users want to synthesize specialized esters or graft a robust fluorinated handle onto molecules used in medicinal chemistry.

    Other fluorinated carboxylic acids, such as difluoropropionic acid or pentafluoropropionic acid, bring their own quirks and challenges. Difluorinated acids lack the same electron-withdrawing punch, limiting their impact on reactivity when compared against TFPA’s trifluoromethyl group. Pentafluoropropionic acid, with its richer fluorine content, often brings increased cost and lower stability under storage. Over repeated reactions and real-world handling, TFPA has hit the sweat spot for many labs. It merges the dramatic reactivity boost of fluorination with the manageability of well-behaved liquids that do not turn nasty after a few weeks in the drum.

    Handling and Practical Safety: A Perspective from the Shop Floor

    Talking about chemical safety means being honest about handling hazards. TFPA, like most fluorinated acids, emits a sharp odor and can irritate skin and mucous membranes. The acid’s volatility, though lower than trifluoroacetic acid, remains a real concern when processing large volumes or when the work takes place in hot conditions. Our own production protocols call for closed systems and dedicated exhaust. Staff use chemical-resistant gloves and safety goggles every time they open transfer lines or sampling ports. While our facility seldom faces accidents, diligent handling prevents most risks before they happen—an essential part of the process, not a box to tick for regulatory sake.

    Long-term service to major pharmaceutical, agrochemical, and fine chemical companies has taught us that customers trust manufacturers who are open about safety measures and limits. We provide clear recommendations on controlled temperature storage and secondary containment for users intending to keep stocks for months. Most process engineers who buy from us run their own safety checks, but they still rely on robust data from our internal reports. We have invested in routine training for new handlers and maintain records of all incidents, even minor ones, to constantly refine our safety protocols.

    Key Applications: Customer Success Stories from Our Perspective

    Once, a client looking to develop next-generation herbicides came to us with concerns about shelf life and field degradation. Traditional carboxylic acids in their active ingredient blend degraded quickly under sunlight and microbial exposure. By switching to 3,3,3-Trifluoropropionic Acid, they extended the life of the active agent. TFPA’s hydrophobic and electron-deficient nature meant the new formula broke down more slowly in the environment, reducing their need for overlapping applications.

    In pharmaceutical research, we have seen our TFPA find its way into drug discovery programs focused on metabolic stability. The trifluoromethyl group resists degradation by most enzymes, allowing medicinal chemists to prolong the circulation time and bioavailability of exploratory drug candidates. While we do not disclose confidential details, it is common practice for our technical team to coordinate directly with research organizations on process optimization. Adjusting reagent ratios or purification steps has sometimes unlocked breakthroughs for partners facing yield losses or unexpected by-products.

    Lessons from Scale-Up: Getting the Details Right

    We went through a challenging scale-up a few years ago, converting a multi-kilogram run from glassware into a continuous stainless-steel reactor. Small batch idiosyncrasies, like trace salt formation or slightly off-target fluorination, quickly became unacceptable at larger scale. We brought in new process control systems to monitor temperature gradients and agitation rates, and set up real-time analysis for every stage of the reaction. Now, every batch delivers the same composition profile we first saw on the bench—without nasty surprises down the shipping line.

    Experienced formulators who have tried both small-scale and industrial volumes often report dramatically different results. Without a production background, it is easy to underestimate how strongly variables such as solvent selection, feed addition rates, or cleaning methods for reactors can impact product purity. Many of our process improvements were the direct result of hands-on troubleshooting and open lines of communication with customers who spotted issues. This feedback loop, more than any specification table, has pushed us to tighten tolerances, streamline logistics, and make real-world usage more predictable.

    Global Trends and Environmental Considerations

    Manufacturing any fluorinated compound in the current era means facing heightened regulatory scrutiny and increasing calls for sustainable practices. As a factory team, we work hard to manage perfluorinated byproducts and have invested heavily in advanced waste treatment. Our facility treats both gaseous and liquid waste, ensuring breakdown of fluorinated residuals before environmental release. Many research partners have asked for information about our production practices, animal testing avoidance, and compliance with international guidelines. Our transparency in these areas has built deeper trust with pharmaceutical and agrochemical partners.

    Globally, demand for TFPA correlates with new advances in crop protection and medicinal chemistry. We track trends by listening to partners working on next-generation pesticides and medicines. Environmental pressures keep tightening, and every year we update our synthesis pathway to minimize side reactions, waste, and reliance on hazardous reagents. This iterative approach means that, as other manufacturers struggle to update older processes, we stay ahead in both product quality and compliance. Our goal is not to produce the cheapest acid, but to guarantee responsible manufacturing practices alongside chemical excellence.

    Ongoing Challenges and Our Solutions

    Supply chain disruptions in raw materials have sometimes posed difficulties. For 3,3,3-Trifluoropropionic Acid, source purity of precursor compounds matters a great deal. Years ago, batches of lower-grade starting materials from overseas suppliers led to months of headaches as we traced new impurities in our final product. In response, we adopted a rigorous supplier audit system and gradually sourced more from local producers, despite higher costs. Maintaining direct oversight of every supply node, even at the expense of margins, means end users do not have to contend with unexplained batch-to-batch variation.

    Occasionally, customers request extremely small impurities, like less than 0.1% water content or total absence of halogenated by-products. Achieving such levels reliably requires dedication and reworking of both the reaction protocol and downstream purification. We re-invest revenue into better distillation setups, analytical tools, and extra hands for custom orders. This focus on continuous improvement has defined our outlook—never treating TFPA as a “commodity” but as a specialty ingredient requiring constant vigilance.

    Why We Take the Long View

    Through direct technical support, joint development ventures, and regular feedback from users, we learned not to rely on assumptions. The needs of a formulary scientist working on blood-brain barrier penetration do not match those of an agrochemist looking to delay soil breakdown. As manufacturers, our responsibility extends beyond selling drums of TFPA—it means sharing the insights gained from countless batches, discussing expected stability, and directly assisting troubleshooting.

    As environmental, technical, and regulatory priorities evolve, TFPA’s specific characteristics ensure its continued role in chemical innovation. Chemists seeking strong electron withdrawal, selectivity, and environmental persistence for new molecules continue to favor our production methods. Years ago, we might have fixated on volumes and throughput. Now, technical accuracy, purity, and safe, responsible handling mean more to both us and our customers. Every kilogram we ship is the result of lessons learned and partnerships nurtured from experience, not simply the execution of a routine order.

    The Future: Collaborative Progress and Evolving Chemistry

    Looking ahead, real advances will hinge on teamwork across the production chain. From reliable sourcing and controlled fluorination to new uses in catalysis, polymer modification, and pharmaceuticals, TFPA’s story is still unfolding. As we improve our synthesis for better selectivity and even greener chemistry, input from the field will continue to steer priorities. For customers, this not only means dependable deliveries of the acid itself, but a growing knowledge base to support their research and manufacturing.

    We make it our business to know both the theory and the day-to-day realities of handling and using 3,3,3-Trifluoropropionic Acid. Lessons from the plant floor guide us just as much as published literature. By grounding our practice in real-world results and open communication, we do more than manufacture a chemical—we help shape how it performs for everyone from bench scientists to process engineers. That is the real difference direct manufacturing experience makes.