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HS Code |
161969 |
| Cas Number | 22064-52-4 |
| Molecular Formula | C3H3F4NO |
| Molecular Weight | 145.06 g/mol |
| Iupac Name | 2,3,3,3-Tetrafluoropropanamide |
| Appearance | White to off-white solid |
| Melting Point | 46-48°C |
| Density | 1.5 g/cm³ (estimated) |
| Solubility In Water | Soluble |
| Smiles | C(C(=O)N)(F)C(F)(F)F |
| Inchi | InChI=1S/C3H3F4NO/c4-1(2(5)6)3(8)7/h1H2,(H2,7,8) |
| Synonyms | Tetrafluoropropionamide, TFPA |
| Storage Conditions | Store at 2-8°C, keep container tightly closed |
As an accredited 2,3,3,3-Tetrafluoropropionamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle with a secure screw cap, labeled "2,3,3,3-Tetrafluoropropionamide" and hazard warnings in black print. |
| Shipping | 2,3,3,3-Tetrafluoropropionamide should be shipped in tightly sealed containers, away from incompatible substances, and clearly labeled. Handle with care, using appropriate protective measures. Transport in accordance with local, national, and international regulations for hazardous chemicals. Store in a cool, dry place, protected from moisture, sunlight, and heat sources during transit. |
| Storage | 2,3,3,3-Tetrafluoropropionamide should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Store in a cool, dry, and well-ventilated area, preferably in a chemical fume hood. Keep away from incompatible substances such as strong acids, bases, and oxidizers. Clearly label the container and restrict access to trained personnel only. |
Applications of 2,3,3,3-Tetrafluoropropionamide in Industrial ManufacturingAs the original manufacturer, we support global industrial customers with high-purity 2,3,3,3-tetrafluoropropionamide for critical applications in chemical synthesis. Below we detail main industrial application scenarios, focusing on compliance, blending ratios, workflow, and downstream final goods. 1. Fluorinated Agrochemical Intermediate SynthesisMajor agrochemical manufacturers use 2,3,3,3-tetrafluoropropionamide as a targeted amide intermediate in the synthesis of next-generation herbicides and insecticides. Leading producers incorporate this material for its unique fluorinated backbone, improving bioavailability and selectivity in active compounds required for crop protection. Technical teams favor the controlled amide functionalization, which provides opportunities for selective coupling or further fluorination under defined process steps. Strictly managed input ratios allow regulated downstream conversion with minimal byproduct formation, supporting efficacy and regulatory acceptability in final agrochemical formulations for field deployment. Industry compliance standards
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2. Fluorine-Containing Pharmaceutical IntermediateAPI manufacturers require 2,3,3,3-tetrafluoropropionamide as a key intermediate in synthesis routes for fluorinated drug candidates, especially in the development of anti-inflammatory, CNS, and antiviral medications. The compound’s amide group and high fluorine substitution allow for selective conversion to various bioactive motifs, facilitating late-stage functionalization in medicinal chemistry pipelines. Process chemists integrating this intermediate achieve clean transformations with enhanced control over purity, facilitating compliance with high-end GMP production requirements. Close attention to input purity and reaction scale enables reliable batch-to-batch reproducibility for downstream pharmaceutical launches. Industry compliance standards
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3. Advanced Fluoropolymer Monomer PrecursorProducers in the specialty polymer sector utilize 2,3,3,3-tetrafluoropropionamide as a monomer precursor for the synthesis of high-performance fluoropolymers. This chemical provides a strategic source of amide functionalities with robust fluorine content, contributing to the development of polymers with advanced resistance to solvents, chemicals, and temperature. Technical formulations incorporate this intermediate during controlled polymerization to manage molecular weight and key end-use performance properties. Final fluoropolymers find application in stringent industrial settings, including electronics and chemical containment industries, where safety and process reliability demand consistently pure input streams. Industry compliance standards
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4. Electronic Grade Fine Chemical ManufactureProducers of electronic-grade fine chemicals incorporate 2,3,3,3-tetrafluoropropionamide in the preparation of functional materials used for microelectronics, including advanced etchants and surface treatments for semiconductor wafer fabrication. Its well-defined fluorinated amide structure enables process engineers to synthesize fluorine-rich surface modifiers exhibiting high thermal and chemical stability. Integration of this material requires ultra-high purity supply and strict adherence to contamination-free protocols critical to semiconductor process yields, driving demand for traceable, lot-based QC and compliance documentation. Industry compliance standards
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In the landscape of specialty fluorochemicals, 2,3,3,3-tetrafluoropropionamide stands out for those seeking a building block with proven performance and distinct handling properties. Direct experience from our manufacturing lines shows that producing this compound requires unwavering attention to purity, as even trace-level impurities can interfere with the work chemists rely on downstream. Our production team routinely analyzes every batch for byproducts such as fluorinated esters or acid remnants to keep the material fit for demanding synthesis environments.
Our current production stream produces 2,3,3,3-tetrafluoropropionamide in a stable form suited for lab, pilot, and scale-up quantities. Over the years, feedback from researchers and production partners pointed us to two main requests: keep the content of free acid exceptionally low and ship promptly to avoid degradation. The latest batches reach purity at or above 99% by HPLC analysis. This level feeds reliably into synthesis—be it for pharma intermediates or performance materials R&D—without unwanted interference.
In daily plant operation, the colorless crystalline form tells us something immediately: no hydrolytic breakdown or polymeric residues developed during packaging or storage. As colleagues who handle chemicals daily know, tactile and olfactory cues speak volumes before paperwork ever appears—the tetrafluoropropionamide gives off a mild, not acrid, odor, a sign solvents have been sufficiently removed during our drying sequence.
Shipping in tightly sealed fluoropolymer or amber glass ensures that moisture and UV do not affect the product between our facility and your lab. Our packagers use both environmental monitoring and regular visual checks to avoid caking or yellowing, which experience shows are signs of compromised product integrity. Shelf stability at ambient conditions remains reliable for at least six months sealed, based on accelerated aging studies with batch retention samples.
Over recent years, R&D customer feedback landed on several use cases where this compound offered an edge. In fluoroalkylation reactions, 2,3,3,3-tetrafluoropropionamide brings in a propionamide substituent already bearing four fluorine atoms—this structure enables introduction of both fluorine and functional amide groups, streamlining synthesis steps for advanced intermediates. Chemists working on active pharmaceutical ingredient routes cited cleaner conversions than with trifluoroacetyl sources, which too often yield nonvolatile byproducts. Our regular customers working in agrochemical development mention this same property, where the selectivity in N-functionalization leaves fewer purification burdens and improves overall project efficiency.
Comparing our tetrafluoropropionamide to similar building blocks, such as trifluoropropionamide or difluoropropionamide, reveals a set of tradeoffs. Our teams have seen that the extra fluorine atom at the 2-position in 2,3,3,3-tetrafluoropropionamide shifts reactivity and alters volatility. Trifluoropropionamide often struggles to provide the same degree of electron-withdrawing strength or results in lower nucleophilicity when constructing target molecules with fluorinated moieties. In kinetic studies done for an industrial partner, the tetrafluorinated compound showed more consistent incorporation into heterocyclic frameworks compared to its less-fluorinated cousins.
The research team in our applications lab recounted an instructive comparison for carbonyl activation. When parallel preparations of activated amide intermediates used trifluoro- and tetrafluoropropionamides, only the tetrafluoro version delivered consistently higher yields and fewer side products, especially under lower temperature regimes. For colleagues in the fine chemicals sector, this difference translated to less material loss and more robust process control.
On the shop floor, processing tetrafluoropropionamide presents unique safety and environmental questions. After years of batch manufacturing, we’ve learned that its vapor pressure, although low, deserves respect. Our operators rely on positive-ventilation fume hoods and maintain nitrogen blanketing through all transfer steps. During large lot preparation, we monitor both workplace air and effluent for low-level emissions; continuous improvement and strict emission control remain part of routine operations.
Unlike some perfluorinated compounds, this amide has not shown persistent environmental accumulation in our discharge audits, largely thanks to rapid break-down in acidic or basic media. Nevertheless, waste management teams avoid blending tetrafluoropropionamide residues with mixed halogenated streams, as we’ve documented that this may cause pH control issues in our on-site neutralization units. Proper segregated disposal and documented chain-of-custody for all outflows formed the core of our compliance approach.
Personal protective equipment expectations do not depart from industry norms, but every new operator must review the specifics on containment in active production bays. The crystalline dust disperses more easily than some heavier amides, so full-face respirators supplement use of splash goggles. Our old line hands remind every trainee not to underestimate this aspect—just because the material appears benign in the vial, careless handling often leads to unnecessary skin or respiratory contact.
Our process development group consistently looks for ways to raise output and cut energy input in fluorination steps. In the move from pilot to commercial-scale synthesis, we tweaked solvent blends and strike conditions, learning that batch control on water content reduced byproduct hydrolysis ninefold relative to early lab runs. Chlorofluorocarbon alternatives, once routine for analogous reactions, no longer enter any step—today, all fluorine source and amide precursors comply with internal standards based on EU REACH and US TSCA guidance. Our documentation stands ready for customer audit, something recent buyers praised as well beyond the industry minimalism they encounter elsewhere.
Capacity expansions in the past year let us shorten lead times even at the high-purity level customers demand in medicinal chemistry. In feedback sessions, large-volume users prioritize not just price and speed, but clarity about any batch-to-batch variation. That transparency can head off lost time during synthesis troubleshooting. While our scale doesn’t yet match global megasuppliers, the level of technical attention and direct communication with buyers gives our mid-sized operation agility lacking in the largest chemical multinationals.
Project chemists reach out to us most often about the suitability of 2,3,3,3-tetrafluoropropionamide for key coupling or substitution reactions. Our analytical group often shares empirical reactivity data, showing how the extra fluorine confers greater metabolic stability in later-stage pharmaceuticals. During medicinal chemistry runs intended for late preclinical work, downstream teams discovered less decomposition in simulated biological matrices compared to products using non-tetrafluorinated amides.
Polymer chemists, working alongside our technical team, have reported more controlled branching in trial fluoroelastomer syntheses. Their reports confirm what our own process engineers suspected: tetrafluoropropionamide links more predictably with activated monomers, particularly where chain-end fidelity must stay high. This reliability and batch consistency also allowed scale-up partners to reduce waste during pilot extrusion trials. These insights grew from months of direct site visits and shared troubleshooting—not theory, but hands-on results.
Within the family of fluorinated amides, 2,3,3,3-tetrafluoropropionamide demonstrates key differences familiar to our product specialists. Commercial trifluoropropionamides, for example, show lower elemental fluorine loading, translating to less dramatic shifts in polarity and less pronounced metabolic shielding. In targets where maximum fluorine content defines performance—be it in agrochemical stability or pharmaceutical clearance—those extra atoms set our product apart. The tetrafluorinated amide also shows less tendency to hydrolysis across a broad pH range, based on both in-house and client-submitted stability data.
R&D teams comparing similar products often reflect on pricing and consistency. Our cost per kilogram remains competitive, due in part to vertical integration from fluorinated acid chloride production through to final amide work-up. We cut out intermediaries, keeping direct control over quality checkpoints and offering better technical support. Users confirmed, in project reviews, that supply disruptions are rare due to our raw material redundancy contracts with upstream fluorine gas and alkyl source providers.
Working on process documentation, we see clearly how often clients want to know about both purity and trace contaminants. Side-by-side assessment with shorter-chain or branched analogs exposes differences in UV absorption, trace metals, and even storage stability. Our QA/QC lab tracks results on every run, sharing full chromatographic profiles when requested. Third-party spot audits consistently verify our internal claims—a point that builds trust among smaller outfits needing confidence while qualifying a new input.
Being manufacturers rather than brokers, we favor conversations with users at every step. Our technical service engineers field questions daily about storage, reactivity, and interfaces with novel synthetic schemes. A recent example involved a customer in emerging materials, stymied by impurity knock-on effects in organocatalyst systems. Our senior chemists evaluated their process, suggested minor temperature and solvent modifications, and followed up until yields reached spec. This kind of engagement, grounded in years of in-house synthesis and plant troubleshooting, consistently reduces risk for downstream users.
Cooperation with academic researchers has led to new application notes, such as using 2,3,3,3-tetrafluoropropionamide for amide bond-forming reactions under green chemistry parameters. Selectivity data from collaborating labs showed how fluorous phase extraction makes this specific amide more amenable to recovery and reuse than others in its class—a distinct edge for those exploring more sustainable approaches to modern synthesis.
Staying current with global regulations, we maintain product documentation that covers all expected safety, compliance, and transport notes. Our teams keep registration dossiers up to date for each jurisdiction where we ship product, and our customers have full access to regulatory status, toxicology summaries, and shipment history. Unlike generic repackers or traders, we provide certificates linking every batch to its origin—crucial for product defense in regulated markets.
Through cooperation with environmental consultants familiar with both REACH and TSCA requirements, incidents of shipment hold-ups or field rejects dropped to nearly zero last fiscal year. For buyers affected by overseas compliance uncertainty, this transparency streamlines both planning and reporting. Our in-house regulatory officers update hazard communication promptly, notify clients about changes ahead of implementation, and support customer audits and questions with specialized expertise—making engagement proactive, not reactive.
Discussions with procurement specialists clarified how reliability goes hand-in-hand with robust supply. Our supply chain model sources precursors both domestically and from longstanding global partners. This policy kept us producing through supply disruptions that sidelined competitors during recent global feedstock crunches. We routinely buffer inventory based on forward orders and historical usage. Value arises not only from stable material but also from ensuring the documentation and compliance support that downstream partners count on at critical moments.
Smaller customers in particular value our readiness to adjust packaging to fit their equipment or storage constraints. Flexible lot sizes and robust pack-out methods—such as PTFE liners or inert-atmosphere shipments for moisture-sensitive lots—cut risk and speed up lab integration. Engineering teams from our clients regularly visit our site to align protocols and cement trust, recognizing the unique position manufacturers occupy in protecting quality from synthesis bench to final application.
We see the role of the manufacturer not just as supplier but as collaborator in solving complex synthetic and process challenges. Regular technical bulletins and open information channels allow customers to learn from our broader experience—successful start-ups, lessons from scale-up mishaps, and troubleshooting oddities—all combine to minimize costly surprises. Workshops hosted at our facility bring users together to swap insights and share real-world outcomes, which ultimately enriches ongoing product development.
Several new applications for 2,3,3,3-tetrafluoropropionamide are now under joint investigation, including as a feedstock in advanced fluorinated surfactants and as a selective modifier for catalyst supports. Our team actively supports customer pilot trials with on-site technical help, quick-response analytical backstops, and direct shipment from production to keep projects moving without interruption.
By centering our operations around long-term customer needs and open technical exchange, we aim to anchor our manufacturing practice in the real requirements of chemical innovators. As the field of fluorochemicals keeps advancing, maintaining this practical, hands-on approach ensures that each new batch of 2,3,3,3-tetrafluoropropionamide meets more than just specs—it also supports safe, innovative, and efficient progress from the chemist’s bench to full-scale production.