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HS Code |
652206 |
| Productname | 4-Amino-1,1,1-Trifluoro-3-Buten-2-One |
| Casnumber | 79456-22-9 |
| Molecularformula | C4H6F3NO |
| Molecularweight | 141.09 |
| Appearance | Pale yellow to brown liquid |
| Purity | Typically ≥ 97% |
| Boilingpoint | No standard data; estimated ~ 105-110°C at reduced pressure |
| Density | Approximately 1.26 g/cm3 |
| Solubility | Soluble in polar organic solvents |
| Smiles | C(C=C(C(=O)N)C)(F)(F)F |
| Inchi | InChI=1S/C4H6F3NO/c5-4(6,7)2-1-3(8)9/h1-2H2,(H2,8,9) |
| Refractiveindex | No standard data; estimated n20/D ~1.41 |
| Storageconditions | Store at 0-4°C, protect from light and moisture |
| Hazardclass | Irritant |
As an accredited 4-Amino-1,1,1-Trifluoro-3-Buten-2-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 4-Amino-1,1,1-Trifluoro-3-Buten-2-One is supplied in a sealed amber glass bottle with a tamper-evident cap. |
| Shipping | 4-Amino-1,1,1-Trifluoro-3-Buten-2-One should be shipped in tightly sealed containers, protected from light and moisture. Transport under cool, dry conditions, following all relevant hazardous material regulations. Ensure proper labeling and documentation, and use secondary containment to prevent leaks or spills during transit. Handle only by trained personnel. |
| Storage | 4-Amino-1,1,1-trifluoro-3-buten-2-one should be stored in a tightly sealed container under an inert atmosphere (such as nitrogen or argon) to prevent reaction with moisture and air. Keep it in a cool, dry, and well-ventilated area away from incompatible substances like strong oxidizers or acids. Store at temperatures recommended by the manufacturer, typically in a refrigerator or a temperature-controlled chemical storage room. |
Applications of 4-Amino-1,1,1-Trifluoro-3-Buten-2-One in Industrial Manufacturing4-Amino-1,1,1-Trifluoro-3-Buten-2-One serves as a critical intermediate in several specialized downstream industries. Its unique structure supports selective reactivity and integration in synthesis pathways where fluorinated functionality provides performance improvements and regulatory compliance. Below, we outline key real-world industrial applications, process details, standards, and resulting end products based on ongoing manufacturing partnerships. 1. Active Pharmaceutical Ingredient (API) Synthesis for Antiviral CompoundsManufacturers use 4-Amino-1,1,1-Trifluoro-3-Buten-2-One as a building block in synthesizing fluorinated heterocyclic scaffolds, which are core structures for novel antiviral APIs. Its high electrophilic reactivity allows precise introduction of trifluoromethyl groups under controlled conditions. At multi-kilogram production scales, operators achieve high yield during the key substitution reaction step, ensuring traceability and raw material purity. Strict system controls govern each process batch, with inline monitoring during aminotransfer and condensation stages to meet pharmaceutical quality demands. Industry compliance standards
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2. Agrochemical Intermediate in Herbicide ManufacturingAgrochemical formulators rely on this compound as a key precursor to synthesize trifluoromethylated pyrazole and pyrimidine derivatives. Its reactivity profile facilitates regioselective introduction of fluorine atoms, which play a crucial role in lowering application rates and increasing soil stability. During large-scale synthesis, plant managers monitor exothermic stages and control solvent recycling to adhere to environmental quality mandates. Industry compliance standards
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3. Specialty Fluorinated Monomers for Performance PolymersProducers in the polymer sector introduce this compound into high-performance fluorinated polymer architectures, especially for membranes and advanced coatings. Its α,β-unsaturated structure allows addition polymerization, imparting both chemical resistance and low surface energy. Quality assurance protocols demand comprehensive analysis of residual starting material and monitoring of reaction kinetics, as small variations can influence the polymer’s molecular weight distribution and end-use coating properties. Industry compliance standards
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4. Fine Chemical Intermediate for Fluorinated Dye SynthesisDye manufacturers select this compound as a functionalized amino-trifluoro precursor during synthesis of reactive dyes for technical textiles and specialty inks. Its structural characteristics enable effective coupling with aromatic aldehydes or ketones via established condensation protocols, yielding colorants with improved photostability. The production environment requires closed-loop recovery of by-products and validated methods for tracking contaminant levels throughout scale-up. Industry compliance standards
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5. Intermediate for Fluorinated Building Blocks in Life Science R&DR&D laboratories and custom synthesis organizations turn to this material for the construction of advanced fluorinated fragments. The electrophilic carbonyl and nucleophilic amino group kinetics support route scouting for isotopically labeled compounds, PET tracers, and probe development. This requires careful control of isotope purity, participating in micro-scale batch analytics, and adherence to documentation, especially in support of regulatory filings for chemical probes. Industry compliance standards
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Every manufacturer faces the challenge of moving research-grade discoveries into concrete production lines. In our case, working directly with 4-Amino-1,1,1-Trifluoro-3-Buten-2-One has shown what it takes to deliver an advanced building block to global labs and plants seeking reliability and utility. Decades in chemical manufacturing have made it clear how easily the entire project—no matter the scale—can turn on the quality and consistency of a single intermediate. We offer this trifluoro enamino ketone as a ready connection between fluoro-organic chemistry and the growing library of fluorinated intermediates in pharmaceuticals, agrochemicals, and specialty chemicals.
Structurally, the molecule bridges aminated butenones and fluorinated fragments in a way few alternatives can. Its 4-amino group brings a reactivity profile sought after in medicinal and crop protection chemistry. We have produced it in kilogram and multi-ton batches—both for custom syntheses and routine supply—favoring a streamlined process that minimizes waste and simplifies downstream purification. Experience has shown trifluoromethyl groups are not only for “effect”; they define a different reactivity toward nucleophiles, broaden bioactivity windows in screening campaigns, and often increase metabolic stability in API development.
Many chemists seek its unique combination of a conjugated amino butenone system alongside full trifluoromethyl substitution at the terminal carbon. Compared to non-fluorinated analogs, there is a practical shift in boiling point, volatility, and even odor characteristics—factors that matter in a synthesis plant as much as a research lab. Our engineers have optimized the storage and handling guidelines based on direct feedback and operational experience, drawing from several pilot campaigns across various climates and geographic regions.
Scalability in organic fluorine chemistry can expose weaknesses in impure reagents or insufficient purification steps. Our method involves a multi-step reaction route, with clinical tracking of byproducts. Process development started from gram-level studies, including exhaustive detection of minor impurities, and has now matured to metric tons with high batch-to-batch reproducibility. The critical points come during final isolation, where rapid removal of volatile fractions and protective atmosphere have proven necessary. Any slip during this stage raises impurity risks or losses that operators downstream never forgive.
Output quality reflects not just technical know-how but an operator’s sense for timing, temperature control, and equipment calibration. Continuous process review, guided by spectral and chromatographic analysis at every stage, allows us to adjust in real-time. Packing and sealing procedures respond to both chemical and regulatory demands—especially since trifluoromethyl materials require careful documentation in international shipping and customs.
Pharmaceutical chemists often request this compound as a nucleophile or building block in heterocyclic synthesis. The amino group and enone backbone form a reactive center that undergoes cyclizations, condensations, and Michael-type additions with predictable results. The fluoroalkyl function can tune physical and medicinal profiles, providing a starting point for blocks that tap into fluorine’s unique properties. It also speeds up discovery in medicinal chemistry campaigns targeting CNS-active compounds, pesticide leads, and fine-tuning of selective biological activity.
Specialty producers of advanced polymers, agrochemical actives, or bioactive compounds have developed their own routes and processes based on the trifluoro-enone unit. In crops, plant protection products using fluorinated cores have demonstrated improved environmental profiles, often needing lower application rates and providing clearer metabolic breakdown profiles for regulatory review.
Amino-enones exist in several chemical spaces—with or without fluorine substitution. Switching from non-fluorinated to CF3-bearing analogs causes a practical shift in stability, reactivity, and safety requirements. Non-fluorinated analogs may seem less expensive at first glance, but the downstream yield and purity improvements often justify the switch in high-value applications. The trifluoromethyl group’s influence on electron density can change product profiles in pharmaceutical applications, offering better binding, different metabolic routes, and greater synthetic flexibility.
Alternative sources of fluoro-enamines or enones lack the controlled reactivity and manageable byproduct profiles our method delivers. In practical terms, we minimized the risk of over-fluorination or under-reacted material in final product streams, removing much of the trial-and-error faced by chemists scaling up from literature procedures. This differs from “off-the-shelf” importers or resellers, who generally do not provide origin guarantees or batch reports connected to actual production data.
In one recent pharmaceutical pilot, a client aimed to synthesize a novel CNS drug candidate. They needed a stable fluorinated amino enone as a key intermediate, with tight limits on trace metal content and process residuals. Because our routine production included proactive impurity monitoring, we supplied a batch with certificates matching the strictest instrumental and clinical requirements. The project moved forward with no unpredictable reaction performance or post-synthesis cleanups. From a purely operational standpoint, the switch to our product eliminated two extra purification steps in their workflow, saving several weeks of man-hours in a single campaign.
Agrochemical customers often evaluate the environmental impact of active ingredients and intermediates. We produced 4-Amino-1,1,1-Trifluoro-3-Buten-2-One for integration into new-generation herbicides intended for low-dose usage. The well-understood breakdown patterns and low volatility of the compound made field testing and regulatory filings easier, reducing the risk of application drift or unexpected soil accumulation—challenges that non-fluorinated or partially fluorinated intermediates sometimes present. Practical fieldwork, supported by our in-house material, allowed early detection of site-specific breakdown products, directly fed back into the design of new application protocols.
Laboratory users, whether from academia or contract research, often share feedback about simple logistics. Real-world packaging and storage matter at all scales. We learned from repeated shipments across continents that moisture control, sealed containers, and tailored labeling for customs streamline import and storage. Site visits have confirmed the reduced presence of hydrolyzed side products in our batches compared to alternatives, meaning less clean-up work for the end-user and more reliable project timelines.
Like most fluorinated building blocks, 4-Amino-1,1,1-Trifluoro-3-Buten-2-One requires exacting process control from the start. Sourcing high-purity starting materials forms the bedrock of each campaign. Our procurement team has built strong supplier relationships to guarantee the integrity of precursor chemicals, favoring traceable, direct-from-source inputs over brokered lots whenever possible. The technical crew has implemented redundant safety checks to detect fluorinated byproducts early, managing risk and keeping operator exposure well below regulatory limits.
On the plant floor, optimizing reactor temperature profiles and solvent choices means getting predictable conversions and limiting hazardous waste. Operators train in the handling of pressure swings and minor thermal excursions, which occur more frequently in fluoro-organic chemistry than in regular amination or condensation processes. By steadily refining batch documentation and reacting quickly to unexpected byproduct profiles, the technical staff maintains a high success rate in final product quality, avoiding downstream headaches at formulation, tableting, or blending stages.
Global markets expect chemical manufacturers to prove stewardship of both employee and environmental safety. Fluorinated intermediates come under increasing regulatory scrutiny due to their persistence and potent bioactivity. Our plant runs audits of emissions, effluent treatment, and hazardous waste with a focus on reducing environmental impact. On-site recycling units capture nearly all process solvents. Operators receive targeted training on the analysis and response to potential release scenarios, including joint drills involving local safety authorities.
Product batches ship with detailed documentation to simplify international clearance. The regulatory landscape, especially for trifluoromethyl compounds, keeps shifting as authorities tighten data requirements on purity, trace residue levels, and degradability. We keep up by running parallel small-scale test lots, supplying samples for client method validation and toxicological evaluation. Our ability to adapt batch composition and documentation for different end-uses builds trust and keeps projects on schedule when time-to-market pressures mount.
Direct conversations with clients keep production close to end-user needs. We collect technical feedback from experienced chemists, plant engineers, and formulation experts. Many process refinements originated from these relationships. Chemists reported back on reactivity in novel synthetic routes; technicians described atmospheric or shipping issues that prompted fresh approaches in container design and labeling. Customer side pilot campaigns uncovered opportunities to further clean up side-product profiles, prompting changes in our own process timing and quenching strategies.
Because we maintain control over primary and secondary synthesis stages, every improvement in yield, purity, or stability comes from hands-on adjustments—not just paperwork or surface-level audits. Our operators hold regular breakdown meetings after campaign close-outs, addressing all working conditions and any technical hiccups. This tight operating loop replaces guesswork with practical know-how.
Demand for fluorinated amino-ketones remains volatile, tracking closely with shifts in pharmaceutical research and changing regulations. Distributor shortages and global shipping snags have pushed many buyers away from indirect suppliers. Our direct-manufacturer supply provides traceability, continuity, and technical support lacking in bulk commodity channels. Standardized lot sizes, flexible fill options, and on-site testing labs mean that orders arrive as promised and substitute solutions come from the same facility, not disconnected warehouses worldwide.
Keeping a steady supply of a specialty intermediate requires both production foresight and agile logistics. We work from live demand forecasts and cross-check our planned runs against market signals—shifting batch size and packaging as needed. During periods of plant maintenance or regulatory inspection, we keep extra stock on hand, prioritizing trusted partners and high-value projects from recurring clients. Remote tracking tools tie shipping, customs, and inventory updates together, cutting out weeks of avoidable “where is my order?” uncertainty.
The march of new chemistry means every established process faces obsolescence. Investment in on-site pilots, QC equipment, and staff training pays off both in product reliability and operator retention. Upgrades in analytical instrumentation have shortened release testing times, allowing us to release fresh batches ahead of schedule. Modern GC, LC, and mass spec tools sharpen impurity detection thresholds, often exceeding even our clients' documented requirements.
Hands-on training keeps process staff current with both safety standards and best practices in handling sensitive fluoro-organic intermediates. Retaining experienced operators means fewer production surprises and a workplace culture built on problem-solving at the shop floor, not just management memos.
Chemistry isn’t only about molecules; it’s about how those molecules get into users’ hands. Experience tells us shortcuts in manufacturing soon catch up with the whole supply chain. The batch records, intermediate QC tests, and shipment reports may only matter when a customer gets a failed reaction or delayed campaign, but by then the losses are real. Our method—developed through years of directly handling both highs and lows—prioritizes hands-on oversight, full documentation, and a willingness to tweak process variables to satisfy real-world requirements.
End-users call on our team not just for supply but for direct technical input. Whether troubleshooting a reaction step or planning storage for a new plant, they value first-hand knowledge and transparency about upstream choices. Close communication bridges lab-scale discovery and full-plant production, giving project leaders confidence in both product quality and delivery timelines.
Pharmaceutical and agrochemical R&D continues to shift toward designer molecules with tailored physicochemical profiles. Trifluoromethyl building blocks offer a clear route to broadened activity, sharpened selectivity, and sometimes lower resistance development. Trends in “green chemistry” and sustainable manufacturing push all suppliers to cut waste, support recycling, and document full life cycles for chemicals like ours. Reliable intermediates like 4-Amino-1,1,1-Trifluoro-3-Buten-2-One allow formulators and process chemists to develop new drugs and agrochemicals that meet rising standards for efficiency and stewardship.
Based on real-world projects and feedback, this compound will keep finding new end-uses as regulatory and technical hurdles clear. Its compatibility with automation, inline QC, and environmentally conscious purification systems positions it as a preferred choice among chemists focused on both performance and responsibility. Trustworthy supply forms the backbone of high-value synthesis and innovative material development; direct manufacturer access means fewer surprises and faster scale-ups.
Drawing from the long view, our ongoing investment in process mastery and technical know-how has made 4-Amino-1,1,1-Trifluoro-3-Buten-2-One more than just a stock number—it functions as a critical link in many innovation pipelines. The real difference, as seen from inside the chemical plant, rests on continuous improvement, operator pride, and working relationships built cell by cell, batch by batch, project by project.