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HS Code |
798976 |
| Productname | 4,4,4-Trifluoro-1-(P-Tolyl)-1,3-Butanedione |
| Casnumber | 720-93-2 |
| Molecularformula | C11H9F3O2 |
| Molecularweight | 230.18 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 73-75°C |
| Boilingpoint | Unknown |
| Density | 1.298 g/cm³ |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically >98% |
| Smiles | CC1=CC=C(C=C1)C(=O)CC(=O)C(F)(F)F |
| Inchi | InChI=1S/C11H9F3O2/c1-7-2-4-9(5-3-7)10(15)6-8(16)11(12,13)14/h2-5H,6H2,1H3 |
| Storagetemperature | Store at room temperature |
As an accredited 4,4,4-Trifluoro-1-(P-Tolyl)-1,3-Butanedione factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g quantity of 4,4,4-Trifluoro-1-(P-Tolyl)-1,3-Butanedione is packaged in a sealed amber glass bottle with hazard labeling. |
| Shipping | 4,4,4-Trifluoro-1-(p-tolyl)-1,3-butanedione should be shipped in tightly sealed containers, protected from light and moisture. It must be labeled as a chemical substance and handled according to relevant safety and transport regulations. Avoid extreme temperatures. Appropriate documentation and hazard classifications (if applicable) should accompany the shipment to ensure regulatory compliance. |
| Storage | 4,4,4-Trifluoro-1-(p-tolyl)-1,3-butanedione should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible materials such as strong oxidizers. The storage environment should be free from moisture. Clearly label the container, and keep it in a designated chemical storage area, following standard laboratory safety protocols. |
Applications of 4,4,4-Trifluoro-1-(P-Tolyl)-1,3-Butanedione in Industrial ManufacturingAs a dedicated manufacturer of 4,4,4-Trifluoro-1-(P-Tolyl)-1,3-Butanedione, we supply this specialty diketone to established downstream segments where it delivers reliable performance, consistent quality, and meets regulated industry protocols. Below are the principal industrial scenarios where downstream companies integrate this raw material into their advanced production lines. 1. Synthesis of Pharmaceutical Intermediates for Fluorinated APIsManufacturers of active pharmaceutical ingredients leverage this compound as a building block in crafting fluorinated heterocycles and advanced pharmaceutical intermediates. Its fluorine-rich structure supports selective introduction of trifluoromethyl groups in target molecules, aiding the development of APIs with enhanced metabolic stability. Precision in batch synthesis is required, as minor byproduct formation can impact downstream purity specifications in API crystallization and formulation. Industry compliance standards
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2. Complexation Agent in Analytical Chemistry ReagentsProducers of specialty analytical reagents incorporate this diketone as a chelating ligand in fluorometric and colorimetric detection kits, especially for trace metal or rare earth ion analysis in laboratory and industrial monitoring. Through controlled condensation with metal ions, it helps generate stable, fluorescent complexes for quantification, requiring precise dissolution and binding to preserve assay reproducibility and reduce matrix interference. Industry compliance standards
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3. Ligand Precursor for Luminescent Materials in OLEDsIn advanced material fabrication for organic light-emitting diodes (OLEDs), compound users deploy this trifluorinated diketone during the synthesis of metal chelate complexes, especially europium and terbium-based emitters. The unique electronic configuration modulates emission wavelength and quantum efficiency in emissive layers, supporting device miniaturization and high brightness displays. Industry compliance standards
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4. Modifier for UV-Curable Fluorinated CoatingsFormulators in the coatings industry utilize this raw material as a specialty modifier to engineer UV-cured resin systems with tailored surface energy, chemical durability, and non-stick characteristics. The trifluorinated group interacts during the prepolymer mixing stage, imparting functional enhancements without compromising cure rates. Proper blending within the reactive diluent matrix ensures complete incorporation and stable film formation post-cure. Industry compliance standards
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5. Precursor for Fluorinated Agrochemical ActivesProducers of specialty crop protection agents adopt this diketone in the synthesis of fluorinated active ingredients, particularly for next-generation herbicides and fungicides. The unique structure facilitates selective ring closure and coupling reactions, yielding high-purity actives with controlled degradation profiles. Careful in-process controls are maintained to meet stringent food safety and residue standards for agricultural applications. Industry compliance standards
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Every batch tells its own story. At our plant, we see that story play out as 4,4,4-Trifluoro-1-(P-Tolyl)-1,3-Butanedione comes together, each molecule shaped both by chemistry and hands-on attention. Synthetic organic chemistry isn’t just about what’s on paper; we spend years learning how raw materials behave and learning from quietly stubborn problems that show up only at scale. Over time, the full behavior of a compound like this reveals itself, and that reality guides what leaves our production line.
Our own teams recognize 4,4,4-Trifluoro-1-(P-Tolyl)-1,3-Butanedione — sometimes referred to by its CAS number, 720-94-5 — as more than another aromatic diketone. In the realm of building fluorine-containing organics, few molecules pull as much interest for downstream synthesis paths. Its trifluoromethyl tail, combined with a p-tolyl ring structure, brings both reactivity and performance advantages sought by pharmaceutical researchers, agrochemical inventors, and OLED material developers.
Once, the only option for such fluorinated diketones was high-cost imports or home-brewed syntheses where purity and reproducibility fluctuated with every supplier’s whim. We know the headaches caused by off-color batches, varying melting points, rogue solvent odor. Bringing control in-house, we have implemented a closed process that holds impurities to levels our own downstream synthesis chemists approve of.
The lot-to-lot reliability our partners demand doesn’t happen by chance. We’ve equipped our reactors with exact temperature and flow controls for each step, and our fractionation removes low-level byproducts that could derail sensitive applications. Specifications vary by user, but a typical outcome leans toward a crystalline powder, pale to off-white, and free-flowing. The target purity exceeds 99 percent in all high-requirement batches, confirmed by HPLC, NMR, and GC analyses, which we perform on every batch—not on a quota basis, but because we also run downstream syntheses ourselves and know how quickly a poor intermediate fouls the next step.
Some researchers settle for crude material when price is the only motivator. Our approach always weighs up-front material cost against the actual yield and time spent on subsequent purifications. Several collaboration partners have found that a slightly higher spend on up-front purity leads to faster process development and less dead time troubleshooting HPLC spikes or crystallization failures.
Anyone synthesizing fluorinated pharmaceuticals or OLED emitters runs into performance gaps with standard butanediones. Adding a trifluoromethyl group at the terminal position cranks up both the electron-withdrawing character and the hydrophobicity. The p-tolyl ring doesn’t just prop up the molecule for analytical identification—it nudges key physical and electronic properties in models for bioactivity and light-emission efficiency.
We have been pressed for years by developers in Asia, North America, and Europe to build kilogram and multi-kilogram lots of 4,4,4-Trifluoro-1-(P-Tolyl)-1,3-Butanedione that consistently meet not just the technical values, but the visual, odor, and handling consistency that matters in rapid R&D or large-batch processing. The reason? Competing diketones either lose critical reactivity or do not offer the stability this compound brings to storage and process.
Our earliest projects started with flask synthesis on the bench; what proved easy at 50 grams became unpredictable at 5 kilograms. Control over moisture content, raw material addition rate, and byproduct removal dictated not just yield, but the simplicity of downstream chromatography or re-crystallization. The more we scaled, the more our internal specialists insisted on tighter batch-log documentation and closed-loop quality checks right at the reactor line.
Several of our biggest improvements came after consultation with process engineers who had fought discoloration issues or unacceptably high residual solvents in the early days. Today, regular inline NMR checks and batch-by-batch tracking cut out the guesswork. Downstream, we’ve developed a post-synthesis workup that tempers particle size for easier dissolution, cuts lot separation headaches, and improves powder-handling safety for every operator along the chain.
It’s not only the active pharmaceutical ingredient (API) pipeline that cares about these improvements; fine chemical users building conjugated materials for electronics or specialty polymers have become some of our most demanding clients simply because they feel the impact of a contaminated batch faster than anyone else. What seemed, on the surface, to be a minor quality slip — maybe a yellow cast or a sticky clump — results in expensive downtime, wasted purification steps, and lost confidence.
We talk regularly with customers moving toward late-stage pharmaceutical research, OLED screen manufacture, and signal-labeling studies who need this diketone as both a core scaffold and a derivatizable handle for complex family trees of end products. The trifluoromethyl group often marks the difference between fleeting drug activity and the required metabolic stability. Meanwhile, the p-tolyl group supports electronic conjugation without introducing undue steric hindrance, so screens show the color and lifetime manufacturers expect.
It isn’t always easy to explain to outsiders what a simple tweak in a molecule can mean for a billion-dollar product line. The proof lands inside the reactor years after the compound leaves our plant, though we always keep an eye for feedback whenever a new screen rolls hot off the presses using our material, or an academic researcher e-mails us about a record-setting fluorinated building block.
Clients often ask where this diketone stands relative to standard 1,3-butanediones or less-fluorinated analogs. There’s no formula that fits all buyers, since the right match depends on the end use. What we do know, from feedstock contracts and hours spent troubleshooting yield losses, is that 4,4,4-Trifluoro-1-(P-Tolyl)-1,3-Butanedione slots into synthesis pathways where other diketones either don't deliver the required electron density or fall short in terms of volatility and final product stability.
Labs pursuing new actives linked to increased membrane permeability or metabolic lifetime rely on the precise presence of both a trifluoro and a tolyl fragment to direct reaction outcomes. Those blending non-fluorinated diketones into their methods may solve short-term sourcing issues, but have repeatedly reported lower end-product performance and more frequent failure to meet downstream regulatory thresholds.
Storing and processing fluorinated aromatics presents realities that rarely make it into published data sheets. Our warehouse teams manage humidity and ambient light for long-term stability, because overlooked conditions mean caking and loss of grade. Hourly checks on our own stock, plus secondary labeling and lot segregation, aren’t a choice but a must. For operators weighing out and transferring open lots, extraction hoods and spill containment have been built into our daily rhythm, since minute particles tend to drift and cause respiratory irritation. Our safety records reflect more than ticking a box for regulatory compliance. Keeping real people safe ensures that expertise stays inside our building, along with the technical know-how learned from years on the floor.
We’ve taken calls from partners caught off guard by products sourced elsewhere showing up out of spec, or with labeling errors that led to process waste and confusion. Our lot traceability systems, run by a team on site rather than a remote office, have pulled several customers back from painful recalls.
Projects in OLED, pharmaceuticals, or specialty agriculture often ramp up from a few grams in the lab to unexpected demands for tens or hundreds of kilograms. Laboratories may miss forecasts when a research hit proves more viable than anyone planned. We plan our own production cycles to set aside capacity for these scaling curves, working closely with several research-driven partners to map projected demand windows and avoid the scramble that comes with sourcing in panic mode.
Our team takes care to not over-promise, especially in the face of raw material crunch, or unpredictable third-party logistics failures. Scaling up too fast or in the wrong direction wastes both time and resources, leaving everyone frustrated. Old hands know the value of steady batch tracking and transparent communication, and we have saved plenty of customer relationships by not chasing short-term wins at the expense of ongoing partnership.
As feedback rolls in from across the research and manufacturing worlds, we focus investment on batch consistency and supply resilience. While we adapt to evolving usage trends, we never take shortcuts or push too hard for volume when it means risking the integrity of a batch. Experience shows that stability, both chemical and operational, means more in the long term than a temporary spike in sales.
Unlike traders looking for the next hot commodity, we actually field questions from the chemists who use our product. These calls cover everything from what the real melting point looks like in their hands, to shared pictures of what purity looks like between batches, or actual troubleshooting advice for an uncooperative reaction. We end up walking through experimental setups, answering why a specific test returns an odd baseline, or how to avoid recrystallization pitfalls during scale-up.
Sometimes, a surprise in process yields or color drags us back to earlier steps in synthesis or packaging. By consistently talking with both industry engineers and academic users, we stay grounded to the daily problems real people face. Connecting user experience with plant process means we evolve our own knowledge base and continuously optimize both our approach and raw material sourcing.
It’s easy to buy a label, but harder to guarantee repeatable properties year in, year out. Manufacturing at scale involves more than pouring chemicals from bottles. Temperatures, moisture, and operator experience write their signature on every drum and bottle that leaves our door. We have seen how competing intermediate-makers treat 4,4,4-Trifluoro-1-(P-Tolyl)-1,3-Butanedione as a check-box, pushing out tons without regard for what happens down the process. Our approach holds every lot up to our own standard before it ever reaches a client’s bench.
Even reliable partners run into interruptions — a supplier’s closure, a logistics stall, a regulatory curveball. We have been called in after buyers lost faith in “cheap and fast” options, only to discover that total project costs skyrocket when bad batches need rework, or deadlines slip. Sourcing from an actual manufacturer, rather than an invisible node in a value chain, translates to fewer surprises in both quality and timeline.
Products such as 4,4,4-Trifluoro-1-(P-Tolyl)-1,3-Butanedione may not always make headlines, but they form the backbone of research and industry. Our daily push for reliability and safety, anchored in hands-on experience and close collaboration, has set benchmarks our customers recognize and return for batch after batch.
As demand for specialized trifluoromethyl diketones grows in emerging applications — from energy-efficient screens to next-generation drug candidates — we keep an eye on both supply chain volatility and evolving user expectations. There are no shortcuts for maintaining quality and delivering technical support, particularly with pressure to compete with no-name suppliers whose quality varies unpredictably.
Solving raw material shortages, investing in better in-process controls, and building stronger ties with key users remain non-stop projects within our walls. Every season brings changes in supply pressures or regulatory shifts, but our accumulated know-how helps buffer against abrupt turns. Anchoring our operation in well-documented production logs and transparent handing of out-of-spec findings means we rarely land unprepared.
With our own chemists and engineers still using what we manufacture, every feedback cycle closes the loop. We take special pride in supporting new users who are stepping up to large-scale synthesis for the first time, guiding them around bottlenecks in process or scale.
Anyone manufacturing 4,4,4-Trifluoro-1-(P-Tolyl)-1,3-Butanedione knows that technical sheets and certificates of analysis cover only part of the reliability story. Performance in the field — in real reactors, under real deadlines, and with the pressure of production — tells the rest. Our team has faced every problem and tried every fix: batch failures, delayed shipments, out-of-spec returns, and unexpected usage needs. Hard-won experience shapes every update we make to process controls, packaging, and follow-up.
This compound may seem routine on a datasheet, but behind each lot we ship runs a line of judgment calls, professional skills, and practical lessons earned on the production floor. Scientific rigor, manufacturing routines, and open talk with users create the real foundation of quality in our operation.
Because we take our responsibility seriously — as the actual manufacturer — the chemical that leaves our facility reflects not just customer expectations, but the accumulated trust built up over many campaigns of hard work, tough problems, and lasting partnerships.