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HS Code |
172202 |
| Product Name | 2-Fluoro-4-(Trifluoromethyl)Phenylacetonitrile |
| Cas Number | 885270-88-0 |
| Molecular Formula | C9H5F4N |
| Molecular Weight | 203.14 |
| Appearance | White to off-white solid |
| Purity | Typically >98% |
| Melting Point | 35-37°C |
| Density | 1.34 g/cm³ (estimated) |
| Smiles | N#CC1=CC(C(F)(F)F)=CC=C1F |
| Inchi | InChI=1S/C9H5F4N/c10-7-2-1-6(5-14)3-8(7)9(11,12)13/h1-3H,5H2 |
| Solubility | Soluble in organic solvents (e.g., DMSO, dichloromethane) |
| Storage Temperature | 2-8°C, protected from light and moisture |
| Synonyms | α-Cyano-2-fluoro-4-(trifluoromethyl)toluene |
As an accredited 2-Fluoro-4-(Trifluoromethyl)Phenylacetonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle with tamper-evident cap, labeled with hazard warnings; contains 25 grams of 2-Fluoro-4-(trifluoromethyl)phenylacetonitrile. |
| Shipping | **Shipping Description**: 2-Fluoro-4-(Trifluoromethyl)Phenylacetonitrile is shipped in tightly sealed containers to prevent moisture ingress and contamination. Packages are clearly labeled with chemical identification and hazard information, and are transported in compliance with relevant regulations. Storage during transit is in a cool, dry, and well-ventilated area, away from incompatible materials. |
| Storage | **2-Fluoro-4-(Trifluoromethyl)Phenylacetonitrile** should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Store it in a cool, dry, well-ventilated chemical storage area, preferably under inert atmosphere (e.g., nitrogen or argon) to prevent degradation. Keep separate from incompatible materials such as strong oxidizers or acids. Label containers clearly and ensure proper secondary containment. |
Applications of 2-Fluoro-4-(Trifluoromethyl)Phenylacetonitrile in Industrial ManufacturingAs a direct producer, we supply 2-Fluoro-4-(Trifluoromethyl)Phenylacetonitrile for advanced synthesis across pharmaceutical, agrochemical, and specialty chemical manufacturing. This intermediate enables efficient downstream integration in regulated environments, supporting precise formulations and demanding process requirements. 1. Pharmaceutical API Intermediate SynthesisPharmaceutical manufacturers use this compound for the synthesis of complex active pharmaceutical ingredient (API) scaffolds requiring fluoroaromatic nitrile moieties. It enters as a key intermediate in multi-step reactions for anti-inflammatory and central nervous system drug candidates, allowing controlled nucleophilic substitution or cyclization routes. Quality assurance teams verify identity and purity before release to synthesis suites, where the material supports strict compliance and scalability, especially in American, European, and Japanese regulatory environments. Industry compliance standards
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2. Agrochemical Intermediate ManufacturingLeading crop protection companies utilize this material as a strategic building block in the synthesis of fungicide and herbicide actives containing high-performance trifluoromethyl-substituted aromatic rings. It supports the creation of nitrile intermediates that undergo chlorination, hydrolysis, or amination in multi-step synthesis plants, ensuring robust input for high-yield agrochemical solid products. Industry compliance standards
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3. Advanced Electronic Chemical Raw MaterialManufacturers in the electronics industry use this compound during the design of specialty fluorinated chemicals for liquid crystal display (LCD) manufacturing and organic electronic components. The material’s stable fluoroaromatic profile fits processes requiring high-purity intermediates for fluorinated polyimide or liquid crystal additives, where contamination control is critical to segment yield and display quality. Industry compliance standards
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4. Fine Chemical Synthesis for Dye and Pigment IntermediatesProducers of specialty dyes and pigments employ this molecule as an advanced aromatic intermediate for synthesizing high-purity colorants, particularly for polar solvent-soluble or fluorine-containing chromophores. The compound participates in controlled condensation or coupling processes under anhydrous and temperature-regulated conditions, essential for pigment stability and optical clarity. Industry compliance standards
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5. Custom Synthesis for Specialty Chemical R&DOur R&D partners in specialty chemistry select this material for developing new molecular entities, including fluorinated ligands for catalysis and advanced materials for battery electrolytes. Its controlled reactivity supports compound library expansion under varied conditions, meeting documentation requirements for patent and process development programs. Industry compliance standards
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Every so often, the landscape of fine chemicals brings forward a molecule that offers more than a niche function. 2-Fluoro-4-(Trifluoromethyl)Phenylacetonitrile (often referenced by its structural designation or CAS number in technical circles) falls into this select group. Conversation on this compound calls to mind the countless hours we, as manufacturers, have spent tuning processes, sampling product from different reactors, and troubleshooting right on the plant floor. The nuances in this molecule’s synthesis challenge even high-volume plants, pushing us to deepen our understanding of both chemistry and customer need.
What sets this compound apart begins at the molecular level. The careful placement of a fluorine and a trifluoromethyl group on the phenyl ring, plus the acetonitrile side chain, results in a structure that pulls attention for routes in advanced synthesis. Each batch inches us closer toward the technical ideal: single-digit ppm in structure-related impurities, moisture levels below 0.1 percent by Karl Fischer titration, and no unexplained peaks in chromatographic analysis. This is not an academic achievement but a practical necessity. Even minute deviations in the fluorinated phenyl motif, detectable through HPLC and NMR, can halt downstream applications or compromise the quality of target APIs or intermediates.
By emphasizing consistency through in-process controls, we keep lot-to-lot variation in check. A big part of this success comes from process controls honed over hundreds of batches, not from templated routines or luck. Copper-catalyzed couplings, controlled temperature ladders in the condensation steps, and pinch-point pH adjustments—each decision on the production line stems from first-hand observations. Chromatographic fingerprinting isn’t just a routine; it’s about safeguarding what comes out of the reactor, ensuring it aligns with published spectra and our own historic benchmarks.
Industry interest in 2-Fluoro-4-(Trifluoromethyl)Phenylacetonitrile comes from its versatility in complex chemical construction. The strong electron-withdrawing trifluoromethyl and cyano groups allow this compound to function as a key intermediate for many active pharmaceutical ingredients, crop protection agents, and specialty materials. These substitutions fine-tune reactivity on neighboring positions of the aromatic ring, granting synthetic chemists a window to build complexity not easily accessed from non-fluorinated analogs.
Feedback from downstream users shapes how we operate. Synthetic organic teams working in pharmaceutical and agrochemical development remind us that even slight shifts in impurity profiles can complicate route scouting or impact reaction selectivity. Equipment engineers at the plant level pass along their observations: subtle differences in melting point behavior, crystal morphology, or flow during transfer operations signal differences in bulk quality many overlook, but which our customers notice immediately during scale-up. Listening to both camps keeps our focus sharp and shows where even incremental process improvements have the greatest return.
Fluorinated benzyl and phenylacetonitrile building blocks populate many catalogs, often appearing superficially similar. The specific profile of 2-Fluoro-4-(Trifluoromethyl)Phenylacetonitrile distinguishes itself in several clear ways. The ortho-fluoro and para-trifluoromethyl combination pushes electron density in a unique way, impacting both nucleophilic and electrophilic aromatic substitution steps. This influences how chemists select for further modifications, often indicating higher yields and fewer by-products than simpler phenylacetonitrile variants.
Process engineers working with more conventional analogs (like unsubstituted or mono-substituted phenylacetonitriles) consistently note that while those compounds offer certain general reactivity, they lack the chemoselectivity and the tunable polarity brought by dual fluorine substitution. Our repeated in-house comparisons—run at both pilot and commercial scales—consistently demonstrate that this particular structural motif reduces the formation of difficult-to-separate side products in multi-step syntheses. Solvent handling and crystallization, measured in both energy requirements and product yield, tend to improve. For every kilogram passing through isolation, fewer resources go into reprocessing or waste remediation.
Every specification document tells only part of the story. Measurement ranges—appearance as white to off-white crystalline solid, melting point ranges, purity by area percent, moisture content, and residual solvents—define customer acceptance criteria. But as manufacturers, our deeper concern centers on making sure each number reflects what happens at the bench.
We report typical melting point ranges within tight boundaries, often corroborated by differential scanning calorimetry and capillary observations. Purity checks, run both by HPLC and GC-FID, back up stated minimums. Depending on end use, we readjust particle size distribution via sieving or controlled crystallization, since flow properties matter during formulation or further chemical conversion. Unlike volume distributors, our team reacts quickly to observed deviations, leveraging our direct oversight of every drum and liner prior to shipment.
Meticulous control of trace metals and particulate contamination has never felt abstract. Clients in regulated environments raise legitimate alarms over sub-ppm levels of iron, copper, or silica residues—sometimes introduced from reactor linings or ancillary equipment, sometimes traced back to raw material sources. Regular audits, third-party analysis, and in-house verification keep these variables managed, so clients avoid headaches downstream.
A chemical’s identity does not rest on purity or CAS registry alone. At our manufacturing site, each kilo of 2-Fluoro-4-(Trifluoromethyl)Phenylacetonitrile reflects hundreds of micro-decisions made by both automation and skilled hands. Process control charts, shift logs, real-time spectroscopic monitoring, and feedback from customer applications all tighten our routine. Oversights or shortcuts rarely remain hidden; our best results follow when we take the time to validate not only finished lots, but also the process steps leading to them.
No plant runs trouble-free forever. Hot spots in a reactor, variability from a new raw materials supplier, or subtle changes in ambient humidity can change reaction kinetics or crystallization behavior. Our technical group addresses these challenges head-on, capturing both recurrence patterns and rare events in a knowledge base spanning years. Solutions—such as staggered feed protocols for exothermic steps or anti-solvent adjustments—stem from careful documentation. We invest in both operator training and automation, ensuring lessons accumulate for the benefit of every subsequent batch.
We put special emphasis on logs from downstream processing: filtration load, drying curve, final cake appearance, and how these predict product transport ability and shelf stability. Such information rarely appears on specification sheets but matters greatly in large-scale protocols, particularly with this molecule's sensitivity to trace hydrolysis or photodegradation.
Direct production puts safety at the center of daily operations. This is not paperwork—each employee understands the risks pictograms not because regulatory posters mandate them, but because we’ve shut down units or initiated corrective actions in real time when alarms signal increased hazard. Handling 2-Fluoro-4-(Trifluoromethyl)Phenylacetonitrile involves awareness of cyanide functionality; our teams use local exhaust, real-time vapor monitoring, and double containment protocols. Occasional drills and actual incidents both shape a culture where prudent skepticism is encouraged and overconfidence is checked.
Environmental controls focus on minimizing process emissions and managing effluent streams with both in-house and contracted waste handling partners. Aqueous streams, containing traces of organics or acid, are separated and neutralized before release. Any vent emissions from solvent recovery pass through activated carbon beds and scrubbers. Every operator knows solvents saved aren’t just billed as revenue but represent less risk and lower community impact.
Transparency feeds into our communications with external stakeholders. Reports don’t get sanitized for outside review. If a batch falls short, or a process tweak is needed, we flag it before it leaves the gate. Customers have a direct channel to senior technical staff, able to discuss not just specs but also process context and future improvement plans. Both technical and commercial staff gain from these conversations, which feed into next generation process development.
Process chemists, formulation scientists, and synthetic route scouts make real choices on the plant floor and at the benchtop. Most begin with trial-scale reactions, learning quickly that reactivity and ease of handling determine whether a material moves up to pilot or full-scale production. With 2-Fluoro-4-(Trifluoromethyl)Phenylacetonitrile, teams cite ease of activation in alkylation or condensation steps as a real asset. Whether bonding to nucleophiles or entering further ring substitutions, the electron-rich ring responds predictably, letting teams push yields without a forest of by-products.
Physical properties also matter. Free-flowing crystalline powder, stable under typical warehouse conditions, eases metering and dosing for batch and semi-continuous processes. Less dust generation equals easier housekeeping and safer handling—points reinforced after each housekeeping audit or spill cleanup. We engineer particle size not simply for flow, but for reproducibility in charging hoppers and weighing vessels.
Feedback leads us to review how storage conditions and packaging influence long-term stability. Some customers prefer sealed foil bags inside high integrity drums, limiting light and oxygen transmission, especially for higher value lots stored over several months. Others convert material promptly, relying on our QA certification and batch reserve samples as the backstop. Adjustments to packaging lines come directly from this feedback loop, not top-down mandates.
Having worked with a variety of phenylacetonitrile derivatives, both fluorinated and non-fluorinated, we see clear contrasts emerge. Some analogs, like 4-(trifluoromethyl)phenylacetonitrile, offer value in cost-sensitive applications, but their electron density and downstream reactivity don’t precisely overlap with the 2-fluoro-substituted variant. Others, such as simple benzyl cyanides, lack the same stability profile under oxidative or basic conditions. The dual influence of ortho-fluoro and para-trifluoromethyl increases hydrolytic stability—a property validated in our own accelerated aging tests and endorsed by users running lengthy reaction cycles.
In purification, the combination of fluorine and cyano moieties leads to differences both in physical handling and in the ability to separate from structurally related impurities. Several contract manufacturing partners report that they see easier fractionation using both normal and reverse phase chromatography, translating to less labor-intensive purification and shorter production timelines. Direct trial runs inform these conclusions, as both yield and purity trace directly to ease of purification from crude reaction masses.
Heat management emerges as another practical concern. During stepwise addition of reagents, the 2-fluoro derivative shows improved stability to thermal excursions compared to some mono-substituted variants; calorimetry data confirm slower exotherm onset and reduced peak temperatures, reducing the likelihood of runaway conditions and unplanned plant shutdowns. This difference, modest in a laboratory jacketed vessel, assumes critical importance in reactors of several tons capacity. The sum total of these practical benefits feeds confidence all the way down to the plant loader.
Markets for advanced organic intermediates thrive not on initial sales, but on consistent, scalable production and technical support. As direct manufacturers, we maintain control over every step: procurement of starting materials, in-process monitoring, and post-production sampling. Access to live production data supports both real-time troubleshooting and after-sales investigations. There is little room to hide behind brokers or second-hand reports when the client faces a production hitch. Our operations group is used to joining end-use teams on conference calls, translating product analytics into problem-solving for their plant teams, not hiding behind disclaimers.
Establishing long-term supply means cultivating stable sourcing partnerships, maintaining process documentation robust enough to weather inspections, and investing in plant capacity upgrades where demand supports larger volumes. Supply chain reliability does not rest on warehousing alone, but also on the ability to flex production schedules and respond to sudden upticks in demand. In the past year, industry disruptions from raw material delays and shifting global freight patterns have tested this capacity. Open communication with customers, both up and downstream, allowed for advance planning and just-in-time production, minimizing gaps and holding costs.
Lab technicians, development chemists, and plant supervisors all bring stories that shape our evolving approach. One batch destined for an agrochemical customer showed increased color and a shift in IR absorption. A deeper dive, prompted by an alert QA staff, led us to trace a minor feedstock impurity that had escaped initial screening. Small deviations in starting material purity, which passed typical QC specs, revealed the need for tighter in-house acceptance criteria. As a result, feedstock specification limits were reduced, triggering better consistency in subsequent batches. Every unexpected observation—color, odor, crystallization habit—adds a data point that tightens our future process windows.
Scale-up brings different lessons. Thermal excursions on initial ton-scale batches showed that direct cooling capacity fell short of peak run requirements. We retrofitted additional cooling loops and updated process automation for better control. Each improvement drew from candid feedback across departments—a luxury that comes from vertical integration rather than fragmented outsourcing.
Customers, for their part, have pushed us to refine container labeling, supply chain tracking, and technical dossier detail. Recent feedback from a regulatory submission team led to modifications in our batch history reporting, making both regulatory approval and customer audit cycles smoother. This isn’t abstract compliance, but a lived process shaped by real questions and urgent deadlines.
Ongoing demand for innovative fluorinated intermediates like 2-Fluoro-4-(Trifluoromethyl)Phenylacetonitrile guarantees continued learning on our factory floor. By resisting shortcuts and investing in both people and equipment, we aim to keep ahead of shifting technical standards. Input from customers, regulators, and our own operations teams continues to drive process fine-tuning and risk management—initiatives that translate directly into higher quality product and strengthened relationships.
As makers, we judge ourselves on more than batch yields or positive test results. We depend on open channels from synthesis to shipment, and on the resilience to meet unexpected challenges head-on. The molecule itself provides an interesting canvas, but it is the daily engagement, problem-solving, and incremental refinements that keep us at the leading edge. 2-Fluoro-4-(Trifluoromethyl)Phenylacetonitrile offers more than just another point on a catalog—it stands as the product of continual improvement, shaped by the direct experience and responsibility that only true manufacturing delivers.