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HS Code |
373539 |
| Chemical Name | 4-Fluoro-2-(Trifluoromethyl)Benzaldehyde |
| Cas Number | 746652-96-2 |
| Molecular Formula | C8H4F4O |
| Molecular Weight | 192.11 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 77-79°C at 15 mmHg |
| Density | 1.384 g/cm3 |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=C(C=C1F)C(F)(F)F)C=O |
| Inchi | InChI=1S/C8H4F4O/c9-6-2-1-5(4-13)7(3-6)8(10,11)12/h1-4H |
| Storage Conditions | Store at 2-8°C, tightly closed |
| Synonyms | 2-(Trifluoromethyl)-4-fluorobenzaldehyde |
| Solubility | Soluble in organic solvents |
As an accredited 4-Fluoro-2-(Trifluoromethyl)Benzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is supplied in a 25g amber glass bottle with a secure screw cap, featuring proper hazard and identification labeling. |
| Shipping | 4-Fluoro-2-(Trifluoromethyl)Benzaldehyde is shipped in a tightly sealed, chemical-resistant container, labeled according to hazardous material regulations. The package is padded and secured to prevent leaks or damage. It is transported via certified carriers, with safety documentation included, ensuring compliance with all relevant local and international chemical shipping regulations. |
| Storage | 4-Fluoro-2-(Trifluoromethyl)benzaldehyde should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from sources of ignition, acids, and incompatible materials. Proper labeling and secondary containment are recommended to prevent leaks or contamination. Always follow local regulations and laboratory safety protocols for hazardous chemicals. |
Applications of 4-Fluoro-2-(Trifluoromethyl)Benzaldehyde in Industrial Manufacturing4-Fluoro-2-(Trifluoromethyl)Benzaldehyde is a specialized aromatic intermediate widely used by leading global manufacturers. Its unique fluorinated structure enables targeted synthesis steps for advanced fine chemicals across pharmaceuticals, agrochemicals, electronics, and liquid crystal industries. The following sections detail direct and high-value application areas handled by production plant users. 1. Active Pharmaceutical Ingredient (API) Building BlockResearch-based and generic drug producers incorporate this compound as a key starting material for small-molecule APIs, especially in CNS and oncology projects. Its electron-deficient aromatic ring enables effective nucleophilic substitutions and controlled functionalization, supporting high-yield coupling reactions. Many drug routes use this aldehyde to introduce fluoroaromatic motifs, increasing metabolic stability and selectivity in final actives. Strict traceability, impurity profiling, and solvent controls apply from intake through each batch. Industry compliance standards
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2. Agrochemical Intermediate for Herbicide SynthesisLarge-scale agrochemical plants employ this benzaldehyde as a foundational moiety for selective herbicide production. It reacts effectively with amine sources and hydrazines to form derivatives critical to the construction of active diketone and triazine herbicides. The material’s thermal stability supports high-pressure, multi-step manufacturing protocols, while process safety teams monitor residuals for field compliance. Industry compliance standards
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3. Liquid Crystal Intermediate for Display MaterialsProducers of liquid crystal mixtures for flat panel displays and advanced optics rely on this fluorinated aromatic aldehyde in the synthesis of key mesogenic compounds. Its chemical profile supports the formation of esters, Schiff bases, and fluorinated biphenyls with precisely defined dipole orientations. These intermediates determine the voltage holding ratio and temperature stability of final display materials. Stringent impurity analytics and trace fluoride determinations remain enforced along every step. Industry compliance standards
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4. Intermediate in Fluorinated Material Synthesis for ElectronicsManufacturers of specialty fluorinated polymers and dielectric materials employ this compound for crafting unique side-chain functionalities. It participates in nucleophilic aromatic substitution and directed ortho-metalation protocols to introduce both fluoro and aldehyde groups, boosting dielectric properties and thermal performance. Its purity and consistent batch quality directly influence reproducibility in electronics applications. Industry compliance standards
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5. Specialty Intermediate for Advanced Dye SynthesisProducers of fluorinated specialty dyes utilize this aromatic aldehyde to access high-performance colorants for fibers, plastics, and security applications. It acts as a core component in condensation reactions with aromatic amines or hydrazides, giving rise to dyes with enhanced fastness and chemical resistance. Control over substitution pattern supports the creation of chromophores tuned to client-specific wavelength and solubility requirements. Production processes align with international and customer-driven regulatory specifications for textile and polymer use. Industry compliance standards
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6. Intermediate for Veterinary Drug SynthesisVeterinary pharmaceutical manufacturers use this compound to synthesize fluorinated actives for antiparasitic and anti-inflammatory agents. Its strong deactivating groups enable selective aromatic modification, crucial in forming high-purity end products with improved bioavailability and metabolic profiles suited to veterinary formulations. All manufacturing steps are validated to meet national and international regulatory frameworks for animal health products. Industry compliance standards
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Producing 4-Fluoro-2-(Trifluoromethyl)Benzaldehyde in our own chemical facilities has given our team a front-row seat to the evolution in specialty building blocks that support industries ranging from pharmaceuticals to advanced materials. This isn’t an off-the-shelf molecule; it takes experience to make with precision, and the degree of interest from research and development departments globally signals how key this molecule has become for next-generation discoveries.
At a glance, this compound looks like another aromatic aldehyde, but its chemical profile draws steady requests from our regular clientele. The presence of both the fluorine atom and the trifluoromethyl group on the aromatic ring sets this material apart from standard benzaldehydes preferred years ago. From first-hand observations in the plant, further modifications downstream tend to benefit from this dual-modified scaffold, especially when exploring structure-activity relationships in medicinal chemistry and agrochemical applications.
Over the last decade, new demands from researchers have shifted the focus from plain aldehylic compounds toward substituted variants that fine-tune not only the electron density on the ring but also lipophilicity and stability. Our synthesis route for 4-Fluoro-2-(Trifluoromethyl)Benzaldehyde brings purity levels typically above 98%, as demonstrated by both HPLC and NMR analyses in our on-site labs. Customer feedback shows that impurities—even minor—isomeric byproducts or incomplete fluorination—quickly cause problems in sensitive reactions. For us, this means additional purification steps and constant process monitoring to minimize batch-to-batch variation.
Our standard material arrives as a colorless to slightly pale yellow liquid, with a molecular formula of C8H4F4O and a formula weight of 192.11 g/mol. The manufacturing setup allows careful temperature control—something crucial for materials that prove both reactive and volatile. So orders arrive fresh, sealed, and ready for rigorous chemistry, without degradation or the buildup of internal pressure you might see with less robust packaging methods.
Handling and storage don’t send out warning signals to trained users, but familiarity reveals a few quirks. The volatility, for instance, demands ventilation and storage out of direct sunlight; the sharp odor reminds one of its aldehydic function and volatility profile. We have watched labs run into problems pouring from inadequately closed bottles over the course of several days. Our packaging choices didn’t come from textbook talks but repeated customer calls about evaporated stocks. It sounds mundane, but double-checking cap tightness and minimizing headspace truly preserves the material quality through long synthetic campaigns.
We routinely test melting points, though users expect a clear liquid at room or slightly lower temperatures. High-performance applications—think enantioselective reactions or cross-coupling experiments—profit from our full analytical panel: NMR, IR, GC-MS, and HPLC documentation. This isn’t paperwork for procurement, it’s the result of real-life troubleshooting in places where subtle contamination can cause painstaking optimization to collapse overnight.
The blend of the trifluoromethyl group with fluorine on the aromatic ring makes this aldehyde much more than a simple precursor. In our experience, the electronic effects from both substituents drive reactivity for downstream transformations, from condensation reactions to nucleophilic additions. Our process control leads to reliable reproducibility, which is a phrase that has saved more experiments than any protocol published in a journal.
Innovation in medicinal chemistry seldom happens without robust building blocks. Adding a CF3 group and a fluorine in these positions reliably alters both pharmacokinetic and metabolic profiles of final products, which explains why the compound appears in new hits for CNS-acting molecules or advanced crop protection candidates. Our internal process avoids trace metallic impurities, which often come from less rigorous fluorinating agents. This consistent profile brings repeat customers from both large multinationals and specialized startups pushing for proprietary scaffolds.
In synthetic method development, the reactivity profile of this benzaldehyde variant—specifically in Pd-catalyzed cross-coupling or novel Grignard additions—sets the stage for diversity-oriented synthesis. Colleagues in medicinal and materials development often comment on predictable para and ortho selectivity for further functionalization. Our in-house teams have trialed this for both small molecule innovation and as a handle for materials chemistry, where the electronic effects govern self-assembly or create persistent dipoles for specialized polymers.
Decades of batch data point to the need for strict control in fluorination and subsequent formylation stages. Too much heat, or a rushed addition schedule, and the ratios of undesired isomers rise. To reduce off-spec material, we invested in in-line analytics and more frequent pilot batches during scale-up. Experience taught us that observer fatigue or poorly calibrated sensors correlate with more customer complaints—something that continuous vigilance overcomes. We document even minor shifts in color or odor, which often presage shifts in chemical purity long before instruments flag an outlier batch.
Packaging stepped out of the shadow of manufacturing. Orders leaving our facility pass through a final hands-on QC step, recognizing labeling mismatches or compromised seals. Those aren’t tasks readily left to automated lines. In our eyes, it pays off: when a German pharmaceutical manufacturer reported consistent yield improvements after switching to our material, we saw the real human impact of these checks.
Over the years, scale-up has triggered its own challenges. Reactors larger than two hundred liters develop minute thermal gradients that never appear in bench-top glassware. We check more probe points and run plant-wide debriefs after each lot destined for pharmaceutical applications. It’s worth noting: bulk production means more heat generation, a greater chance of runaway exotherms, and even static electricity matters. Steps as simple as ensuring grounding straps on filling drums keep everyone safer in the plant—one incident long ago convinced us never to get complacent. Our operational safety procedures aren’t inspired by regulatory expectations alone, but by direct lessons learned on the line.
Users approach us with a range of target applications. Leading pharma groups investigate aryl fluoro compounds for improved metabolic stability and lower clearance rates in vivo, making this benzaldehyde a favorite for key intermediate formation. Analytical and process chemists engaged in SAR studies often value the distinctive NMR and mass spectrometric fingerprints for tracking intermediates and confirming reaction sequence outcomes.
Contract manufacturers account for another consistent application, using the aldehyde motif for multicomponent condensations. In agricultural research, the electron-deficient aromatic ring, influenced by the trifluoromethyl and fluorine substituents, reportedly delivers higher herbicidal or fungicidal activity when incorporated into more advanced structures. Our contacts in materials science comment on the polarity and packing interactions the compound imparts to complex polymers. This direct user feedback loops into minor process tweaks and packaging updates.
We’ve handled a full spectrum of benzaldehyde derivatives. Compared to 4-fluorobenzaldehyde, the addition of the trifluoromethyl motif causes a notable increase in volatility and overall reactivity. This influences both storage protocols and performance in reactions needing precise control. In classic Wittig or hydrazone chemistry, the electron-withdrawing groups accelerate reaction rates for more demanding or less nucleophilic partners—feedback that comes directly from our customers’ process optimization reports.
Using non-fluorinated benzaldehydes often leads chemists into modifications seeking improved metabolic resilience. Our product shortcut this step. The dual-substitution pattern reduces the number of post-condensation transformations. In our users’ hands, that translates to real resource savings and faster project timelines. The low aqueous solubility and higher vapor pressure compared to less fluorinated analogs mean users trust our unit-specific recommendations for safe handling and transport.
Some competitors have struggled with supplier-to-supplier variability. Batches purchased from non-specialist sources routinely fail to hit purity and water content specs. Experienced chemists note that even a small presence of positional isomers reduces selectivity or yield in final key step reactions. Our familiar relationship with this chemistry helps us spot and eliminate the pain points.
Another critical difference comes in regulatory scrutiny. Monitoring for trace solvents and heavy metals sits high on both our and our clients’ to-do lists, given progressively stringent environmental and pharmaceutical regulations. Our internal quality system, constantly refined, anticipates evolving expectations so our material continues to fit both R&D and commercial launch projects.
Manufacturing this aldehyde at scale means addressing both obvious and subtle hurdles. Fluorinated reagents demand careful storage and handling, with strict exclusion of moisture. At our plant, redundant drying lines and sealed reactor ports prevent contamination and safeguard our operators. The unforgiving nature of fluorinating agents leaves no room for shortcuts—a single process deviation can trigger hazardous byproduct formation. Our experienced chemists have built in real-time monitoring and staged additions to minimize risk.
Product identity always reflects the integrity of both reagents and procedures. Counterfeit or misidentified chemicals disrupt research and production pipelines, with downstream financial and experimental consequences. Our team tackles this through end-to-end chain-of-custody protocols and batch archiving. From the procurement of raw materials to final finished bottles, we log and reconcile every lot. A rare mislabeling incident taught us to double-source barcodes and audit bottle counts prior to each shipment. Such painstaking tracking isn’t a marketing point; it’s the foundation that research departments rely on.
On the technical front, achieving consistency in physical properties like color and odor signals purity, and assures researchers that the batch they used last month will behave the same this time around. We map minor impurity patterns to their process origin, supporting troubleshooting efforts when clients report anomalous results. Periodic customer site visits uncover usage challenges or storage issues that don’t show up in lab-based stability testing. These exchanges shape our drive for better packaging, clearer labeling, and even revised documentation practices.
Our commitment to product stewardship includes evolving environmental practices. Waste fluorinated solvents and byproducts don’t leave site in unmonitored barrels; in-house treatment systems reclaim reusable components and neutralize hazardous waste according to strict standards. This isn’t just box-checking: site audits, often with customer participation, keep us accountable to higher benchmarks than minimum regulation, protecting workers and local communities alike.
The demand for 4-Fluoro-2-(Trifluoromethyl)Benzaldehyde won’t fade. Each year, our order book reflects a wider range of application areas, as synthetic chemists and formulators chase unique pharmacophores and advanced materials. In response, we regularly review our raw material streams to secure consistent, high-quality starting reagents, minimizing the risk of upstream disruptions.
Advanced analytics boost our edge, as clients request certificates of analysis with deeper impurity profiling: 19F NMR, trace metals scans below pharmaceutical cutoffs, water content measured by Karl Fischer titration. Such requests shape our internal benchmarks—what passes for good enough elsewhere often prompts process tightening. Researchers need this molecular consistency to spend less time checking and more time innovating.
Keeping pace with green chemistry goals drives us to explore new synthetic routes. Electrophilic fluorination and catalytic formylation, both under continuous flow conditions, create the potential for safer, more sustainable manufacturing. Our plant engineers engage researchers who envision pilot production that not only increases throughput but slashes hazardous waste. We don’t advertise blue-sky thinking until we’ve proven feasibility on the ground; our scale-up efforts take pragmatic steps, knowing that change must fit industrial realities.
The evolving regulatory climate draws our continued attention. Pharmaceuticals and crop protection molecules derived from advanced building blocks now face more pre-market scrutiny, including extended impurity profiles and assurance of process robustness. Our relationships with regulatory consultants, along with participation in industry quality forums, help us anticipate—not just react to—these shifts. Processing documentation, batch certification, and safety documentation rise with new requirements, and manufacturing adapts.
Continuous two-way communication with our clients shapes both product quality and service. We know that users want material that works right the first time, delivered as promised. We share our analytical methods and adapt packaging and shipping practices in response to real-world challenges that researchers report. Research teams around the world have taught us that minor impurities or trace leftover solvents, undetectable in some specs, still present issues in formulation or bioassays. Listening and proactively responding keeps our material at the front of their ordering lists.
Long-term customer partnerships influence our choices in raw material sourcing and logistics, propelling investments in both traceability and advanced packaging. Comments about late shipments or confusing labeling have pointed us toward improved logistics chains and clearer bottle coding. When a research group in Japan highlighted a trend in trace impurities affecting their high-throughput screens, our technical service collaborated to identify the offending byproduct and modify purification accordingly—improving results for all clients.
Feedback does not only improve what we send out, but instructs our own technical teams. Users running scaled syntheses or pilot plant runs share data about how micro-scale deviations translate into kilo-scale problems. These insights return to our process development group, feeding incremental improvement.
Producing 4-Fluoro-2-(Trifluoromethyl)Benzaldehyde consistently and safely is a team effort, demanding attentive eyes and open communication. The technical challenges of chemical manufacturing intersect with regulatory, environmental, and customer service dimensions daily. Having lived through years of demand spikes, regulatory changes, and raw material constraints, our approach blends practical caution with an appetite for innovation.
Above all, our experience shows that real relationships—internally and with customers—drive both the product and the progress of the field. Those pushing forward in medicinal chemistry, agrochemical innovation, or materials development see their work supported by careful, responsible manufacturing rooted in the realities of modern chemistry. Our goal remains unchanged: supplying a molecule that reliably meets, or often exceeds, the evolving expectations of serious research and development teams.