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HS Code |
302655 |
| Compound Name | 2-Fluoro-4-(Trifluoromethyl)Benzaldehyde |
| Cas Number | 92450-63-0 |
| Molecular Formula | C8H4F4O |
| Molecular Weight | 192.11 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 140-142°C (at 29 mmHg) |
| Density | 1.414 g/cm3 |
| Purity | Typically ≥98% |
| Solubility | Soluble in organic solvents (e.g., dichloromethane, ethanol) |
| Smiles | C1=CC(=C(C=C1C=O)F)C(F)(F)F |
| Inchi | InChI=1S/C8H4F4O/c9-7-2-1-5(4-13)3-6(7)8(10,11)12/h1-4H |
| Synonyms | 2-Fluoro-4-(trifluoromethyl)benzaldehyde; 4-(Trifluoromethyl)-2-fluorobenzaldehyde |
As an accredited 2-Fluoro-4-(Trifluoromethyl)Benzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2-Fluoro-4-(trifluoromethyl)benzaldehyde, sealed with a PTFE-lined cap, labeled for laboratory use. |
| Shipping | 2-Fluoro-4-(Trifluoromethyl)Benzaldehyde is shipped in tightly sealed, chemically-resistant containers to prevent leaks and contamination. Packaging complies with international regulations for hazardous materials, ensuring protection against moisture, light, and physical damage. Accompanied by proper labeling and documentation, the shipment is handled by certified carriers specializing in chemical transport. |
| Storage | Store **2-Fluoro-4-(trifluoromethyl)benzaldehyde** in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Keep away from sources of ignition and direct sunlight. Recommended storage temperature is between 2–8 °C (refrigerated). Handle under an inert atmosphere if possible to prevent degradation. Ensure proper chemical labeling and follow all safety protocols. |
Applications of 2-Fluoro-4-(Trifluoromethyl)Benzaldehyde in Industrial ManufacturingAs a specialist upstream manufacturer of 2-Fluoro-4-(Trifluoromethyl)Benzaldehyde, we supply this key aromatic intermediate to enterprises operating in advanced pharmaceuticals, crop protection, and specialty chemical synthesis. The following application scenarios illustrate industry-validated downstream usages, detailed with compliance standards, formulation levels, process integration, and typical demanded end products. 1. Advanced Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers employ this compound in constructing fluorinated heteroaromatics for next-generation active pharmaceutical ingredients, especially in oncology and CNS categories. Due to fluorine’s contribution to metabolic stability and target affinity, this aldehyde forms part of the core framework in synthesizing clinical trial and commercial APIs through Grignard and condensation reactions. Industry compliance standards
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2. Agrochemical Active Ingredient ManufacturingProducers of crop protection agents incorporate this aromatic building block to synthesize innovative fungicides and herbicides with enhanced bioavailability and environmental stability. Its electron-deficient ring structure enables downstream halogenation or coupling to produce high-performance active ingredients demanded in regulated markets. Industry compliance standards
Typical usage ratio
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3. Specialty Monomer and Polymer SynthesisIndustries focused on high-performance polymers exploit the reactivity of this fluorinated benzaldehyde to produce specialty monomers, which impart enhanced hydrophobicity and chemical resistance in finished engineering plastics and coatings. The material is vital in the design of fluorinated polyimides and aryl ether-based polymers. Industry compliance standards
Typical usage ratio
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4. Fine Chemical Intermediate for Electronic MaterialsElectronic chemical manufacturers rely on this raw material to design intermediates for advanced photoresists and organic semiconductors, where controlled fluorination strategies are crucial for thermal, chemical, and dielectric performance. Its precise substitution pattern supports the needs of microfabrication and optoelectronic specialty chemicals. Industry compliance standards
Typical usage ratio
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5. Custom Synthesis in Research and Analytical ReagentsProducers specializing in custom chemical synthesis and analytical standard manufacturing use this material for developing reference compounds and labelled standards, particularly where selective fluorine or trifluoromethyl incorporation enables enhanced detection and quantification in advanced instrumental methods such as LC-MS and NMR. Industry compliance standards
Typical usage ratio
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Producing 2-Fluoro-4-(Trifluoromethyl)Benzaldehyde over the years has given us a close look at what customers really expect from a specialty benzaldehyde. Our chemists, line workers, and QC staff invest their daily efforts to ensure that each batch reflects consistency, reliability, and the kind of purity that research chemists and process engineers require. This compound, a crystalline solid or sometimes a clear pale-yellow liquid at room temperature, delivers the structural features necessary for specialized synthesis, especially in pharmaceutical intermediate development and advanced materials research.
As a manufacturer, my involvement goes beyond the paperwork and MSDS reports—I've supervised the distillation and scrutinized the infrared spectra to confirm its signature carbon-fluorine and aldehyde stretches. 2-Fluoro-4-(Trifluoromethyl)Benzaldehyde, bearing the CAS number 142732-23-6, earns its reputation through a unique substitution pattern: a fluorine at the ortho position to the aldehyde, along with a trifluoromethyl further down the aromatic ring. These groups do more than decorate the molecule—them shape reactivity and make this compound suitable for chemistries where electron-withdrawing strength matters. This is common in late-stage functionalization strategies and when manipulating electron-deficient aromatic rings.
Manufacturing this compound in our plant challenged us to refine our halogenation and formylation processes. Direct fluorination is rarely straightforward and patience pays off in product quality; aggressive methods, such as selecting the right temperatures and handling hazardous reagents, must be balanced against the purity we promise. We've invested in closed-system reactors, on-line purity monitoring, and post-synthesis purification by distillation and recrystallization. Handling fluorinated intermediates invites safety considerations that only robust procedural discipline and vigilant operator training can address.
The way a 2-Fluoro-4-(Trifluoromethyl)Benzaldehyde batch leaves our facility says a lot about our day-to-day standards. Moisture, air, and temperature shifts can compromise stability, so we rely on tightly sealed amber glass and fluoropolymer-lined containers. We avoid polyolefin plastics, learned from past compatibility tests—some plastics degrade or leach trace contaminants. From loading lines to outgoing inspection, product integrity sits squarely on not cutting corners.
Customers who keep the chemical in their own dry storerooms often ask about long-term stability. From our own retention samples, we have seen it maintain purity above 99% for at least 24 months when stored below 25°C, away from direct sunlight, with desiccants in the secondary packaging. Fluctuations can lead to slow hydrolysis or oxidation, so environmental control remains every bit as important on the user’s end as ours.
Our routine lot testing involves NMR, GC-MS, HPLC, and water content by Karl Fischer, all performed in-house. We cite a minimum purity specification of 98% for the standard product, though regular manufacturing runs often deliver greater than 99.5%. Residual solvents, key to understanding impact on downstream synthesis, test below 500 ppm for qualified batches. We track trace metals during raw material selection; most lots show metal content measured in the single-digit ppb. These values stem from empirical data, not aspirational targets. Anyone buying directly from us gets full access to batch analytical reports, not simplified summaries.
Chirality isn't a concern with this molecule due to its symmetrically substituted ring, but we’ve fielded questions about isomerism, and supply customers with authentic NMR spectra to confirm correct substitution.
We regularly ship this product to labs engaged in high-value pharmaceutical R&D, agrochemical innovation, and materials chemistry programs. Its main draw lies in the electron-deficient aromatic system, which steers reactivity in palladium-catalyzed couplings, condensation reactions, and nucleophilic aromatic substitutions. Our long-term partners in pharma intermediate synthesis favor this aldehyde for its predictable reaction profile, especially when controlling for regioselectivity and ensuring a consistent starting point for complex molecule assembly. Formulators in crop protection compounds use this building block to prepare fluorinated analogs of known actives, probing for improved metabolic stability.
We've seen interesting developments in the field of fluorinated OLED materials, where designers look for aromatic aldehydes to anchor small-molecule semiconductors. The compound’s robust electron-withdrawing properties enhance performance in some of these niche applications. From my conversations with material scientists, small changes in substitution pattern can mean the difference between a compound that works and one that fails—and that's why this particular structure wins repeat attention.
Those familiar with benzaldehyde chemistry know that fluorination and trifluoromethylation often serve to fine-tune physicochemical properties. Compared to classic benzaldehyde or plain 4-trifluoromethylbenzaldehyde, the extra fluorine atom increases resistance to oxidation and boosts volatility safeguards, resulting in longer shelf life and decreased incidence of unwanted interaction with reagents in sensitive syntheses. From working with similar compounds, I can say the ortho-fluorine especially narrows the spread of electrophilic reactions, offering more control during condensation or organometallic additions.
We’ve handled both mono- and polyfluorinated benzaldehydes, learning that each pattern influences boiling point, solubility, and even sensory characteristics—unwanted odors get suppressed in compounds with increased fluorination. In direct client feedback sessions, customers pointed out this aldehyde’s reduced tendency to form oxidation by-products in storage and its cleaner reaction profiles compared to derivatives without the trifluoromethyl group.
Our production facilities operate under strict emission control. The move to high-purity solvents and minimized waste generation is not about abstract “sustainability” goals alone. Compliance audits in the past revealed trace emissions that needed real-time changes—better vent cleaning, solvent recycling, and effluent management. Each kilogram we ship comes stamped by actual process improvements, rather than just certificate paperwork.
Increasing regulatory attention on fluorinated organics has brought more scrutiny in the industry. Our teams work to ensure that every outgoing batch stays below legal notification thresholds in major jurisdictions. RoHS, REACH, and local directives shape our day-to-day plant practices. Our regulatory team’s boots-on-the-ground involvement in designing closed-loop reactions and careful solvent handling makes a measurable difference in both compliance and operator safety.
Every run gets sampled at multiple stages—after reaction, finishing, and before packing. Our staff checks for impurity signatures using our in-house GC-MS, HPLC, and NMR instruments calibrated against certified standards. It’s one thing to claim “high purity” on a website, it’s another to stand behind it with accessible, traceable data. Incoming raw materials—fluorobenzene, trifluoromethylating agents—are qualified in small pilot batches before scale-up. I’ve seen firsthand that skipping early pilot work invites disaster in either yield, impurity, or reproducibility.
We’ve learned a lot about what can go wrong at scale: atmospheric moisture in product lines, trace metal contamination from piping, and non-uniform heating during distillation all show up as real problems, not just theoretical risks. Our engineering team invested serious time into flow control upgrades, which now allow us to achieve temperature uniformity within a degree or two. Any deviation outside of our set range means the batch gets diverted for review rather than rework. This accountability holds from plant floor technicians to QA leads.
All our lots trace back through documented batch sheets, raw material certifications, and instrument calibration routines. Customers with validation requirements for cGMP or ISO-9001 regularly ask for full manufacturing histories, which we provide, rather than just tossing out a compliance box on a form.
Shipping 2-Fluoro-4-(Trifluoromethyl)Benzaldehyde presents a unique set of complications. This is a classified chemical by IATA and IMDG guidelines—requiring UN-approved packaging, completed shipping declarations, and trained dangerous goods handlers. Over the years, we’ve run into deadlines missed by customs or rejected paperwork, resulting in us partnering with freight agents who already know the idiosyncrasies of moving specialty chemicals across borders. From experience, shipments routed through the Middle East or South Asia need extra scrutiny to avoid customs delays, and we communicate that transparently with customers.
Temperature sensitivity during transit matters. One summer, as temperatures at international cargo centers spiked above 40°C, we noticed impurity levels creep up in a few shipments. Insulated shipping with cold packs became our next line of defense, and this now forms part of our high-value batch protocol. It's these iterative lessons that ensure reliability for end-users, not mere regulatory paperwork.
Direct feedback from established partners shapes how we make and deliver 2-Fluoro-4-(Trifluoromethyl)Benzaldehyde. One research chemist in the northeast US provided valuable insights after noticing batch-to-batch color differences—turns out, trace iron from unlined reaction vessels skewed product color. Adjustments to a PTFE lining cleared up the color variation and improved batch-to-batch reliability. It’s this back-and-forth—the chemist’s eye on their end, our technical team on our end—that distinguishes what factory-direct supply should look like.
We owe much to university labs and R&D partners, whose demanding synthetic protocols sometimes require tailored purity, dried product, or custom solvent packaging. Our flexibility to run short custom lots or tweak drying protocols has cemented relationships and keeps us knowledgeable for future synthesis questions.
Being a direct manufacturer means the questions come to us, not a faceless sales rep or distributor. Every query—why oximes form under certain storage conditions or how to shift a condensation product’s selectivity—lands on our technical team’s desks. That real-world challenge keeps us honest and makes us better at what we do. We update our methods, not because a consultant told us to, but because customer discussions spark improvement ideas.
We do more than make a commodity. Each kilogram reflects hundreds of hands-on hours troubleshooting, improving, and documenting. We pride ourselves on giving customers access to the very people responsible for production, analytical support, and ongoing technical problem-solving. You’re never days removed from the people who understand production, from raw material sourcing to final packaging.
Fluorinated aromatics remain in high demand as researchers in pharmaceuticals and advanced materials look to fine-tune molecular activity. Combinatorial chemistry and high-throughput screening often need unique aldehydes like this one because small differences in substitution drive big changes in end-use profiles. We've partnered with academic groups to explore new transformations—palladium/photoredox combinations, metal-catalyzed cross-coupling, and organocatalytic condensations—that all depend on clean, consistent starting materials.
Our R&D team tracks regulatory developments that will shape future production—PFAS scrutiny, new persistent organic pollutant rules, and solvent replacement strategies. As countries adjust their policies regarding fluorinated chemicals, our chemists already test pilot routes employing greener solvents and improved yield optimization. We believe that success in tomorrow’s specialty chemical supply means moving faster and more transparently, not just keeping pace.
Supplying 2-Fluoro-4-(Trifluoromethyl)Benzaldehyde isn't just about getting the right CAS number into a bottle. It means understanding what downstream chemists, engineers, and regulatory shepherds expect. Having produced, analyzed, and shipped this aldehyde batch after batch, we can say production offers daily lessons. From tackling stubborn impurities to adjusting packaging to match end-users’ evolving storage standards, our hands-on experience—poured into every shipment—makes sure our customers can work with total confidence.
The difference for anyone sourcing this product directly from us comes from our skin in the game—factory-floor know-how, problem-solving mentality, and a commitment to real, verifiable performance. Our drive to improve doesn’t come from sales targets; it comes from living up to customer trust and our own standards for chemical manufacturing done right.