3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde

    • Product Name: 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde
    • Chemical Name (IUPAC): 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde
    • CAS No.: 876521-89-6
    • Chemical Formula: C7H3F4NO
    • Form/Physical State: Liquid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    514113

    Chemical Name 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde
    Molecular Formula C7H3F4NO
    Molecular Weight 195.10
    Cas Number 885276-00-8
    Appearance Pale yellow to colorless liquid
    Purity Typically ≥98%
    Density Approx. 1.45 g/cm³ (estimated)
    Solubility Soluble in common organic solvents (e.g., DMSO, DMF, chloroform)
    Smiles C1=CC(=NC=C1C(=O)C(F)(F)F)F
    Inchi InChI=1S/C7H3F4NO/c8-5-2-1-4(3-13)12-6(5)7(9,10)11
    Storage Conditions Store at 2-8°C, tightly sealed

    As an accredited 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 5 grams, with a tamper-evident cap and hazard label, sealed in a protective secondary container.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde: Securely packed drums, moisture-protected, properly labeled, meeting international transport regulations.
    Shipping The chemical 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde is shipped in a tightly sealed, chemically resistant container under ambient or refrigerated conditions, depending on stability requirements. Properly labeled, it is packaged according to international regulations for hazardous materials, ensuring protection from moisture, light, and physical damage during transit.
    Storage Store 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, in a cool, dry, and well-ventilated area away from light. Keep it separated from acids, bases, and strong oxidizing agents. Store at temperatures recommended by the supplier, typically at 2–8 °C or lower. Avoid moisture and prolonged exposure to air.
    Shelf Life Shelf life of 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde: Stable for 1–2 years when stored in a cool, dry, dark place.
    Application of 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde

    Purity 98%: 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction efficiency and minimal by-product formation.

    Melting Point 42°C: 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde with a melting point of 42°C is used in agrochemical development, where its well-defined phase transition enables precise formulation processes.

    Stability Temperature 80°C: 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde with stability up to 80°C is used in high-temperature catalytic reactions, where it maintains chemical integrity for reliable product yields.

    Molecular Weight 193.08 g/mol: 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde at molecular weight 193.08 g/mol is used in heterocyclic compound synthesis, where it provides predictable stoichiometric calculations and scalable process control.

    Particle Size <100 µm: 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde with particle size less than 100 µm is used in fine chemical manufacturing, where increased surface area enhances reaction rates and product uniformity.

    Solubility in DMSO: 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde soluble in DMSO is used in medicinal chemistry research, where superior solubility facilitates compound screening in biological assays.

    Moisture Content <0.2%: 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde with moisture content below 0.2% is used in moisture-sensitive organic syntheses, where low water levels prevent undesired hydrolysis and maintain product quality.

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    Certification & Compliance
    More Introduction

    3-Fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde: A Versatile Building Block From Our Laboratory

    Real-World Insight From the Manufacturer’s Bench

    Developing advanced chemical intermediates calls for both hands-on craftsmanship and scientific rigor. We have poured years of expertise into producing 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde, and its journey reflects the practicality and challenges of modern chemical manufacturing. It has become a crucial compound for our partners in pharmaceuticals and agrochemicals, where purity and consistent quality support high-stakes innovation.

    Every batch that leaves our facility carries the mark of close monitoring, tight process control, and attention to physical characteristics that truly matter in the lab. Over time, we fine-tuned temperature profiles and solvent choices to avoid over-fluorination and aldehyde loss. Scaling up from gram-scale research to reactors handling scores of kilograms, we adjusted for airflow, filter efficiency, and even the humidity on production days. That dedication impacts yields you can rely on and lets downstream chemists work confidently, batch after batch.

    Model, Specifications, and Physical Profile

    We make 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde to support the strictest requirements in method development and advanced syntheses. The compound’s CAS number helps with traceability and audit trails, while consistency defines our philosophy. During production, most steps take place under inert conditions because even a brief exposure to moist air can degrade sensitive moieties. This isn’t just academic—the aldehyde group in this molecule provides a crucial reaction handle, but it also makes the compound more reactive than many fluorinated pyridines, meaning stability starts with everything from how we pack it to how quickly it reaches your lab bench.

    Our product exhibits the pale yellow crystalline appearance expected of high-grade aromatic aldehydes, and routine NMR scans confirm the clean, sharp signals characteristic of the intended structure: a six-membered aromatic ring with pyridine nitrogen, a fluorine at position 3, a bulky trifluoromethyl at position 6, and an aldehyde at position 2. This arrangement imparts both electron-withdrawing properties and distinct reactivity, making it a workhorse for chemists designing more stable, more selective molecules.

    Purity standards matter greatly here. We use GC and LC purity checks on top of established wet-chemical tests. With this approach, we routinely achieve purity levels above 98%, but the proof comes when downstream partners build out their target libraries without needing excess purification. Moisture content, residual solvents, and particulate matter receive attention because issues at tiny scales can snowball in API development or material science.

    Applications and Front-Line Experiences

    Research chemists tell us one of the main draws is the unique combination of electron-withdrawing power and aldehyde function. The electron-deficient ring enhances cross-coupling reactions, creating opportunities for biaryl synthesis where other aldehydes would stall or give mixed results. In our experience, the compound fares well as a precursor for heterocyclic cores used in next-generation anti-infectives and herbicidal actives. One project involved Suzuki-Miyaura couplings under basic conditions, where the 3-fluorine and 6-trifluoromethyl pattern delivered yields 10–15% higher compared to less-fluorinated analogs. Our team worked directly with process chemists to dial in reaction stoichiometry and minimize side reactions.

    The aldehyde group at the 2-position stands out for rapid condensation with amines and hydrazines. Medicinal chemists value this for building SAR libraries in kinase inhibitor programs. We’ve also supported R&D teams as they use the compound in reductive amination, quickly introducing complexity without risking fouling catalysts with persistent impurities. Having the work-up process streamlined helps speed up synthesis, and projects can clear hit-confirmation bottlenecks much faster.

    The compound has differences from its cousins like 2-fluoro-6-(trifluoromethyl)pyridine-3-carbaldehyde or unsubstituted pyridinecarbaldehydes. By shifting the fluorine and trifluoromethyl groups to the observed positions, substitution reactivity and electronic effects change dramatically. Some customers looking for less reactivity in the aldehyde have found related molecules provide slower background hydrolysis, but for a compound-pool buildout or specifically challenging condensation, ours consistently comes up as the preferred choice. Differences in solubility and reactivity translate directly to costs and timelines—a lesson we’ve learned after watching failed reactions with less-optimized products from elsewhere.

    Safety, Handling, and Logistics—From Our Floor to Yours

    We know firsthand that aromatic aldehydes with heavy fluorination can behave unpredictably in bulk. Our production staff wear specialized PPE, and we keep air-handling in check due to the strong odor and volatility. The packaging has evolved over the years, now relying on lined, airtight containers that cut down on degradation and evaporation. Logistics teams trained in chemical handling regularly troubleshoot minor shipping hiccups, especially during high-humidity seasons. That level of practical feedback feeds right back into our continuous improvement loop, with real observations from the loading dock, not just desk-bound theory.

    Partner feedback sharpened our response to instability in storage and transit. Temperature excursions during distribution can cause color changes or off-specification material, eating into the shelf life. In response, we upgraded both the packaging lining and the insulation used for larger lots, reducing the number of customer complaints about discoloration or aldehyde “ghosting” by more than half in the last three years. This hands-on approach grew out of watching the material’s quirks over hundreds of shipments rather than relying on generic safety data.

    Environmental and Regulatory Considerations

    Our long-term production has taught us the ecological impact of fluorinated intermediates is a real concern, both in waste management and residual emissions. We’ve reduced the use of high-hazard solvents where possible and set up closed-loop systems to recycle byproducts. The byproducts of this particular synthetic route have relatively low volatility, though they require careful disposal and neutralization. Over ongoing years of auditing, we’ve tackled emissions with activated carbon scrubbers and improved condensation traps. These measures have both regulatory and community trust implications. We respond to inquiries from environmental oversight bodies about solvent recovery and fluorinated waste because our local relationships matter as much as finished product output.

    Increasingly, downstream partners in pharma and agrochemicals look for clean audit trails. We track lot numbers, maintain detailed process records, and retain samples for post-release investigation if a regulatory question comes up—an all-too-common reality as rules around fluorinated intermediates evolve. Responsible handling from synthesis through to delivery not only streamlines partner audits, it has preempted a number of past supply-chain holdups, once international standards for fluorinated chemicals tightened.

    One practical lesson: even if regulatory status differs by region, adhering to stricter standards on purity, labeling, and safety keeps us prepared for audits or rapid customer scaling. We document everything, not because regulators ask—though they do—but because small process lapses snowball into lost batches or, worst case, end-user safety issues. That’s not news to anyone running analytical QC for active intermediates, but dedication in the trenches makes a difference to the final user.

    What Sets This Product Apart

    Over the years, customers often ask whether it makes sense to use 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde compared to older, less functionalized pyridine aldehydes. The real point of difference leans on the push-pull effect between the fluorine atoms and the aldehyde, which enables unique reactivity for C–C and C–N bond formation. For manufacturing scale and bench-scale development, the compound handles purification without persistent dimerization or resin fouling, which can bog down prep HPLC on less stable candidates.

    Having feedback from teams across pharma, material science, and crop protection means we see what works, where it stalls, and what adjustments to make upstream. We once retooled our filtration process after a partner reported trace particulates fouling their microfluidizer columns. We switched filter providers, ran trial batches, and confirmed tighter particulate control, preventing a repeat. These lessons stick with us, and they manifest every time a batch is loaded, sampled, and released.

    Evaluating cost-effectiveness, we routinely compare input costs, solvent usage, and labor. The unique structure of our high-fluorine pyridinecarbaldehyde means expensive fluorinated building blocks pay for themselves when fewer isolation steps and cleaner downstream conversions translate to overall process gains. From the synthetic lab to the pilot plant, time really does mean money, especially when handling sensitive functional groups.

    Lessons From Scaling Up and Supporting Applied Research

    Expanding production from multi-gram research batches to metric ton capability isn’t a straight line. Fluorinated pyridine chemistry requires engineering modifications that only come from direct experience. We retrofitted our reactor lids and transfer lines after noting corrosion in pilot-scale hardware, learning that even with good material specifications on paper, the nuances of leaching, gasket compatibility, and solvent swelling make a real difference to throughput and long-range cost control.

    Testing for scale-dependent properties, such as heat release and off-gassing during high-volume distillations, formed its own discipline in our shop. Over time, we deployed real-time monitoring of temperature and pressure, which let us catch runaway exotherms early and respond instantly—headache avoided for both our team and our customers. Lab-scale notes cannot substitute for pilot-plant feedback; both are needed to ensure safe, reliable supply.

    In research support, we provide access not just to the material but to our observations—where purification issues crop up, what glassware coatings improve shelf life, and how to optimize dissolution for slow-release formulations. We pull from a running log of field experience rather than recycling generic academic insight. The value comes from direct troubleshooting, such as adjusting the mixing protocol for problematic emulsions or swapping out the final drying medium after noticing small but critical trends in aldehyde retention.

    Supporting Innovation in Customer Applications

    Partnerships often develop when teams face a bottleneck with a difficult reaction. One pharma group approached us after traditional pyridine aldehydes failed to deliver on selectivity, risking a year-long delay. Our technical group worked hands-on with theirs, reviewing NMR spectra, narrowing down minor side products, and identifying minor changes in reaction conditions that helped them reach their yield targets. That kind of support does not appear in catalogs, but it shapes genuine collaboration and speeds the route from lab discovery to commercial product.

    The material’s market demand reflects both reactivity and reliability. Peers in agricultural chemistry report gains in seed coating adhesion due to the molecule’s specific polarity, which drives more uniform application compared to less-fluorinated aldehydes. Projects in advanced polymers harness its ring-fluorination to achieve new electrical properties—potentially a growing field as electronics miniaturization leans on specialty materials. Our vantage point inside the production chain gives us firsthand exposure to how far creative application stretches beyond the datasheet.

    Facing Tomorrow: Continuous Improvement From Production Floor

    Feedback loops in specialty chemical manufacturing run deep. Our operators note even minor temperature swings during final distillation, tweaking protocols in response. Years of hands-on troubleshooting have built up a deep well of practical knowledge. Recently, we overhauled our solvent recovery to further lower VOC emissions—a change that not only satisfied upcoming environmental requirements, but actually improved material throughput, lowering back-orders by nearly 20%.

    Lessons learned in one synthesis often carry over to others. Observing how aldehyde content drifted in old storage bottles prompted us to reformulate inert atmosphere techniques not just here, but for our entire aldehyde range. We learn in motion, not just from isolated incidents. By building a team culture where floor operators, analysts, and technical support share notes, we catch trends that no spreadsheet or algorithm would highlight. The result surfaces in partner labs months later—in higher throughput, fewer purification steps, or simply in not having to pause a project halfway for batch retesting.

    The Ongoing Value of Reliable Sourcing

    Chemists tell us regularly that delays in intermediate supply—especially for functionally dense building blocks like 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde—translate into costly program slowdowns. From the manufacturer’s perspective, consistent communication across all stages of planning and logistics keeps product flowing and timelines manageable. We routinely share lead-time updates, stock levels, and technical insights. Small adjustments on our end—such as rerouting finished goods during weather disruptions—yield large reliability dividends down the line.

    In a landscape where method reproducibility has become a key hurdle, our focus on batch-to-batch consistency goes beyond internal QC. We coordinate with partners as they troubleshoot new synthesis schemes or transfer processes to scale-up. Often, a failed scale-up elsewhere traces back to small inconsistencies in the supply chain: solvent content drift, lot-to-lot color shifts, or even unnoticed labeling errors. Having walked through these missteps ourselves, we built cross-team systems to track, and rapidly resolve, outliers.

    Partnering for Better Chemistry

    From our laboratory benches to finished project pipelines, 3-fluoro-6-(trifluoromethyl)pyridine-2-carbaldehyde represents the blend of technical achievement and experience-driven refinement. As synthetic targets become more challenging and market needs evolve, we invest in staying ahead—not just by delivering a molecule that meets its spec sheet, but by actively supporting every stage of use, troubleshooting, and scale-up. Whether it’s process innovation, reduced environmental footprint, or faster access to enabling intermediates, the product’s value is felt in real results on the ground, shaped by years of hands-on manufacturing.

    Our ongoing vigil at every stage—synthesis, purification, packing, logistics, and technical support—grows from direct manufacturer experience, not from behind a desk. Through that, we offer more than a building block. We offer partnership, reliability, and a practical voice in the demanding, ever-changing world of advanced chemistry.