2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile

    • Product Name: 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile
    • Chemical Name (IUPAC): 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile
    • CAS No.: 950241-89-5
    • Chemical Formula: C7H2ClF3N2
    • Form/Physical State: Powder
    • 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

    447224

    Iupac Name 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile
    Molecular Formula C7H2ClF3N2
    Molecular Weight 206.56 g/mol
    Cas Number 898781-58-7
    Appearance White to off-white solid
    Melting Point 56-60 °C
    Solubility In Water Poorly soluble
    Smiles C1=CN=C(C(=C1C#N)Cl)C(F)(F)F
    Inchi InChI=1S/C7H2ClF3N2/c8-6-5(3-12)4(7(9,10)11)1-2-13-6/h1-2H
    Pubchem Cid 25079754
    Logp 2.4

    As an accredited 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, white powder with tightly sealed cap, labeled with chemical name, formula, hazard pictograms, and safety information.
    Container Loading (20′ FCL) Container Loading (20′ FCL): 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile is securely packed in sealed drums/pallets, maximizing container capacity.
    Shipping 2-Chloro-4-(trifluoromethyl)pyridine-3-carbonitrile is shipped in tightly sealed containers under dry, cool conditions. It must be handled with appropriate protective equipment and in compliance with relevant chemical and hazardous material shipping regulations. Proper labeling, safety data sheets, and documentation must accompany the shipment to ensure safe and legal transportation.
    Storage Store **2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile** in a tightly sealed container in a cool, dry, well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers and bases. Keep away from sources of ignition and moisture. Label the storage container clearly, and use appropriate secondary containment to prevent leaks or spills. Follow all relevant chemical safety guidelines.
    Shelf Life Shelf life of 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile is typically 2-3 years when stored in a cool, dry, airtight container.
    Application of 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile

    Purity 98%: 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and minimal by-product formation.

    Melting Point 85°C: 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile with a melting point of 85°C is used in agrochemical formulation, where it provides precise blending and stable processing.

    Molecular Weight 222.57 g/mol: 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile with a molecular weight of 222.57 g/mol is used in custom catalyst production, where it allows accurate stoichiometric calculations in catalytic cycles.

    Moisture Content ≤0.2%: 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile with moisture content ≤0.2% is used in electronic material synthesis, where it supports consistent electrical properties and device performance.

    Stability Temperature 120°C: 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile stable up to 120°C is used in polymer modification reactions, where it maintains compound integrity during thermal processing.

    Particle Size <50 μm: 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile with particle size <50 μm is used in advanced pharmaceutical formulations, where it facilitates uniform dispersion and enhanced bioavailability.

    Residual Solvent <0.5%: 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile with residual solvent below 0.5% is used in fine chemical manufacturing, where it reduces impurities and meets regulatory standards.

    Chromatographic Purity >99%: 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile with chromatographic purity above 99% is used in medicinal chemistry research, where it enables reliable structure-activity relationship studies.

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    Certification & Compliance
    More Introduction

    Introducing 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile: Real Production Insights

    Understanding the Makeup of This Important Intermediate

    Each day, our teams interact with molecules like 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile, but this one stands out. It draws attention because it seamlessly balances structural complexity with valuable chemical properties. Chemists across the agricultural and pharmaceutical sectors have relied on this building block for its reliability in synthesis. We see this firsthand as the demand for more targeted chemical scaffolds continues to shape modern organic chemistry.

    Working batches of this product, we notice the molecule’s defining attributes: the interplay of a chloro group, a trifluoromethyl moiety, and a reactive nitrile function. This set of features empowers it to fit into a variety of advanced transformations—Suzuki couplings, nucleophilic substitutions, and further derivatization all come up in regular production planning. The reactivity profile isn’t just theoretical. Lab results have matched pilot plant runs, and we see downstream flexibility that opens doors in both laboratory research and commercial fine chemical manufacturing.

    What Sets Our Material Apart

    Not every 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile sample behaves the same way. In-house, we take every precaution, refining synthesis routes and sharpening purification strategies until the material reaches solid, repeatable benchmarks. Impurity profiles sit at the front of these efforts. Halogenated byproducts, acid sensitivity, and trace moisture all threaten reaction outcomes, particularly at larger scale. So, our analytical team runs batch releases through a suite of confirming tests, not just spot checks. NMR, mass spectrometry, and HPLC all combine to give a tight window of accepted product performance.

    Feedback from our customers often circles around these practical details. Synthetic chemists are wary of trace impurities causing unwanted side reactions or yield drop-off in critical steps. Our experience reflects this concern. By tracking stability throughout the process, we work to keep incoming material dry and to confirm each shipment holds up over practical storage intervals. Our standard specs hit a minimum purity threshold exceeding 98 percent—typically, delivered lots peak higher, holding on color and solubility as well.

    Having tried multiple crystallization solvents and column setups during scale-up, we can speak to the practical side of purification. Each batch is checked for unwanted halides and possible mother liquor contaminants. We listen to downstream users who voice frustration when unreliable material slows research or production. No batch leaves our plant without tight scrutiny on these points.

    Why These Attributes Make a Difference in Synthesis

    Ask a bench chemist why a specific intermediate matters. One might say it unlocks key fragments in crop protection actives, another might note its central position in trial pharmaceutical runs. Our conversations with development partners have highlighted these roles. The electron-withdrawing trifluoromethyl and nitrile groups on the pyridine ring shape regioselectivity in metal-catalyzed couplings. This affects what comes next in a multi-step synthesis, which can spell the difference between a successful active ingredient lead and a wasted campaign.

    Our synthetic campaigns show this compound handles oxidative and basic conditions better than several related structures. By contrast, simple pyridine derivatives containing only halogen or only nitrile substituents fall short in some Suzuki and Buchwald-Hartwig procedures. Customers who run scale-ups with these simpler analogues sometimes return to us after running into yield, solubility, or reproducibility troubles. The combination of three distinct substituents on this pyridine framework keeps pathways open, especially when pushing for high yield, selectivity, or challenging coupling steps.

    The Realities and Opportunities in Manufacturing This Intermediate

    Producing 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile occupies more than just shelf space in our facility. Each lot involves selecting reliable sources for raw pyridine compounds, ensuring reagents like chlorinating agents and trifluoromethylating agents arrive within narrow specifications, and carefully monitoring every step. Scale brings new hurdles: exothermic additions, phase separations, and solvent recovery demand constant vigilance from shift chemists and engineers. Plant operators continually check the rig for tight junctions, as fugitive emissions can’t be tolerated in a high-value run.

    Learning from earlier hiccups—occasional incomplete conversions, precipitation issues in cooler months, or inconvenient hydrolysis from trace water—our process now bakes in checks at critical control points. We rotate team members through every stage of the plant workflow, so lessons and experience circulate throughout the workforce, not just among a specialist group.

    Waste management has evolved. Residual solvents and spent reagents no longer pile up. Our waste streams now run through dedicated onsite recovery units to minimize environmental impact, and we log these metrics for regulatory review and internal improvement. Process analytics track material balance and highlight scope for further yield optimization projects. Each batch of this intermediate reflects not just market demand, but a company’s ethos in resourcefulness and environmental awareness.

    Comparing Against Similar Building Blocks

    Chemists often ask us how 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile stacks up against other nitrogen heterocycles—especially those containing just two substituents instead of three. Take plain 3-cyanopyridine as an example. It works for certain syntheses, but falls short where trifluoromethyl groups are needed to stabilize a transition state or shield a site from undesired nucleophilic attack. Building the extra electronic and steric complexity into the molecule upfront pays dividends downstream, as fewer functionalization steps are required and less time is spent chasing side products.

    The story is similar with 2-chloropyridine-3-carbonitrile, which lacks the trifluoromethyl group. Many users chase similar coupling reactions only to hit solubility or selectivity barriers. When both speed and yield top the list, our target molecule emerges as the tool of choice, especially in emerging agricultural R&D pipelines seeking next-generation active ingredients.

    Synthetic access also differs. Adding trifluoromethyl at a late stage often leads to incomplete conversion and low isolated yields. By producing the fully decorated pyridine ring directly, we support customers looking to simplify route scouting and pilot runs. Many move on to large-scale production with fewer supply chain hiccups and tighter timeline control because of it.

    Usage in Everyday R&D and Production Pipelines

    The feedback loop between our manufacturing site and downstream partners shapes how we refine both product and service. Agrochemical researchers push for new active scaffolds that meet tightening regulatory requirements on selectivity and environmental fate. Here, the unique pattern of substituents on this pyridine ring makes all the difference, as they influence both biological activity and metabolic stability. External development teams often relay that this intermediate enables them to run clean substitutions and cross-coupling reactions, opening doors to analogs that weren’t feasible before.

    In pharmaceutical labs, the presence of a nitrile group offers routes into aminopyridine, amide, or carboxylic acid derivatives without extensive manipulation. Medicinal chemists prize this, as convergent synthesis paths speed up access to diverse compounds needed in hit-to-lead optimization or patent space exploration. We’ve followed numerous contracts where this starting material enabled a four- or five-step journey to novel clinical candidates targeting CNS, anti-infective, or cardiovascular applications. Partners seek out our lots specifically for clean transitions and minimal protection-deprotection requirements.

    Formulation chemists often review our certificates of analysis to ensure no residual catalyst traces threaten downstream biological assays or stability studies. By keeping a stringent eye on residual metal content and residual solvent levels, our QC teams support both compliance and real-world reactivity in these key sectors.

    Tackling Practical Manufacturing Hurdles

    Every campaign through the plant brings a chance to fine-tune operations. Initial pilot runs revealed that modulating reaction conditions—temperature ramping, solvent composition, and agitation speed—unlocks more efficient conversion rates. Over time, we’ve gone from batch trial-and-error toward a more controlled, reproducible operation. This transition didn’t come overnight; it required collecting batch data, learning from the occasional off-spec lot, and swapping out a few legacy reactor vessels that showed poor temperature homogeneity.

    Quality isn’t only about the numbers on a spec sheet. From time to time, we received calls from returning customers who struggled with batch variability from other suppliers. A few rough shipments can drag down a whole project or force expensive rework. Our response has been to prioritize transparency: customers know precisely which analytical measurements tie to each shipment, and our support teams include lead chemists who manage technology transfer discussions. This hands-on approach puts us in a position to help, whether it’s troubleshooting a stalled cross-coupling or suggesting alternative purification protocols downstream.

    Another practical step involves how we handle packaging. This compound arrives in solid form, but has an affinity for atmospheric moisture. Repeated exposure can hamper performance in moisture-sensitive reactions. We’ve implemented moisture-barrier drums and heat-sealed liners, paired with instructive labeling based on observed user handling errors. Our plant floor staff follows set routines for desiccant changes and residual moisture checks before each outbound shipment.

    Supporting Scale-Up and Custom Applications

    Developing new applications in fine chemicals and custom synthesis requires a flexible relationship between producer and customer. We field requests from researchers targeting entirely novel transformations built off the 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile core. Sometimes, a contract arrives requiring kgs rather than tons, but with tighter specs on particle size or impurity content. Rather than take a cookie-cutter approach, our technical group develops side-by-side with the customer’s own team, sharing sample material for route testing, and gathering direct feedback on each milestone.

    Scaling up always brings the risk of new bottlenecks. A reaction that works perfectly in 100 ml flasks can behave unpredictably in a 1000-liter vessel. Plant engineers and synthetic chemists collaborate to match the dynamics of batch-to-batch addition, mixing, and heat control, making small adjustments that will keep the process within safety and spec limits. Together, they head off common pain points: incomplete reactions, hard-to-separate byproducts, or changes to crystal habit. In these moments, knowledge built by years of hands-on plant work makes a difference that spreadsheets alone can’t capture.

    We’ve learned that open communication with end users lets us shape the product to the demands of both routine production runs and cutting-edge research campaigns. This two-way feedback loop heads off potential snags in formulation, solids handling, or wet chemistry adaptation, preventing costly missteps and keeping innovation flowing.

    Building Trust Through Real Quality

    In the modern world, reliability sits at the center of any technology platform. For customers developing agrochemicals or pharma leads, a missed delivery or off-spec batch can halt an entire R&D week. Repeat business comes from trust built not only on the identity and purity of the product, but on consistent performance, regular communication, and the willingness to dig into process snags. Chemists who order our material count on each drum matching the last in both purity and consistency, enabling them to rely confidently on their results and timelines.

    Our internal checks focus on more than meeting laboratory test results. Seasoned staff scrutinize each batch for color, flow, and caking during transfer, which often indicate subtle physical inconsistencies. A tightly controlled process serves as the backbone for stability in delivery and performance. Process documentation—batch logs, in-process analytics, sampling notes—becomes both a record and a tool for continuous improvement.

    Beyond analytical reports, our team runs periodic stability and reactivity challenge tests, simulating user environments such as prolonged storage or combined exposure to light and air. Results from these tests circle back to packaging improvements and recommendations for storage at the customer site.

    Prioritizing Sustainable Production

    As environmental regulation tightens and public expectations for sustainable manufacturing grow, chemicals like 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile get renewed scrutiny. We review our synthesis steps and waste disposal yearly, searching for chances to lower solvent consumption and streamline recycling. Inventory tracking and process mapping reveal opportunities to cut reaction times or optimize solvent swap-outs, reducing both cost and footprint.

    Waste is more than a regulatory burden: it reflects missed opportunity for resource recovery. Instead of treating all byproducts simply as hazardous waste, our process engineers actively reclaim reusable solvents and seek safer alternatives to legacy reagents where practical. Emission traps, in-line scrubbers, and operator training sharpen this focus, helping us stay compliant and ahead of changing standards.

    Throughout the value chain, we discuss these priorities directly with customers. Many development programs now require documented environmental data and life-cycle analysis for key intermediates. We’ve responded by tightening our batch documentation and adding traceablility features for both raw materials sourcing and finished batch disposition. This strategy meets not just organizational goals, but the wider expectations of researchers, regulators, and end-consumers.

    Building Knowledge and Expertise for the Next Decade

    Long-term viability in fine chemical manufacturing demands knowledge, not just hardware. The most successful production cycles blend technical skills, safety culture, and deep process understanding. Our teams—chemists, operators, analysts, and engineers—cross-train to ensure that lessons learned propagate through the organization. Experience from one campaign improves controls for the next; line operators share insights from day-to-day hands-on practice while chemists apply the latest synthetic literature.

    Investing in the next generation of chemical workers pays off in reliability and innovation. We mentor new hires, foster continuing education, and maintain partnerships with academic and industrial groups. On the plant floor, seasoned workers model safe handling of energetic reagents and careful raw material checks. In the QC lab, analysts double-check data integrity, knowing that customer projects often hinge on one reliable supply line.

    Plants do not run on automation alone. Each batch benefits from repeated inspections, seasoned intuition about potential process upsets, and rapid troubleshooting support. This sets a manufacturer apart from traders or bulk commodity suppliers. A hand-crafted approach means slower throughput but steps up overall product value. Our people embody this difference every day, putting evidence of real experience into each delivered drum.

    Conversations with the Field: Real-World Applications

    Companies working with 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile bring field stories that guide improvements on the production side. For instance, agrochemical partners shared how optimal solubility and high purity levels sidestepped crop formulation challenges that plagued previous development cycles. Pharma researchers confirmed that predictable performance in carbon-nitrogen bond-forming reactions led to fewer purification bottlenecks.

    On the research bench and in bulk plant reactions, the value of well-characterized intermediates shines through. Shorter timelines, more reliable documentation packages, and reduced troubleshooting mean scientists spend less time navigating side issues and more time hitting core project milestones. These conversations shape new approaches, from how we select starting materials to how final products move through inventory into customers’ hands.

    We learn that each use case can prompt small, meaningful changes to production and support practice. The faster we close the loop between manufacturer and user, the stronger both sides become.

    Why Choosing the Right Source Matters

    In today’s market, not all chemical material is manufactured with the same attention to detail, traceability, or process knowledge. Experience delivering reliable, high-purity 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile in both custom and catalog formats makes a difference not only for routine runs but for project launches where unexpected variable costs and delays can cripple next steps. Our direct line from process to product brings agility and accountability that third-party distributors struggle to match.

    Decay in quality or lack of support can come from too many parties between producer and end-user. Direct manufacture means rapid solutions, tailored support, and the willingness to engage at the level users require. Continued ability to deliver well-characterized, stable product reinforces both credibility in the market and long-term project viability for every partner involved.

    The Ongoing Journey

    Manufacturing 2-chloro-4-(trifluoromethyl)pyridine-3-carbonitrile is not a static achievement. Each new project, regulatory shift, or customer request sends our teams back to process logs, analytical instruments, and synthesis options to identify improvement opportunities. This constant engagement drives both scientific progress and practical success. In serving partners worldwide, our core values of expertise, transparency, and sustainable practice remain constant. Day by day, we strive to deliver not just a molecule, but a foundation for scientific discovery and commercial success.