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6-(Trifluoromethyl)Nicotinonitrile

    • Product Name 6-(Trifluoromethyl)Nicotinonitrile
    • Alias 6-(Trifluoromethyl)nicotinonitrile
    • Einecs 703-278-5
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    652018

    Chemical Name 6-(Trifluoromethyl)nicotinonitrile
    Cas Number 349-57-7
    Molecular Formula C7H3F3N2
    Molecular Weight 172.11 g/mol
    Appearance White to off-white solid
    Boiling Point 229°C
    Melting Point 49-51°C
    Density 1.36 g/cm3
    Purity Typically ≥ 98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=CC(=NC=C1C#N)C(F)(F)F
    Inchi InChI=1S/C7H3F3N2/c8-7(9,10)5-2-1-4(3-11)12-6-5/h1-2,6H
    Storage Conditions Store in a cool, dry place, away from direct sunlight
    Refractive Index 1.458 (predicted)
    Ec Number 620-969-2

    As an accredited 6-(Trifluoromethyl)Nicotinonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g bottle of 6-(Trifluoromethyl)nicotinonitrile is packaged in an amber glass container with a tightly sealed screw cap.
    Shipping **Shipping Description:** 6-(Trifluoromethyl)nicotinonitrile is shipped in tightly sealed containers to prevent moisture and air exposure. Packaging complies with chemical safety regulations, ensuring protection from physical damage and contamination. The shipment includes all necessary hazard labeling and documentation for safe transport, whether by ground, air, or sea, according to international chemical shipping standards.
    Storage Store **6-(Trifluoromethyl)nicotinonitrile** in a tightly sealed container within a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers. Protect from moisture and direct sunlight. Ensure access to proper chemical spill containment and follow local chemical storage regulations. Clearly label all containers and restrict access to authorized personnel only.
    Application of 6-(Trifluoromethyl)Nicotinonitrile

    Applications of 6-(Trifluoromethyl)Nicotinonitrile in Industrial Manufacturing

    As a direct manufacturer of 6-(Trifluoromethyl)Nicotinonitrile, we work closely with downstream industries to supply this compound for advanced synthesis workflows. Its unique trifluoromethyl and nitrile functionalities drive targeted performance in pharmaceutical development, agrochemical intermediates, specialty dyes, and electronic material processing. Below we outline the key application routes adopted by leading industry participants, including integration levels, compliance standards, recommended process ratios, and representative finished products.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Innovator and generic pharma manufacturers utilize this compound as a building block in custom synthetic routes to novel APIs, particularly for fluoroquinolone and pyridine derivative pipelines. The molecule enters late-intermediate steps that require reliable purity, with batch documentation matching regulated sector oversight. Process chemists adjust input volumes to balance cost, impurity profile, and subsequent functionalization efficiency in GMP conditions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA cGMP (21 CFR Parts 210/211)
    • European Pharmacopoeia (Ph. Eur.), where relevant
    • USP–NF for intermediates destined for US market drugs

    Typical usage ratio

    • 10–28% w/w as a key intermediate, adjusting based on target molecule structure and yield optimization in multi-step pharmaceutical synthesis workflows

    Downstream process integration

    • Introduced post-nitration or halogen exchange steps, following initial aromatic ring construction, and prior to asymmetric hydrogenation, cyclization, or amination stages in small-molecule drug manufacturing

    Final product types

    • Quinolone-class antibacterial APIs
    • Nicotinonitrile-based antiviral lead compounds
    • Pyridine-derived kinase inhibitors
    • Other fluorinated pharmaceutical intermediates

    2. Agrochemical Intermediate for Crop Protection Actives

    Agrochemical formulation firms rely on the chemical's electron-withdrawing pattern to construct active ingredients used in new-generation insecticides and herbicides. Precision in addition rate impacts isomeric purity crucial for field efficacy, while all bulk handling and blending steps adhere to occupational and environmental stewardship systems aligned with regional regulations.

    Industry compliance standards

    • FAO/WHO Technical Grade Specifications
    • EPA (US) Pesticide Registration Regulations 40 CFR Part 158
    • REACH (EU Regulation 1907/2006)
    • ISO 9001:2015 for quality management in agrochemical production

    Typical usage ratio

    • 7–18% by weight as a key intermediate during multi-step synthesis of trifluoromethylated crop protection agents; input adjusted to optimize downstream conversion rates depending on target molecule and impurity tolerance

    Downstream process integration

    • Added during intermediate stages of active ingredient synthesis, especially after aromatic ring formation, followed by condensation, cyclization, or chlorination as required by the crop protection formulation

    Final product types

    • Fluorinated insecticidal active ingredients
    • Nicotinonitrile-based herbicidal compounds
    • Seed treatment agents featuring trifluoromethyl pyridine cores
    • Intermediates for regulated crop safety chemicals

    3. Dye and Pigment Precursor Manufacture

    Producers of specialty dyes for textiles and technical applications use this compound’s structure to enhance colorfastness, photostability, and solvent resistance in custom pigment synthesis. High-purity input allows consistent chromophore function, integrating at key aromatic modification points and requiring compliance with global contamination and toxicity limits in colorant production.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile safety
    • REACH (Annex XVII) for restricted substances in dyestuffs
    • ISO 9001:2015 for pigment and dye production QC
    • EN 71-3 (Safety of Toys – migration of hazardous elements) for pigment use in children’s products

    Typical usage ratio

    • 2–12% by weight based on target dye structure and intensity requirements, with adjustments for solubility and batch color precision

    Downstream process integration

    • Incorporated following initial condensation or alkylation, prior to sulfonation or chelation in the colorant synthesis chain; precise addition enables targeted chromophore construction for specialty pigments

    Final product types

    • High-performance textile dyes
    • Fluorinated pigment dispersions for inks
    • UVA-resistant technical colorants
    • Specialty pigments for plastics, coatings, and electronics

    4. Electronics and Liquid Crystal Material Synthesis

    Producers of advanced materials for electronic display and optoelectronic devices incorporate this intermediate in liquid crystal and organic semiconductor synthesis. Selection focuses on its electron-withdrawing capacity and rigid aromatic backbone, which modify dielectric and optical properties in finished functional layers. Material stewardship includes tight QC and trace metal control per microelectronics industry requirements.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) for lead, mercury, cadmium, and hexavalent chromium content
    • IEC 62474 declarable substances for electrical/electronic products
    • IPC-1752A for electronics material content reporting
    • ISO 14001 for environmental management in electronic material manufacturing

    Typical usage ratio

    • 0.5–4% weight fraction, adjusted depending on the degree of fluorination and molecular alignment needed for final liquid crystal or organic transistor properties

    Downstream process integration

    • Added at high-purity synthesis stages for LC host compounds, following initial oligomer construction, before final cross-coupling or purification; critical for performance in microdisplay thin films and device substrates

    Final product types

    • Liquid crystal display (LCD) host materials
    • Organic electronic semiconductors
    • OLED active matrix components
    • Specialized display alignment films
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    Certification & Compliance
    More Introduction

    6-(Trifluoromethyl)Nicotinonitrile: Direct Insights from the Manufacturer

    Stepping Into Real Synthesis: The Backbone of Our Daily Lab Work

    6-(Trifluoromethyl)Nicotinonitrile belongs to the family of trifluoromethyl-substituted pyridines. In our experience, this particular compound, with its molecular structure anchored by the trifluoromethyl group at the 6-position and the nitrile functional group, brings a unique advantage for anyone working on pharmaceutical intermediates, agrochemical development, or active molecule synthesis. Our daily production batches run under tightly controlled parameters, not for show but for chemical reliability. The true measure comes to light only after you see the purity results and test the material inside your own synthetic sequence.

    About the Compound: What Sets It Apart in Our Portfolio

    You notice the difference between 6-(Trifluoromethyl)Nicotinonitrile and simply substituted nicotinonitriles at the bench, not only on paper. The presence of the trifluoromethyl group extends not only the electronic properties but also increases the lipophilicity of the molecule, which often translates to enhanced ability to cross biological barriers. Having this moiety on the aromatic ring changes the chemical behavior dramatically when attached to the pyridine core, particularly for entities seeking to design novel APIs or crop protection agents.

    We've learned that introducing a trifluoromethyl group changes the game in terms of reactivity and stability. This property isn't just theoretical; you'd see it after storing the compound, running high-performance liquid chromatography, or watching yields improve in your next reaction route. Compared with general nicotinonitriles, this molecule stands out with consistently low water content, sharp melting point, and robust stability under ambient storage conditions. It lets researchers and process chemists avoid repeated purification work that comes with more labile analogues.

    Specification Data: From Batch Production to Bottling

    Daily manufacturing doesn't run on generalizations. Our quality control focuses on batch-to-batch reproducibility. With 6-(Trifluoromethyl)Nicotinonitrile, each shipment undergoes routine tests for purity by HPLC (often exceeding 98%), GC-MS confirmation of mass, and NMR checks for isomeric integrity. Trace impurities, residual solvents, and color all undergo direct quantification. We rely on actual numbers rather than certificate templates. The consistency in crystalline habit—mostly as pale yellow or white solid—and absence of unusual odors confirm process control.

    Our team packages the compound in containers designed for low permeability and minimal headspace. This approach reduces any contact with moisture and airborne contaminants. We ship under inert atmosphere primarily for multi-kilogram orders, knowing that even a brief exposure can degrade lesser analogues but rarely disturbs the stability of this aromatic nitrile. Customers often remark on the compound’s fresh and unchanged state, even after weeks in transit.

    Applications: Insights from Years of Supplying Synthesis Labs

    Researchers rely on trifluoromethylated pyridines for developing bioactive molecules, often starting with our 6-(Trifluoromethyl)Nicotinonitrile as a core building block. In pharmaceutical settings, the compound brings a step forward for medicinal chemists probing new kinase inhibitors or modulation pathways, thanks to its role in structure-activity relationship studies. We’ve watched several projects pivot mid-synthesis to our product due to its higher reaction compatibility and the downstream security it provides for scale-up. Agrochemical innovation embraces the same advantages, with developers aiming for high-value crop protection agents that require firm aromatic stability and synthetic resilience.

    Process development teams repeatedly mention that their reason for shifting from standard pyridine nitriles to our product lies in reliable downstream transformation. Nucleophilic substitution proceeds with fewer side-reactions. Hydrogenation or cyclization steps demand less reprocessing after initial product isolation. By using 6-(Trifluoromethyl)Nicotinonitrile, teams often shorten project timelines due to batch cleanliness and the simplicity of post-reaction work-up.

    The Production Perspective: What True Manufacturing Control Looks Like

    Our plant runs this molecule through a series of proprietary steps, designed from first principles up to industrial scale. Sourcing the starting materials—even at scale—requires a disciplined approach to raw-material verification; we learned this lesson years ago during a period when market shortages caused visible purity fluctuations. Each lot gets sampled and verified with reference spectra backed by internally retained samples, not just against out-of-date standards.

    After reaction, we isolate and dry the intermediate under reduced pressure, still fighting the same real-world things every lab faces: dust, static charge, and moisture. Technicians monitor for trace oxygen, and production staff manage sodium drying agents, slab chromatography, and extra filtration for fractions destined for high-sensitivity applications. Each process step chases away potential for batch contamination, a discipline learned through years of lost material and repeated root-cause investigations.

    Warehouse staff finalize packaging not by rote, but by verifying each order per client specifications. Special packaging or cold-chain transport stands ready for extra-sensitive end-users. Shipping logs confirm environment and handoff, ensuring materials reach facilities as we prepared them.

    What Real Customers Tell Us

    Feedback comes straight when you manufacture chemicals long enough. Medicinal chemistry groups routinely compare the performance of our 6-(Trifluoromethyl)Nicotinonitrile against competitor sources. They usually point out fewer resinous impurities, no trace solvent, and a consistent crystal habit. One client described their earlier experience of “invisible yield loss” in a cyclization step, which vanished upon switching to our batches. Another synthetic lead told us that the compound’s ability to remain free-running even after repeated jar opening and closing saves them from time lost to screening and re-drying.

    Pilot plant chemists in process development value that the material resists caking and remains distinctly pourable, even after exposure to typical lab environments. They speak less about theoretical advantages and more about actual differences in pilot reactor cleaning or downstream chromatography—practical, day-to-day improvements.

    Working With Regulatory and Safety Needs

    Direct chemical handling carries safety requirements that come not from regulation alone, but practical experience. We scale production under fume extraction, observe dust minimization, and apply antistatic packaging for shipment. For research organizations producing kilogram quantities of new pharmaceuticals, knowing the exact composition and trace impurity profile of each order matters, not just for documentation, but to avoid setbacks in regulatory filings.

    Our in-house compliance team works with customers’ regulatory groups, sharing detailed batch histories, analytic chromatograms, and storage condition records. Open communication reduces surprises and adds a path of confidence that has real impact during audit season or quality management inspections. Anyone in chemistry knows that surprises can destroy project budgets and timelines.

    Market Trends: Why This Compound Holds Steady

    We have witnessed demand grow in step with rising focus on fluorinated scaffolds in medicinal chemistry and crop science. Industry journals and scientific publications regularly highlight how trifluoromethyl groups bring improved metabolic stability and broaden the chemical space available for screening. In practice, this means more research centers request this building block, not only for established applications but also for novel molecular libraries.

    In earlier years, many organizations viewed fluorinated analogues as niche, but that’s changed. Over the last five years, major pharmaceutical R&D pipelines and agrochemical start-ups both reach for this chemistry early in lead optimization. One catalyst is the tightening focus on green chemistry and selective synthetic methodologies; for example, direct couplings that take advantage of trifluoromethyl substitution follow less waste-generating routes compared with older functional groups.

    Stable and ready-to-use products reduce the real cost of research, and we see this reflected in orders increasingly requesting multi-kilogram lots straight to pilot plants and, sometimes, bulk supply agreements.

    What Sets Our 6-(Trifluoromethyl)Nicotinonitrile Apart From Standard Grades

    Chemists who work at the bench learn to spot differences between seemingly identical samples. Our batches deliver high purity, absence of colored by-products, and a consistent melting point—a sign of controlled crystallization. We reject sub-batch mixtures, segregate off-standard lots, and reserve select runs for toxicology or high-throughput screening.

    Compared to other pyridine nitrile derivatives, our product provides a combination of lipophilicity (from the trifluoromethyl group), sharp reactivity balance, and stability. The difference appears during late-stage functionalizations, especially for groups attaching to the aromatic ring or performing nucleophilic substitutions at remote positions. Chemists in medchem often report that these characteristics translate to fewer synthetic bottlenecks and more predictable process performance.

    We refrain from blending different production lots, believing that product traceability drives real confidence for downstream processing. Warehouse and QC teams connect order numbers to retained samples at every stage, making retrospective analysis possible if a customer’s process shows unexpected results. By doing so, we help researchers uncover factors behind unexpected impurities or yields, reducing both cost overruns and investigation delays.

    Supporting Customers, Solving Problems

    Real work in a chemical facility never unfolds as perfectly as the brochures suggest. We’ve seen batches of lab reagents from general suppliers occasionally fall short under heavy-synthesis conditions—unexpected clogging of filters, polymorphic shifts, even changes in solubility after storage. Our teams address such issues by providing direct access to our production chemists—something that only real manufacturers can offer. This support has, on several occasions, enabled customer R&D teams to bypass days of troubleshooting by shifting quickly to a new lot or pulling historical data from our archives.

    Chemists working on process scale-up sometimes discover obscure side-products not previously encountered at gram scale. We help by reviewing production records, and if a contaminant traces back to an earlier raw material run, we pivot our own process or offer replacement lots. This reliability keeps customers coming back, knowing each order comes with both product and practical experience.

    Environmental Practices and Responsibility

    Our manufacturing facility invests in solvent recovery and waste reclamation systems, minimizing emissions at both reaction and packaging stages. This isn’t just for compliance checks—it saves process costs and fosters safer working conditions indoors. Early investment in fluorine-handling protocols taught us the importance of robust venting, pressure controls, and closed-loop solvent recapture; smaller plants sometimes overlook these needs.

    By keeping process streams separate, managing spent catalyst discharge responsibly, and monitoring for air and water emissions, we anchor environmental performance at a measurable level. These controls let us promise more than a paper guarantee—we maintain real operational oversight, ready to respond to customer or regulatory inquiry at any shipment stage.

    Why Real-World Experience Matters

    Our leadership, many of whom once spent years as bench chemists and pilot plant supervisors, keep a hand in daily production review. Decisions about raw material selection, solvent choice, and process adjustments come straight from firsthand trials, not only management meetings. This lived experience shapes how we train staff, troubleshoot issues, and keep our focus on consistent quality.

    We view our relationship with downstream users as collaborative. Medicinal chemists, process development leads, and academic researchers interact with the people who actually make and test the compound. A quick phone call to our lab often resolves process uncertainty faster than an endless cycle of emails and secondary certifications.

    Moving Forward: Innovation and Adaptability

    Our R&D group methods evolve based on what customers ask and the real challenges coming out of new research fields. As synthetic techniques shift towards more environmentally conscious processes, we evaluate alternative routes, sustainable solvents, and catalysts for making 6-(Trifluoromethyl)Nicotinonitrile. Process trials focus on reduced reagent excess, cleaner waste streams, and safer handling at every step.

    Several years ago, a customer project required material meeting a unique impurity threshold, and we delivered by tweaking purification steps and scaling extra analytic work. Since then, this flexibility influences every batch review. Adapting to new regulatory frameworks, documentation needs, or analytical requirements forms part of our daily routine—driven not by external demands, but by a belief that reliable chemical supply springs from practical, hands-on problem-solving.

    Conclusion: Beyond Standard Supply

    For every kilogram of 6-(Trifluoromethyl)Nicotinonitrile produced in our plant, knowledge and commitment shape the outcome far more than standard procedure. The real differences emerge in client labs, when process steps run smoother, synthetic bottlenecks shrink, and researchers find time to push projects forward instead of chasing rework. Working directly with the manufacturer means access to expertise, historical data, and material made specifically for applied research and development. Our commitment stands for every batch, every shipment, every customer partnership.