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2,6-Dichloro-4-(Trifluoromethyl)Nicotinamide

    • Product Name 2,6-Dichloro-4-(Trifluoromethyl)Nicotinamide
    • Alias DTN
    • Einecs 253-348-7
    • 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
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    Specifications

    HS Code

    688161

    Chemicalname 2,6-Dichloro-4-(Trifluoromethyl)Nicotinamide
    Casnumber 82692-97-5
    Molecularformula C7H3Cl2F3N2O
    Molecularweight 259.02 g/mol
    Appearance White to off-white solid
    Meltingpoint 134-138°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Synonyms 2,6-Dichloro-4-(trifluoromethyl)nicotinamide; DCTFNA
    Smiles C1=CN=C(C(=C1Cl)C(F)(F)F)C(=O)NCl
    Inchi InChI=1S/C7H3Cl2F3N2O/c8-4-1-3(7(12,13)14)2-15-6(4)5(16)11/h1-2H,(H2,11,16)
    Storagetemperature 2-8°C

    As an accredited 2,6-Dichloro-4-(Trifluoromethyl)Nicotinamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, tamper-evident, screw-cap amber glass bottle labeled “2,6-Dichloro-4-(Trifluoromethyl)Nicotinamide, 25g,” with hazard warnings and CAS number.
    Shipping 2,6-Dichloro-4-(Trifluoromethyl)Nicotinamide is shipped in tightly sealed containers to prevent moisture ingress. It is transported as a chemical substance, with appropriate labeling according to international regulations. Packaging ensures protection against physical damage, and all relevant safety data sheets (SDS) accompany the shipment for regulatory compliance and safe handling.
    Storage Store 2,6-Dichloro-4-(trifluoromethyl)nicotinamide in a tightly closed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Recommended storage temperature is 2-8°C (refrigerated). Ensure that the container is clearly labeled, and avoid prolonged or repeated exposure. Follow all appropriate safety protocols when handling.
    Application of 2,6-Dichloro-4-(Trifluoromethyl)Nicotinamide

    Applications of 2,6-Dichloro-4-(Trifluoromethyl)Nicotinamide in Industrial Manufacturing

    As a producer specializing in the synthesis and bulk supply of 2,6-Dichloro-4-(Trifluoromethyl)Nicotinamide, we focus on core, established industrial applications validated by international regulatory standards and downstream manufacturing requirements. Below, we present verified use cases, detailing exact compliance frameworks, formulation references, process steps, and end product types as encountered by our direct partners and the broader sector.

    1. Crop Protection Intermediate for Pyridine-based Agrochemicals

    This compound remains a key building block in the synthesis of a select range of next-generation pyridine-derived herbicides and insecticides, prized for their broad-spectrum action and residue control. In industrial production, formulators integrate the material at the early stage of heterocyclic ring construction, ensuring high-purity intermediates for further derivatization under strictly monitored GMP-controlled processes. The agricultural sector’s move towards precise actives with established residue profiles necessitates rigorous compliance and documentation throughout synthesis and final formulation.

    Industry compliance standards

    • FAO/WHO Food and Agriculture Organization pesticide specifications;
    • EPA (United States Environmental Protection Agency) registration criteria;
    • China GB/T agricultural chemical regulations;
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals, ECHA) for European market entry;
    • ISO 9001:2015 quality management for agrochemical intermediates.

    Typical usage ratio

    • Formulators typically use 15–25% by molar ratio during the active ingredient precursor stage, adjusted for target molecule and yield optimization in batch and semi-continuous processes.

    Downstream process integration

    • Enters the multi-step synthesis as the halogenated pyridine scaffold, following chloro-dehydrohalogenation and amidation. Used directly prior to cyclization or further functional group modifications. Entire reaction sequence carried out in controlled environments to prevent cross-contamination and guarantee traceability.

    Final product types

    • Herbicides targeting grass and broadleaf weeds in cereal and vegetable cultivation;
    • Selective insecticides for integrated pest management (IPM);
    • Seed-treatment active concentrates;
    • Technical-grade agrochemical active ingredients (AIs) for formulation plants.

    2. Pharmaceutical Intermediate for Advanced Nicotinamide Derivatives

    Our material is used by major pharmaceutical CDMOs and API manufacturers to construct key intermediates for complex, fluorinated nicotinamide derivatives. These intermediates form core fragments in anti-inflammatory, anti-neoplastic, and CNS-targeting development pipelines. All production occurs in GMP-regulated cleanrooms, involving strict in-process monitoring and full traceability from raw material intake to final drug substance purification.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients;
    • USP-NF monograph standards (where applicable);
    • EU GMP Part II (active substance manufacture);
    • Comprehensive Certificate of Analysis compliant with DMF filings;
    • ISO 13485 and ISO 9001:2015 QA/QC frameworks.

    Typical usage ratio

    • In pharmaceutical synthesis, usage varies from 10–18% molar equivalent, depending on route selection and required fluorination degree in the downstream product. Adjustments depend on the efficiency of subsequent amide bond formation and purification loss projections.

    Downstream process integration

    • Introduced during the late-stage condensation or amidation in the heterocyclic assembly for fluorinated drug intermediates; often followed by catalytic hydrogenation or selective halide substitution, depending on final structure.

    Final product types

    • Nicotinamide-based oncology intermediates;
    • Lead compounds for CNS disorder APIs;
    • Clinical candidate fragments in anti-inflammatory therapeutic lines;
    • Custom fluorinated pyridine synthons for further contract research.

    3. Fine Chemical Synthesis for Specialty Electronic Materials

    Advanced electronics manufacturing, including specialty coatings and semiconductors, utilizes this compound as a functionalized halogenated pyridine source for constructing high-performance electronic transport layers. Stringent batch-to-batch consistency, trace metals control, and minimized fluorine loss are enforced throughout every stage of blending and reaction. The electronics field demands precise documentation of each precursor lot, including residual solvent and trace contaminant analysis.

    Industry compliance standards

    • RoHS (Restriction of Hazardous Substances Directive), for electronic-grade chemicals;
    • IPC-1752 and IPC-4101 standards for electronic materials;
    • ISO 9001:2015 with integrated SPC/QC for electronic chemical production;
    • QC benchmarks for trace-level elemental and halogen impurities (ICP-MS, GC-MS release).

    Typical usage ratio

    • Direct precursor integrations typically use 6–10% by weight, with the precise level benchmarked against desired dielectric constant and film thickness in downstream coating or semiconductor transport layer application.

    Downstream process integration

    • Fed into step-growth polymerization or condensation reactions as the critical halogenated segment provider; subsequent spin-coating, sputtering, or vapor-phase deposition applied for final component fabrication. Complete batch traceability and in-process impurity monitoring required.

    Final product types

    • Thin-film transistor (TFT) specialty resins;
    • Photolithography masks and imaging layers;
    • Advanced dielectric films;
    • Specialty organic semiconductors for OLED display modules.

    4. Active Ingredient Intermediate for Veterinary Drug Synthesis

    Veterinary pharmaceutical producers use this halogenated nicotinamide in the targeted synthesis of new-generation anti-parasitic and antimicrobial agents. Production lines employ validated reaction protocols ensuring traceability and batch compliance with pharmacopoeial standards, from intermediate building block formation to the purification of actives intended for companion and food-producing animals.

    Industry compliance standards

    • Veterinary International Cooperation on Harmonization (VICH) GL guidelines;
    • Pharmacopoeia of the People’s Republic of China (ChP), EP, and USP-Veterinary monographs as applicable;
    • GMP for Veterinary Medicinal Products (EU 2019/6 and related national statutes);
    • ISO 9001:2015 process control audits for veterinary intermediates.

    Typical usage ratio

    • Standard synthesis protocols use 8–16% by molar input, tailored to the exact target molecule. The ratio is typically calibrated to ensure full conversion and ease of purification for veterinary drug compliance.

    Downstream process integration

    • Serves as an input at the key amidation or heterocycle formation step in veterinary compound synthesis, followed by catalytic or enzymatic coupling in dedicated GMP zones. Full QA/QC monitoring before final API delivery or formulation.

    Final product types

    • Anti-parasitic veterinary drugs for livestock and aquaculture;
    • Active pharmaceutical intermediates for animal health products;
    • Pre-mix and final injectables for companion animals;
    • Intermediate blocks for veterinary diagnostic agents.

    5. Intermediate for Industrial Anti-Fouling Coatings

    This compound acts as a reactive intermediate in producing polymerized biocidal additives for industrial anti-fouling coatings, especially for marine, shipping, and submerged infrastructure. Regulatory requirements enforce strict limitations on leachate and active ingredient profile, necessitating process controls from blending through to resin curing and finished formulation.

    Industry compliance standards

    • BPR (Biocidal Products Regulation 528/2012/EU) for marine coatings;
    • US EPA registration for biocidal active substance;
    • IMO (International Maritime Organization) AFS Convention for anti-fouling paints;
    • ISO 12944-6 for high-durability industrial coatings production.

    Typical usage ratio

    • Polymer blend integration typically requires 4–9% by weight, adjusted by activity profiling and desired curing properties of the target formulation for specific marine application use cases.

    Downstream process integration

    • Enters reaction during biocidal moiety attachment to resin or copolymer base, combined under controlled agitation and monitored temperature cycles. Subsequent blending with other resins or pigment dispersions finalized before curing and packaging.

    Final product types

    • Marine anti-fouling paints for vessel hulls;
    • Industrial water-treatment coating systems;
    • Protective linings for submerged pipelines and offshore structures;
    • Coatings for desalination plant infrastructure.
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    Certification & Compliance
    More Introduction

    2,6-Dichloro-4-(Trifluoromethyl)Nicotinamide: Experience on the Production Line

    Work on the factory floor has a way of teaching any chemist the real language of molecules. 2,6-Dichloro-4-(Trifluoromethyl)Nicotinamide stands out in our year-round schedules, mostly because of how frequently it turns up on the production calendar and the specialized attention it commands. In our plant, batches of this compound move straight off the reactor with a pungency that hints at the linkage between its structure and performance. You notice it long before anyone starts quoting CAS numbers or pulling off certificates of analysis.

    What Sets This Compound Apart

    In the chemistry world—especially agrochemical and pharmaceutical synthesis—2,6-Dichloro-4-(Trifluoromethyl)Nicotinamide isn’t a household name. Yet for those of us responsible for making it, every shift reminds us just how critical each atom’s position is. The two chlorine atoms at positions 2 and 6, plus the trifluoromethyl group on the 4-position ring, change everything about its reactivity. Major customers talk about this molecule’s reliability as an intermediate when formulating newer crop protection chemistries or designing active pharmaceutical ingredients. That reliability doesn’t happen by chance; it grows out of consistent process control, attention to purity, and a refusal to settle for off-spec physical properties.

    In the past, we’ve trialed other substituted nicotinamides—sometimes single-chlorinated rings or those lacking fluorine modifications. They’ll often yield a product, but scaling up reveals weaknesses. Lower yields, unpredictable crystallization, solubility annoyances—all of those slow a production line down and eat margins alive. With this compound, reproducibility shows up through every inspection checkpoint: consistent melting point, color, particle size, no trace of unreacted starting material. People often overlook how much trouble a tiny amount of isomeric impurity can cause, possibly making an entire multi-ton batch worthless downstream. Our refining distillation setups are purpose-built and maintain those stringent requirements without compromise.

    Specifications We Sweat Over

    Production starts with raw materials that haven’t always been predictable. Procurement colleagues will tell you stories about unannounced changes from suppliers: a drum that sits longer in the sun, a shipment delayed at customs, purity levels swinging up and down. For our powder, only pharmaceutical grade solvents touch the product stream. Thin-layer chromatography spots are checked by hand—twice on release days. Modern analytical equipment, such as HPLC and NMR, finds its place after the eyes and instincts of those with decades of batch experience have signed off. Specifications become a living agreement, daily reaffirmed by the people running the machines.

    As for physical characteristics, we aim for off-white, fine powder material with no clumping or discoloration. Moisture levels stay below a tight threshold, since even a bit of residual water can trigger hydrolysis or spoil blending. Particle sizing runs through several precise screens post-synthesis, because the downstream synthetic steps—often in continuous reactors off-site—demand near-absolute uniformity. Simple things like how the powder falls from a scoop, or how it disperses into solvents, guide us more than any data sheet could.

    Common Uses and Transformations

    Unlike with some bulk chemicals, no two users treat 2,6-Dichloro-4-(Trifluoromethyl)Nicotinamide exactly the same. Some clients blend it directly into formulations for fungicides; others count on it as a coupling piece for more complex molecules with pyridine rings. Its halogenated structure helps lock in stability during downstream reactions where gentler intermediates would decompose or racemize. Every few months an R&D partner brings news of a new patent or an updated synthetic pathway using our compound, reminding us that even small tweaks in our crystallization step can ripple out into global product launches.

    On rare occasions, we’ve seen customers run into bottlenecks—not on our end, but because their own solvent handling systems weren’t tuned for a powder with this kind of volatility and density. We run pilot-scale collaboration batches in our own labs to help diagnose that. Sometimes it just comes down to offering samples processed with a different grind or water content. Little fixes like these matter much more than some idealized “generic” specification you’ll find in other catalogs. Those don’t take into account what a customer’s pump, reactor, or mixing vessel actually faces.

    Why Not Stick With Simpler Pyridine Derivatives?

    The market overflows with milder pyridine products: mono-chlorinated, simple amides, unsubstituted varieties. We’ve made those in the past and still do when needed, but you learn quickly that added complexity on the ring—specifically with two chlorines and a CF3—completely reshapes the reactivity and safety profile. Customers developing patent-protected molecules stress over specific electronic effects: less accessible protons, precise activation for nucleophilic substitution, better control in step-growth polymerizations. This trifluoromethyl-nicotinamide gives them options no other ring can rival, and we hear about that in field results and feedback sessions.

    In our own early development runs, we tried to shortcut the synthesis using cheaper or more available pyridine stocks, but never matched the yields or cleanliness. Even small process upsets—too much agitation, a temperature blip—would create side-products easily flagged downstream. It cost real money fixing off-grade batches and forced us to engineer extra purification steps. That’s why our current route, with careful halogen introduction and a late-stage amide coupling, has stuck. Most clients won’t see those choices directly, but they feel it in how smoothly our intermediate fits into their flow chemistry systems or batch processes.

    Production Realities: Making It Work, Every Run

    Talk with anyone on the line, and you’ll hear that regularity is king. Our methods keep headspace contamination low, which matters since these halogenated organics can foul gasket material if left unchecked. Workers inspect hands-on for flask residue after every crystallization and double check that our drying ovens don’t stray from the target temperature. On unusually humid days, the flexibility to adjust nitrogen sparging rates preserves product quality; we are always watching for the telltale sheen of surface moisture or odor changes. Ignoring these tiny operational cues causes trouble, both in the plant and for any customer running high-stakes projects on tight timelines.

    Large batch reactors introduce unpredictability—differences between jacket cooling efficiency, mixing rate, or simply the way suspended solids behave as the solution clarifies. Each crew learns fast that the devil is in the details: rinse protocol, time in hold tanks, membrane filtration steps. Relying solely on specifications offered by literature or technical data sheets quickly proves risky: unique plant layouts, different access to cooling towers, or slight differences in vacuum pumps all mean the same recipe can behave very differently across facilities. Over years of experience, we got to the point where each crew can compare notes and catch slight changes batch to batch. This tribal knowledge, more than any digitized control panel, keeps the line moving at high yield each season.

    Lessons from Scale-Up: Avoiding the Usual Pitfalls

    Scale-up doesn’t always play fair. Some reactions look beautifully crisp in the flask but don’t cooperate in a 1-ton reactor. With this chemical, we had to iron out quirks like exotherms that ramped up faster than our cooling systems could manage, or media that clumped and refused to disperse. Simple agitation tricks—changing impeller pitch, sequence of additions, timing on anti-foam dosing—proved critical. We tuned these through short-cycle repetition, watching each adjustment’s impact in real time and keeping careful records of every tweak. This empirical process taught us that for halogenated, fluorinated specialties, a one-size-fits-all approach never succeeds. Flexibility, vigilance, and keeping experienced operators involved make the difference.

    Consistency Across Lots: More than Just a Lot Number

    Quality teams track every gram of input, making sure traceability isn’t just a line item. Maintaining a consistent melting range and color profile batch after batch means re-calibrating sensors, validating cleaning protocols, and never assuming last month’s filter cake will behave the same this week. Customer feedback has flagged minor changes in powder flow or compaction as causes of headache on automated lines. That led us to invest in finer screens and more precise dry milling, saving clients untold downtime.

    Returning customers, especially those with highly regulated or high-value applications, appreciate this level of constancy. They don’t want to re-validate batches or troubleshoot variances. We invite their teams to visit and walk the line, showing them each control we’ve put in place to safeguard their investment downstream. Any deviation triggers detailed root cause analysis, not just a replacement shipment. This ongoing dialogue with customers keeps our standards high and opens channels for new process or product improvements nobody’s considered yet.

    Handling and Shipping: Reality Beyond the Factory Gate

    Shipping halogenated powders is an exercise in timing, method, and packaging. These materials demand airtight, water-impermeable containers with anti-static liners. Our crews monitor loading for trace leaks and atmospheric exposure. We warehouse only in controlled environments; open warehouses and uncontrolled climates undo weeks of careful work in a single night. Drivers sign off at dispatch, and the logistics teams frequently cross-check documentation against actual condition at each handoff. Stories abound in the industry of containers arriving clumped, compacted, or even partially hydrolyzed after being delayed at port or left in humid transit sheds. To guard against these, we trained every handler, from line supervisors to truck load crew, on spot-checking seals and protecting shipments from spill or moisture incursion.

    Regulatory compliance extends beyond shipping: not every country welcomes organohalogens or fluorinated compounds equally. We track all jurisdictional demands and update product labels and declarations accordingly. Failing to do so leads to returns, fines, or lost shelf life. Few customers see these steps but they directly benefit from a product that arrives on time, in spec, without regulatory headache or quality loss.

    How We’ve Helped Solve Real-World Challenges

    The real test of our compound’s value comes from scenarios that wouldn’t show up on any safety data sheet. We’ve supported clients facing yield drops on new fungicidal actives. After running parallel synthesis using off-brand intermediates, it turned out small but critical impurities in those substitutes caused performance losses in their downstream reactions. Switching over to our tightly monitored supply, outcomes improved and complaints about “mystery by-products” disappeared. Similar cases pop up in pilot pharmaceutical plants, where every impurity not flagged by standard chromatograms ends up complicating purification or triggering batch rejections. Sharing spectral data and, occasionally, even opening our lab so their analysts can review our runs in person, builds trust that standard catalogs just can’t replace.

    Years back, a partner firm encountered challenges in blending this compound with another nitrogenous intermediate that tended to agglomerate. Collaborating directly, our shop floor tested alternative grades, fineness levels, and tighter water content batches. Through cooperation—not just transactional selling—we kept their project timeline intact and generated new internal specs for both partners that shaped future campaigns.

    We have on occasion uncovered upstream contamination issues—ironically, usually invisible to the naked eye but disastrous for certain downstream catalysts. After catching a recurrent, almost undetectable particulate matter, we revamped our filtration and partnered with new raw material sources. Those extra steps cost more but save end users from lost production days, scrapped product, and failed validation runs. This sort of shared problem-solving defines long-term supplier relationships and creates opportunities for both sides to deepen technical knowhow.

    Continuous Improvement in the Production Loop

    Years of production and customer feedback shape every improvement. Periodic investment in better dust control, solvent recovery, and green chemistry initiatives reduces workplace risk and boosts staff retention. In turn, high morale and low turnover mean old shop-floor hands—who catch off-odors or spot unusual filter cake texture—are always nearby. We learn from every run and know the value of a workforce that takes ownership. Chemists, line operators, and logistics handlers offer input during regular reviews so incremental fixes don’t get overlooked. We record each minor process deviation, combining digital logs with handwritten shifts notes. Though the production and commercial landscape is always evolving, stability built over time creates a knowledge base that customers trust implicitly.

    What the Future Holds

    Long-term, our plant invests in flexibility: better reactor automation, more robust filtration, environmental controls that can handle climate extremes. Demand for advanced pyridine intermediates, especially those harnessing halogen and trifluoromethyl influences, keeps growing in response to regulatory shifts and new market requirements. Rapid prototyping, in-plant pilot runs, and tighter customer partnerships will drive the next phase. Every improvement in yield, every reduction in process loss, and each elimination of trace impurity adds up. Close collaboration with our clients, not just product delivery, defines our approach.

    This is the reality of making 2,6-Dichloro-4-(Trifluoromethyl)Nicotinamide—not just a molecule from a catalog, but a living example of the care, discussion, and shared expertise that goes into producing a specialty chemical that supports real-world advances in medicine, agriculture, and materials science. Those daily lessons, fixes, and collaborations keep us learning, adapting, and delivering on the high standards that customers rely on season after season.