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HS Code |
417796 |
| Chemical Name | 2,6-Dichloro-4-(Trifluoromethyl)Benzamide |
| Molecular Formula | C8H4Cl2F3NO |
| Molecular Weight | 260.03 g/mol |
| Cas Number | 86404-63-9 |
| Appearance | White to off-white crystalline solid |
| Melting Point | 134-137°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Synonyms | Benzamide, 2,6-dichloro-4-(trifluoromethyl)- |
| Storage Conditions | Store in a cool, dry, well-ventilated area |
| Smiles | C1=CC(=C(C=C1C(=O)N)Cl)C(F)(F)F |
| Inchikey | KOZDZPICLYZZRX-UHFFFAOYSA-N |
As an accredited 2,6-Dichloro-4-(Trifluoromethyl)Benzamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, sealed HDPE bottle containing 25 grams of 2,6-Dichloro-4-(trifluoromethyl)benzamide, labeled with hazard warnings and product details. |
| Shipping | This product is shipped in tightly sealed containers to prevent moisture and contamination. Appropriate labeling ensures compliance with regulatory standards for hazardous materials. Packaging includes cushioning to avoid breakage, and the item is transported in temperature-stable, secure conditions, following all relevant chemical transport guidelines for safety and environmental protection. |
| Storage | Store 2,6-Dichloro-4-(trifluoromethyl)benzamide in a tightly sealed container, in a cool, dry, well-ventilated area away from direct sunlight. Keep away from moisture, acids, bases, and incompatible substances. Use only in a chemical fume hood, and avoid exposure to heat and ignition sources. Properly label the container and ensure access is restricted to trained personnel. |
Applications of 2,6-Dichloro-4-(Trifluoromethyl)Benzamide in Industrial Manufacturing2,6-Dichloro-4-(Trifluoromethyl)Benzamide serves as a critical intermediate across select chemical manufacturing chains, supporting high-value synthesis in specialty chemicals, crop protection, pharmaceuticals, polymer modification, electronics chemistry, and dye production. The material’s physical and chemical stability allows integration into demanding process environments with strict quality oversight. 1. Agrochemical Synthesis: Herbicide IntermediateLeading agrochemical formulators specify this compound for advanced herbicide synthesis, especially where strong electron-withdrawing substituents support the targeted activity profiles. Manufacturers introduce this intermediate during condensation steps for amide-linkage herbicide scaffolds, improving downstream yield and molecule selectivity. Plant operators manage temperature-sensitive batch reactions under closed-loop control, ensuring raw material quality aligns with active ingredient registration dossiers. Industry compliance standards
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2. Pharmaceutical API Intermediate: Anilide DerivativesThis benzamide derivative enters pharmaceutical pipelines as an amide coupling reactant for preparing select anilide-based active pharmaceutical ingredients. Process chemists value its stability during multistep synthesis and its capacity to facilitate regioselective modifications. The material integrates before final API crystallization steps. Systematic in-process controls and material lot validation support cGMP compliance throughout the API chain. Industry compliance standards
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3. Specialty Polymer Modification: Fluorinated Functional AdditivePolymer manufacturers utilize this material to introduce halogenated benzamide structures into specialty copolymers. It allows resin formulators to adjust surface energy, chemical resistance, and wetting properties in engineering plastics. The compound is metered into extrusion or solution polymerization reactors, following precise dosing protocols to prevent unreacted residue. Downstream technical teams perform QC on the resin batch to confirm modified copolymer attributes for high-performance industrial applications. Industry compliance standards
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4. Electronic Chemicals: Photoresist IngredientManufacturers in the electronics sector employ this compound as a functional group modifier in advanced photoresist formulations. It modifies the solubility profile and etch selectivity of negative-tone resist chemistries. QC teams handle material within cleanroom environments, maintaining strict contamination control and traceability. This step takes place prior to resist blending, with subsequent lithography tests confirming the impact on fine-line patterning and feature resolution. Industry compliance standards
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5. Dyes and Pigments: Intermediate for Halogenated ColorantsProducers of specialty dyes and technical pigments incorporate this compound to develop halogenated benzamide-based colorants with increased fastness and solvent resistance. The intermediate reacts during the azo or acridine dye synthesis cycle, typically in tandem with coupling or diazotization agents. Coloristics teams specify reactant proportions by target color strength and application substrate, and regularly confirm residue clearance via spectroscopic QC analysis. Industry compliance standards
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Our journey manufacturing 2,6-Dichloro-4-(Trifluoromethyl)Benzamide did not begin in response to fleeting demand. We have worked with this compound through decades of industry change, adapting production methods to continue meeting rigorous needs in agrochemical, pharmaceutical, and specialty chemical segments. This material, recognized under the model DCTB-99, stems from chloro- and trifluoromethyl-substituted benzamides that consistently support demanding research and commercial projects.
Producing DCTB-99 relies on thorough knowledge of halogenated aromatic chemistry. Every synthesis batch follows carefully mapped-out reaction steps, examining both intermediates and finished product by HPLC and NMR. We favor tried-and-true conditions for ensuring the ring substitutions land in the 2,6-dichloro and 4-trifluoromethyl positions. Our purification approach relies on recrystallization, extraction, and polishing steps that avoid crossover contamination from other benzamide lines. This lets our clients focus on their R&D or production work instead of troubleshooting variability in incoming raw materials.
DCTB-99 often appears as an off-white to faintly yellow crystalline solid. We regularly measure purity beyond 99%, not just by HPLC but with orthogonal approaches for certainty. Trace moisture and residual solvents sit far below relevant thresholds. Our packaging lines charge product in airtight, light-resistant containers, minimizing degradation from air, moisture, or ambient light during transit and storage.
The melting point typically holds tight to our measured 146–151°C range. Particle size sits in a reliable distribution, tailored for both research and pilot scale dissolution or suspension needs. Handling safety is maximized by our attention to dust minimization and by supplying information from direct experience with batch-scale and pilot-scale operations.
2,6-Dichloro-4-(Trifluoromethyl)Benzamide sits at a crucial crossroad for groups investigating potential herbicide scaffolds, new crop protection chemistry, and emerging pharmaceutical intermediates. Many synthetic routes for advanced molecules require aromatic amides with both halogen and fluorine substitutions to introduce the right reactivity, solubility, or metabolic stability. DCTB-99 supports Suzuki and Buchwald-Hartwig couplings, classical amidations, and other transformations where selectivity and reliability at each functional group mean project timelines hold steady.
Pharmaceutical teams reach out when exploring amide modifications for enhanced potency or altered pharmacokinetics. Agrochemical innovators test our batches for their pre-emergent herbicidal properties or as scaffolds for new chemical analogs. Our material helps address real-world synthetic bottlenecks, letting teams maximize their own throughput without backtracking due to inconsistent intermediates.
Not all substituted benzamides deliver the unique balance found in DCTB-99. Structural modifications, such as positioning a trifluoromethyl group at the para site and placing chlorines at both ortho positions, change physicochemical behavior compared to mono-chloro or non-fluorinated variants. This layout impacts solubility in polar and non-polar solvents as well as reactivity toward various nucleophiles and electrophiles.
Our direct manufacturing experience reveals that similar analogs frequently fall short in stability under basic or acidic conditions. Purity often drifts over time without strict control on moisture, especially for multi-gram to kilogram users relying on months of storage. Those who have tried cheaper variants or resold material routinely report clogging in reactors, persistent color impurities, or off-target reactions in downstream chemistry batches. DCTB-99 from our facility minimizes these risks, year after year.
Clients do not wait long for material availability, as we schedule batch production in anticipation of both established demand and cyclical project upticks—such as springtime agrochemical research or quarterly pharmaceutical synthesis campaigns. We document every lot, tracking not only analytical results but also observed handling notes from packaging through shipment. If a new project needs a small trial batch with a tighter particle size distribution, we accommodate that experience-based request, and we later scale up to full campaign volumes with unchanged physical and chemical profiles.
Seasoned chemists in our plant learned early that finer details—static buildup during drum filling, clumping during humid days, slight color shift under halogen lighting—impact customer outcomes. By sharing these insights directly, we minimize wasted labor and unplanned interruptions for chemists and engineers downstream.
Quality routines at our site evolve from routine lab work and pilot batch learnings. Instead of checking boxes for routine parameters, we look for subtle shifts in FTIR and NMR signals and act on them promptly. If trace byproducts show up with certain raw material lots, we switch suppliers, adjust our distillation, and retest before declaring readiness for shipment. Our hands-on approach, built on years of practice, outpaces generic pass/fail data.
We archive full analytical datasets for every production run, documenting how batches behave under varying humidity and temperature for clients with global shipping environments. Return rates for DCTB-99 remain near zero after implementing extra QA steps that address field-specific concerns like container compatibility and thermal shock risk. Each request for batch documentation or usage advice gets routed to chemists with actual synthesis and scale-up experience, rather than to customer service intermediaries unfamiliar with the realities of handling benzamides.
Researchers contact us not just for a source of 2,6-Dichloro-4-(Trifluoromethyl)Benzamide but to solve bottlenecks in synthesis and product deployment. Over the years, we have fielded hundreds of inquiries ranging from solvent compatibility issues to downstream byproduct formation questions. We have modified particle size, sped up project turnaround during time-sensitive campaigns, and shared methods for minimizing loss during process transfer. This kind of peer-to-peer technical sharing builds deeper trust and long-term partnerships.
Production teams managing kilogram to multi-tonne projects gain confidence from our willingness to advise on storage, transfer, and reaction charging based on what worked and what did not in our own operations. Even details like labeling or customized lot traceability arise from recurring customer requests and our field experience navigating regulatory or audit tasks.
Waste-handling in halogenated benzamide manufacture presents direct challenges. From the earliest days, we have designed processes with solvent recycling and high-yield conversion rates at the forefront. Solvent use is tracked in detail, vigorously recovering and purifying for repeated cycles. Embedded energy in heating, cooling, and distillation does not go unchecked, and our initiative to recover and reuse spent mother liquors has minimized halogenated waste sent to incineration.
Operators work continuously to reduce the need for hazardous solvents and to improve washing and filtration. Early experience taught us that unchecked venting or spills risked both safety and compliance. We closely monitor air, water, and solid waste streams, applying in-line testing and direct operator oversight rather than trusting only automated systems. Compliance with prevailing environmental and safety regulations is a priority, but we also pursue practices that support sustainability and offer predictability for users needing documentation or eco-impact data.
Handling DCTB-99 requires vigilance, not only in controlling dust and exposure but in ensuring consistent reactivity during complex syntheses. Our team has learned the hard way that moisture sensitivity and contact with incompatible solvents can degrade both product and process consistency. Each time an unforeseen challenge arose—say, clumping after a cross-continental shipment or a yellow discoloration after a new filtration upgrade—we tracked causes, adjusted process or packaging, and built those lessons into future manufacturing runs.
Clients often underestimate the cost of low-quality intermediates, leading to batch rejection, yield losses, or time-consuming troubleshooting. By discussing these concrete examples and demonstrating the steps we take to avoid them, we empower users to better predict and manage their own process outcomes. This direct communication sets the stage for solutions instead of recurring problems.
Effective support for users of specialized benzamides relies on more than just certificates of analysis or response times. Over years of direct feedback, we have gathered a network of technical liaisons with laboratory and pilot plant backgrounds who listen to the deeper concerns of R&D teams. Whether a client faces regulatory audit, needs a specialized lot history, or simply wants a consistent high-purity source for scaling up, we speak from the vantage point of those who have faced similar hurdles.
Instead of relying on sales scripts or marketing language, our team translates real operational history into relevant advice. Customers benefit from lessons hard-won through hundreds of process iterations and from a manufacturing backbone where every improvement comes directly from plant operations and product handling.
Production of 2,6-Dichloro-4-(Trifluoromethyl)Benzamide continues to evolve with technological advances and growing field demands. As the landscape for synthetic chemistry tools widens, we track new coupling protocols, alternative green solvents, and application-specific quality demands for pharma and agro applications. Our in-house R&D experiments focus on increasing conversion rates, lowering impurity levels, and extending shelf stability without resorting to unnecessary stabilizers.
Across each stage—from raw material selection to shipment—field notes, customer feedback, and real-time batch analysis guide our investment in process upgrades. We also maintain open lines with academic and industrial collaborators to vet emerging approaches that might further reduce costs or increase throughput. This commitment to honest improvement underpins years of reliable supply and customer trust.
Working with substituted aromatic benzamides—especially 2,6-Dichloro-4-(Trifluoromethyl)Benzamide—means adapting fast thinking and long-earned process knowledge. Real advancements in this space rarely arise from textbook chemistry alone. They stem from teams willing to invest years addressing operational chokepoints, anticipating seasonal demand shifts, and learning from every customer objective, success, and misstep.
For groups looking beyond generic, commodity intermediates, a consistent supply chain for DCTB-99 makes advanced syntheses feasible at scale. Our continued focus on open communication, technical guidance, and transparent documentation ensures long-term value and project stability for innovators everywhere.