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HS Code |
147794 |
| Cas Number | 214779-22-9 |
| Molecular Formula | C7H2ClF3N2O4 |
| Molecular Weight | 270.55 |
| Iupac Name | 1-chloro-2,4-dinitro-5-(trifluoromethyl)benzene |
| Appearance | Yellow crystalline powder |
| Melting Point | 67-72°C |
| Solubility | Slightly soluble in organic solvents |
| Smiles | C1=C(C=C(C(=C1Cl)[N+](=O)[O-])C(F)(F)F)[N+](=O)[O-] |
As an accredited 1,3-Dinitro-2-Chloro-5-Trifluoromethylbenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed 100g amber glass bottle, labeled "1,3-Dinitro-2-Chloro-5-Trifluoromethylbenzene," with hazard warnings and lot number for laboratory use. |
| Shipping | 1,3-Dinitro-2-Chloro-5-Trifluoromethylbenzene must be shipped in compliance with hazardous materials regulations. It requires packaging in tightly sealed, corrosion-resistant containers, with clear hazard labeling. Transport should be arranged via certified carriers, with documentation meeting local and international chemical shipping requirements, ensuring protection from heat, shock, and incompatible substances during transit. |
| Storage | **1,3-Dinitro-2-Chloro-5-Trifluoromethylbenzene** should be stored in a cool, dry, well-ventilated area, away from heat, sparks, and open flames. Keep the container tightly closed and clearly labeled. Store separately from incompatible substances such as strong reducing agents, bases, and combustible materials. Use secondary containment to prevent spills and ensure appropriate personal protective equipment (PPE) is available nearby. |
Applications of 1,3-Dinitro-2-Chloro-5-Trifluoromethylbenzene in Industrial Manufacturing1,3-Dinitro-2-Chloro-5-Trifluoromethylbenzene functions as a critical building block in multiple specialized chemical manufacturing sectors. As a direct producer, we support customers with material traceability, technical formulation advice, and continued regulatory updates throughout each downstream application. 1. Agrochemical Active Ingredient SynthesisThis compound serves as an essential intermediate in the multi-step synthesis of certain pre-emergent and post-emergent herbicide molecules, especially within triazine- and sulfonylurea-based crop protection frameworks. Advanced process control governs its reaction stage, influencing both regioselectivity and crop safety profiles in the resultant actives. Manufacturers employ this intermediate to ensure compliance with evolving residue and toxicity standards for modern plant protection products. Industry compliance standards
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2. Pharmaceutical Intermediate for API SynthesisThe compound operates as a pharmaceutically relevant precursor in the high-purity synthesis of active pharmaceutical ingredients (APIs) containing trifluoromethylated aromatic rings for anti-infective or anti-inflammatory agents. GMP-controlled facilities process this intermediate for further transformation, maximizing purity and minimizing genotoxic impurities for registration under stringent health authority requirements. Industry compliance standards
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3. Electronic Chemicals—Specialty Fluorinated Compound ManufacturingSemiconductor and display manufacturers use this compound in custom fluorinated aromatic monomer synthesis, feeding into the production of advanced liquid crystal and photoresist materials. Precision in stoichiometry and reaction condition control is critical to maintain electronic grade purity and low ion content, contributing to optimal device performance and reducing defect rates on high-value substrates. Industry compliance standards
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4. Industrial Dye and Pigment SynthesisThe material features as a key aromatic precursor in the synthesis of nitro- and chloro-substituted pigments for high-durability industrial coatings, plastic coloration, and inkjet printing systems. Chemical engineers employ the compound in strictly controlled steps to influence final pigment hue, solubility, lightfastness, and weathering characteristics, all under strict environmental safety monitoring of by-product streams. Industry compliance standards
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The journey of 1,3-Dinitro-2-Chloro-5-Trifluoromethylbenzene starts inside a facility shaped by decades of technical development. Every kilogram reflects the precise control over temperature, pressure, and purity that only comes from repeatedly refining each step of the reaction. The core process involves selective nitration and halogenation in vessels designed for strict exclusion of moisture and airborne contaminants. Quality standards guide every batch, whether destined for agrochemicals, pharmaceuticals, or specialty chemical applications. Our team knows that even subtle deviations in raw material quality or process timing can fall short of purity requirements set by leading formulators, so each lot sees rigorous instrumental analysis before packaging for shipment.
Material suppliers sometimes underestimate the headaches impurities create for formulators and end-users. Years of feedback from real-world usage make it clear: product purity and homogeneity deserve sharp focus. Our 1,3-Dinitro-2-Chloro-5-Trifluoromethylbenzene distinguishes itself with a melting point consistently within the narrowest published range. High-performance liquid chromatography verifies low levels of related isomers and any trace hydrolysis byproducts. The outcome is predictable, reliable performance for downstream reactions—especially during further substitution or reduction, where even trace contaminants might stall a catalyst. Chemical engineers on both sides exchange technical data, ensuring alignment between batch analytics and customer specifications. This level of partnership is only possible for a manufacturer that controls every step—from raw ingredient validation through to custom packaging formats.
Finished batches move into diverse chemical syntheses, especially where nitroaromatic building blocks drive product innovation or regulatory pressure demands recalibration of old formulas. Agricultural intermediate formulators often select this product for its ortho-chloro, para-nitro reactivity pattern, which allows selective transformations not feasible with simpler nitroaromatics. Pharma innovators prize this molecule as a key intermediate for libraries where electron-withdrawing groups determine molecular target affinity. In polymer chemistry, the trifluoromethyl group offers unique chemical and thermal stability, opening ways to create specialty coatings or high-durability films. These sectors push us to keep process impurities far below the levels tolerated in generic solvent-grade materials.
Anyone who manufactures fine chemicals long enough faces unforeseen hurdles. Over the years, we’ve found ambient humidity swings, overlooked trace metals, and even seemingly minor equipment surface finishes can bleed through to product consistency. Throughout product history, we’ve retooled reactors, upgraded in-line purification, and redrawn analytical protocols to resolve minor issues—long before customer labs ever discovered them. Spectral fingerprinting and advanced chromatography became standard after we learned how difficult it can be to remove positional isomers post-synthesis. This continuous feedback loop cuts waste, reduces downtime for our customers’ own processes, and means end-users receive the reliable quality essential for regulated applications.
Quality should prove itself in laboratory results, not in marketing copy or flowery phrases. Our product achieves a typical assay of more than 99.5 percent by area normalization and less than 0.05 percent each of related positional isomers. Moisture content after final packaging reads under 0.1 percent, thanks to controlled environment packaging lines. Each drum or pail bears a lot-specific certificate of analysis, never generics or “typical data,” because we recognize that suppliers must stand behind each individual lot. Visual clarity, melting range, and detailed spectra are always archived, available to partners who want transparency in their own regulatory filings or technical dossiers.
On the manufacturing floor, we’ve seen how customers push this intermediate to its limits: use in high-pressure vessel alkylations, on-demand reductions, and coupling reactions where substituent orientation matters. Some intermediates attempt to swap in lower-cost nitro-chloroaromatics with weaker positional purity or higher water content, but these rarely deliver the conversion rates or downstream selectivity end-users require. Over time, repeat customers emerge not from advertisements, but from the word-of-mouth credibility earned on the basis of empirical results—batch after batch, cycle after cycle.
Decades of hands-on manufacturing shape every conversation our technical team has with partners. Questions might start with “how tolerant is the material to vigorous oxidation,” or “what happens if we push nucleophilic aromatic substitution at higher temperatures?” These aren’t theoretical puzzles; they reflect daily production reality for those who actually run reactors. Years of lab trials show that the para-trifluoromethyl motif pushes electron density, creating a slightly higher activation energy for nucleophilic attack at the ortho chlorinated site. That nuance only reveals itself to chemists actually running syntheses, not simply reading structures off a screen. Reactivity differences between this molecule and similar nitrobenzene analogues leave direct fingerprints in conversion data and impurity profiles from our partners’ pilot lines.
Strict environmental controls keep us accountable to both legislative frameworks and responsible stewardship. Modern fine chemical production always invites scrutiny on waste streams, air emissions, and packaging cycles. Anticipating regulatory shifts, our process employs closed-loop recovery for acidic and basic process fractions; solvent recovery units keep hazardous discharge volumes minimal. Customers value this not because it provides a talking point for audits, but because unnecessary regulatory triggers in supply chains introduce uncertainty. Limiting known contaminants and providing full batch traceability boost confidence for anyone subject to national or international chemical inventory registrations.
Chemists sometimes begin their search by comparing chlorinated dinitrobenzenes with or without fluoroalkyl substituents. Many discover that the trifluoromethyl group tethers unique performance—and price premium, for some. From direct feedback, the advantage isn’t just in downstream chemical reactivity, but in the resulting physicochemical handling: improved solubility in select organic media, sharper chromatographic profiles, and higher crystallinity for downstream fractionation. Removing the trifluoromethyl, or shifting chloro and nitro groups, often leads to melting point suppression and broader impurity bands after work-up. That translates into more challenging purifications, lost material, and longer process cycles. Our in-house test batches continually stress these differences, so we don’t rely on suppliers’ word or literature guesses. Side-by-side reactivity screens detail where our grade makes the critical difference between a stalled process and a high-yield outcome.
Transporting fine chemicals requires a grounded understanding of real-world logistics. Material may head overseas, face weeks of temperature fluctuation, or move directly into critical-path batch synthesis without days of staging. We’ve adopted moisture-sealable, chemical-resistant containers, sized for both research applications and pilot-plant scale-ups. Partners avoid supply chain delays because our lot tracking dovetails directly with their own batch records, making recalls or tracebacks fast, but more importantly, rare. Real-time notification systems trigger at every shipping milestone, based on decades spent finding places where delays and shortfalls creep into global logistics.
Manufacturing facilities that produce multi-nitrated, halogenated aromatics face one truth: complacency is the enemy of safety. Ventilation controls, continuous spill monitoring, and regular staff retraining grew directly out of field lessons—not just regulations on paper. Nitration remains an exothermic, potentially runaway reaction; only teams who log thousands of safe cycles develop that kind of technical intuition. Custodianship stretches beyond our walls; we share updated safety data periodically with our partners, reflecting shifts in handling protocols or new analytical insights. End-users know our production teams tackle real hazards head-on, never relying on generic checklists or periodic audits alone.
Questions never stop once material leaves the plant. Industrial chemists ring up asking about “unexpected crystalline forms,” or tweaks needed for in-line blending. We connect their teams directly with our senior chemists, not just sales reps. Having grown up within the laboratory and production environment, these technical minds already faced most issues at a bench or reactor scale: solubility failures, exotherm management, even color shifts during scale-up. This real-world experience brings practical advice, honed through collaboration rather than textbook responses. Problem-solving together creates lasting relationships, and batch-specific know-how beats generalized guidance every time.
Manufacturing this advanced aromatic intermediate delivers fresh lessons with each cycle. Observing even minor shifts during production—like a slight uptick in crystallization time or a color tone departure—can signal upstream changes in material or process chemistry. Teams quickly swap notes, analyze data, and document these learnings. Downstream partners spot increased reproducibility, fewer intermediate side reactions, and better assay closure in final targets. These details form the heart of continuous improvement, not idle compliance. Manufacturing fine chemicals asks for deep respect for empirical data over process folklore, and real manufacturers never stop learning from their own product’s behavior, both in-house and in the field.
Change comes fast in regulated and high-performance chemical sectors. Our R&D team develops process tweaks aimed at minimizing waste and streamlining time-to-market for custom derivatives. Direct customer conversations push this product’s evolution, sometimes leading to novel crystalline forms, cleaner impurity profiles, or new packaging tailored to on-site automation systems. The commitment to real technical collaboration drives product upgrades that deliver tangible benefits, not just incremental tweaks for catalog variety. Product refinement often unfolds on the shop floor, supported by chemists who listen as much as they innovate. We prioritize investments where they matter—in specialized purification lines, tighter analytical cutoff protocols, and staff technical training—so customer feedback never gathers dust on a shelf.
No process runs flawlessly forever; supply risk grows when intermediate sources dry up or competition for precursors stiffens. Lessons from past supply disruptions taught us to diversify our upstream networks and validate critical raw material sources on a rolling basis. We warehouse backup reagents and train staff to adapt processes across different input grades, so customers’ orders keep moving even when global logistics falter. These safeguards minimize gaps that might jeopardize a partner’s clinical trial window or regulatory timeline, because being a true material partner means thinking far ahead of the next order cycle.
Handling, packaging, and shipping a compound like 1,3-Dinitro-2-Chloro-5-Trifluoromethylbenzene creates a deeper awareness that goes beyond chemical structures or bullet-pointed attributes. Fixed daily process checks, rapid analytical feedback, and honest sharing of field data create a product both laboratories and production plants trust. Colleagues across the world rely on timely deliveries and accurate certificates. The working relationships built from this hands-on approach let us adjust in real time—whether for a surge in demand, a technical challenge, or a new compliance mandate. Staying close to the product from reactor to shipping dock keeps us grounded in the needs of those who transform this intermediate into tomorrow’s innovations.