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HS Code |
811984 |
| Chemical Name | 5-Chloro-2-Fluoronitrobenzene |
| Molecular Formula | C6H3ClFNO2 |
| Cas Number | 446-34-4 |
| Appearance | Pale yellow to light brown solid |
| Boiling Point | 244-246°C |
| Melting Point | 38-41°C |
| Density | 1.544 g/cm3 |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Synonyms | 1-Chloro-4-fluoro-3-nitrobenzene |
| Refractive Index | 1.556 (predicted) |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Smiles | C1=CC(=C(C=C1Cl)[N+](=O)[O-])F |
| Inchi | InChI=1S/C6H3ClFNO2/c7-4-1-2-5(8)6(3-4)9(10)11 |
As an accredited 5-Chloro-2-Fluoronitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 5-Chloro-2-Fluoronitrobenzene, sealed with a chemical-resistant cap and labeled with hazard warnings. |
| Shipping | 5-Chloro-2-Fluoronitrobenzene is shipped in tightly sealed containers, compliant with hazardous material regulations. It must be labeled as a toxic and irritant substance, with transport adhering to UN and DOT guidelines. Avoid exposure to heat, sunlight, and incompatible substances. Proper documentation and handling procedures are required to ensure safety during transit. |
| Storage | 5-Chloro-2-Fluoronitrobenzene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong reducing agents and bases. It should be kept away from direct sunlight and heat. Properly label the container and avoid exposure to moisture. Store in accordance with local, state, and federal regulations. |
Applications of 5-Chloro-2-Fluoronitrobenzene in Industrial Manufacturing5-Chloro-2-Fluoronitrobenzene plays a critical role as an intermediate in several advanced chemical sectors. Our production delivers consistent quality for customers in pharmaceuticals, agrochemicals, pigment synthesis, polymer additives, and advanced material intermediates. We outline key industrial application scenarios and precise integration details below. 1. Pharmaceutical Intermediate SynthesisThis compound serves as a key starting material in the synthesis of certain active pharmaceutical ingredient (API) scaffolds, especially in the production of heterocyclic functional groups for targeted therapies. Our facility provides custom-tailored specifications compatible with multi-step organic synthesis, enabling direct halogen exchange and nucleophilic aromatic substitution in common pharmaceutical routes. Customers commonly employ this intermediate for developing fluoro- and chloro-substituted aniline or benzoxazole derivatives, which are essential in modern small-molecule drug portfolios. Industry compliance standards
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2. Agrochemical Synthesis (Herbicide and Fungicide Intermediates)The molecule is widely used by agrochemical manufacturers for synthesizing halogenated benzenes bearing nitro or amine groups, particularly in production of pre- and post-emergence herbicide intermediates. Its structure provides selective reactivity for condensation or reduction steps used to prepare anilines or heterocyclic moiety-containing pesticides. Our plant ensures high-purity lots, avoiding batch cross-contamination and residual solvents, which can impact downstream catalyst lifetimes and field product quality. Industry compliance standards
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3. Colorant and Pigment Intermediate ManufacturingDownstream pigment and colorant manufacturers use this compound to produce high-stability azo and disperse dyes. The chemical’s dual halogen and nitro functionality support diazo coupling, and subsequent reduction steps facilitate coupling to phenols and amines, resulting in intensely colored pigment bases. Material undergoes strict purification at our site, ensuring minimal metal ion contamination—a critical factor for textile and plastics pigment reliability. Industry compliance standards
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4. Polymer Additive and Material Modification AgentChemical producers integrate this intermediate to prepare halogenated or nitroaromatic monomers, which get grafted onto polymer chains to improve flame retardancy, chemical resistance, or UV stability for specialty plastics and elastomers. Controlled reactivity prevents degradation during extrusion or copolymerization, supporting requirements in electronic component encapsulation and high-end composite materials. We maintain product batch trackability for stringent QC documentation. Industry compliance standards
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5. Advanced Material and Battery Electrolyte PrecursorProducers of specialty chemicals for high-performance batteries and electronic materials use this intermediate in the preparation of functionalized aromatic compounds for electrolyte salts or electrode surface treatments. The molecular structure allows for fine electronic tuning in lithium-ion and solid-state battery component design. Strict moisture and trace metal controls during packaging at our facility help maintain electrolyte formulation stability demanded by battery manufacturers. Industry compliance standards
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Competitive 5-Chloro-2-Fluoronitrobenzene prices that fit your budget—flexible terms and customized quotes for every order.
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Every batch of 5-Chloro-2-Fluoronitrobenzene we produce reflects the experience and precision of years on the chemical manufacturing floor. This compound, known among chemists as a key halogenated nitrobenzene derivative, carries a consistent demand in both pharmaceutical and agrochemical development pipelines. From upstream synthesis all the way to quality control, we've learned that nothing replaces tried-and-tested process control—especially for a nitrobenzene with such a delicate fluorine and chlorine arrangement.
Our manufacturing line has handled substituted nitrobenzenes since the early 2000s. Over time, we’ve refined the reaction process for higher selectivity, purity, and scalability. Every improvement starts on the floor—hearing a distillation operator share a minor adjustment or re-checking the crystallization temperature with a few early test runs. This real-world feedback has shaped our in-line sampling frequencies and monitoring routines. You only know a chemical’s true quirks after running it at scale for years, day in, day out.
The needs of customers using 5-Chloro-2-Fluoronitrobenzene often differ from those of end-users of general-purpose nitrobenzenes or chloro-fluoro derivatives. Many are developing new pharmaceuticals, crop protection actives, or dyes. They depend on reliable, repeatable quality, which only comes from consistency across every production batch. Each lot is sampled not just at completion, but at strategic points throughout synthesis and purification.
We check purity using both gas chromatography and HPLC, targeting results well above 98% for the main component—purity that allows for smooth downstream chemistry. Even minor impurities like isomeric contaminants or hydrolyzed by-products can affect subsequent steps. We long ago adopted extra analytical checkpoints. These mean a slightly longer shift some days, but we see the payoff in long-term trust and fewer surprise calls from labs dealing with unexpected offcuts.
As a manufacturer, our understanding of specifications doesn’t come from handbooks—it’s drawn from hands-on experience handling hundreds of runs over the years. Moisture, for instance, represents more than a figure on a data sheet. Controlling water content in 5-Chloro-2-Fluoronitrobenzene pushes our team to monitor drying temperatures and vacuum parameters closely. Certain downstream processes—like nucleophilic substitutions leading toward complex heterocycles—prove extremely sensitive to traces of water.
Particle size distribution and melting point matter to us because they’re direct indicators of crystallization conditions and compound stability. If we see an outlier value, we track back to each crystalization step, sometimes as granular as reviewing the agitator speed late in the process. Our standard lots typically show a clear, yellow crystalline powder with a melting range that matches reference values, and deviations are investigated on the same day.
Odor has its own story—unlike many halogen-substituted aromatics, 5-Chloro-2-Fluoronitrobenzene gives off a distinct, pungent aroma during handling. We outfit our operators accordingly, but we’ve found that even subtle changes in odor sometimes indicate an unwanted impurity or incomplete washing. This sort of insight only comes from spending real time on the line, handling the substance shift after shift.
Most of the 5-Chloro-2-Fluoronitrobenzene we provide enters multi-step syntheses as an intermediate. Its unique dual substitution (chlorine at the 5-position, fluorine at the 2-position) gives rise to distinctive reactivity. We’ve watched the molecule serve as the backbone for active pharmaceutical ingredient (API) routes where precise halogen management prevents undesired side reactions.
Many research groups favor this nitrobenzene because both the nitro and halogen groups remain available for further transformations—nucleophilic aromatic substitution, reduction, or even palladium-catalyzed coupling. In pesticide research, it’s commonly chosen to introduce electron-withdrawing attributes to aromatic rings, often resulting in active ingredients that can handle environmental degradation better than their non-fluorinated peers.
Working directly as the producer, we regularly adjust delivery forms based on customer feedback. While powder dominates for most R&D benches, some scale-up groups want the product pre-dissolved in select solvents. As a team that manages every step from raw material sourcing to final packaging, we adapt to these requests, provided stability and quality stay uncompromised.
It’s easy to lump 5-Chloro-2-Fluoronitrobenzene with other halonitrobenzenes, but years of manufacturing both commonplace and specialty aromatics reveal subtle, crucial differences. Unlike 4-chloro-2-fluoronitrobenzene, the 5-position substitution provides slightly different electronic effects. Chemists often tell us that small changes in substitution pattern can mean markedly different reactivity, yield, and by-product profiles in later synthesis stages.
We’ve also run batches of 2-chloro-5-fluoronitrobenzene and 3-chloro-4-fluoronitrobenzene for custom projects, and the differences in process complexity stand out. The 5-chloro substitution, for example, allows for cleaner nitration profiles and easier separation at purification. For customers working on patent-protected actives, this specificity can make—or break—a new molecular entity.
Comparing with standard nitrobenzene or mono-substituted chloronitrobenzenes, the added fluorine not only introduces unique reactivity but also complications in waste handling and environmental monitoring. Our own operations carried out upgrades to exhaust scrubbing and effluent treatment after seeing the trends in regulatory oversight, particularly on organofluorine emissions.
Every large-scale manufacturer finds its own rhythm. We’ve built ours around openness with users about what makes each batch tick. Instead of focusing on abstract numbers, we welcome audits and plant visits. Over the years, we’ve walked many chemists and purchasing teams through our process flow—right from raw materials, through reaction, to final packing and documentation. They see firsthand how process tweaks show up in product performance down the line.
We mark every drum and carton with a batch number, linking directly to all test results, logs, and operator notes. This helps users connect the dots if any surprises crop up in their own synthesis or formulation work. Transparency makes for fewer headaches, and we’ve found most users appreciate being shown the reality, rather than just being handed a product and a certificate.
Experience on the shop floor has taught us not to underestimate handling risks. 5-Chloro-2-Fluoronitrobenzene, with its nitro group and dual halogens, deserves respect in transport, storage, and processing. Extra containment and fume extraction have long been part of our operations. We audit our storage rooms regularly, keeping temperatures tight and minimizing exposure to open heat or incompatible chemicals.
Waste minimization has become more than a talking point. We’ve reduced mother liquor disposal by introducing more effective solvent recovery and refining our washing cycles. This benefits both the environment and the cost structure—factoring in tighter environmental regulations. We no longer view spent process solvents as a necessary evil; with advances in distillation and solvent exchange, most can be routed back into earlier process steps.
Safety isn’t just about compliance. Our crew handles nitroaromatics regularly. Before any new process step takes off, we run small-scale hazard assessments and real-world simulations. For this product, we’ve paid extra attention to static control and personal protective equipment, since dust from finely powdered halogenated aromatics poses real risks. Experience has hardened our stance on pre-emptive risk management, far more than any checklist requirement could.
Relying on single-source intermediates can feel risky in a business with so many moving parts. We’ve weathered tight times by keeping direct control of every manufacturing stage, from starting materials to outbound logistics. Whenever possible, our own team manages the movement and storage of finished product, favoring dedicated containers and clear chain of custody. This brings down the odds of mix-ups or quality dips.
Periodic shortages—often tied to upstream raw material markets or geopolitical disruptions—mean we keep both inventory buffers and flexible production schedules. We learned early that over-promising on fast-turn supply ends up hurting trust. Instead, we share updates about inventory and possible shipment timelines, so users can plan with real facts in hand. Production planning runs on both our forecast and honest feedback from long-term partners.
Over the years, we’ve helped support hundreds of new syntheses, scale-ups, and reformulations built around 5-Chloro-2-Fluoronitrobenzene. Our technical team stays in direct touch with users—answering questions about solubility in nonpolar solvents, best storage practices, or possible side-products during downstream transformations. This isn’t just about ticking off ISO documentation. We invest time answering process questions or pulling out archived GC traces and crystallization notes.
Sometimes, a user flags unexpected reactivity in their own lab. In those moments, we don’t just refer to specification sheets—we review our batch notes, check if there’s a history of similar reports, and even re-run extra characterization if needed. This two-way connection creates stronger relationships, and we see the results in the steady growth of repeat orders and collaborative problem-solving.
Many classic nitrobenzene derivatives have matured into high-volume commodities, but 5-Chloro-2-Fluoronitrobenzene remains a specialty chemical that benefits from targeted, hands-on production. New research continues to spotlight the unique properties imparted by its combination of two halogens and a reactive nitro group. Having handled similar compounds for decades, we notice upticks in demand as more chemists recognize its value in complex syntheses—especially where both electron-withdrawing effects and selective future substitution are needed.
Some of the latest work we’ve supported involves high-throughput screening of halogenated aromatics for pharmaceutical and advanced polymer development. Real-world usage sometimes veers into unanticipated territory, and we relish these challenges. For example, we worked closely with one process team to tweak particle size for continuous flow chemistry, which called for narrowly defined sieving. These kinds of collaborations extend beyond mere supply; they’re about real partnership driven by an understanding of both molecule and market.
Production of halogenated nitrobenzenes falls under close scrutiny, especially as regulators keep a close eye on organofluorine emissions and general chemical safety. Decades of compliance auditing have made us proactive, not reactive. Our effluent treatment processes, air handling upgrades, and documented handling procedures have evolved as both requirements and our own standards rose.
Maintaining detailed batch records and traceability systems isn’t just about ticking regulatory boxes—it ensures we can look back across years of production runs, troubleshooting or confirming any questions users have. Whether for toxicological registration or environmental reporting, our batch sheets and storage facility logs reflect every production detail. Each modification in our facility comes after practical feedback from both shop-floor operators and user experience.
Differences in regulatory treatment around the world mean shipments sometimes face extra customs or documentation demands. We keep our shipping and compliance team trained in market-specific requirements. These aren’t just hurdles—they’re opportunities to show that real manufacturing commitment means seeing the process through, right to the end user’s door.
Manufacturing 5-Chloro-2-Fluoronitrobenzene doesn’t lend itself to shortcuts. Our experience over the years has taught us that every process tweak, every run improvement, and every new analytical check makes a difference in both product quality and user confidence. When a customer reports a good outcome—a higher yield downstream, a smoother conversion, a lack of unexpected contaminants—our whole team sees that as the true measure of what experienced manufacturing really delivers.
We remain grounded in the details, always open to direct communication. Direct insight from both the lab and the warehouse floor steers our improvements more than outside opinion ever could. That’s what sets truly experienced and dedicated manufacturing apart in the specialty chemical sector.