|
HS Code |
458560 |
| Name | 2,3,4,6-Tetrafluoronitrobenzene |
| Cas Number | 446-15-1 |
| Molecular Formula | C6F4NO2 |
| Molecular Weight | 191.06 |
| Appearance | Pale yellow solid |
| Melting Point | 50-54°C |
| Boiling Point | 204-209°C |
| Density | 1.737 g/cm3 |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | c1c(c(c(c(c1F)F)[N+](=O)[O-])F)F |
| Inchi | InChI=1S/C6F4NO2/c7-2-1-3(8)5(11(12)13)6(10)4(2)9 |
| Refractive Index | 1.522 (predicted) |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Hazard Class | H315 (causes skin irritation) |
As an accredited 2,3,4,6-Tetrafluoronitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 2,3,4,6-Tetrafluoronitrobenzene, sealed with a PTFE-lined cap and labeled with hazard warnings. |
| Shipping | **2,3,4,6-Tetrafluoronitrobenzene** is shipped as a chemical substance, typically in sealed, chemical-resistant containers with clear hazard labeling. It should be handled in compliance with relevant transport regulations (such as DOT or IATA), as it may be classified under hazardous materials due to its toxicity and potential environmental risks. |
| Storage | 2,3,4,6-Tetrafluoronitrobenzene should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from sources of ignition, heat, and incompatible materials such as strong bases or reducing agents. Protect from moisture and direct sunlight. Ensure proper chemical labeling and keep away from food, drink, and animal feed. Use appropriate secondary containment to prevent spills. |
Applications of 2,3,4,6-Tetrafluoronitrobenzene in Industrial Manufacturing2,3,4,6-Tetrafluoronitrobenzene serves as a key intermediate in manufacturing processes where high-purity fluorinated building blocks are essential. Its defined reactivity profile and substitution pattern make it valuable in several specialized chemical industries. Below, we provide substantive details on real downstream use cases, formulation parameters, regulatory frameworks, integration points in the production stream, and representative end-use products. 1. Synthesis of Active Pharmaceutical Ingredient (API) PrecursorsMany pharmaceutical production lines require fluorinated aromatic intermediates to create active molecules with improved metabolic stability and bioavailability. 2,3,4,6-Tetrafluoronitrobenzene acts as a fluoroaromatic precursor in selective nucleophilic aromatic substitution reactions, facilitating the introduction of pharmacophores in complex molecules. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Synthesis IntermediatesThe nitro-fluorobenzene scaffold is routinely transformed in agrochemical plants to create protected fluorinated aniline derivatives. These intermediates are crucial for the downstream manufacture of crop protection agents, including novel herbicides and fungicides with enhanced target specificity. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. High-Performance Polymer Monomer PreparationSpecialty polymer manufacturers use this compound to introduce fluorinated moieties into polyaryletherketones or other engineering plastic monomers, conferring chemical resistance and thermal stability. These downstream applications demand consistent purity and reactivity. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Specialty Dye and Pigment ManufacturingManufacturers of high-performance specialty dyes employ fluoronitrobenzenes to synthesize molecular fragments that impart UV stability and solvent resistance. This building block features in the design of advanced colorants for printing inks and industrial coatings. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Electronic Material IntermediatesProducers of specialty materials for printed circuit boards and semiconductors utilize this chemical to synthesize insulating and photoresist monomers. Its electron-withdrawing substituents are essential for controlling dielectric properties in advanced electronic components. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
6. Fluorinated Agrochemical Analytical Reference StandardsCertified analytical laboratories source ultra-pure reference standards based on this compound to validate residue and degradation pathway studies for environmental monitoring of modern fluorinated agrochemicals as required by regulatory agencies. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2,3,4,6-Tetrafluoronitrobenzene prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Producing 2,3,4,6-tetrafluoronitrobenzene brings real challenges to the floor, yet years spent scaling reactors and fine-tuning purifications have shaped our methods. This compound attracts attention across fine chemical synthesis and specialty intermediates, not because it is simply another halonitro aromatic in the catalogue, but due to its genuine difference in reactivity, purity, and process stability in active manufacturing. Chemical structure forms the heart of any reaction, and two ortho fluorines, another fluorine at position 4, and one at position 6 fundamentally set its properties apart from isomeric or lower-fluorinated alternatives. The strong electron-withdrawing effect of the nitro group, reinforced by the four fluorines, confers one of the more robust platforms for nucleophilic aromatic substitution or downstream transformations. These qualities directly impact what happens in a plant—real yields, impurity handling, and safety demands.
Anyone who has handled direct fluorination or aromatic nitration at scale knows where risks and costly mistakes hide. Our plant never treats tetrafluoronitrobenzene just as another number on a batch sheet. Tight temperature and pressure controls keep formation of regioisomers in check, especially when moving from lab glassware to tonnage. Water-white product may look good in a bottle, but real validation comes from running GC and NMR in-house after every crude cut and wash. This approach has chased away more than one off-the-shelf process. We stopped using shortcuts on workup years ago; batch consistency counts for more than brochure data. Having eyes on every distillation and workers who know their craft ensures this product retains its fine edge for demanding applications, not only standard purity levels.
Our last five years’ batches average above 99% GC purity, but the downstream reactions driving this focus on minimising organic, inorganics, or trace water. The money is in details: off-colour products usually mean poorly controlled second-phase byproducts have not been managed. Deep halogenation sometimes brings over-fluorinated debris or trace acids that ruin downstream amination or cross-coupling. Even minor changes in residual nitrobenzene ghost through into hydrogenation or substitution steps. We stay vigilant: internal standards calibrate what the lab sees versus what the market truly values, and we discuss impurity drift openly with partners, not just behind closed laboratory doors. Years of seeing how this intermediate impacts next-step and final-pot yields means habits grow cautious, not careless.
Many of the companies that source our tetrafluoronitrobenzene feed it into agrochemical, material science, or pharmaceutical intermediates. Its halogenation pattern enables direct nucleophilic aromatic substitution at position 1 or 5—a versatility not seen with 2,4-difluoronitrobenzenes or unsubstituted analogs. In the world of heteroaromatic construction, this effect unlocks possibilities for coupling reactions, amination, or metal-catalyzed aryl-aryl bond formation. While some folks focus on the classical SNAr profile, others seek stability for bioconjugation or electronic component synthesis. Experience shows that these real-world features only reach potential when the upstream material keeps a clean impurity and isomer baseline. Any deviation in those parameters comes back as phone calls or emails from the customer line—not just in data, but in downtime or trouble tickets in their own plant.
It is easy enough to say one nitrobenzene derivative is like another, yet no experienced operator believes that on the production floor. Compare tetrafluoronitrobenzene to 2,4-difluoronitrobenzene or 2,6-difluoronitrobenzene; the differences show up quickly. Four fluorine atoms not only make the ring more electron-poor and resistant to unwanted side reactions, but shift boiling point, solubility, and handling requirements. Purification is harder but the reward is less side-product formation in demanding bond-making reactions downstream. Early in our manufacturing journey, we ran a direct comparison through a kilo-scale Suzuki coupling sequence. The tetrafluorinated material actually showed cleaner conversion, less need for silica gel clean-up, and higher isolated yield, especially in one-pot multi-step syntheses. We documented these runs and drew lessons for later optimization: some plants accept a higher input cost for this product because it means reducing subsequent processing headaches, waste disposal loads, and quality reprocessing.
Batch failures most often trace back to moisture management, heat history, or cross-contamination. During winter, we have seen ambient humidity sneak up, causing cloudy solutions and knock-on hydrolysis issues down the supply chain. Even a few ppm of leftover acid from incomplete neutralization during acid wash can eat through nickel in storage tanks or show up in accelerated container corrosion. Real manufacturers plan not just to hit a spec one time, but to avoid these pitfalls batch after batch. The plant keeps a log of lessons learned, because making 2,3,4,6-tetrafluoronitrobenzene safely and stably means understanding the cumulative micro-problems: hidden acid residue, secondary halide traces, even the effect of metallic stirring paddles, which sometimes catalyze unwanted reduction in warm holding tanks.
We often get calls from chemists looking to use this intermediate over other polynitrobenzenes or differently halogenated aromatics. The difference is not just a matter of melting point or bottle label. Our long-term partners point to three factors that set 2,3,4,6-tetrafluoronitrobenzene apart for them: reactivity tuning due to electronic effects, predictable handling in glovebox or open-air bench chemistry, and options for selective substitutions. Fluorines at all but para to the nitro group steer almost every step, from rate of nucleophilic attack to byproduct minimization. In one long campaign, a client found that using our tetrafluoronitrobenzene cut post-reaction purification time by almost half compared to the 2,4- version—most of the side reactions simply never occurred, which we corroborated in-house. This benefit translates directly to sustainability, less solvent use, less energy spent, and ultimately tighter quality tracking overall.
Not every supplier of tetrafluoronitrobenzene has invested in stable scaling from pilot batches up to industrial production. We learned years ago that churning out laboratory-purity product in 100-gram bottles is not the same as providing every barrel or drum at scale with robust, repeatable quality. Our staff monitor every parameter: packing density, blender turnover, distillation cut points, and cool-down cycle times. By training every shift supervisor in both best practices and likely points of failure, we have weathered more than one production hiccup. Long-term relationships with raw material vendors—especially those who provide guaranteed low-chlorine precursors—help us dodge hidden halide side reactions and manage synthetic risks upstream. We find that customers come for product, but stay for a level of technical conversation and troubleshooting that only another manufacturer can offer.
Some improvements only become clear once hundreds of kilograms move through our customer's benches and pilot lines. Field feedback rarely comes as glowing praise—it’s far more likely to flag a haze in a late-stage filtrate, a faint yellowing in a recrystallized solid, or a downstream instrument calibration shift. These early warnings guide our own QA/QC tweaks and have resulted in nearly a dozen micro-refinements to the crystallization and drying steps. We treat field complaints as direct inputs into shop-floor practice: we shifted to higher-purity solvent grades, invested in in-line microfiltration, and tuned our vacuum pumps to avoid broadening impurity tails. Decades of direct conversations with formulators and engineers mean these changes reflect reality—not marketing speak or regulatory minimums. The product evolves by demand and direct result, not by committee.
Four-fluorine processes pose unique compliance and handling burdens. Each run brings us in contact with high-strength acids and fluorinated waste, so containment, waste management, and worker safety gain equal attention. From the earliest days at our site, we kept audit trails for all utility streams and invested in fume scrubbing and heat recovery, not just to stay compliant but to protect both people and equipment. Environmental oversight teams walk every batch report and waste manifest for this product. We joined benchmark outreach efforts on fluorinated chemical emissions—not because regulators required it, but because we understand downstream users care about environmental reputation as much as reaction performance. No plant can afford to treat its rivers, air, or soil casually when dealing with halonitro intermediates, and our decades of continuous improvement mean audits go smoothly and records stay open to customer queries.
Product quality in tetrafluoronitrobenzene production rarely stands still. What set the bar last decade reads as minimum compliance now, both in purity and process traceability. Each year brings better in-line analytics, new impurity trap designs, more granular tracking of solvent and raw material bills. We realized early that simplicity in batch sheets brings speed, but documenting every change prevents lost knowledge whenever headcount rotates or a line retools. Our blending, filtration, and drying have changed in small but measurable ways nearly every year, reflecting direct input either from analytical improvements or field feedback. By measuring both our best and worst runs, we avoid overconfidence. Our rivals sometimes promise purity from a blurb, but our own experience teaches that only consistent process control keeps a product like this from turning into a liability, both for us and every partner downstream.
2,3,4,6-Tetrafluoronitrobenzene stands out not simply for its chemical profile, but for what experience and attention to process bring to finished product. From first gram to bulk shipment, we invest in every batch and keep documentation honest and accessible. Users who depend on specific downstream performance in high-value or regulated spaces will find that the cost of quality here more than pays for itself in uptime, yield, and fewer fire drills on the laboratory or production line. Chemical manufacturing is not just about reaction conditions or spec sheets; it lives in day-to-day care, attention to detail, and shared ambition to push the boundaries of what’s possible in synthesis. Our story with tetrafluoronitrobenzene grows from decades spent on the plant floor, where every decision feeds forward to the next innovation or improvement.