|
HS Code |
764188 |
| Cas Number | 954-97-8 |
| Molecular Formula | C6H2F5N |
| Molecular Weight | 183.08 |
| Iupac Name | 2,3,4,5,6-Pentafluoroaniline |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point C | 139-141 |
| Melting Point C | -18 |
| Density G Per Cm3 | 1.593 |
| Solubility In Water | Slightly soluble |
| Flash Point C | 54 |
As an accredited 2,3,4,5,6-Pentafluoroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g amber glass bottle is tightly sealed, labeled "2,3,4,5,6-Pentafluoroaniline," featuring a hazard warning and CAS number. |
| Shipping | 2,3,4,5,6-Pentafluoroaniline should be shipped in tightly sealed containers, protected from light and moisture. It is classified as a hazardous material and should be handled according to regulations for toxic and potentially flammable chemicals. Proper labeling, UN numbers, and documentation are required during transport to ensure safe and legal shipment. |
| Storage | **2,3,4,5,6-Pentafluoroaniline** should be stored in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers and acids. Keep the container tightly closed and protected from moisture. Store in a chemical-resistant container, and ensure proper labeling. Use appropriate personal protective equipment when handling to avoid inhalation and skin contact. |
Applications of 2,3,4,5,6-Pentafluoroaniline in Industrial ManufacturingAs a direct manufacturer of 2,3,4,5,6-pentafluoroaniline, we support industrial customers with technical-grade material positioned for use in select downstream sectors with well-defined compliance and processing frameworks. Below we present verified industry scenarios where this compound integrates into specialized formulations and advanced synthesis routes. 1. Agrochemical Active Ingredient SynthesisAgrochemical producers use 2,3,4,5,6-pentafluoroaniline as a key fluorinated aromatic amine intermediate for building selective herbicides and fungicide molecules. Its electron-withdrawing pentafluoro substitution supports enhanced metabolic stability in target actives, especially in triazole, pyridine, and anilide compound frameworks. The material typically undergoes direct condensation or amide-forming reactions in the advanced stages of API synthesis, requiring close control of reaction kinetics and impurity formation throughout the manufacturing QC process. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Pharmaceutical Intermediate for Specialty API SynthesisPharmaceutical companies employ 2,3,4,5,6-pentafluoroaniline as a secondary amine intermediate during multistage synthesis of certain active pharmaceutical ingredients, particularly those requiring high fluorine-content aromatic subunits. Reaction schemes leverage its nucleophilicity for aromatic substitution and condensation reactions specific to high-performance CNS and oncology drug molecules. All integration happens under stringent cGMP controls to guarantee traceability and impurity reduction from raw material through final API generation. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Fluorinated Liquid Crystal Precursor ManufacturingSpecialty electronics chemical manufacturers rely on 2,3,4,5,6-pentafluoroaniline as a core building block to create custom fluorinated aniline derivatives incorporated in advanced liquid crystal materials. The heavily fluorinated aromatic ring imparts low viscosity, high chemical resistance, and unique dielectric anisotropy to final liquid crystal mixtures used in LCD and display technologies. Precise stoichiometric addition and rigorous purification are demanded to maintain optical purity and electrical performance in the final formulations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Fluorinated Polymer Additive and Monomer SynthesisPolymer manufacturers utilize 2,3,4,5,6-pentafluoroaniline to synthesize high-performance specialty monomers and as a chemical modifier to improve film-forming and barrier properties in niche fluorinated polymer products. The compound integrates during functionalization steps in the creation of polyimides, polyamides, or copolymers, conferring enhanced thermal stability and reduced water absorption desirable in advanced electronic insulation coatings and aerospace material applications. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Building Block for Advanced Dye and Pigment SynthesisManufacturers of specialty dyes and pigments apply 2,3,4,5,6-pentafluoroaniline as a fluorinated amine scaffold in synthesizing colorants with extraordinary chemical and thermal resistance. These compounds find use in niche inkjet printer formulations, microelectronic labeling, or anti-counterfeiting print technologies, where specific shade properties and chemical inertness are demanded by downstream OEMs. Process reliability, purity of the amine, and precision in diazotization or coupling reactions are central to downstream quality. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 2,3,4,5,6-Pentafluoroaniline 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!
At our chemical plant, we deal with many aromatic amines, but 2,3,4,5,6-Pentafluoroaniline holds its own in the specialty segment. The model we most often supply comes as a clear to slight pale liquid, sometimes presenting a faint brown tint if stored for longer periods. Our production team carefully manages distillation to minimize traces of related compounds – typically 98% minimum purity by GC. We package it in tight-sealed fluorinated bottles to avoid any seepage or hydrolysis, a practice born from decades of observing subtle storage and handling challenges. Most customers request small lots: 50g, 100g, or up to 1kg, thanks to its potency in downstream synthesis.
Chemical synthesis always balances reactivity and selectivity. With 2,3,4,5,6-Pentafluoroaniline, the unique arrangement of fluorine atoms boosts both. Water and oxygen don’t degrade it easily; humidity doesn’t trigger polymerization. The molecule offers high thermal stability so it survives harsher reaction environments than other anilines. Many chemists notice how the pentafluorination blocks unwanted side reactions on the benzene ring, helping synthesize novel heterocycles or ligands. High-end material science and agrochemical research regularly call us for batches, especially for developing fluorinated pharmaceuticals or advanced dyes.
Pentafluoroaniline works as a sturdy anchor in multi-step syntheses. Our partners in medicinal chemistry often mention how its fluorinated backbone helps introduce superb metabolic stability and fine-tune electronic effects. By offering a consistent model and clean impurity profile, we take headaches out of reproducibility for early-stage drug research. In polymer science, adding pentafluoroaniline lets manufacturers tweak polymer properties: more resistance to solvents, greater UV durability, and tighter control over dielectric characteristics. Not all aromatic amines contribute these qualities.
Over the years, we’ve worked with a range of substituted anilines, including trifluoroaniline, pentafluorobenzene, and even mono-substituted variants. Each brings something different to the bench. Regular aniline or para-substituted fluoroaniline don’t pack the same electron-withdrawing punch or steric hindrance. The all-around ring fluorination in pentafluoroaniline means one can count on predictable, clean reactivity, especially in metal-catalyzed couplings. It rarely succumbs to over-reduction or accidental oxidation. Chemists who tried to substitute in trifluoro often circle back, citing inconsistent yields or unexpected byproducts when they test at scale. The repeatability with pentafluoro stands out – orders have steadily increased as more customers realize it saves cleanup and lessens variable screening. We’ve never seen another aromatic amine that travels from theory to kilo-scale synthesis with so few hiccups.
Some of our long-term collaborators create advanced ligands for catalysis. They tell us pentafluoroaniline introduces unique bite angles and binding affinities not easily accessed with lower fluorinated analogues. The strong inductive effect from the five fluorines modifies the amine electron density, shifting reaction windows. This opens doors for C-N cross-coupling, or nucleophilic aromatic substitution, that just doesn’t happen with plain aniline. Agrochemical innovators particularly love its firepower: halogenated herbicides, fungicides, and pest control molecules that demand durable chemical skeletons. The most successful formulations in the last ten years, at least among our direct buyers, often start their journey in R&D with a gram or two from our facility.
Industrial realities inform every step of our process. Even stable compounds like pentafluoroaniline require respect. It’s not volatile, but its amine function can still cause skin or eye irritation. We run regular safety drills and supply safety data sheets along with each shipment. In the warehouse, our staff wear double-layer gloves and operate chemical fume hoods during repackaging. We keep storage rooms at stable temperatures to keep product color and purity intact, logging temperature and humidity every shift. In a few rare instances, exposure to high heat and open air changed the appearance slightly, though not the purity profile. Lessons like these, learned from experience, steer us toward tighter quality checks long before product hits the dock.
The synthesis of 2,3,4,5,6-Pentafluoroaniline is neither trivial nor forgiving. Our synthesis route avoids hazardous intermediates and excessive waste. Early pilot trials showed that trace iron contamination could knock yields down by half and seed premature decomposition in storage. To combat this, we upgraded glass-lined reactors and added careful filtration to every run – even though it slows things down. We selected distillation ranges based on hundreds of small-scale purifications to ensure minimal residues, which means our clients do not run into ghost peaks during their HPLC analyses. Many downstream users report greater batch-to-batch consistency when sourcing from us, an outcome only possible through constant feedback between our manufacturing and QC teams.
Manufacturing fluorinated intermediates poses undeniable waste challenges. We capture evolved halogens and recover solvents where feasible, using actively monitored scrubbers. Waste stream composition changes with each run, and we tweak process parameters to cut off-spec product. Our spent solvents are sent for chemical recycling; every liter saved reduces environmental burden. Auditors routinely review our plant for emissions, and over the last five years, data shows a steady drop in both VOCs and halogenated wastes leaving the premises. We always look for third-party partners in green chemistry research, because waste stream reduction never has a single end point.
Our primary clients work in material innovation hubs and pharmaceutical research parks. They appreciate high-purity pentafluoroaniline for building bespoke chemical libraries. In specialty coatings, the compound helps improve water and oil repellency for textile and electronics applications. Several next-generation OLED and liquid crystal displays use components based on derivatives of pentafluoroaniline. As research into high-performance polymers and drug discovery moves forward, the demand for more intricate fluorinated intermediates has only grown. The health sector, especially antiviral and anticancer research, pushes us to new consistency standards—one misstep in purity shows up fast in lead optimization programs where every side product might hide important biological activity. Collaborators in Japan and Europe remark how switching to pentafluoroaniline impacts their timelines, compressing steps and boosting reliability on scaleup.
Scientists working on rapid library development or SAR (structure-activity relationship) frequently choose pentafluoroaniline as a start point. They mention how its reactivity profiles mesh with click chemistry and Suzuki-Miyaura coupling, especially when compared with lower fluorinated analogs. We have sent samples for pilot trials on other continents, with feedback highlighting simple workups and less time spent troubleshooting. Where similar products required extra steps or rare catalysts, pentafluoroaniline proved more straightforward, needing only standard reagent suites common in most synthetic labs.
Compared to classic aromatic amines, pentafluoroaniline handles extended storage better. Our longest-retained batch dates back nearly three years, with only minor color shift and no change in GC profile. This shelf life means customers do not need to rush through inventory or replace lots mid-project. Several partners even share logistics pools to capitalize on larger-frequent orders, knuckling down on cost saving without sacrificing chemical integrity. No other fluorinated aniline we supply matches its tenacity under long-term storage conditions.
All chemicals require vigilance in their use. Pentafluoroaniline, while robust, reacts strongly with some acids and oxidizers, more so than typical aromatic amines. Any spill or leak requires prompt neutralization and disposal. We train all new hires on response protocols to cut down workplace accidents. Older literature and outdated MSDS copies occasionally give misleading advice about volatility or fire risk; close reading and real-world handling always show pentafluoroaniline isn’t a significant vapor hazard under normal usage, but a live environment and appropriate PPE matter for safety on production and lab floors.
Since making upscaling practical, we’ve streamlined contractor relationships for packaging and export. Our product moves direct from reactor to jerrican, avoiding excess handling. Cold-chain logistics are not usually necessary, but shipments face less risk from seasonal temperature swings. The main bottleneck remains precursor sourcing, as global fluorine chemicals have grown tighter with new regulations. By holding our own stocks and running smaller, more frequent campaigns, we keep lead times short, rarely leaving partners waiting on crucial intermediates. Careful forecasting based on regular customer check-ins lets us plan for even volatile segments like electronics or pharmaceuticals.
Being a manufacturer means not just supplying product but also troubleshooting with customers. Our technical team regularly reviews reaction outcomes and adapts production if issues recur downstream. Several drug R&D partners shared that pentafluoroaniline’s distinct NOE (Nuclear Overhauser Effect) patterns helped them confirm reaction sites, speeding up iterative synthesis. We pass along detailed analytical spectra for every lot, enhancing transparency. Where issues with solubility or color have come up, we’ve adjusted distillation or optimized purification until partners were happy with performance. In a world full of molecular options, direct feedback shapes our evolution.
Changing compliance laws affect us directly. Fluorinated aromatics now draw more regulatory scrutiny, especially around downstream toxicology and environmental fate. All our lots are fully traceable, from raw material through to end user, aligning with new chemical inventory systems in multiple jurisdictions. Where new guidelines ask for extended impurity profiling, our QC teams adapt. Regular audits from external authorities keep us in line and support our buyers’ needs for Registration, Evaluation, Authorization and Restriction of Chemicals compliance in Europe, or similar frameworks elsewhere. Some application fields, such as active pharmaceutical ingredient synthesis, require even more rigorous data, and we commit resources to meet those requirements.
From the operator’s bench to compliance teams, pentafluoroaniline’s value shows up across multiple axes. Research groups increasingly reach for highly fluorinated intermediates to unlock new chemical spaces, and our experience as a manufacturer keeps us tuned to the next set of demands. Our approach centers on mutual problem-solving, open information sharing, and constant refinement, which has nurtured a virtuous cycle—clients succeed, we re-invest, and both sides advance together. Because new targets in diagnostics or electronics need solid building blocks, having a responsive and knowledgeable partner on manufacturing leads to better, faster progress. Most custom synthesis routes we now explore started as a single application request for pentafluoroaniline, and scaling these up shapes the future of many industries we support.
Few chemicals combine stability, reactivity, and consistency the way 2,3,4,5,6-Pentafluoroaniline does. From the earliest days in our plant to recent innovations, every batch represents decades of accumulated experience across synthesis, purification, and technical troubleshooting. We root our approach in what we learn from hands-on handling, careful observation, and feedback from partners at every stage. This mindset means we champion transparency in supply, open dialogue in technical development, and a continued push toward better, safer ways to bring high-quality fluorinated intermediates to the world.