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2,3,4,5,6-Pentafluoroaniline

    • Product Name 2,3,4,5,6-Pentafluoroaniline
    • Alias Pentafluoroaniline
    • Einecs 217-496-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    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 & Storage
    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.
    Application of 2,3,4,5,6-Pentafluoroaniline

    Applications of 2,3,4,5,6-Pentafluoroaniline in Industrial Manufacturing

    As 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 Synthesis

    Agrochemical 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

    • ISO 9001:2015 (Quality Management for Chemical Manufacturing)
    • FAO/WHO Specifications for Pesticide Actives
    • REACH Regulation (EC) No 1907/2006, Annex II (Safety Use of Intermediates)
    • Globally Harmonized System (GHS) for hazard communication

    Typical usage ratio

    • 5–15% molar ratio in final active ingredient synthetic pathway, adjusted based on required fluorination pattern and downstream yield optimization

    Downstream process integration

    • Introduced during targeted amination or acylation steps after initial core scaffold assembly; fed through glass-lined reactors with controlled addition rates for exothermic steps; reaction monitored by HPLC/GC for endpoint validation

    Final product types

    • Selective herbicide actives (e.g., fluorinated triazoles)
    • Systemic fungicides with enhanced environmental persistence
    • Intermediate compounds for final crop-protection product formulation

    2. Pharmaceutical Intermediate for Specialty API Synthesis

    Pharmaceutical 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

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP/NF General Chapters <467> and <232> (Residual Solvents and Elemental Impurities)
    • EU GMP Directives, Part II (Basic Requirements for APIs)
    • Ph. Eur. monograph reference when referenced in specification

    Typical usage ratio

    • 2–8% by mol during intermediate coupling or ring-closure operation, variable depending on the complexity of downstream pharmacophore construction

    Downstream process integration

    • Charged to reactor during intermediate amine-aryl coupling or nucleophilic aromatic substitution step; followed by precise thermal control and aqueous workup; subjected to in-process testing for fluorine distribution and aniline residue

    Final product types

    • Small-molecule APIs for CNS indication
    • Advanced pharmaceutical intermediates for fluorinated drug development
    • Reference standards for method validation in pharmaceutical QC

    3. Fluorinated Liquid Crystal Precursor Manufacturing

    Specialty 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

    • IEC 61249-2-34 (Materials for Printed Boards - Halogen Content)
    • RoHS 3 (Directive (EU) 2015/863) compliance for restricted substances
    • JIS C 61000-4 (Japanese Standards for Electronic Materials)
    • ISO 9001 for specialty material synthesis

    Typical usage ratio

    • 0.5–3% w/w incorporated into precursor feed for downstream fluorinated aromatic synthesis, with scale variance determined by targeted mesogen performance and manufacturer’s proprietary blend requirements

    Downstream process integration

    • Enters as limiting reagent in aromatic alkylation or Suzuki coupling during initial precursor synthesis; requires inert atmosphere and stepwise purification to ensure trace halide removal; quality confirmed via NMR and GC-MS before final blending

    Final product types

    • Advanced liquid crystal compounds for LCD displays
    • Dielectric anisotropic materials for touch panels and mobile screens
    • Custom fluorinated aromatic building blocks for optoelectronics

    4. Fluorinated Polymer Additive and Monomer Synthesis

    Polymer 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

    • ASTM D5207 (Standard for Fluoropolymer Raw Materials in Coatings)
    • UL 94 (Flammability Standard for Plastic Materials)
    • ISO 14001 (Environmental Management for Handling Fluorinated Compounds)
    • REACH Annex XVII (Restrictions on Manufacture and Use of Certain Hazardous Substances)

    Typical usage ratio

    • 0.1–2% by weight in copolymer modification or as an end-group modifier in specialty polymerizations, adjusted per desired property enhancement and end-use certification

    Downstream process integration

    • Added during controlled-stage copolymerization with diamines or dianhydrides; process necessitates real-time FTIR/DSC monitoring for conversion and structural uniformity; full batch certification post-synthesis per customer QC protocol

    Final product types

    • Fluorinated polyimide films
    • High-performance insulating coatings for electronics
    • Water- and oil-repellent engineering plastics

    5. Building Block for Advanced Dye and Pigment Synthesis

    Manufacturers 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

    • EN 71-3 (Safety of Toys: Migration of Certain Elements for ink/pigment safety)
    • ISO 2846-1 (Pigment Specification for Offset Inks)
    • California Proposition 65 (Safe Drinking Water and Toxic Enforcement Act for print chemicals)
    • ISO 14021 (Environmental Claims for Secondary Chemical Use)

    Typical usage ratio

    • 1–5% molar ratio as primary amine or diazo compound precursor, adjusted to reach calibrated fluorination and colorfastness benchmarks per OEM ink/pigment specification

    Downstream process integration

    • Fed into diazotization or azo-coupling reaction vessel under chilled, buffered aqueous conditions; intermediates isolated and processed to colorant standard using high-vacuum drying and precision filtration steps; end-product validated for photostability and chromatographic profile

    Final product types

    • Fluorinated specialty inkjet dyes
    • High-stability pigments for electronic device marking
    • Security printing inks with tamper-evident features
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    Competitive 2,3,4,5,6-Pentafluoroaniline prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    2,3,4,5,6-Pentafluoroaniline: A Closer Look from the Manufacturer’s Perspective

    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.

    Why Pentafluoroaniline?

    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.

    Role in Fluorinated Intermediates

    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.

    Comparison with Related Anilines

    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.

    Synthesizing New Molecules with Pentafluoroaniline

    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.

    Product Handling and Safety from a Manufacturer’s View

    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.

    Practical Challenges and Solutions in Production

    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.

    Environmental Impact and Sustainable Practices

    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.

    Applications in Modern Industry

    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.

    Ease of Integration into Research Pipelines

    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.

    Looking at Longevity and Shelf Life

    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.

    Limitations and Potential Risks

    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.

    Supply Chain Considerations

    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.

    Supporting Innovation with Technical Feedback

    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.

    Regulatory and Compliance Landscape

    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.

    Partnering for the Future

    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.

    Reliable Quality Backed by Experience

    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.