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2-Fluoroaniline

    • Product Name 2-Fluoroaniline
    • Alias 2-Fluoro-1-aminobenzene
    • Einecs 209-075-6
    • 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
    VTB
    Specifications

    HS Code

    519221

    CAS Number 578-54-1
    Molecular Formula C6H6FN
    Molar Mass 111.12 g/mol
    Appearance Colorless to pale yellow liquid
    Odor Aromatic
    Melting Point -19 °C
    Boiling Point 182 °C
    Density 1.18 g/cm³
    Solubility in Water Slightly soluble
    Flash Point 71 °C
    Refractive Index 1.584
    Vapor Pressure 0.3 mmHg (25 °C)

    As an accredited 2-Fluoroaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Fluoroaniline, 100g, supplied in a sealed amber glass bottle with tamper-evident cap and clear hazard labeling for safe handling.
    Shipping 2-Fluoroaniline should be shipped as a hazardous material in compliance with relevant regulations (DOT, IATA, IMDG). It must be packed in tightly sealed containers, cushioned to prevent breakage, and labeled with hazard warnings (toxic, flammable liquid). Store and transport it in a cool, well-ventilated area, away from incompatible substances.
    Storage 2-Fluoroaniline should be stored in a cool, dry, well-ventilated area away from sources of ignition, heat, and incompatible materials such as strong oxidizers and acids. Store in a tightly sealed container made of compatible material, and protect from light. Keep away from moisture and ensure proper labeling. Use secondary containment to prevent leaks or spills.
    Application of 2-Fluoroaniline

    Applications of 2-Fluoroaniline in Industrial Manufacturing

    2-Fluoroaniline serves as a high-value intermediate in specialized industrial segments, linking advanced chemical synthesis to key end markets. As a direct manufacturer, we maintain strict quality and regulatory alignment for each application, based on extensive process experience and real batch feedback. Below we provide detailed application scenarios grounded in actual downstream adoption.

    1. Agrochemical Intermediate Synthesis

    Leading agrochemical producers incorporate 2-fluoroaniline as a tailored building block in the synthesis of select phenylurea and aniline-based herbicides. The compound’s reactivity with isocyanates and carboxylic acid derivatives supports efficient manufacture of active ingredients designed for selective weed control in cereal and rice cropping systems. During scale-up, processing teams monitor purity and impurity profiles to remain within environmental and product safety thresholds.

    Industry compliance standards

    • EPA (US Environmental Protection Agency) registration guidelines for pesticide actives
    • European Union Regulation (EC) No 1107/2009 for plant protection products
    • China GB/T 1604-2016 for technical grade agrochemicals
    • ISO 9001:2015 for quality management in chemical production

    Typical usage ratio

    • 5–12% mass fraction in intermediate coupling; optimized through molar conversion efficiency, adjusted for specific herbicide formulations and yield requirements

    Downstream process integration

    • Directly charged into condensation or acylation reactors for synthesis of herbicidal scaffolds, prior to downstream formulation and granulation steps

    Final product types

    • Selective herbicide actives (e.g., fluoroaniline-derived urea and anilide herbicides)
    • Suspension concentrate and water-dispersible granule herbicide formulations

    2. Pharmaceutical Intermediate in API Manufacture

    Regulated pharmaceutical synthesis uses 2-fluoroaniline as a precursor in the multipart synthesis of certain fluorinated aromatic APIs, especially within the anti-infective and CNS therapy categories. Medicinal chemists leverage its aryl amine and fluorine substitution for regioselective coupling reactions, improving metabolic stability of target drug molecules. All process steps strictly follow cGMP requirements, with dedicated documentation of material flow, impurity tracking, and validation data.

    Industry compliance standards

    • ICH Q7 GMP guidelines for API synthesis
    • US FDA 21 CFR Part 211 for finished pharmaceuticals
    • European Pharmacopoeia monographs (when relevant for trace residuals)
    • ISO 13485:2016 for applicable medical chemical manufacturing

    Typical usage ratio

    • 2–6 mol% relative to final API target; adjusted based on stoichiometry and chemoselectivity requirements in multi-step processes

    Downstream process integration

    • Charged into aromatic substitution and amidation reactions during early- or mid-stage API synthesis, followed by subsequent isolation, purification, and crystallization steps

    Final product types

    • Fluorinated active pharmaceutical ingredients (APIs) for CNS drugs and anti-infectives
    • Pharmaceutical intermediates for further medicinal chemistry derivatization

    3. Dye and Pigment Intermediate Production

    The dye manufacturing sector utilizes 2-fluoroaniline to prepare specialized azo, anthraquinone, and disperse dye precursors. Its fluorinated aromatics contribute to brightness, wash-fastness, and light stability in textile and plastic coloration. During large-scale production, our technical team monitors diazotization and coupling regimes to maintain batch-to-batch chromatographic profiles compliant with textile and polymer applications.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile chemicals
    • REACH (EC) No 1907/2006 registration for dyes and pigments
    • ISO 9001:2015 for dye manufacturing quality systems
    • ISO 14001:2015 for environmental management in colorant production

    Typical usage ratio

    • 5–15% molar input during precursor synthesis, modulated by hue intensity and chromophore design requirements

    Downstream process integration

    • Introduced during diazotization or direct aromatic amination to generate fluorinated dye intermediates, followed by coupling with coloristic partners and subsequent purification or blending

    Final product types

    • Disperse dyes for polyester and synthetics
    • Fluorinated pigments for plastics and packaging inks
    • Textile reactive dyes with enhanced washfastness

    4. Specialty Polymeric Material Modification

    Polymer manufacturers introduce 2-fluoroaniline during custom synthesis of high-performance polyamides and thermoset resins. The fluorinated aromatic group increases chemical and thermal resistance in specialty engineering plastics. This application requires strict monomer feed control, as well as in-process QC to track amine end-group conversion and ensure regulatory approval for industrial and limited consumer contact materials.

    Industry compliance standards

    • UL 94 flammability rating for plastics
    • ISO 10993 for biocompatibility, if destined for medical-grade applications
    • REACH and TSCA for registration of monomers and finished polymers
    • ISO 9001:2015 for process verification and lot traceability

    Typical usage ratio

    • 1–7 mol% of overall monomer batch, adjusted for target molecular weight and crosslinking density during chain extension or curing processes

    Downstream process integration

    • Added at the polycondensation or curing stage, participating in backbone or pendant group formation within engineered resin matrices

    Final product types

    • High-performance polyamides for automotive and electronic components
    • Specialty fluorinated thermoset resins for coatings and adhesives
    • Modified engineering plastics requiring enhanced resistance profiles

    5. Electronic Chemicals Precursor

    The electronics industry applies 2-fluoroaniline in synthesis routes for specific functional materials such as fluorinated aryl compounds used in OLED and advanced display technologies. Its electronic characteristics benefit hole transport material (HTM) development and photoactive layer design. Production requires levels of purity and trace metals control that satisfy sector-specific analytical benchmarks, ensuring consistent device performance in downstream integration.

    Industry compliance standards

    • JEITA standards for electronic chemicals purity
    • SEMATECH guidelines for trace contaminants in materials
    • ISO 9001:2015 for specialty electronic grade chemical production
    • Restriction of Hazardous Substances (RoHS) directives for electronic components

    Typical usage ratio

    • 0.5–3% by weight in precursor solution, controlled for specific conductivity, band gap properties, and process yield in electronic materials

    Downstream process integration

    • Introduced into organic synthesis steps for functional arylamines in photoactive components, often followed by vacuum sublimation and film deposition in cleanroom environments

    Final product types

    • Organic light-emitting diode (OLED) transport layers
    • Fluorinated aryl intermediates for display and sensor devices
    • Electronic chemical additives for precision materials
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    Certification & Compliance
    More Introduction

    Quality 2-Fluoroaniline from a Trusted Chemical Manufacturer

    Our Experience with 2-Fluoroaniline Production

    Over years of manufacturing fine chemicals, our approach to 2-fluoroaniline grew out of countless hours spent fine-tuning reaction conditions, optimizing purification steps, and tracking real-world variations in product quality. We’ve stood side-by-side with R&D chemists and plant operators who rely on consistent performance batch-to-batch, so we see the real demand behind words like “purity” in their daily work. 2-Fluoroaniline appears simple on paper—an aniline ring with a single fluorine at the ortho position—but the practical effort behind it can get overlooked. Shortcuts in purification or shortcuts in reaction controls trigger frustration on the user’s end, so we keep those potential weak spots top of mind.

    Chemists choose 2-fluoroaniline for several reasons: it’s a direct building block for fluoro-substituted pharmaceuticals, agrochemicals, and specialty materials, or it’s a key intermediate along a production route with little room for error. Each batch we produce is defined by its clarity, odor, color, and analytical profile. Standard analytical specs include GC purity, content of related anilines, water content, and color—details that matter far more on the plant floor than they do behind a desk. Colleagues in API research, custom manufacturing, and dye synthesis come to us because our control over those specs reduces headaches during scale-up or downstream processing.

    Differences Between Fluoroaniline Isomers

    In conversation with process teams, the distinction between ortho-, meta-, and para-fluoroaniline comes up often. 2-Fluoroaniline, or ortho-isomer, functions differently from its meta (3-fluoroaniline) or para (4-fluoroaniline) cousins. The fluorine in the ortho position changes electron distribution and reactivity—details that make a difference during subsequent steps like coupling reactions, nitrations, or diazotizations. Analysts working through NMR spectra or managing exotherms during scale-up frequently point this out. We’ve seen cases in dye intermediates and active pharmaceutical ingredients where using the wrong isomer actually derails a campaign. Trading houses occasionally mislabel isomers in the rush to fill an order, but as a manufacturer, we don’t face that temptation—traceability matters here.

    2-Fluoroaniline’s boiling point, density, and viscosity also differ from its isomeric relatives. These details matter during solvent swaps, vacuum distillation steps, and QC. A process designed for 4-fluoroaniline doesn’t always function the same with our product—this comes up in technical discussions where heat transfer or blending timings make a difference in batch control. While structurally these molecules look similar, downstream practitioners care about more than the CAS number. Small changes at the bench amplify during production-scale runs, so our team keeps information about impurity profiles and stability in real-world storage conditions ready for questions.

    Practical Aspects of 2-Fluoroaniline in Manufacturing

    A lot of research groups and production teams come to us looking for 2-fluoroaniline material that supports their process without introducing unnecessary risk or waste. Sometimes this means a tighter color spec to reduce byproduct formation in azo dye synthesis. Other times, a major concern is keeping secondary amine byproducts and iron below a particular threshold—the latter matters for photostability in certain intermediates. Those details guide our in-plant controls. There’s pressure to guarantee stability through shipping and warehousing in varied climates; nothing ruins trust in a supplier faster than product that darkens or decomposes while in transit.

    Years of feedback from scale-up chemists led us to devote significant resources to storage containers, stabilization methods, and data tracking between intermediate and final production steps. We ship 2-fluoroaniline in containers that stand up to both corrosive residue and temperature variation. In practical terms, that means seamless transitions from pilot plant to kilo-plant—groups from the US, Europe, and Asia confirm these choices spare them rework or contamination headaches.

    Current Trends in Applications and Challenges

    Demand for 2-fluoroaniline shifted over the past decade. Early on, most orders came from dye houses and pigment formulators looking to impart specific hue and solubility combinations. These days, pharmaceutical manufacturers and custom synthesis shops form our largest customer segment, targeting new fluoro-containing molecules for oncology, CNS, or anti-infective drugs. An increasing share of research contracts now specify ortho-fluorine placement for its impact on biological activity or metabolic pathway, not just its effect on solubility or base sensitivity.

    This shift means tighter controls across every stage—from initial fluorination to final drum filling. We track lot genealogy for each barrel, ensuring the process remains consistent even if the application changes from bulk tonnage for pigments to kilogram batches for pharma reference standards. Our ongoing discussions with QA teams and external auditors focus on trace levels of related amines, non-aromatic byproducts, and trace metals, since these influence downstream biological or physical properties.

    Another trend relates to regulatory scrutiny and evolving toxicology data. We keep up with new studies on skin sensitization, inhalation exposure risk, and effluent management. Many clients want certificates or third-party audits verifying our environmental and occupational controls, especially with heightened attention to aromatic amine handling in multiple regions. Our team helped shape new containment, PPE, and disposal practices based on both regulatory shifts and practical incidents—there’s little substitute for lessons learned during an actual on-site review.

    Optimizing Quality for End Users: Experience from Routine QC

    Repeated stress tests on our 2-fluoroaniline lots, conducted both in-house and in customer pilot lines, reveal clear links between production parameters and downstream outcomes: peak area ratios in GC traces, clarity post-storage, reactivity in Buchwald-Hartwig couplings, and color formation after prolonged warehouse storage. Because we rerun full specs on retained reference samples from each batch, users receive consistent answers when conducting their own verifications.

    On dozens of occasions, researchers and QA teams have shown us how even small differences in impurity content or starting material quality will affect product development timelines. There’s an expectation now that a manufacturer supplies not just a drum of chemical, but the confidence that each lot will perform as needed during scale-ups. Our decisions on process stabilization and post-synthesis workup flow directly from those real-world observations, not marketing templates.

    The difference from generic distribution is obvious—cosmetic clarity, analytical backup, and process history all go beyond minimum requirements. By keeping internal communication lines open with long-term user partners, we’ve refined our analytical intervention points to match both expected and unexpected needs, instead of running all materials through the same old template. The result: fewer customer complaints, less returned inventory, and a stronger sense of trust in our sample transparency.

    Switching to 2-Fluoroaniline from Other Aniline Derivatives

    Pharmaceutical chemists or plant managers evaluating a switch from standard aniline or another fluoroisomer encounter multiple technical hurdles. Ortho fluorination affects both the electron-rich position for downstream functionalization and the volatility profile compared to unsubstituted or para-fluoro units. Our own R&D experiments confirm that certain steps—like Suzuki coupling or benzoylation—run under different temperatures and catalyst loads with 2-fluoroaniline than with its structural relatives. Over the years, we’ve accumulated dozens of customer reports and in-house notes documenting those distinctions.

    We see regular requests for side-by-side comparisons or detailed impurity breakdowns when research groups are considering that initial switch. Process control teams spending weeks on pilot runs cannot afford unexpected effects due to overlooked differences. Our QC team works closely with client labs asking those extra questions about peroxide formation, color retention, and iron, especially when regulatory or internal standards ramp up. Our hand in manufacturing—not merely sourcing—lets us act on unique requests without depending on upstream suppliers to care about the difference.

    Supporting Innovation Across Industries

    Clients in pharmaceuticals, fine chemicals, dyes, and agricultural intermediates push for new applications where a single atom switch—like fluorine at position 2—changes process economics or product efficacy. We contribute by not just supplying a molecule but also tracking and sharing process observations relevant to each application. Some look for high-purity 2-fluoroaniline for structure-activity relationship studies, others need tighter specs for downstream registrations. Technical customs audits and third-party validation have grown more frequent, and as a manufacturer, our responsibility extends to transparent process histories and traceability.

    Requests come in from global sites needing multilingual documentation, real-time support, and product configuration to meet customs or environmental compliance in their home countries. Each region holds its own baseline expectations for analytical proof, documentation, or material traceability. Our facility’s continuous improvement plans keep us ready to revise practices as applications expand or regulatory regimes shift focus. Decade-long relationships with both multinational and specialty partners enable a cross-industry perspective on where 2-fluoroaniline fits best or what needs to change as end-user requirements evolve.

    Managing Supply Chain and Sustainability Concerns

    As direct, primary manufacturers, our concerns stretch beyond just reaction optimization. Raw material sourcing, energy usage per ton, process waste handling, and effluent treatment now attract as much attention as final product quality. Clients increasingly request sustainability data or audit our plant for carbon impact, and the demand to show real-world improvements in solvent recycling, emissions, and raw material origin grows each year.

    That pressure led us to overhaul portions of our process to favor closed-loop gas handling, minimized solvent footprint, and on-site waste neutralization that reduces both environmental impact and regulatory risk. Our commitment to continuous improvement comes from both internal values and decades of customer pushback against outdated, “business as usual” approaches. We share batch-level waste reports and energy usage breakdowns for clients investing in green chemistry or tracking their own carbon footprints.

    Partners further up the supply chain appreciate reliable reporting on compliance status, traceability, and ongoing improvements. These are not distant corporate goals—they shape daily operations and ongoing relationships with customers who carry high expectations for data access and non-greenwashed reporting. We see collaboration with clients as a two-way street, improving both product quality and environmental outcomes.

    Solutions for Downstream Processing Challenges

    2-Fluoroaniline users often run into difficulties during scale-up phases: suppressed crystallization rates, side reaction formation, volatility under certain extraction regimes, or color instability during storage. Our internal pilot team regularly shares notes and improvement suggestions for these common bottlenecks—details not found in academic papers or dry safety data sheets. By collaborating with these users, we’ve incorporated additional drying, stabilization, or container design modifications, raising confidence through repeated lot checks and field testing.

    On more than one occasion, we’ve been called in to help troubleshoot unexpected color shift or trace impurity in downstream intermediates traced back to minor instability events or overlooked trace contamination. Solutions often include in-line analytical monitoring, continuous review of process steps, and feedback loops with downstream process teams. Where large traders chase volumes, we learn from each production issue and bring those lessons directly into updated SOPs, technical bulletins, and customer guidance.

    Maintaining a real partnership with users dealing with the complexity of fluorinated aromatic intermediates shapes our entire approach to process design, risk commmunication, and support. The focus is not just selling, but ensuring the molecule supports a broader technical or regulatory purpose, avoiding rework waste or regulatory setbacks further down the line.

    Conclusion: Value from a Manufacturer’s Standpoint

    As a direct producer, we offer more than just a chemical. Reliable, quality 2-fluoroaniline represents thousands of hours of invested expertise, lessons from failed batches, and incremental improvements driven by user demands. The learning we gather from one campaign feeds into improved specs and better troubleshooting for the next. No batch leaves our facility without confidence that it matches application requirements, industry standards, and evolving environmental concerns.

    By staying grounded in real-world process experience, ongoing regulatory shifts, and the technical goals of chemists, product developers, and production managers, we don’t just provide a product, but a foundation for innovation and trust. Our history manufacturing 2-fluoroaniline—backed by a continual commitment to improvement—means partners gain not only on-paper specifications, but hands-on insight ready for next-generation challenges.