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4-Fluoro-2-Nitrobenzeneamine

    • Product Name 4-Fluoro-2-Nitrobenzeneamine
    • Alias 4-Fluoro-2-nitroaniline
    • Einecs 225-009-5
    • 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

    980379

    Chemical Name 4-Fluoro-2-nitroaniline
    Molecular Formula C6H5FN2O2
    Molecular Weight 156.12 g/mol
    Cas Number 324-10-9
    Appearance Yellow to brown crystalline powder
    Melting Point 73-77 °C
    Solubility In Water Slightly soluble
    Density 1.47 g/cm³
    Purity Typically ≥98%
    Synonyms 2-Amino-4-fluoronitrobenzene
    Smiles Nc1cc(F)ccc1[N+](=O)[O-]
    Storage Conditions Store in a cool, dry, and well-ventilated place
    Hazard Classification Irritant

    As an accredited 4-Fluoro-2-Nitrobenzeneamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25 grams, with tamper-evident cap and hazard labeling for 4-Fluoro-2-Nitrobenzeneamine; includes safety data sheet.
    Shipping 4-Fluoro-2-Nitrobenzeneamine is shipped in tightly sealed containers to prevent moisture and contamination. It is classified as a hazardous material, requiring appropriate labeling and documentation. Shipment should comply with local, national, and international regulations, ensuring protection from heat, ignition sources, and physical damage during transit. Use of secondary containment is recommended.
    Storage Store 4-Fluoro-2-nitroaniline (4-Fluoro-2-Nitrobenzeneamine) in a tightly sealed container in a cool, dry, well-ventilated area away from sources of ignition, moisture, and incompatible substances such as oxidizing agents and strong acids. Avoid exposure to direct sunlight. Properly label the container and handle with appropriate protective equipment to prevent inhalation, ingestion, or skin contact.
    Application of 4-Fluoro-2-Nitrobenzeneamine

    Applications of 4-Fluoro-2-Nitrobenzeneamine in Industrial Manufacturing

    As a direct manufacturer, we supply 4-Fluoro-2-Nitrobenzeneamine to multiple specialized industrial sectors. Its unique electronic and functional group characteristics enable targeted use in pharmaceuticals, agrochemicals, dye intermediates, advanced materials, and specialty polymers. This section details how established downstream manufacturers incorporate this chemical into their production environments.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers employ 4-Fluoro-2-Nitrobenzeneamine in the synthesis of active pharmaceutical ingredients requiring aromatic fluorinated amine fragments. Custom synthesis routes take advantage of its clean reactivity in aromatic nucleophilic substitution and reduction reactions. Customers use it predominantly in intermediate steps for anti-infective and central nervous system compounds, where the substitution pattern enhances metabolic stability and bioavailability. Its role in GMP-compliant environments makes raw material quality traceability and contaminant control critical throughout procurement and use.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (FDA)
    • European Pharmacopoeia applicable sections
    • Chinese Pharmacopoeia for registered drug substances

    Typical usage ratio

    • Intermediate concentrations between 0.1 to 2.5 mol equivalents per synthetic step, based on the stoichiometry of target API formation
    • Adjusted per route efficiency and regulatory specifications for impurity control

    Downstream process integration

    • Introduced during aryl amination, reduction, or coupling reactions in multi-step API synthesis
    • Transfers from chemical reactors directly to downstream isolation and purification units
    • Subject to in-process QC for trace-level fluorinated impurities

    Final product types

    • Anti-infective drug intermediates
    • Neuroactive compound intermediates
    • GMP-compliant active pharmaceutical ingredients (APIs)

    2. Agrochemical Active Ingredient Production

    Producers of advanced agrochemical actives, such as selective herbicides and insecticides, incorporate this compound as a key aromatic building block in their process chemistry. Its electron-withdrawing substituents help modulate the activity spectrum and persistence profile. The downstream usage occurs in highly automated continuous production environments, requiring stringent material traceability and batch segregation for identity-preserved output. Regulatory focus extends to environmental residue controls and worker safety during handling and processing.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for agrochemicals
    • FAO/WHO Specifications for Plant Protection Products
    • REACH (EU) for registration and safe handling
    • China ICAMA pesticide registration protocols

    Typical usage ratio

    • Applied at 0.5 to 1.7 mol equivalents per batch, according to the structural complexity of the target active compound
    • Adjusted based on downstream conversion yield and waste minimization requirements

    Downstream process integration

    • Fed into nitration or reduction units for further transformation to bioactive moieties
    • Occupies early to mid-stage synthesis position before technical-grade formulation
    • Isolated intermediates routed to purification and micronization plants as needed

    Final product types

    • Selective herbicide actives
    • Systemic insecticide intermediates
    • Technical-grade crop protection agents

    3. Colorant and Pigment Intermediate Manufacturing

    Specialty dye manufacturers use 4-Fluoro-2-Nitrobenzeneamine to introduce both nitro and fluoro-substituted phenyl structures into dye molecules. The material actively participates in diazotization and coupling stages to generate unique chromophores with strong light and wash fastness. Control of reaction temperature and pH is crucial to avoid over-reduction and loss of color stability. Large-scale processes require integration with automated bulk handling and precise metering systems, with emphasis on effluent treatment for aromatic amines.

    Industry compliance standards

    • OEKO-TEX Standard 100 limits for aryl amine residues
    • EN 71-3 Safety of Toys (migration of certain elements in pigments)
    • China GB/T 5009.70-2003 for food contact dye substances
    • ISO 14001 for environmental management in dye production

    Typical usage ratio

    • 0.3 to 1.2 molar equivalents per coupling batch, dependent on target color intensity and solubility profile
    • Adjusted for downstream blending compatibility and final hue requirements

    Downstream process integration

    • Fed to azotization and coupling reactors for formation of aryl diazonium compounds
    • Combined with coupling agents to generate mono- and di-azo dye bases
    • Direct feed to pigment precipitation units for insoluble dye forms

    Final product types

    • Water-soluble textile dyes
    • Inkjet printer pigment dispersions
    • Plastics colorants for engineering polymers

    4. Specialty Polymeric Material Synthesis

    Chemical formulators use this aromatic nitro compound as a comonomer or chain modifier in the synthesis of specialty polymers for advanced engineering applications. Fluorination and nitro groups impart both chemical resistance and altered refractive index, making the output suitable for coatings, films, and electrical encapsulants. Precise adjustment of addition rates and curing environments ensures controlled chain length and crosslink density. Raw material feed must meet strict specifications for residual alkali and particle size to avoid final product defects.

    Industry compliance standards

    • ISO 9001:2015 for industrial polymer production
    • UL 94 Flame Class for encapsulation materials
    • RoHS Directive for electronics-associated polymers
    • ASTM D638 for physical property testing

    Typical usage ratio

    • 0.1 to 0.8 weight percent of total monomer mass, variable by required mechanical and dielectric properties
    • Modified upward for increased chemical resistance applications

    Downstream process integration

    • Added at pre-polymerization blending stage with other aromatic or aliphatic monomers
    • Participates in chain-extension or cross-linking reactions initiated under controlled heating
    • Direct feed to continuous casting or extrusion lines for final form shaping

    Final product types

    • High-performance engineering plastics
    • Chemical-resistant polymer coatings
    • Optical films for electronics and displays

    5. Fine Chemical Intermediate for Electronic Materials

    Manufacturers of advanced electronic materials employ this compound as a fine intermediate, exploiting its high purity and regioselective reactivity for functionalization steps in liquid crystal and organic semiconductor synthesis. Strict control over trace metal and particle contamination is mandatory due to downstream device performance sensitivity. Integration within closed-loop production environments safeguards material integrity and prevents cross-contamination during scale-up.

    Industry compliance standards

    • IATF 16949 for automotive electronics supply chain
    • IPC-4101B/123 for base materials in PCB laminates
    • REACH Substances of Very High Concern (SVHC) assessment protocols
    • IEC 61249-2-7 halogen content limits

    Typical usage ratio

    • Typically 0.15 to 0.4 mol equivalents per functionalization batch, calculated based on electronic grade material demand
    • Adjusted to ensure consistent molecular alignment and optoelectronic uniformity

    Downstream process integration

    • Fed to aryl amination and coupling units in organic electronic material synthesis modules
    • Integrated into thin-film precursor processing lines
    • Transitions to downstream purification and substrate deposition operations

    Final product types

    • Liquid crystal monomers for display technologies
    • Organic semiconductors for flexible electronics
    • Specialty chemical intermediates for printed circuit boards
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    Certification & Compliance
    More Introduction

    Understanding 4-Fluoro-2-Nitrobenzeneamine: Purpose, Value, and Hands-On Perspective from the Manufacturer

    Direct from the Factory Floor: What Matters in Producing 4-Fluoro-2-Nitrobenzeneamine

    Chemical production often comes down to crafting the right molecule with consistency, purity, and reliability. Over decades on the job, I’ve learned that 4-Fluoro-2-Nitrobenzeneamine stands as a foundation for countless specialty projects around the world—especially across pharmaceuticals, agrochemicals, and dye intermediates. Our expertise grows from being hands-on, not just supplying, but actively engaging in the process. We scrutinize every detail during manufacturing, which shows in the stability and predictability of the batches leaving our plant.

    Scientists and engineers searching for dependable building blocks often turn to this compound because of its unique orientation of functional groups on the benzene ring: a fluorine atom at the para-position and a nitro group ortho to the amine. This may sound like dry technical jargon, but it’s crucial. The substitution pattern in 4-Fluoro-2-Nitrobenzeneamine (CAS number 450-91-9) creates a molecule that can undergo further transformation for specialty end groups—giving greater flexibility in synthesis compared to simpler aminobenzenes or less reactive nitroanilines. The result: easier downstream chemistry and higher selectivity in product development.

    From Raw Material to Fine Chemical: The Realities of Large-Scale Synthesis

    While lab-scale processes make it look simple, the real hurdles start on the production floor. Scaling up involves more than just multiplying your recipe. Batch-to-batch consistency lies at the heart of our operations. In practice, raw fluorinated nitrobenzenes demand precise temperature control, careful solvent management, and a grown respect for exothermic reactivity. Inconsistent impurities or temperature spikes can immediately ruin quality, forcing costly rework or, in the worst case, disposal. Years of real-world production have tuned our systems, so the end user receives material that performs as expected—with no surprises, no unpleasant batch-to-batch variation.

    The model of 4-Fluoro-2-Nitrobenzeneamine that we supply usually appears as a pale yellow to beige crystalline powder. What sets our approach apart is not just the color or form, but the purity cut-offs we enforce after high-vacuum distillation or crystallization and the characterization performed by our in-house HPLC and GC-MS systems. Typical purities exceed 99%, but we have found that careful monitoring of trace metals and solvent residues can make or break performance in sensitive downstream reactions such as catalytic hydrogenations or Suzuki couplings.

    What Does This Compound Actually Do?—Beyond the Molecular Formula

    Industries now routinely require more than just a bucket of aniline or a plain nitrobenzene; niche reactivities call for fine-tuned building blocks. Take medicinal chemistry and its constant drive for novel scaffolds. The trifecta of fluoro, nitro, and amino groups on this specific benzene ring enables site-selective functionalization, a key advantage during lead optimization. Unlike many off-the-shelf aminobenzenes, our fluorinated nitroaniline derivative slots directly into synthetic schemes for kinase inhibitors or anti-infective candidates. One example: the fluorinated amino group confers metabolic stability—crucial for improving half-life in drug candidates.

    Process chemists in agrochemical development have also leaned on this molecule, using its electron-withdrawing nitro group to facilitate subsequent nucleophilic aromatic substitution. The selective fluoro group creates opportunities for ligand-coupling, helping drive green chemistry trends that reduce hazardous byproducts. In dye chemistry, 4-Fluoro-2-Nitrobenzeneamine’s combination of reactivity and color-modifying properties allows for tailored pigment design, supporting vivid, thermally stable colorant options demanded by today’s multi-industry markets.

    Beyond Commodity: Where Our Version Stands Apart

    Most differences in chemical building blocks stem from the production approach. In the early years, differentiation often centered on simple purity metrics. With 4-Fluoro-2-Nitrobenzeneamine, that’s only the start. Many producers rely on cost-saving shortcuts, or accept wider impurity ranges to boost output. In our experience, such trade-offs may pass a cursory external audit, but surface flaws during tough downstream syntheses—especially in pharmaceutical or electronic materials, where side products can ruin both yield and regulatory compliance.

    Our method keeps focus on molecular integrity and process transparency. Material qualification at our site isn’t just paperwork. Trained QC chemists monitor reaction kinetics, impurity profiles, and lot histories, catching trends before they become issues. Requests for custom grades—such as ultra-dry powder, particle size tuning for solid-phase synthesis, or minimized halide content—start with direct, candid discussion between our chemists and the client’s technical team. This formula, built on real production experience, helps achieve the best possible result for specialized needs without adding unnecessary steps or costs.

    Working Around Limitations and Addressing Issues Upfront

    Major bottlenecks with nitroaniline derivatives often revolve around safety and waste handling. Few outside the industry appreciate the real challenges that come with scaling reactions involving nitro groups and halogen substituents—particularly under high-heat or catalytic conditions. Over years, we have upgraded reactor and distillation technology to mitigate risk and keep yields high. In practice, this means active scrubbing systems for off-gassing, robust secondary containment, and careful solvent recovery. Skilled operators know that a minor lapse spells trouble; institutional knowledge makes all the difference.

    Another persistent challenge: minimizing trace contaminants that can sabotage advanced catalysis or downstream biochemistry. A producer’s work does not end at “good enough for sale.” We invest in advanced analytical feedback loops, process filtration, and additional drying. We analyze for low-ppm levels of residual solvents and trace heavy metals—parameters that do not concern traders or resellers, but matter greatly in real-world industrial use. This consistently pays off for customers working in regulated environments, where trace volatiles or cross-contamination mean lost time, failed campaigns, or regulatory headaches.

    Application-Centric Manufacturing: Bridging the Lab and Plant

    We have seen a shift where buyers want more than just raw material—they want consultation, troubleshooting advice, and a route to scale-up. Our track record shows real value here. Project technical leads approach us with questions about reactivity under microwave conditions, hydrolysis under mild acid, or behavior during solid-phase coupling. Every month brings new feedback, prompting us to revisit reaction work-ups or drying cycles. In one case, a pharma client struggled with a stubborn byproduct during hydrogenation. With a direct dialog about our process intermediates and micro-impurity levels, we jointly developed an alternative work-up that allowed their route to succeed.

    We don’t shy from raw truth: sometimes, production economics clash with technical needs. There are limits to purity, and at times the most “ideal” grade is economically unsound. Open discussion early in the process saves resources and matches expectation to reality. The feedback loop between our manufacturing floor and users shapes ongoing process design—lessons learned are rolled into subsequent batches.

    The Role of 4-Fluoro-2-Nitrobenzeneamine Amidst Competing Analogues

    Chemists frequently ask how this product compares to other aromatic amines or nitro-substituted compounds. Over time, I’ve seen that subtle differences in reactivity can mean breakthrough or dead-end for a synthetic target. While classic nitroanilines answer for many bulk needs, once selective functionality is required, these lack precision. 4-Fluoro-2-Nitrobenzeneamine steps in effectively due to the electron-donating and withdrawing effect of its substituents. Modifying reactivity patterns, it favors selective substitutions at predefined ring positions—significantly more adaptable than single-substituted anilines or fluorobenzenes alone.

    Comparing with its close relatives, such as 4-chloro or 4-bromo derivatives, the fluoro group’s small size and high electronegativity allow for cleaner, more predictable reaction outcomes, often less steric hindrance, and greater stability in oxidative conditions. These traits enable successful extension to multi-step synthesis, increasing isolation efficiency and overall yields.

    Higher-tier alternatives, such as polyfluorinated or trifluoromethylated nitroanilines, offer advanced properties but at sharply rising cost and decreased reaction generality. Our compound balances performance and affordability. Customers working in combinatorial chemistry have cited improvement in reaction cleanliness and less “off-pathway” side product formation after switching to our version of this product.

    A Hands-On Understanding of Specifications and Quality Calls

    Specifications only matter if they translate to reliable performance. We produce 4-Fluoro-2-Nitrobenzeneamine in standard batch sizes, supplying quantities tailored to research or pilot plant scale. Purity is only part of the equation. Key attributes such as particle morphology, solubility in specific solvents, and moisture content affect how the compound behaves in both manual and automated systems.

    We have tailored drying and milling steps based on direct customer feedback. Dye manufacturers, who often dissolve it in organic bases, asked for a crystal fraction that minimizes particulate hang-up and delivers rapid dissolution. Pharma innovators using solid-phase peptide synthesis requested product lots with narrow particle size distribution, avoiding caking and streamlining their material handling. Our plant installed new screening and drying systems to deliver on these needs—never as a checkbox exercise, always informed by practical outcomes. This is where manufacturer experience makes the difference.

    Addressing Safety and Environmental Responsibilities

    As a chemical manufacturer, we can’t overlook environmental impact and worker safety. Nitro- and fluorinated intermediates derive from potentially hazardous chemistry. Years of professional work made clear that environmental compliance rises in importance annually, not just from legislation but from the collective drive of our industry. Investment in efficient solvent recovery, closed handling, and responsible effluent management aren’t just optional; they help maintain our license to operate and reduce risk for our customers down the chain.

    Exposure controls—ranging from proper PPE and automated containment, to real-time monitoring for air- and water-borne emissions—bring daily experience to the forefront. No two runs or operators are quite the same; culture matters. We focus on continuous improvement, learning from incidents, and running thorough hazard analyses during each process update. These steps may not seem obvious to the buyer but make a world of difference in reliable global supply.

    Building a Bridge: Collaboration Beyond the Sale

    Product stewardship extends far beyond the bulk shipment. We often work with users who must modify purification schemes, optimize reaction conditions, or align analytical testing to suit this compound’s behavior. Questions about shelf-life, storage temperature, or compatibility with uncommon solvents arise often. Our history of direct, open communication creates trust and problem-solving, helping avoid costly setbacks or safety missteps.

    For international shipments, logistics coordination and documentation transparency become critical—ensuring every drum or pallet meets import, packaging, and hazard labeling rules in the destination country. We proactively support these needs, offering the paperwork, analytical validation, and global regulatory insight our customers need—freeing them to focus on what they do best.

    Why Quality, Experience, and Consistency Outlast Pretense or Cutting Corners

    From manufacturing floor to final formulation, our approach keeps clear that supply of 4-Fluoro-2-Nitrobenzeneamine is not a narrowly defined procurement exercise. Only by threading technical expertise, on-the-ground experience, and ongoing customer engagement can a manufacturer deliver high-value chemical components. Market surges and supply turbulence happen; established, rigorous processes and industry learning stand between a smooth project and a costly failure.

    Nobody gets to mastery through shortcuts. Each kilogram shipped reflects the cumulative impact of safe practices, dedicated chemists, and an openness to feedback and adaptation. This compound’s importance will continue to grow alongside the industries it supports. With each new challenge or application, we remain engaged—not as a commodity seller, but as a committed manufacturing partner who knows the nuances and realities of the trade.