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2-Fluoro-4-Nitroaniline

    • Product Name 2-Fluoro-4-Nitroaniline
    • Alias 2-Fluoro-4-nitrobenzenamine
    • Einecs 226-954-1
    • 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

    578102

    Chemical Name 2-Fluoro-4-Nitroaniline
    Cas Number 369-37-1
    Molecular Formula C6H5FN2O2
    Molecular Weight 156.12 g/mol
    Appearance Yellow solid
    Melting Point 109-112 °C
    Solubility In Water Slightly soluble
    Smiles c1cc([N+](=O)[O-])ccc1F
    Inchi InChI=1S/C6H5FN2O2/c7-4-1-2-5(9)3-6(4)8-10/h1-3H,(H2,8,9,10)
    Synonyms 2-Fluoro-4-nitrobenzenamine
    Pubchem Cid 136551
    Storage Temperature Room temperature
    Hazard Statements Harmful if swallowed, causes skin irritation

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

    Packing & Storage
    Packing A 25-gram amber glass bottle with a white, tamper-evident cap, labeled "2-Fluoro-4-Nitroaniline" and safety hazard symbols.
    Shipping 2-Fluoro-4-Nitroaniline should be shipped in tightly sealed containers, protected from physical damage and moisture. Transport in compliance with local, national, and international regulations for hazardous chemicals. Ensure appropriate labeling and documentation. Use secondary containment and cushioning to prevent spillage or leakage during transit. Store and ship at ambient temperature unless specified otherwise.
    Storage Store 2-Fluoro-4-nitroaniline in a tightly closed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from light and moisture. Ensure appropriate chemical labeling, and keep away from heat sources or ignition. Use secondary containment if possible, and limit access to trained personnel only. Handle with appropriate personal protective equipment.
    Application of 2-Fluoro-4-Nitroaniline

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

    As the original manufacturer of 2-Fluoro-4-Nitroaniline, we focus on consistent quality and suitability for diverse downstream processing. Our material supports critical intermediate roles within several industrial value chains. Below, we detail primary application segments, each with specific compliance, process, and integration factors validated by large-scale users.

    1. Pharmaceutical Intermediate Synthesis

    2-Fluoro-4-Nitroaniline serves as a key building block in the preparation of active pharmaceutical ingredient (API) intermediates, especially in the anti-infective and anti-inflammatory drug categories. Pharmaceutical companies favor its electron-withdrawing groups for selective aromatic substitution, supporting complex molecule assembly. Consistency in purity and impurity control is essential due to strict downstream regulatory environments, and QC labs assess each lot for compliance before use in multi-stage synthesis processes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP for Starting Materials, Directive 2001/83/EC
    • USP/EP/JP Pharmacopoeial guidance on intermediate use, as applicable to downstream API
    • REACH registration for intermediates

    Typical usage ratio

    • 1.2–2.0 molar equivalents per main API precursor, optimized based on target yield and impurity pathway control in pilot-scale route development

    Downstream process integration

    • Charged during initial condensation or coupling stage, typically after solvent exchange and control of basic/acidic conditions to minimize undesired side reactions
    • Purity pivotal before downstream hydrogenation or amination

    Final product types

    • Nitrofluoroaniline-derived antibiotics
    • Intermediates for anti-tumor agents
    • Non-steroidal anti-inflammatory drug precursors
    • Specialty heterocyclic APIs using fluoroaromatic linkers

    2. Agrochemical Intermediate Production

    Major agrochemical groups utilize this material as a core intermediate for synthesizing active ingredients in herbicides and fungicides where selective fluorination and nitration allow for targeted biological activity. Process chemists prefer its substitution pattern for cost-effective access to downstream heterocycles and benzimidazoles. Each shipment must align with regional registration status, thorough certification, and batch-to-batch reproducibility.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP) for test item manufacturing
    • FAO/WHO Specifications and Codes of Practice
    • China ICAMA and EPA TSCA notification for agrochemical intermediates
    • REACH and CLP compliance for import/export in EEA markets

    Typical usage ratio

    • 0.8–1.5 molar equivalents per final active ingredient unit, adjusted according to yield and by-product management in scale-up reactions

    Downstream process integration

    • Introduced early in the synthetic route for chloro-substitution or cyclization
    • Integrated into closed-system reactors with in-line monitoring for residual nitration by-products

    Final product types

    • Selective herbicide actives (e.g., substituted benzimidazoles)
    • Fungicide precursors for cereal crops
    • Seed treatment intermediates with fluoro/nitro moieties
    • Safener additives for crop protection formulations

    3. Dyes and Pigments Synthesis

    2-Fluoro-4-Nitroaniline enters the dye and pigment industry as an intermediate for synthesizing disperse and metal-complex dyes. Color chemists rely on its stable aromatic framework and substituent effect to modify color fastness and shade. Control over impurity profiles is crucial for consistent coloration in textile and plastics applications, while all operations prioritize occupational safety and environmental compliance during synthesis and finishing.

    Industry compliance standards

    • EN 71-3 Safety of Toys (Migration of Certain Elements)
    • Oeko-Tex Standard 100 for dye limits in textiles
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • GHS/CLP labelling requirements for import/export

    Typical usage ratio

    • 0.9–1.3 equivalents per target azo or anthraquinone dye molecule, tailored to chromophore design

    Downstream process integration

    • Used in diazotization or coupling reactions following purification and solvent replacement
    • Entry point determined by targeted color index and intended application (textile, plastics)

    Final product types

    • Disperse dyes for synthetic fibers
    • Reactive dyes for cellulosic substrates
    • High-performance pigments for plastics
    • Colorants in printing inks and leather applications

    4. Specialty Fluorochemical Manufacturing

    In the specialty chemicals sector, the compound finds use as a precursor for advanced fluorinated materials. Manufacturers use it to introduce both electron-deficient nitro groups and fluorine atoms onto aromatic rings, facilitating downstream modifications for engineering plastics, photoinitiators, and advanced materials. Lot-to-lot traceability and documentation are essential, given downstream applications in electronics and photonics. All manufacturing adheres to customer-specific and regulatory-driven purity profiles for functionally critical end uses.

    Industry compliance standards

    • ISO 9001:2015 Quality Management in chemical manufacturing
    • RoHS Directive 2011/65/EU for restricted substances in electronics
    • UL 94 flammability test documentation for polymer additives
    • REACH substance of very high concern (SVHC) guidelines

    Typical usage ratio

    • 0.7–1.4 equivalents per monomer or functional additive batch, finetuned based on targeted modification degree and downstream purification yield

    Downstream process integration

    • Dosed during the intermediate building step leading to further fluorination or cross-coupling (e.g., Suzuki, Buchwald–Hartwig)
    • Purity confirmation prior to chemical vapor deposition or extrusion into engineering compounds

    Final product types

    • Fluorinated photoinitiators for UV-curing resins
    • Specialty polymers with engineered dielectric properties
    • Performance additives for polyimides
    • Fluorinated aryl intermediates for OLED and LCD display manufacturing
    Free Quote

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