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4-Fluorobenzamide

    • Product Name 4-Fluorobenzamide
    • Alias 4-Fluorobenzamide; Benzamide, 4-fluoro-; p-Fluorobenzamide; NSC 85708; RA 7
    • Einecs 209-783-2
    • 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
    VTB
    Specifications

    HS Code

    843667

    Chemical Name 4-Fluorobenzamide
    Cas Number 456-78-4
    Molecular Formula C7H6FNO
    Molecular Weight 139.13 g/mol
    Appearance White to off-white solid
    Melting Point 159-161 °C
    Boiling Point 324.6 °C at 760 mmHg
    Density 1.282 g/cm³
    Solubility Slightly soluble in water
    Smiles C1=CC(=CC=C1C(=O)N)F
    Inchi InChI=1S/C7H6FNO/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,(H2,9,10)
    Pubchem Cid 10597

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

    Packing & Storage
    Packing The 25g quantity of 4-Fluorobenzamide is supplied in a tightly sealed amber glass bottle with a secure screw cap.
    Shipping 4-Fluorobenzamide is shipped in tightly sealed containers, protected from moisture and light, and labeled according to hazardous material regulations. The package includes safety data sheets and complies with international transport guidelines. Handle with care, ensuring proper ventilation and use of personal protective equipment during unpacking and handling to prevent exposure.
    Storage 4-Fluorobenzamide should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible materials such as strong oxidizing agents. Keep the storage area secure and clearly labeled. Avoid moisture and sources of ignition. Handle using appropriate personal protective equipment to prevent inhalation, ingestion, or skin contact.
    Application of 4-Fluorobenzamide

    Applications of 4-Fluorobenzamide in Industrial Manufacturing

    4-Fluorobenzamide serves as a key intermediate in several specialized chemical production workflows. Our manufacturing process ensures high purity and quality to meet stringent industrial requirements. Below are principal downstream application scenarios drawn directly from practical global industrial usage.

    1. Pharmaceutical API Intermediate Synthesis

    This material plays a role in synthetic pathways for select active pharmaceutical ingredients. Producers utilize it specifically in benzamide-containing drug structures where fluorination improves metabolic stability and target specificity. Our customers apply it during late-stage intermediate formation, focusing on central nervous system (CNS) medications and select antipsychotic agents. Process development must consider trace element control and strict impurity profiles due to regulatory demands in regulated markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • European Pharmacopoeia monographs for CNS drugs
    • US FDA 21 CFR Part 211 (Finished Pharmaceuticals)
    • CEP (Certificate of Suitability) submissions in the EU

    Typical usage ratio

    • 0.6–1.2 molar equivalents per reaction stage, adjusted per target API and synthesis protocol

    Downstream process integration

    • Charged after initial condensation step; enters either amidation or direct substitution depending on pathway
    • Implementation requires anhydrous conditions and impurity monitoring via HPLC
    • Reacts at 90–120°C under nitrogen or argon atmosphere

    Final product types

    • Antipsychotic pharmaceutical ingredients
    • CNS drug intermediates
    • Pain management compound precursors

    2. Agrochemical Intermediate Production

    Formulation chemists in crop protection industries use this compound as a building block to synthesize modern benzamide-based herbicides and fungicides. Its introduction into target molecules enables adjustable lipophilicity and bioactivity profiles, necessary for new patentable active substances. Scale-up batches require precise mass balance and process reproducibility under controlled conditions, with routine sampling for structural verification.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Ingredients
    • ISO 9001:2015 Accredited QM Systems
    • REACH Registration for Industrial Chemical Use (EU)

    Typical usage ratio

    • 5–10% of total mass input per target molecule crop protection synthesis

    Downstream process integration

    • Added at nucleophilic coupling step following halogenation
    • Requires temperature control (80–110°C) and closed reactor due to reaction off-gas
    • Subsequent purification through acid-base extraction

    Final product types

    • Benzamide herbicide actives (preformulation stage)
    • Next-generation fungicide intermediate blends
    • Active ingredients for integrated pest management solutions

    3. Specialty Dyes and Pigments Synthesis

    The electronics and printing industries utilize this compound for building blocks in high-performance dye molecules. Its benzamide ring with fluorine substitution is integral to achieving desired color fastness, solvent resistance, and electrochemical properties. These applications involve multistep coupling reactions where stringent control of side-product formation and batch reproducibility is essential for QC release.

    Industry compliance standards

    • Global Organic Textile Standard (GOTS) for input chemicals
    • OEKO-TEX Standard 100, Class II
    • ISO 13320 for pigment particle size analysis
    • REACH SVHC Substances Monitoring

    Typical usage ratio

    • 2–7% of total mass in pigment or dye precursor synthesis

    Downstream process integration

    • Introduced post-sulfonation in azo-coupling or condensation reactions
    • Process includes solvent phase change and crystallization under vacuum conditions
    • QC via UV-Vis and FTIR ensures correct chromophore formation

    Final product types

    • High-stability inkjet printer dyes
    • Specialty electronics-grade colorants
    • Lightfast textile dyestuffs

    4. Liquid Crystal (LC) Intermediate Manufacturing

    Producers of advanced display technologies select this compound as a key intermediate for synthesizing fluorinated benzamide derivatives, which contribute favorable mesophase ranges and thermal stability in LC mixtures. These selections depend on high-purity input, with continuous monitoring of isomeric composition and moisture content. Multi-step batch operations commonly use inert atmosphere handling and specialized glass-lined reactors.

    Industry compliance standards

    • IEC 61249-2-21 Standard for Base Materials in Electronics
    • RoHS Directive 2011/65/EU (EU Restriction of Hazardous Substances)
    • REACH Annex XVII for chemicals in consumer electronics

    Typical usage ratio

    • Varies based on design: typically 0.5–2 parts by weight per 100 parts LC blend

    Downstream process integration

    • Feeding at first ring formation or subsequent acylation in LC precursor production
    • Temperature-controlled crystallization and solvent exchange steps
    • Analytical verification includes DSC and NMR for mesogen structure

    Final product types

    • Liquid crystal mixture precursors for display panels
    • LC compounds for advanced e-paper and signage
    • Specialty mesogens for scientific instrumentation

    5. Polymer Crosslinker Intermediate for Engineering Plastics

    Advanced polymer manufacturers deploy this intermediate in the synthesis of functional crosslinkers and chain extenders. The fluorine atom imparts enhanced thermal and chemical resistance, making derived polymers suitable for application in high-performance engineering materials. Production must apply rigorous cleaning protocols and real-time process analytics to avoid batch contamination and to maintain precise molecular weights.

    Industry compliance standards

    • ASTM D638/D3039 for polymer mechanical properties
    • ISO 9001:2015 for process documentation and traceability
    • Underwriters Laboratories UL 94 for flame retardancy rating

    Typical usage ratio

    • 1–3% of total monomer mass depending on targeted polymer network

    Downstream process integration

    • Introduced during the chain extension or crosslinking stage in copolymerization
    • Batch process control using GPC and FT-NIR monitoring
    • Post-reaction blending or direct molding for initial product shaping

    Final product types

    • Fluorinated engineering plastics
    • Thermoset resins for automotive and aerospace components
    • Specialty polymers for microelectronic encapsulation
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