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4-(4-Fluorobenzoyl)Butyric Acid

    • Product Name 4-(4-Fluorobenzoyl)Butyric Acid
    • Alias 4F-BzB
    • Einecs EINECS 425-040-4
    • 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

    201788

    Compound Name 4-(4-Fluorobenzoyl)butyric acid
    Chemical Formula C11H11FO3
    Molecular Weight 210.20 g/mol
    Cas Number 83432-60-8
    Appearance White to off-white solid
    Purity Typically >98%
    Melting Point 78-82°C
    Boiling Point No data available
    Solubility Soluble in DMSO, methanol, and ethanol
    Storage Conditions Store at room temperature, away from light and moisture
    Inchi Key XQRFHESHNLHPNP-UHFFFAOYSA-N
    Smiles C1=CC(=CC=C1C(=O)CCCC(=O)O)F

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

    Packing & Storage
    Packing The product is supplied in a 25g amber glass bottle with a secure screw cap, labeled clearly with chemical name and hazard warnings.
    Shipping **Shipping Description:** 4-(4-Fluorobenzoyl)butyric acid is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. Packages include clear hazard labeling and are handled in accordance with relevant chemical safety regulations. Transport is conducted via ground or air, with appropriate documentation, to ensure safe and compliant delivery.
    Storage 4-(4-Fluorobenzoyl)butyric acid should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature (15–25°C). Avoid sources of ignition and incompatible materials such as strong oxidizers. Label the container clearly and ensure access is restricted to trained personnel. Use appropriate personal protective equipment when handling.
    Application of 4-(4-Fluorobenzoyl)Butyric Acid

    Applications of 4-(4-Fluorobenzoyl)Butyric Acid in Industrial Manufacturing

    As a direct manufacturer with extensive experience in advanced aromatic acid intermediates, we provide 4-(4-Fluorobenzoyl)butyric acid for several downstream sectors. This material supports regulated syntheses across pharmaceuticals, agrochemicals, specialty polymers, and fine chemical intermediates, where precision and regulatory alignment guide every production stage.

    1. Pharmaceutical API Synthesis

    Pharmaceutical manufacturers use this raw material as a benzoyl moiety donor in the synthesis of specific active pharmaceutical ingredients, particularly in the development of anti-inflammatory and central nervous system (CNS) agents. Its fluorinated aromatic structure grants metabolic stability and improved pharmacokinetics. Process engineers directly introduce this intermediate into the acylation or condensation stages to construct advanced building blocks. Quality assurance teams employ stringent batch traceability to satisfy GMP and registration needs throughout the chain.

    Industry compliance standards

    • ICH Q7 GMP Guideline for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211
    • EU GMP Directive 2003/94/EC
    • Chinese Pharmacopoeia (when applicable for local supply)

    Typical usage ratio

    • 1.2 – 1.4 molar equivalents relative to primary amine/ketone reactants, adjustable depending on specific API synthesis route and yield optimization

    Downstream process integration

    • Introduced during acylation, condensation, or key step intermediate coupling in multi-step API synthesis flows
    • Serves as a protected intermediate that is deprotected or modified in downstream transformation steps

    Final product types

    • Anti-inflammatory drug actives for clinical development
    • CNS-targeted APIs with enhanced blood-brain barrier penetration
    • Small-molecule pharmaceutical intermediates for contract manufacturing
    • Research compounds for medicinal chemistry screening

    2. Agrochemical Active Ingredient Synthesis

    Agrochemical producers utilize this building block for synthesizing selective herbicide and plant growth regulator candidates, leveraging the fluoroaromatic functionality for increased bioactivity and environmental stability. Formulators precisely dose and activate this intermediate during active ingredient construction, commonly incorporating halogen management protocols and yield optimization steps. Continuous analytics ensure batch compliance and trace impurity elimination.

    Industry compliance standards

    • FAO/WHO Guidelines for Pesticide Specifications
    • OECD Principles of Good Laboratory Practice
    • REACH Regulation (EC) No 1907/2006 for chemical registration
    • ISO 9001 Quality Management for agrochemicals

    Typical usage ratio

    • 5–15% by mass, typically controlled according to the desired concentration and reactivity in heterocyclic or acylated herbicide precursor synthesis

    Downstream process integration

    • Added during pre-condensation of agrochemical active nucleus, often under alkaline or Lewis acid-catalyzed conditions
    • Processed in closed-systems to comply with halogenated waste handling and environmental safeguards

    Final product types

    • Herbicide technical concentrates (active ingredients before formulation)
    • Plant growth modification agents
    • Precursor compounds for patented crop protection formulations
    • R&D batches for new pesticide screening

    3. Specialty Polymer Modification

    Polymer manufacturers incorporate this specialty acid during functional monomer synthesis to build fluorinated polymer chains with controlled hydrophobicity, chemical resistance, and mechanical properties. Material scientists add this intermediate to improve adhesion and solvent resistance of engineered plastics used in demanding industrial environments. All input batches undergo chemical identity testing and end-use performance simulation to verify property distribution across the polymer matrix.

    Industry compliance standards

    • ISO 9001 Quality Management in polymers
    • ISO 14001 Environmental Management for chemical processing
    • REACH (Europe) and TSCA (US) for chemical content reporting
    • RoHS Directive for electrical/electronics applications, if incorporated into E&E polymers

    Typical usage ratio

    • 0.3 – 2 weight-% as a co-monomer or chain modifier, with precise dosing based on required fluorine incorporation and final plastic specification

    Downstream process integration

    • Fed into the monomer reactor during pre-polymerization or direct co-polymerization stages
    • May be used as a chain stopper or side-group modifier in functionalized copolymer architectures

    Final product types

    • Fluorinated engineering plastics for automotive housings
    • Specialty films with high barrier properties
    • Industrial coatings for anti-fouling applications
    • Electronic encapsulants with improved moisture resistance

    4. Fine Chemical Intermediate for Advanced Synthesis

    Fine chemical producers implement this benzoyl acid in multi-stage syntheses, especially where a para-fluorophenyl group is necessary for downstream reactivity or to impart electronic effects in final molecules. Chemists typically handle precise reaction monitoring and purification to enable reliable scale-up. All lots receive full traceability, and analytical teams document impurity profiles to support specialty chemical applications or additional contract manufacturing.

    Industry compliance standards

    • ISO 9001 and ISO 17025 for lab process traceability
    • PAT (Process Analytical Technology) for in-process monitoring
    • REACH registration for multi-tonne shipments within the EU
    • Standard operating procedures for specialty chemicals as per client NDA/MQA agreements

    Typical usage ratio

    • Variable, typically 0.5 – 3.5 equivalents depending on reaction partner and scale, with stoichiometry optimized according to conversion yield and downstream structure complexity

    Downstream process integration

    • Charged during key ring-forming, acylation, ortho/para-substitution, or other custom multistep syntheses
    • Isolated as a purified intermediate or carried through to subsequent transformations in batch campaigns

    Final product types

    • Specialty pharmaceutical intermediates beyond generic APIs
    • Advanced intermediates for catalyst ligand production
    • Performance additives for industrial blends
    • Custom-synthesized molecular probes and research reagents
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