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2-(4-Fluorophenyl)Benzaldehyde

    • Product Name 2-(4-Fluorophenyl)Benzaldehyde
    • Alias MFBA
    • Einecs 629-008-3
    • 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

    450844

    Chemical Name 2-(4-Fluorophenyl)Benzaldehyde
    Cas Number 446-14-0
    Molecular Formula C13H9FO
    Molecular Weight 200.21
    Appearance White to light yellow solid
    Melting Point 52-54°C
    Boiling Point 344.4°C at 760 mmHg
    Density 1.18 g/cm3
    Purity Typically >98%
    Smiles C1=CC=C(C=C1)C2=CC=C(C=C2)F
    Inchi InChI=1S/C13H9FO/c14-12-8-6-10(7-9-12)11-3-1-2-4-13(11)15/h1-9H
    Solubility Slightly soluble in water, soluble in organic solvents
    Refractive Index 1.618
    Storage Conditions Store at room temperature, protect from light and moisture
    Synonyms 2-(4-Fluorophenyl)benzaldehyde; o-(p-Fluorophenyl)benzaldehyde

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

    Packing & Storage
    Packing The chemical is packaged in a 25g amber glass bottle with a secure screw cap, labeled with hazard and identification information.
    Shipping 2-(4-Fluorophenyl)Benzaldehyde is shipped in tightly sealed containers, protected from light and moisture. It is classified as a chemical substance requiring proper labeling and documentation. Handling guidelines, including safety data sheets, are included to comply with regulatory standards. Transport follows local and international hazardous material shipping regulations.
    Storage 2-(4-Fluorophenyl)benzaldehyde should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from direct sunlight, moisture, and sources of ignition. It should be segregated from incompatible substances such as strong oxidizing agents. Proper labeling and handling are essential, and appropriate personal protective equipment should be used when handling the chemical.
    Application of 2-(4-Fluorophenyl)Benzaldehyde

    Applications of 2-(4-Fluorophenyl)Benzaldehyde in Industrial Manufacturing

    2-(4-Fluorophenyl)Benzaldehyde serves as a specialized intermediate in fine chemical, pharmaceutical, and advanced material synthesis. The chemical’s unique structure provides targeted reactivity for downstream transformations, supporting rigorous manufacturing protocols. Below, we detail genuine industrial application sectors where this raw material plays a critical role.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Antipsychotic Compounds

    Pharmaceutical manufacturers incorporate this benzaldehyde derivative as a key building block in the production of certain antipsychotic drug substances. The aldehyde group ensures selective condensation in multistep organic synthesis, especially in the preparation of benzyl alcohol analogues and diarylmethane frameworks. Production takes place under close regulatory oversight, demanding traceability at every batch and phase.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for active pharmaceutical ingredients
    • United States Pharmacopoeia (USP) quality monographs
    • EU EMA guidelines and GMP Part II
    • ISO 9001:2015 certified quality management systems

    Typical usage ratio

    • Applied at 0.8–1.3 molar equivalents in relation to core substrate, with minor adjustments based on route optimization and impurity profile control

    Downstream process integration

    • Utilized during the first coupling stage for diaryl compound backbone assembly, then followed by catalytic reduction or functionalization

    Final product types

    • Finished API for atypical antipsychotics (e.g., derivatives of fluorenone or fluorinated phenylpiperazines)
    • Reference standards for pharmaceutical QC laboratories

    2. Fine Chemical Intermediates for Liquid Crystal Synthesis

    Electronic material firms employ this compound as a tailored aromatic aldehyde precursor in the synthesis of liquid crystal monomers. It offers precise substitution patterns needed for controlling electro-optical behavior. Process conditions require anhydrous environments with high-purity input chemicals and careful by-product monitoring to ensure suitability in high-end display devices.

    Industry compliance standards

    • REACH Registration, Evaluation, Authorization and Restriction of Chemicals (EU)
    • RoHS Directive (EU)
    • ISO 14001:2015 for environmental management
    • Internal QC based on JIS K standards for liquid crystal chemicals

    Typical usage ratio

    • Introduced at 2–7% weight-to-weight in monomer mix; precise ratios depend on bespoke mesogen structure requirements and target dielectric anisotropy

    Downstream process integration

    • Employed in condensation or Wittig reactions for constructing biphenyl or terphenyl moieties; follows purification and final polymerization steps

    Final product types

    • Liquid crystal monomers for thin-film transistor LCD (TFT-LCD) production
    • High performance nematic and smectic liquid crystal mixtures

    3. Agrochemical Intermediate for Fungicide Synthesis

    Agrochemical producers adopt 2-(4-Fluorophenyl)Benzaldehyde in the synthesis of triazole-based fungicides. Its fluorinated aromatic ring ensures robust binding properties in the final agroactives. Manufacturing processes require chlorinated solvent handling and advanced waste management systems, monitored for trace contaminants and residual solvents.

    Industry compliance standards

    • FAO/WHO Specification for Pesticides
    • OECD Good Laboratory Practice (GLP) Principles
    • ISO 9001:2015 for process standardization
    • China National Standards for Agrochemicals (GB/T)

    Typical usage ratio

    • Ranges from 0.5–1.6 equivalents depending on targeted triazole ring formation efficiency and specific crop application spectrum

    Downstream process integration

    • Added as primary aromatic aldehyde for azole cyclization, preceding methylation or sulfonation steps to complete the active ingredient

    Final product types

    • Technical-grade triazole fungicides
    • Active ingredient concentrates for emulsion or granule formulations

    4. Specialty Materials – OLED and Photonic Polymer Manufacturing

    The electronics and photonics sector utilizes this chemical for the design of novel fluorinated aromatic scaffolds in organic light-emitting diode (OLED) emitters and high-refractive-index polymers. Its structural features enable the introduction of specific functionalities required for color accuracy and charge transport properties in thin films. Downstream fabrication is tightly controlled to prevent incorporation of trace impurities that could impact device reliability.

    Industry compliance standards

    • RoHS (Restriction of Hazardous Substances) compliance for electronic materials
    • UL 94 standards for flammability in polymers
    • ISO 14644 Cleanroom Standards in material handling
    • IEC 62321 determination protocols for substances in electrotechnical products

    Typical usage ratio

    • Commonly 1–5% molar in precursor cocktails; precise proportions based on chromophore intensity, quantum yield targets, and processing temperature windows

    Downstream process integration

    • Activated during Suzuki–Miyaura or Heck coupling to form extended π-conjugated structures, followed by casting, spin-coating, or vapor deposition

    Final product types

    • OLED emitter molecules for display backplanes
    • Polymeric photoresists and high-index optical polymers

    5. Synthesis of Fragrance Intermediates in Aroma Chemicals

    Aroma chemical manufacturers incorporate this benzaldehyde species for controlled aldol and condensation reactions, leading to complex aromatic ingredients found in perfumery and personal care products. Its fluorophenyl group imparts lasting scent profiles and improves hydrolytic stability. All reactions run under food-grade or cosmetic-grade protocols, with robust impurity and allergen screening.

    Industry compliance standards

    • IFRA Code of Practice for fragrance safety
    • Cosmetic Ingredient Review (CIR) recommendations
    • ISO 22716:2007 GMP for cosmetics
    • REACH compliance for aroma chemicals

    Typical usage ratio

    • Used at 1–4% in key intermediates, with adjustment based on end-use regulatory limits and stability studies of the target fragrance component

    Downstream process integration

    • Participates in aldol condensation and subsequent cyclization or etherification to yield macrocyclic or linear aroma lactones

    Final product types

    • Aroma intermediates for fine fragrances
    • Base chemicals for personal care and cosmetic scent formulations
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