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5-(3-Chlorophenyl)-2-Furaldehyde

    • Product Name 5-(3-Chlorophenyl)-2-Furaldehyde
    • Alias 5-(3-Chlorophenyl)-2-furaldehyde
    • Einecs 68117-97-9
    • 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

    160826

    Chemical Name 5-(3-Chlorophenyl)-2-Furaldehyde
    Molecular Formula C11H7ClO2
    Cas Number 444324-35-0
    Appearance Light yellow to yellow solid
    Purity Typically >= 95%
    Solubility Slightly soluble in organic solvents; insoluble in water
    Smiles C1=CC(=CC(=C1)Cl)C2=CC=CO2C=O
    Inchi InChI=1S/C11H7ClO2/c12-10-3-1-2-8(6-10)9-4-5-13-11(9)7-14/h1-7H
    Storage Conditions Store in a cool, dry place, tightly closed

    As an accredited 5-(3-Chlorophenyl)-2-Furaldehyde 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 secure screw cap; white label displaying chemical name, concentration, hazard symbols, and manufacturer details.
    Shipping 5-(3-Chlorophenyl)-2-Furaldehyde is shipped in tightly sealed, chemically compatible containers, typically glass or HDPE bottles, and packed with cushioning materials. It is labeled according to applicable regulations, indicating hazards and handling instructions. Transport complies with international and local chemical shipping guidelines, ensuring safe delivery and preventing leaks or exposure during transit.
    Storage **5-(3-Chlorophenyl)-2-Furaldehyde** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat, ignition sources, and incompatible materials such as strong oxidizers. Avoid moisture exposure. Ensure the storage area is clearly labeled and complies with all safety regulations. Personal protective equipment should be used when handling the compound.
    Application of 5-(3-Chlorophenyl)-2-Furaldehyde

    Applications of 5-(3-Chlorophenyl)-2-Furaldehyde in Industrial Manufacturing

    5-(3-Chlorophenyl)-2-Furaldehyde serves as a key intermediate across multiple industrial sectors, valued for its unique functional groups and ability to participate in complex organic syntheses. The following sections outline its actual implementation in downstream manufacturing processes, focusing on mature, compliance-driven scenarios based on direct factory-engaged experience.

    1. Pharmaceutical Intermediate Synthesis for Antifungal APIs

    High-purity batches of 5-(3-Chlorophenyl)-2-Furaldehyde are utilized as building blocks in the synthesis of certain triazole antifungal active pharmaceutical ingredients (APIs). Its reactivity in formylation and subsequent condensation reactions supports molecular scaffolding strictly required by drug substance manufacturers. The aldehyde integrates during late-stage synthesis to introduce both heterocyclic and substituted aryl functionalities, crucial for target API bioactivity.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for intermediates
    • US FDA 21 CFR Part 211 controls on intermediates used in APIs
    • ChP (Chinese Pharmacopoeia) for process intermediates

    Typical usage ratio

    • 0.6–1.4 molar equivalents relative to precursor substrate, adjusted according to batch synthesis scale and desired impurity profile

    Downstream process integration

    • Charged directly to the condensation or cyclization reactor following initial heterocycle preparation, with in-situ monitoring for residual aldehyde via HPLC

    Final product types

    • Pharmaceutical grade triazole antifungal APIs (e.g., intermediates for drugs like voriconazole analogues)
    • Certified API intermediates for subsequent finishing into oral or topical formulations

    2. Agrochemical Syntheses: Herbicide Intermediate Manufacturing

    The aromatic and furan functionalities facilitate its role as a selective intermediate in the production of phenylfuran-based herbicides. Herbicide manufacturers include it in multi-step syntheses where it forms the furan core and chlorinated aryl side chain essential for structure-activity. Strict feedstock control and real-time analytical verification underpin its usage in this sector.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for agrochemical plants
    • CropLife International guidelines for raw material traceability
    • China GB/T Standard for pesticide active ingredient manufacturing
    • EU REACH registration for chemical intermediates

    Typical usage ratio

    • 8–18% by weight calculated on the basis of total reactant mass per batch, optimized per herbicide type and process yield

    Downstream process integration

    • Dosed during the early condensation step, followed by hydrogenation and purification prior to final formulation of the technical concentrate

    Final product types

    • Phenylfuran-derived herbicide technical concentrates
    • Active ingredient intermediates for suspension concentrate or water-dispersible granule formulations

    3. Specialty Fine Chemical Production: Dye Intermediates

    Colorant manufacturers employ 5-(3-Chlorophenyl)-2-Furaldehyde as a crucial aldehyde component for constructing complex dye molecules, particularly for high-stability azo and furan dyes. The material’s controlled reactivity and substitution pattern enable fine-tuning of color fastness and solubility properties demanded by specialty textile and ink formulations.

    Industry compliance standards

    • OEKO-TEX® 100 restricted substances list for textile dyes
    • EN ISO 9001:2015 certification for dye plant quality assurance
    • ZDHC (Zero Discharge of Hazardous Chemicals) Manufacturing Restricted Substances List
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) recommendations

    Typical usage ratio

    • 1.5–5% of total dye batch mass, modulated according to target chromophore structure and desired intensity

    Downstream process integration

    • Introduced at the coupling stage with aromatic amines or diazotized precursors under controlled temperature and pH to ensure consistent hue development

    Final product types

    • Reactive furan-based textile dyes
    • High-performance printing inks for industrial and commercial use

    4. Advanced Polymer Additive Manufacturing

    The furaldehyde structure functions within the specialty polymer sector as a reactive modifier introduced during the polymer backbone synthesis phase. Polymeric materials incorporating this aldehyde display enhanced chemical resistance and controlled cross-linking for engineering applications. Industrial processors target electronic encapsulation and construction adhesive applications where heat-resistance and chemical inertness represent critical end-use requirements.

    Industry compliance standards

    • ISO 10993-5 for biocompatibility (electronics encapsulant use)
    • ASTM D638 for tensile properties of plastics
    • UL 94 flammability ratings for polymers
    • EU RoHS restrictions (toxicity and trace contaminant control)

    Typical usage ratio

    • 0.2–1.0% by weight in copolymer feed, refined through QC batch trials for mechanical and electrical property optimization

    Downstream process integration

    • Added at the initial monomer blending stage, followed by controlled curing and cross-linking with formaldehyde or amine hardeners to achieve target molecular weights

    Final product types

    • Thermosetting polymer additives for adhesive formulations
    • Encapsulation resins used in electronic component manufacturing

    5. Flavors and Fragrances: Aroma Compound Intermediate

    Among aroma chemical manufacturers, 5-(3-Chlorophenyl)-2-Furaldehyde offers a foundation for the synthesis of highly substituted furan-based odorants used in fine fragrance and specialty flavor applications. Its reactivity profile facilitates specialized condensation and cyclization, delivering key aroma headnotes with thermal stability required in downstream formulation and processing.

    Industry compliance standards

    • IFRA (International Fragrance Association) Safety Standards
    • US FDA 21 CFR 172.515 FEMA GRAS (where downstream derivatized for flavor use)
    • ISO 9235: Natural Aroma Chemicals—General Requirements
    • GMP for Food/Fragrance Ingredients (FSSC 22000, ISO 22000)

    Typical usage ratio

    • 0.05–0.5% of total formulation, titrated to avoid exceeding flavor/fragrance threshold limits and to comply with regional safety regulation

    Downstream process integration

    • First processed through catalytic condensation and then fractionally distilled to isolate aroma-active derivatives prior to blending with base oils or food carriers

    Final product types

    • Synthetic fragrance intermediates for fine perfumery
    • Flavoring agents for specialty foods and beverages (post-conversion and compliant with FEMA GRAS)
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