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2,4-Difluorobenzaldehyde Oxime

    • Product Name 2,4-Difluorobenzaldehyde Oxime
    • Alias 2,4-DFBA Oxime
    • Einecs 693-358-5
    • 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

    408429

    Product Name 2,4-Difluorobenzaldehyde Oxime
    Cas Number 163633-79-8
    Molecular Formula C7H5F2NO
    Molecular Weight 157.12 g/mol
    Appearance White to off-white solid
    Melting Point 73-77 °C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=CC(=C(C=C1F)F)C=NO
    Inchi InChI=1S/C7H5F2NO/c8-6-1-2-7(9)5(3-6)4-10-11/h1-4,11H
    Storage Conditions Store at 2-8 °C, keep container tightly closed

    As an accredited 2,4-Difluorobenzaldehyde Oxime 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, tightly sealed with a plastic screw cap, labeled with product name, purity, CAS number, and hazard symbols.
    Shipping 2,4-Difluorobenzaldehyde Oxime should be shipped in tightly sealed containers under dry, cool conditions, protected from light and incompatible substances. Proper labeling is required, adhering to local, national, and international regulations. Transport in accordance with hazardous material guidelines, ensuring secure packaging to prevent leaks and exposure during transit.
    Storage 2,4-Difluorobenzaldehyde Oxime should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect it from direct sunlight, moisture, and heat. Proper chemical labeling and secondary containment are recommended to prevent accidental exposure or spills. Store according to all applicable chemical safety regulations.
    Application of 2,4-Difluorobenzaldehyde Oxime

    Applications of 2,4-Difluorobenzaldehyde Oxime in Industrial Manufacturing

    As a specialized manufacturer of 2,4-Difluorobenzaldehyde Oxime, our facility provides consistent quality for industrial customers integrating this material into advanced chemical synthesis. The following application scenarios detail real downstream processes where this raw material delivers technical and compliance value in everyday production.

    1. Pharmaceutical Intermediate Synthesis for Active Pharmaceutical Ingredients (APIs)

    In the pharmaceutical sector, 2,4-Difluorobenzaldehyde Oxime acts as a building block for synthesizing fluorinated intermediates required in antihypertensive and antiviral drug manufacturing. Its specific difluoro substitution supports the introduction of metabolically stable groups into API molecules, enhancing final product profiles. The material is introduced at the initial condensation or protection steps, reacting with amine or acid partners under controlled temperature and pH, with formulation concentration adjusted based on molecular target and subsequent synthetic steps. Pharmaceutical-grade supply requires certified traceability throughout batch production, and rigorous analytical verification during both incoming inspection and post-reaction QC.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients (APIs)
    • EU GMP Part II (APIs)
    • USP-NF and European Pharmacopoeia for relevant impurity testing
    • ISO 9001 Quality Management System

    Typical usage ratio

    • Applied at molar ratios of 0.90 to 1.05 per target intermediate, depending on synthetic route and required conversion efficiency. Slight molar excess or deficit is determined by desired yield and minimization of by-products.

    Downstream process integration

    • Added in the oxime protection stage or direct condensation with amines during early-stage intermediate synthesis, preceding deprotection or further fluorination.

    Final product types

    • Antihypertensive drug intermediates (e.g., fluorinated pyridine derivatives)
    • Antiviral API precursors
    • Specialty small-molecule pharmaceutical compounds for clinical pipelines

    2. Agrochemical Active Ingredient Manufacturing

    Leading agrochemical companies incorporate 2,4-Difluorobenzaldehyde Oxime in the multi-step synthesis of advanced fluorinated herbicide and fungicide actives. Its chemical structure enables selective introduction of difluorinated aromatic rings into target molecules, providing critical improvement in field persistency and resistance properties. During scale-up, the raw material is combined with specific acetyl or sulfonamide partners via catalyzed reactions, requiring controlled pH and solvent choices to maximize selectivity. Formulation dosing is optimized by final product efficacy data and regulatory limits on total fluorine content in outflow.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001 Quality Management System
    • European Union Regulation (EC) No 1107/2009 (Plant Protection Products)
    • China GB2763 for pesticide residue control

    Typical usage ratio

    • Included at 0.85 to 1.10 mol equivalents relative to the main reactant in the active ingredient synthesis step, based on the desired final substitution pattern and conversion yield, optimized during pilot runs.

    Downstream process integration

    • Charged at the aromatic oxime formation or halogenation stages, prior to the construction of the full active core scaffold. Real-time reaction monitoring controls addition rate and temperature.

    Final product types

    • Difluorinated herbicide actives (e.g., novel triazoles or substituted phenylpyridines)
    • Fungicide intermediates with enhanced weathering resistance
    • Crop protection molecule building blocks

    3. Electronic Chemicals – Synthesis of Advanced Organic Semiconductors

    Within the electronic materials industry, manufacturers utilize 2,4-Difluorobenzaldehyde Oxime as a precursor in producing difluorinated aromatic monomers for use in advanced polymer semiconductors and organic light-emitting diode (OLED) emitters. The oxime group enables specific functionalization routes to achieve controlled solubility and electronic properties in the target intermediates. Product is dosed in precision-controlled batch or continuous-flow reactors, with purity and trace metals stringently monitored to meet strict device manufacturing criteria. The concentration and addition strategy depend on oligomer chain length targets and ultimate film formation characteristics.

    Industry compliance standards

    • IPC-4101E Electronic Interconnect Material Specification
    • IEC 61249-2 for base materials standards
    • ISO 14001 Environmental Management (manufacturing facilities)
    • RoHS Directive 2011/65/EU (lead and halogen content limits for electronic components)

    Typical usage ratio

    • Formulated at 0.95–1.08 mol equivalents per coupling partner in initial monomer formation, with dose refined for target molecular weight control and defect mitigation.

    Downstream process integration

    • Integrated during the monomer synthesis step, typically via oxime-condensation or reduction, prior to polymerization into functional electronic materials.

    Final product types

    • Organic semiconductors for display technology
    • Difluorinated monomers in advanced dielectric materials
    • OLED intermediate compounds

    4. Fine Chemical Synthesis for Specialty Chemical Building Blocks

    In the fine chemical manufacturing sector, the oxime derivative serves as a strategic intermediate for constructing fluorinated benzene and pyridine derivatives, which are subsequently functionalized into advanced specialty chemicals. The material enters reactions such as Beckmann rearrangement, nucleophilic aromatic substitution, or selective oxidations, where its controlled reactivity allows for tailored product distribution shaped by customer specifications. Dosage and reaction conditions are customized after bench trials and scaled in batch or fed-batch reactors for reliability and minimization of unwanted side products.

    Industry compliance standards

    • REACH Regulation (Registration, Evaluation, Authorisation and Restriction of Chemicals), EU
    • ISO 9001 Quality Management System
    • Globally Harmonized System of Classification and Labelling of Chemicals (GHS)
    • Responsible Care Management System for specialty chemical producers

    Typical usage ratio

    • Dosed at 0.95–1.15 mol per equivalent target, depending on subsequent synthetic transformations and customer specification for purity/yield optimization.

    Downstream process integration

    • Charged at the relevant oxime formation, reduction, or rearrangement step for downstream functional group placement, before isolation, and purification of advanced intermediates.

    Final product types

    • Fluorinated benzene and pyridine derivatives
    • Niche specialty chemical intermediates found in dyes, fragrances, and advanced materials
    Free Quote

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