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2,4-Difluoro-Alpha-(1H-1,2,4-Triazolyl)Acetophenone

    • Product Name 2,4-Difluoro-Alpha-(1H-1,2,4-Triazolyl)Acetophenone
    • Alias DFTA
    • Einecs 685-174-9
    • 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
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    Specifications

    HS Code

    960965

    Productname 2,4-Difluoro-Alpha-(1H-1,2,4-Triazolyl)Acetophenone
    Molecularformula C10H6F2N3O
    Molecularweight 221.17 g/mol
    Casnumber 864376-37-2
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Soluble in DMSO, DMF, and slightly in water
    Storagetemperature Store at 2-8°C
    Smiles C1=CC(=C(C=C1F)F)C(=O)CN2C=NC=N2
    Inchi InChI=1S/C10H6F2N3O/c11-7-2-1-6(9(12)3-7)10(16)5-15-8-13-4-14-15/h1-4,8H,5H2

    As an accredited 2,4-Difluoro-Alpha-(1H-1,2,4-Triazolyl)Acetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 10g sample is packaged in a sealed amber glass bottle with a tamper-evident cap and labeled with full chemical identification.
    Shipping Shipping of 2,4-Difluoro-Alpha-(1H-1,2,4-Triazolyl)Acetophenone is carried out in accordance with chemical safety regulations. The substance is securely packaged in appropriate containers, labeled clearly, and transported with documentation. Handling precautions are followed, ensuring stable temperature conditions and preventing exposure to moisture, sunlight, or incompatible substances during transit.
    Storage Store 2,4-Difluoro-Alpha-(1H-1,2,4-Triazolyl)Acetophenone in a tightly sealed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers. Protect from light and moisture. Keep refrigerated if recommended by the supplier. Ensure proper labeling, and use secondary containment to prevent spills. Follow all relevant safety guidelines and consult the SDS for further instructions.
    Application of 2,4-Difluoro-Alpha-(1H-1,2,4-Triazolyl)Acetophenone

    Applications of 2,4-Difluoro-Alpha-(1H-1,2,4-Triazolyl)Acetophenone in Industrial Manufacturing

    2,4-Difluoro-Alpha-(1H-1,2,4-Triazolyl)Acetophenone, an advanced triazole-functionalized aromatic ketone, plays a critical role in several specialized chemical synthesis fields due to its unique fluorinated structure and triazole moiety. Below, we detail its downstream industrial applications, focusing on the active requirements, processing integration, regulatory context, and end-product types relevant to manufacturing sectors.

    1. Triazole-based Agrochemical Synthesis

    Manufacturers in the agrochemical sector incorporate this material as a triazole core intermediate for systemic fungicide actives, such as triazole fungicides used in crop protection. The compound enables efficient selective modifications to the molecular structure, improving activity and environmental stability. Chemical engineers generally introduce it during the heterocyclic condensation stage, achieving high conversion rates in scalable batch reactors for further derivatization. Plants standardize formula variations based on targeted pathogenic species and local compliance restrictions, matching residue levels and specific crop registrations.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • ISO 23195:2022 (Triazole content and purity requirements)
    • REACH (EC) No 1907/2006 for intermediates registration
    • China GB 2763 Maximum Residue Limits (for finished crop use)

    Typical usage ratio

    • Ranges from 2% to 8% of reaction input; adjusted according to desired fungicidal activity and downstream derivatization for registration requirements

    Downstream process integration

    • Charged during synthesis of key intermediate en route to active triazole compounds; added after initial fluorination, prior to ring closure or side-chain functionalization

    Final product types

    • Systemic triazole fungicides (e.g., prothioconazole, difenoconazole derivatives)
    • Crop protection formulations (suspension concentrates, emulsifiable concentrates)

    2. Pharmaceutical Intermediate for Antifungal APIs

    Research and production units in the pharma sector employ this material as a key building block for synthesizing triazole-based antifungal active pharmaceutical ingredients. The compound’s dual fluorination pattern enhances metabolic stability and antifungal spectrum by participating in core coupling reactions during multi-step synthesis. GMP production sites precisely monitor the charge and conversion ratio of this substance to support both bulk API output and regulatory dossier consistency for global market submissions.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • USP-NF for API identity, purity, and safety
    • European Pharmacopoeia (Ph. Eur.) monographs for triazole antifungals
    • FDA Drug Master File (DMF) requirements

    Typical usage ratio

    • Commonly 1.5%–6%, depending on target molecule yield and impurity profiling; batch-to-batch adjustment based on process validation results

    Downstream process integration

    • Introduced during the core coupling step for triazole ring assembly, crucial in the build-up to the antifungal active, followed by purification and crystallization

    Final product types

    • Fluconazole, itraconazole, and voriconazole APIs
    • Generic and branded antifungal pharmaceuticals (tablets, injectables)

    3. Fine Chemical Synthesis for Specialty Triazole Additives

    Producers in the specialty chemicals sector rely on this raw material to introduce both fluorine and triazole functionalities into advanced additives and performance enhancers. It serves as a molecular precursor when manufacturing heat- and UV-resistant triazole-based stabilizers for plastics and coatings. Selection of the dosing regimen stems from required functional group incorporation and desired polymer compatibility, with precision-controlled incorporation into large-scale continuous reactors.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems for additives manufacturing)
    • EU Regulation (EC) No 1272/2008 (CLP Regulation for chemical hazard classification)
    • ASTM D5208-21 (Light stability in plastics)
    • OECD Guidelines for the Testing of Chemicals (safety and eco-toxicity)

    Typical usage ratio

    • 0.7%–2.5% in additive intermediate synthesis; level tailored based on desired triazole loading and polymer base compatibility

    Downstream process integration

    • Added at intermediate stage during fine chemical synthesis for triazole stabilizers, prior to coupling or grafting onto polymer backbones

    Final product types

    • Fluorinated triazole light stabilizers
    • High-performance anti-aging additives for plastics and coatings

    4. Agrochemical Analytical Reference Standard Production

    Certified reference material (CRM) labs and agrochemical R&D centers use this compound in the production of analytical reference standards for residue analysis and environmental monitoring of triazole fungicides. The high chemical purity and structural stability of the material are critical to generate traceable and reproducible calibration solutions, ensuring validity across various LC-MS/MS and GC-MS analytical platforms. The precision adjustment of formulation standards depends on instrument sensitivity and method validation parameters as defined by international guidelines.

    Industry compliance standards

    • ISO/IEC 17025:2017 (Testing and calibration laboratories)
    • ISO Guide 34 (General requirements for CRM production)
    • SANTE/12682/2019 (Residue analytical methods for pesticides)
    • OECD GLP for analytical batch release

    Typical usage ratio

    • Analytical reference standards prepared at concentrations from 0.01 mg/mL to 10 mg/mL, based on targeted residue limits and instrumental method sensitivity

    Downstream process integration

    • Weigh-out of high-purity compound for stock solution preparation, then serial dilution and aliquoting under validated conditions

    Final product types

    • Certified analytical reference standards for triazole fungicide residues
    • Calibration solutions for environmental and food safety testing laboratories
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