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3,4-Difluorobenzoyl Chloride

    • Product Name 3,4-Difluorobenzoyl Chloride
    • Alias DFBC
    • Einecs 219-010-4
    • 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
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    Specifications

    HS Code

    932722

    Product Name 3,4-Difluorobenzoyl Chloride
    Cas Number 452-81-1
    Molecular Formula C7H3ClF2O
    Molecular Weight 176.55
    Appearance Colorless to pale yellow liquid
    Boiling Point 98-100°C at 18 mmHg
    Melting Point -5°C
    Density 1.404 g/cm3
    Purity Typically ≥98%
    Solubility Reacts with water, soluble in organic solvents
    Synonyms 3,4-Difluorobenzoyl chloride; Benzoyl chloride, 3,4-difluoro-
    Refractive Index 1.506
    Storage Conditions Store under inert gas, keep container tightly closed, cool and dry place

    As an accredited 3,4-Difluorobenzoyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g amber glass bottle with secure screw cap, labeled "3,4-Difluorobenzoyl Chloride," includes hazard warnings and handling instructions.
    Shipping 3,4-Difluorobenzoyl Chloride is shipped in tightly sealed containers, protected from moisture and incompatible substances. It should be transported under cool, dry conditions as a corrosive, hazardous chemical, in accordance with local, national, and international regulations for dangerous goods. Proper labeling and documentation must accompany all shipments to ensure safe handling.
    Storage 3,4-Difluorobenzoyl chloride should be stored in a cool, dry, well-ventilated area away from moisture and incompatible substances such as bases, alcohols, and oxidizers. Keep the container tightly closed in a corrosion-resistant container with a resistant inner liner. Protect from direct sunlight and sources of ignition. Store under an inert atmosphere if possible to prevent hydrolysis and degradation.
    Application of 3,4-Difluorobenzoyl Chloride

    Applications of 3,4-Difluorobenzoyl Chloride in Industrial Manufacturing

    As a direct manufacturer of 3,4-Difluorobenzoyl Chloride, we supply this specialty acid chloride to major industries engaged in the synthesis of high-performance chemicals. The following industrial sectors represent the realistic, primary downstream markets utilizing this material in their precise formulations and advanced process steps.

    1. Pharmaceutical Active Ingredient Synthesis

    3,4-Difluorobenzoyl Chloride serves as an essential acylating agent in the synthesis of precursor molecules for non-steroidal anti-inflammatory drugs and other pharmaceutical intermediates. Pharmaceutical manufacturers incorporate this intermediate during the benzoylation step to prepare specialty APIs following multi-stage synthetic routes. We support cGMP-oriented production, ensuring traceability for regulated import and export flows.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • 21 CFR Parts 210/211
    • USP-NF Monographs (where applicable for intermediates)
    • REACH Regulation (EC) No 1907/2006 compliance

    Typical usage ratio

    • Used at 0.9–1.2 molar equivalents per target intermediate step; adjusted to minimize residuals per batch validation.

    Downstream process integration

    • Integrated after amine or phenol substrate charging in acylation reactors; controlled addition at 0–5°C to manage exotherm and selectivity.

    Final product types

    • N-(3,4-difluorobenzoyl) substituted APIs (e.g., advanced NSAID intermediates)
    • Pyridine-based antineoplastic precursors
    • Anti-infective agent intermediates
    • Aromatic amide-based bulk APIs

    2. Agrochemical Active and Intermediate Synthesis

    Downstream agrochemical manufacturers utilize this specialty acid chloride in the formation of difluorinated benzamide structures. It is critical in the acylation steps for selective herbicide and fungicide synthesis. Our product adheres to purity and consistency requirements specific for scalable crop protection manufacture, ensuring consistent field performance and regulatory compliance.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 certified production controls
    • EU Regulation (EC) No 1107/2009 (plant protection products)
    • Regulatory Registration Dossiers (e.g., China ICAMA, US EPA)

    Typical usage ratio

    • Applied at 1.0–1.1 molar equivalents to technical intermediate synthesis, with ratios validated per specific crop-protection molecule production.

    Downstream process integration

    • Continuous or batchwise addition to acid scavenger-containing reactors post-amide formation; temperature controlled at 10–20°C for optimal conversion.

    Final product types

    • Difluorobenzamide herbicide actives
    • Fungicidal intermediate compounds
    • Seed treatment chemicals
    • Weed control agent pre-mixtures

    3. Liquid Crystal Display (LCD) Intermediate Manufacturing

    In the electronic chemicals segment, 3,4-Difluorobenzoyl Chloride is a specialty building block for the synthesis of difluorinated esters and biphenyl units used in advanced liquid crystal mixtures. Materials science teams formulate these mixtures to ensure high birefringence, thermal stability, and response speed in display applications. Process control emphasizes minimizing metal and residual chloride impurities for electronic grade demands.

    Industry compliance standards

    • IPC-4101/99 (base materials for printed boards)
    • IEC 61249-2-41 for organic electronic chemicals
    • RoHS Directive (2011/65/EU) for restricted substances
    • Customer-specific non-conductive residue (NCR) limits

    Typical usage ratio

    • Employed at 0.95–1.05 molar equivalents per liquid crystal intermediate, with adjustments to target specific phase transition temperatures.

    Downstream process integration

    • Added post-biphenyl core formation; strict control under dry nitrogen to prevent moisture-sensitive side reactions; transferred to subsequent esterification reactors under inert atmosphere.

    Final product types

    • Advanced nematic and smectic liquid crystal compounds
    • Polarizer and alignment layer chemicals
    • LCD panel raw materials
    • Organic electronic display intermediates

    4. High-Performance Polymer Synthesis

    Polymer manufacturers use 3,4-Difluorobenzoyl Chloride to introduce difluorobenzoyl moieties into polyamide-imide and polyetherketone backbones. These modifications enhance chemical resistance and dimensional stability for high-performance engineering plastics. The product supports melt and solution polymerization routes, providing precisely controlled reactivity and end-group functionality demanded in advanced molding and film applications.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • ASTM D5336-15 (Polyimide Test Methods)
    • EN ISO 1874-1:2019 (Polyamide Resins)
    • UL 94 Flame Classification (for finished resin parts)

    Typical usage ratio

    • Used at 0.98–1.05 molar equivalents with respect to diamine or dihydroxy co-monomers, adjusted to match polymer chain length and processing viscosity targets.

    Downstream process integration

    • Metered into closed-system reactors between co-monomer charging and cyclization; controlled atmosphere; integrated with inline viscosity and molecular weight monitoring.

    Final product types

    • High-performance polyamide-imide resins
    • PEEK copolymers for electrical insulation
    • Automotive under-hood plastic compounds
    • Specialty film extrusion resins
    Free Quote

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