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3,5-Dichlorobenzoyl Chloride

    • Product Name 3,5-Dichlorobenzoyl Chloride
    • Alias m-Dichlorobenzoyl chloride
    • Einecs 221-009-2
    • 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

    399715

    Chemical Name 3,5-Dichlorobenzoyl Chloride
    Cas Number 2905-62-6
    Molecular Formula C7H3Cl3O
    Molecular Weight 209.46 g/mol
    Appearance White to off-white crystalline solid
    Melting Point 50-53 °C
    Boiling Point 273-274 °C
    Density 1.51 g/cm³
    Solubility In Water Reacts with water
    Refractive Index 1.573
    Storage Conditions Store in a cool, dry place; keep tightly closed and away from moisture
    Synonyms Benzoyl chloride, 3,5-dichloro-
    Smiles C1=C(C=C(C=C1Cl)Cl)C(=O)Cl

    As an accredited 3,5-Dichlorobenzoyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of 3,5-Dichlorobenzoyl Chloride is packaged in a sealed amber glass bottle with hazard labels and tamper-evident cap.
    Shipping 3,5-Dichlorobenzoyl Chloride is shipped as a hazardous material due to its corrosive and reactive properties. It is securely packaged in airtight, chemical-resistant containers, clearly labeled, and transported following international regulations for dangerous goods. Specialized handling and storage conditions, including temperature control and spill containment, are strictly maintained during shipping.
    Storage 3,5-Dichlorobenzoyl chloride should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from incompatible substances like water, alcohols, bases, and strong oxidizers. Protect it from moisture and direct sunlight. Store under inert gas if possible. Use suitable corrosion-resistant materials for containers. Keep away from heat sources and ignition points.
    Application of 3,5-Dichlorobenzoyl Chloride

    Applications of 3,5-Dichlorobenzoyl Chloride in Industrial Manufacturing

    As an established producer of 3,5-Dichlorobenzoyl Chloride, we supply this high-purity intermediate to key industries, powering synthesis steps demanding strict regulatory and quality control. Below we detail concrete application segments, typical formulation ranges, compliance considerations, process roles, and resultant finished products in actual practice.

    1. Agrochemical Synthesis: Herbicide and Fungicide Active Ingredient Production

    Major agrochemical manufacturers employ this raw material primarily in the synthesis of selective herbicide and fungicide actives. Its dichlorinated benzoyl moiety delivers targeted reactivity for coupling with specific heterocycles. Raw material lot consistency directly affects the purity of key intermediates, which downstream contractual farming regulations scrutinize during audits and import registrations.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • REACH SVHC registration (EU)
    • EPA Pesticide Ingredient Registration (US FIFRA)
    • China ICAMA Technical Material Registration

    Typical usage ratio

    • Batch reactions: 0.9–1.2 molar equivalents as acylating agent relative to amine substrate; ratio refined based on target impurity thresholds and downstream purity specs.

    Downstream process integration

    • Charged to controlled-acidification reactors after base-neutralization of precursor amines or hydrazines; often follows exothermic addition under nitrogen atmosphere with temperature monitoring. Acid chloride is consumed during the final condensation step before workup.

    Final product types

    • Triazole-based fungicides (e.g., difenoconazole precursor synthesis)
    • Chloro-substituted herbicide technical concentrates
    • Registered pesticide active technical materials for formulation plants

    2. Pharmaceutical Intermediates: Sartan Antihypertensive Synthesis

    Leading API companies use 3,5-Dichlorobenzoyl Chloride in protected-stage synthesis of sartan-class antihypertensives, where reproducible reactivity ensures batch-ro-batch consistency. Strict traceability and GMP validation demand high analytical transparency and upstream supplier auditability.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • EDQM CEP documentation (Europe)
    • USP-NF and/or European Pharmacopoeia impurity limits (where applicable)
    • FDA DMF referencing, site inspection readiness

    Typical usage ratio

    • 1.0–1.05 equivalents per coupling step, with minor excess to drive reaction completion; ratio depends on API impurity control and yield optimization studies.

    Downstream process integration

    • Introduced into solvent-controlled reactors during the penultimate step of biphasic acylation, prior to hydrolysis and final deblocking; product then isolated under controlled filtration and re-crystallization protocols.

    Final product types

    • Losartan, valsartan, and related sartan intermediate compounds
    • Fully synthetic routes to chloroarene pharmaceutical building blocks
    • Validated GMP intermediates for onward finished-dosage manufacture

    3. Specialty Polymerization: Photopolymer Cross-Linker Precursors

    Advanced materials companies utilize this dichlorinated acid chloride for preparing high-performance benzoyl cross-linkers in UV-curable polymer systems. The product’s specific substitution enables tailored molecular weight build-up and glass transition behaviors, essential for coatings and resins subject to demanding end-use performance requirements.

    Industry compliance standards

    • ISO 9001:2015 and QC stability protocols
    • ROHS Directive (for electronics coatings, where applicable)
    • Specific end-use regulatory review for industrial coatings (e.g., automotive and microelectronics)
    • SDS/M SDS for chemical workplace safety

    Typical usage ratio

    • Typically 0.1–2.0 wt% as chain terminator or cross-linker precursor relative to prepolymer content; levels set based on mechanical properties specification and curing window.

    Downstream process integration

    • Charged into polyol/acrylate melt reactors following catalyst introduction; participates in in-situ formation of benzoylated prepolymer chains prior to UV curing tank transfer.

    Final product types

    • Photoresist systems for printed circuit fabrication
    • UV-curable industrial varnishes
    • Adhesive and encapsulant matrix resins with defined cross-link density

    4. Fine Chemical Synthesis: Custom Aromatic Derivatives for Dyes and Pigments

    Producers of specialty colorants use this compound as a controlled acyl donor in custom aromatic substitution, ensuring precise positioning of dichloro functionalities. It permits synthesis of unique chromophores that require consistent, reproducible input purity and low by-product profiles for colorfastness and light stability.

    Industry compliance standards

    • ISO 14001 Environmental Management (for waste control)
    • ZEK 01-08 Hausfarbenverordnung (where pigments for children’s products are involved, EU)
    • Compliance with local chemical safety control (e.g., TSCA inventory for US sales)
    • Internal batch records per end-customer approved specification

    Typical usage ratio

    • Ranging 0.5–1.5 equivalents per aromatic substrate, set by targeted substitution pattern and final product hue; adjusted for yield vs. color strength tradeoff.

    Downstream process integration

    • Dosed during the acylation stage of multi-step condensation reactions in stirrer-equipped glass-lined reactors, followed by aqueous workup and chromophore stabilization.

    Final product types

    • Dichloro-functionalized pigments for plastics coloration
    • Custom dye intermediates for automotive and textile applications
    • High-performance organic colorants for specialty ink formulations

    5. Electronic Chemicals: Precursors for Liquid Crystal Monomer Synthesis

    Manufacturers in the advanced display materials sector utilize the dichlorinated acid chloride for precise synthesis of aromatic intermediates required in specialty liquid crystal monomers. Accurate batch-to-batch consistency and low residual contaminants are critical for downstream optical and electrical properties, affecting end-product performance in high-resolution display panels.

    Industry compliance standards

    • ISO 9001:2015 for supplier and process qualification
    • IPC-4101B specification for base materials (as applicable)
    • ROHS/REACH compliance for global electronics value chain
    • Customer-specific impurity limits (ppm-level requirements in display applications)

    Typical usage ratio

    • 0.8–1.2 equivalents in stepwise acylation of biphenyl or cyclohexyl substrates; fine-tuned according to device performance QC results.

    Downstream process integration

    • Introduced during final acylation or halogenation steps in liquid crystal monomer synthesis lines, with care to control moisture and avoid hydrolysis; downstream distillation and chromatographic purification follow.

    Final product types

    • Mono- and di-functional liquid crystal monomers
    • Pre-polymers for display alignment layers
    • High-specification intermediates for specialty display and touch panel manufacturers
    Free Quote

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