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2',4'-Dichloroacetophenone

    • Product Name 2',4'-Dichloroacetophenone
    • Alias CN code 44
    • Einecs 219-047-6
    • 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

    671056

    Cas Number 2234-16-4
    Molecular Formula C8H6Cl2O
    Molecular Weight 189.04
    Iupac Name 1-(2,4-dichlorophenyl)ethan-1-one
    Appearance White to off-white solid
    Melting Point 46-48 °C
    Boiling Point 286-287 °C
    Density 1.33 g/cm³
    Solubility In Water Slightly soluble
    Pubchem Cid 176463
    Smiles CC(=O)C1=C(C=C(C=C1)Cl)Cl
    Inchi InChI=1S/C8H6Cl2O/c1-5(11)6-2-3-8(10)7(9)4-6/h2-4H,1H3

    As an accredited 2',4'-Dichloroacetophenone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 2',4'-Dichloroacetophenone, sealed with a screw cap, labeled with safety and chemical information.
    Shipping **2',4'-Dichloroacetophenone** is shipped in tightly sealed containers to prevent leaks or contamination. It is typically packaged in glass or high-density plastic bottles, labeled with hazard information. The chemical is transported under cool, dry conditions in compliance with regulations for hazardous substances, ensuring minimal risk during transit.
    Storage 2',4'-Dichloroacetophenone should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Keep it protected from light and sources of ignition. Store at room temperature and avoid humidity. Use safety labeling and limit access to trained personnel to ensure safe handling and storage.
    Application of 2',4'-Dichloroacetophenone

    Applications of 2',4'-Dichloroacetophenone in Industrial Manufacturing

    2',4'-Dichloroacetophenone serves as a functional intermediate in multiple industrial value chains, distinguished by its reactivity and selective substitution pattern. Our plant-grade material integrates directly into downstream production workflow, supporting quality, safety, and regulatory alignment in each sector. Below we outline principal application scenarios, implementation practices, and relevant use frameworks based on real-world customer requirements and industry mandates.

    1. Pharmaceutical Intermediate Synthesis for API Manufacturing

    In advanced pharmaceutical manufacturing, 2',4'-Dichloroacetophenone operates as a key building block for the preparation of certain active pharmaceutical ingredients (APIs), particularly those involving substituted aryl ketone scaffolds. Process engineers employ it for sequential functionalization steps, where its clean halogenation supports precise selectivity and minimizes purification burdens. Formulators rely on validated input specifications when integrating this intermediate into GMP-controlled processes, ensuring full traceability throughout multi-step syntheses for oncology, anti-inflammatory, and CNS-targeted APIs.

    Industry compliance standards

    • ICH Q7 GMP Guidelines for Active Pharmaceutical Ingredients
    • EU GMP (Part II: Basic Requirements for Starting Materials)
    • US FDA 21 CFR Part 211 & 210
    • Ph.Eur., USP, JP Pharmacopoeias (for downstream API batches)

    Typical usage ratio

    • Reaction input loading: 0.9 - 1.2 molar equivalents per synthetic step; adjusted by desired yield and downstream conversion rate

    Downstream process integration

    • Used in initial acylation or halogenation stages; introduced in solvent-bonded batch or continuous stirred tank reactors; intermediate isolation and stepwise purification precede API assembly

    Final product types

    • Active pharmaceutical ingredients (aromatic ketone derivatives for investigational or generic drugs)
    • Advanced pharmaceutical intermediates destined for final API conversion

    2. Fine Chemical Synthesis for Agrochemical Manufacturing

    Agrochemical formulators use 2',4'-Dichloroacetophenone as a precursor in the synthesis of chlorinated acyl compounds and heterocyclic ring systems employed for crop protection agents. Its substitution pattern provides site-specific entry for additional functional groups, facilitating tight control over the physicochemical properties of herbicides or fungicides. Compliance and batch traceability are critical, with all raw input material quality records retained for subsequent end-product registration dossiers.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Fine Chemical Production
    • FAO/WHO Specifications for Plant Protection Products
    • REACH Registration (EC 1907/2006) for European supply chains
    • China GB 2763 National Food Safety Standard—regarding residues in pesticide technical materials

    Typical usage ratio

    • Formulation input: 5%—20% by weight relative to overall active ingredient mass; variation aligned with synthesis throughput and desired precursor loading

    Downstream process integration

    • Typically undergoes nucleophilic aromatic substitution or Grignard reactions in jacketed glasslined reactors; integrated in batchwise or semi-continuous processes up to precursor isolation

    Final product types

    • Herbicide or fungicide technical concentrates
    • Heterocyclic pesticide intermediates
    • Crop protection active substances for commercial formulation

    3. Performance Polymer Additive Synthesis

    In the advanced polymer segment, manufacturers utilize 2',4'-Dichloroacetophenone to produce specialty monomers or polymer chain modifiers, targeting the production of custom high-performance resins. The aryl ketone structure allows fine-tuned control of cross-link densities and mechanical characteristics in specialty copolymer formulations, especially where chlorine-containing substituents enable thermal stability and flame retardancy. Polymers produced using this intermediate supply industries such as electronics encapsulation and coated wire insulation.

    Industry compliance standards

    • ISO 14001 Environmental Management (for controlled emissions)
    • EN 45545-2 Requirements for Fire Behavior of Materials (for rail applications)
    • RoHS Directive 2011/65/EU (as relates to downstream polymer additives)
    • REACH Regulation EC 1907/2006—Annex XVII (for restricted substances monitoring)

    Typical usage ratio

    • Intermediate monomer input: 1%—15% by mass in copolymer feed streams, defined by target end-use flame retardancy or thermal stability specification

    Downstream process integration

    • Polymerization step/chain extension: input as a functional comonomer; typically undergoes condensation or radical copolymerization, based on process recipe

    Final product types

    • Flame-retardant thermoset resins
    • Halogenated engineering plastics
    • Specialty encapsulation polymers

    4. Organic Synthesis for Colorant and Dye Manufacturing

    Producers in the dye and pigment industry apply 2',4'-Dichloroacetophenone as a controlled halogenated building block for azo dye precursors and chromophore intermediates, allowing for the introduction of specific electronic effects and improved colorfastness. The halogen pattern here enables stability and performance in fabric or technical textile dyeing applications, demanding consistent material input for batch-to-batch shade reproducibility. All production adheres to industry-wide constraints on banned aromatic amines and hazardous residues.

    Industry compliance standards

    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • OEKO-TEX Standard 100 for textile chemicals
    • EU REACH Annex XVII (Aromatic Amine Restrictions)
    • ASTM D4282 Textiles—Colorfastness Testing Protocols

    Typical usage ratio

    • Dye precursor batch: 0.5%—6% by mass depending on chromophoric group extension and required intensity

    Downstream process integration

    • Employed in diazotization or coupling reactions in reflux condensers or flow reactors; precursor then isolated and introduced to finishing steps for dye formulation

    Final product types

    • High-performance azo dyes
    • Industrial pigments for plastics and coatings
    • Textile colorants used for cellulose and polyester fibers
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