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2-Amino-4,4'-Dichlorodiphenyl Ether

    • Product Name 2-Amino-4,4'-Dichlorodiphenyl Ether
    • Alias Amino DPE 2,4-Cl
    • Einecs 221-016-5
    • 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
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    Specifications

    HS Code

    107270

    Chemical Name 2-Amino-4,4'-Dichlorodiphenyl Ether
    Cas Number 20103-09-7
    Molecular Formula C12H9Cl2NO
    Molecular Weight 254.11 g/mol
    Appearance Pale yellow to brown crystalline solid
    Melting Point 127-129°C
    Boiling Point No data available
    Solubility Insoluble in water
    Density No data available
    Storage Temperature Store at 2-8°C
    Synonyms 4,4'-Dichloro-2-aminodiphenyl ether
    Structure Diphenyl ether core with 4,4'-dichloro and 2-amino substitution
    Pubchem Cid 130879

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

    Packing & Storage
    Packing A 100-gram amber glass bottle labeled "2-Amino-4,4'-Dichlorodiphenyl Ether," featuring hazard symbols, lot number, and safety instructions.
    Shipping `2-Amino-4,4'-Dichlorodiphenyl Ether` should be shipped in tightly sealed containers, protected from light and moisture. It must be labeled according to relevant hazardous materials regulations and transported by qualified carriers. Ensure proper documentation accompanies the shipment, and store at room temperature away from incompatible substances to prevent contamination or reaction.
    Storage 2-Amino-4,4'-Dichlorodiphenyl Ether should be stored in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Keep the container tightly closed and protected from light and moisture. Store away from heat and ignition sources. Proper labeling and secondary containment are recommended to prevent spills and accidental exposure.
    Application of 2-Amino-4,4'-Dichlorodiphenyl Ether

    Applications of 2-Amino-4,4'-Dichlorodiphenyl Ether in Industrial Manufacturing

    2-Amino-4,4'-Dichlorodiphenyl Ether is a specialty aromatic intermediate utilized in several advanced manufacturing sectors, serving as a building block and performance-enhancing component in carefully controlled chemical syntheses. Our technical team supports global industrial clients with consistent purity and supply chain reliability, ensuring every batch meets the specific technical requirements of regulated and competitive downstream markets. Below, we detail key application fields and integration methods based on customer production specifications and industry standards.

    1. Agrochemical Active Ingredient Synthesis

    Major agrochemical companies use this compound as an intermediate in the synthesis of selective herbicides and fungicides—especially where halogenated aromatic structures improve biological activity and application stability. Its introduction occurs during the condensation or coupling stages of active ingredient manufacture, ensuring the formulated pesticides meet regulatory residue and reactivity limits.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Chemical Manufacturing
    • FAO Specification for Agricultural Pesticide Ingredients
    • REACH Annex II: Safety Data requirements for chemical substances
    • US EPA 40 CFR Part 180 (Tolerances and exemptions for pesticide residues)

    Typical usage ratio

    • Generally 5–18% w/w of total batch mass during key active ingredient synthesis; the exact proportion depends on molecule being targeted and reaction yield requirements.

    Downstream process integration

    • Introduced at the condensation or coupling step in multi-stage synthesis. Reacts with halo-acids or other aromatic intermediates under controlled temperature and pH, followed by purification and crystallization processes.

    Final product types

    • Selective triazole fungicides
    • Phenoxy herbicide technical concentrates
    • Crop protection suspensions
    • Premix formulations for integrated pest management (IPM) programs

    2. Specialty Polymer Additives

    Manufacturers of engineering plastics select this compound as a functional additive to introduce targeted halogenated aromatic groups, imparting improved high-temperature stability and flame-retardant properties. Production lines apply it at the compounding or co-polymerization phases, where precise dosing is essential to meeting international flammability and migration standards for finished plastics.

    Industry compliance standards

    • UL 94 Flammability Standard for Plastics
    • EN 71-3: Chemical Safety of Toy Materials
    • IEC 61249-2-21: Halogen-free Base Materials Standard (for electronics grade plastics)
    • ISO 10993-5: Biological evaluation for medical device plastics (where applicable)

    Typical usage ratio

    • Typically 0.5–4% by weight in polymer melt or solution; loading adjusted for balance between flame resistance and mechanical properties, depending on resin system and application field.

    Downstream process integration

    • Added during compounding (extrusion or internal mixing) or as a reactive monomer in step-growth polymerizations for specialty resins. Requires uniform dispersion prior to molding or shaping.

    Final product types

    • Flame-retardant polyamide and polyester granules
    • Halogenated plasticizer masterbatches
    • High-performance molded components for automotive and electronics
    • Specialty fiber-forming polymers

    3. Pharmaceutical Intermediate for Active Compound Synthesis

    Research-based pharmaceutical companies use this chlorinated ether as an advanced intermediate in the manufacture of specific APIs (active pharmaceutical ingredients), especially where electron-withdrawing or hydrophobic aromatic groups are structurally essential. Each batch must comply with medicinal-grade impurity profiles and process validation requirements for GMP environments.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF and Ph. Eur. monographs for relevant APIs
    • Japanese Pharmacopoeia standards
    • FDA 21 CFR Part 210/211: Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs

    Typical usage ratio

    • Range is 2–8% as a precursor or coupling reactant, set by the stoichiometry of target API synthesis step; exact percentage confirmed by process scale-up and GMP validation data.

    Downstream process integration

    • Charged into heterocyclic formation or aromatic coupling reactions under nitrogen atmosphere, often followed by hydrogenation, crystallization, and multi-stage purification to produce GMP-compliant intermediates and API final crystallizate.

    Final product types

    • Intermediate APIs for anti-inflammatory and anti-allergy formulations
    • Niche oncology drug intermediates
    • Building blocks for structure-activity relationship (SAR) research in medicinal chemistry
    • Quality-controlled reference standards

    4. High-Performance Dye and Pigment Manufacture

    Producers of specialty colorants use this intermediate during the synthesis of chlorinated aniline-based dyes and pigments. The aromatic ether structure and dichloro substitution promote color fastness and thermal stability, benefitting coatings or fiber coloration subject to stringent lightfastness and migration criteria.

    Industry compliance standards

    • ISO 105-B02: Color Fastness to Light (for textiles)
    • OEKO-TEX® Standard 100 (chemical safety for textile colorants)
    • 42 CFR Part 74: FDA Color Additive Regulations (for food-contact and pharma use pigments)
    • GB/T 5211.5-2014: General Methods for Testing Pigments and Extenders (China National Standards)

    Typical usage ratio

    • Usually 1–6% of total dye or pigment synthesis mass, adjusted for tint strength, application substrate, and reaction consistency in batch or continuous synthesis.

    Downstream process integration

    • Reacted in nucleophilic aromatic substitution or condensation reactions to build up functionalized pigment molecules. Post-reaction, the mixture is filtered, milled, and optionally spray dried for pigment grade stability.

    Final product types

    • Chlorinated azo and aniline-based textile dyes
    • High-fastness organic pigments for plastic and coatings
    • Colorant masterbatches
    • Printing ink concentrates
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