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2-Chloro-N-[4-Chloro-2-(2-Chlorobenzoyl)Phenyl]Acetamide

    • Product Name 2-Chloro-N-[4-Chloro-2-(2-Chlorobenzoyl)Phenyl]Acetamide
    • Alias CKD-712
    • Einecs 629-456-4
    • 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
    VTB
    Specifications

    HS Code

    643505

    Chemicalname 2-Chloro-N-[4-Chloro-2-(2-Chlorobenzoyl)Phenyl]Acetamide
    Molecularformula C15H10Cl3NO2
    Molecularweight 342.61 g/mol
    Casnumber 197197-73-2
    Appearance White to off-white solid
    Solubility Slightly soluble in DMSO, insoluble in water
    Purity Typically >98%
    Storagetemperature 2-8°C (Refrigerated)
    Synonyms 2-Chloro-N-(4-chloro-2-(2-chlorobenzoyl)phenyl)acetamide
    Iupacname 2-chloro-N-[4-chloro-2-(2-chlorobenzoyl)phenyl]acetamide
    Hazardstatements May cause skin and eye irritation

    As an accredited 2-Chloro-N-[4-Chloro-2-(2-Chlorobenzoyl)Phenyl]Acetamide 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, with tamper-evident cap, chemical label displaying product name, formula, hazard symbols, and lot number.
    Shipping This chemical ships in secure, leak-proof containers suitable for hazardous materials. Packaging complies with international safety regulations for transport. Material safety data sheets (MSDS) are included. Shipping is available via certified carriers with tracking and mandatory adult signature upon delivery. Temperature and handling instructions are clearly labeled to ensure product integrity.
    Storage 2-Chloro-N-[4-Chloro-2-(2-Chlorobenzoyl)phenyl]acetamide should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from heat, light, moisture, and incompatible substances such as strong oxidizing agents. Properly label the storage container, and avoid prolonged exposure to air. Recommended storage temperature is at room temperature (15–25°C), unless otherwise specified by the manufacturer.
    Application of 2-Chloro-N-[4-Chloro-2-(2-Chlorobenzoyl)Phenyl]Acetamide

    Applications of 2-Chloro-N-[4-Chloro-2-(2-Chlorobenzoyl)Phenyl]Acetamide in Industrial Manufacturing

    As a direct manufacturer of 2-Chloro-N-[4-Chloro-2-(2-Chlorobenzoyl)Phenyl]Acetamide, we supply this advanced intermediate for downstream industries that rely on precision synthesis, stringent quality assurance, and regulatory compliance. Below we detail key application scenarios where this raw material forms an essential component in large-scale value chains, with technical insight into standards, integration modes, and final product outcomes.

    1. Non-Steroidal Anti-Inflammatory Drug (NSAID) Active Pharmaceutical Ingredient (API) Synthesis

    Large pharmaceutical companies utilize this intermediate for the synthesis of select NSAID APIs through multi-step organic processes. It acts as a crucial acylating reagent in API formation, ensuring the molecular structure and purity demanded by health authorities. Our material meets the high-quality requirements controlling genotoxic impurity limits and trace residuals vital for regulatory approval of finished APIs.

    Industry compliance standards

    • United States Pharmacopeia (USP) Monographs
    • EU Guidelines for Good Manufacturing Practice for Medicinal Products for Human and Veterinary Use (EudraLex, Volume 4, Part II)
    • Chinese Pharmacopoeia for API Quality
    • ICH Q7 GMP for Active Pharmaceutical Ingredients

    Typical usage ratio

    • Dosage in synthesis varies between 0.13–0.21 molar equivalents relative to the starting aromatic amine, adjusted based on desired API output and process yield optimization

    Downstream process integration

    • Forms part of the acylation reaction in Stage 2 or 3 of NSAID API multi-step synthesis sequence; followed by crystallization, purification, and salt formation as per route-specific process validation

    Final product types

    • Bulk NSAID active pharmaceutical ingredients (e.g. emerging chlorinated acetanilide derivatives)
    • Prescription pharmaceutical tablets
    • Injectable solutions post-formulation

    2. Specialty Agrochemical Active Ingredient Manufacturing

    Agrochemical formulators harness this compound for the production of selective herbicides active against dicot weeds. As a key structural building block, it enables the preparation of higher-order intermediates which undergo further condensation and chlorination, tailored for application-specific efficacy with crop safety maintained under residue analysis guidelines.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • ISO 9001:2015 for agrochemical manufacturing
    • Chinese GB/T 1605-2001 Regulation for Herbicide Raw Material Purity
    • OECD Guidelines for Quality Control of Pesticide Production

    Typical usage ratio

    • Standard incorporation is 5–8% by batch mass in the initial active ingredient preparation; specific dosage depends on targeted molecule and stepwise yield calculations during pilot trials

    Downstream process integration

    • Used at first or second stage of synthesis involving esterification and chlorination; intermediates proceed through closed reactor processing, distillation, organic phase washings, and formulation into technical concentrates

    Final product types

    • Technical-grade selective herbicide actives
    • Emulsifiable concentrate (EC) agrochemical formulations
    • Wettable powder (WP) weed control products

    3. Photoinitiator Intermediate for Advanced Polymer Systems

    Producers of UV-curable resins employ this molecule in the synthesis of specialized photoinitiators, which are essential for high-precision coatings and adhesives. Its molecular framework supports subsequent aryl substitution steps required in modern photoinitiator chemistry, which must align with current performance and toxicological standards for electronics and optical applications.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for chemical management
    • RoHS Directive 2011/65/EU for restricted substances in electronics
    • ISO 9001:2015 Quality Management for resin and coatings manufacturing
    • UL 94 Flammability Testing for polymers

    Typical usage ratio

    • Ranges from 2–4% by weight as input during intermediate synthesis; process chemists adjust levels to control photoinitiator structural yield and side product minimization in multi-step pathways

    Downstream process integration

    • Introduced during first or second condensation phase in photoinitiator precursor production; completion involves purification, etherification, and further transformation to the target active for UV curing systems

    Final product types

    • Photoinitiator compounds for UV-cured inks
    • Crosslinking agents in protective optical coatings
    • Resin additives for 3D printing photoresists

    4. Fine Chemical Intermediate for Liquid Crystal Material Synthesis

    Manufacturers specializing in advanced display technology leverage this compound as an upstream intermediate in the synthesis of aromatic liquid crystal materials. Its multiple chloro and amide substitutions enable it to serve as a coupling component in the formation of mesogenic core structures required for high-purity LCM production in TFT-LCD device fabrication.

    Industry compliance standards

    • IEC 61249-2-41 Safety Requirements for Display Materials
    • ISO 14001:2015 Environmental Management for electronics chemicals
    • Quality system certified to GB/T 19001
    • RoHS/REACH conformity in downstream supply chain

    Typical usage ratio

    • Loading level varies from 3–6 mol% in the targeted synthetic step, modulated during process scale-up studies to achieve liquid crystal structure and display uniformity benchmarks

    Downstream process integration

    • Chemists introduce the compound during aromatic coupling, alongside solvent and catalyst management under inert atmosphere; followed by repeated recrystallization and vacuum stripping to ensure functional purity

    Final product types

    • Liquid crystal mixture intermediates
    • LCM material for LCD and OLED screens
    • Conductive alignment layer compositions for advanced panels
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