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2-Chloro-N-Phenylacetamide

    • Product Name 2-Chloro-N-Phenylacetamide
    • Alias Acetochlor
    • Einecs 214-402-2
    • 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
    VTB
    Specifications

    HS Code

    311186

    Chemicalname 2-Chloro-N-Phenylacetamide
    Casnumber 621-24-1
    Molecularformula C8H8ClNO
    Molecularweight 169.61
    Appearance White to off-white solid
    Meltingpoint 104-107°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.286 g/cm3
    Purity Typically ≥98%
    Synonyms N-Phenyl-2-chloroacetamide
    Iupacname 2-chloro-N-phenylacetamide
    Smiles ClCC(=O)NC1=CC=CC=C1
    Inchi InChI=1S/C8H8ClNO/c9-6-8(11)10-7-4-2-1-3-5-7/h1-5H,6H2,(H,10,11)
    Storageconditions Store at room temperature, keep container tightly closed

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

    Packing & Storage
    Packing The 100g package of 2-Chloro-N-Phenylacetamide comes in a sealed amber glass bottle with hazard labels and a secure screw cap.
    Shipping 2-Chloro-N-Phenylacetamide is shipped in tightly sealed containers, protected from moisture and light. It is handled as a hazardous chemical, complying with regulations for safe transport. Shipping includes appropriate labeling, documentation, and, if necessary, temperature control to ensure product stability and worker safety during transit and storage.
    Storage 2-Chloro-N-Phenylacetamide should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect it from light, heat, and moisture. Ensure appropriate labeling and keep it away from sources of ignition. Use chemical safety cabinets if available and restrict access to authorized personnel only.
    Application of 2-Chloro-N-Phenylacetamide

    Applications of 2-Chloro-N-Phenylacetamide in Industrial Manufacturing

    2-Chloro-N-Phenylacetamide supports pivotal synthesis routes for multiple industries where precision formulation, regulatory adherence, and clear downstream integration dictate real-world adoption. Our focus as a manufacturer centers on major material segments where this intermediate delivers process-specific advantages and supports end-product quality control, as outlined in verified downstream applications below.

    1. Pharmaceutical Intermediate for Analgesic Compound Synthesis

    Downstream pharmaceutical producers use this raw material as a core building block in the preparation of several non-opioid analgesics, where the compound’s structural attributes enable selective functional group transformations under controlled conditions. The material enters amidation reactions for active pharmaceutical ingredient (API) generation, with traceability and impurity profiling aligned with regional submission batches.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) for bulk drug substances
    • European Pharmacopoeia (Ph. Eur.) for intermediate validation
    • U.S. FDA 21 CFR Part 211 (Current Good Manufacturing Practice)

    Typical usage ratio

    • Integrated in stepwise syntheses at 0.8–1.2 molar equivalents, relative to parent acid/amine precursor; sensitive to batch scale and downstream yield requirements

    Downstream process integration

    • Dosed into controlled amidation stages under nitrogen atmosphere after precursor preparation, followed by purification, crystallization, and analytical QC for residuals and splits

    Final product types

    • Bulk analgesic APIs (e.g., paracetamol derivatives)
    • Finished oral solid dose medications
    • Pharmaceutical intermediate stock

    2. Agrochemical Intermediate for Herbicide Manufacturing

    Large-scale agrochemical formulations incorporate this material as an acetamide-type intermediate in the synthesis of various chloro- and phenyl-substituted herbicides. The reactivity profile enables the selective formation of target molecules during multi-stage plant protection chemistry workflows, especially where environmental residue tracking mandates stringent process transparency.

    Industry compliance standards

    • FAO/WHO Manual on Development and Use of FAO and WHO Specifications for Agricultural Pesticides
    • ISO 9001:2015 Quality Management System
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EU)
    • US EPA 40 CFR Part 180: Tolerances and Exemptions for Pesticide Chemical Residues

    Typical usage ratio

    • Typically 3–7% by total process input weight, subject to molecular target and downstream chlorination efficiency parameters

    Downstream process integration

    • Charged to primary amide condensation tanks in the initial stage of herbicide precursor manufacturing; integrates post-activation of chlorinated intermediates with process control of exothermic reaction rates

    Final product types

    • Selective pre-emergent herbicide technical concentrate
    • Suspension and emulsifiable agricultural formulations
    • Bulk actives for granulated and liquid herbicide end products

    3. Dye and Pigment Intermediate in Azo Compound Production

    This material serves as a critical amide-containing intermediate in the controlled synthesis of azo-based colorants, where downstream pigment manufacturers require consistency for both fastness and solubility parameters in textile, leather, and ink sectors. The defined halogen substitution supports diazotization and coupling reactions, facilitating targeted hue and shade development based on precise demand specifications from color manufacturers.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for textile auxiliary substances)
    • EN 71-3:2019 Safety of Toys – Migration of certain elements (for pigment migration)
    • ISO 9001:2015 and ISO 14001:2015 for colorant manufacturing
    • REACH Annex XVII restricted substances list (for azo dyes)

    Typical usage ratio

    • Used within 1.5–6% by mass depending on coupling requirements and final shade intensity; fine-tuned for each pigment lot based on spectral analysis

    Downstream process integration

    • Reacted in diazotization-coupling sequences following primary amine mixing; subsequent purification by filtration and milling ahead of finished pigment paste or dispersion formulation

    Final product types

    • High-fastness azo pigments for synthetic fiber dyeing
    • Stable organic dye dispersions for digital and screen inks
    • Coloring agents for rubber and plastics compounding

    4. Specialty Chemical Synthesis for Fine Chemical Building Blocks

    Producers of specialty and fine chemicals apply this intermediate during multi-step syntheses of custom halogenated and substituted aromatic compounds, often in toll manufacturing environments where trace impurities and reactivity windows must be closely managed. Detailed batch records and analytical data support each run for markets demanding process-specific verification, such as electronics chemicals or custom reagents.

    Industry compliance standards

    • ISO 9001:2015 for specialty chemical manufacturing
    • Custom-defined in-house specifications (based on client NDA projects)
    • REACH full registration for specialty intermediates
    • Chemical industry Responsible Care Management System

    Typical usage ratio

    • Ranges from 0.2 to 1.0 molar equivalent based on synthesis design; adjusted for desired halogenation density and substituted aromatic output purity control

    Downstream process integration

    • Dosed into custom batch reactors following aniline or substituted benzene activation, coordinated with in-line analytical tracking for reaction completion and yield assessment

    Final product types

    • Halogenated benzene derivatives for electronics-grade polymers
    • Aromatic functional intermediates for research reagents
    • Building blocks for fine chemical catalogs
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