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2-Chloro-N-Methyl-N-Phenylacetamide

    • Product Name 2-Chloro-N-Methyl-N-Phenylacetamide
    • Alias N-methyl-N-phenyl-2-chloroacetamide
    • Einecs 207-361-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    769368

    Iupac Name 2-Chloro-N-methyl-N-phenylacetamide
    Molecular Formula C9H10ClNO
    Molecular Weight 183.64 g/mol
    Cas Number 5827-97-8
    Appearance White to off-white solid
    Melting Point 54-57°C
    Solubility Soluble in organic solvents like ethanol, methanol, and acetone
    Purity Typically ≥98%
    Smiles CN(C1=CC=CC=C1)C(=O)CCl
    Inchi InChI=1S/C9H10ClNO/c1-11(8-4-2-3-5-8)9(12)6-7-10/h2-5H,6-7H2,1H3
    Synonyms N-Methyl-N-phenyl-2-chloroacetamide
    Storage Temperature Store at room temperature, protected from light and moisture

    As an accredited 2-Chloro-N-Methyl-N-Phenylacetamide 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 100 grams of 2-Chloro-N-Methyl-N-Phenylacetamide; sealed with a white screw cap and labeled for laboratory use.
    Shipping 2-Chloro-N-Methyl-N-Phenylacetamide is shipped in tightly sealed containers, protected from moisture and direct sunlight. It is classified for transport according to local and international chemical safety regulations. Appropriate labeling, hazard identification, and relevant documentation ensure compliance and safe handling during transit. Store in a cool, dry location upon arrival.
    Storage 2-Chloro-N-Methyl-N-Phenylacetamide should be stored in a tightly closed container, in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Label the container clearly and keep it in a designated chemical storage area, following all local regulations for handling hazardous chemicals. Wear appropriate personal protective equipment when handling.
    Application of 2-Chloro-N-Methyl-N-Phenylacetamide

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

    2-Chloro-N-Methyl-N-Phenylacetamide serves as an essential building block in the synthesis of specialty chemicals for high-value industrial manufacturing sectors. Below, we outline key application fields, highlighting compliance requirements, formulation practices, process stages, and end-product specifications relevant to downstream manufacturers.

    1. Pharmaceutical Intermediate Synthesis

    This compound functions as a key intermediate in the preparation of several active pharmaceutical ingredients (APIs), particularly for central nervous system and anti-inflammatory drug classes. Regulatory frameworks require careful traceability and documentation from raw material sourcing through synthesis stages to final API production, ensuring both product safety and therapeutic consistency. Producers adjust usage ratios depending on the target molecule’s yield requirements and impurity control plans. Strict process validation, impurity profiling, and risk management measures guide process setup, while the compound typically enters during the acylation or amidation sequence of multi-step syntheses within GMP-qualified facilities. Customers expect material that meets stringent quality benchmarks suitable for high-purity pharmaceuticals.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU Regulation (EC) No 1907/2006 (REACH)
    • USP/NF and EP pharmacopoeial standards for intermediates
    • FDA 21 CFR Part 211 (where applicable)

    Typical usage ratio

    • 0.5 to 1.4 molar equivalents relative to target amine group, with adjustments based on desired selectivity and downstream isolation efficiency

    Downstream process integration

    • Enters as acylation agent in Step 2 or 3 during intermediate stage of multi-step API manufacturing; involved in direct amidation, followed by purification and crystallization prior to further derivatization steps

    Final product types

    • Non-steroidal anti-inflammatory drugs (NSAIDs) intermediates
    • Tranquilizer and antiepileptic drug precursors
    • Central nervous system (CNS) agent intermediates
    • Custom-developed molecular entity building blocks

    2. Agrochemical Synthesis

    The chemical supports the synthesis of selective herbicide pre-mixes and fungicidal agents. Agrochemical producers utilize it for targeted acylation during the construction of protective groups or as a masking agent that modifies active ingredient activity. Compliance involves alignment with global crop protection regulation, adherence to hazard communication, and stewardship standards from raw material through to formulated product. Usage ratios vary depending on the molecular design and crop specificity, with precise dosing guided by target molecule substitution patterns. Integration typically occurs in the mid-stage of chemical route, preceding formulation and encapsulation into finished goods, under monitored batch production and analytical quality control.

    Industry compliance standards

    • FAO/WHO International Code of Conduct on Pesticide Management
    • REACH chemical safety assessment (for Europe-bound export)
    • OECD Principles of Good Laboratory Practice (GLP) for agrochemical testing
    • US EPA 40 CFR Part 180 residue and purity standards

    Typical usage ratio

    • 0.6–1.2 molar equivalents per functionalized core, depending on the degree of acyl protection required; optimized for minimal by-product formation

    Downstream process integration

    • Used in mid-stage acylation or masking step, prior to hydrolysis and active ingredient finalization; typically followed by purification, blending, and microencapsulation

    Final product types

    • Pre-mix triazine herbicides
    • Prothioconazole fungicide intermediates
    • Custom crop protection active ingredient scaffolds
    • Herbicide-tolerant trait chemistry building blocks

    3. Dye and Pigment Intermediate Production

    In the fine chemical sector, this material is widely adopted for the synthesis of specialty azo and anthraquinone dye intermediates where targeted acylation is required. Colorant producers demand high batch-to-batch consistency and regulated impurity levels to ensure superior color development and lightfastness in downstream applications. Industry accreditation and environmental regulation dictate hazardous substance management and emission controls throughout manufacturing. The chemical most often reacts at intermediate steps prior to coupling, followed by distillation or filtration. Precise dosing relies on the complexity and functionalization of dye precursors, which producers calculate based on shade, yield, and cost targets.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (for textile dyes)
    • REACH SVHC monitoring (Substances of Very High Concern)
    • ETAD Quality Standards for colorant intermediates
    • ISO 9001:2015 for quality management systems

    Typical usage ratio

    • 0.7–1.3 molar equivalents per colorant core structure; lower end favored for pale shades, higher for dark or high-purity tones

    Downstream process integration

    • Feeds into acylation step during synthesis of dye precursor; followed by diazotization, coupling, then granulation or spray drying for stabilization

    Final product types

    • Azo dye intermediates for textile and paper
    • Anthraquinone pigments for plastics or inks
    • Disperse dye bases for polyester fibers
    • Organic pigment intermediates

    4. Specialty Polymer Modifier Synthesis

    Producers of engineering plastics and elastomers use the compound as a reactive intermediate to introduce aromatic acylamido functionalities, improving polymer resilience, thermal properties, and processability. Application demands close process control and rigorous chemical inventory management, complying with polymer-grade raw material protocols and product stewardship standards. Usage ratio varies by targeted modification effect and substrate reactivity, with pilot studies guiding final formulation ratios. The compound typically enters post-polymerization, during chain modification by grafting or block copolymer extension, or as a precursor for synthesizing performance modifiers prior to compounding and extrusion. End-users specify intermediate purity and kinetics data to achieve consistent final material properties.

    Industry compliance standards

    • ISO 9001:2015 for process quality management
    • REACH pre-registration for polymer production
    • Chemical Industry Regulatory Guidelines for intermediates use
    • ASTM D256 and D638 for polymer performance testing

    Typical usage ratio

    • 1–5 wt% relative to the polymer or copolymer batch; adjust based on chain length and degree of functionalization required in finished resin

    Downstream process integration

    • Added post-polymerization as chain modifier; introduced during grafting or end-group functionalization in solution or melt phase, followed by blending and pelletizing

    Final product types

    • High-performance engineering thermoplastics
    • Heat-resistant elastomer blends
    • Specialty copolymers for automotive and electronics
    • Polymer-based structural composite intermediates
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