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2-Acetoxy-2-Phenylacetyl Chloride

    • Product Name 2-Acetoxy-2-Phenylacetyl Chloride
    • Alias Mandelic acid 2-acetoxyacetyl chloride
    • Einecs 406-880-8
    • 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

    487176

    Iupac Name 2-acetoxy-2-phenylacetyl chloride
    Molecular Formula C10H9ClO3
    Molecular Weight 212.63 g/mol
    Cas Number 21205-45-4
    Appearance Colorless to pale yellow liquid
    Density 1.27 g/cm³ (approximate)
    Solubility Reacts with water; soluble in organic solvents
    Functional Groups Acetoxy, acyl chloride, phenyl
    Smiles CC(=O)OC(C(=O)Cl)C1=CC=CC=C1
    Inchi InChI=1S/C10H9ClO3/c1-7(12)14-10(9(11)13)8-5-3-2-4-6-8/h2-6,10H,1H3
    Hazard Classification Corrosive

    As an accredited 2-Acetoxy-2-Phenylacetyl Chloride 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 with a tightly sealed cap, clearly labeled "2-Acetoxy-2-Phenylacetyl Chloride" and hazard symbols.
    Shipping 2-Acetoxy-2-Phenylacetyl Chloride is shipped in tightly sealed, chemical-resistant containers to prevent moisture ingress and ensure stability. It must be handled as a corrosive and lachrymatory substance, shipped under cool, dry conditions, with appropriate hazard labeling and documentation, complying with local and international transport and safety regulations.
    Storage 2-Acetoxy-2-Phenylacetyl Chloride should be stored tightly sealed in a cool, dry, well-ventilated area, away from moisture, heat, and incompatible materials such as strong bases, oxidizers, and alcohols. Keep the container tightly closed and protected from light. Use appropriate corrosion-resistant containers and avoid prolonged exposure to air, as the compound is moisture-sensitive and may hydrolyze or emit harmful fumes.
    Application of 2-Acetoxy-2-Phenylacetyl Chloride

    Applications of 2-Acetoxy-2-Phenylacetyl Chloride in Industrial Manufacturing

    2-Acetoxy-2-Phenylacetyl Chloride serves as a specialty acylation agent and intermediate in several advanced chemical manufacturing segments. Our production controls comply with international quality standards and deliver consistent purity for reliable downstream integration. Below, we detail core industrial sectors and practical end-use cases based on authentic market demand.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Major API manufacturers use this material as an efficient acylating agent in the multi-step synthesis of several non-steroidal anti-inflammatory drugs and beta-lactam antibiotics. In these high-value pharmaceutical processes, the compound plays a role in regioselective acylation, helping form key intermediate structures with controlled impurity profiles. Effective for creating side-chain derivatives, customers implement tailored in-process analytics to ensure compliance throughout GMP manufacturing.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • European Pharmacopoeia (Ph. Eur.) and United States Pharmacopeia (USP) monographs for APIs
    • ICH Q3A(R2) guideline for impurities in new drug substances
    • FDA 21 CFR Parts 210/211 for finished pharmaceuticals

    Typical usage ratio

    • 0.8 – 1.2 molar equivalents relative to the target core structure
    • Dosing varies based on specific pathway and impurity rejection criteria
    • Adjustments made for batch vs. continuous process schemes

    Downstream process integration

    • Acylation of heterocyclic amines or phenolic precursors during advanced intermediate formation
    • Incorporated during telescoped coupling steps with in-line purification (e.g., crystallization or extraction)
    • Monitored via HPLC or LC-MS at the reaction stage for residual chloride assessment

    Final product types

    • Non-steroidal anti-inflammatory drug (NSAID) APIs
    • Beta-lactam and cephalosporin side-chain intermediates
    • Custom chiral intermediates for clinical candidate libraries

    2. Agrochemical Intermediate Manufacturing

    Producers of specialized agrochemical actives employ this acyl chloride for synthesizing aromatic and heterocyclic building blocks found in herbicides and pesticides. Its use facilitates controlled incorporation of acetoxy-phenyl motifs, which can enhance both volatility and biological activity. Our material meets rigorous trace impurity specifications to support large-scale, multi-ton crop protection synthesis workflows.

    Industry compliance standards

    • ISO 9001:2015 for quality management in agrochemical production
    • FAO/WHO Specifications for Plant Protection Products
    • Globally Harmonized System (GHS) of Classification and Labelling of Chemicals
    • REACH registration for import or market in the European Union

    Typical usage ratio

    • 0.5 – 1.5 molar equivalents, based on active ingredient synthesis route
    • Ratio calculated according to optimal yield for the desired target structure
    • Batch-to-continuous integration may alter requirements as process intensifies

    Downstream process integration

    • Stepwise aromatic acylation under controlled temperature (<10°C) in nitrogen atmosphere
    • Post-acylation workup with aqueous quench and solvent extraction
    • Intermediate undergoes further modifications (e.g., chlorination, oxidation) for downstream actives

    Final product types

    • Herbicide active base molecules
    • Fungicide precursor intermediates
    • Insecticide chiral building blocks
    • Growth regulator core precursors

    3. Fine Chemical Synthesis for Fragrance and Flavor Ingredients

    Industry formulators use 2-Acetoxy-2-Phenylacetyl Chloride in multi-step construction of complex aromatic esters, which contribute to key accords in high-end fragrances and select food flavorings. The material enables selective acetylation while maintaining the structural fidelity of aromatic cores. Its batch-to-batch purity meets IFRA and food grade restrictions for non-pharmaceutical downstream preparation.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards
    • Food Chemicals Codex (FCC) standards for intermediates
    • ISO 9235:2013 for aromatic raw materials
    • US FDA 21 CFR §172 for flavoring substance approvals

    Typical usage ratio

    • 0.7 – 1.1 molar equivalents within aromatic ester formation
    • Blending adjusted for target purity (≥99% GC) and residual acid control
    • Process variables: solvent selection, reaction time, and downstream neutralization

    Downstream process integration

    • Introduction in esterification reactors after precursor alcohols or phenols charging
    • Purification via vacuum distillation for removal of by-product chloroacetic acid
    • Quality screening by GC-FID and organoleptic analysis in the finished blend

    Final product types

    • High-purity aromatic esters for perfumery bases
    • Flavoring additives in beverage or dairy formulations
    • Aroma intermediates for personal care and air care products
    • Functionalized aromatics for luxury candle and soap manufacturing

    4. Specialty Polymer and Resin Modification

    2-Acetoxy-2-Phenylacetyl Chloride is adopted by advanced polymer manufacturers for introducing functional aromatic groups into thermoset and thermoplastic resins. This functionalization improves polymer rigidity, solvent resistance, and compatibility in high-performance coatings and engineered composites. Our QC ensures that chloride and organic impurity concentrations remain below user-defined thresholds for materials performance.

    Industry compliance standards

    • ISO 9001:2015 for chemical production quality management
    • ASTM D2567 and D4715 for synthetic resin standards
    • RoHS for limiting hazardous substances in polymer components (where end use applies)
    • EU Regulation No 10/2011 for food contact materials, if appropriate

    Typical usage ratio

    • 0.3 – 0.8 molar equivalents per polymer repeat unit
    • Higher concentration for rigid thermoset resins, lower for thermoplastics
    • Exact formulation optimized for desired end-use properties

    Downstream process integration

    • Incorporated during polymer chain extension or grafting steps (solution or bulk phase)
    • Monitored for grafting yield via gel permeation chromatography (GPC)
    • Volatile removal and neutralization before extrusion or molding

    Final product types

    • Rigid polyesters for automotive components
    • High-durability epoxy resins used in coatings and adhesives
    • Specialty copolymers for filtration membranes
    • Composite sheet molding compounds (SMC) with enhanced physicochemical properties
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