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Diethyl (2-Oxopropyl)Phosphonate

    • Product Name Diethyl (2-Oxopropyl)Phosphonate
    • Alias DEP
    • Einecs 249-665-6
    • 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

    238145

    Chemical Name Diethyl (2-Oxopropyl)Phosphonate
    Molecular Formula C7H15O4P
    Molecular Weight 194.17 g/mol
    Cas Number 808-52-4
    Appearance Colorless to pale yellow liquid
    Boiling Point 132-134°C at 14 mmHg
    Density 1.128 g/mL at 25°C
    Refractive Index n20/D 1.430
    Solubility Soluble in organic solvents such as ethanol and ether
    Purity Typically ≥97%
    Smiles CCOP(=O)(OCC)CC(=O)C
    Storage Store at 2-8°C in a cool, dry place
    Synonyms Diethyl (1-oxopropan-2-yl)phosphonate

    As an accredited Diethyl (2-Oxopropyl)Phosphonate 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 of Diethyl (2-Oxopropyl)Phosphonate, sealed with a screw cap and proper hazard labeling.
    Shipping Diethyl (2-Oxopropyl)phosphonate is shipped in tightly sealed containers under dry, cool conditions, away from heat and incompatible substances. Proper hazard labeling and documentation are included, following all applicable local and international chemical transport regulations. Protective packaging prevents leakage or breakage during transit to ensure safe delivery.
    Storage Diethyl (2-Oxopropyl)phosphonate should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep it in a cool, dry, and well-ventilated area, separated from oxidizing agents and strong bases. Store at room temperature, and ensure proper labeling to avoid accidental misuse. Always follow local regulations and safety guidelines for chemical storage.
    Application of Diethyl (2-Oxopropyl)Phosphonate

    Applications of Diethyl (2-Oxopropyl)Phosphonate in Industrial Manufacturing

    Diethyl (2-Oxopropyl)phosphonate serves critical synthesis roles in several industrial chemical production routes. As the original manufacturer, we supply this compound for downstream applications requiring strict adherence to safety, purity, and regulatory compliance. Below, we detail recognized industrial uses with relevant standards, process considerations, and finished product types.

    1. Synthesis of Pharmaceutical Intermediates

    Manufacturers use diethyl (2-oxopropyl)phosphonate as a key enolate component during the synthesis of active pharmaceutical ingredient (API) intermediates, particularly those involving substituted phosphonates for oncology and antiviral compounds. The compound participates in selective alkylation and condensation stages, providing critical phosphonate moieties to heterocyclic scaffolds. Strict adherence to established pharmacopeial and GMP frameworks is essential to ensure consistent downstream production quality and patient safety.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for intermediates
    • USP Guidelines for Bulk Pharmaceuticals
    • FDA 21 CFR Part 211 for finished pharmaceuticals

    Typical usage ratio

    • 5–15 mol% relative to limiting substrate
    • Adjusted according to desired yield and stoichiometry in enolate alkylation or Michael addition reactions

    Downstream process integration

    • Entry at early or mid-stage step during scaffold formation
    • Direct addition to condensation reactors for enolate formation
    • Purification follows by preparative chromatography and crystallization
    • Quality control sampling prior to final active ingredient assembly

    Final product types

    • Pyridine-based antitumor agents
    • Phosphonate-modified peptide drugs
    • Antiviral nucleotide analogues
    • API intermediates for further downstream synthesis

    2. Agrochemical Active Agent Production

    Agrochemical formulators incorporate this phosphonate as a phosphorus donor and building block during the synthesis of herbicide and fungicide active substances. The compound’s reactivity enables controlled introduction of phosphonate groups under regulated process environments, supporting production of stable, bioactive molecules. Process lines are designed to avoid cross-contamination, especially when producing dual-use intermediates for multiple crop protection classes.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for agrochemical production
    • FAO/WHO Codex for pesticide manufacturing
    • REACH Registration for chemical safety assessment within Europe
    • Globally Harmonized System (GHS) labeling and documentation

    Typical usage ratio

    • 2–10% by weight in initial synthesis batch
    • Adjusted based on targeted active content in final technical concentrate

    Downstream process integration

    • Reacts with haloester substrates in early organophosphorus synthesis phase
    • Incorporated in solvents under inert atmosphere to prevent premature hydrolysis
    • Intermediate isolation before downstream functionalization (e.g., oxidation, halogenation)
    • Process water monitoring as per GHS aquatic impact guidelines

    Final product types

    • Fosetyl-based systemic fungicide technical concentrate
    • Herbicide actives with phosphonate substituents
    • Insecticide intermediates tailored for crop protection
    • Pesticide formulations for export and domestic use

    3. Flame Retardant Additive Synthesis

    Industrial polymer and plastics companies rely on diethyl (2-oxopropyl)phosphonate for production of halogen-free flame retardant additives. The molecule introduces phosphorus content under condensation or grafting procedures, directly contributing to the fire resistance of resins and thermoplastics. Careful dosing ensures compliance with emissions and safety standards required for resin applications in electrical and construction sectors.

    Industry compliance standards

    • UL 94 Standard for Safety of Flammability of Plastic Materials
    • RoHS Directive 2011/65/EU for hazardous substances
    • EN 13501 for fire classification of construction products
    • REACH/CLP hazard classification for flame retardants

    Typical usage ratio

    • 3–8 wt% in polymer matrix (polyester, epoxy, polyurethane)
    • Adjusted per target LOI (Limiting Oxygen Index) of final compound

    Downstream process integration

    • Mixed directly into polymer melt during compounding
    • Feedstock for phosphorus esterification or grafting with polyols or epoxides
    • Monitored by in-line FTIR and TGA for phosphorus content control
    • Final homogenization before extrusion or molding operations

    Final product types

    • Low-smoke polycarbonate flame retardant granules
    • Fire-resistant polyurethane foams
    • Epoxy resin compounds for printed circuit boards
    • Halogen-free cable insulation formulations

    4. Organic Synthesis for Specialty Chemicals

    Research and industrial synthesis groups employ this compound as a stabilized enolate and phosphorus donor during the preparation of advanced specialty intermediates. Typical downstream transformations include Horner–Wadsworth–Emmons reactions, which yield substituted alkenes or allylic phosphonates with unique physicochemical properties. Usage must reflect strict process safety and solvent compatibility guidelines, especially when scale exceeds pilot plant levels.

    Industry compliance standards

    • ISO 14001 Environmental Management for chemical synthesis sites
    • GMP-like documentation for specialty and fine chemicals
    • REACH chemical inventory registration (if exported to Europe)
    • Local fire and occupational safety codes due to flammable solvent usage

    Typical usage ratio

    • 0.5–2 equivalents in Horner–Wadsworth–Emmons or Michael addition reactions
    • Adjusted based on scale, solvent volume, and conversion requirements

    Downstream process integration

    • Introduced at condensation or alkylation step in batch reactor
    • Works in dry aprotic solvents to minimize side reactions
    • Followed by aqueous work-up and extraction
    • Yield and purity tracking by HPLC or NMR at each stage

    Final product types

    • Allylic and vinyl phosphonate intermediates for dyes
    • Custom reagents for photoresist manufacturing
    • Performance additives for specialty coatings
    • Building blocks for optoelectronic materials
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