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Dimethyl (2-Oxo-4-Phenylbutyl)Phosphonate

    • Product Name Dimethyl (2-Oxo-4-Phenylbutyl)Phosphonate
    • Alias Dimethyl (2-oxo-4-phenylbutyl)phosphonate
    • Einecs 248-487-2
    • 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
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    Specifications

    HS Code

    622324

    Productname Dimethyl (2-Oxo-4-Phenylbutyl)Phosphonate
    Casnumber 42042-71-7
    Molecularformula C12H17O4P
    Molecularweight 256.24
    Appearance Colorless to pale yellow liquid
    Density 1.169 g/cm3
    Refractiveindex 1.486
    Purity Typically ≥ 97%
    Smiles COP(=O)(CCC(=O)CC1=CC=CC=C1)OC
    Storageconditions Store at 2-8°C, keep container tightly closed
    Solubility Soluble in common organic solvents

    As an accredited Dimethyl (2-Oxo-4-Phenylbutyl)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 Dimethyl (2-Oxo-4-Phenylbutyl)Phosphonate, with tamper-evident cap and hazard labeling.
    Shipping Dimethyl (2-Oxo-4-Phenylbutyl)phosphonate is shipped in tightly sealed containers, protected from moisture and light. The packaging complies with all relevant hazardous material regulations. During transport, temperature and handling precautions are followed to prevent leaks or degradation, ensuring safe delivery while maintaining chemical integrity and adhering to legal safety standards.
    Storage Dimethyl (2-Oxo-4-Phenylbutyl)phosphonate should be stored in a cool, dry, and well-ventilated area, away from heat, sparks, and direct sunlight. Keep the container tightly closed and protected from moisture. Store separately from incompatible substances such as strong oxidizers, acids, or bases. Use only in a chemical fume hood and follow all relevant safety guidelines and regulations.
    Application of Dimethyl (2-Oxo-4-Phenylbutyl)Phosphonate

    Applications of Dimethyl (2-Oxo-4-Phenylbutyl)Phosphonate in Industrial Manufacturing

    As the direct manufacturer of Dimethyl (2-Oxo-4-Phenylbutyl)Phosphonate, we supply this specialty intermediate for advanced chemical synthesis in high-value sectors. Its reactivity and molecular design support crucial transformations in downstream applications. Below, we outline clearly defined industrial uses, focusing on real-world implementation and the technical, regulatory, and process specifics demanded by B2B partners across specialized segments.

    1. Active Pharmaceutical Ingredient (API) Synthesis for CNS Drug Development

    Pharmaceutical companies utilize this phosphonate as a building block during the multi-step synthesis of certain central nervous system (CNS) active compounds, such as anticonvulsant and neuroprotective APIs. Its incorporation at the intermediate stage enables efficient construction of phosphorus-carbon frameworks required for subsequent pharmacophore elaboration. Stringent quality standards and batch traceability are critical throughout processing to ensure suitability for API manufacture targeting regulated markets.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF Monograph Specific Testing (where applicable)
    • EU GMP Guide Parts I & II
    • FDA 21 CFR Part 210/211

    Typical usage ratio

    • 0.08–0.18 molar equivalents per target stage, adjusted based on purity and reaction yield optimization studies.

    Downstream process integration

    • Charged to catalytic coupling stage following aromatic precursor activation in small-molecule synthesis workflows.

    Final product types

    • Active pharmaceutical ingredients for CNS drug candidates (e.g., anti-epileptics, neuroprotectives)
    • Regulatory-submitted clinical trial substances

    2. Synthesis of Organophosphorus Flame Retardants for High-Performance Polymers

    Polymer compounders and masterbatch formulators employ Dimethyl (2-Oxo-4-Phenylbutyl)Phosphonate in the production of modern organophosphorus flame retardant additives. Its structural attributes enable direct participation in transesterification reactions, introducing phosphorus-containing groups into polyester and polyamide matrices. This approach meets demanding flammability requirements for electronics, electronics housings, and automotive interior components subject to international fire safety regulations.

    Industry compliance standards

    • UL 94: Standard for Safety of Flammability of Plastic Materials
    • REACH Regulation (EC) 1907/2006: Registration, Evaluation, Authorisation and Restriction of Chemicals
    • IEC 60695-11: Fire hazard testing for polymeric materials
    • RoHS Directive (EU) 2015/863

    Typical usage ratio

    • 6–15% by weight in additive masterbatches; precise ratio determined by resin compatibility and required LOI (Limiting Oxygen Index) results.

    Downstream process integration

    • Introduced as a reaction intermediate during reactive extrusion or in batch blending before pelletization of functionalized flame retardant resins.

    Final product types

    • Flame-retarded polyesters and polyamides
    • Electronics and electrical device components (e.g., housings, connectors)
    • Automotive polymer parts with certified FR performance

    3. Agrochemical Intermediate for Selective Herbicide Synthesis

    Chemical producers in the crop protection sector leverage this organophosphonate for the synthesis of select phosphonate-based herbicidal active ingredients. The compound’s carbon-phosphorus bond facilitates further functionalization through alkylation and conjugation reactions, supporting access to actives targeting resistant weed species in regulated agricultural markets. Formulation, handling, and documentation must comply with global pesticide regulatory frameworks.

    Industry compliance standards

    • FAO/WHO Specification and Evaluation for Plant Protection Products
    • OECD Guidelines for the Testing of Chemicals
    • China ICAMA Registration Requirements
    • EPA 40 CFR Part 180 (U.S. Tolerances for Pesticide Residues)

    Typical usage ratio

    • 0.10–0.21 molar equivalents in stepwise synthesis of herbicidal actives, controlled by targeted activity screen and downstream demand.

    Downstream process integration

    • Engaged during the key phosphonylation or Michael addition step, preceding final formulation and crystallization of the herbicide technical concentrate.

    Final product types

    • Technical-grade selective herbicides for grain and vegetable crops
    • Commercial herbicide formulations (e.g., wettable powders, suspension concentrates)

    4. Fine Chemical Intermediate for Aroma Chemical Synthesis

    Manufacturers of high-purity aroma chemicals for fragrances and flavors use this phosphonate as a functional synthon to construct complex aromatic ketones and aldehydes. Its participation in carbon-phosphorus bond formation and subsequent hydrolysis/oxidation reactions enables access to target molecules valued for their sensory attributes. Units handling such specialty intermediates operate under rigorous purity control and traceability systems supporting food-grade and perfumery applications.

    Industry compliance standards

    • FEMA GRAS (Flavor and Extract Manufacturers Association, U.S.)
    • IFRA Standards (International Fragrance Association) for restricted substances
    • ISO 9001:2015 Quality Management Systems
    • EU Regulation (EC) 1334/2008 on Flavorings

    Typical usage ratio

    • 0.05–0.11 equivalents relative to the aromatic starting material; ratio tailored for conversion yield and substrate selectivity in pilot and commercial-scale runs.

    Downstream process integration

    • Fed to the controlled organophosphonate addition or Wittig-type reaction vessel, usually followed by acid or enzymatic hydrolysis prior to final distillation and refining.

    Final product types

    • Aroma intermediates for fine fragrance bases
    • Flavoring compounds for beverages and confectionery
    • High-purity restaurant and consumer-grade aroma substances
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