|
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 | 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. |
Applications of Diethyl (2-Oxopropyl)Phosphonate in Industrial ManufacturingDiethyl (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 IntermediatesManufacturers 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
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Active Agent ProductionAgrochemical 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
Typical usage ratio
Downstream process integration
Final product types
3. Flame Retardant Additive SynthesisIndustrial 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
Typical usage ratio
Downstream process integration
Final product types
4. Organic Synthesis for Specialty ChemicalsResearch 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
Typical usage ratio
Downstream process integration
Final product types
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