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Bis(2-Oxo-3-Oxazolidinyl)Phosphinic Chloride

    • Product Name Bis(2-Oxo-3-Oxazolidinyl)Phosphinic Chloride
    • Alias BOC-Cl
    • Einecs 410-160-2
    • 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

    814679

    Chemicalname Bis(2-Oxo-3-Oxazolidinyl)Phosphinic Chloride
    Casnumber 66070-58-4
    Molecularformula C6H8ClN2O5P
    Molecularweight 266.57
    Appearance White to off-white crystalline solid
    Meltingpoint 104-110°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥ 98%
    Boilingpoint Decomposes before boiling
    Storagetemperature 2-8°C (Refrigerated)
    Synonyms Phosphinic chloride, bis(2-oxo-3-oxazolidinyl)-
    Smiles C1C(=O)N(CO1)P(=O)(Cl)N2CCOC2=O

    As an accredited Bis(2-Oxo-3-Oxazolidinyl)Phosphinic Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25-gram Bis(2-Oxo-3-Oxazolidinyl)Phosphinic Chloride is securely sealed in an amber glass bottle with a tamper-evident cap.
    Shipping Bis(2-Oxo-3-Oxazolidinyl)Phosphinic Chloride is shipped in tightly sealed containers under inert atmosphere to prevent moisture contamination. The chemical is classified as hazardous; shipping follows all relevant regulations, including labeling and documentation requirements. It must be handled and transported by trained personnel, ensuring appropriate temperature controls and safety precautions during transit.
    Storage Bis(2-Oxo-3-Oxazolidinyl)Phosphinic Chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as water, strong bases, and oxidizing agents. It should be kept at room temperature and protected from light. Proper labeling and appropriate chemical storage protocols should be followed to ensure safety.
    Application of Bis(2-Oxo-3-Oxazolidinyl)Phosphinic Chloride

    Applications of Bis(2-Oxo-3-Oxazolidinyl)Phosphinic Chloride in Industrial Manufacturing

    Bis(2-Oxo-3-Oxazolidinyl)Phosphinic Chloride provides unique reactivity and selectivity for various synthesis routes in specialty chemicals, electronics, and polymer modification. Our manufacturing facility supports stable, on-spec supply by strict batch control, making it suitable for critical industrial production environments worldwide.

    1. Organophosphorus Fine Chemicals Synthesis

    Major pharmaceutical and agrochemical companies utilize this compound as a core phosphorus donor in the construction of advanced intermediates, such as P-containing heterocycles and related ligands. The compound enters the organophosphate synthesis process where controlled chlorination and subsequent substitution optimize yields for structures where both oxazolidinone and phosphinic groups are essential. Reaction scale-up in pilot and full-scale settings depends on tight control of reagent feed and in-process monitoring by in-house QC teams.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice
    • EU REACH Regulation (EC) No 1907/2006
    • US EPA TSCA Inventory
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • Generally 0.8–1.2 molar equivalents, adjusted based on target intermediate structure and desired purity targets.

    Downstream process integration

    • Charged to closed reactors during key phosphorus coupling steps, usually post-primary amine or oxazolidinone activation, under nitrogen atmosphere and monitored for heat release control.

    Final product types

    • Phosphinic acid derivatives
    • P-containing heterocycles
    • Active pharmaceutical ingredient intermediates
    • Crop protection precursor molecules

    2. Flame Retardant Additive Manufacturing

    Chemical formulators for plastics and electronic encapsulants depend on this reagent as an intermediate in generating phosphorus-based flame inhibiting agents. Functional group placement supports downstream reactivity for binding within epoxy matrices, delivering required retardant properties without significant volatility. The product enables in-situ resin modification lines with reliable phosphorus incorporation rates, critical for downstream thermal stability of molded parts.

    Industry compliance standards

    • IEC 60695 (Fire hazard testing of electrical equipment)
    • UL 94 (Flammability of plastic materials)
    • RoHS Directive (2011/65/EU, for electronics)
    • ISO 14001:2015 Environmental Management Systems

    Typical usage ratio

    • Flame retardant synthesis: 3–10% w/w of polymer resin input, depending on V-0, V-1, or V-2 fire safety targets and resin type.

    Downstream process integration

    • Added to resin melt blending reactors before final compounding; integration point calibrated to achieve uniform phosphorus distribution and meet product pass rates in flame testing.

    Final product types

    • Flame-resistant composite panels
    • Epoxy resin-based circuit board laminates
    • Wire insulation compounds
    • Consumer electronics enclosures

    3. Functionalized Polymer Crosslinkers

    Specialty polymer manufacturers employ this raw material to introduce phosphinic linkages during reactive extrusion or batch polymer modification. The chloro functionality facilitates precise incorporation into copolymer backbones, offering improved hydrolytic stability and functional handle density. Our QC-monitored production batches support consistent viscosity and molecular weight distribution critical for downstream film extrusion and performance film manufacturing.

    Industry compliance standards

    • ISO 11357-2 (Differential scanning calorimetry for polymers)
    • EN 12814 (Plastics welding standards)
    • REACH Annex XVII (Polymer additives restrictions)
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 0.5–5% w/w within the formulation, based on polymer backbone compatibility, desired crosslinking density, and final mechanical property requirements.

    Downstream process integration

    • Fed to twin-screw extruders or gas-phase batch reactors during crosslinking, with dosing controlled by in-line spectroscopic analysis to prevent overreaction and maintain target elasticity indexes.

    Final product types

    • Hydrolytically stable specialty films
    • High-performance elastomers
    • Polymer-based adhesives
    • Flexible packaging materials

    4. Specialty Ligands for Catalytic Process Development

    Producers of homogeneous and heterogeneous catalysts rely on this compound to synthesize bidentate and tridentate phosphinic ligands supporting advanced catalyst architectures. The dual oxazolidinone functionality enables creation of ligand frameworks matched to specific metal centers for improved selectivity and turnover rates in catalytic transformations including hydroformylation and asymmetric hydrogenation. Integration in R&D pilot labs and scale-up environments depends on batch-to-batch consistency managed by our production analytics.

    Industry compliance standards

    • ISO 17025 (Analytical testing in catalyst R&D)
    • OECD Guideline 109 (Catalyst materials assessment)
    • REACH compliance (for specialty chemicals)
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 0.05–0.2 molar equivalents in ligand-metal complexation; optimized in multi-step syntheses by iterative analytical control and catalytic screening results.

    Downstream process integration

    • Introduced in the final ligand assembly stage prior to metal salt addition, with stoichiometry controlled for complete conversion and analytical verification of phosphorus source utilization.

    Final product types

    • Chiral phosphinic ligands
    • Custom palladium and rhodium catalyst complexes
    • Process chemistry catalyst packages
    • R&D catalyst kits for fine chemical development
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