Phosphazene base P2-Et

≥98.0% (NT)

  • Product Code: 76865
  Alias:    Polybis(ethoxypyrrolidone)phosphazene
  CAS:    165535-45-5
Molecular Weight: 339.40 g./mol Molecular Formula: C₁₂H₃₅N₇P₂
EC Number: MDL Number: MFCD00145113
Melting Point: Boiling Point: 383.4ºC at 760mmHg
Density: 1.05g/mL Storage Condition: room temperature
Product Description: Phosphazene base P2-Et is widely utilized in organic synthesis as a strong, non-nucleophilic base. It is particularly effective in deprotonation reactions, where it facilitates the generation of highly reactive anions. This makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals. Its application extends to polymerization processes, where it acts as a catalyst or initiator, enabling the production of high-performance polymers. Additionally, it is employed in the preparation of specialty materials, such as advanced coatings and adhesives, due to its ability to enhance reaction efficiency and control molecular structure. Its stability and low nucleophilicity make it a preferred choice in reactions requiring precise pH control and minimal side reactions.
Product Specification:
Test Specification
Purity 98 100%
Appearance Yellow liquid
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿28,000.00
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Phosphazene base P2-Et
Phosphazene base P2-Et is widely utilized in organic synthesis as a strong, non-nucleophilic base. It is particularly effective in deprotonation reactions, where it facilitates the generation of highly reactive anions. This makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals and fine chemicals. Its application extends to polymerization processes, where it acts as a catalyst or initiator, enabling the production of high-performance polymers. Additionally, it is employed in the preparation of specialty materials, such as advanced coatings and adhesives, due to its ability to enhance reaction efficiency and control molecular structure. Its stability and low nucleophilicity make it a preferred choice in reactions requiring precise pH control and minimal side reactions.
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