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  • Diphenylphosphonic azide, 97%, Thermo Scientific Chemicals

    A12124.06
    CAS Number: 26386-88-9See All CAS: 26386-88-9 In Stock

      CAT NUM
      PRODUCT NAME
      Pack Size
      PRICE
      QUANTITY
       
      CAT NUM: A12124.06
      Diphenylphosphonic azide, 97%, Thermo Scientific Chemicals
      Pack Size: 5GR
      PRICE: 
      CAT NUM: A12124.14
      Diphenylphosphonic azide, 97%, Thermo Scientific Chemicals
      Pack Size: 25GR
      PRICE: 
      CAT NUM: A12124.22
      Diphenylphosphonic azide, 97%, Thermo Scientific Chemicals
      Pack Size: 100GR
      PRICE: 

      CAS Number
      26386-88-9
      Hazard Class
      6.1
      Pack Size
      5GR, 25GR, 100GR
      Molecular Formula
      C12 H10 N3 O3 P
      Molecular Weight
      275.2
      MFCD
      00001987
      Density
      1.275
      UN Number
      3278
      Flash Point
      >110
      Storage Temp
      Refrigerator +4°C
      Brand
      Thermo Scientific - Alfa Aesar

      Diphenylphosphonic azide acts as a reagent for the synthesis of peptides and phosphoramidates by reacting with amines. It is also used in the preparation of oligosaccharides linked with carbamate and urea bonds utilizing modified Curtis rearrangement. It is involved in pseudohalogen replacement of the azido group by treatment with nucleophilic reagents, such as water, butanol, ammonia, and various amines. Further, it is used as a hydroazidation catalyst for preparation of organoazides.

      This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.


      Applications
      Diphenylphosphonic azide acts as a reagent for the synthesis of peptides and phosphoramidates by reacting with amines. It is also used in the preparation of oligosaccharides linked with carbamate and urea bonds utilizing modified Curtis rearrangement. It is involved in pseudohalogen replacement of the azido group by treatment with nucleophilic reagents, such as water, butanol, ammonia, and various amines. Further, it is used as a hydroazidation catalyst for preparation of organoazides.

      Solubility
      Immiscible with water.

      Notes
      Store in a cool place. Incompatible with acids and oxidizing agents.
      Certifications
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