| | Identification | More |  | [Name] 
 7-Azabenzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate
 |  | [CAS] 
 156311-85-2
 |  | [Synonyms] 
 7-Azabenzotriazol-1-yloxytris(dimethylamino)phosph
 7-Azabenzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate
 AOP
 Tris(dimethylamino)(3H-1,2,3-triazolo[4,5-b]pyridin-3-yloxy)phosphorus hexafluorophosphate
 7-Aza-1H-benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate
 AOP [7-(Azabenzotriazol-1-yl)oxy tris(dimethylamino)phosphonium hexafluorosphate]
 |  | [EINECS(EC#)] 
 681-486-7
 |  | [Molecular Formula] 
 C11H21F6N7OP2
 |  | [MDL Number] 
 MFCD09263289
 |  | [Molecular Weight] 
 443.27
 |  | [MOL File] 
 156311-85-2.mol
 | 
 | Chemical Properties | Back Directory |  | [Melting point ] 
 180°C
 |  | [storage temp. ] 
 under inert gas (nitrogen or Argon) at 2-8°C
 |  | [Usage] 
 An intermediate in the synthesis of biotin. Pimeloyl-CoA is transformed into AOP in the presence of L-alanine by the enzyme AOP synthase.  The catalytic mechanism of AOP synthase has been studied for the elucidation of inhibitors as potential antimi
 |  | [CAS DataBase Reference] 
 156311-85-2(CAS DataBase Reference)
 | 
 | Hazard Information | Back Directory |  | [Chemical Properties] 
 White to almost white crystalline powder
 |  | [Uses] 
 An intermediate in the synthesis of biotin. Pimeloyl-CoA is transformed into AOP in the presence of L-alanine by the enzyme AOP synthase.  The catalytic mechanism of AOP synthase has been studied for the elucidation of inhibitors as potential antimi
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 |  |