Propanephosphonic acid anhydride

Propanephosphonic acid anhydride
Names
	IUPAC name 2,4,6-Tripropyl-1,3,5,2λ5,4λ5,6λ5-trioxatriphosphinane 2,4,6-trioxide
	Other names PPACA; PPAA; T3P; Propylphosphonic anhydride
Identifiers
CAS Number	68957-94-8;
3D model (JSmol)	Interactive image;
ChemSpider	100355;
ECHA InfoCard	100.102.078
EC Number	422-210-5;
PubChem CID	111923;
UNII	I6EGD8839N;
CompTox Dashboard (EPA)	DTXSID20219011 ;
	InChI InChI=1S/C9H21O6P3/c1-4-7-16(10)13-17(11,8-5-2)15-18(12,14-16)9-6-3/h4-9H2,1-3H3 Key: PAQZWJGSJMLPMG-UHFFFAOYSA-N;
	SMILES CCCP1(=O)OP(=O)(OP(=O)(O1)CCC)CCC;
Properties
Chemical formula	C9H21O6P3
Molar mass	318.182 g·mol−1
Hazards
GHS pictograms
GHS Signal word	Warning
GHS hazard statements	H290, H314
GHS precautionary statements	P234, P260, P264, P280, P301+330+331, P303+361+353, P304+340, P305+351+338, P310, P321, P363, P390, P404, P405, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Propanephosphonic acid anhydride (PPAA, T3P) is an anhydride of propanephosphonic acid. Its structure is a cyclic trimer, with a phosphorus–oxygen core and propyl groups and additional oxygens attached.[1] The chemical is a useful reagent for peptide synthesis reactions, where it activates the carboxylic acid partner for subsequent reaction with amines. It is commercially available as 50 % solution in DMF or ethyl acetate as a slightly yellow mixture.

References

"Propanephosphonic acid anhydride". Sigma-Aldrich.

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[1] "Propanephosphonic acid anhydride". Sigma-Aldrich.