Triphosphoric acid
This articleneeds additional citations forverification.(December 2014) |
Names | |
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IUPAC name
Diphosphono hydrogenphosphate
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Systematic IUPAC name
Triphosphoric acid Tripolyphosphoric acid | |
Other names
Diphosphonophosphoric acid
Phosphono trihydrogenpyrophosphate Phosphonopyrophosphoric acid | |
Identifiers | |
3D model (JSmol)
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ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.030.752 |
EC Number |
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KEGG | |
PubChemCID
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UNII | |
CompTox Dashboard(EPA)
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Properties | |
H5P3O10 | |
Molar mass | 257.95 g/mol |
Acidity(pKa) | See body |
Conjugate base | Triphosphate |
Hazards | |
Occupational safety and health(OHS/OSH): | |
Main hazards
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Corrosive (C) |
Except where otherwise noted, data are given for materials in theirstandard state(at 25 °C [77 °F], 100 kPa).
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Triphosphoric acid(alsotripolyphosphoric acid), with formula H5P3O10,is acondensedform ofphosphoric acid.In the family ofphosphoric acids,it is the nextpolyphosphoric acidafterpyrophosphoric acid,H4P2O7,also called diphosphoric acid.
Compounds such as ATP (adenosine triphosphate) areestersof triphosphoric acid.
Triphosphoric acid has not been obtained in crystalline form. The equilibrium mixture with an overall composition corresponding to H5P3O10contains about 20% of triphosphoric acid. A solution of the pure species can be obtained by ion exchange of the sodium salt,sodium triphosphate,at 0 °C.[1]
Triphosporic acid is apentaprotic acid,meaning that it can release five protons in basic enough conditions. Sources differ on the corresponding pKavalues:
- 1.0; 2.2; 2.3; 5.7; 8.5[1]
- 1.0; 2.2; 2.3; 3.7; 8.5[2]
- small; small; 2.30; 6.50; 9.24[citation needed]
References
[edit]- ^abCorbridge, D. (1995). "Chapter 3: Phosphates".Studies in inorganic Chemistry vol. 20.Elsevier Science B.V. pp. 169–305.ISBN0-444-89307-5.
- ^Holleman, Arnold Frederik; Wiberg, Egon (2001), Wiberg, Nils (ed.),Inorganic Chemistry,translated by Eagleson, Mary; Brewer, William, San Diego/Berlin: Academic Press/De Gruyter, p. 729,ISBN0-12-352651-5