Tripotassium phosphate
Chemical compound
From Wikipedia, the free encyclopedia
Tripotassium phosphate, also called tribasic potassium phosphate[3] is a water-soluble salt with the chemical formula K3PO4.(H2O)x (x = 0, 3, 7, 9).[4] Tripotassium phosphate is basic: a 1% aqueous solution has a pH of 11.8.[4]
Unit cell of tripotassium phosphate. | |
| Names | |
|---|---|
| IUPAC name
Potassium phosphate | |
| Systematic IUPAC name
Potassium tetraoxidophosphate(3−) | |
| Other names
Potassium phosphate, tribasic | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.029.006 |
| EC Number |
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| E number | E340(iii) (antioxidants, ...) |
PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| K3PO4 | |
| Molar mass | 212.27 g/mol |
| Appearance | White deliquescent powder |
| Density | 2.564 g/cm3 (17 °C) |
| Melting point | 1,380 °C (2,520 °F; 1,650 K) |
| 90 g/100 mL (20 °C) | |
| Solubility in ethanol | Insoluble |
| Basicity (pKb) | 1.6 |
| Structure[1] | |
| Primitive orthorhombic | |
| Pnma, No. 62 | |
| Hazards[2] | |
| Occupational safety and health (OHS/OSH): | |
Main hazards |
Irritant |
| GHS labelling: | |
| Warning | |
| H319 | |
| P264, P280, P305+P351+P338, P337+P313 | |
| NFPA 704 (fire diamond) | |
| Flash point | Non-flammable |
| Safety data sheet (SDS) | MSDS |
| Related compounds | |
Other cations |
Trisodium phosphate Triammonium phosphate Tricalcium phosphate |
Related compounds |
Monopotassium phosphate Dipotassium phosphate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Production
Tripotassium phosphate is produced by the neutralization of phosphoric acid with potassium hydroxide:[4]
- H3PO4 + 3KOH → K3PO4 + 3H2O
Use in organic chemistry

Tripotassium phosphate has few industrial applications, however it is commonly used as a base in laboratory-scale organic chemistry. Being insoluble in organic solvents, it is an easily removed proton acceptor in organic synthesis. The anhydrous salt is especially basic.[5] Some of the reactions are listed below:
- The hydrate (K3PO4·H2O) has been used to catalyze the deprotection of BOC amines. Microwave radiation is used to aid the reaction.[6]
- As a catalyst for the synthesis of unsymmetrical diaryl ethers using [Bmim]BF4 as the solvent. Aryl methane-sulfonates are deprotected and then followed by a nucleophilic aromatic substitution (SNAr) with activated aryl halides.[7]
- As a base in the cross-coupling reaction of aryl halides with terminal alkynes. It also plays a role in the deacetonation of 4-aryl-2-methylbut-3-yn-2-ol intermediates.[8]
- As the base in the cross-coupling reaction between aryl halides and phenols or aliphatic alcohols.[9]
Use in foods
Tripotassium phosphate can be used in foods as a buffering agent, emulsifying agent, and for nutrient fortification. It can serve as a sodium-free substitute for trisodium phosphate. The ingredient is most common in dry cereals but is also found in meat, sauces, and cheeses.[10]


