Tripotassium phosphate, also called tribasic potassium phosphate is a water-soluble salt with the chemical formula K3PO4.(H2O)x (x = 0, 3, 7, 9). Tripotassium phosphate is basic: a 1% aqueous solution has a pH of 11.8.
Unit cell of tripotassium phosphate. | |
| Names | |
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| IUPAC name Potassium phosphate | |
| Systematic IUPAC name Potassium tetraoxidophosphate(3−) | |
| Other names Potassium phosphate, tribasic | |
| Identifiers | |
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| ECHA InfoCard | 100.029.006 |
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| E number | E340(iii) (antioxidants, ...) |
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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 | |
| Primitive orthorhombic | |
| Pnma, No. 62 | |
a = 1.123772 nm, b = 0.810461 nm, c = 0.592271 nm | |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards | Irritant |
| GHS labelling: | |
Signal word | Warning |
| H319 | |
| P264, P280, P305+P351+P338, P337+P313 | |
| NFPA 704 (fire diamond) | 2 0 0 |
| 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). verify (what is ?) Infobox references | |
Production
Tripotassium phosphate is produced by the neutralization of phosphoric acid with potassium hydroxide:
- 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. 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.
- 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.
- 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.
- As the base in the cross-coupling reaction between aryl halides and phenols or aliphatic alcohols.
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.
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