Tripotassium phosphate

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.

Tripotassium phosphate
Unit cell of tripotassium phosphate.
Names
IUPAC name
Potassium phosphate
Systematic IUPAC name
Potassium tetraoxidophosphate(3−)
Other names
Potassium phosphate, tribasic
Identifiers
  • 7778-53-2 Y
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:190301
ChemSpider
  • 56408 Y
ECHA InfoCard 100.029.006
EC Number
  • 231-907-1
E number E340(iii) (antioxidants, ...)
  • 62657
UNII
  • 16D59922JU Y
  • DTXSID3043994
  • InChI=1S/3K.H3O4P/c;;;1-5(2,3)4/h;;;(H3,1,2,3,4)/q3*+1;/p-3 Y
    Key: LWIHDJKSTIGBAC-UHFFFAOYSA-K Y
  • [K+].[K+].[K+].[O-]P([O-])([O-])=O
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).
Y verify (what is YN ?)
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:

  1. The hydrate (K3PO4·H2O) has been used to catalyze the deprotection of BOC amines. Microwave radiation is used to aid the reaction.
  2. 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.
  3. 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.
  4. 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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