Sodium trimetaphosphate

Chemical compound From Wikipedia, the free encyclopedia

Sodium trimetaphosphate

Sodium trimetaphosphate (also STMP), with formula Na3P3O9, is one of the metaphosphates of sodium. It has the formula Na3P3O9 but the hexahydrate Na3P3O9·(H2O)6 is also well known. It is the sodium salt of trimetaphosphoric acid. It is a colourless solid that finds specialised applications in food and construction industries: it is used as a phosphorylating agent for ascorbic acid to stabilize vitamin C mixtures against thermal decomposition; in the construction industry, sodium trimetaphosphate is used to prevent the shrinkage of gypsum plaster boards (US Pat. 03/0154888) and as a setting retarder for gypsum plaster.[2]

Quick Facts Names, Identifiers ...
Sodium trimetaphosphate[1]
Thumb
Names
Other names
Sodium trimetaphosphate
Identifiers
3D model (JSmol)
ECHA InfoCard 100.029.171
EC Number
  • 232-088-3
UNII
  • InChI=1S/3Na.H3O9P3/c;;;1-10(2)7-11(3,4)9-12(5,6)8-10/h;;;(H,1,2)(H,3,4)(H,5,6)/q3*+1;/p-3
  • O=P(OP(O1)([O-])=O)([O-])OP1([O-])=O.[Na+].[Na+].[Na+]
Properties
Na3P3O9
Molar mass 305.885 g/mol
Appearance colorless or white crystals
Density 2.49 g/cm3 (anhydrous)
1.786 g/cm3 (hexahydrate)
Melting point 53 °C (127 °F; 326 K) (hexahydrate, decomposes to anyhdrous)
22 g/100 mL
Solubility insoluble in alcohol
1.433 (hexahydrate)
Structure
triclinic (hexahydrate)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Close

Although drawn with a particular resonance structure, the trianion has high symmetry.[3]

Thumb
Portion of the solid state structure of Na3P3O9·(H2O)6, as determined by X-ray crystallography. Highlighted is the P3O9 ring and some hydrogen bonding. Atoms are color coded as: purple = P, red = O, cyan = Na, white = H.[4]

Synthesis and reactions

Trisodium trimetaphosphate is produced industrially by heating sodium dihydrogen phosphate to 550 °C, a method first developed in 1955:[5]

3 NaH2PO4 → Na3P3O9 + 3 H2O

The trimetaphosphate dissolves in water and is precipitated by the addition of sodium chloride (common ion effect), affording the hexahydrate.[6] STMP can also prepared by heating samples of sodium polyphosphate,[2] or by a thermal reaction of orthophosphoric acid and sodium chloride at 600°C.[7][8]

3 H3PO4 + 3 NaCl → Na3P3O9 + 3 H2O + 3 HCl

Hydrolysis of the ring leads to the acyclic sodium triphosphate:

Na3P3O9 + H2O → H2Na3P3O10

The analogous reaction of the metatriphosphate anion involves ring-opening by amine nucleophiles.[9]

References

Wikiwand - on

Seamless Wikipedia browsing. On steroids.