Praseodymium(III) Sulfate
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Praseodymium III Sulfate
Praseodymium(III) sulfate
Praseodymium sulphate octahydrate crystals.JPG
Praseodymium sulfate octahydrate
IUPAC name
praseodymium(3+); trisulfate
Other names
Praseodymium sulphate, dipraseodymium trisulphate, praseodymium(III) sulfate
3D model (JSmol)
ECHA InfoCard 100.030.553
EC Number
  • 233-622-8
Pr2(SO4)3·nH2O, n=2,5,8
Molar mass 570.0031 g/mol
714.12534 g/mol (octahydrate)
Appearance green crystalline solid
Density 3.72 g/cm3[1]
Melting point 1,010 °C (1,850 °F; 1,280 K) (decomposes)[1]
113.0 g/l (20 °C)
108.8 g/l (25 °C)
+9660·10-6 cm3/mol
Main hazards Xi
R-phrases (outdated) 36/37/38
S-phrases (outdated) 26-36
Flash point Non-flammable
Related compounds
Other anions
Praseodymium carbonate
Praseodymium chloride
Other cations
Neodymium sulfate
Related compounds
Praseodymium(III) oxide
Praseodymium(III) sulfide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
?N verify (what is ?Y?N ?)
Infobox references

Praseodymium(III) sulfate is a praseodymium compound with formula Pr2(SO4)3. It is an odourless whitish-green crystalline compound. The anhydrous substance readily absorbs water forming pentahydrate and octahydrate.[1]


Praseodymium sulfate is stable under standard conditions. At elevated temperatures, it gradually loses water and becomes more whitish. Like all rare earth sulfates, its solubility decreases with temperature, a property once used to separate it from other, non-rare earth compounds.

Pentahydrate and octahydrate have monoclinic crystal structures with densities of 3.713 and 2.813 g/cm3, respectively. The octahydrate crystals are optically biaxial, with refractive index components of n? = 1.5399, n? = 1.5494 and n? = 1.5607.[1] They belong to the space group C12/c1 (No. 15) and have lattice constants a = 1370.0(2) pm, b = 686.1(1) pm, c = 1845.3(2) pm, ? = 102.80(1)° and Z = 4.[2]


Crystals of octahydrate can be grown from solution obtained by dissolving wet Pr2O3 powder with sulfuric acid. This procedure can be optimised by adding a few evaporation/dissolution steps involving organic chemicals.[2]


  1. ^ a b c d National Research Council (U.S.) (1919). Bulletin of the National Research Council. National Academies. pp. 3-. NAP:12020. Retrieved 2011.
  2. ^ a b Y.-Q. Zheng, Y.-J. Zhu and J.-L. Lin (2002). "Redeterminaton of the crystal structure of praseodymium sulfate octahydrate, Pr2(SO4)3·8H2O". Zeitschrift für Kristallographie - New Crystal Structures. 217: 299-300.PDF copy[permanent dead link]

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