Strontium perchlorate

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Strontium perchlorate
Names
Other names
Strontium(II) perchlorate; Strontium diperchlorate
Identifiers
3D model (JSmol)
ChemSpider
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EC Number
  • 236-614-2
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  • InChI=1S/2ClHO4.Sr/c2*2-1(3,4)5;/h2*(H,2,3,4,5);/q;;+2/p-2
    Key: MXRFIUHRIOLIIV-UHFFFAOYSA-L
  • [O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O.[Sr+2]
Properties
Sr(ClO4)2
Molar mass 286.51 g·mol−1
Appearance White crystals
Density 2.973 g/cm3[1]
Melting point 477 °C (891 °F; 750 K)[1] (decomposes vigorously)
309.7 g/100 g
Solubility in ethyl acetate 136.9 g/100 g
Solubility in methanol 221.0 g/100 g
Solubility in ethanol 180.7 g/100 g
Solubility in 1-propanol 140.4 g/100 g
Solubility in 1-butanol 113.5 g/100 g
Solubility in isobutanol 77.9 g/100 g
Solubility in acetone 140.1 g/100 g
Structure[2]
orthorhombic
Pbca
a = 14.18206 Å, b = 9.78934 Å, c = 9.37624 Å
α = 10.009°, β = 90°, γ = 90°
1301.73 Å3
8
Hazards
GHS labelling:[3]
GHS03: OxidizingGHS07: Exclamation mark
Danger
H272, H315, H319, H335
P210, P221, P280, P305+P351+P338, P403+P233, P501
NFPA 704 (fire diamond)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Strontium perchlorate is a deliquescent white crystalline compound with the formula Sr(ClO4)2.[1]

It is a strong oxidizer which gives red flames. It can be used in pyrotechnics; however, usually the more common strontium nitrate is used. Strontium perchlorate has been used in gelled flame compositions where its hygroscopic nature isn't an issue, in a polymerized candle composition that excluded water, and in an experimental high-atmosphere flash powder.[1]

It is also used in Liquid Injection Thrust Vector Control (LITVC) in solid-propellant rockets to enable steering control with a simple fixed nozzle.[citation needed]

Strontium perchlorate has been characterized in multiple hydrated forms; a trihydrate (Sr(ClO4)2·3H2O), tetrahydrate (Sr(ClO4)2·4H2O) and nonahydrate (Sr(ClO4)2·9H2O).[2]

Synthesis

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Hydrated forms may be prepared by dissolving pure strontium nitrate in an excess of perchloric acid, neutralizing the excess acid with strontium carbonate, centrifuging off solids, and chilling to precipitate crystals.

The anhydrous form may be prepared by drying the hydrate at 250 °C (482 °F), which gives a yield of 50%, or by the addition of anhydrous perchloric acid to a solution of strontium ion in anhydrous trifluoroacetic acid followed by filtration of the precipitated solid and removal of excess acid under vacuum.[1]

References

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