Sodium aluminium hydride or sodium alanate is an inorganic compound with the chemical formula NaAlH4. It is a white solid that dissolves in tetrahydrofuran (THF), but not in diethyl ether or hydrocarbons. It has been evaluated as an agent for the reversible storage of hydrogen and it is used as a reagent for the chemical synthesis of organic compounds. Similar to lithium aluminium hydride, it is a salt consisting of separated sodium cations and tetrahedral AlH anions.J. W. Lauher, D. Dougherty P. J. Herley "Sodium tetrahydroaluminate" Acta Crystallogr. 1979, volume B35, pp.1454-1456.

Structure, preparation, and reactions Sodium tetrahydroaluminate adopts the structure of (is isostructural with) calcium tungstate. As such, the tetrahedral AlH centers are linked with eight-coordinate Na+ cations. The compound is prepared from the elements under high pressures of H2 at 200 °C using triethylaluminium catalyst:Peter Rittmeyer, Ulrich Wietelmann "Hydrides" in Ullmann's Encyclopedia of Industrial Chemistry, 2002, Wiley-VCH, Weinheim. Na + Al + 2 H2 → NaAlH4

As a suspension in diethyl ether, it reacts with lithium chloride to give the popular reagent lithium aluminium hydride: LiCl + NaAlH4 → LiAlH4 + NaCl

The compound reacts rapidly, even violently, with protic reagents, such as water, as described in this idealized equation: 4 H2O + NaAlH4 → "NaAl(OH)4" + 4 H2

Applications

Hydrogen storage Sodium alanateComputational Study of Pristine and Titanium-doped Sodium Alanates for ... has been explored for hydrogen storage in hydrogen tanks. The relevant reactions are: 3 NaAlH4 → Na3AlH6+ 2 Al + 3 H2 Na3AlH6 → 3 NaH + Al + 3/2 H2

Sodium tetrahydroaluminate can release up to 7.4 wt % of hydrogen when heated at . Absorption can be slow, with several minutes being required to fill a tank. Both release and uptake are catalysed by titanium.

Reagent in organic chemistry Sodium aluminium hydride is a strong reducing agent, very similar in reactivity to lithium aluminium hydride (LAH) and, to some extent, diisobutylaluminium hydride (DIBAL) in organic reactions.Melinda Gugelchuk "Sodium Aluminum Hydride" Encyclopedia of Reagents for Organic Synthesis, 2001, John Wiley. It is much more powerful reducing agent than sodium borohydride due to the weaker and more polar Al-H bond compared to the B-H bond. Like LAH, it reduces esters to alcohols.

Safety Sodium aluminium hydride is highly flammable. It does not react in dry air at room temperature but is very sensitive to moisture. It ignites or explodes on contact with water.

See also Complex metal hydride

References