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Key Documents

199877

Sigma-Aldrich

Lithium aluminum hydride

greener alternative

powder, reagent grade, 95%

Synonym(s):

LAH, Lithium alanate, Lithium tetrahydroaluminate

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About This Item

Linear Formula:
LiAlH4
CAS Number:
Molecular Weight:
37.95
EC Number:
MDL number:
UNSPSC Code:
26111700
PubChem Substance ID:
NACRES:
NA.22

grade

reagent grade

Quality Level

Assay

95%

form

powder

reaction suitability

reagent type: reductant

greener alternative product characteristics

Design for Energy Efficiency
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sustainability

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mp

125 °C (dec.) (lit.)

greener alternative category

SMILES string

[Li].[AlH3]

InChI

1S/Al.Li.4H/q-1;+1;;;;

InChI key

OCZDCIYGECBNKL-UHFFFAOYSA-N

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General description

Atomic number of base material: 3
In Europe, packaged and shipped in plastic bags. Bags are soluble at 45-60 °C in hydrocarbons, THF and dioxane.
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency. Find details here.

Application

Lithium aluminum hydride (LiAlH4) is an effective reducing agent that can be used in chemical synthesis to reduce esters, carboxylic acids, acyl chlorides, aldehydes, epoxides, and ketones into the corresponding alcohols. In addition, amide, nitro, nitrile, imine, oxime, and azide compounds are converted into amines.
LiAlH4 is a promising substance for hydrogen storage applications. Its properties include high gravimetric and volumetric hydrogen densities . It can also be used as a reducing agent in the preparation of reduced graphene oxide (rGO).

Pictograms

FlameCorrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1A - Water-react 1

Storage Class Code

4.3 - Hazardous materials which set free flammable gases upon contact with water

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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Lithium Aluminum Hydride
Paquette LA, et al.
Encyclopedia of Reagents for Organic Synthesis, Second Edition (2001)
Synthesis and characterization of lithium aminoborohydrides: A new class of powerful reducing agents
Fisher GB, et al.
Tetrahedron Letters, 33(32), 4533-4536 (1992)
A first-principles study of the electronic structure and stability of a lithium aluminum hydride for hydrogen storage
Song Y, et al.
The Journal of Physical Chemistry B, 110(13), 6906-6910 (2006)
Reversible hydrogen storage via titanium-catalyzed LiAlH4 and Li3AlH6
Chen J, et al.
The Journal of Physical Chemistry B, 105(45), 11214-11220 (2001)
Reduction of organic compounds by lithium aluminum hydride. I. Aldehydes, ketones, esters, acid chlorides and acid anhydrides.
Nystrom RF and Brown WG
Journal of the American Chemical Society, 69(5), 1197-1199 (1947)

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