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Merck

199877

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
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
26111700
EC Number:
240-877-9
MDL number:
assay:
95%
grade:
reagent grade
form:
powder

Product Name

Lithium aluminum hydride, powder, reagent grade, 95%

InChI key

OCZDCIYGECBNKL-UHFFFAOYSA-N

InChI

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

SMILES string

[Li].[AlH3]

grade

reagent grade

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.)

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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).

General description

Atomic number of base material: 3
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.

pictograms

FlameCorrosion

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Danger

hcodes

Hazard Classifications

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

Storage Class

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


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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)
Lithium aluminum hydride as reducing agent for chemically reduced graphene oxides
Ambrosi A, et al.
Chemistry of Materials, 24(12), 2292-2298 (2012)
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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