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Merck

62421

Lithium aluminum hydride

≥97.0% (gas-volumetric), tablet (5 g each)

Synonym(s):

LAH, Lithium alanate, Lithium tetrahydroaluminate

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About This Item

Linear Formula:
LiAlH4
CAS Number:
16853-85-3
Molecular Weight:
37.95
NACRES:
NA.22
PubChem Substance ID:
57651883
UNSPSC Code:
26111700
EC Number:
240-877-9
MDL number:
MFCD00011075

Product Name

Lithium aluminum hydride, ≥97.0% (gas-volumetric), tablet (5 g each)

InChI key

OCZDCIYGECBNKL-UHFFFAOYSA-N

InChI

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

SMILES string

[Li].[AlH3]

assay

≥97.0% (gas-volumetric)

form

tablet (5 g each)

reaction suitability

reagent type: reductant

mp

125 °C (dec.) (lit.)

Quality Level

100

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Other Notes

Review

pictograms

FlameCorrosion
GHS02,GHS05

signalword

Danger

hcodes

H260,H314

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

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
STBJ7389
STBJ5737
STBJ1716
STBH8878
STBH3514

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H.C. Brown et al.
Tetrahedron, 35, 567-567 (1979)
Pseudo-allosteric recognition of mandelic acid with an enantioselective coordination complex.
Jungseok Heo et al.
Angewandte Chemie (International ed. in English), 45(6), 941-944 (2005-12-31)
Seiji Takeda et al.
Journal of biomedical nanotechnology, 9(2), 303-306 (2013-05-01)
Measurement of oxidized low-density lipoprotein (LDL) generated by oxidative stress of various kinds might be useful for evaluating the risk of cardiovascular disease. We evaluated some electrode materials to detect oxidized LDL electrochemically. Some carbon nanotube dispersions were studied as
Matthias D'hooghe et al.
Organic & biomolecular chemistry, 8(3), 607-615 (2010-01-22)
trans- and cis-1-Alkyl-4-aryl-3-chloroazetidin-2-ones, prepared through cyclocondensation of chloroketene and the appropriate imines in a diastereoselective way, were transformed into the corresponding non-activated trans- and cis-2-aryl-3-(hydroxymethyl)aziridines via reductive ring contraction using LiAlH(4) in Et(2)O. Furthermore, trans-2-aryl-3-(hydroxymethyl)aziridines were transformed into 2-amino-3-arylpropan-1-ols and
Sonja Stanković et al.
Organic & biomolecular chemistry, 8(19), 4266-4273 (2010-08-05)
A new synthetic protocol for the LiAlH(4)-promoted reduction of non-activated aziridines under microwave conditions was developed. Thus, ring opening of 2-(acetoxymethyl)aziridines provided the corresponding beta-amino alcohols, which were then used as eligible substrates in the synthesis of 5-methylmorpholin-2-ones via condensation
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