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222356

Sigma-Aldrich

Lithium borohydride

greener alternative

≥90%

Synonym(s):

Lithium boron hydride, Lithium hydroborate

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About This Item

Linear Formula:
LiBH4
CAS Number:
Molecular Weight:
21.78
EC Number:
MDL number:
UNSPSC Code:
26111700
PubChem Substance ID:
NACRES:
NA.22

Assay

≥90%

form

solid

reaction suitability

reagent type: reductant

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sustainability

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mp

275 °C (dec.)

density

0.666 g/mL at 25 °C (lit.)

greener alternative category

SMILES string

[Li+].[BH4-]

InChI

1S/BH4.Li/h1H4;/q-1;+1

InChI key

UUKMSDRCXNLYOO-UHFFFAOYSA-N

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General description

Lithium borohydride, a white solid, may be prepared from the exchange reaction of LiCl and sodium borohydride in isopropylamine. The orthorhombic crystal structure converts to tetragonal at 108oC and eventually melting at 278oC. Infrared and Raman spectral studies at 80oC have been reported in a study.
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Application

Versatile reducing agent for aldehydes, ketones, acid chlorides, lactones, epoxides, and esters. Applied in the lithiation of 2H-WS2 giving high yields of exfoliated WS2, and opening the way to new intercalation compounds and nanocomposites. Lithium borohydride is used as hydrogen storage system. It regenerates hydrogen at 320-380oC at 10atm (H2 pressure).

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B - Water-react 1

Storage Class Code

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

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Fieser, M.
Reagents for Organic Synthesis, 14, 191-191 (1989)
Tsai, H-L. et al.
Chemistry of Materials, 9, 879-879 (1997)
Low temperature infrared and raman spectra of lithium borohydride.
Harvey KB and McQuaker NR
Canadian Journal of Chemistry, 49(21), 3282-3286 (1971)
Mita Dasog et al.
Chemical communications (Cambridge, England), 47(30), 8569-8571 (2011-06-28)
In the presence of large excesses of borohydride salts, gold monolayer protected-clusters can be grown to larger sizes simply by controlling the amount of reducing agent added to smaller clusters. In addition, gold monolayer clusters can be used as catalysts
Sumalee Supothina et al.
The Journal of antibiotics, 57(11), 732-738 (2005-02-17)
Optimal fermentation conditions for enniatin production using the entomopathogenic fungus Verticillium hemipterigenum BCC 1449 have been investigated. Among various liquid media tested, highest efficiency of enniatin production was achieved by fermentation in yeast extract sucrose. Application of this condition to

Articles

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