Skip to Content
MilliporeSigma
All Photos(3)

Documents

62460

Sigma-Aldrich

Lithium borohydride

≥95.0%

Synonym(s):

Lithium boron hydride, Lithium hydroborate

Sign Into View Organizational & Contract Pricing


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

≥95.0%

form

solid

reaction suitability

reagent type: reductant

mp

275 °C (dec.)

density

0.666 g/mL at 25 °C (lit.)

SMILES string

[Li+].[BH4-]

InChI

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

InChI key

UUKMSDRCXNLYOO-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Lithium borohydride is a general reducing agent commonly used to reduce aldehydes, ketones esters, lactones, and epoxides. It catalyzes hydroboration of alkenes. It is also used in the preparation of other borohydrides such as aluminum borohydride.

Other Notes

Review; Smooth reduction of esters; Reduction of acids and other functional groups with LiBH4/Me3SiCl

signalword

Danger

Hazard Classifications

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

Storage Class

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

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Lithium borohydride-catalyzed selective reduction of the carbonyl group of conjugated and unconjugated alkenones with borane in tetrahydrofuran.
Arase, Akira et al.
Journal of the Chemical Society. Chemical Communications, 51(7), 855-856 (1994)
Mixed solvents containing methanol as useful reaction media for unique chemoselective reductions within lithium borohydride.
Soai, Kenso and Ookawa, Atsuhiro
The Journal of Organic Chemistry, 51(21), 4000-4005 (1986)
Lithium Borohydride.
eEROS (Encyclopedia of Reagents for Organic Synthesis) (2001)
H.C. Brown et al.
The Journal of Organic Chemistry, 47, 1604-1604 (1982)
H.C. Brown et al.
The Journal of Organic Chemistry, 47, 4702-4702 (1982)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service