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About This Item
Linear Formula:
LiOH · H2O
CAS Number:
Molecular Weight:
41.96
EC Number:
215-183-4
UNSPSC Code:
12352300
MDL number:
InChI key
GLXDVVHUTZTUQK-UHFFFAOYSA-M
InChI
1S/Li.2H2O/h;2*1H2/q+1;;/p-1
SMILES string
[Li+].O.[OH-]
grade
reagent grade
assay
98%
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General description
Crystals of Lithium hydroxide monohydrate belong to the monoclinic crystal system. It can be prepared by reacting Li metal with H2O, followed by the evaporation of the aqueous solution.
Application
Lithium hydroxide monohydrate (LiOH.H2O) may be employed as a catalyst for the melt transesterification of diphenyl carbonate and bisphenol A. It can also be used for the synthesis of 3,4-disubstituted pyrrole derivatives.
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B
Storage Class
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 1
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Regulatory Information
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Lithium hydroxide mediated synthesis of 3, 4-disubstituted pyrroles.
Sharma R, et al.
Royal Society of Chemistry Advances, 3(34), 14521-14527 (2013)
Kinetics of melt transesterification of diphenyl carbonate and bisphenol A to polycarbonate with lithium hydroxide monohydrate catalyst.
Kim Y, et al.
Industrial & Engineering Chemistry Research, 31(9), 2118-2127 (1992)
Refinement of the crystal structure of lithium hydroxide monohydrate.
Alcock NW.
Acta Crystallographica Section B, Structural Science, Crystal Engineering and Materials, 27(8), 1682-1683 (1971)
Infrared active vibrational modes of lithium hydroxide monohydrate.
Hase Y.
Inorganic and Nuclear Chemistry Letters, 16(3), 159-163 (1980)
Jinyoung Jeong et al.
Advanced materials (Deerfield Beach, Fla.), 24(15), 1999-2003 (2012-03-21)
Highly water-soluble and color-tunable photoluminescent fullerene nanoparticles are synthesized by using tetraethylene glycol (TEG) and lithium hydroxide as a catalyst. The maximum PL emission changes depend on the contents of the remaining π-conjugation in oxidized C(60), which is partially covalently
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