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Merck

449873

Lithium bromide

AnhydroBeads, −10 mesh, ≥99.9% trace metals basis

Synonym(s):

Lithium monobromide

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About This Item

Linear Formula:
LiBr
CAS Number:
Molecular Weight:
86.85
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
231-439-8
MDL number:
Assay:
≥99.9% trace metals basis
Grade:
synthesis grade
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grade

synthesis grade

product line

AnhydroBeads

assay

≥99.9% trace metals basis

reaction suitability

core: lithium

impurities

≤1000.0 ppm Trace Metal Analysis

particle size

−10 mesh

mp

550 °C (lit.)

application(s)

battery precursors
catalysts
material synthesis precursor

SMILES string

[Li+].[Br-]

InChI

1S/BrH.Li/h1H;/q;+1/p-1

InChI key

AMXOYNBUYSYVKV-UHFFFAOYSA-M

Legal Information

AnhydroBeads is a trademark of Sigma-Aldrich Co. LLC


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pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

No data available

flash_point_c

No data available



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Ngoc-Ly Hoang et al.
Journal of chromatography. A, 1205(1-2), 60-70 (2008-08-30)
The structure of starch molecules is relevant to nutrition and industrial applications. Size-exclusion chromatography (SEC, also known as GPC) of native starch generally suffers non-satisfactory repeatability and reproducibility of the dissolution and separation. This work combines two polar organic solvents:
Mohammad M Mojtahedi et al.
Organic letters, 9(15), 2791-2793 (2007-06-22)
A room temperature convenient disproportionation or reduction of aldehydes prompted by lithium bromide and triethylamine is described in a solvent-free environment. Distribution of the products to selectively direct the process toward Cannizzaro or Tishchenko reactions is controlled by the type
R Quaderer et al.
Organic letters, 3(20), 3181-3184 (2001-09-28)
[reaction: see text] The alkanesulfonamide "safety-catch" resin has proven useful for Fmoc-based synthesis of C-terminal peptide thioesters. We now report that the yield of isolated thioester can increase significantly when the cleavage reaction is carried out in 2 M LiBr/THF