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Lithium bromide

AnhydroBeads™, −10 mesh, 99.999% trace metals basis

Synonym(s):

Lithium monobromide

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About This Item

Linear Formula:
LiBr
CAS Number:
7550-35-8
Molecular Weight:
86.85
EC Number:
231-439-8
MDL number:
MFCD00011077
UNSPSC Code:
12352302
PubChem Substance ID:
24866863
NACRES:
NA.23

product line

AnhydroBeads™

Quality Level

100

assay

99.999% trace metals basis

form

beads

impurities

≤15.0 ppm Trace Metal Analysis

particle size

−10 mesh

mp

550 °C (lit.)

SMILES string

[Li+].[Br-]

InChI

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

InChI key

AMXOYNBUYSYVKV-UHFFFAOYSA-M

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General description

Lithium bromide is a crystalline solid with high refractive index. It is widely used in the field of rechargeable batteries, organic synthesis, and optical lenses.

Application

Lithium bromide(LiBr) can be used:
  • An electrolyte additive for lithium-sulfur batteries to enhance their rate performance and cycling stability.
  • To prepare poly (vinyl alcohol) (PVA) fibers. The addition of LiBr improves the mechanical properties of the polymer fibers.
  • To fabricate a surface passivation layer for silicon solar cells to enhance photoluminescence intensity.

Legal Information

AnhydroBeads is a trademark of Sigma-Aldrich Co. LLC

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Product No.
Description
Pricing

pictograms

Exclamation mark
GHS07

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Warning

Hazard Classifications

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

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

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’.

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Zhongli Cai et al.
Radiation research, 159(3), 411-419 (2003-02-26)
An investigation of electron and hole transfer to oxidized guanine bases in DNA is reported. Guanine in DNA was preferentially oxidized by Br(2)(*-) at 298 K to 8-oxo-7,8-dihydro-guanine (8-oxo-G) and higher oxidation products. HPLC-EC analysis of irradiated DNA shows that
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
Arlette Solladié-Cavallo et al.
The Journal of organic chemistry, 70(5), 1605-1611 (2005-02-26)
Both symmetrical and nonsymmetrical trans-2,3-diaryloxiranes are regio- and stereoselectively opened by the LiBr/Amberlyst 15 system. In the case of symmetrical trans-stilbene oxide, the syn- versus anti-bromohydrins ratio ranged between 88/12 and 30/70, by varying the reaction temperature from 20 to
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
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