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429465

Sigma-Aldrich

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:
Molecular Weight:
86.85
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.23

product line

AnhydroBeads

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

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Storage Class Code

13 - Non Combustible Solids

WGK

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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LiBr treated porous silicon used for efficient surface passivation of crystalline silicon solar cells
Ahmed Zarroug, et al.
Superlattices and Microstructures, 80, 181-187 (2015)
Modification of poly(vinyl alcohol) fibers with lithium bromide
Riza Asmaa Saari, et al.
Polymer, 213, 123193-123193 (2021)
Toward in-situ protected sulfur cathodes by using lithium bromide and pre-charge
Feixiang Wu, et al
Nano Energy, 40, 170-179 (2017)
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

Articles

Solid-state lithium fast-ion conductors are crucial for safer, high-energy-density all-solid-state batteries, addressing conventional battery limitations.

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