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229733

Sigma-Aldrich

Lithium bromide

powder and chunks, ≥99.995% trace metals basis

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Synonym(s):
Lithium monobromide
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:
24853301
NACRES:
NA.23

Quality Level

100

Assay

≥99.995% trace metals basis

form

powder and chunks

impurities

≤50.0 ppm Trace Metal Analysis

mp

550 °C (lit.)

application(s)

battery manufacturing

SMILES string

[Li+].[Br-]

InChI

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

InChI key

AMXOYNBUYSYVKV-UHFFFAOYSA-M

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Related Categories

Application


  • Space cooling using geothermal single‐effect water/lithium bromide absorption chiller: This research explores the use of lithium bromide in geothermal absorption chillers for space cooling applications (M El Haj Assad, M Sadeghzadeh, 2021).

  • A facile and fast method for quantitating lignin in lignocellulosic biomass using acidic lithium bromide trihydrate (ALBTH): The paper introduces a novel method for lignin quantification using lithium bromide trihydrate (N Li, X Pan, J Alexander, 2016).

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H317,H319

Hazard Classifications

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

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

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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
Sophie Nocquet-Thibault et al.
Organic letters, 15(8), 1842-1845 (2013-04-02)
Using (diacetoxyiodo)benzene in conjunction with simple bromide salts in ethanol allows the regioselective ethoxybromination of a wide range of enamides, thus yielding highly versatile α-bromo hemiaminals, which can then be engaged in a broad array of transformations.
B Saake et al.
Bioresource technology, 80(3), 195-204 (2001-10-17)
Four xylan samples from different origin were investigated, using a multi-detector, size exclusion, chromatographic system with two chromatographic column sets and mobile phases differing in the DMSO:water ratio. Molar mass distribution could be analysed best using a mobile phase of
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