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Documentos

229733

Sigma-Aldrich

Bromuro de litio

powder and chunks, ≥99.995% trace metals basis

Sinónimos:

Lithium monobromide

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About This Item

Fórmula lineal:
LiBr
Número de CAS:
7550-35-8
Peso molecular:
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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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

signalword

Warning

Hazard Classifications

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

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

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2,4-Dimethylphenol

Lithium oxide 97%, powder, −60 mesh

Sigma-Aldrich

374725

Lithium oxide

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
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:
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
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.
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