229733
Bromure de lithium
powder and chunks, ≥99.995% trace metals basis
Synonyme(s) :
Lithium monobromide
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A propos de cet article
Formule linéaire :
LiBr
Numéro CAS:
Poids moléculaire :
86.85
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
231-439-8
MDL number:
Assay:
≥99.995% trace metals basis
Form:
powder and chunks
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≥99.995% trace metals basis
form
powder and chunks
reaction suitability
core: lithium
greener alternative product characteristics
Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
impurities
≤50.0 ppm Trace Metal Analysis
mp
550 °C (lit.)
application(s)
battery precursors
catalysts
material synthesis precursor
greener alternative category
SMILES string
[Li+].[Br-]
InChI
1S/BrH.Li/h1H;/q;+1/p-1
InChI key
AMXOYNBUYSYVKV-UHFFFAOYSA-M
General description
We are committed to bringing you Greener Alternative Products that adhere to one of the four categories of Greener Alternatives. This is an enabling product that enhances cyclic stability in lithium-ion batteries, significantly improving energy storage performance and contributing to more efficient energy solutions. Click here for more information.
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).
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1
Classe de stockage
11 - Combustible Solids
wgk
WGK 2
flash_point_f
No data available
flash_point_c
No data available
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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
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