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229733

Sigma-Aldrich

Bromure de lithium

powder and chunks, ≥99.995% trace metals basis

Synonyme(s) :

Lithium monobromide

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About This Item

Formule linéaire :
LiBr
Numéro CAS:
7550-35-8
Poids moléculaire :
86.85
Numéro CE :
231-439-8
Numéro MDL:
MFCD00011077
Code UNSPSC :
12352302
ID de substance PubChem :
24853301
Nomenclature NACRES :
NA.23

Qualité

for analytical purposes

Essai

≥99.995% trace metals basis

Forme

powder and chunks

Impuretés

≤50.0 ppm Trace Metal Analysis

Pf

550 °C (lit.)

Application(s)

battery manufacturing

Chaîne SMILES 

[Li+].[Br-]

InChI

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

Clé InChI

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).

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H302,H315,H317,H319

Classification des risques

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

Code de la classe de stockage

13 - Non Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

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Certificats d'analyse (COA)

Lot/Batch Number
MKCD1658
MKCD1655
MKCC3732
MKBX0228V
MKBX5394V

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Lithium oxide 97%, powder, −60 mesh

Sigma-Aldrich

374725

Lithium oxide

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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