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Sigma-Aldrich

Lithiumbromid

powder and chunks, ≥99.995% trace metals basis

Synonym(e):

Lithium monobromide

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About This Item

Lineare Formel:
LiBr
CAS-Nummer:
7550-35-8
Molekulargewicht:
86.85
EG-Nummer:
231-439-8
MDL-Nummer:
MFCD00011077
UNSPSC-Code:
12352302
PubChem Substanz-ID:
24853301
NACRES:
NA.23

Assay

≥99.995% trace metals basis

Form

powder and chunks

Verunreinigungen

≤50.0 ppm Trace Metal Analysis

mp (Schmelzpunkt)

550 °C (lit.)

Anwendung(en)

battery manufacturing

SMILES String

[Li+].[Br-]

InChI

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

InChIKey

AMXOYNBUYSYVKV-UHFFFAOYSA-M

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Anwendung


  • 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).

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Lagerklassenschlüssel

13 - Non Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Analysenzertifikate (COA)

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Lithiumcarbonat 99.99% trace metals basis

Sigma-Aldrich

431559

Lithiumcarbonat

Lanthan(III)-Oxid suitable for AAS, ≥99.9%

Supelco

289205

Lanthan(III)-Oxid

2,4-Dimethylphenol 98%

Sigma-Aldrich

D174203

2,4-Dimethylphenol

Lithiumoxid 97%, powder, −60 mesh

Sigma-Aldrich

374725

Lithiumoxid

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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