Skip to Content
Merck

429465

Lithium bromide

AnhydroBeads™, −10 mesh, 99.999% trace metals basis

Synonym(s):

Lithium monobromide

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
LiBr
CAS Number:
7550-35-8
Molecular Weight:
86.85
NACRES:
NA.23
PubChem Substance ID:
24866863
UNSPSC Code:
12352302
EC Number:
231-439-8
MDL number:
MFCD00011077
Assay:
99.999% trace metals basis
Grade:
synthesis grade
Form:
beads

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

particle size

−10 mesh

InChI key

AMXOYNBUYSYVKV-UHFFFAOYSA-M

InChI

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

SMILES string

[Li+].[Br-]

grade

synthesis grade

product line

AnhydroBeads™

assay

99.999% trace metals basis

form

beads

reaction suitability

core: lithium

impurities

≤15.0 ppm Trace Metal Analysis

mp

550 °C (lit.)

application(s)

battery precursors
catalysts
material synthesis precursor

Quality Level

100

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Lithium bromide(LiBr) can be used:
  • An electrolyte additive for lithium-sulfur batteries to enhance their rate performance and cycling stability.
  • To prepare poly (vinyl alcohol) (PVA) fibers. The addition of LiBr improves the mechanical properties of the polymer fibers.
  • To fabricate a surface passivation layer for silicon solar cells to enhance photoluminescence intensity.

General description

Lithium bromide is a crystalline solid with high refractive index. It is widely used in the field of rechargeable batteries, organic synthesis, and optical lenses.

Legal Information

AnhydroBeads is a trademark of Sigma-Aldrich Co. LLC

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

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCB6469
MKBR5328V
MKBV0924V
MKBR1169V
MKBR4802V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service