Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

62463

Sigma-Aldrich

Lithium bromide

purum p.a., ≥98.0% (dried material, AT), powder, crystals or chunks

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
LiBr
CAS Number:
Molecular Weight:
86.85
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
assay:
≥98.0% (dried material, AT)
form:
powder, crystals or chunks

grade

purum p.a.

assay

≥98.0% (dried material, AT)

form

powder, crystals or chunks

loss

≤2% loss on drying, 400 °C

mp

550 °C (lit.)

anion traces

sulfate (SO42-): ≤200 mg/kg

cation traces

Ca: ≤100 mg/kg
Cd: ≤50 mg/kg
Co: ≤50 mg/kg
Cu: ≤50 mg/kg
Fe: ≤50 mg/kg
K: ≤100 mg/kg
Na: ≤500 mg/kg
Ni: ≤50 mg/kg
Pb: ≤50 mg/kg
Zn: ≤50 mg/kg

SMILES string

[Li+].[Br-]

InChI

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

InChI key

AMXOYNBUYSYVKV-UHFFFAOYSA-M

Looking for similar products? Visit Product Comparison Guide

General description

Lithium bromide (LiBr) is a lithium salt. LiBr/Chlorotrimethylsilane reagent has been employed for the transformations of alcohols to bromides.[1] LiBr/Ceric ammonium nitrate (CAN) reagent system has been used for the chemo- and regioselective bromination of aromatic compounds.[2]

Application

Lithium bromide (LiBr) may be employed as a catalyst in the following studies:
  • Solvent-free dithioacetalization of (aromatic- and α,β-unsaturated) aldehydes.[3]
  • Synthesis of olefins, via condensation reaction of carbonyl compounds with active methylene compounds.[4]
  • Synthesis of β-amino alcohols, via ring opening reaction of epoxides with amines.[5]

pictograms

Exclamation mark

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


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

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.

Already Own This Product?

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

Visit the Document Library

Lithium Bromide, an Inexpensive and Efficient Catalyst for Opening of Epoxide Rings by Amines at Room Temperature under Solvent-Free Condition.
Chakraborti AK, et al.
European Journal of Organic Chemistry, 2004(17), 3597-3600 (2004)
An efficient chemo and regioselective oxidative nuclear bromination of activated aromatic compounds using lithium bromide and ceric ammonium nitrate.
Roy SC, et al.
Tetrahedron Letters, 42(39), 6941-6942 (2001)
Lithium bromide as a new catalyst for carbon-carbon bond formation in the solid state.
Prajapati D, et al.
Journal of the Chemical Society. Perkin Transactions 1, 9, 959-960 (1996)
Lithium bromide-catalyzed highly chemoselective and efficient dithioacetalization of α,β-unsaturated and aromatic aldehydes under solvent-free conditions.
Firouzabadi H, et al.
Synthesis, 58-60 (1999)
Chlorotrimethylsilane/lithium bromide and hexamethyldisilane/pyridinium bromide perbromide: effective and selective reagents for the conversion of alkyl (cycloalkyl and aralkyl) alcohols into bromides.
Olah GA, et al.
The Journal of Organic Chemistry, 45(9), 1638-1639 (1980)

Questions

Reviews

No rating value

Active Filters

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