Skip to Content
Merck
All Photos(3)

Documents

212865

Sigma-Aldrich

Copper(I) bromide

98%

Synonym(s):

Cuprous bromide

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Linear Formula:
CuBr
CAS Number:
7787-70-4
Molecular Weight:
143.45
EC Number:
232-131-6
MDL number:
MFCD00010969
UNSPSC Code:
12352302
PubChem Substance ID:
329752131
NACRES:
NA.21

Quality Level

100

Assay

98%

form

solid

reaction suitability

reaction type: click chemistry
reagent type: catalyst
core: copper

mp

504 °C (lit.)

density

4.71 g/mL at 25 °C (lit.)

SMILES string

[Cu]Br

InChI

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

InChI key

NKNDPYCGAZPOFS-UHFFFAOYSA-M

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Copper(I) bromide (CuBr) may be used in the synthesis of the following:
  • enantioenriched, functionalized and protected propargylamines
  • polyvinylchloride bearing benzoxazine side groups
  • polybutadiene having benzoxazine side-groups (PB-benzoxazine)
  • mononuclear complexes [Cu(L)(PPh3)2Br]
  • Copper(I) bromide along with N-(n-octyl)-2-pyridylmethanimine participates in the living-radical polymerization of methyl methacrylate.

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

Copper (I) bromide/N-(n-octyl)-2-pyridylmethanimine-mediated living-radical polymerization of methyl methacrylate using carbosilane dendritic initiators.
Hovestad NJ, et al.
Macromolecules, 33(11), 4048-4052 (2000)
Enantioselective synthesis of propargylamines by copper-catalyzed addition of alkynes to enamines.
Christopher Koradin et al.
Angewandte Chemie (International ed. in English), 41(14), 2535-2538 (2002-08-31)
Copper (I) bromide complexes with heterocyclic thiones and triphenylphosphine as ligands. The X-ray crystal structure of copper (I) pyrimidine-2-thione bis (triphenylphosphine) bromide [Cu (PPh 3) 2 (PymtH) Br].
Lecomte C, et al.
Polyhedron, 8(8), 1103-1109 (1989)
Thermally curable polyvinylchloride via click chemistry.
Kiskan B, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 46(11), 3512-3518 (2008)
B Podobnik et al.
Bioconjugate chemistry, 26(3), 452-459 (2015-01-30)
The covalent attachment of poly(ethylene glycol) (PEG) to therapeutic proteins is a commonly used approach for extending in vivo half-lives. A potential limitation of this PEGylation strategy is the adverse effect of PEG on conjugate viscosity. Interferon-alpha (IFN) was conjugated
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