Skip to Content
Merck
All Photos(3)

Documents

254185

Sigma-Aldrich

Copper(I) bromide

99.999% trace metals basis

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:
24855364
NACRES:
NA.23

Assay

99.999% trace metals basis

form

powder

reaction suitability

reagent type: catalyst
core: copper

impurities

≤15.0 ppm Trace Metal Analysis

mp

504 °C (lit.)

density

4.71 g/mL at 25 °C (lit.)

application(s)

battery manufacturing

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

General description

Copper(I) bromide is a faint green inorganic diamagnetic solid that has a polymeric structure like zinc sulfide. It is insoluble in water and widely used in the field of catalysis, nanomaterial synthesis, and solar cells.

Application

Copper(I) bromide can be used:
  • As a solution-processable hole transport layer (HTL) for organic solar cells (OSCs). CuBr enhances the power conversion efficiency of solar cells.
  • As a precursor to synthesize photoluminescent metal organic frameworks(MOFs).
  • To synthesize highly emissive three-coordinate copper(I) complexes as a dopant in OLEDs with maximum external quantum efficiency of 21.3%.
  • As a catalyst with ligands for atom transfer radical polymerization (ATRP) reaction of tertiary alkyl halides in 14 different solvents to determine the rate constant.
  • To synthesize macrocyclic polymer via intramolecular radical trap-assisted atom transfer radical coupling.

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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

Denissova I and Barriault L et al.
Handbook of Reagents for Organic Synthesis null
Carla Sardo et al.
International journal of pharmaceutics, 563, 347-357 (2019-04-03)
Sustained pulmonary delivery of tobramycin from microparticles composed of drug/polymer nanocomplexes offers several advantages against traditional delivery methods. Namely, in patients with cystic fibrosis, microparticle delivery can protect the tobramycin being delivered from strong mucoadhesive interactions, thus avoiding effects on
Thomas F Cooke et al.
Cell, 171(2), 427-439 (2017-10-07)
Parrot feathers contain red, orange, and yellow polyene pigments called psittacofulvins. Budgerigars are parrots that have been extensively bred for plumage traits during the last century, but the underlying genes are unknown. Here we use genome-wide association mapping and gene-expression
Fang Sun et al.
Nature communications, 7, 13437-13437 (2016-11-12)
Surface-enhanced Raman spectroscopy (SERS) is an ultrasensitive analytical technique with molecular specificity, making it an ideal candidate for therapeutic drug monitoring (TDM). However, in critical diagnostic media including blood, nonspecific protein adsorption coupled with weak surface affinities and small Raman
Xiao-Yan Tu et al.
Macromolecular bioscience, 18(7), e1800022-e1800022 (2018-05-11)
The cyclic brush polymers, due to the unique topological structure, have shown in the previous studies higher delivery efficacy than the bottlebrush analogues as carriers for drug and gene transfer. However, to the best of knowledge, the preparation of reduction-sensitive
View All Related Papers

Articles

Reagents for C–C Bond Formation

Reagents for C–C Bond Formation

A Micro Review of Reversible Addition/Fragmentation Chain Transfer (RAFT) Polymerization

We presents an article about a micro review of reversible addition/fragmentation chain transfer (RAFT) polymerization. RAFT (Reversible Addition/Fragmentation Chain Transfer) polymerization is a reversible deactivation radical polymerization (RDRP) and one of the more versatile methods for providing living characteristics to radical polymerization.

Tools for Performing ATRP

Tools for Performing ATRP

Applying ARGET ATRP to the Growth of Polymer Brush Thin Films by Surface-initiated Polymerization

Applying ARGET ATRP to the Growth of Polymer Brush Thin Films by Surface-initiated Polymerization

See All

Protocols

Concepts and Tools for RAFT Polymerization

Sigma-Aldrich presents an article about RAFT, or Reversible Addition/Fragmentation Chain Transfer, which is a form of living radical polymerization.

Typical Procedures for Polymerizing via RAFT

We presents an article featuring procedures that describe polymerization of methyl methacrylate and vinyl acetate homopolymers and a block copolymer as performed by researchers at CSIRO.

Typical Procedures for Polymerizing via ATRP

Sigma-Aldrich presents an article about the typical procedures for polymerizing via ATRP, which demonstrates that in the following two procedures describe two ATRP polymerization reactions as performed by Prof. Dave Hadddleton′s research group at the University of Warwick.

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