Skip to Content
Merck

451665

Copper(II) chloride

anhydrous, powder, ≥99.995% trace metals basis

Synonym(s):

Cupric chloride

Sign In to View Organizational & Contract Pricing.

Select a Size

All Photos(1)

About This Item

Linear Formula:
CuCl2
CAS Number:
7447-39-4
Molecular Weight:
134.45
NACRES:
NA.23
PubChem Substance ID:
24868644
UNSPSC Code:
12352302
EC Number:
231-210-2
MDL number:
MFCD00010972
assay:
≥99.995% trace metals basis
grade:
anhydrous
form:
powder

Product Name

Copper(II) chloride, anhydrous, powder, ≥99.995% trace metals basis

InChI key

ORTQZVOHEJQUHG-UHFFFAOYSA-L

InChI

1S/2ClH.Cu/h2*1H;/q;;+2/p-2

SMILES string

Cl[Cu]Cl

grade

anhydrous

assay

≥99.995% trace metals basis

form

powder

reaction suitability

core: copper

impurities

≤50.0 ppm Trace Metal Analysis

mp

620 °C (lit.)

density

3.386 g/mL at 25 °C (lit.)

application(s)

electroplating
material synthesis precursor

Quality Level

100

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Catalyst for oxidation of alcohols under aerobic conditions.

Modified Markó′s aerobic oxidation of alcohols under atmospheric pressure with air or molecular oxygen at room temperature
Effective catalyst for the tetrahydropyranylation of alcohols, using mild conditions and in high yields.

Features and Benefits

  • High purity of ≥99.995% Copper(II) chloride minimizes impurities, boosting efficiency and selectivity in catalytic processes essential for organic synthesis and industrial chemical production.
  • The presence of low metal impurities in ≥99.995% copper(II) chloride ensure consistent quality in electroplating applications, enhancing adhesion and achieving uniform coatings on substrates without contamination that could compromise the finish.
  • Anhydrous CuCl₂ reduces the risk of hydrolysis, preventing unwanted by-products and enhancing the efficiency of chemical processes.

General description

CuCl2 was used in studies investigating pleural fibrosis resulting from chronic inhalation of indium phosphide (InP) particles in mice.

signalword

Danger

Hazard Classifications

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

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000497283
0000497294
0000497294
0000497283
0000456589

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

Chen Hou et al.
Nanomaterials (Basel, Switzerland), 10(3) (2020-03-04)
In this work, magnetic CuFe2O4/Ag nanoparticles activated by porous covalent organic frameworks (COF) was fabricated to evaluate the heterogenous reduction of 4-nitrophenol (4-NP). The core-shell CuFe2O4/Ag@COF was successfully prepared by polydopamine reduction of silver ions on CuFe2O4 nanoparticles, followed by
Jing Li et al.
ChemSusChem, 12(19), 4471-4479 (2019-08-02)
A simple one-pot method has been developed to synthesize a palladium/cuprous oxide-copper (Pd/Cu2 O-Cu) material with a well-defined structure, by modification of Cu2 O-Cu with Pd through a galvanic replacement reaction. Compared with the well-known copper/cuprous oxide (Cu/Cu2 O) catalysts
Bhalerao, U.T. et al.
Synthetic Communications, 26, 3081-3081 (1996)
Julia Mazurków et al.
Sensors (Basel, Switzerland), 21(3) (2021-02-04)
The constant progress in novel nanomaterials synthesis has contributed to the rapid development of nonenzymatic glucose sensors. For working electrodes preparation, drop casting proved to be the most convenient and thus most widely applied method. However, appropriate interpretation of obtained
Kenji Funaki et al.
Organic letters, 14(24), 6186-6189 (2012-12-12)
Direct arylation of thiophenes and benzothiophenes with aryltrimethylsilanes was effectively catalyzed by PdCl(2)(MeCN)(2) in the presence of CuCl(2) as an oxidant. The reaction preferentially occurred at the β-position of both thiophenes and benzothiophenes.
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