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751944

Sigma-Aldrich

Copper(II) chloride

powder, 99%

Synonym(s):

Copper dichloride, Cupric chloride

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About This Item

Linear Formula:
CuCl2
CAS Number:
7447-39-4
Molecular Weight:
134.45
EC Number:
231-210-2
MDL number:
MFCD00010972
UNSPSC Code:
12352302
PubChem Substance ID:
329766251
NACRES:
NA.23

Quality Level

100

Assay

99%

form

powder

composition

Cl, 51.9-53.5% silver nitrate titration

mp

620 °C (lit.)

density

3.386 g/mL at 25 °C (lit.)

application(s)

battery manufacturing

SMILES string

Cl[Cu]Cl

InChI

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

InChI key

ORTQZVOHEJQUHG-UHFFFAOYSA-L

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Application

Copper chloride was used as a reagent solution in the preparation of silver nanowires by the polyol synthesis process.

Signal Word

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 Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
0000107053
0000105911
0000363073
0000107053
0000105911

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Synthesis and Characterization of Silver Nanowire Suspensions for Printable Conductive Media
Hemmati S, et al.
ECS Journal of Solid State Science and Technology, 4(4), P3075-P3079 (2015)
Joseph R Lizza et al.
Organic letters, 20(21), 6760-6764 (2018-10-24)
The 2,2,6,6-tetramethylpiperidin-1-yloxycarbonyl (Tempoc) protecting group is readily introduced by the reaction of amines with a new acyl transfer reagent, 4-nitrophenyl (2,2,6,6-tetramethylpiperidin-1-yl) carbonate (NPTC). Tempoc has a reactivity profile that complements the commonly used t-butyloxycarbonyl (Boc) and benzyloxycarbonyl (Cbz) protecting groups.
Olga Guselnikova et al.
Sensors (Basel, Switzerland), 19(9) (2019-05-10)
In this contribution, we propose a novel functional surface-enhanced Raman spectroscopy (SERS) platform for the detection of one of the most hazardous heavy metal ions, Hg2+. The design of the proposed sensor is based on the combination of surface plasmon-polariton
Iron(II)-catalyzed trifluoromethylation of potassium vinyltrifluoroborates.
Andrew T Parsons et al.
Angewandte Chemie (International ed. in English), 51(12), 2947-2950 (2012-02-14)
Francesca Cima et al.
Chemosphere, 89(1), 19-29 (2012-05-01)
After the widespread ban of TBT, due to its severe impact on coastal biocoenoses, mainly related to its immunosuppressive effects on both invertebrates and vertebrates, alternative biocides such as Cu(I) salts and the triazine Irgarol 1051, the latter previously used
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