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Sigma-Aldrich

Copper(II) acetate

greener alternative

powder, 99.99% trace metals basis

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Synonym(s):
Cupric acetate
Linear Formula:
Cu(CO2CH3)2
CAS Number:
142-71-2
Molecular Weight:
181.63
Beilstein:
3595638
EC Number:
205-553-3
MDL number:
MFCD00008690
UNSPSC Code:
12352300
PubChem Substance ID:
24873953
NACRES:
NA.23

vapor density

6.9 (vs air)

Quality Level

100

Assay

99.99% trace metals basis

form

powder

reaction suitability

core: copper

greener alternative product characteristics

Catalysis
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sustainability

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Aligned

SMILES string

CC(=O)O[Cu]OC(C)=O

InChI

1S/2C2H4O2.Cu/c2*1-2(3)4;/h2*1H3,(H,3,4);/q;;+2/p-2

InChI key

OPQARKPSCNTWTJ-UHFFFAOYSA-L

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General description

Copper acetate (Cu (OAc)2) occurs in dimeric structure in solid state and in non-aqueous solution. Anhydrous Cu (OAc)2 may be manufactured by heating or refluxing the monohydrate Cu (OAc)2 at 90oC and then washing the insoluble product with diethyl ether.
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Application

Copper acetate forms complexes which may be used in biochemical reactions such as; DNA extraction, binding ribose hydroxyls of purine and pyrimidine nucleosides. A study has shown Cu (OAc)2 to fix and remove tannins in samples from Pyrus yielding high quality DNA. The complexes have been studied for anticancer, anti-bacterial and antifungal activities.

Signal Word

Danger

Hazard Statements

H302,H314,H410

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Skin Corr. 1B

WGK

WGK 3

Flash Point(F)

does not flash

Flash Point(C)

does not flash

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Manpreet Kaur et al.
Nanoscale research letters, 13(1), 182-182 (2018-06-20)
Here, we report efficient composition-tunable Cu-doped ZnInS/ZnS (core and core/shell) colloidal nanocrystals (CNCs) synthesized by using a colloidal non-injection method. The initial precursors for the synthesis were used in oleate form rather than in powder form, resulting in a nearly
Stereoselective differentiation between ribonucleosides and deoxynucleosides by reaction with the copper(II) acetate dimer.
N A Berger et al.
Nature: New biology, 239(95), 237-240 (1972-10-25)
Quantitative densitometric thin-layer chromatography of lipids using copper acetate reagent.
M E Fewster et al.
Journal of chromatography, 43(1), 120-126 (1969-08-05)
Michael Devereux et al.
Journal of inorganic biochemistry, 98(6), 1023-1031 (2004-05-20)
Thiabendazole (TBZH) reacts with iron(III) nitrate causing protonation of the ligand to yield the nitrate salt [TBZH(2)NO(3)] (1). Reaction of TBZH with copper(II) acetate results in the deprotonation of the ligand yielding [Cu(TBZ)2.(H2O)2] (2). Reactions of TBZH with the chloride
Microwave-assisted efficient copper-promoted N-arylation of amines with arylboronic acids.
Shiyu Chen et al.
Journal of combinatorial chemistry, 10(3), 358-360 (2008-04-09)
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