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517453

Sigma-Aldrich

Copper(II) acetate

greener alternative

powder, 99.99% trace metals basis

Synonym(s):

Cupric acetate

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About This Item

Linear Formula:
Cu(CO2CH3)2
CAS Number:
142-71-2
Molecular Weight:
181.63
Beilstein/REAXYS Number:
3595638
EC Number:
205-553-3
MDL number:
MFCD00008690
UNSPSC Code:
12352103
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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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.

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Danger

Hazard Classifications

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

Storage Class

8B - Non-combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

does not flash

flash_point_c

does not flash

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCT8667
MKCR3186
MKCP5073
MKCN3463
MKCL6239

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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)
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
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
Sarayut Radapong et al.
Molecules (Basel, Switzerland), 25(11) (2020-06-05)
Artocarpus lakoocha Wall. ex Roxb. (family: Moraceae) has been used as a traditional Thai medicine for the treatment of various parasitic diseases. This species has been reported to be the source of phytochemicals, which show potent biological activities. The objective
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