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517453

Sigma-Aldrich

Kupfer(II)-acetat

greener alternative

powder, 99.99% trace metals basis

Synonym(e):

Cupric acetate

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About This Item

Lineare Formel:
Cu(CO2CH3)2
CAS-Nummer:
142-71-2
Molekulargewicht:
181.63
Beilstein:
3595638
EG-Nummer:
205-553-3
MDL-Nummer:
MFCD00008690
UNSPSC-Code:
12352103
PubChem Substanz-ID:
24873953
NACRES:
NA.23

Dampfdichte

6.9 (vs air)

Qualitätsniveau

100

Assay

99.99% trace metals basis

Form

powder

Eignung der Reaktion

core: copper

Grünere Alternativprodukt-Eigenschaften

Catalysis
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

Grünere Alternativprodukt-Kategorie

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

InChIKey

OPQARKPSCNTWTJ-UHFFFAOYSA-L

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Allgemeine Beschreibung

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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Anwendung

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.

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

8B - Non-combustible corrosive hazardous materials

WGK

WGK 3

Flammpunkt (°F)

does not flash

Flammpunkt (°C)

does not flash

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
MKCP5073
MKCN3463
MKCL6239
MKCJ7951
MKCG6061

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Eisen(II)-acetat ≥99.99% trace metals basis

Sigma-Aldrich

517933

Eisen(II)-acetat

Benzoin for synthesis

Sigma-Aldrich

8.01776

Benzoin

Benzoin purified by sublimation, ≥99.5%

Sigma-Aldrich

399396

Benzoin

Kupfer(II)-chlorid 99.999% trace metals basis

Sigma-Aldrich

203149

Kupfer(II)-chlorid

Kupfer(II)-sulfat anhydrous, powder, ≥99.99% trace metals basis

Sigma-Aldrich

451657

Kupfer(II)-sulfat

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
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
Hanmei Zheng et al.
The Journal of organic chemistry, 74(2), 943-945 (2008-12-11)
A novel copper-catalyzed protocol for the synthesis of carbinol derivatives has been developed. In the presence of copper(II) acetate and dppf, carbinol derivatives were prepared by the addition of arylboronic acids to aromatic aldehydes in good to excellent yields. Moreover
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