517453
Copper(II) acetate
powder, 99.99% trace metals basis
Sinónimos:
Cupric acetate
Iniciar sesión para ver los precios por organización y contrato.
Seleccione un Tamaño
Acerca de este artículo
Fórmula lineal:
Cu(CO2CH3)2
Número CAS:
Peso molecular:
181.63
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
205-553-3
Beilstein/REAXYS Number:
3595638
MDL number:
Servicio técnico
¿Necesita ayuda? Nuestro equipo de científicos experimentados está aquí para ayudarle.
Permítanos ayudarleServicio técnico
¿Necesita ayuda? Nuestro equipo de científicos experimentados está aquí para ayudarle.
Permítanos ayudarlevapor density
6.9 (vs air)
Quality Level
assay
99.99% trace metals basis
form
powder
reaction suitability
core: copper
greener alternative product characteristics
Catalysis
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
bp
100 °C (212 °F)
greener alternative category
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
¿Está buscando productos similares? Visita Guía de comparación de productos
General description
Copper(II) acetate, also known as cupric acetate, is commonly used as a precursor in the synthesis of copper-containing materials such as nanoparticles and thin films. Its good solubility in water and organic solvents makes it well-suited for solution-based methods like sol-gel processing and spin coating. It serves as a reliable source of Cu²⁺ ions, which are essential for producing copper-based nanomaterials, metal–organic frameworks (MOFs), and various catalysts. Additionally, it decomposes into copper oxides (CuO, Cu₂O) at moderate temperatures, making it valuable for thin-film deposition in applications like sensors, solar cells, and semiconductor devices
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Green Chemistry. This product has been enhanced for catalytic efficiency. Click here for more information.
Application
Copper acetate (Cu(OAc)₂) is used as a precursor:
- For the synthesis of copper(I) oxide (Cu₂O) thin films via atomic layer deposition (ALD) which are used in the fabrication of photoconductor devices solar cells, and thin film transistors.
- In the synthesis of Cu-Doped ZnO Thin Films via Sol–Gel process for Optoelectronic Applications.
- In the green synthesis of copper and copper oxide nanoparticles. The resulting nanoparticles exhibited antibacterial and antifungal activities, making them valuable in biomedical applications and environmental remediation.
Features and Benefits
- (99.99% trace metals basis) ensures that there are minimal impurities, which enhances the efficiency and selectivity of the catalytic processes, such as oxidation and coupling reactions leading to higher yields and fewer by-products.
- The absence of impurities in high purity copper(II) acetate leads to vibrant colours and improved stability of the pigments, enhancing the overall quality of the final products
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 2 - Skin Corr. 1B
Clase de almacenamiento
8B - Non-combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
does not flash
flash_point_c
does not flash
ppe
dust mask type N95 (US), Eyeshields, Gloves
Elija entre una de las versiones más recientes:
¿Ya tiene este producto?
Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.
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
Nuestro equipo de científicos tiene experiencia en todas las áreas de investigación: Ciencias de la vida, Ciencia de los materiales, Síntesis química, Cromatografía, Analítica y muchas otras.
Póngase en contacto con el Servicio técnico