403342
Copper(I) acetate
97%
Synonym(s):
Copper monoacetate, Cuprous acetate
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About This Item
Linear Formula:
CuCO2CH3
CAS Number:
Molecular Weight:
122.59
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352103
EC Number:
209-938-7
MDL number:
Quality Level
assay
97%
form
powder and chunks
reaction suitability
core: copper, reagent type: catalyst
mp
250 °C (dec.) (lit.)
SMILES string
CC(=O)O[Cu]
InChI
1S/C2H4O2.Cu/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1
InChI key
RFKZUAOAYVHBOY-UHFFFAOYSA-M
General description
Copper(II) acetate hydrate is a high-purity (98%), blue crystalline solid widely used as a versatile precursor for copper-based materials. Its hydrate form enhances solubility in aqueous/organic solvents, facilitating solution processing for advanced applications. Recent research emphasizes its role in sustainable energy technologies, catalysis, and functional nanomaterials, aligning with trends in green chemistry and renewable energy.
Application
Copper(II) acetate hydrate can be used as:
- A copper source in synthesizing CuS@C nanocomposites for sodium-ion battery anodes, delivering 485 mAh/g capacity after 200 cycles.
- A precursor to synthesize copper oxide thin films through deposition techniques like atomic layer deposition (ALD) and pulsed spray pyrolysis, enabling p-type semiconductor layers for optoelectronic applications.
- A electrocatalyst precursor for CO2 reduction to ethanol.
- A Precursor for superhydrophobic coatings via electrochemical deposition.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Articles
Copper metal deposition processes are an essential tool for depositing interconnects used in microelectronic applications, giving group 11 (coinage metals: Copper, Silver, and Gold) an important place in atomic layer deposition (ALD) process development.
Qiuyan Jin et al.
European journal of mass spectrometry (Chichester, England), 25(1), 30-43 (2019-02-19)
Gas-phase ion trap mass spectrometry experiments and density functional theory calculations have been used to examine the routes to the formation of the 1,8-naphthyridine (napy) ligated geminally dimetallated phenyl complexes [(napy)Cu2(Ph)]+, [(napy)Ag2(Ph)]+ and [(napy)CuAg(Ph)]+ via extrusion of CO2 or SO2
Jan Lorkowski et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 25(48), 11365-11374 (2019-07-06)
Cyclic (amino)(aryl)carbenes (cAArCs) based on the isoindoline core were successfully generated in situ by α-elimination of 3-alkoxyisoindolines at high temperatures or by deprotonation of isoindol-2-ium chlorides with sodium or copper(I) acetates at low temperatures. 3-Alkoxy-isoindolines 2 a,b-OR (R=Me, Et, iPr) have
Room?Temperature Formation of Hollow Cu2O Nanoparticles.
Hung LI, et al.
Advanced Materials, 22.17, 1910-1914 (2010)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 403342-1G | 04061831986563 |
| 403342-10G | 04061831986556 |