204374
醋酸银
99.99% trace metals basis
别名:
醋酸 银盐
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线性分子式:
CH3COOAg
化学文摘社编号:
分子量:
166.91
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
209-254-9
Beilstein/REAXYS Number:
3595636
MDL number:
产品名称
醋酸银, 99.99% trace metals basis
InChI key
CQLFBEKRDQMJLZ-UHFFFAOYSA-M
InChI
1S/C2H4O2.Ag/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1
SMILES string
CC(O[Ag])=O
assay
99.99% trace metals basis
form
powder or crystals
reaction suitability
core: silver
reaction type: C-H Activation
reagent type: catalyst
Quality Level
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Application
用于高反射性、导电性银聚合物膜的新型制备方法。亦可用于有效催化异氰基乙酸酯与多种烯烃的环加成反应。
Silver acetate is used as:
- A dopant in the synthesis of tetrahedrite Cu10-x-yAgyZnxS thin film via polyol method
- A precursor in the synthesis of AgBiS2 nanocrystals (NCs), which are then employed in the fabrication of photodetectors.
- Precursor in the synthesis of silver phosphate (Ag3PO4) crystals, specifically rhombic dodecahedrons with well-defined {1 1 0} facets. These Ag3PO4 crystals exhibit high photocatalytic activity, making them effective for water photooxidation and the reduction of CO2 into renewable fuels.
Features and Benefits
- High purity (99.99% trace metals basis) improves the conductivity and stability of silver-based inks, ensuring reliable performance in electronic applications.
- High purity ensures effective antimicrobial action with 64% silver content while preventing harmful contaminants that could compromise safety.
- The high purity (99.99% trace metals basis) minimizes impurities that could inhibit catalytic activity, leading to higher reaction rates and improved selectivity, along with a high silver loading of 64%
General description
Silver acetate is a high-purity (99.99% trace metals basis) white to off-white crystalline solid that is moderately soluble in water and highly soluble in polar organic solvents such as ethanol. This solubility makes it well-suited for use in formulating conductive inks and coatings for flexible electronics. It exhibits moderate thermal stability, decomposing at temperatures above 150–200 °C. This characteristic enables its application in thermal processing techniques, including thin-film formation, nanoparticle synthesis, and metal coating processes.
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Chemistry of Materials, FL501-FL501 (1999)
Jed E Rose et al.
Experimental and clinical psychopharmacology, 18(6), 462-469 (2010-12-29)
Oral topical silver-containing formulations were marketed in the 1970s and 1980s as smoking deterrents, based on the finding that when using such formulations, an unpleasant taste occurs upon smoking. This approach has not been widely adopted, however, in part because
Dewi Susanti et al.
The Journal of organic chemistry, 77(17), 7166-7175 (2012-08-17)
A method to prepare (Z)-2-methylene-1-sulfonylindolin-3-ols efficiently that relies on silver acetate catalyzed hydroamination of 1-(2-(sulfonylamino)phenyl)prop-2-yn-1-ols is reported. The reactions proceed rapidly at room temperature with catalyst loadings as low as 1 mol % under conditions that did not require the
Tim Lancaster et al.
The Cochrane database of systematic reviews, 9(9), CD000191-CD000191 (2012-09-14)
Silver acetate produces an unpleasant taste when combined with cigarettes, thereby producing an aversive stimulus. It has been marketed in various forms with the aim of extinguishing the urge to smoke, by pairing the urge with an unpleasant stimulus. The
Siddappa Patil et al.
Metallomics : integrated biometal science, 3(1), 74-88 (2010-12-08)
From the reaction of 1-methylimidazole (1a), 4,5-dichloro-1H-imidazole (1b(I)) and 1-methylbenzimidazole (1c) with p-cyanobenzyl bromide (2a), non-symmetrically substituted N-heterocyclic carbene (NHC) [(3a-c)] precursors, 5,6-dimethyl-1H-benzimidazole (1d) and 4,5-diphenyl-1H-imidazole (1e) with p-cyanobenzyl bromide (2a) and benzyl bromide (2b), symmetrically substituted N-heterocyclic carbene (NHC)
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