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216674

Sigma-Aldrich

Silver acetate

ReagentPlus®, 99%

Synonym(s):

Acetic acid silver salt

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About This Item

Linear Formula:
CH3COOAg
CAS Number:
563-63-3
Molecular Weight:
166.91
Beilstein/REAXYS Number:
3595636
EC Number:
209-254-9
MDL number:
MFCD00012446
UNSPSC Code:
12352103
PubChem Substance ID:
329752191
NACRES:
NA.21

Quality Level

100

product line

ReagentPlus®

assay

99%

form

powder or chunks

reaction suitability

reagent type: catalyst
core: silver

SMILES string

CC(O[Ag])=O

InChI

1S/C2H4O2.Ag/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1

InChI key

CQLFBEKRDQMJLZ-UHFFFAOYSA-M

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Application

Used in a novel preparation of highly reflective, conductive silvered polymer films. Also effectively catalyzes cycloaddition reactions of isocyanoacetates with a variety of olefins.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

Hazard Classifications

Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Study of thermal decomposition of silver acetate.
Logvinenko V, et al.
Journal of Thermal Analysis and Calorimetry, 90(3), 813-816 (2007)
cis-Hydroxylation of a synthetic steroid intermediate with iodine, silver acetate and wet acetic acid.
Woodward RB and Brutcher Jr FV.
Journal of the American Chemical Society, 80(1), 209-211 (1958)
Silver acetate catalysed cycloadditions of isocyanoacetates.
Grigg R, et al.
Tetrahedron, 55(7), 2025-2044 (1999)
Chemistry of Materials, FL501-FL501 (1999)
Silver acetate-assisted formation of amides from acyl chlorides.
Leggio A, et al.
Tetrahedron Letters, 56(1), 199-202 (2015)
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