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Sigma-Aldrich

Silver trifluoroacetate

≥99.99% trace metals basis

Synonym(s):

Trifluoroacetic acid silver salt

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About This Item

Linear Formula:
CF3COOAg
CAS Number:
Molecular Weight:
220.88
Beilstein:
3634022
EC Number:
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.23

Assay

≥99.99% trace metals basis

form

crystalline powder
powder, crystals or chunks

reaction suitability

core: silver

mp

257-260 °C (dec.) (lit.)

SMILES string

FC(F)(F)C(=O)O[Ag]

InChI

1S/C2HF3O2.Ag/c3-2(4,5)1(6)7;/h(H,6,7);/q;+1/p-1

InChI key

KZJPVUDYAMEDRM-UHFFFAOYSA-M

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General description

Silver trifluoroacetate is a versatile reagent used in organic synthetic reactions, including acylation, alkylation, and cyclization reactions. It is also used to fabricate silver nanomaterials.

Application

Silver trifluoroacetate can be used:
  • As a precursor to synthesize silver nanoparticles.
  • As a starting material to fabricate conducting silver networks with high transmittance and low resistance via a polymer-assisted electrospinning technique.
  • As a reagent to prepare polynuclear luminescent complexes.
  • As a bifunctional reagent for oxidative carbonylative [4 + 1] annulation of aromatic acid.

Pictograms

Skull and crossbonesEnvironment

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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Direct Synthesis of Narrowly Dispersed Silver Nanoparticles Using a Single-Source Precursor
Xue Zhang Lin, et al.
Langmuir, 19, 10081-10085 (2003)
Silver trifluoroacetate as a bifunctional reagent for palladium-catalyzed oxidative carbonylative [4+ 1] annulation of aromatic acids
Zhuang-Zhuang Li, et al
Organic Chemistry Frontiers : An International Journal of Organic Chemistry / Royal Society of Chemistry, 10, 2243-2250 (2023)
Perhalophenyl(tetrahydrothiophene)gold(I) Complexes as Lewis Bases in Acid?Base Reactions with Silver Trifluoroacetate
Eduardo J. Fernandez, et al.},
Organometallics, 26, 5931-5939 (2007)
Conducting Silver Networks Based on Electrospun Poly(Methyl Methacrylate) and Silver Trifluoroacetate
Hung-Tao Chen, et al.
ACS Applied Materials & Interfaces, 7, 9479-9485 (2015)

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