Silver acetate - ≥99.95% metals basis , CAS No.563-63-3

CAS: 563-63-3 Cat. No.: S104731 Molecular Weight: 166.91 EC Number: 209-254-9 PubChem CID: 11246

GRADE & PURITY ≥99.95% metals basis

Synonyms

SILVER ACETATE [WHO-DD] | silver(1+) ion acetate | Silver(1+ ) acetate | D74466 | UNII-19PPS85F9H | Acetic acid, silver(1+) salt (1:1) | Silver acetate Ag(OAc) | Acetic acid silver salt | NSC112212 | NSC-112212 | SILVER ACETATE [MI] | AKOS025243287 | SILV

Storage

Protected from light,Room temperature,Argon charged,Desiccated

Shipped In

Normal

Overview

Used in a novel preparation of highly reflective, conductive silvered polymer films. Also effectively catalyzes cycloaddition reactions of isocyanoacetates with a variety of olefins.Reaction of silver carbonate with acetic acid at 45-60°C has been reported to afford silver acetate. It participates in the conversion of carboxylic acid chlorides to amides, via aminolysis.

Specifications

Synonyms

SILVER ACETATE [WHO-DD] | silver(1+) ion acetate | Silver(1+ ) acetate | D74466 | UNII-19PPS85F9H | Acetic acid, silver(1+) salt (1:1) | Silver acetate Ag(OAc) | Acetic acid silver salt | NSC112212 | NSC-112212 | SILVER ACETATE [MI] | AKOS025243287 | SILV

Specifications & Purity

≥99.95% metals basis

Storage

Protected from light, Room temperature, Argon charged, Desiccated

Shipped In

Normal

Purity

≥99.95% metals basis

Names and Identifiers

• Canonical Smiles: CC(=O)[O-].[Ag+]
• IUPAC Name: silver;acetate
• InChIKey: CQLFBEKRDQMJLZ-UHFFFAOYSA-M
• INCHI: 1S/C2H4O2.Ag/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1
• Isomeric SMILES: CC(=O)[O-].[Ag+]
• PubChem CID: 11246
• Molecular Weight: 166.91

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives
        • Level5 Carboxylic acid salts
          • Level6 Acetate salts

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Carboxylic acid salts
• Direct Parent: Acetate salts
• Alternative Parents: Monocarboxylic acids and derivatives Organic silver salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Acetate salt - Organic metal salt - Organic transition metal salt - Monocarboxylic acid or derivatives - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic silver salt - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as acetate salts. These are organic compounds containing acetic acid as its acid component.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Mechanisms of Action

Chemical and Physical Properties

• Solubility: Soluble in water (10.2 mg/ml at 20 °C), and nitric acid.
• Sensitivity: Light sensitive
• Molecular Weight: 166.910 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 165.918 Da
• Monoisotopic Mass: 165.918 Da
• Topological Polar Surface Area: 40.100 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 25.500
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3

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