241245

Acetate de sodium

ACS reagent, ≥99.0%

• Synonyme(s) : Acide acétique sodium salt
• Formule linéaire : CH₃COONa
• Numéro CAS: 127-09-3
• Poids moléculaire : 82.03
• Numéro Beilstein : 3595639
• Numéro CE : 204-823-8
• Numéro MDL: MFCD00012459
• Code UNSPSC : 12352300
• eCl@ss : 39021906
• ID de substance PubChem : 329752574
• Nomenclature NACRES : NA.21

Propriétés

• Qualité: ACS reagent
• Niveau de qualité: 200
• Pureté: ≥99.0%
• Forme: solid
• Température d'inflammation spontanée: 1112 °F
• Impuretés: ≤0.01% insolubles
• Perte: ≤1.0% loss on drying
• pH: 7.0-9.2 (25 °C, 5%)
• pKa: 4.76 (acetic acid)
• Pf: >300 °C (dec.) (lit.)
• Traces d'anions: chloride (Cl^-): ≤0.002%; phosphate (PO₄^3-): ≤0.001%; sulfate (SO₄^2-): ≤0.003%
• Traces de cations: Ca: ≤0.005%; Fe: ≤0.001%; Mg: ≤0.002%; heavy metals: ≤0.001% (by ICP-OES)
• Adéquation: complies for IR spectroscopy
• Chaîne SMILES: [Na+].CC([O-])=O
• InChI: 1S/C2H4O2.Na/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1
• Clé InChI: VMHLLURERBWHNL-UHFFFAOYSA-M

Description

Description générale

Sodium acetate is a hydrophilic organic compound that can be prepared by treating acetic acid with sodium carbonate or sodium hydroxide. It acts as neutralizing agent, catalyst, food additive, and buffer to maintain a specific pH.

Application

Sodium acetate can be used as a base to synthesize:

• Oxazolones via Erlenmeyer Plochl condensation reaction of aromatic aldehydes and hippuric acid.
• Cinnamic acids via Perkin reaction between aromatic aldehydes and acid anhydrides.

A mixture of sodium acetate-acetic acid buffer can be employed in the polybromination of substituted imidazoles to synthesize polybrominated imidazoles.

It can also be used as a catalyst in tandem Knoevenagel-Michael multicomponent reactions.

Autres remarques

Go to Redi-Dri^™ Product Listing 791741

Informations légales

Redi-Dri is a trademark of Sigma-Aldrich Co. LLC

Informations sur la sécurité

• Code de la classe de stockage: 11 - Combustible Solids
• Classe de danger pour l'eau (WGK): WGK 1