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Merck

32319

Sodium acetate

puriss. p.a., ACS reagent, reag. Ph. Eur., anhydrous

Sinónimos:

Acetic acid sodium salt

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About This Item

Fórmula lineal:
CH3COONa
Número CAS:
Peso molecular:
82.03
UNSPSC Code:
12352302
NACRES:
NA.21
PubChem Substance ID:
EC Number:
204-823-8
Beilstein/REAXYS Number:
3595639
MDL number:

Nombre del producto

Sodium acetate, puriss. p.a., ACS reagent, reag. Ph. Eur., anhydrous

InChI key

VMHLLURERBWHNL-UHFFFAOYSA-M

InChI

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

SMILES string

[Na+].CC([O-])=O

grade

ACS reagent
puriss. p.a.

agency

reag. Ph. Eur.

assay

≥99.0% (perchloric acid titration)

form

solid

autoignition temp.

1112 °F

impurities

≤0.01% in water soluble matter

loss

≤1% loss on drying, 120 °C

pH

7.5-9.2 (20 °C, 5%)

pKa 

4.76 (acetic acid)

mp

>300 °C (dec.) (lit.)

anion traces

chloride (Cl-): ≤0.002%
phosphate (PO43-): ≤0.001%
sulfate (SO42-): ≤0.003%

cation traces

Al: ≤10 mg/kg
Ca: ≤0.005%
Cd: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤0.001%
K: ≤200 mg/kg
Mg: ≤0.002%
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg
heavy metals: ≤0.001% (by ICP-OES)

suitability

in accordance for appearance of solution

Quality Level

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Application

Sodium acetate can be used as a catalyst to synthesize:
  • 1,2-Dihydropyridines by reacting 3-formylchromones, N-nucleophiles, and active methylene molecules.
  • 2(3H)-Furanone derivatives by using cinnamaldehyde and 5-aryl-2(3H) furanone.

Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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Visite la Librería de documentos

A Facile Route to Synthesize 1, 2-Dihydropyridine and 1, 6 Pyrimidinone Analogues from 4-Oxo-4H-Chromene-3-Carbaldehyde
Bari A
Journal of Heterocyclic Chemistry, 53, 461-466 (2016)
Synthesis, Characterization and Photophysical Properties of New 2 (3H) Furanone Derivatives
Soliman M, et al.
Journal of Molecular Structure, 134543-134543 (2022)
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