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Merck

32319

Sodium acetate

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

Synonym(s):

Acetic acid sodium salt

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About This Item

Linear Formula:
CH3COONa
CAS Number:
Molecular Weight:
82.03
UNSPSC Code:
12352302
NACRES:
NA.21
PubChem Substance ID:
EC Number:
204-823-8
Beilstein/REAXYS Number:
3595639
MDL number:

Product Name

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.

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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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)
Mari Endo et al.
Journal of gastroenterology, 49(6), 1026-1039 (2013-07-13)
Daikenchuto (DKT), a gastrointestinal prokinetic Japanese herbal medicine, is prescribed for patients with postoperative ileus (POI) and adhesive bowel obstruction following abdominal surgery. Several mechanisms for the amelioration of POI by DKT have been suggested; however, it has remained unclear
Carol L Ladner-Keay et al.
PloS one, 9(6), e98753-e98753 (2014-06-04)
The formation of β-sheet rich prion oligomers and fibrils from native prion protein (PrP) is thought to be a key step in the development of prion diseases. Many methods are available to convert recombinant prion protein into β-sheet rich fibrils
Andrew D Shaw et al.
Annals of surgery, 255(5), 821-829 (2012-04-04)
To assess the association of 0.9% saline use versus a calcium-free physiologically balanced crystalloid solution with major morbidity and clinical resource use after abdominal surgery. 0.9% saline, which results in a hyperchloremic acidosis after infusion, is frequently used to replace

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