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32319

Sodium acetate

Name: Sodium acetate
Brand: SIGALD

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:

127-09-3

Molecular Weight:

82.03

UNSPSC Code:

12352302

NACRES:

NA.21

PubChem Substance ID:

329754137

EC Number:

204-823-8

Beilstein/REAXYS Number:

3595639

MDL number:

MFCD00012459

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Properties

Quality Level

200

agency

reag. Ph. Eur.

grade

ACS reagent, puriss. p.a.

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 (PO₄^3-): ≤0.001%, sulfate (SO₄^2-): ≤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

SMILES string

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

InChI

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

InChI key

VMHLLURERBWHNL-UHFFFAOYSA-M

Description

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.

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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)

Shaking alone induces de novo conversion of recombinant prion proteins to β-sheet rich oligomers and fibrils.

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

Daikenchuto, a traditional Japanese herbal medicine, ameliorates postoperative ileus by anti-inflammatory action through nicotinic acetylcholine receptors.

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

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Global Trade Item Number

SKU	GTIN
32319-500G-F	04061826708415
32319-500G-R	04061826708422
32319-100G-F	04061835570485
32319-1KG-R	04061835562756