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この商品について
化学式:
CH3COONa
CAS番号:
分子量:
82.03
UNSPSC Code:
12352302
NACRES:
NA.21
PubChem Substance ID:
EC Number:
204-823-8
Beilstein/REAXYS Number:
3595639
MDL number:
Quality Level
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 (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
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
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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.
保管分類
11 - Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Synthesis, Characterization and Photophysical Properties of New 2 (3H) Furanone Derivatives
Soliman M, et al.
Journal of Molecular Structure, 134543-134543 (2022)
A Facile Route to Synthesize 1, 2-Dihydropyridine and 1, 6 Pyrimidinone Analogues from 4-Oxo-4H-Chromene-3-Carbaldehyde
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