Description
Potassium acetate, 100G
ACS reagent, ≥99.0%
Linear Formula:
CH3COOK
CAS Number:
127-08-2
Molecular Weight:
98.14
Beilstein/REAXYS Number:
3595449
EC Number:
204-822-2
MDL number:
MFCD00012458
PubChem Substance ID:
329752436
NACRES:
NA.21
PROPERTIES
InChI key
SCVFZCLFOSHCOH-UHFFFAOYSA-M
grade
ACS reagent
Quality Level
200
vapor pressure
<0.0000001 hPa ( 25 °C)
assay
≥99.0%
form
powder or crystals
impurities
≤0.005% insolubles
pH
6.5-9.0 (25 °C, 5%)
solubility
water: soluble 98.2 g/L at 20 °C
density
1.57 g/cm3 at 25 °C (lit.)
anion traces
chloride (Cl-): ≤0.003%
phosphate (PO43-): ≤0.001%
sulfate (SO42-): ≤0.002%
cation traces
Ca: ≤0.005%
Fe: ≤5 ppm
Mg: ≤0.002%
Na: ≤0.03%
heavy metals: ≤5 ppm (as Pb)
suitability
complies for IR spectroscopy
SMILES string
[K+].CC([O-])=O
InChI
1S/C2H4O2.K/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1
General description
Potassium acetate is a hygroscopic material used as a base in organic synthesis. It can also be used as a buffer and neutralizing agent.
Application
Potassium acetate can be used:
Potassium acetate can also be used as a base:
- As a catalyst in the glycolysis of rigid polyurethane (PU) using DEG (diethylene glycol) as a solvent.
- As a nucleophilic catalyst for addition and polymerization reaction.
- As a nucleophilic catalyst in the regioselective reaction of epoxides with S-phenyl thioesters.
- As a promoter/base in transition metal-catalyzed reactions.
- As a source of methyl radical in photo-decarboxylative nucleophilic additions to phthalimides and source of potassium ion for templating reactions.
Potassium acetate can also be used as a base:
- In the Lossen rearrangement of hydroxamic acid.
- In the E2 elimination′s reaction.
- In the fragmentation of α,α-dichloroketoesters and deprotonation of alcohols.
Other Notes
Go to Redi-Dri™ Product Listing 791733
Legal Information
Redi-Dri is a trademark of Sigma-Aldrich Co. LLC
SAFETY INFORMATION
Storage Class
13 - Non Combustible Solids
wgk_germany
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable