모든 사진(5)
About This Item
Linear Formula:
CH3COOK
CAS Number:
Molecular Weight:
98.14
Beilstein:
3595449
EC Number:
MDL number:
UNSPSC 코드:
12352106
PubChem Substance ID:
NACRES:
NA.21
solubility:
water: soluble 98.2 g/L at 20 °C
추천 제품
Grade
ACS reagent
Quality Level
vapor pressure
<0.0000001 hPa ( 25 °C)
분석
≥99.0%
양식
powder or crystals
불순물
≤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.)
음이온 미량물
chloride (Cl-): ≤0.003%
phosphate (PO43-): ≤0.001%
sulfate (SO42-): ≤0.002%
양이온 미량물
Ca: ≤0.005%
Fe: ≤5 ppm
Mg: ≤0.002%
Na: ≤0.03%
heavy metals: ≤5 ppm (as Pb)
적합성
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
InChI key
SCVFZCLFOSHCOH-UHFFFAOYSA-M
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일반 설명
Potassium acetate is a hygroscopic material used as a base in organic synthesis. It can also be used as a buffer and neutralizing agent.
애플리케이션
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.
법적 정보
Redi-Dri is a trademark of Sigma-Aldrich Co. LLC
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 1
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
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시험 성적서(COA)
Lot/Batch Number
이미 열람한 고객
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Steady-state and time-resolved emission techniques were employed to study the effect of acetate, a mild base, on the luminescence of curcumin in methanol and ethanol. We found that the steady-state emission intensity as well as the average fluorescence decay time
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