ログインで組織・契約価格をご覧ください。
サイズを選択してください
表示を変更する
この商品について
化学式:
CH3COOK
CAS番号:
分子量:
98.14
UNSPSC Code:
12352302
NACRES:
NA.21
PubChem Substance ID:
EC Number:
204-822-2
Beilstein/REAXYS Number:
3595449
MDL number:
Assay:
99-101%
Form:
crystalline
vapor pressure
<0.0000001 hPa ( 25 °C)
Quality Level
grade
puriss.
assay
99-101%
form
crystalline
quality
meets analytical specification of Ph. Eur., BP, E261
impurities
residual solvents, complies, ≤0.0004% heavy metals (as Pb), ≤0.05% KMnO4 red. matter (as HCOOH)
loss
≤1% loss on drying, 150 °C, 2 h
pH
7.5-9 (20 °C, 5%)
density
1.57 g/cm3 at 25 °C (lit.)
anion traces
chloride (Cl-): ≤50 mg/kg, sulfate (SO42-): ≤100 mg/kg
cation traces
Al: ≤1 mg/kg, As: ≤2 mg/kg, Ca: ≤50 mg/kg, Cu: ≤4 mg/kg, Fe: ≤10 mg/kg, Mg: ≤30 mg/kg, Na: ≤5000 mg/kg, Pb: ≤4 mg/kg, Zn: ≤10 mg/kg
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
General description
Potassium acetate is a hygroscopic potassium salt. It can be prepared by the neutralization of acetic acid with potassium hydroxide or potassium carbonate. It can be used as nucleophilic catalyst for polymerization and addition reactions, source of acetate anion in substitution and addition reaction. It can be used as a base and promoter in various organic reactions.
Application
Potassium acetate is used as a catalyst:
Potassium acetate is also used as a promoter:
- In the preparation of 2-hexadecylfuran from furfuraldehyde and palmitic anhydride.
- Potassium acetate can be used as a base:,In Lossen rearrangement of hydroxamic acids to carbamic acids.
- In E2 elimination reactions.
- In the formation of lactones from alkoxyamide substrates.
Potassium acetate is also used as a promoter:
- In the borylation of aryl chlorides with bis(pinacolato)diboron in presence of palladium catalyst.
- In the β-boration of α, β-unsaturated ketones.
Still not finding the right product?
Explore all of our products under 酢酸カリウム
保管分類
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
Eagleson M.
Concise Encyclopedia Chemistry, 886-886 (1994)
Saša Haberl et al.
The Journal of membrane biology, 246(11), 861-867 (2013-07-09)
The use of plasmid DNA (pDNA) as a pharmaceutical tool has increased since it represents a safer vector for gene transfer compared to viral vectors. Different pDNA extraction methods have been described; among them is alkaline lysis, currently the most
Jay D Gralla et al.
The EMBO journal, 25(7), 1515-1521 (2006-03-17)
Potassium glutamate accumulates upon hyper-osmotic shock and serves as a temporary osmoprotectant. This salt leads to transcriptional activation of sets of genes that allow the cell to achieve long-term adaptation to high osmolarity. The current experiments show that potassium glutamate