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Ethyl potassium malonate, 98%, Thermo Scientific Chemicals
$122.73 - $1597.90
Chemical Identifiers
| CAS | 6148-64-7 |
|---|---|
| Molecular Formula | C5H7KO4 |
| Molecular Weight (g/mol) | 170.205 |
| MDL Number | MFCD00035603 |
| InChI Key | WVUCPRGADMCTBN-UHFFFAOYSA-M |
| Synonym | ethyl potassium malonate, potassium 3-ethoxy-3-oxopropanoate, potassium ethyl malonate, potassium monoethyl malonate, monoethyl malonate potassium salt, malonic acid monoethyl ester potassium salt, monoethyl potassium malonate, ethyl malonate potassium salt, propanedioic acid, monoethyl ester, potassium salt, ethylpotassiummalonate |
| PubChem CID | 3446434 |
| IUPAC Name | potassium;3-ethoxy-3-oxopropanoate |
| SMILES | CCOC(=O)CC(=O)[O-].[K+] |
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
|---|---|---|---|---|---|---|---|---|---|
| Catalog Number | Mfr. No. | Quantity | Price | Quantity | |||||
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AAA1072014
|
Thermo Scientific Chemicals
A1072014 |
25 g |
Each for $122.73
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AAA1072022
|
Thermo Scientific Chemicals
A1072022 |
100 g |
Each for $334.19
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AAA1072036
|
Thermo Scientific Chemicals
A1072036 |
500 g |
Each for $1,597.90
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Description
Ethyl potassium malonate is used as a competitive inhibitor of the enzyme succinate dehydrogenase. It acts as a precursor to produce (trimethylsilyl)ethyl malonate, which is utilized to prepare beta-ketoesters by acylation. Further, it reacts with aryl nitriles to prepare beta-amino acrylates in the presence of zinc chloride and a catalytic amount of Hünig's base. In addition to this, it serves as an intermediate for the preparation of ethyl tert-butyl malonate.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
ApplicationsEthyl potassium malonate is used as a competitive inhibitor of the enzyme succinate dehydrogenase. It acts as a precursor to produce (trimethylsilyl)ethyl malonate, which is utilized to prepare beta-ketoesters by acylation. Further, it reacts with aryl nitriles to prepare beta-amino acrylates in the presence of zinc chloride and a catalytic amount of Hünig′s base. In addition to this, it serves as an intermediate for the preparation of ethyl tert-butyl malonate.
Solubility
Soluble in water.
Notes
Hygroscopic. Incompatible with strong oxidizing agents.
Chemical Identifiers
| 6148-64-7 | |
| 170.205 | |
| WVUCPRGADMCTBN-UHFFFAOYSA-M | |
| 3446434 | |
| CCOC(=O)CC(=O)[O-].[K+] |
| C5H7KO4 | |
| MFCD00035603 | |
| ethyl potassium malonate, potassium 3-ethoxy-3-oxopropanoate, potassium ethyl malonate, potassium monoethyl malonate, monoethyl malonate potassium salt, malonic acid monoethyl ester potassium salt, monoethyl potassium malonate, ethyl malonate potassium salt, propanedioic acid, monoethyl ester, potassium salt, ethylpotassiummalonate | |
| potassium;3-ethoxy-3-oxopropanoate |
Specifications
| 6148-64-7 | |
| 9.1 | |
| C5H7KO4 | |
| MFCD00035603 | |
| 3721682 | |
| ethyl potassium malonate, potassium 3-ethoxy-3-oxopropanoate, potassium ethyl malonate, potassium monoethyl malonate, monoethyl malonate potassium salt, malonic acid monoethyl ester potassium salt, monoethyl potassium malonate, ethyl malonate potassium salt, propanedioic acid, monoethyl ester, potassium salt, ethylpotassiummalonate | |
| WVUCPRGADMCTBN-UHFFFAOYSA-M | |
| potassium;3-ethoxy-3-oxopropanoate | |
| 3446434 | |
| 98% |
| ∼200°C (decomposition) | |
| Odorless | |
| KO2CCH2CO2CH2CH3 | |
| 25 g | |
| Hygroscopic | |
| Soluble in water. | |
| CCOC(=O)CC(=O)[O-].[K+] | |
| 170.205 | |
| 170.21 | |
| Ethyl potassium malonate |
Safety and Handling
P261-P264b-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P362-P501c
H315-H319-H335
EINECSNumber : 228-156-7
TSCA : No
Recommended Storage : Ambient temperatures
RUO – Research Use Only