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Diethyl malonate, 99%
CAS: 105-53-3 | C7H12O4 | 160.169 g/mol
41.25 EUR - 443.00 EUR
Chemical Identifiers
| CAS | 105-53-3 |
|---|---|
| Molecular Formula | C7H12O4 |
| Molecular Weight (g/mol) | 160.169 |
| MDL Number | MFCD00009195 |
| InChI Key | IYXGSMUGOJNHAZ-UHFFFAOYSA-N |
| Synonym | diethyl malonate, malonic ester, propanedioic acid, diethyl ester, dicarbethoxymethane, malonic acid, diethyl ester, carbethoxyacetic ester, malonic acid diethyl ester, 1,3-diethyl propanedioate, ethyl propanedioate, ethyl malonate van |
| PubChem CID | 7761 |
| IUPAC Name | diethyl propanedioate |
| SMILES | CCOC(=O)CC(=O)OCC |
| Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
|---|---|---|---|---|---|---|---|---|---|
| Product Code | Brand | Quantity | Price | Quantity & Availability | |||||
|
11452837
|
Thermo Scientific Alfa Aesar
A15468.36 |
500 g |
41.25 EUR
500g |
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|
11462837
|
Thermo Scientific Alfa Aesar
A15468.0E |
2500 g |
118.00 EUR
2500g |
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|
11472837
|
Thermo Scientific Alfa Aesar
A15468.0C |
10,000 g |
443.00 EUR
10000g |
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Description
Diethyl malonate is used in organic synthesis for the preparation of alpha-aryl malonates, mono-substituted and di-substituted acetic acid, barbiturates and artificial flavorings. It is also involved in the synthesis of pharmaceuticals like chloroquine, butazolidin and barbital. It acts as intermediate in the synthesis of vitamin B1, vitamin B6, non-steroidal anti-inflammatory agents agrochemicals and perfumes. In Knoevenagel condensation reaction, it reacts with benzaldehyde to get diethyl benzylidenemalonate.
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.
ApplicationsDiethyl malonate is used in organic synthesis for the preparation of alpha-aryl malonates, mono-substituted and di-substituted acetic acid, barbiturates and artificial flavorings. It is also involved in the synthesis of pharmaceuticals like chloroquine, butazolidin and barbital. It acts as intermediate in the synthesis of vitamin B1, vitamin B6, non-steroidal anti-inflammatory agents agrochemicals and perfumes. In Knoevenagel condensation reaction, it reacts with benzaldehyde to get diethyl benzylidenemalonate.
Solubility
Miscible with ethyl alcohol, ether, chloroform and benzene. Slightly miscible with water.
Notes
Incompatible with acids, bases, oxidizing agents and reducing agents.
Chemical Identifiers
| 105-53-3 | |
| 160.169 | |
| IYXGSMUGOJNHAZ-UHFFFAOYSA-N | |
| 7761 | |
| CCOC(=O)CC(=O)OCC |
| C7H12O4 | |
| MFCD00009195 | |
| diethyl malonate, malonic ester, propanedioic acid, diethyl ester, dicarbethoxymethane, malonic acid, diethyl ester, carbethoxyacetic ester, malonic acid diethyl ester, 1,3-diethyl propanedioate, ethyl propanedioate, ethyl malonate van | |
| diethyl propanedioate |
Specifications
| 105-53-3 | |
| 1.055 | |
| 90°C (194°F) | |
| C7H12O4 | |
| MFCD00009195 | |
| 14,3823 | |
| Miscible with ethyl alcohol,ether,chloroform and benzene. Slightly miscible with water. | |
| CCOC(=O)CC(=O)OCC | |
| 160.169 | |
| 160.17 | |
| Liquid |
| °C to 50°C | |
| 198°C to 200°C | |
| 99% | |
| 1.414 | |
| 774687 | |
| diethyl malonate, malonic ester, propanedioic acid, diethyl ester, dicarbethoxymethane, malonic acid, diethyl ester, carbethoxyacetic ester, malonic acid diethyl ester, 1,3-diethyl propanedioate, ethyl propanedioate, ethyl malonate van | |
| IYXGSMUGOJNHAZ-UHFFFAOYSA-N | |
| diethyl propanedioate | |
| 7761 | |
| 99% | |
| Diethyl Malonate |
Safety and Handling
P210-P280-P370+P378q-P501c
H227
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missing translation for 'rtecsNumber' : OO0700000
missing translation for 'tsca' : Yes
Recommended Storage : Ambient temperatures
RUO – Research Use Only
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Product Title
Diethyl malonate, 99%