Thermo Scientific Chemicals

Diethyl malonate, 99%, Thermo Scientific Chemicals

Catalog number: A15468.0C
10,000 g, Each
Thermo Scientific Chemicals

Diethyl malonate, 99%, Thermo Scientific Chemicals

Catalog number: A15468.0C
10,000 g, Each
Quantity
Informational:Informational:This chemical may require us to obtain additional information for our regulatory and chemical compliance records. If required, we will contact you for this information once your order is placed.
Catalog number: A15468.0C
also known as A15468-0C
Price (USD)
Price: 374.00
Online price: 317.65
Your price:
Quantity
-

Chemical Identifiers

CAS
105-53-3
IUPAC Name
1,3-diethyl propanedioate
Molecular Formula
C7H12O4
InChI Key
IYXGSMUGOJNHAZ-UHFFFAOYSA-N
SMILES
CCOC(=O)CC(=O)OCC
Assay (GC)
≥98.5%
Water Content (Karl Fischer Titration)
≤0.5%
Appearance (Color)
Clear colorless
Identification (FTIR)
Conforms
Refractive Index
1.4125-1.4155 @ 20?C

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.

Applications
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.

Solubility
Miscible with ethyl alcohol, ether, chloroform and benzene. Slightly miscible with water.

Notes
Incompatible with acids, bases, oxidizing agents and reducing agents.
RUO – Research Use Only

Figures

Documents & Downloads

Certificates

    Frequently asked questions (FAQs)

    Citations & References

    Search citations by name, author, journal title or abstract text