Malonic acid

Description

Malonic acid (IUPAC systematic name: propanedioic acid) is a dicarboxylic acid with structure CH₂(COOH)₂. The ionized form of malonic acid, as well as its esters and salts, are known as malonates. For example, diethyl malonate is malonic acid's diethyl ester. The name originates from the Greek word (malon) meaning 'apple'.

Description

Malonic acid, formally propanedioic acid, is the second-smallest aliphatic dicarboxylic acid. (Oxalic acid?is the smallest.) It should not be confused with malic or maleic acid, both of which also contain two carboxyls.
Malonic acid is a white crystalline solid with a decomposition point of ≈135 °C. It is highly soluble in water and oxygenated solvents. It has numerous commercial uses: It is a precursor to specialty polyesters; it is used in the manufacture of barbiturates, coatings, and biodegradable containers; and it is even a component of surgical adhesives.
French chemist Victor Dessaignes reported the first synthesis of malonic acid in 1858; he made it by oxidatively decomposing four-carbon malic acid with potassium dichromate. Since then, it has been synthesized commercially starting from chloroacetic acid, diethyl malonate, and even sodium acetate.
In the past two decades, much work has been done on biobased syntheses of malonic acid. Most recently, the Berkeley, CA, venture-capital startup Lygos raised US$13 million to scale up a process that uses bioengineered yeast strains to?produce malonic acid from sugars.
Lygos, by the way, was reported by Pliny the Elder as a former name of the “town of Byzantium”. Today, of course, it’s the city of Istanbul.

The Uses of Malonic acid

Malonic acid is used as an intermediate in the manufacture of barbiturates and other pharmaceuticals. It is a component used as a stabilizer in many high-end cosmetic and pharmaceutical products. Malonic acid is also used as building block in chemical synthesis, specifically to introduce the molecular group -CH2-COOH. It is used for the introduction of an acetic acid moiety under mild conditions by Knoevenagel condensation and subsequent decarboxylation.