Malonic acid

Malonic acid
IUPAC name propanedioic acid
Other names methanedicarboxylic acid
Identifiers
CAS number	141-82-2 Y
PubChem	867
ChemSpider	844 Y
DrugBank	DB02175
ChEBI	CHEBI:30794 Y
ChEMBL	CHEMBL7942 Y
Jmol-3D images	Image 1
SMILES C(C(=O)O)C(=O)O
InChI InChI=1S/C3H4O4/c4-2(5)1-3(6)7/h1H2,(H,4,5)(H,6,7) Y Key: OFOBLEOULBTSOW-UHFFFAOYSA-N Y InChI=1/C3H4O4/c4-2(5)1-3(6)7/h1H2,(H,4,5)(H,6,7) Key: OFOBLEOULBTSOW-UHFFFAOYAJ
Properties
Molecular formula	C3H4O4
Molar mass	104.06 g mol−1
Density	1.619 g/cm3
Melting point	135–136 °C
Boiling point	decomposes
Solubility in water	Miscible
Acidity (pKa)	pKa1 = 2.83[1] pKa2 = 5.69[1]
Related compounds
Other anions	malonate
Related carboxylic acids	acetic acid oxalic acid propionic acid tartronic acid acrylic acid butyric acid succinic acid fumaric acid
Related compounds	propanone propionaldehyde propanedial dimethyl malonate
Hazards
MSDS	External MSDS
Y (verify) (what is: Y/N?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

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 μᾶλον (malon) meaning 'apple'.

Biochemistry

The calcium salt of malonic acid occurs in high concentrations in beetroot. It exists in its normal state as white crystals. Malonic acid is the classic example of a competitive inhibitor: It acts against succinate dehydrogenase (complex II) in the respiratory electron transport chain.

Preparation

A classical preparation of malonic acid starts from chloroacetic acid:^[2]

Sodium carbonate generates the sodium salt, which is then reacted with sodium cyanide to provide the cyano acetic acid salt via a nucleophilic substitution. The nitrile group can be hydrolyzed with sodium hydroxide to sodium malonate, and acidification affords malonic acid.

Organic reactions

In a well-known reaction, malonic acid condenses with urea to form barbituric acid. Malonic acid is also frequently used as an enolate in Knoevenagel condensations or condensed with acetone to form Meldrum's acid. The esters of malonic acid are also used as a ⁻CH₂COOH synthon in the malonic ester synthesis.

References

External links

• pH-Spectrum of Disodium Malonate
• pH-Spectrum of Malonate-copper-complex
• Calculator: Water and solute activities in aqueous malonic acid