Discover

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| Chemical name
|
|-
| Other names
| methanedicarboxylic acid
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| Chemical formula
|
|-
| pK_a
| 2.83 (pK₁)
5.69 (pK₂)
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| Molecular mass
| g/mol
|-
| CAS number
| []
|-
| Melting point
| °C ''decomp.''
|-
| SMILES
|
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! | Properties
|-
| Density and phase
| ? g/cm³, Solid
|-
| Solubility in water
| Completely Soluble
|-
| Melting point
| 135-136°C (408-409 K)
|-
| Boiling point
| Decomposes
|-
| Acidity (p''K''_a1)
| 2.83
|-
| Acidity (p''K''_a2)
| 5.69
|-
| |
|-
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'Malonic acid' (IUPAC systematic name: 'propanedioic acid') is a dicarboxylic acid with structure CH₂(COOH)₂. The ionised form of malonic acid, as well as its esters and salts, are known as 'malonates'. For example, diethyl malonate is malonic acid's ethyl ester. The name originates from Latin ''malum'', meaning ''apple''.

Contents

Biochemistry

Organic synthesis

Organic reactions

External links

References

Biochemistry

The calcium salt of malonic acid occurs in high concentrations in beetroot.

Organic synthesis

A classical preparation of malonic acid starts from acetic acid ^[1]. This acid is chlorinated to chloroacetic acid. Sodium carbonate generates the sodium salt which is then reacted with sodium cyanide to the cyano acetic acid salt in a nucleophilic substitution. The nitrile group can be hydrolysed with sodium hydroxide to sodium malonate and acidification affords malonic acid.

Organic reactions

In a well known reaction malonic acid condenses with urea to barbituric acid. Malonic acid is frequently used as an enolate in Knoevenagel condensations or condensed with acetone to form Meldrum's acid.

External links

★ MSDS http://physchem.ox.ac.uk [1]

★ MSDS http://avogadro.chem.iastate.edu [2]

★ pH spectrum http://www.Theoprax-Research.com Disodium Malonate

★ pH spectrum http://www.Theoprax-Research.com Malonic acid copper complex

References

1. ''Malonic acid'' Nathan Weiner Organic Syntheses, Coll. Vol. 2, p.376; Vol. 18, p.50 Online article