Mellitic acid

Mellitic acid^[1]

Names
IUPAC name Benzene-1,2,3,4,5,6-hexacarboxylic acid
Other names Graphitic acid Benzenehexacarboxylic acid
Identifiers
CAS Number	517-60-2
ChEBI	CHEBI:41089
ChEMBL	ChEMBL1231329
ChemSpider	2244
DrugBank	DB01681
Jmol interactive 3D	Image
PubChem	2334
InChI InChI=1S/C12H6O12/c13-7(14)1-2(8(15)16)4(10(19)20)6(12(23)24)5(11(21)22)3(1)9(17)18/h(H,13,14)(H,15,16)(H,17,18)(H,19,20)(H,21,22)(H,23,24) Key: YDSWCNNOKPMOTP-UHFFFAOYSA-N InChI=1/C12H6O12/c13-7(14)1-2(8(15)16)4(10(19)20)6(12(23)24)5(11(21)22)3(1)9(17)18/h(H,13,14)(H,15,16)(H,17,18)(H,19,20)(H,21,22)(H,23,24) Key: YDSWCNNOKPMOTP-UHFFFAOYAB
SMILES O=C(O)c1c(c(c(c(c1C(=O)O)C(=O)O)C(=O)O)C(=O)O)C(=O)O
Properties
Chemical formula	C12H6O12
Molar mass	342.16 g/mol
Density	1.68 g/cm^3, 2.078 (calc.)[2]
Melting point	> 300 °C (572 °F; 573 K)
Boiling point	678 °C (1,252 °F; 951 K) (calc.)[2]
Acidity (pKa)	1.40, 2.19, 3.31, 4.78, 5.89, 6.96[3]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Mellitic acid, also called graphitic acid or benzenehexacarboxylic acid, is an acid first discovered in 1799 by M. H. Klaproth in the mineral mellite (honeystone), which is the aluminium salt of the acid.^[4]

Preparation

Mellitic acid may be prepared by warming mellite with ammonium carbonate, boiling off the excess of the ammonium salt, and adding ammonia to the solution. The precipitated alumina is filtered off, the filtrate evaporated, and the ammonium salt of the acid purified by recrystallization. The ammonium salt is then converted into the lead salt by precipitation with lead acetate, and the lead salt is then decomposed by hydrogen sulfide. The acid may also be prepared by the oxidation of pure carbon, graphite or hexamethyl benzene, by alkaline potassium permanganate in the cold, or by hot concentrated nitric acid.^[5]

Reactions

Mellitic acid crystallizes in fine silky needles and is soluble in water and alcohol. It is a very stable compound; chlorine, concentrated nitric acid and hydriodic acid do not react with it. It is decomposed, on dry distillation, into carbon dioxide and pyromellitic acid, C₁₀H₆O₈; when distilled with lime it gives carbon dioxide and benzene. Long digestion of the acid with an excess of phosphorus pentachloride forms the acid chloride, which crystallizes in needles, and melts at 190 °C. By heating the ammonium salt of the acid to 150–160 °C while ammonia is evolved, a mixture of paramide (mellimide, molecular formula C
6(CONHCO)
3), and ammonium euchroate is obtained. The mixture may be separated by dissolving out the ammonium euchroate with water. Paramide is a white amorphous powder, insoluble in water and alcohol.

The high stability of mellitic acid salts and their presence as an endproduct of the oxidation of polycyclic aromatic hydrocarbons, which are present in the solar system, make them a possible organic substance in Martian soil.^[6]

Mellitates (and salts of other benzene polycarboxylic acids) of iron and cobalt have interesting magnetic properties.^[7]

See also

• Mellitic anhydride

References

1. MSDS for mellitic acid
2. Curate Data: Predicted Properties: 2244. ChemSpider.com.
3. Brown, H.C., et al., in Baude, E.A. and Nachod, F.C., Determination of Organic Structures by Physical Methods, Academic Press, New York, 1955.
4. Beiträge zur chemischen Kenntniss der Mineralkörper, Band 3 (in German). p. 114.
5. WebElements.com
6. S. A. Benner, K. G. Devine, L. N. Matveeva, D. H. Powell (2000). "The missing organic molecules on Mars". Proceedings of the National Academy of Sciences 97 (6): 2425–2430. doi:10.1073/pnas.040539497. PMC 15945. PMID 10706606.
7. Kurmoo M, Estournes C, Oka Y, Kumagai H, Inoue K (2005) Inorganic Chemistry volume 44, page 217

Further reading

Henry Enfield Roscoe, Carl Scholemmer, "Mellitene Group", "A Treatise on Chemistry: V.III: The Chemistry of the Hydrocarbons and their Derivatives on Organic Chemistry: P.V:529. D. Appleton and Co. (1889).

 This article incorporates text from a publication now in the public domain: Chisholm, Hugh, ed. (1911). Encyclopædia Britannica (11th ed.). Cambridge University Press.