Phthalic acid
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| Names | |
|---|---|
| Preferred IUPAC name
Benzene-1,2-dicarboxylic acid | |
| Other names
Phthalic acid Benzene-1,2-dioic acid ortho-Phthalic acid | |
| Identifiers | |
88-99-3  | |
| 3D model (Jmol) | Interactive image |
| ChEBI | CHEBI:29069  |
| ChemSpider | 992 |
| ECHA InfoCard | 100.001.703 |
| EC Number | 201-873-2 |
| PubChem | 1017 |
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| Properties | |
| C8H6O4 | |
| Molar mass | 166.14 g/mol |
| Appearance | white solid |
| Density | 1.593 g/cm3, solid |
| Melting point | 207 °C (405 °F; 480 K)[1] |
| 0.6 g / 100 mL [2][3] | |
| Acidity (pKa) | 2.89, 5.51[4] |
| Hazards | |
| NFPA 704 | |
| Related compounds | |
| Related carboxylic acids |
Isophthalic acid Terephthalic acid |
| Related compounds |
Phthalic anhydride Phthalimide Phthalhydrazide Phthaloyl chloride Benzene-1,2- dicarboxaldehyde |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| verify (what is ?) | |
| Infobox references | |
Phthalic acid is an aromatic dicarboxylic acid, with formula C6H4(CO2H)2. It is an isomer of isophthalic acid and terephthalic acid. Although phthalic acid is of modest commercial importance, the closely related derivative phthalic anhydride is a commodity chemical produced on a large scale.[5]
Production
Phthalic acid is produced by the catalytic oxidation of naphthalene or ortho-xylene directly to phthalic anhydride and a subsequent hydrolysis of the anhydride.[5]
Phthalic acid was first obtained by French chemist Auguste Laurent in 1836 by oxidizing naphthalene tetrachloride. Believing the resulting substance to be a naphthalene derivative, he named it "naphthalic acid".[6] After the Swiss chemist Jean Charles Galissard de Marignac determined its correct formula,[7] Laurent gave it its present name.[8] Manufacturing methods in the nineteenth century included oxidation of naphthalene tetrachloride with nitric acid, or, better, oxidation of the hydrocarbon with fuming sulfuric acid, using mercury or mercury(II) sulfate as a catalyst.
Reactions and uses
It is a dibasic acid, with pKa's of 2.89 and 5.51. The monopotassium salt, potassium hydrogen phthalate is a standard acid in analytical chemistry. Typically phthalate esters are prepared from the widely available phthalic anhydride. Reduction of phthalic acid with sodium amalgam in the presence of water gives the 1,3-cyclohexadiene derivative.[9]
Isomers
Phthalic acid is one of three isomers of benzenedicarboxylic acid, the others being isophthalic acid and terephthalic acid. Sometimes the term "phthalic acids" is used to refer to this family of isomers, but in the singular, "phthalic acid", refers exclusively to the ortho- isomer.
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| phthalic acid | isophthalic acid | terephthalic acid |
| (ortho-phthalic acid) | (meta-phthalic acid) | (para-phthalic acid) |
Safety
The toxicity of phthalic acid is low with LD50 (mouse) of 550 mg/kg. However, many phthalate esters have been implicated as endocrine disruptors.
Biodegradation
The bacteria Pseudomonas sp. P1 degrades phthalic acid.[10]
See also
- Isophthalic acid
- Phthalate
- Phthalic anhydride
- Potassium hydrogen phthalate, a primary standard for acid-base titrations
- Terephthalic acid
References
- ↑ Several melting points are reported, for example: (i) 480. K (NIST website), (ii) 210−211 °C with decomposition (Sigma-Aldrich on-line), (iii) 191 °C in a sealed tube (Ullmann's Encyclopedia of Industrial Chemistry), (iv) 230 °C with conversion to phthalic anhydride and water (J.T.Baker MSDS).
- ↑ http://hazard.com/msds/mf/baker/baker/files/p4270.htm
- ↑ http://actrav.itcilo.org/actrav-english/telearn/osh/ic/88993.htm
- ↑ 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.
- 1 2 Peter M. Lorz, Friedrich K. Towae, Walter Enke, Rudolf Jäckh, Naresh Bhargava, Wolfgang Hillesheim "Phthalic Acid and Derivatives" in Ullmann's Encyclopedia of Industrial Chemistry, 2007, Wiley-VCH, Weinheim. doi:10.1002/14356007.a20_181.pub2
- ↑ See:
- Auguste Laurent (1836) "Sur l'acide naphtalique et ses combinaisons" (On naphthalic acid and its compounds), Annales de Chimie et de Physique, 61 : 113-125. (Note: The empirical formulae of the compounds that were analyzed in this article are incorrect, in part because, during this period, chemists used incorrect atomic masses for carbon (6 instead of 12) and other elements.)
- Reprinted in German as: Auguste Laurent (1836) "Ueber Naphthalinsäure und ihre Verbindungen" (On naphthalenic acid and its compounds), Annalen der Pharmacie, 19 (1) : 38-50; for the preparation of phthalic acid, see page 41.
- ↑ C. de Marignac (1841) "Ueber die Naphtalinsäure und ein bei ihrer Darstellung entstehendes flüchtiges Produkt" ("On naphthalinic acid and a volatile product that arises during its preparation"), Annalen der Chemie und Pharmacie, 38 (1) : 13-20. (Note: Again, Marignac's empirical formulae are wrong because chemists at this time used incorrect atomic masses.)
- ↑ See:
- Auguste Laurent (1841) "Sur de nouvelles combinaisons nitrogénées de la naphtaline et sur les acides phtalique et nitrophtalique" (On new nitrogenous compounds of naphthalene, and on phthalic acid and nitrophthalic acid), Revue Scientifique et Industrielle, 6 : 76-99; on page 92, Laurent coins the name "acide phtalique" (phthalic acid) and admits that his earlier empirical formula for phthalic acid was wrong.
- Reprinted in German as: Auguste Laurent (1842) "Ueber neue stickstoffhaltige Verbindungen des Naphtalins, über Phtalinsäure und Nitrophtalinsäure" (On new nitrogenous compounds of naphthalene, on phthalic acid and nitrophthalic acid), Annalen der Chemie und Pharmacie, 41 (1) : 98-114; on page 108, Laurent coins the name "Phtalinsäure" (phthalic acid).
- ↑ Richard N. McDonald and Charles E. Reineke (1988). "trans-1,2-Dihydrophthalic Acid". Org. Synth.; Coll. Vol., 6, p. 461
- ↑ Ishtiaq Ali, Muhammad (2011). Microbial degradation of polyvinyl chloride plastics (PDF) (Ph.D.). Quaid-i-Azam University. p. 47.
- Merck Index, 9th ed, #7178
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This article incorporates text from a publication now in the public domain: Chisholm, Hugh, ed. (1911). "article name needed". Encyclopædia Britannica (11th ed.). Cambridge University Press.