|Preferred IUPAC name
|3D model (Jmol)||Interactive image|
|Molar mass||148.1 g/mol|
|Density||1.53 g/cm3, solid; 1.20 g/mL, molten|
|Melting point||131.6 °C (268.9 °F; 404.8 K)|
|Boiling point||295 °C (563 °F; 568 K) sublimates|
|0.62 g/100g (20—25 °C);
19.0 g/100g (100 °C);
|Vapor pressure||0.0015 mmHg (20°C)|
|R-phrases||R22, R37/38, R41, R42/43|
|S-phrases||(S2), S23, S24/25, S26, S37/39, S46|
|Flash point||152 °C (306 °F; 425 K)|
|Lethal dose or concentration (LD, LC):|
LD50 (median dose)
|4020 mg/kg (oral, rat)
1520 mg/kg (oral, mouse)
800 mg/kg (oral, cat)
800-1600 mg/kg (oral, rat)
2210 mg/kg (oral, mouse)
|US health exposure limits (NIOSH):|
|TWA 12 mg/m3 (2 ppm)|
|TWA 6 mg/m3 (1 ppm)|
IDLH (Immediate danger)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Phthalic anhydride is the organic compound with the formula C6H4(CO)2O. It is the anhydride of phthalic acid. Phthalic anhydride is a principal commercial form of phthalic acid. It was the first anhydride of a dicarboxylic acid to be used commercially. This colourless solid is an important industrial chemical, especially for the large-scale production of plasticizers for plastics. In 2000, the worldwide production volume was estimated to be about 3 million tonnes per year.
Synthesis and production
Phthalic anhydride was first reported in 1836 by Auguste Laurent. More contemporary routes include catalytic oxidation of ortho-xylene and naphthalene ("Gibbs phthalic anhydride process"), although use of naphthalene has declined. Starting from o-xylene, the oxidation follows the following stoichiometry:
- C6H4(CH3)2 + 3 O2 → C6H4(CO)2O + 3 H2O
The reaction proceeds with about 70% selectivity. About 10% of maleic anhydride is also produced:
- C6H4(CH3)2 + 7.5 O2 → C4H2O3 +4 H2O + 4 CO2
The reaction is catalyzed by a vanadium pentoxide (V2O5) between 320 - 400 °C. The phthalic anhydride is separated from byproducts by a series of "switch condensers". Phthalic anhydride and maleic anhydride are recovered by distillation. Phthalic anhydride can also be prepared from phthalic acid:
The primary use of phthalic anhydride is as a chemical intermediate in the production of plastics from vinyl chloride. Phthalate esters, which function as plasticizers, are derived from Phthalic Anhydride. Phthalate plasticizers are used for the production of flexible PVC products such as cables, pipes and hoses, leather cloth, shoes, film for packaging etc. Phthalic anhydride has another major use in the production of polyester resins and other minor uses in the production of alkyd resins used in paints and lacquers; certain dyes (anthraquinone, phthalein, rhodamine, phthalocyanine, fluorescin, and xanthene dyes); insect repellents; and polyester polyols for polyurethanes. It is also utilized as a rubber scorch inhibitor and retarder.
Phthalic anhydride is a versatile intermediate in organic chemistry, in part because it is bifunctional and cheaply available. Hydrolysis by hot water forms ortho-phthalic acid. Hydrolysis of anhydrides is not typically a reversible process. Phthalic acid is however easily dehydrated to form phthalic anhydride. Above 180 °C, phthalic anhydride re-forms.
Preparation of phthalate esters
As with other anhydrides, the alcoholysis reaction is the basis of the manufacture of phthalate esters, which are widely used (and controversial - see endocrine disruptor) plasticizers. In the 1980s, approximately 6.5×109 kg of these esters were produced annually, and the scale of production was increasing each year, all from phthalic anhydride. The process begins with the reaction of phthalic anhydride with alcohols, giving the monoesters:
- C6H4(CO)2O + ROH → C6H4(CO2H)CO2R
The second esterification is more difficult and requires removal of water:
- C6H4(CO2H)CO2R + ROH ⇌ C6H4(CO2R)2 + H2O
Phthalic anhydride is a precursor to a variety of reagents useful in organic synthesis. Important derivatives include phthalimide and its many derivatives. Chiral alcohols form half-esters (see above), and these derivatives are often resolvable because they form diastereomeric salts with chiral amines such as brucine. A related ring-opening reaction involves peroxides to give the useful peroxy acid:
- C6H4(CO)2O + H2O2 → C6H4(CO3H)CO2H
Preparation of aliphatic nitroalkenes
Precursor to dyestuffs
Phthalic anhydride is widely used in industry for the production of certain dyes. A well-known application of this reactivity is the preparation of the anthroquinone dye quinizarin by reaction with para-chlorophenol followed by hydrolysis of the chloride.
Phthalic anhydride treated with cellulose acetate gives cellulose acetate phthalate (CAP), a common enteric coating excipient that has also been shown to have antiviral activity. Phthalic anhydride is a degradation product of CAP.
The most probable human exposure to phthalic anhydride is through skin contact or inhalation during manufacture or use. Studies show that exposure to phthalic anhydride can cause rhinitis, chronic bronchitis, and asthma. Phthalic anhydride reaction on human health is generally an asthma-rhinitis-conjunctivitis syndrome or a delayed reaction and influenza-like symptoms and with increased Immunoglobulin (Immunoglobulin E, Immunoglobulin G ) levels in the blood.
- Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 835. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.
- "NIOSH Pocket Guide to Chemical Hazards #0512". National Institute for Occupational Safety and Health (NIOSH).
- "Phthalic anhydride". Immediately Dangerous to Life and Health. National Institute for Occupational Safety and Health (NIOSH).
- 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
- Noller, Carl R. (1965). Chemistry of Organic Compounds, 3rd ed. Philadelphia: W. B. Saunders. p. 602.
- Joseph Kenyon (1941). "d- and l-Octanol-2". Org. Synth.; Coll. Vol., 1, p. 418
- George B. Payne (1973). "Monoperphthalic acid". Org. Synth.; Coll. Vol., 5, p. 805
- Ranganathan, Darshan; Rao, Bhushan; Ranganathan, Subramania; Mehrotra, Ashok & Iyengar, Radha (1980). "Nitroethylene: a stable, clean, and reactive agent for organic synthesis". The Journal of Organic Chemistry. 45 (7): 1185–1189. doi:10.1021/jo01295a003. Retrieved 5 January 2014.
- L. A. Bigelow and H. H. Reynolds (1941). "Quinizarin". Org. Synth.; Coll. Vol., 1, p. 476
- Neurath AR. (2000). "Microbicide for prevention of sexually transmitted diseases using a pharmaceutical excipient.". AIDS Patient Care STDS. 14 (4): 215–9. doi:10.1089/108729100317830. PMID 10806641.
- Mayhew JW, Gideon LT, Ericksen B, Hlavaty JJ, Yeh SM, Chavdarian CG, Strick N, Neurath AR (2009). "Development of a gel permeation chromatographic assay to achieve mass balance in cellulose acetate phthalate stability studies.". J Pharm Biomed Anal. 49 (2): 240–6. doi:10.1016/j.jpba.2008.10.039. PMC . PMID 19070984.