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Acetic anhydride

Acetic anhydride
IUPAC name Ethanoyl ethanoate
Other names Acetic anhydride
Acetic acid anhydride
Acetyl oxide
Acetic oxide
Ethanoic anhydride
CAS number 108-24-7
RTECS number AK1925000
InChI InChI=1/C4H6O3/c1-3(5)
Molecular formula C4H6O3
Molar mass 102.1 g/mol
Appearance clear liquid
Density 1.08 g/cm³, liquid
Melting point

−73.1 °C

Boiling point

139.8 °C

Solubility in water 2.6% by weight; rapidly reacts to
form acetic acid
EU classification Corrosive (C)
R-phrases R10, R20/22, R34
S-phrases (S1/2), S26, S36/37/39, S45
Flash point 54 °C
Related Compounds
Related acid anhydrides Propionic anhydride
Related compounds Acetic acid
Acetyl chloride
Except where noted otherwise, data are given for
materials in their standard state
(at 25 °C, 100 kPa)
Infobox disclaimer and references

Acetic anhydride is the chemical compound with the formula (CH3CO)2O. Commonly abbreviated Ac2O, it is one of the simplest acid anhydrides and is a widely used reagent in organic synthesis. It is a colorless liquid that smells strongly of acetic acid, which is formed by its reaction with the moisture in the air.



Acetic anhydride is produced by carbonylation of methyl acetate:[1]

CH3CO2CH3 + CO → (CH3CO)2O

This process involves the conversion of methyl acetate to methyl iodide and an acetate salt. Carbonylation of the methyl iodide in turn affords acetyl iodide, which reacts with acetate salts or acetic acid to give the product. Rhodium and lithium iodides are employed as catalysts. Because acetic anhydride is not stable in water, the conversion is conducted under anhydrous conditions. In contrast, the Monsanto acetic acid synthesis, which also involves a rhodium catalyzed carbonylation of methyl iodide, is at least partially aqueous.

To a decreasing extent, acetic anhydride is also prepared by the reaction of ketene with acetic acid. Ketene is generated by dehydrating acetic acid at elevated temperatures.

Due to its low cost, acetic anhydride is purchased, not prepared, for use in research laboratories.


Ac2O is mainly used for the acetylation of cellulose to cellulose acetate for photographic film and other applications.

In general alcohols and amines are acetylated.[2] For example, the reaction of acetic anhydride with ethanol is:


Often a base such as pyridine is added to function as catalyst. Lewis acidic scandium salts are also effective catalysts.[3]

Aspirin, acetyl salicylic acid, is prepared by the acetylation of salicylic acid using acetic anhydride. Because of its use for the synthesis of heroin by the diacetylation of morphine, acetic anhydride (known as 'AA' in clandestine chemistry circles) is listed as a DEA List II Precursor,[4] and restricted in many other countries.


Acetic anhydride dissolves in water to approximately 2.6% by weight.[5] Aqueous solutions have limited stability because, like most acid anhydrides, acetic anhydride hydrolyses to give acetic acid:[6]

(CH3CO)2O + H2O → 2 CH3CO2H


  Acetic anhydride is an irritant and flammable. Because of its reactivity toward water, alcohol foam or carbon dioxide are preferred for fire suppression.[7] The vapour of acetic anhydride is harmful.[8]

Notes and references

  1. ^ Zoeller, J. R.; Agreda, V. H.; Cook, S. L.; Lafferty, N. L.; Polichnowski, S. W.; Pond, D. M. "Eastman Chemical Company Acetic Anhydride Process" Catalysis Today (1992), volume 13, pp.73-91. doi:10.1016/0920-5861(92)80188-S
  2. ^ Science is Fun…. Chemical of the Week. Retrieved on 2006-03-25.
  3. ^ Macor, J.; Sampognaro, A. J.; Verhoest, P. R.; Mack, R. A. "(R)-(+)-2-Hydroxy-1,2,2-Triphenylethyl Acetate" Organic Syntheses, Collected Volume 10, p.464 (2004).
  4. ^ ChemGuide. Acid Anhydrides. Retrieved on 2006-03-25.
  5. ^ British Petroleum. Acetic Anhydride: Frequently Asked Questions (PDF). Retrieved on 2006-05-03.
  6. ^ Celanese. Acetic Anhydride: Material Safety Data Sheet (PDF). Retrieved on 2006-05-03.
  7. ^ Data Sheets. International Occupational Safety and Health Information Centre. Retrieved on 2006-04-13.
  8. ^ NIOSH. Pocket Guide to Chemical Hazards. Retrieved on 2006-04-13.

See also

  • Acid anhydride
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Acetic_anhydride". A list of authors is available in Wikipedia.
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