|Preferred IUPAC name
|Systematic IUPAC name
3D model (JSmol)
|E number||E1504 (additional chemicals)|
CompTox Dashboard (EPA)
|Molar mass||88.106 g·mol−1|
|Melting point||−83.6 °C (−118.5 °F; 189.6 K)|
|Boiling point||77.1 °C (170.8 °F; 350.2 K)|
|8.3 g/100 mL (at 20 °C)|
|Solubility in ethanol, acetone, diethyl ether, benzene||Miscible|
|Vapor pressure||73 mmHg (9.7 kPa) at 20 °C|
Refractive index (nD)
|Viscosity||426 μPa·s (0.426 cP) at 25 °C|
|Safety data sheet||See: data page|
|R-phrases (outdated)||R11, R36, R66, R67|
|S-phrases (outdated)||S16, S26, S33|
|Flash point||−4 °C (25 °F; 269 K)|
|Lethal dose or concentration (LD, LC):|
LD50 (median dose)
|11.3 g/kg, rat|
LC50 (median concentration)
|16,000 ppm (rat, 6 h)|
12,295 ppm (mouse, 2 h)
1600 ppm (rat, 8 h)
LCLo (lowest published)
|21 ppm (guinea pig, 1 h)|
12,330 ppm (mouse, 3 h)
|US health exposure limits (NIOSH):|
|TWA 400 ppm (1400 m3)|
|TWA 400 ppm (1400 mg/m3)|
IDLH (Immediate danger)
Related carboxylate esters
|Supplementary data page|
|Refractive index (n),|
Dielectric constant (εr), etc.
|UV, IR, NMR, MS|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Ethyl acetate (systematically ethyl ethanoate, commonly abbreviated EtOAc, ETAC or EA) is the organic compound with the formula CH
3, simplified to C
2. This colorless liquid has a characteristic sweet smell (similar to pear drops) and is used in glues, nail polish removers, decaffeinating tea and coffee. Ethyl acetate is the ester of ethanol and acetic acid; it is manufactured on a large scale for use as a solvent. The combined annual production in 1985 of Japan, North America, and Europe was about 400,000 tonnes. In 2004, an estimated 1.3 million tonnes were produced worldwide.
The reaction can be accelerated by acid catalysis and the equilibrium can be shifted to the right by removal of water.
A specialized industrial route entails the catalytic dehydrogenation of ethanol. This method is more cost effective than the esterification but is applied with surplus ethanol in a chemical plant. Typically, dehydrogenation is conducted with copper at an elevated temperature but below 250 °C. The copper may have its surface area increased by depositing it on zinc, promoting the growth of snowflake-like fractal structures (dendrites). Surface area can be again increased by deposition onto a zeolite, typically ZSM-5. Traces of rare-earth and alkali metals are beneficial to the process. Byproducts of the dehydrogenation include diethyl ether, which is thought to arise primarily due to aluminum sites in the catalyst, acetaldehyde and its aldol products, higher esters, and ketones. Separations of the byproducts are complicated by the fact that ethanol forms an azeotrope with water, as does ethyl acetate with ethanol and water, and methyl ethyl ketone (MEK, which forms from 2-butanol) with both ethanol and ethyl acetate. These azeotropes are broken by pressure swing distillation or membrane distillation.
Ethyl acetate is used primarily as a solvent and diluent, being favored because of its low cost, low toxicity, and agreeable odor. For example, it is commonly used to clean circuit boards and in some nail varnish removers (acetone and acetonitrile are also used). Coffee beans and tea leaves are decaffeinated with this solvent. It is also used in paints as an activator or hardener. Ethyl acetate is present in confectionery, perfumes, and fruits. In perfumes, it evaporates quickly, leaving only the scent of the perfume on the skin.
In the laboratory, mixtures containing ethyl acetate are commonly used in column chromatography and extractions. Ethyl acetate is rarely selected as a reaction solvent because it is prone to hydrolysis and transesterification.
Ethyl acetate is fairly volatile at room temperature and has a boiling point of 77 °C (171 °F). Due to these properties, it can be removed from a sample by heating in a hot water bath and providing ventilation with compressed air.
Ethyl acetate is the most common ester in wine, being the product of the most common volatile organic acid – acetic acid, and the ethyl alcohol generated during the fermentation. The aroma of ethyl acetate is most vivid in younger wines and contributes towards the general perception of "fruitiness" in the wine. Sensitivity varies, with most people having a perception threshold around 120 mg/L. Excessive amounts of ethyl acetate are considered a wine fault. Global ethyl acetate market to be valued at $3.3 billion in 2018 according to international research agency visiongain .
In the field of entomology, ethyl acetate is an effective asphyxiant for use in insect collecting and study. In a killing jar charged with ethyl acetate, the vapors will kill the collected insect quickly without destroying it. Because it is not hygroscopic, ethyl acetate also keeps the insect soft enough to allow proper mounting suitable for a collection.
Ethyl acetate can be hydrolyzed in acidic or basic conditions to regain acetic acid and ethanol. The use of an acid catalyst accelerates the hydrolysis, which is subject to the Fischer equilibrium mentioned above. In the laboratory, and usually for illustrative purposes only, ethyl esters are typically hydrolyzed in a two-step process starting with a stoichiometric amount of a strong base, such as sodium hydroxide. This reaction gives ethanol and sodium acetate, which is unreactive toward ethanol:
Overexposure to ethyl acetate may cause irritation of the eyes, nose, and throat. Severe overexposure may cause weakness, drowsiness, and unconsciousness. Humans exposed to a concentration of 400 ppm in 1.4 mg/L ethyl acetate for a short time were affected by nose and throat irritation. Ethyl acetate is an irritant of the conjunctiva and mucous membrane of the respiratory tract. Animal experiments have shown that, at very high concentrations, the ester has central nervous system depressant and lethal effects; at concentrations of 20,000 to 43,000 ppm (2.0–4.3%), there may be pulmonary edema with hemorrhages, symptoms of central nervous system depression, secondary anemia and liver damage. In humans, concentrations of 400 ppm cause irritation of the nose and pharynx; cases have also been known of irritation of the conjunctiva with temporary opacity of the cornea. In rare cases exposure may cause sensitization of the mucous membrane and eruptions of the skin. The irritant effect of ethyl acetate is weaker than that of propyl acetate or butyl acetate.