Rahul Sharma (Editor)


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Appearance  Colorless liquid
Density  862 kg/m³
Molar mass  62.13404 g/mol
Formula  C2H6S
Boiling point  35 °C
Ethanethiol httpsuploadwikimediaorgwikipediacommonsff
Related compounds  Methanethiol Butanethiol Ethanol thiophenol

Ethanethiol, commonly known as ethyl mercaptan, is a clear liquid with a distinct odor. It is an organosulfur compound with the formula CH3CH2SH. Abbreviated EtSH, it consists of an ethyl group (Et), CH3CH2, attached to a thiol group, SH. Its structure parallels that of ethanol, but with sulfur in place of oxygen. The odor of EtSH is infamous. Ethanethiol is more volatile than ethanol due to a diminished ability to engage in hydrogen bonding. Ethanethiol is toxic. It occurs naturally as a minor component of petroleum, and may be added to otherwise odorless gaseous products such as liquefied petroleum gas (LPG) to help warn of gas leaks. At these concentrations, ethanethiol is not harmful.


Ethanethiol FileEthanethiolskeletalpng Wikimedia Commons


Ethanethiol FileEthanethiolpng Wikimedia Commons

Ethanethiol is prepared by the reaction of ethylene with hydrogen sulfide over a catalyst. The various producers utilize different catalysts in this process. It has also been prepared commercially by the reaction of ethanol with hydrogen sulfide gas over an acidic solid catalyst, such as alumina.

Ethanethiol ethanethiollewispng

Ethanethiol was originally reported by Zeise in 1834. Zeise treated calcium ethyl sulfate with a suspension of barium sulfide saturated with hydrogen sulfide. He is credited with naming the C2H5S- group as mercaptum.

Ethanethiol ethanethiollewis2png

Ethanethiol can also be prepared by a halide displacement reaction, where ethyl halide is reacted with aqueous sodium bisulfide. This conversion was demonstrated as early as 1840 by Henri Victor Regnault.


Ethanethiol Ethanethiol C2H6S ChemSpider

Ethanethiol has a strongly disagreeable odor that humans can detect in minute concentrations. The threshold for human detection is as low as one part in 2.8 billion parts of air (0.36 parts per billion). Its odor resembles that of leeks, onions, durian or cooked cabbage, but is quite distinct.

Ethanethiol FileEthanethiol2svg Wikimedia Commons

Employees of the Union Oil Company of California reported first in 1938 that turkey vultures would gather at the site of any gas leak. After finding that this was caused by traces of ethanethiol in the gas it was decided to boost the amount of ethanethiol in the gas, to make detections of leaks easier.


Ethanethiol is intentionally added to butane and propane (see: LPG) to impart an easily noticed smell to these normally odorless fuels that pose the threat of fire, explosion, and asphyxiation.

In the underground mining industry, ethanethiol or ethyl mercaptan is referred to as "stench gas". The gas is released into mine ventilation systems to alert mine workers during an emergency. In Ontario, mining legislation dictates that "The alarm system in an underground mine shall, consist of the introduction into all workplaces of sufficient quantities of ethyl mercaptan gas or similar gas to be readily detectable by all workers".


Ethanethiol is a reagent in organic synthesis. In the presence of sodium hydroxide, it gives the powerful nucleophile SEt. The salt can be generated quantitatively by reaction with sodium hydride.

Ethanethiol can be oxidized to ethyl sulfonic acid, using strong oxidizing agents. Weaker oxidants, such as ferric oxide or hydrogen peroxide give the disulfide, diethyl disulfide:

2 EtSH + H2O2 → EtS-SEt + 2 H2O

Like other thiols, it behaves comparably to hydrogen sulfide. For example, it binds, concomitant with deprotonation to "soft" transition metal cations, such as Hg2+, Cu+, and Ni2+ to give polymeric thiolato complexes, Hg(SEt)2, CuSEt, and Ni(SEt)2, respectively.


Ethanethiol Wikipedia

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