Ethanethiol

Chembox new
Reference = ["Merck Index", 12th edition, 3771]
Name = Ethanethiol
ImageFileL1 = Ethanethiol-skeletal.png ImageSizeL1 = 100px
ImageNameL1 = Skeletal structure of ethanethiol
ImageFileR1 = Ethanethiol-3D-balls.png ImageSizeR1 = 100px
ImageNameR1 = Ball-and-stick model of the ethanethiol molecule
IUPACName = Ethanethiol
OtherNames = Ethyl mercaptan
Section1 = Chembox Identifiers
CASNo = 75-08-1
SMILES = CCS
RTECS = KI9625000
Section2 = Chembox Properties
Formula = C₂H₆S
MolarMass = 62.13404 g·mol⁻¹
Density = 0.8617 g·cm⁻³
MeltingPt = -148 °C
BoilingPt = 35 °C
Section7 = Chembox Hazards
MainHazards = Nauseating
RPhrases = 11-20-50/53
SPhrases = 16-25-60-61
Section8 = Chembox Related
OtherCpds = Methanethiol
Ethanol
thiophenol

Ethanethiol is the organic compound with the formula CH₃CH₂SH. It consists of an ethyl group, CH₃CH₂, attached to a thiol group, SH. The compound is structurally similar to ethanol by replacement of O by S. This change leads to many different properties, the most infamous of which is the strong odour of EtSH. Ethanethiol is also more volatile than ethanol due to its diminished ability to engage in hydrogen bonding. Ethanethiol is toxic. It occurs naturally as a minor component of petroleum, and may be added to liquefied petroleum gas (LPG) to warn of a gas leak. At these concentrations, ethanethiol is not harmful.

Odour

Ethanethiol has a strongly disagreeable odour 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. Its odour resembles that of leeks or onions. Ethanethiol is intentionally added to butane and propane (see: LPG) to impart an easily noticed smell to these odourless fuels, that otherwise pose the threat of fire and explosion.

According to the 2000 edition of the "Guinness Book Of World Records", ethanethiol is the "smelliest substance" in existence. Other more specialized chemicals were probably not examined, however. Most volatile thiols are comparably offensive. Thiols can be oxidized to sulfoxides, which have only a faint smell, using bleach or related oxidants.

Reactions

Ethanethiol is a valued reagent in organic synthesis. In the presence of sodium hydroxide, it forms the powerful nucleophile NaSEt. The salt can also be generated quantitatively by reaction with sodium hydride. [OrgSynth | author = Mirrington, R. N.; Feutrill, G. I. | title = Orcinol Monomethyl Ether | collvol = 6 | collvolpages = 859 | year = 1988 | prep = CV6P0859]

Mild oxidation of EtSH gives the disulfide, diethyl disulfide::2 EtSH + H₂O₂ → EtS-SEt + 2 H₂OLike 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.

References

External links

* [http://toxnet.nlm.nih.gov/cgi-bin/sis/search/r?dbs+hsdb:@term+@na+Ethanethiol NLM Hazardous Substances Databank – Ethyl mercaptan]