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Ethanethiol

CAS No.
75-08-1
Chemical Name:
Ethanethiol
Synonyms
ETHYL MERCAPTAN;C2H5SH;Ethanthiol;Thioethanol;MERCAPTAN C2;1-ETHANETHIOL;Ethylmerkaptan;EM RT;EM(TM) RT;Etantiolo
CBNumber:
CB7854211
Molecular Formula:
C2H6S
Lewis structure
c2h6s lewis structure
Molecular Weight:
62.13
MDL Number:
MFCD00004887
MOL File:
75-08-1.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-08-25 20:17:46
Product description Number Pack Size Price
Ethanethiol ≥97% W425800 1 each $63.5
Ethanethiol for synthesis 8.00796 250ML $79.2
Ethanethiol for synthesis 8.00796 1L $174
Ethanethiol ≥97% W425800 1 unit $58.61
Ethanethiol analytical standard 80534 1ml $63.9
More product size

Ethanethiol Properties

Melting point -148 °C
Boiling point 35 °C(lit.)
Density 0.839 g/mL at 25 °C(lit.)
vapor density 2.1 (vs air)
vapor pressure 8.51 psi ( 20 °C)
refractive index n20/D 1.4306(lit.)
FEMA 4258 | ETHANETHIOL
FLAVIS Number 12.017 | Ethanethiol
Flash point 1 °F
storage temp. Store below +30°C.
solubility Soluble in Ether, Alcohol, Acetone
pka 10.6(at 25℃)
form Liquid
color Colorless
Odor Strong chunk; offensive garlic.
explosive limit 2.8-18%(V)
Odor Threshold 0.0000087ppm
biological source synthetic
Water Solubility Slightly miscible with water.
Specific Heat Capacity Cp(liquid): 1.9 J/(g·K); Cp(gas): 1.17 J/(g·K), at 25℃
JECFA Number 1659
Merck 14,3726
BRN 773638
Henry's Law Constant 3.57(x 10-3 atmm3/mol) at 25 °C (Przyjazny et al., 1983)
Exposure limits ACGIH:TLV-TWA 0.5 ppm (1 mg/m3)
OSHA:PEL-Ceiling 10 ppm (25 mg/m3)
NIOSH:REL-Ceiling 0.5 ppm [15-min]
Dielectric constant 6.9(14℃)
Stability Stable. Extremely flammable - note low flash point. Incompatible with oxidizing agents, strong acids. May form explosive mixtures with air.
Major Application cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care
InChI 1S/C2H6S/c1-2-3/h3H,2H2,1H3
InChIKey DNJIEGIFACGWOD-UHFFFAOYSA-N
SMILES CCS
LogP 1.44
CAS DataBase Reference 75-08-1(CAS DataBase Reference)
Substances Added to Food (formerly EAFUS) ETHANETHIOL
EWG's Food Scores 1
FDA UNII M439R54A1D
NIST Chemistry Reference Ethanethiol(75-08-1)
EPA Substance Registry System Ethyl mercaptan (75-08-1)
UNSPSC Code 85151701
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  Flame (GHS02)Skull and Crossbones (GHS06)Health Hazard (GHS08)Environment (GHS09)
GHS02,GHS06,GHS08,GHS09
Signal word  Danger
Hazard statements  H331-H302-H316-H320-H370-H335-H410-H225
Precautionary statements  P501-P273-P270-P240-P260-P210-P233-P243-P241-P242-P271-P264-P280-P370+P378-P391-P337+P313-P305+P351+P338-P308+P311-P303+P361+P353-P332+P313-P301+P312+P330-P304+P340+P311-P403+P233-P403+P235-P405
Hazard Codes  F,Xn,N,F+
Risk Statements  11-20-50/53-51/53-12-20/22
Safety Statements  16-25-60-61
RIDADR  UN 2363
OEL Ceiling: 0.5 ppm (1.3 mg/m3) [15-minute]
WGK Germany  3
RTECS  KI9625000
13
Autoignition Temperature 570 °F
TSCA  TSCA listed
HS Code  2930 90 98
HazardClass  3
PackingGroup  I
Storage Class 3 - Flammable liquids
Hazard Classifications Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Aquatic Acute 1
Aquatic Chronic 1
Flam. Liq. 1
Hazardous Substances Data 75-08-1(Hazardous Substances Data)
Toxicity LD50 orally in Rabbit: 682 mg/kg
IDLA 500 ppm
REACH Registrations Active
Excepted Quantities Not Permitted as Excepted Quantity
NFPA 704
4
2 1

Ethanethiol price More Price(22)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich W425800 Ethanethiol ≥97% 75-08-1 1 each $63.5 2026-04-30 Buy
Sigma-Aldrich 8.00796 Ethanethiol for synthesis 75-08-1 250ML $79.2 2026-04-30 Buy
Sigma-Aldrich 8.00796 Ethanethiol for synthesis 75-08-1 1L $174 2026-04-30 Buy
Sigma-Aldrich W425800 Ethanethiol ≥97% 75-08-1 1 unit $58.61 2025-07-31 Buy
Sigma-Aldrich 80534 Ethanethiol analytical standard 75-08-1 1ml $63.9 2022-05-15 Buy
Product number Packaging Price Buy
W425800 1 each $63.5 Buy
8.00796 250ML $79.2 Buy
8.00796 1L $174 Buy
W425800 1 unit $58.61 Buy
80534 1ml $63.9 Buy

Ethanethiol Chemical Properties,Uses,Production

Description

Ethane thiol, commonly known as ethyl mercaptan, is a colorless gas or 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 S instead of O. 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 other wise odorless gaseous products such as liquefied petroleum gas (LPG) to help warn of gas leaks. At these concentrations, ethanethiol is not harmful.

Chemical Properties

A yellowish liquid (or a colorless gas above the BP). fruity, sulfur aroma. Strong, sharp odor of garlic or skunklike odor.

Physical properties

Colorless liquid with a strong, disagreeable, skunk-like or rotten egg odor. Extremely flammable liquid or gas. An experimentally determined odor threshold concentration of 1 ppbv was reported by Leonardos et al. (1969). Katz and Talbert (1930) reported experimental detection odor threshold concentrations in the range 0.66–7.6 μg/m3 (0.26 to 3.0 ppbv).

Uses

Ethanethiol is used as an intermediate inthe manufacture of insecticides, plastics, andantioxidants; and as an additive to natural gasto give odor. It occurs in illuminating gas andin petroleum distillates.

Uses

Stenching agent for liquefied petroleum gases; adhesive stabilizer; manufacture of plastics, insecticides, and antioxidants

Uses

LPG odorant, adhesive, stabilizer, chemical intermediate.

Preparation

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

Definition

ChEBI: Ethanethiol is an alkanethiol that is ethane substituted by a thiol group at position 1. It is added to odorless gaseous products such as liquefied petroleum gas (LPG) to provide a garlic scent which helps warn of gas leaks. It has a role as a rodenticide.

Application

Ethanethiol can be used as a reactant for the synthesis of:
Functionalized oxazolidinones by conjugated nucleophilic addition- electrophilic amination reaction.
Ethyl phenyl sulfide by C-S coupling with iodobenzene.
Chain transfer agent in the RAFT polymerization of N-isopropylacrylamide.

Production Methods

Ethyl mercaptan is prepared by distilling ethyl potassium sulfate with potassium hydrogen sulfide. Additional mercaptans can be prepared in a similar manner with the corresponding proper ingredients.

Reactions

Ethane thiol is a valued 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.
Ethane thiol can be oxidized to ethyl sulfonic acid, using bleach and related strong aqueous oxidants. Weaker oxidants, such as ferric oxide 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.

Aroma threshold values

High strength odor, sulfurous fruity type; recommend smelling in a 0.01% solution or less.

General Description

A clear colorless low-boiling liquid (boiling point 97°F) with an overpowering, garlic-like/skunk-like odor. Flash point -55°F. Less dense than water and very slightly soluble in water. Vapors are heavier than air. Vapors may irritate nose and throat. May be toxic if swallowed, by inhalation or by contact. Added to natural gas as an odorant. Used as a stabilizer for adhesives.

Air & Water Reactions

Highly flammable. A very dangerous fire hazard. Very slightly soluble in water.

Reactivity Profile

Ethanethiol reacts violently with calcium hypochlorite, May react vigorously with other oxidizing reagents. On contact with strong acids or when heated to decomposition Ethanethiol emits highly toxic fumes of sulfur oxides [Sax, 9th ed., 1996, p. 1575].

Hazard

Toxic by ingestion and inhalation. Flammable, dangerous fire risk.

Health Hazard

Inhalation of vapor causes muscular weakness, convulsions, respiratory paralysis. High concentrations may cause pulmonary irritation. Liquid irritates eyes and skin. Ingestion causes nausea and irritation of mouth and stomach.

Health Hazard

The inhalation toxicity of ethanethiol islower than that of methanethiol. Intraperitoneal administration in rats at sublethaldoses caused deep sedation, followed bylethargy, restlessness, lack of muscular coordination, and skeletal muscle paralysis.Higher doses produced cyanosis, kidney andliver damage, respiratory depression, coma,and death. The intraperitoneal LD50 value inrats was 450 mg/kg (ACGIH 1986).
Ethanethiol is metabolized to inorganicsulfate and ethyl methyl sulfone, and excreted. The oral LD50 value in rats is 680 mg/kg.
In humans, repeated exposures to itsvapors at about 5 ppm concentration canproduce irritation of the nose and throat,headache, fatigue, and nausea.

Chemical Reactivity

Reactivity with Water No reaction; Reactivity with Common Materials: No reaction; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.

Mechanism of action

Non-toxic mode of action. Repellent properties due to odour

Safety Profile

Moderately toxic by ingestion, inhalation, and intraperitoneal routes. A skin and eye irritant. Inhalation causes central nervous system effects in humans. A very dangerous fire hazard when exposed to heat or flame; can react vigorously with oxidizing materials. A moderate explosion hazard when exposed to spark or flame. Violent reaction with Ca(OCl)2. Will react with water or steam to produce toxic and flammable vapors. To fight fire, use CO2, dry chemical. When heated to decomposition or on contact with acid or acid fumes it emits hghly toxic fumes of SOx. See also MERCAPTANS.

Potential Exposure

This material is used as a warning odorant for liquefied petroleum gases. It is used as an intermediate in the manufacture of many pesticides and other organic chemicals

Environmental Fate

Biological. Ethyl mercaptan did not degrade in anaerobic sediments and sludges nor in anaerobic freshwater conditions (van Leerdam et al., 2006).
Photolytic. A second-order rate constant of 1.21 x 10-12 cm3/moleculesec was reported for the reaction of ethyl mercaptan and NO3 radicals in the atmosphere at 297 K (Atkinson, 1991).
Chemical/Physical. In the presence of nitric oxide, ethyl mercaptan reacted with OH radicals forming ethyl thionitrite. The rate constant for this reaction is 2.7 x 10-11 at 20 °C (MacLeod et al., 1984).

Shipping

UN2363 Ethyl mercaptan, Hazard Class: 3; Labels: 3-Flammable liquid

Purification Methods

Dissolve the thiol in aqueous 20% NaOH, extract it with a small amount of *benzene and then steam distil until clear. After cooling, the alkaline solution is acidified slightly with 15% H2SO4 and the thiol is distilled off, dried with CaSO4, CaCl2 or 4A molecular sieves, and fractionally distilled under nitrogen [Ellis & Reid J Am Chem Soc 54 1674 1932]. It has a foul odour. [Beilstein 1 IV 1390.]

Incompatibilities

May form explosive mixture with air. Slowly forms peroxides. This material is a weak acid. Reacts with oxidizers, causing fire and explosion hazard. Reacts with strong acids evolving toxic and flammable hydrogen sulfide. May accumulate static electrical charges, and may cause ignition of its vapors. Attacks some forms of plastics, coatings and rubber. Aldehydes are frequently involved in self-condensation or polymerization reactions. These reactions are exothermic; they are often catalyzed by acid. Aldehydes are readily oxidized to give carboxylic acids. Flammable and/or toxic gases are generated by the combination of aldehydes with azo, diazo compounds, dithiocarbamates, nitrides, and strong reducing agents. Aldehydes can react with air to give first peroxo acids, and ultimately carboxylic acids. These autoxidation reactions are activated by light, catalyzed by salts of transition metals, and are autocatalytic (catalyzed by the products of the reaction). The addition of stabilizers (antioxidants) to shipments of aldehydes retards autoxidation

Toxics Screening Level

The initial threshold screening level (ITSL) for ethyl mercaptan (CAS # 75-08-1) is 13 μg/m3 with a 1-hour averaging time.

Waste Disposal

Incineration (1093℃) followed by scrubbing with a caustic solution

Pesticide Type

Rodenticide; Metabolite

74-93-1
74-85-1
75-18-3
624-89-5
352-93-2
75-08-1
Synthesis of Ethanethiol from METHYL MERCAPTAN and Ethylene
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