Potency and safety analysis of hemp-derived delta-9 products: The hemp vs. cannabis demarcation problem

Hydrogen sulfide
Skeletal formula of hydrogen sulfide with two dimensions
Ball-and-stick model of hydrogen sulfide
Ball-and-stick model of hydrogen sulfide
Spacefill model of hydrogen sulfide
Spacefill model of hydrogen sulfide
  Sulfur, S
  Hydrogen, H
Systematic IUPAC name
Hydrogen sulfide[1]
Other names
  • Dihydrogen monosulfide
  • Sour gas
  • Dihydrogen sulfide
  • Sewer gas
  • Egg gas
  • Sulfane
  • Sulfurated hydrogen
  • Sulfureted hydrogen
  • Sulfuretted hydrogen
  • Sulfur hydride
  • Hydrosulfuric acid
  • Hydrothionic acid
  • Thiohydroxic acid
  • Sulfhydric acid
3D model (JSmol)
ECHA InfoCard 100.029.070 Edit this at Wikidata
EC Number
  • 231-977-3
MeSH Hydrogen+sulfide
RTECS number
  • MX1225000
UN number 1053
  • InChI=1S/H2S/h1H2 checkY
  • InChI=1/H2S/h1H2
  • S
Molar mass 34.08 g·mol−1
Appearance Colorless gas
Odor Foul, pungent, like that of rotten eggs
Density 1.539 g.L−1 (0°C)[2]
Melting point −85.5[3] °C (−121.9 °F; 187.7 K)
Boiling point −59.55[3] °C (−75.19 °F; 213.60 K)
3.980 g dm−3 (at 20 °C) [4]
Vapor pressure 1740 kPa (at 21 °C)
Acidity (pKa) 7.0[5][6]
Conjugate acid Sulfonium
Conjugate base Bisulfide
−25.5·10−6 cm3/mol
1.000644 (0 °C)[2]
0.97 D
1.003 J K−1 g−1
206 J mol−1 K−1[7]
−21 kJ mol−1[7]
Occupational safety and health (OHS/OSH):
Main hazards
Flammable and highly toxic
GHS labelling:
GHS02: FlammableGHS06: ToxicGHS09: Environmental hazard
H220, H330, H400
P210, P260, P271, P273, P284, P304+P340, P310, P320, P377, P381, P391, P403, P403+P233, P405, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 4: Very short exposure could cause death or major residual injury. E.g. VX gasFlammability 4: Will rapidly or completely vaporize at normal atmospheric pressure and temperature, or is readily dispersed in air and will burn readily. Flash point below 23 °C (73 °F). E.g. propaneInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
Flash point −82.4 °C (−116.3 °F; 190.8 K)[10]
232 °C (450 °F; 505 K)
Explosive limits 4.3–46%
Lethal dose or concentration (LD, LC):
  • 713 ppm (rat, 1 hr)
  • 673 ppm (mouse, 1 hr)
  • 634 ppm (mouse, 1 hr)
  • 444 ppm (rat, 4 hr)[9]
  • 600 ppm (human, 30 min)
  • 800 ppm (human, 5 min)[9]
NIOSH (US health exposure limits):
PEL (Permissible)
C 20 ppm; 50 ppm [10-minute maximum peak][8]
REL (Recommended)
C 10 ppm (15 mg/m3) [10-minute][8]
IDLH (Immediate danger)
100 ppm[8]
Related compounds
Related hydrogen chalcogenides
Related compounds
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Hydrogen sulfide is a chemical compound with the formula H2S. It is a colorless chalcogen-hydride gas, and is poisonous, corrosive, and flammable, with trace amounts in ambient atmosphere having a characteristic foul odor of rotten eggs.[11] Swedish chemist Carl Wilhelm Scheele is credited with having discovered the chemical composition of purified hydrogen sulfide in 1777.[12]

Hydrogen sulfide is toxic to humans and most other animals by inhibiting cellular respiration in a manner similar to hydrogen cyanide. When it is inhaled or its salts are ingested in high amounts,[clarification needed] damage to organs occurs rapidly with symptoms ranging from breathing difficulties to convulsions and death.[13][14] Despite this, the human body produces small amounts of this sulfide and its mineral salts, and uses it as a signalling molecule.[15]

Hydrogen sulfide is often produced from the microbial breakdown of organic matter in the absence of oxygen, such as in swamps and sewers; this process is commonly known as anaerobic digestion, which is done by sulfate-reducing microorganisms. It also occurs in volcanic gases, natural gas deposits, and sometimes in well-drawn water.


Hydrogen sulfide is slightly denser than air. A mixture of H2S and air can be explosive.


In general, hydrogen sulfide acts as a reducing agent, as indicated by its ability to reduce sulfur dioxide in the Claus process. Hydrogen sulfide burns in oxygen with a blue flame to form sulfur dioxide (SO2) and water:

2 H2S + 3 O2 → 2 SO2 + 2 H2O

If an excess of oxygen is present, sulfur trioxide (SO3) is formed, which quickly hydrates to sulfuric acid:

H2S + 2 O2 → H2SO4

Acid-base properties

It is slightly soluble in water and acts as a weak acid (pKa = 6.9 in 0.01–0.1 mol/litre solutions at 18 °C), giving the hydrosulfide ion HS. Hydrogen sulfide and its solutions are colorless. When exposed to air, it slowly oxidizes to form elemental sulfur, which is not soluble in water. The sulfide anion S2− is not formed in aqueous solution.[16]

Extreme temperatures and pressures

At pressures above 90 GPa (gigapascal), hydrogen sulfide becomes a metallic conductor of electricity. When cooled below a critical temperature this high-pressure phase exhibits superconductivity. The critical temperature increases with pressure, ranging from 23 K at 100 GPa to 150 K at 200 GPa.[17] If hydrogen sulfide is pressurized at higher temperatures, then cooled, the critical temperature reaches 203 K (−70 °C), the highest accepted superconducting critical temperature as of 2015. By substituting a small part of sulfur with phosphorus and using even higher pressures, it has been predicted that it may be possible to raise the critical temperature to above 0 °C (273 K) and achieve room-temperature superconductivity.[18]

Hydrogen sulfide decomposes without a presence of a catalyst under atmospheric pressure around 1200 °C into hydrogen and sulfur.[19]


Hydrogen sulfide reacts with metal ions to form metal sulfides, which are insoluble, often dark colored solids. Lead(II) acetate paper is used to detect hydrogen sulfide because it readily converts to lead(II) sulfide, which is black. Treating metal sulfides with strong acid or electrolysis often liberates hydrogen sulfide. Hydrogen sulfide is also responsible for tarnishing on various metals including copper and silver; the chemical responsible for black toning found on silver coins is silver sulfide (Ag2S), which is produced when the silver on the surface of the coin reacts with atmospheric hydrogen sulfide.[20] Coins that have been subject to toning by hydrogen sulfide and other sulfur-containing compounds may have the toning add to the numismatic value of a coin based on aesthetics, as the toning may produce thin-film interference, resulting in the coin taking on an attractive coloration.[21] Coins can also be intentionally treated with hydrogen sulfide to induce toning, though artificial toning can be distinguished from natural toning, and is generally criticised among collectors.[22]


Hydrogen sulfide is most commonly obtained by its separation from sour gas, which is natural gas with a high content of H2S. It can also be produced by treating hydrogen with molten elemental sulfur at about 450 °C. Hydrocarbons can serve as a source of hydrogen in this process.[23]

S + H2 → H2S

The very favorable thermodynamics for the hydrogenation of sulfur implies that the dehydrogenation (or cracking) of hydrogen sulfide would require very high temperatures.[24]

A standard lab preparation is to treat ferrous sulfide with a strong acid in a Kipp generator:

FeS + 2 HCl → FeCl2 + H2S

For use in qualitative inorganic analysis, thioacetamide is used to generate H2S:

CH3C(S)NH2 + H2O → CH3C(O)NH2 + H2S

Many metal and nonmetal sulfides, e.g. aluminium sulfide, phosphorus pentasulfide, silicon disulfide liberate hydrogen sulfide upon exposure to water:[25]

6 H2O + Al2S3 → 3 H2S + 2 Al(OH)3

This gas is also produced by heating sulfur with solid organic compounds and by reducing sulfurated organic compounds with hydrogen. It can also be produced by mixing ammonium thiocyanate to concentrated sulphuric acid and adding water to it.


Hydrogen sulfide can be generated in cells via enzymatic or non-enzymatic pathways. Three enzymes catalyze formation of H
: cystathionine γ-lyase (CSE), cystathionine β-synthetase (CBS), and 3-mercaptopyruvate sulfurtransferase (3-MST).[26] CBS and CSE are the main proponents of H2S biogenesis, which follows the trans-sulfuration pathway.[27] These enzymes have been identified in a breadth of biological cells and tissues, and their activity is induced by a number of disease states.[28] These enzymes are characterized by the transfer of a sulfur atom from methionine to serine to form a cysteine molecule.[27] 3-MST also contributes to hydrogen sulfide production by way of the cysteine catabolic pathway.[28][27] Dietary amino acids, such as methionine and cysteine serve as the primary substrates for the transulfuration pathways and in the production of hydrogen sulfide. Hydrogen sulfide can also be derived from proteins such as ferredoxins and Rieske proteins.[28]

Sulfate-reducing (resp. sulfur-reducing) bacteria generate usable energy under low-oxygen conditions by using sulfates (resp. elemental sulfur) to oxidize organic compounds or hydrogen; this produces hydrogen sulfide as a waste product.

Water heaters can aid the conversion of sulfate in water to hydrogen sulfide gas. This is due to providing a warm environment sustainable for sulfur bacteria and maintaining the reaction which interacts between sulfate in the water and the water heater anode, which is usually made from magnesium metal.[29]

Signalling role

H2S in the body acts as a gaseous signaling molecule with implications for health and in diseases.[26] [30][31]

Hydrogen sulfide is involved in vasodilation in animals, as well as in increasing seed germination and stress responses in plants.[32] Hydrogen sulfide signaling is moderated by reactive oxygen species (ROS) and reactive nitrogen species (RNS).[32] H2S has been shown to interact with NO resulting in several different cellular effects, as well as the formation of another signal called nitrosothiol.[32] Hydrogen sulfide is also known to increase the levels of glutathione, which acts to reduce or disrupt ROS levels in cells.[32]

The field of H2S biology has advanced from environmental toxicology to investigate the roles of endogenously produced H2S in physiological conditions and in various pathophysiological states.[33] H2S has been implicated in cancer and Down syndrome and vascular disease.[34][35][36][37]

It inhibits Complex IV of the mitochondrial electron transport chain, which effectively reduces ATP generation and biochemical activity within cells.[32]


Production of sulfur

Hydrogen sulfide is mainly consumed as a precursor to elemental sulfur. This conversion, called the Claus process, involves partial oxidation to sulfur dioxide. The latter reacts with hydrogen sulfide to give elemental sulfur. The conversion is catalyzed by alumina.[38]

2H2S + SO2→ 3S + 2H2O

Production of thioorganic compounds

Many fundamental organosulfur compounds are produced using hydrogen sulfide. These include methanethiol, ethanethiol, and thioglycolic acid.[23] Hydrosulfides can be used in the production of thiophenol.[39]

Production of metal sulfides

Upon combining with alkali metal bases, hydrogen sulfide converts to alkali hydrosulfides such as sodium hydrosulfide and sodium sulfide:

H2S + NaOH → NaSH + H2O
NaSH + NaOH → Na2S + H2O

Sodium sulfides are used in the paper making industry. Specifically, salts of SH break bonds between lignin and cellulose components of pulp in the Kraft process.[23]

As indicated above, many metal ions react with hydrogen sulfide to give the corresponding metal sulfides. Oxidic ores are sometimes treated with hydrogen sulfide to give the corresponding metal sulfides which are more readily purified byy flotation.[23] Metal parts are sometimes passivated with hydrogen sulfide. Catalysts used in hydrodesulfurization are routinely activated with hydrogen sulfide.

Hydrogen sulfide was a reagent in the qualitative inorganic analysis of metal ions. In these analyses, heavy metal (and nonmetal) ions (e.g., Pb(II), Cu(II), Hg(II), As(III)) are precipitated from solution upon exposure to H2S. The components of the resulting solid are then identified by their reactivity.

Miscellaneous applications

Hydrogen sulfide is used to separate deuterium oxide, or heavy water, from normal water via the Girdler sulfide process.

A suspended animation-like state has been induced in rodents with the use of hydrogen sulfide, resulting in hypothermia with a concomitant reduction in metabolic rate. Oxygen demand was also reduced, thereby protecting against hypoxia. In addition, hydrogen sulfide has been shown to reduce inflammation in various situations.[40]


Deposit of sulfur on a rock, caused by volcanic gas

Volcanoes and some hot springs (as well as cold springs) emit some H2S. Hydrogen sulfide can be present naturally in well water, often as a result of the action of sulfate-reducing bacteria.[41][better source needed] Hydrogen sulfide is produced by the human body in small quantities through bacterial breakdown of proteins containing sulfur in the intestinal tract, therefore it contributes to the characteristic odor of flatulence. It is also produced in the mouth (halitosis).[42]

A portion of global H2S emissions are due to human activity. By far the largest industrial source of H2S is petroleum refineries: The hydrodesulfurization process liberates sulfur from petroleum by the action of hydrogen. The resulting H2S is converted to elemental sulfur by partial combustion via the Claus process, which is a major source of elemental sulfur. Other anthropogenic sources of hydrogen sulfide include coke ovens, paper mills (using the Kraft process), tanneries and sewerage. H2S arises from virtually anywhere where elemental sulfur comes in contact with organic material, especially at high temperatures. Depending on environmental conditions, it is responsible for deterioration of material through the action of some sulfur oxidizing microorganisms. It is called biogenic sulfide corrosion.

In 2011 it was reported that increased concentrations of H2S were observed in the Bakken formation crude, possibly due to oil field practices, and presented challenges such as "health and environmental risks, corrosion of wellbore, added expense with regard to materials handling and pipeline equipment, and additional refinement requirements".[43]

Besides living near gas and oil drilling operations, ordinary citizens can be exposed to hydrogen sulfide by being near waste water treatment facilities, landfills and farms with manure storage. Exposure occurs through breathing contaminated air or drinking contaminated water.[44]

In municipal waste landfill sites, the burial of organic material rapidly leads to the production of anaerobic digestion within the waste mass and, with the humid atmosphere and relatively high temperature that accompanies biodegradation, biogas is produced as soon as the air within the waste mass has been reduced. If there is a source of sulfate bearing material, such as plasterboard or natural gypsum (calcium sulfate dihydrate), under anaerobic conditions sulfate reducing bacteria converts this to hydrogen sulfide. These bacteria cannot survive in air but the moist, warm, anaerobic conditions of buried waste that contains a high source of carbon – in inert landfills, paper and glue used in the fabrication of products such as plasterboard can provide a rich source of carbon[45] – is an excellent environment for the formation of hydrogen sulfide.

In industrial anaerobic digestion processes, such as waste water treatment or the digestion of organic waste from agriculture, hydrogen sulfide can be formed from the reduction of sulfate and the degradation of amino acids and proteins within organic compounds.[46] Sulfates are relatively non-inhibitory to methane forming bacteria but can be reduced to H2S by sulfate reducing bacteria, of which there are several genera.[47]

Removal from water

A number of processes have been designed to remove hydrogen sulfide from drinking water.[48]

Continuous chlorination
For levels up to 75 mg/L chlorine is used in the purification process as an oxidizing chemical to react with hydrogen sulfide. This reaction yields insoluble solid sulfur. Usually the chlorine used is in the form of sodium hypochlorite.[49]
For concentrations of hydrogen sulfide less than 2 mg/L aeration is an ideal treatment process. Oxygen is added to water and a reaction between oxygen and hydrogen sulfide react to produce odorless sulfate.[50]
Nitrate addition
Calcium nitrate can be used to prevent hydrogen sulfide formation in wastewater streams.

Removal from fuel gases

Hydrogen sulfide is commonly found in raw natural gas and biogas. It is typically removed by amine gas treating technologies. In such processes, the hydrogen sulfide is first converted to an ammonium salt, whereas the natural gas is unaffected.

RNH2 + H2S ⇌ [RNH3]+ + SH

The bisulfide anion is subsequently regenerated by heating of the amine sulfide solution. Hydrogen sulfide generated in this process is typically converted to elemental sulfur using the Claus Process.

Process flow diagram of a typical amine treating process used in petroleum refineries, natural gas processing plants and other industrial facilities


The underground mine gas term for foul-smelling hydrogen sulfide-rich gas mixtures is stinkdamp. Hydrogen sulfide is a highly toxic and flammable gas (flammable range: 4.3–46%). It can poison several systems in the body, although the nervous system is most affected.[citation needed] The toxicity of H2S is comparable with that of carbon monoxide.[51] It binds with iron in the mitochondrial cytochrome enzymes, thus preventing cellular respiration. Its toxic properties were described in detail in 1843 by Justus von Liebig.[52]

Even before hydrogen sulfide was discovered, Italian physician Bernardino Ramazzini hypothesized in his 1713 book De Morbis Artificum Diatriba that occupational diseases of sewer-workers and blackening of coins in their clothes may be caused by an unknown invisible volatile acid (moreover, in late 18th century toxic gas emanation from Paris sewers became a problem for the citizens and authorities).[53]

Although very pungent at first (it smells like rotten eggs[54]), it quickly deadens the sense of smell, creating temporary anosmia,[55] so victims may be unaware of its presence until it is too late. Safe handling procedures are provided by its safety data sheet (SDS).[56]

Low-level exposure

Since hydrogen sulfide occurs naturally in the body, the environment, and the gut, enzymes exist to metabolize it. At some threshold level, believed to average around 300–350 ppm, the oxidative enzymes become overwhelmed. Many personal safety gas detectors, such as those used by utility, sewage and petrochemical workers, are set to alarm at as low as 5 to 10 ppm and to go into high alarm at 15 ppm. Metabolism causes oxidation to sulfate, which is harmless.[57] Hence, low levels of hydrogen sulfide may be tolerated indefinitely.

Exposure to lower concentrations can result in eye irritation, a sore throat and cough, nausea, shortness of breath, and fluid in the lungs.[51] These effects are believed to be due to hydrogen sulfide combining with alkali present in moist surface tissues to form sodium sulfide, a caustic.[58] These symptoms usually subside in a few weeks.

Long-term, low-level exposure may result in fatigue, loss of appetite, headaches, irritability, poor memory, and dizziness. Chronic exposure to low level H2S (around 2 ppm) has been implicated in increased miscarriage and reproductive health issues among Russian and Finnish wood pulp workers,[59] but the reports have not (as of 1995) been replicated.

High-level exposure

Short-term, high-level exposure can induce immediate collapse, with loss of breathing and a high probability of death. If death does not occur, high exposure to hydrogen sulfide can lead to cortical pseudolaminar necrosis, degeneration of the basal ganglia and cerebral edema.[51] Although respiratory paralysis may be immediate, it can also be delayed up to 72 hours.[60] Diagnostic of extreme poisoning by H2S is the discolouration of copper coins in the pockets of the victim.[citation needed]

Inhalation of H2S resulted in about 7 workplace deaths per year in the U.S. (2011–2017 data), second only to carbon monoxide (17 deaths per year) for workplace chemical inhalation deaths.[61]

Exposure thresholds

  • Exposure limits stipulated by the United States government:[62]
    • 10 ppm REL-Ceiling (NIOSH): recommended permissible exposure ceiling (the recommended level that must not be exceeded, except once for 10 min. in an 8-hour shift, if no other measurable exposure occurs)
    • 20 ppm PEL-Ceiling (OSHA): permissible exposure ceiling (the level that must not be exceeded, except once for 10 min. in an 8-hour shift, if no other measurable exposure occurs)
    • 50 ppm PEL-Peak (OSHA): peak permissible exposure (the level that must never be exceeded)
    • 100 ppm IDLH (NIOSH): immediately dangerous to life and health (the level that interferes with the ability to escape)
  • 0.00047 ppm or 0.47 ppb is the odor threshold, the point at which 50% of a human panel can detect the presence of an odor without being able to identify it.[63]
  • 10–20 ppm is the borderline concentration for eye irritation.
  • 50–100 ppm leads to eye damage.
  • At 100–150 ppm the olfactory nerve is paralyzed after a few inhalations, and the sense of smell disappears, often together with awareness of danger.[64][65]
  • 320–530 ppm leads to pulmonary edema with the possibility of death.[51]
  • 530–1000 ppm causes strong stimulation of the central nervous system and rapid breathing, leading to loss of breathing.
  • 800 ppm is the lethal concentration for 50% of humans for 5 minutes' exposure (LC50).
  • Concentrations over 1000 ppm cause immediate collapse with loss of breathing, even after inhalation of a single breath.


Treatment involves immediate inhalation of amyl nitrite, injections of sodium nitrite, or administration of 4-dimethylaminophenol in combination with inhalation of pure oxygen, administration of bronchodilators to overcome eventual bronchospasm, and in some cases hyperbaric oxygen therapy (HBOT).[51] HBOT has clinical and anecdotal support.[66][67][68]


Hydrogen sulfide was used by the British Army as a chemical weapon during World War I. It was not considered to be an ideal war gas, partially due to its flammability and because the distinctive smell could be detected from even a small leak, alerting the enemy to the presence of the gas. It was nevertheless used on two occasions in 1916 when other gases were in short supply.[69]

On September 2, 2005, a leak in the propeller room of a Royal Caribbean Cruise Liner docked in Los Angeles resulted in the deaths of 3 crewmen due to a sewage line leak. As a result, all such compartments are now required to have a ventilation system.[70][71]

A dump of toxic waste containing hydrogen sulfide is believed to have caused 17 deaths and thousands of illnesses in Abidjan, on the West African coast, in the 2006 Côte d'Ivoire toxic waste dump.

In September 2008, three workers were killed and two suffered serious injury, including long term brain damage, at a mushroom growing company in Langley, British Columbia. A valve to a pipe that carried chicken manure, straw and gypsum to the compost fuel for the mushroom growing operation became clogged, and as workers unclogged the valve in a confined space without proper ventilation the hydrogen sulfide that had built up due to anaerobic decomposition of the material was released, poisoning the workers in the surrounding area.[72] An investigator said there could have been more fatalities if the pipe had been fully cleared and/or if the wind had changed directions.[73]

In 2014, levels of hydrogen sulfide as high as 83 ppm were detected at a recently built mall in Thailand called Siam Square One at the Siam Square area. Shop tenants at the mall reported health complications such as sinus inflammation, breathing difficulties and eye irritation. After investigation it was determined that the large amount of gas originated from imperfect treatment and disposal of waste water in the building.[74]

In 2014, hydrogen sulfide gas killed workers at the Promenade shopping center in North Scottsdale, Arizona, USA [75] after climbing into 15ft deep chamber without wearing personal protective gear. "Arriving crews recorded high levels of hydrogen cyanide and hydrogen sulfide coming out of the sewer."

In November 2014, a substantial amount of hydrogen sulfide gas shrouded the central, eastern and southeastern parts of Moscow. Residents living in the area were urged to stay indoors by the emergencies ministry. Although the exact source of the gas was not known, blame had been placed on a Moscow oil refinery.[76]

In June 2016, a mother and her daughter were found dead in their still-running 2006 Porsche Cayenne SUV against a guardrail on Florida's Turnpike, initially thought to be victims of carbon monoxide poisoning.[77][78] Their deaths remained unexplained as the medical examiner waited for results of toxicology tests on the victims,[79] until urine tests revealed that hydrogen sulfide was the cause of death. A report from the Orange-Osceola Medical Examiner's Office indicated that toxic fumes came from the Porsche's starter battery, located under the front passenger seat.[80][81]

In January 2017, three utility workers in Key Largo, Florida, died one by one within seconds of descending into a narrow space beneath a manhole cover to check a section of paved street.[82] In an attempt to save the men, a firefighter who entered the hole without his air tank (because he could not fit through the hole with it) collapsed within seconds and had to be rescued by a colleague.[83] The firefighter was airlifted to Jackson Memorial Hospital and later recovered.[84][85] A Monroe County Sheriff officer initially determined that the space contained hydrogen sulfide and methane gas produced by decomposing vegetation.[86]

On May 24, 2018, two workers were killed, another seriously injured, and 14 others hospitalized by hydrogen sulfide inhalation at a Norske Skog paper mill in Albury, New South Wales.[87][88] An investigation by SafeWork NSW found that the gas was released from a tank used to hold process water. The workers were exposed at the end of a 3-day maintenance period. Hydrogen sulfide had built up in an upstream tank, which had been left stagnant and untreated with biocide during the maintenance period. These conditions allowed sulfate-reducing bacteria to grow in the upstream tank, as the water contained small quantities of wood pulp and fiber. The high rate of pumping from this tank into the tank involved in the incident caused hydrogen sulfide gas to escape from various openings around its top when pumping was resumed at the end of the maintenance period. The area above it was sufficiently enclosed for the gas to pool there, despite not being identified as a confined space by Norske Skog. One of the workers who was killed was exposed while investigating an apparent fluid leak in the tank, while the other who was killed and the worker who was badly injured were attempting to rescue the first after he collapsed on top of it. In a resulting criminal case, Norske Skog was accused of failing to ensure the health and safety of its workforce at the plant to a reasonably practicable extent. It pleaded guilty, and was fined AU$1,012,500 and ordered to fund the production of an anonymized educational video about the incident.[89][90][87][91]

In October 2019, an Odessa, Texas employee of Aghorn Operating Inc. and his wife were killed due to a water pump failure. Produced water with a high concentration of hydrogen sulfide was released by the pump. The worker died while responding to an automated phone call he had received alerting him to a mechanical failure in the pump, while his wife died after driving to the facility to check on him.[92] A CSB investigation cited lax safety practices at the facility, such as an informal lockout-tagout procedure and a nonfunctioning hydrogen sulfide alert system.[93]


The gas, produced by mixing certain household ingredients, was used in a suicide wave in 2008 in Japan.[94] The wave prompted staff at Tokyo's suicide prevention center to set up a special hotline during "Golden Week", as they received an increase in calls from people wanting to kill themselves during the annual May holiday.[95]

As of 2010, this phenomenon has occurred in a number of US cities, prompting warnings to those arriving at the site of the suicide.[96][97][98][99][100] These first responders, such as emergency services workers or family members are at risk of death or injury from inhaling the gas, or by fire.[101][102] Local governments have also initiated campaigns to prevent such suicides.

In 2020, H2S ingestion was used as a suicide method by Japanese pro wrestler Hana Kimura.[103]

Hydrogen sulfide in the natural environment

Microbial: The sulfur cycle

Sludge from a pond; the black color is due to metal sulfides

Hydrogen sulfide is a central participant in the sulfur cycle, the biogeochemical cycle of sulfur on Earth.[104]

In the absence of oxygen, sulfur-reducing and sulfate-reducing bacteria derive energy from oxidizing hydrogen or organic molecules by reducing elemental sulfur or sulfate to hydrogen sulfide. Other bacteria liberate hydrogen sulfide from sulfur-containing amino acids; this gives rise to the odor of rotten eggs and contributes to the odor of flatulence.

As organic matter decays under low-oxygen (or hypoxic) conditions (such as in swamps, eutrophic lakes or dead zones of oceans), sulfate-reducing bacteria will use the sulfates present in the water to oxidize the organic matter, producing hydrogen sulfide as waste. Some of the hydrogen sulfide will react with metal ions in the water to produce metal sulfides, which are not water-soluble. These metal sulfides, such as ferrous sulfide FeS, are often black or brown, leading to the dark color of sludge.

Several groups of bacteria can use hydrogen sulfide as fuel, oxidizing it to elemental sulfur or to sulfate by using dissolved oxygen, metal oxides (e.g., iron oxyhydroxides and manganese oxides), or nitrate as electron acceptors.[105]

The purple sulfur bacteria and the green sulfur bacteria use hydrogen sulfide as an electron donor in photosynthesis, thereby producing elemental sulfur. This mode of photosynthesis is older than the mode of cyanobacteria, algae, and plants, which uses water as electron donor and liberates oxygen.

The biochemistry of hydrogen sulfide is a key part of the chemistry of the iron-sulfur world. In this model of the origin of life on Earth, geologically produced hydrogen sulfide is postulated as an electron donor driving the reduction of carbon dioxide.[106]


Hydrogen sulfide is lethal to most animals, but a few highly specialized species (extremophiles) do thrive in habitats that are rich in this compound.[107]

In the deep sea, hydrothermal vents and cold seeps with high levels of hydrogen sulfide are home to a number of extremely specialized lifeforms, ranging from bacteria to fish.[which?][108] Because of the absence of sunlight at these depths, these ecosystems rely on chemosynthesis rather than photosynthesis.[109]

Freshwater springs rich in hydrogen sulfide are mainly home to invertebrates, but also include a small number of fish: Cyprinodon bobmilleri (a pupfish from Mexico), Limia sulphurophila (a poeciliid from the Dominican Republic), Gambusia eurystoma (a poeciliid from Mexico), and a few Poecilia (poeciliids from Mexico).[107][110] Invertebrates and microorganisms in some cave systems, such as Movile Cave, are adapted to high levels of hydrogen sulfide.[111]

Interstellar and planetary occurrence

Hydrogen sulfide has often been detected in the interstellar medium.[112] It also occurs in the clouds of planets in our solar system.[113][114]

Mass extinctions

A hydrogen sulfide bloom (green) stretching for about 150km along the coast of Namibia. As oxygen-poor water reaches the coast, bacteria in the organic-matter rich sediment produce hydrogen sulfide, which is toxic to fish.

Hydrogen sulfide has been implicated in several mass extinctions that have occurred in the Earth's past. In particular, a buildup of hydrogen sulfide in the atmosphere may have caused, or at least contributed to, the Permian-Triassic extinction event 252 million years ago.[115][116][117]

Organic residues from these extinction boundaries indicate that the oceans were anoxic (oxygen-depleted) and had species of shallow plankton that metabolized H2S. The formation of H2S may have been initiated by massive volcanic eruptions, which emitted carbon dioxide and methane into the atmosphere, which warmed the oceans, lowering their capacity to absorb oxygen that would otherwise oxidize H2S. The increased levels of hydrogen sulfide could have killed oxygen-generating plants as well as depleted the ozone layer, causing further stress. Small H2S blooms have been detected in modern times in the Dead Sea and in the Atlantic Ocean off the coast of Namibia.[115]

See also


  1. ^ "Hydrogen Sulfide - PubChem Public Chemical Database". The PubChem Project. USA: National Center for Biotechnology Information.
  2. ^ a b Patnaik, Pradyot (2002). Handbook of Inorganic Chemicals. McGraw-Hill. ISBN 978-0-07-049439-8.
  3. ^ a b William M. Haynes (2016). CRC Handbook of Chemistry and Physics (97th ed.). Boca Raton: CRC Press. pp. 4–87. ISBN 978-1-4987-5429-3.
  4. ^ "Hydrogen sulfide". pubchem.ncbi.nlm.nih.gov.
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