Not Available
Common NameHydrogen sulfide
DescriptionHydrogen sulfide is a highly toxic and flammable gas. Because it is heavier than air it tends to accumulate at the bottom of poorly ventilated spaces. Although very pungent at first, it quickly deadens the sense of smell, so potential victims may be unaware of its presence until it is too late. H2S arises from virtually anywhere where elemental sulfur comes into contact with organic material, especially at high temperatures. Hydrogen sulfide is a covalent hydride chemically related to water (H2O) since oxygen and sulfur occur in the same periodic table group. It often results when bacteria break down organic matter in the absence of oxygen, such as in swamps, and sewers (alongside the process of anaerobic digestion). It also occurs in volcanic gases, natural gas and some well waters. It is also important to note that Hydrogen sulfide is a central participant in the sulfur cycle, the biogeochemical cycle of sulfur on Earth. As mentioned above, sulfur-reducing and sulfate-reducing bacteria derive energy from oxidizing hydrogen or organic molecules in the absence of oxygen by reducing sulfur or sulfate to hydrogen sulfide. Other bacteria liberate hydrogen sulfide from sulfur-containing amino acids. Several groups of bacteria can use hydrogen sulfide as fuel, oxidizing it to elemental sulfur or to sulfate by using oxygen or nitrate as oxidant. The purple sulfur bacteria and the green sulfur bacteria use hydrogen sulfide as electron donor in photosynthesis, thereby producing elemental sulfur. (In fact, this mode of photosynthesis is older than the mode of cyanobacteria, algae and plants which uses water as electron donor and liberates oxygen). Hydrogen sulfide can be found in Alcaligenes, Chromobacteriumn, Klebsiella, Proteus and Pseudomonas (PMID: 13061742 ).
Structure
Molecular FormulaH2S
Average Mass34.08100
Monoisotopic Mass33.98772
IUPAC Namehydrogen sulfide
Traditional NameHydrogen sulfide
CAS Registry Number7783-06-04
SMILES[SH-]
InChI IdentifierInChI=1S/H2S/h1H2
InChI KeyRWSOTUBLDIXVET-UHFFFAOYSA-N
CHEBI IDCHEBI:29919
HMDB IDHMDB0003276
Pathways
NameSMPDB/PathBank
Cysteine Metabolism
Beta-mercaptolactate-cysteine disulfiduria
Cystinosis, ocular nonnephropathic
StateLiquid
Water SolubilityNot Available
logSNot Available
pKa (Strongest Acidic)Not Available
pKa (Strongest Basic)Not Available
Hydrogen Acceptor Count0
Hydrogen Donor Count1
Polar Surface Area0 Ų
Rotatable Bond Count0
Physiological Charge-1
Formal Charge0
Refractivity7.36 m³·mol⁻¹
Polarizability3.45

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