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2D Structure
Also known as: Sulphur dioxide, Sulfurous anhydride, 7446-09-5, Sulfurous oxide, Sulfon, Sulfur superoxide
Molecular Formula
O2S
Molecular Weight
64.07  g/mol
InChI Key
RAHZWNYVWXNFOC-UHFFFAOYSA-N
FDA UNII
0UZA3422Q4

A highly toxic, colorless, nonflammable gas. It is used as a pharmaceutical aid and antioxidant. It is also an environmental air pollutant.
1 2D Structure

2D Structure

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
sulfur dioxide
2.1.2 InChI
InChI=1S/O2S/c1-3-2
2.1.3 InChI Key
RAHZWNYVWXNFOC-UHFFFAOYSA-N
2.1.4 Canonical SMILES
O=S=O
2.2 Other Identifiers
2.2.1 UNII
0UZA3422Q4
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Sulfurous Anhydride

2.3.2 Depositor-Supplied Synonyms

1. Sulphur Dioxide

2. Sulfurous Anhydride

3. 7446-09-5

4. Sulfurous Oxide

5. Sulfon

6. Sulfur Superoxide

7. Sulfur Oxide (so2)

8. Fermenicide Liquid

9. Fermenicide Powder

10. Sulfurous Acid Anhydride

11. Schwefeldioxid

12. Oxosulfane Oxide

13. Siarki Dwutlenek

14. Sulfur Dioxide (so2)

15. Dioxidosulfur

16. Schwefeldioxyd

17. Surfur Dioxide (anhydrous)

18. Fema No. 3039

19. Sulfur Dioxide (nf)

20. Sulfur-dioxide

21. So2

22. Un 1079

23. Chebi:18422

24. 0uza3422q4

25. Sulfur Dioxide (so2) 10% By Volume Or More So2

26. 67015-63-8

27. Sulfur Dioxide [nf]

28. E220

29. Sulfur Dioxide, >=99.9%

30. Sulfurdioxide

31. Caswell No. 813

32. Schwefeldioxyd [german]

33. Siarki Dwutlenek [polish]

34. Sulfonyl

35. Sulfuryl

36. Sulphonyl

37. Sulfer Dioxide

38. Ccris 9001

39. Hsdb 228

40. Dioxide, Sulfur

41. Fermenticide Liquid

42. Oxosulfane Oxide #

43. Schwefel(iv)-oxid

44. Einecs 231-195-2

45. Anhydride, Sulfurous

46. Un1079

47. Sulfuroxide

48. Epa Pesticide Chemical Code 077601

49. Sulfur Dioxide [un1079] [poison Gas]

50. Sulfur Dioxide [ii]

51. Sulfur Dioxide [mi]

52. Sulfur Dioxide [fcc]

53. Sulfur Dioxide [fhfi]

54. Sulfur Dioxide [hsdb]

55. Sulfur Dioxide [iarc]

56. Unii-0uza3422q4

57. Ins No.220

58. Sulfur Dioxide [mart.]

59. Sulfur Dioxide, >=99.98%

60. Chembl1235997

61. Dtxsid6029672

62. Fema 3039

63. Rahzwnyvwxnfoc-uhfffaoysa-

64. Ins-220

65. [so2]

66. Sulfur Dioxide (e 220)

67. Sulfurous Anhydride (e220)

68. Akos015904447

69. Sulfur Dioxide, Puriss., >=99.9%

70. Sulfur Dioxide [un1079] [poison Gas]

71. E-220

72. Q5282

73. R-764

74. U0147

75. U0148

76. C09306

77. D05961

78. Ec 231-195-2

79. Sulfur Dioxide (ca. 2.5% In Dichloromethane, Ca. 0.5 Mol/l)

80. Sulfur Dioxide (ca. 8% In Tetrahydrofuran, Ca. 1.2 Mol/l)

2.4 Create Date
2004-09-16
3 Chemical and Physical Properties
Molecular Weight 64.07 g/mol
Molecular Formula O2S
XLogP30.1
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count3
Rotatable Bond Count0
Exact Mass63.96190041 g/mol
Monoisotopic Mass63.96190041 g/mol
Topological Polar Surface Area35.1 Ų
Heavy Atom Count3
Formal Charge0
Complexity18.3
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count1
4 Pharmacology and Biochemistry
4.1 MeSH Pharmacological Classification

Air Pollutants

Any substance in the air which could, if present in high enough concentration, harm humans, animals, vegetation or materials. Substances include GASES; PARTICULATE MATTER; and volatile ORGANIC CHEMICALS. (See all compounds classified as Air Pollutants.)


4.2 Absorption, Distribution and Excretion

Although the major route of absorption of the relevant sulfur compounds and particulate matter into the body is through the intestinal tract, the respiratory tract is the most vulnerable area for airborne materials. Most studies on both man and animals have indicated that 40 to 90% or more of inhaled sulfur dioxide is absorbed in the upper respiratory tract. Taken into the blood stream, it appears to be widely distributed throughout the body, metabolized, and excreted via the urinary tract. The deposition pattern of particulate matter varies with particle size, shape, and density, and also with airflow conditions. Deposited particles are largely phagocytized and transported to the mucociliary escalator, into the interstitium, or to the lymphatic system. The biological half-times range from days to years depending on their chemical composition. Soluble particles may dissolve in the mucous or aqueous lining of the lungs. In the first case, they will be eliminated via the mucociliary route. In the second, they may diffuse into the lymph or blood.

WHO; Environmental Health Criteria 8: Sulfur Oxides and Suspended Particulate Matter (1979); Available from, as of November 21, 2017: https://www.inchem.org/pages/ehc.html


Sulfur dioxide is highly soluble in aqueous media. Absorption after inhalation has been studied in rabbits and man. In rabbits, about 40% of the inhaled sulfur dioxide is absorbed in the nose and pharynx when concentrations of about 290 ug/cu m (0.1 ppm) are inhaled. At higher concentrations (29-290 mg/cu m, 10-100 ppm), the fraction absorbed is much higher (about 95%). The reasons for these different rates of absorption are not clear. In dogs, more than 99% of the inhaled sulfur dioxide is absorbed by the nose at exposure levels of 2.9-140 mg/cu m (1-50 ppm).

WHO; Environ Health Criteria: Sulfur Oxides and Suspended Particulate Matter p.50 (1979);


Sulfur dioxide is highly soluble in water and, therore, is absorbed efficiently in the upper respiratory tract. Two factors affecting the efficiency of absorption are the mode of breathing (oral versus oronasal) and ventilation rate. The nose filters out most inhaled sulfur dioxide, preventing its passage to sensitive irritant receptors at and below the larynx. At rest, most people (about 85%) breathe through the nose, providing protection against the pulmonary toxicity of sulfur dioxide. Mouth breathing, particularly at higher airflow rates, substantially increases the fraction of sulfur dioxide reaching the lung. Thus, voluntary hyperventilation or exercise at a level of exertion requiring oronasal breathing lowers the threshold for sulfur dioxide-induced respiratory symptoms and bronchomotor responsiveness. Deep lung penetration and toxicity are enhanced by oxidation and adsorption to submicrometer acidic particles.

Sullivan, J.B., Krieger G.R. (eds). Clinical Environmental Health and Toxic Exposures. Second edition. Lippincott Williams and Wilkins, Philadelphia, Pennsylvania 1999., p. 826


Radiolabeled sulfur dioxide is absorbed from the respiratory tract of experimental animals in the blood and is distributed throughout the body, concentrating in the liver, spleen, esophagus, and kidneys. It is metabolized to a variety of sulfur-containing compounds and is excreted principally via the urine as sulfate. Significant quantities of sulfur dioxide may be retained for a week or more in the lungs and trachea of experimental animals.

Sullivan, J.B., Krieger G.R. (eds). Clinical Environmental Health and Toxic Exposures. Second edition. Lippincott Williams and Wilkins, Philadelphia, Pennsylvania 1999., p. 826


While sulfur dioxide (SO(2)) has been previously known for its toxicological effects, it is now known to be produced endogenously in mammals from sulfur-containing amino acid L-cysteine. L-cysteine is catalyzed by cysteine dioxygenase (CDO) to L-cysteine sulfinate, which converts to beta-sulfinylpyruvate through transamination by aspartate aminotransferase (AAT), and finally spontaneously decomposes to pyruvate and SO(2). The present study explored endogenous SO(2) production, and AAT and CDO distribution in different rat tissue. SO(2) content was highest in stomach, followed by tissues in the right ventricle, left ventricle, cerebral gray matter, pancreas, lung, cerebral white matter, renal medulla, spleen, renal cortex and liver. AAT activity and AAT1 mRNA expression were highest in the left ventricle, while AAT1 protein expression was highest in the right ventricle. AAT2 and CDO mRNA expressions were both highest in liver tissue. AAT2 protein expression was highest in the renal medulla, but CDO protein expression was highest in liver tissue. In all tissues, AAT1 and AAT2 were mainly distributed in the cytoplasm rather than the nucleus. These observed differences among tissues endogenously generating SO(2) and associated enzymes are important in implicating the discovery of SO(2) as a novel endogenous signaling molecule.

PMID:22020076 Luo L et al; Biochem Biophys Res Commun 415 (1): 61-7 (2011)


4.3 Metabolism/Metabolites

... Sulfur dioxide (SO2) can be produced endogenously from normal metabolism of sulfur-containing amino acids. L-cysteine is oxidized via cysteine dioxygenase to L-cysteinesulfinate, and the latter can proceed through transamination by glutamate oxaloacetate transaminase (GOT) to beta-sulfinylpyruvate which decomposes spontaneously to pyruvate and SO2 ... Endogenous production of SO2 /was detected in spontaneous hypertensive rats/ in all cardiovascular tissues, including in heart, aorta, pulmonary artery, mesenteric artery, renal artery, tail artery and the plasma SO2 content. As the key enzyme producing SO2, GOT mRNA in cardiovascular system was detected and found to be located enrichedly in endothelial cells and vascular smooth muscle cells near the endothelial layer ...

Jin HF et al; Beijing da xue xue bao. Yi xue ban 39 (4): 423-5 (2007)


Once absorbed, sulfur dioxide appears to be metabolized rapidly to sulfate by the widely distributed enzyme sulfite oxidase. After it has been oxidized to sulfate, it becomes part of the large sulfate pool within the body. /It was reported/ relatively large differences in sulfite oxidase activity among five species: rats had the highest levels and rabbits the lowest. An inverse correlation was shown between enzyme activity and sensitivity to bisulfite toxicity. These results reflect species differences in rate of S-sulfonate formation.

IARC. Monographs on the Evaluation of the Carcinogenic Risk of Chemicals to Humans. Geneva: World Health Organization, International Agency for Research on Cancer, 1972-PRESENT. (Multivolume work). Available at: https://monographs.iarc.fr/ENG/Classification/index.php, p. V54 166 (1992)


4.4 Biological Half-Life

No reports found; [TDR, p. 1098]

TDR - Ryan RP, Terry CE, Leffingwell SS (eds). Toxicology Desk Reference: The Toxic Exposure and Medical Monitoring Index, 5th Ed. Washington DC: Taylor & Francis, 1999., p. 1098