| IUPAC name
| Systematic IUPAC name
| Other names
|Molar mass||80.066 g/mol|
|Appearance||White crystalline solid or liquid, which fumes in air|
|Odor||Sulfurous, highly corrosive|
|Density|| 1.96 g/cm3 (10 °C)|
1.929 g/cm3 (15 °C)
1.911 g/cm3 (20 °C)
1.893 g/cm3 (25 °C)
1.875 g/cm3 (30 °C)
1.857 g/cm3 (35 °C)
1.84 g/cm3 (40 °C)
1.809 g/cm3 (45 °C)
1.783 g/cm3 (50 °C)
1.7552 g/cm3 (55 °C)
|Melting point||45 °C (113 °F; 318 K)|
|Boiling point||16.9 °C (62.4 °F; 290.0 K)|
|Reacts highly exothermically|
|Solubility|| Reacts with alcohols|
Soluble in bromine trifluoride, bromoacetic acid, dichloromethane, halocarbons, hydrogen cyanide, cold nitromethane, sulfuryl chloride fluoride, tetrachloroethylene
|Vapor pressure||263 mmHg at 25 °C|
Std enthalpy of
|Safety data sheet||Sigma-Aldrich|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Sulfur trioxide, chemical formula SO3, is a highly corrosive and easily melted white solid at room temperature. It is the acid anhydride of sulfuric acid.
Sulfur trioxide is an extremely strong dehydrating agent that causes immediate and highly exothermic charring of virtually any organic material it comes into contact with. Sulfur trioxide reacts with water in the air to form a dense fog of concentrated sulfuric acid.
- SO3 + SCl2 → SOCl2 + SO2
Sulfur trioxide is a volatile liquid that fumes in contact with open air. This compounds reacts violently with water and alcohols, releasing a fine mist of sulfuric acid and alkyl sulfates. It has a relative narrow liquid range, melting at 16.9 °C and boiling at 45 °C.
SO3 is available for purchase only to professional chemists due to its extreme hazards. It is commonly sold as a solution in sulfuric acid known as oleum.
The preparation of this compound is extremely dangerous and should only be attempted by chemists with experience working with hazardous volatile reagents.
SO3 can be made in low yield through the pyrolosys of sodium persulfate, first forming ozone and then SOSO3. A catalytic amount of 100% sulfuric acid is required.
Nearly the same reaction takes place when sodium bisulfate is very strongly heated, first evolving water and then SO3.
There are reports that heating sodium pyrosulfate with concentrated sulfuric acid to 150°C results in SO3 and bisulfate.
Heating iron(II) sulfate at 700 °C with carbon yields iron(III) oxide, sulfur dioxide and sulfur trioxide. The same reaction also works with manganese(II) sulfate.
Adding phosphorus pentoxide to extremely concentrated sulfuric acid will release sulfur trioxide, which can be extracted via distillation. Metaphosphoric acid can also be used instead of the pentoxide.
Roasting calcium sulfate with silicon dioxide (ground silica gel can be used) at 1000 °C for 1 hour yields calcium silicate and sulfur trioxide. Adding small amounts of chromium(III) oxide or tungsten(IV) oxide improves the process.
In industry sulfur trioxide is produced via the contact process. Purified sulfur dioxide is mixed with dry air and injected through a bed of V2O5 catalyst heated to temperatures between 400-600 °C (the optimum temperature is 450 °C), at 1-2 atm. The resulting hot sulfur trioxide is recirculated and passed through more layers of catalyst to increase the yield. The gaseous SO3 is cooled by passing it through a heat exchanger and can be collected if required. The condensed trioxide is dissolved in concentrated H2SO4 in the absorption tower to form oleum.
Sulfur trioxide can also be obtained by oxidizing sulfur dioxide in the presence of several metal oxides, such as copper(II) oxide at high temperatures or chromium(III) oxide (at temperatures between 180-400 °C).
- SO3 reacts with SCl2 to form thionyl chloride
- SO3 reacts (violently) with water to form sulfuric acid, with dilute sulfuric acid to form concentrated sulfuric acid, and with the concentrated acid to form oleum.
- A mixture of SO3 and sulfuric acid is effective at sulfonating aromatic compounds, forming useful reagents like benzenedisulfonic acid and toluensulfonic acid.
Sulfur trioxide is highly corrosive and will fume in open air, resulting in a highly dangerous and corrosive sulfuric acid mist. Since this mist is incredibly hazardous, standard protection clothing is insufficient, as the acid mist will attack most organic fibers as well as wreck most air filtration systems and may condense on the cloth. A showering installation may be required in the worst case scenario.
Sulfur trioxide reacts violently with plain water 1.
Sulfur trioxide is best stored as a solution in sulfuric acid, also known as disulfuric acid.
Pure sulfur trioxide should only be stored in sealed ampoules, as it will corrode most metal and plastic containers and their lids. Teflon containers, sealed with PTFE tape can also be used, but are very expensive. Lastly, SO3 containers can also be kept in a glovebox, to limit the hazard in the event of spill.
Due to its relative narrow liquid range, between 16.9 °C 45 °C, it's mandatory to keep sulfur trioxide away from any source of heat, although if kept in a place too cold it will freeze.
Sulfur trioxide has a tendency to violently polymerize, much faster in contact with moisture, and samples should never stored without inhibitors. Some inhibitors used are antimony pentafluoride or antimony pentachloride.
The neutralization of SO3 is a nightmare. It reacts explosively with water and most bases, so dilution must be performed very slowly. The sulfate salt can then be washed down the sink. A safer way involves slowly adding sulfur trioxide over dry calcium carbonate powder, which results in anhydrous calcium sulphate and carbon dioxide. However this process produces large amounts of heat, which causes some sulfur trioxide to become airborne, forming a dangerous corrosive mist. Neutralizing SO3 is not something that can be done in lab, and instead it should be done in either a special enclosed chamber fitted with washing shower or outside in the presence of draft. Neutralizing large amounts of sulfur trioxide is very dangerous for the amateur chemist.
- Appel, R.; Goehring, M.; Zeitschrift fuer Anorganische und Allgemeine Chemie; vol. 271; (1953); p. 171 - 175
- Adadurov, L. E.; Pligunov, V. P.; Zhurnal prikladnoi Khim. (russ.); vol. 5; (1932); p. 149 - 156