1,3,5-Trioxane
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1,3,5-Trioxane | |
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IUPAC name | 1,3,5-Trioxane |
Other names | s-Trioxane
1,3,5-Trioxacyclohexane Trioxymethylene Metaformaldehye Trioxin |
Identifiers | |
CAS number | [110-88-3] |
RTECS number | YK0350000 |
SMILES | C1OCOCO1 |
Properties | |
Molecular formula | C3H6O3 |
Molar mass | 90.08 g/mol |
Appearance | white crystalline solid |
Density | 1.17 g/cm³ (65 °C) |
Melting point |
64 °C |
Boiling point |
114.5 °C |
Solubility in water | 17.2 g/100 ml (18 °C) |
Hazards | |
NFPA 704 | |
R-phrases | 22 |
S-phrases | 24/25 |
Flash point | 45 °C |
Related compounds | |
Related compounds | Formaldehyde |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
1,3,5-Trioxane is a stable cyclic trimer of formaldehyde with a chloroform-like odor. Being a trioxane, it has the molecular formula C3H6O3 and consists of a six membered ring with three carbon atoms and three oxygen atoms.
Contents |
[edit] Uses
In chemistry, it is used as a stable, easily handled source of anhydrous formaldehyde. In acidic solutions, it decomposes to generate three molecules of formaldehyde. It may also be used in polymerization to form acetal resins, such as polyoxymethylene plastic.
When combined with hexamine and compressed into solid bars, it is used by the military and outdoorsmen as a cooking fuel similar to Esbit.
1,3,5-Trioxane is a mortician's restorative chemical that repairs cells and maintains the corpse's contours after postmortem tissue constriction.[citation needed]
Trioxane is also occasionally known by the synonym trioxin, sometimes mistaken for the fictional 2,4,5-trioxin.
[edit] Derivatives
The only possible mono-bromo derivative of trioxane is C3H5BrO3.
[edit] See also
[edit] References
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