| 1,3,5-Trioxane |
|---|
| |
| General | |
|---|---|
| Systematic name | 1,3,5-Trioxane |
| Other names | ''s''-Trioxane 1,3,5-Trioxacyclohexane Trioxymethylene Metaformaldehye Trioxin |
| Molecular formula | C3H6O3 |
| SMILES | C1OCOCO1 |
| Molar mass | 90.08 g/mol |
| Appearance | white crystalline solid |
| CAS number | [110-88-3] |
| Properties |
|---|
| Density and phase | 1.17 g/cm³ (65 °C) |
| Solubility in water | 17.2 g/100 ml (18 °C) |
| Melting point | 64 °C |
| Boiling point | 114.5 °C |
| Hazards |
|---|
| MSDS | External MSDS |
| Main hazards | ? |
| NFPA 704 | 2 2 0 |
| Flash point | 45 °C |
| R/S statement | R: 22 S: 24/25 |
| RTECS number | YK0350000 |
| Related compounds |
|---|
| Related compounds | Formaldehyde 1,2,4-Trioxane Polyoxymethylene |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
|
'1,3,5-Trioxane' is a stable cyclic
trimer of
formaldehyde with a
chloroform-like odor. Being a
trioxane, it has the
molecular formula C
3H
6O
3 and consists of a six membered ring with three
carbon atoms and three
oxygen atoms.
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.
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.
Trioxane is also occasionally known by the synonym trioxin, sometimes mistaken for the fictional
2,4,5-trioxin.
Derivatives
The only possible mono-bromo derivative of trioxane is C
3H
5BrO
3.
External links