Threitol
From Sciencemadness Wiki
Revision as of 20:56, 13 August 2017 by Mabus (Talk | contribs) (Created page with "{{Stub}} {{Chembox | Name = Threitol | Reference = | IUPACName = (2R,3R)-Butane-1,2,3,4-tetrol | PIN = | SystematicName = | OtherNames = <!-- Images --> | ImageFile = | Imag...")
 |
This article is a stub. Please help Sciencemadness Wiki by expanding it, adding pictures, and improving existing text.
|
| Names | |
|---|---|
| IUPAC name
(2R,3R)-Butane-1,2,3,4-tetrol
| |
| Properties | |
| C4H10O4 | |
| Molar mass | 122.12 g/mol |
| Appearance | White crystalline solid |
| Odor | Odorless |
| Density | 1.401 g/cm3 |
| Melting point | 88–90 °C (190–194 °F; 361–363 K) |
| Boiling point | Decomposes |
| 880 g/100 ml (25 °C)[1] | |
| Solubility | Soluble in ethanol, methanol |
| Vapor pressure | ~0 mmHg |
| Hazards | |
| Safety data sheet | Sigma-Aldrich |
| Related compounds | |
| Related compounds
|
Erythritol |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Threitol is a four-carbon sugar alcohol with the molecular formula C4H10O4, diastereomer of erythritol.
Contents
Properties
Chemical
Threitol can be nitrated to threitol tetranitrate.
Physical
Threitol is a colorless solid, soluble in water.
Availability
It is sold by chemical suppliers.
Occurs naturally in the edible fungus Armillaria mellea, though you will need a large amount of said fungus to obtain significant amounts of threitol.
Preparation
Best to buy it than make it yourself.
Projects
- Swettener
- Threitol tetranitrate
Handling
Safety
Threitol has low toxicity.
Storage
In closed bottles.
Disposal
No special disposal is required.
References
- ↑ Cohen, Shlomo; Marcus, Yizhak; Migron, Yoelit; Dikstein, Shabtay; Shafran, Avi; Journal of the Chemical Society, Faraday Transactions; vol. 89; nb. 17; (1993); p. 3271 - 3275
