Trehalose
| Names | |
|---|---|
| IUPAC name α-D-glucopyranosyl-(1→1)-α-D-glucopyranoside | |
| Systematic IUPAC name (2R,3S,4S,5R,6R)-2-(Hydroxymethyl)-6-[(2R,3R,4S,5S,6R)-3,4,
5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-3,4,5-triol | |
| Other names α,α‐Trehalose | |
| Identifiers | |
| 3D model (JSmol) | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.002.490 | 
| PubChem CID | |
| UNII | |
| CompTox Dashboard (EPA) | |
| 
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| 
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| Properties | |
| C12H22O11 (anhydride) | |
| Molar mass | 342.296 g/mol (anhydrous) 378.33 g/mol (dihydrate) | 
| Appearance | White orthorhombic crystals | 
| Density | 1.58 g/cm3 at 24 °C | 
| Melting point | 203 °C (397 °F; 476 K) (anhydrous) 97 °C (dihydrate) | 
| 68.9 g per 100 g at 20 °C | |
| Solubility | Slightly soluble in ethanol, insoluble in diethyl ether and benzene | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Trehalose (from Turkish tıgala – a sugar derived from insect cocoons + -ose) is a sugar consisting of two molecules of glucose. It is also known as mycose or tremalose. Some bacteria, fungi, plants and invertebrate animals synthesize it as a source of energy, and to survive freezing and lack of water.
Trehalose has high water retention capabilities, and is used in food, cosmetics and as a drug.