Volemitol
Volemitol
Chemical structure of volemitol |
Names
|
IUPAC name D-glycero-D-manno-Heptitol |
Systematic IUPAC name (2R,3R,5R,6R)-Heptane-1,2,3,4,5,6,7-heptol |
Other names
- D-glycero-D-talo-Heptitol
- α-Sedoheptitol
- β-Mannoheptitol
|
Identifiers
|
| |
| |
ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.006.978  |
EC Number | |
KEGG | |
| |
UNII | |
| |
InChI=1S/C7H16O7/c8-1-3(10)5(12)7(14)6(13)4(11)2-9/h3-14H,1-2H2/t3-,4-,5-,6-/m1/s1 YKey: OXQKEKGBFMQTML-KVTDHHQDSA-N Y
|
O[C@@H]([C@@H](O)C(O)[C@H](O)[C@H](O)CO)CO
|
Properties
|
| C7H16O7 |
Molar mass | 212.198 g·mol−1 |
Melting point | 152 to 153 °C (306 to 307 °F; 425 to 426 K)
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
Chemical compound
Volemitol is a naturally occurring seven-carbon sugar alcohol. It is a substance widely distributed in plants, red algae, fungi, mosses, and lichens. It was also found in lipopolysaccharides from E. coli. In certain higher plants, such as Primula, volemitol plays several important physiological roles. It functions as a photosynthetic product, phloem translocate, and storage carbohydrate.
It is used as a natural sweetening agent.
Volemitol was first isolated as a white crystalline substance from the mushroom Lactarius volemus by the French scientist Émile Bourquelot in 1889.[1]
See also
References
- ^ E. Bourquelot, Bull. Soc. Mycol. Fr., 5 (1889) 132.
External links
Media related to Volemitol at Wikimedia Commons
|
---|
By consumption | |
---|
Primary alcohols (1°) | Methanol | |
---|
Ethanol | |
---|
Butanol | |
---|
Straight-chain saturated C1 — C9 | |
---|
Straight-chain saturated C10 — C19 | |
---|
Straight-chain saturated C20 — C29 | |
---|
Straight-chain saturated C30 — C39 | - 1-Triacontanol (melissyl / myricyl)
- 1-Hentriacontanol
- 1-Dotriacontanol (lacceryl)
- 1-Tritriacontanol
- 1-Tetratriacontanol (geddyl)
- 1-Pentatriacontanol
- 1-Hexatriacontanol
- 1-Heptatriacontanol
- 1-Octatriacontanol
- 1-Nonatriacontanol
|
---|
Straight-chain saturated C40 — C49 | - 1-Tetracontanol
- 1-Hentetracontanol
- 1-Dotetracontanol
- 1-Tritetracontanol
- 1-Tetratetracontanol
- 1-Pentatetracontanol
- 1-Hexatetracontanol
- 1-Heptatetracontanol
- 1-Octatetracontanol
- 1-Nonatetracontanol
|
---|
|
---|
Secondary alcohols (2°) | |
---|
Tertiary alcohols (3°) | |
---|
Hydric alcohols | |
---|
Amyl alcohols | |
---|
Aromatic alcohols | |
---|
Saturated fatty alcohols | |
---|
Branched and unsaturated fatty alcohols | |
---|
Sugar alcohols | C1 — C7 | |
---|
Deoxy sugar alcohols | |
---|
Cyclic sugar alcohols | |
---|
Glycylglycitols | |
---|
|
---|
Terpene alcohols | Monoterpene alcohols | |
---|
Sesquiterpene alcohols | |
---|
Diterpene alcohols | |
---|
|
---|
Dialcohols | |
---|
Trialcohols | |
---|
Sterols | |
---|
Fluoroalcohols | |
---|
Preparations | |
---|
Reactions | |
---|
|