Names | |
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IUPAC name
(2S,3R,4R,5R)-Hexane-1,2,3,4,5,6-hexol
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Other names
D-glucitol; D-Sorbitol; Sorbogem; Sorbo
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Identifiers | |
50-70-4 | |
3D model (Jmol) | Interactive image |
ChEBI | CHEBI:17924 |
ChEMBL | ChEMBL1682 |
ChemSpider | 5576 |
DrugBank | DB01638 |
ECHA InfoCard | 100.000.056 |
E number | E420 (thickeners, ...) |
MeSH | Sorbitol |
PubChem | 5780 |
UNII | 506T60A25R |
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Properties | |
C6H14O6 | |
Molar mass | 182.17 g/mol |
Appearance | White crystalline powder |
Density | 1.49 g/cm3 |
Melting point | 94–96 °C (201–205 °F; 367–369 K) |
2350 g/L | |
-107.80·10−6 cm3/mol | |
Pharmacology | |
A06AD18 (WHO) A06AG07 (WHO) B05CX02 (WHO) V04CC01 (WHO) | |
Hazards | |
NFPA 704 | |
Flash point | >100 °C |
420 °C | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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what is ?) | (|
Infobox references | |
Sorbitol (/ˈsɔərbᵻˌtɒl/), less commonly known as glucitol (/ˈɡluːsᵻˌtɒl/), is a sugar alcohol with a sweet taste which the human body metabolizes slowly. It can be obtained by reduction of glucose, changing the aldehyde group to a hydroxyl group. Most sorbitol is made from corn syrup, but it is also found in apples, pears, peaches, and prunes. It is converted to fructose by sorbitol-6-phosphate 2-dehydrogenase. Sorbitol is an isomer of mannitol, another sugar alcohol; the two differ only in the orientation of the hydroxyl group on carbon 2. While similar, the two sugar alcohols have very different sources in nature, melting points, and uses.
Sorbitol is a sugar substitute. It may be listed under the inactive ingredients listed for some foods and products. Its INS number and E number is 420. Sorbitol has approximately 60% the sweetness of sucrose (table sugar).