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| Names | |
|---|---|
| IUPAC name
 D-Arabinitol[2]  | |
| Systematic IUPAC name
 (2R,4R)-Pentane-1,2,3,4,5-pentol  | |
| Other names
 (2R,4R)-Pentane-1,2,3,4,5-pentaol (not recommended) Arabitol Lyxitol  | |
| Identifiers | |
3D model (JSmol)  | 
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| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.006.988 | 
PubChem CID  | 
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| UNII | |
CompTox Dashboard (EPA)  | 
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| Properties | |
| C5H12O5 | |
| Molar mass | 152.146 g·mol−1 | 
| Appearance | Prismatic crystals | 
| Melting point | 103 °C (217 °F; 376 K) | 
| Miscible | |
| Hazards | |
| NFPA 704 (fire diamond) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). 
Infobox references  | |
Arabitol, or arabinitol, is a sugar alcohol. It can be formed by the reduction of either arabinose or lyxose. Some organic acid tests check for the presence of D-arabitol, which may indicate overgrowth of intestinal microbes such as Candida albicans or other yeast/fungus species.[3]
References
- ↑ Merck Index, 11th Edition, 789
 - ↑ "2-Carb-19".
 - ↑ "Candida and Yeast Overgrowth". Archived from the original on 2010-03-02. Retrieved 2010-03-16.
 
Further reading
- Herman, Anna; Herman, Andrzej Przemysław (15 January 2022). "Could Candida Overgrowth Be Involved in the Pathophysiology of Autism?". Journal of Clinical Medicine. 11 (2): 442. doi:10.3390/jcm11020442. PMC 8778531. PMID 35054136.
 
External links
 Media related to Arabitol at Wikimedia Commons
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