Cannabis Ruderalis

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Arabitol[1]
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)
ChEBI
ChemSpider
ECHA InfoCard 100.006.988 Edit this at Wikidata
UNII
  • InChI=1S/C5H12O5/c6-1-3(8)5(10)4(9)2-7/h3-10H,1-2H2/t3-,4-/m1/s1 checkY
    Key: HEBKCHPVOIAQTA-QWWZWVQMSA-N checkY
  • InChI=1/C5H12O5/c6-1-3(8)5(10)4(9)2-7/h3-10H,1-2H2/t3-,4-/m1/s1
    Key: HEBKCHPVOIAQTA-QWWZWVQMBW
  • OC[C@@H](O)C(O)[C@H](O)CO
Properties
C5H12O5
Molar mass 152.146 g·mol−1
Appearance Prismatic crystals
Melting point 103 °C (217 °F; 376 K)
729 g/L[3]
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 0: Exposure under fire conditions would offer no hazard beyond that of ordinary combustible material. E.g. sodium chlorideFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
0
0
0
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

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.[4]

References[edit]

  1. ^ Merck Index, 11th Edition, 789
  2. ^ "2-Carb-19".
  3. ^ Arabitol at the Human Metabolome Database
  4. ^ "Candida and Yeast Overgrowth". Archived from the original on 2010-03-02. Retrieved 2010-03-16.

Further reading[edit]

External links[edit]

  • Media related to Arabitol at Wikimedia Commons


source: https://en.wikipedia.org/wiki/Arabitol

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