Misplaced Pages

Arabitol

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
(Redirected from Arabinitol)
Arabitol
Names
IUPAC name D-Arabinitol
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
CAS Number
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.006.988 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C5H12O5/c6-1-3(8)5(10)4(9)2-7/h3-10H,1-2H2/t3-,4-/m1/s1Key: HEBKCHPVOIAQTA-QWWZWVQMSA-N
  • InChI=1/C5H12O5/c6-1-3(8)5(10)4(9)2-7/h3-10H,1-2H2/t3-,4-/m1/s1Key: HEBKCHPVOIAQTA-QWWZWVQMBW
SMILES
  • OC(O)C(O)(O)CO
Properties
Chemical formula C5H12O5
Molar mass 152.146 g·mol
Appearance Prismatic crystals
Melting point 103 °C (217 °F; 376 K)
Solubility in water 729 g/L
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 , 100 kPa). ☒verify (what is  ?) Infobox references
Chemical compound

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.

References

  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

External links

  • Media related to Arabitol at Wikimedia Commons
Alcohols
By consumption
Alcohols found in
alcoholic drinks
Medical alcohol
Toxic alcohols
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
Straight-chain
saturated
C40 — C49
Secondary
alcohols (2°)
  • 1-Phenylethanol
  • 2-Butanol
  • 2-Deoxyerythritol
  • 2-Heptanol
  • 3-Heptanol
  • 2-Hexanol
  • 3-Hexanol
  • 3-Methyl-2-butanol
  • 2-Nonanol
  • 2-Octanol
  • 2-Pentanol
  • 3-Pentanol
  • Cyclohexanol
  • Cyclopentanol
  • Cyclopropanol
  • Diphenylmethanol
  • Isopropanol
  • Pinacolyl alcohol
  • Pirkle's alcohol
  • Propylene glycol methyl ether
  • Tertiary
    alcohols (3°)
    Hydric alcohols
    Monohydric alcohols
    Dihydric alcohols
    Trihydric alcohols
    Polyhydric alcohols (sugar 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


    Stub icon

    This article about an alcohol is a stub. You can help Misplaced Pages by expanding it.

    Categories: