-
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...
-
Ribitol is one of four
stereoisomers having the
formula C5H12O5: D-
arabitol and L-
arabitol Ribitol (non-chiral)
Xylitol (non-chiral) "2-Carb-19". Advances...
- are
arabitol and ribitol.
These three compounds differ in the
stereochemistry of the
three secondary alcohol groups. 5-carbon
sugar alcohols Arabitol Ribitol...
- D-
arabitol-phosphate
dehydrogenase (EC 1.1.1.301, APDH, D-
arabitol 1-phosphate dehydrogenase, D-
arabitol 5-phosphate dehydrogenase) is an
enzyme with systematic...
- synthesis.
Another possibility is that the ac****ulation of D-ribitol and D-
arabitol may be toxic. However,
Klussman et al.
evaluated the
toxicity of polyols...
- For example, d-ribulose is an
intermediate in the
fungal pathway for d-
arabitol production. Also, as the 1,5-bisphosphate, d-ribulose
combines with carbon...
- (2-carbon)
Glycerol (3-carbon)
Erythritol (4-carbon)
Threitol (4-carbon)
Arabitol (5-carbon)
Xylitol (5-carbon)
Ribitol (5-carbon)
Mannitol (6-carbon) Sorbitol...
- (C1)
Ethylene glycol (C2)
Glycerol (C3)
Erythritol (C4)
Threitol (C4)
Arabitol (C5)
Ribitol (C5)
Xylitol (C5)
Mannitol (C6)
Sorbitol (C6)
Galactitol (C6)...
- and the
formation of
higher levels of
sugar alcohols (such as glycerol,
arabitol, mannitol, sorbitol, and inositol)
contribute to the
complexity and mouthfeel...
- Fischer's ****ignment of
Configuration to d-Glucose. The
Pentaacetates of d-
Arabitol and d-Xylitol".
Journal of the
American Chemical Society. 57 (9): 1753...
