| Weight | 182.172 g/mol |
|---|---|
| Formula | C6H14O6 |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 6 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 5 |
galactitol (608-66-2)
Dulcitol
Score:
#1461 in Biochemistry
,
#3453 in Biology
,
#4312 in Chemistry
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- Synthesis of 5-amino-5-deoxy-d-galactopyranose and 1,5-dideoxy-1,5-imino-d-galactitol, and their inhibition of - and -d-galactosidases (Carbohydrate Research, 1986)
- RENAL EXCRETION OF HEXITOLS (SORBITOL, MANNITOL, AND DULCITOL) AND THEIR DERIVATIVES (SORBITAN, ISOMANNIDE, AND SORBIDE) AND OF ENDOGENOUS CREATININE-LIKE CHROMOGEN IN DOG AND MAN (Journal of Biological Chemistry, 1940)
- Osmotic Changes caused by the Accumulation of Dulcitol in the Lenses of Rats fed with Galactose (Nature, 1962)
- Mutations affecting transport of the hexitols D-mannitol, D-glucitol, and galactitol in Escherichia coli K-12: isolation and mapping. (Journal of Bacteriology, 1975)
- Molecular analysis of the gat genes from Escherichia coli and of their roles in galactitol transport and metabolism. (Journal of Bacteriology, 1996)
- Galactitol in the Tissues of a Galactosemic Child (JAMA Pediatrics, 1966)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Dulcitol
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SMILESC(C(C(C(C(CO)O)O)O)O)O
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InChIKeyFBPFZTCFMRRESA-UHFFFAOYSA-N
- Pubchem - galactitol
- Wikipedia - galactitol
Galactitol (dulcitol) is a sugar alcohol, the reduction product of galactose. It has a slightly sweet taste. In people with galactokinase deficiency, a form of galactosemia, excess dulcitol forms in the lens of the eye leading to cataracts.
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