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Updating {{chembox}} (no changed fields - added verified revid - updated 'DrugBank_Ref', 'UNII_Ref', 'ChEMBL_Ref', 'ChEBI_Ref', 'KEGG_Ref') per Chem/Drugbox validation (report [[Wikipedia_talk:Wi
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{{chembox
{{chembox
| Verifiedfields = changed
| verifiedrevid = 443830856
| Watchedfields = changed
|ImageFile=Dulcitol.svg
| verifiedrevid = 443831933
|ImageSize=
| ImageFile=Dulcitol.svg
|IUPACName=(2''R'',3''S'',4''R'',5''S'')-hexane-1,2,3,4,5,6-hexol
|OtherNames= <small>D</small>-Galactitol; Dulcitol
| ImageFile2=D-Galactitol.png
| ImageSize=
|Section1= {{Chembox Identifiers
| IUPACName=<small>D</small>-Galactitol
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
|SystematicName=(2''R'',3''S'',4''R'',5''S'')-hexane-1,2,3,4,5,6-hexol
| OtherNames=Dulcitol
|Section1={{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 11357
| ChemSpiderID = 11357
| InChI = 1/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2/t3-,4+,5+,6-
| InChI = 1/C6H14O6/c7-1-3(9)5(11)6(12)4(10)2-8/h3-12H,1-2H2/t3-,4+,5+,6-
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| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo=608-66-2
| CASNo=608-66-2
| UNII_Ref = {{fdacite|correct|FDA}}
| PubChem=11850
| UNII = 113ZQ1Y7DD
| ChEBI_Ref = {{ebicite|correct|EBI}}
| PubChem=11850
| ChEMBL_Ref = {{ebicite|changed|EBI}}
| ChEMBL = 1773904
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 16813
| ChEBI = 16813
| SMILES = O[C@H]([C@@H](O)CO)[C@@H](O)[C@H](O)CO
| SMILES = O[C@H]([C@@H](O)CO)[C@@H](O)[C@H](O)CO
}}
}}
|Section2= {{Chembox Properties
|Section2={{Chembox Properties
|C=6|H=14|O=6
| C=6 | H=14 | O=6
| MolarMass=182.172 g/mol
| MolarMass=182.172 g/mol
| Appearance=
| Appearance=
| Density=
| Density=
| MeltingPt=
| MeltingPt=
| BoilingPt=
| BoilingPt=
| Solubility=
| Solubility=
| MagSus = -112.40·10<sup>−6</sup> cm<sup>3</sup>/mol
}}
}}
|Section3= {{Chembox Hazards
|Section3={{Chembox Hazards
| MainHazards=
| MainHazards=
| FlashPt=
| FlashPt=
| AutoignitionPt =
| Autoignition=
}}
}}
}}
}}


'''Galactitol''' ('''dulcitol''') is a [[sugar alcohol]], the [[redox|reduction]] product of [[galactose]].<ref name=pubchem>{{cite web|url=http://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=11850|title=Galactitol - Compound Summary |publisher=[[National Center for Biotechnology Information]]|accessdate=2008-08-06}}</ref> In people with [[galactokinase deficiency]], a form of [[galactosemia]], excess dulcitol forms in the [[lens (anatomy)|lens]] of the eye leading to [[cataract]]s.<ref name=eMedicine>{{cite web |url = http://www.emedicine.com/ped/TOPIC815.HTM |title = Galactokinase Deficiency |accessdate = 2008-08-08 |author = Roth, KS |date = September 10, 2007 |work = [[eMedicine]] |publisher = [[WebMD]]}}</ref>
'''Galactitol''' ('''dulcitol''') is a [[sugar alcohol]], the [[redox|reduction]] product of [[galactose]].<ref name=pubchem>{{cite web|url=https://pubchem.ncbi.nlm.nih.gov/summary/summary.cgi?cid=11850|title=Galactitol - Compound Summary |publisher=[[National Center for Biotechnology Information]]|access-date=2008-08-06}}</ref> It has a slightly sweet taste.<ref name=pubchem/> In people with [[galactokinase deficiency]], a form of [[galactosemia]], excess dulcitol forms in the [[lens (anatomy)|lens]] of the eye leading to [[cataract]]s.<ref name=eMedicine>{{cite web |url = http://www.emedicine.com/ped/TOPIC815.HTM |title = Galactokinase Deficiency |access-date = 2008-08-08 |author = Roth, KS |date = September 10, 2007 |work = [[eMedicine]] |publisher = [[WebMD]]}}</ref>


Galactitol is produced from [[galactose]] in a reaction catalyzed by [[aldose reductase]]. Galactose itself comes from the metabolism of the disaccharide [[lactose]] into [[glucose]] and galactose.
Galactitol is produced from [[galactose]] in a reaction catalyzed by [[aldose reductase]].


The other common galactose metabolism defect is a defect in [[galactose-1-phosphate uridylyltransferase]], an [[autosomal recessive disorder]], which also causes a buildup of galactitol as a result of increased concentrations of galactose-1-phosphate and galactose. The toxicity associated with [[galactose-1-phosphate uridylyltransferase]] deficiency is associated with symptoms of [[hepatosplenomegaly]] and [[mental retardation]] in addition to the cataracts caused by galactitol buildup.
The other common galactose metabolism defect is a defect in [[galactose-1-phosphate uridylyltransferase]], an [[autosomal recessive disorder]], which also causes a buildup of galactitol as a result of increased concentrations of galactose-1-phosphate and galactose. This disorder leads to cataracts caused by galactitol buildup.


==References==
==References==
{{reflist}}
{{reflist}}


==External links==
[[Category:Sugar alcohols]]
*{{Commonscatinline}}



{{Alcohols}}
{{Fructose and galactose metabolic intermediates}}
{{Fructose and galactose metabolic intermediates}}


[[Category:Sugar alcohols]]
[[de:Galaktit]]
[[Category:Sugar substitutes]]
[[es:Dulcitol]]
[[fr:Dulcitol]]
[[ja:ガラクチトール]]