Sorbitol: Difference between revisions

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==Synthesis==
<!-- linked from redirect [[Glucose reduction reaction]] -->
Sorbitol may be synthesised via a glucose reduction reaction<ref>{{cite web|title=Reduction of Glucose|url=http://butane.chem.uiuc.edu/pshapley/GenChem2/B8/1.html|website=butane.chem.uiuc.edu|access-date=2017-10-03|archive-date=2017-09-25|archive-url=https://web.archive.org/web/20170925133922/http://butane.chem.uiuc.edu/pshapley/GenChem2/B8/1.html|url-status=dead}}</ref> in which the converted [[aldehyde]] group is converted into a [[hydroxyl]] group. The reaction requires [[NADH]] and is catalyzed by [[aldose reductase]]. Glucose reduction is the first step of the [[polyol pathway]] of [[glucose metabolism]], and is implicated in multiple diabetic complications. [[File:Net reaction of glucose reduction reaction.png|center]] The mechanism involves a [[tyrosine]] residue in the active site of aldehyde reductase. The hydrogen atom on NADH is transferred to the electrophilic aldehyde carbon atom; electrons on the aldehyde carbon-oxygen double bond are transferred to the oxygen that abstracts the proton on tyrosine side chain to form the hydroxyl group. The role of aldehyde reductase tyrosine phenol group is to serve as a general acid to provide proton to the reduced aldehyde oxygen on glucose. [[File:Mechanism of glucose reduction reaction.png|center]] Glucose reduction is not the major [[glucose metabolism]] pathway in a normal human body, where the [[Blood sugar|glucose level]] is in the normal range. However, in diabetic patients whose blood glucose level is high, up to 1/3 of their glucose could go through the glucose reduction pathway. This will consume NADH and eventually leads to cell damage.
 
<chem display="block">C6H12O6 + NADH + H+ -> C6H14O6 + NAD+</chem>The mechanism involves a [[tyrosine]] residue in the active site of aldehyde reductase. The hydrogen atom on NADH is transferred to the electrophilic aldehyde carbon atom; electrons on the aldehyde carbon-oxygen double bond are transferred to the oxygen that abstracts the proton on tyrosine side chain to form the hydroxyl group. The role of aldehyde reductase tyrosine phenol group is to serve as a general acid to provide proton to the reduced aldehyde oxygen on glucose.
Sorbitol also may be synthesized through a catalytic hydrogenation of d-glucose to form d-sorbitol.<ref>SRINIVASAN, K.; GUNDEKARI, S. India Patent WO2017/60922. April 13, 2017.</ref>{{nonspecific|date=November 2017}} This reaction has a 100% yield of d-sorbitol when d-glucose is reacted with hydrogen in water at 120 degrees Celsius, under 150001.5 Torr, for 1 hour.{{Citation needed|date=November 2017}}
 
[[File:Glucose reduction to sorbitol.svg|535x535px|Mechanism of glucose aldehyde reduction into sorbitol]]
 
Glucose reduction is not the major [[glucose metabolism]] pathway in a normal human body, where the [[Blood sugar|glucose level]] is in the normal range. However, in diabetic patients whose blood glucose level is high, up to 1/3 of their glucose could go through the glucose reduction pathway. This will consume NADH and eventually leads to cell damage.
 
==Uses==
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===Miscellaneous uses===
A mixture of sorbitol and [[potassium nitrate]] has found some success as an [[amateur rocketry|amateur]] solid [[rocket fuel]]. It has similar performance to sucrose-based [[rocket candy]], but is easier to cast, less hygroscopic and does not [[caramelization|caramelize]].<ref>{{citeCite web |last=Nakka |first=Richard |title=KNSB Propellant |url=http://www.nakka-rocketry.net/sorb.html |titleaccess-date=Richard12 Nakka'sJuly Experimental Rocketry Web2015 Site|workwebsite=nakka-rocketry.net|access-date=12 July 2015}}</ref>
 
Sorbitol is identified as a potential key chemical intermediate<ref>{{cite journal