Sorbitol

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Sorbitol
2D structure for Sorbitol
Chemical Name (2R,3R,4R,5S)-1,2,3,4,5,6-hexanol
Chemical Formula C6H14O6
CAS Number 50-70-4
Chemical Information HMDB00247
Biochemical Taxonomy

  • Alcohols and Polyols

Functional Taxonomy Not Available
Nutritional Taxonomy Not Available
Metabolic Pathways

  • Aminosugars Metabolism
  • Fructose and Mannose Metabolism
  • Galactose Metabolism
  • Glycerolipid Metabolism
  • Glycolysis
  • Glycosphingolipid Metabolism
  • Pentose and Glucuronate Interconversions
  • Pyruvate Metabolism
  • Starch and Sucrose Metabolism
  • Streptomycin Biosynthesis

Biofluid Location

  • Blood
  • Cerebrospinal Fluid (CSF)
  • Saliva

Tissue Location

  • Adrenal Medulla
  • Bladder
  • Erythrocyte
  • Eye Lens
  • Fibroblasts
  • Kidney
  • Lens
  • Liver
  • Nerve
  • Nerves
  • Neurons
  • Placenta
  • Platelet
  • Red Blood Cells
  • Retina
  • Sciatic Nerve
  • Adipose Tissue

Normal Biofluid Concentrations

  • Blood: 1.10 (0.72-1.47) uM
  • Blood: 13.0 (4.0-24.0) uM
  • Cerebrospinal Fluid (CSF): 13.0 (9.49-16.5) uM
  • Cerebrospinal Fluid (CSF): 15.6 +/- 1.9 uM
  • Cerebrospinal Fluid (CSF): 17.2 +/- 4.6 uM
  • Cerebrospinal Fluid (CSF): 19.4 +/- 5.6 uM
  • Cerebrospinal Fluid (CSF): 19.43 +/- 5.65 uM
  • Saliva: <1.00 uM

Normal Tissue Concentrations Not Available
Diseases / Conditions Related to Nutrition

  • Alzheimer
  • Alzheimer's disease

Other (Monogenic Disorders) Not Available
Abnormal Biofluid Concentrations

  • Cerebrospinal Fluid (CSF) (Alzheimer's disease): 22.89 +/- 3.34 uM
  • Cerebrospinal Fluid (CSF) (Alzheimer): 23.3 +/-3.3 uM

Abnormal Tissue Concentrations Not Available
Physiological Processes Not Available
Authors:
Affiliations:

Contents

Introduction

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A polyhydric alcohol with about half the sweetness of sucrose. Sorbitol occurs naturally and is also produced synthetically from glucose. It was formerly used as a diuretic and may still be used as a laxative and in irrigating solutions for some surgical procedures. It is also used in many manufacturing processes, as a pharmaceutical aid, and in several research applications. Ascorbic acid fermentation; in solution form for moisture-conditioning of cosmetic creams and lotions, toothpaste, tobacco, gelatin; bodying agent for paper, textiles, and liquid pharmaceuticals; softener for candy; sugar crystallization inhibitor; surfactants; urethane resins and rigid foams; plasticizer, stabilizer for vinyl resins; food additive (sweetener, humectant, emulsifier, thickener, anticaking agent); dietary supplement. (Hawley's Condensed Chemical Dictionary) Biological Source: Occurs widely in plants ranging from algae to the higher orders. Fruits of the plant family Rosaceae, which include apples, pears, cherries, apricots, contain appreciable amounts. Rich sources are the fruits of the Sorbus and Crataegus spp. Use/Importance: Used for manuf. of sorbose, propylene glycol, ascorbic acid, resins, plasticizers and as antifreeze mixtures with glycerol or glycol. Tablet diluent, sweetening agent and humectant, other food uses. Used in photometric determination of Ru(VI) and Ru(VIII); in acid-base titration of borate (Dictionary of Organic Compounds)

Biological Function

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Catabolism

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Diseases / Conditions Related to Nutrition

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  • Alzheimer
  • Alzheimer's disease

Other (Monogenic) Disorders

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Nutritional Information

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Drivers for biological variation

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Vulnerable groups

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Other resources

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Links

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