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D-Sorbitol
[CAS# 50-70-4]

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Identification
Classification API >> Urinary system medication >> Dehydrated medicine
Name D-Sorbitol
Synonyms D-Glucitol; Sorbitol BP
Molecular Structure CAS # 50-70-4, D-Sorbitol, D-Glucitol, Sorbitol BP
Molecular Formula C6H14O6
Molecular Weight 182.17
CAS Registry Number 50-70-4
EC Number 200-061-5
FEMA 3029
SMILES C([C@H]([C@H]([C@@H]([C@H](CO)O)O)O)O)O
Properties
Melting point 95-99 ºC
alpha 4 º (per eur. pharm.)
Water solubility SOLUBLE
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315-H319-H335    Details
Precautionary Statements P261-P305+P351+P338    Details
SDS Available
up Discovory and Applicatios
D-sorbitol was first discovered in 1872 by French chemist Jean-Baptiste Boussingault, who extracted it from the berries of the sorbus tree (Sorbus aucuparia), hence the name sorbitol. It occurs naturally in many fruits and berries, including apples, pears, peaches, and plums. Sorbitol's ability to retain moisture and mild sweetness make it of interest in a variety of applications. Commercial production of D-sorbitol involves hydrogenation of glucose derived from corn or wheat starch. The process converts glucose into sorbitol, resulting in a stable and versatile product. The production method is efficient and affordable, which has led to its widespread use.

Sorbitol is commonly used as a low-calorie sweetener in a variety of foods. Its mild sweetness (about 60% of sucrose) and low glycemic index make it suitable for sugar-free and diabetic-friendly foods. It is used in sugar-free gum, candies, and baked goods to provide sweetness without adding calories or causing a spike in blood sugar levels.

In addition to being a sweetener, sorbitol is also used as a humectant, helping to retain moisture in foods, thereby extending their shelf life and maintaining texture. It is used in products such as cookies, cakes and frozen desserts to prevent drying out and improve consistency.

Sorbitol is an important ingredient in the pharmaceutical industry, used as an excipient in syrups, tablets and oral solutions. It improves the taste of liquid medicines as a sugar substitute without causing tooth decay. Sorbitol is valuable in pharmaceutical formulations due to its ability to enhance the stability and bioavailability of active ingredients.

In cosmetics, sorbitol is used as a humectant and thickener in lotions, creams and gels. Its ability to absorb and retain water helps keep the skin moisturized, making it a popular ingredient in moisturizers and other skin care products. Sorbitol is mild and non-irritating, making it suitable for sensitive skin formulations.

Sorbitol is a polyol in the synthesis of surfactants and emulsifiers, which are important in the production of detergents and cleaners. Its chemical properties also make it a precursor for the production of ascorbic acid (vitamin C), highlighting its role in industrial chemistry.

In the plastics industry, sorbitol is used as a plasticizer and stabilizer to enhance the flexibility and durability of products such as resins and adhesives. Its ability to improve the physical properties of materials extends its usefulness to a variety of manufacturing processes.

D-Sorbitol is generally recognized as safe (GRAS) by regulatory agencies such as the FDA. It is non-toxic and well tolerated in food and drug applications. However, excessive consumption can cause gastrointestinal upset as it has a laxative effect. In industrial applications, handling guidelines should be followed to ensure safety and prevent environmental contamination.

References

2023. Identification, Synthesis, and Characterization of Potential Dichloro Impurity: N,N-Dimethyl-3-Phenyl-2, 3-Dichloropropylamine in the Synthesis of Atomoxetine. Pharmaceutical Chemistry Journal, 56(11).
DOI: 10.1007/s11094-024-03039-8

2022. N,N-dimethyl fluorosulfonamide for suppressed aluminum corrosion in lithium bis(trifluoromethanesulfonyl)imide-based electrolytes. Nano Research, 15(12).
DOI: 10.1007/s12274-022-4669-8

1948. The Addition of Dimethylamine to Benzoquinone. Journal of the American Chemical Society, 70(2).
DOI: 10.1021/ja01182a502
Market Analysis Reports
List of Reports Available for D-Sorbitol
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