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Glucose pentaacetate CAS:604-68-2

Glucose pentaacetate is a derivative of glucose, in which all five hydroxyl (-OH) groups of the glucose molecule are acetylated, resulting in an acyclic structure. This compound appears as a colorless, viscous liquid and is primarily used in organic synthesis and research applications. The acetylation of glucose serves to enhance its stability and solubility in organic solvents, making it suitable for various chemical reactions. Additionally, glucose pentaacetate can be employed as a protective group in carbohydrate chemistry, allowing chemists to modify other functional groups without interfering with the sugar moiety’s reactivity.


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Application and Effect:

Glucose pentaacetate is an important derivative of glucose formed through the complete acetylation of all five hydroxyl (-OH) groups present in the glucose molecule. This conversion yields a more hydrophobic compound that exhibits enhanced stability and solubility in organic solvents compared to its parent sugar. As a result, glucose pentaacetate is widely utilized in organic synthesis and carbohydrate chemistry. One of the primary applications of glucose pentaacetate is as a protective group for hydroxyl functionalities in carbohydrate derivatives. Protecting groups are crucial in synthetic chemistry as they allow chemists to selectively modify specific functional groups without affecting others. By introducing acetyl groups, researchers can carry out further reactions on other parts of the glucose molecule while preserving the integrity of the acetylated hydroxyls. This versatility makes glucose pentaacetate a valuable tool in the synthesis of complex carbohydrates and glycosides. In addition to its role in synthetic organic chemistry, glucose pentaacetate serves as a useful substrate for studying reaction mechanisms and the properties of carbohydrate derivatives. Its reactivity under various conditions can provide insights into how structural changes affect the behavior of sugars and their derivatives. Furthermore, glucose pentaacetate may also find applications in medicinal chemistry, where modifications of glucose can lead to the development of bioactive compounds. Research indicates that certain glucosamine derivatives possess pharmacological activities, and glucose pentaacetate can serve as a precursor for such compounds. In conclusion, glucose pentaacetate is a significant compound in both academic and industrial settings, offering unique properties that facilitate various chemical transformations. Its role as a protective group and its use in exploring carbohydrate chemistry underscore its importance in advancing organic synthesis, medicinal chemistry, and related fields. Ongoing research on glucose pentaacetate and its derivatives continues to expand our understanding of carbohydrate chemistry and its potential applications.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C16H22O11
Assay 99%
Appearance white powder
CAS No.  604-68-2
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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