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CAS 604-69-3 Skin Whitening Ingredients β-D-Glucose Pentaacetate Solid
  • CAS 604-69-3 Skin Whitening Ingredients β-D-Glucose Pentaacetate Solid
  • CAS 604-69-3 Skin Whitening Ingredients β-D-Glucose Pentaacetate Solid

CAS 604-69-3 Skin Whitening Ingredients β-D-Glucose Pentaacetate Solid

Place of Origin China
Brand Name FIRSKY
Model Number 604-69-3
Document Product Brochure PDF
Product Details
Product Name:
β-D-Glucose Pentaacetate
CAS NO:
604-69-3
Molecular Formula:
C₁₆H₂₂O₁₁
Molecular Weight:
390.34
Highlight: 

604-69-3 Skin Whitening Ingredients

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Skin Whitening Ingredients Pentaacetate

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Β-D-Glucose Pentaacetate Solid

Payment & Shipping Terms
Minimum Order Quantity
1KG
Packaging Details
1kg, 5kg, 15kg, 20kg, 25kg can be packed in different specifications. Packaging can be customized according to customer requirements. Aluminium foil bag and carton.
Delivery Time
7-15days
Payment Terms
T/T, Western Union, MoneyGram
Supply Ability
2000T
Product Description

β-D-Glucose Pentaacetate CAS 604-69-3

Chemical Nameβ-D-Glucose Pentaacetate
Synonymsβ-D-Glucopyranose 1,2,3,4,6-Pentaacetate; 1,2,3,4,6-Penta-O-acetyl-β-D-
CAS Number604-69-3
Molecular FormulaC₁₆H₂₂O₁₁
AppearanceWhite to Off-White Solid
Melting Point128-130°C
Molecular Weight390.34
Storage4°C
SolubilityChloroform (Slightly), Methanol (Slightly)
CategoryBuilding Blocks; Carbohydrates;
ApplicationsD-Glucose pentaacetate was reported to stimulate insulin release in rat pancreatic islets. Only a-D-glucose pentaacetate caused an immediate increase in insulin output. The b-anomer of D-glucose pentaacetate first transiently inhibited insulin release, this initial effect being followed by a secondary rise in secretory rate.

 

Description


β-D-Glucose Pentaacetate, CAS 604-69-3: A Precious Derivative of a Sweet Molecule
Prepare to explore the captivating world of β-D-Glucose Pentaacetate, CAS 604-69-3, a remarkable chemical derivative of glucose with diverse applications in chemistry, science, and industry.
 

  • Chemical Transformation: β-D-Glucose Pentaacetate is the result of a chemical reaction that replaces hydroxyl (-OH) groups in glucose with acetyl (-OCOCH3) groups. This transformation imparts unique properties to the molecule.
  • Hydrophobic Nature: Due to the acetyl groups, this compound becomes less soluble in water and more soluble in organic solvents, making it valuable in various chemical processes.
  • Chemical Reactions: It serves as a reagent in numerous chemical reactions, including acetylation and protection of hydroxyl groups in organic synthesis.
  • Analytical Chemistry: In analytical chemistry, β-D-Glucose Pentaacetate is used to derivatize carbohydrates, enabling their analysis and quantification through techniques like gas chromatography.
  • Biological and Medicinal Research: This compound can find applications in pharmaceutical research, particularly in drug development involving carbohydrate-based molecules.
  • Scientific Innovation: Researchers continue to explore the potential applications of β-D-Glucose Pentaacetate, making it a molecule of interest in various scientific fields.
  • Elevate Your Chemical Understanding: Understanding the significance and potential of β-D-Glucose Pentaacetate, CAS 604-69-3, underscores its importance in the fields of organic chemistry, analytical chemistry, and chemical research.

Whether you're a chemist conducting innovative experiments, a researcher unlocking the secrets of complex molecules, or someone intrigued by the diverse applications of chemistry, unveiling the potential of β-D-Glucose Pentaacetate offers profound insights into its pivotal role in advancing scientific knowledge and driving chemical progress.
Your journey to discover the significance of this compound, from its chemical transformations to its contributions to research and industry, begins here. Delve into its uses to gain a deeper understanding of its vital place in advancing scientific knowledge and supporting innovation in the world of chemistry. Embrace the possibilities of a molecule that transforms our understanding of the sweet world of glucose.
 

Application


β-D-Glucose pentaacetate, with the CAS number 604-69-3, is a chemically modified form of glucose. It is also known as glucose pentaacetate. Here is its main usage:

  1. Chemical synthesis: β-D-Glucose pentaacetate is commonly used in organic chemical synthesis as a protecting group for the hydroxyl (OH) groups of glucose. By acetylating the hydroxyl groups, β-D-glucose pentaacetate can temporarily block their reactivity during chemical reactions. This protection allows selective functionalization or modification of other parts of the glucose molecule. After completing the desired reactions, the acetyl groups can be removed to regenerate the original glucose molecule.

It's important to note that β-D-Glucose pentaacetate is primarily used in laboratory settings for chemical research and synthesis purposes. It is not intended for human consumption or application in food, drugs, or other consumer products.
If you are considering using or working with β-D-Glucose pentaacetate or any other chemical compound, it is essential to adhere to proper safety precautions, handle the substance in a well-equipped laboratory, and follow the guidance and regulations provided by relevant authorities, such as safety data sheets (SDS) and local regulations for chemical handling and disposal.
 


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