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Catalog Number:
22004
CAS Number:
4064-06-6
1,2,3,4-Di- O -isopropylidène-α-D-galactopyranose
Purity:
≥ 96,5 % (CG)
Documents
$36.65 /5G
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Product Information

1,2,3,4-Di-O-isopropylidene-a-D-galactopyranose is a versatile carbohydrate derivative that plays a significant role in organic synthesis and carbohydrate chemistry. This compound is recognized for its protective group capabilities, particularly in the synthesis of glycosides and oligosaccharides. Its unique structure allows for selective reactions, making it an essential reagent in the development of complex carbohydrates. Researchers and industry professionals utilize this compound to enhance the stability and solubility of sugars during various chemical processes, facilitating the study of carbohydrate interactions and properties.

In addition to its synthetic applications, 1,2,3,4-Di-O-isopropylidene-a-D-galactopyranose is also valuable in the pharmaceutical industry for drug formulation and delivery systems. Its ability to form stable complexes with other molecules can improve the bioavailability of active pharmaceutical ingredients. This compound's distinctive features, such as its high stability and ease of handling, make it a preferred choice for researchers looking to streamline their synthesis processes and improve the efficiency of their experiments.

CAS Number
4064-06-6
Purity
≥ 96,5 % (CG)
Molecular Formula
C12H20O6
Molecular Weight
260.28
MDL Number
MFCD00063225
PubChem ID
19984
Appearance
Huile jaune
Optical Rotation
[a] 20 D = -57 à -61 ° (C=3 dans CHCl 3 )
Conditions
Conserver à 0 - 8 °C
General Information
CAS Number
4064-06-6
Purity
≥ 96,5 % (CG)
Molecular Formula
C12H20O6
Molecular Weight
260.28
MDL Number
MFCD00063225
PubChem ID
19984
Appearance
Huile jaune
Optical Rotation
[a] 20 D = -57 à -61 ° (C=3 dans CHCl 3 )
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

1,2,3,4-Di-O-isopropylidene-a-D-galactopyranose is widely utilized in research focused on:

  • Carbohydrate Chemistry: This compound serves as a protective group in the synthesis of various carbohydrates, allowing researchers to manipulate sugar structures without affecting their functional groups.
  • Drug Development: It plays a crucial role in the formulation of glycosylated drugs, enhancing their stability and bioavailability, which is vital for effective therapeutic applications.
  • Biotechnology: The compound is used in the preparation of glycoproteins, which are essential for vaccine development and other biopharmaceuticals, providing a means to improve immune responses.
  • Food Industry: It can be applied in the development of sugar substitutes and sweeteners, offering a way to create low-calorie products without sacrificing taste.
  • Analytical Chemistry: This chemical is utilized in the analysis of carbohydrate structures, aiding researchers in understanding complex carbohydrate interactions and behaviors in various environments.

Citations