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Catalog Number:
32337
CAS Number:
220017-47-0
1,2,3,4,6-Penta-O-pivaloyl-D-mannopyranose
Purity:
≥ 98% (GC)
Documents
$79.22 /100MG
Pack Size Availability Price
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Product Information

1,2,3,4,6-Penta-O-pivaloyl-D-mannopyranose is a versatile carbohydrate derivative that plays a significant role in the field of organic synthesis and carbohydrate chemistry. This compound is recognized for its protective group capabilities, particularly in glycosylation reactions, where it enhances the stability and reactivity of sugar moieties. Its unique structure allows for selective reactions, making it an invaluable tool for researchers aiming to develop complex carbohydrates and glycosides. The pivaloyl groups provide steric hindrance, which can be advantageous in controlling reaction pathways and improving yields in synthetic processes.

In addition to its synthetic applications, 1,2,3,4,6-Penta-O-pivaloyl-D-mannopyranose is utilized in the pharmaceutical industry for the development of glycosylated drugs and biologically active compounds. Its ability to modulate the solubility and bioavailability of drug candidates makes it a crucial component in drug formulation. Researchers and industry professionals can leverage this compound to streamline their synthesis processes, enhance product stability, and ultimately improve the efficacy of their pharmaceutical products.

CAS Number
220017-47-0
Purity
≥ 98% (GC)
Molecular Formula
C31H52O11
Molecular Weight
600.75
MDL Number
MFCD11112186
PubChem ID
13829681
Melting Point
167-171° C
Appearance
White to almost white crystalline powder
Optical Rotation
[a]20/D= +37 to +43° (C=1 in CHCl3
Conditions
Store at 2-8 °C
General Information
CAS Number
220017-47-0
Purity
≥ 98% (GC)
Molecular Formula
C31H52O11
Molecular Weight
600.75
MDL Number
MFCD11112186
PubChem ID
13829681
Melting Point
167-171° C
Appearance
White to almost white crystalline powder
Optical Rotation
[a]20/D= +37 to +43° (C=1 in CHCl3
Conditions
Store at 2-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

1,2,3,4,6-Penta-O-pivaloyl-D-mannopyranose is widely utilized in research focused on:

  • Carbohydrate Chemistry: This compound serves as a versatile protecting group in the synthesis of complex carbohydrates, allowing chemists to manipulate functional groups without affecting the sugar backbone.
  • Drug Development: Its unique structure can enhance the solubility and stability of pharmaceutical compounds, making it valuable in the formulation of new drugs.
  • Biotechnology: Used in glycosylation reactions, it helps in the production of glycoproteins, which are crucial for vaccine development and therapeutic proteins.
  • Food Industry: As a food additive, it can improve the texture and shelf-life of certain products, appealing to manufacturers looking for natural solutions.
  • Research Applications: It is employed in various analytical techniques, such as NMR and mass spectrometry, to study carbohydrate structures and interactions, aiding researchers in understanding biological processes.

Citations