1,2,3,4,6-Penta-O-acetyl-b-D-mannopyranose

≥98%

Reagent Code: #103607
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CAS Number 4026-35-1

science Other reagents with same CAS 4026-35-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 390.34 g/mol
Formula C₁₆H₂₂O₁₁
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of complex carbohydrates and glycoconjugates. It is widely employed in the pharmaceutical industry for the development of glycosylated drugs, which are crucial in treatments targeting cancer, infections, and immune disorders. Additionally, it plays a significant role in carbohydrate chemistry research, facilitating the study of glycosylation processes and the synthesis of oligosaccharides. Its acetylated form enhances stability and reactivity, making it a valuable reagent in the preparation of mannose derivatives for biochemical and medicinal applications.

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Test Parameter Specification
Appearance White To Off-White Solid
Purity (%) 97.5-100
Infrared Spectrum Conforms To Structure

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,120.00
inventory 250mg
10-20 days ฿10,680.00
inventory 1g
10-20 days ฿25,740.00

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1,2,3,4,6-Penta-O-acetyl-b-D-mannopyranose
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Used primarily in organic synthesis, this compound serves as a key intermediate in the production of complex carbohydrates and glycoconjugates. It is widely employed in the pharmaceutical industry for the development of glycosylated drugs, which are crucial in treatments targeting cancer, infections, and immune disorders. Additionally, it plays a significant role in carbohydrate chemistry research, facilitating the study of glycosylation processes and the synthesis of oligosaccharides. Its acetylated for

Used primarily in organic synthesis, this compound serves as a key intermediate in the production of complex carbohydrates and glycoconjugates. It is widely employed in the pharmaceutical industry for the development of glycosylated drugs, which are crucial in treatments targeting cancer, infections, and immune disorders. Additionally, it plays a significant role in carbohydrate chemistry research, facilitating the study of glycosylation processes and the synthesis of oligosaccharides. Its acetylated form enhances stability and reactivity, making it a valuable reagent in the preparation of mannose derivatives for biochemical and medicinal applications.

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