1,3,4,6-Tetra-O-acetyl-β-D-galacosamine Hydrochloride

≥98%

Reagent Code: #103627
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CAS Number 34948-62-4

science Other reagents with same CAS 34948-62-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 383.10 g/mol
Formula C₁₄H₂₂ClNO₉
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used primarily in biochemical research, this compound serves as a key intermediate in the synthesis of complex carbohydrates and glycoconjugates. It is particularly valuable in the preparation of glycosylated molecules, which are essential for studying cell-surface interactions and carbohydrate-based drug development. Its acetylated form allows for controlled deprotection, enabling precise modification of sugar moieties in oligosaccharide synthesis. Additionally, it plays a role in the production of glycosaminoglycans, which are important for understanding extracellular matrix biology and developing therapeutics for conditions like osteoarthritis and wound healing. Its hydrochloride form enhances solubility, making it suitable for various organic and aqueous reaction conditions.

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

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,190.00
inventory 5g
10-20 days ฿5,360.00

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1,3,4,6-Tetra-O-acetyl-β-D-galacosamine Hydrochloride
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Used primarily in biochemical research, this compound serves as a key intermediate in the synthesis of complex carbohydrates and glycoconjugates. It is particularly valuable in the preparation of glycosylated molecules, which are essential for studying cell-surface interactions and carbohydrate-based drug development. Its acetylated form allows for controlled deprotection, enabling precise modification of sugar moieties in oligosaccharide synthesis. Additionally, it plays a role in the production of glycosa
Used primarily in biochemical research, this compound serves as a key intermediate in the synthesis of complex carbohydrates and glycoconjugates. It is particularly valuable in the preparation of glycosylated molecules, which are essential for studying cell-surface interactions and carbohydrate-based drug development. Its acetylated form allows for controlled deprotection, enabling precise modification of sugar moieties in oligosaccharide synthesis. Additionally, it plays a role in the production of glycosaminoglycans, which are important for understanding extracellular matrix biology and developing therapeutics for conditions like osteoarthritis and wound healing. Its hydrochloride form enhances solubility, making it suitable for various organic and aqueous reaction conditions.
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