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*For research and further manufacturing use only, not for direct human use.
Structure of 34948-62-4
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This acetylated galactosamine derivative features four acetyl groups strategically positioned at the 1,3,4,6-positions, enhancing solubility and stability in organic media. The hydrochloride salt form ensures improved crystallinity and handling ease, enabling reliable use in glycoconjugate synthesis and carbohydrate chemistry workflows.
1,3,4,6-Tetra-O-acetyl-β-D-galacosamine (hydrochloride) serves as a stable, bench-ready glycosyl donor for the synthesis of β-linked galactosides. The acetyl groups provide enhanced solubility and protection of hydroxyl functionalities, enabling high-fidelity glycosylation reactions under standard activation conditions. Its defined stereochemistry facilitates reliable construction of complex oligosaccharides and glycoconjugates in medicinal chemistry and glycobiology applications.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: