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Structure of 98266-33-2
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Boc-D-3-Pal-OH features a protected D-3-palmitic acid derivative with enhanced stability and solubility in organic solvents. This bench-stable reagent integrates seamlessly into peptide synthesis workflows, enabling efficient incorporation of hydrophobic side chains. The Boc group facilitates straightforward deprotection under mild acidic conditions, while the primary alcohol supports further functionalization.
Boc-D-3-Pal-OH serves as a key chiral building block for the synthesis of bioactive peptides and heterocyclic scaffolds. The Boc-protected D-3-phenylalanine moiety offers enhanced stability and compatibility with standard peptide coupling protocols, enabling efficient incorporation into complex molecular architectures. Its orthogonality to other functional groups and favorable purification profile make it well-suited for iterative synthetic sequences in medicinal chemistry and process development.
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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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: