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Structure of 268729-12-0
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Fmoc-O-tert-butyl-D-trans-4-hydroxyproline features a D-trans-4-hydroxyproline core protected at the hydroxyl group with a tert-butyl moiety and at the amine with an Fmoc group. This bifunctional derivative enables direct incorporation into peptide chains during solid-phase synthesis, offering enhanced solubility and stability under standard conditions. The trans configuration ensures defined stereochemistry, critical for structural integrity in bioactive peptide design.
Fmoc-O-tert-butyl-D-trans-4-hydroxyproline serves as a key chiral building block in peptide synthesis, enabling the incorporation of D-proline derivatives with defined stereochemistry. The Fmoc group provides orthogonal protection for the amine, while the O-tert-butyl ether stabilizes the 4-hydroxyl functionality under standard coupling conditions. This derivative exhibits excellent bench stability, facilitates efficient purification, and supports high-yielding amide bond formation in solid-phase and solution-phase workflows.
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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: