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Structure of 2304-94-1
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Z-β-Ala-OH features a stabilized Z-configured enolizable amide with enhanced resistance to racemization under standard conditions. This bench-stable derivative integrates readily into peptide synthesis workflows, offering reliable access to stereodefined β-amino acid scaffolds without requiring cryogenic handling or specialized reagents.
Z-β-Ala-OH serves as a valuable building block in peptide synthesis, offering enhanced stability and reduced racemization during coupling. Its Z (benzyloxycarbonyl) protection group provides excellent orthogonality and facilitates selective deprotection in multi-step sequences. The β-alanine backbone enables incorporation into peptidomimetics and bioactive oligomers, with proven utility in solid-phase and solution-phase syntheses.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H318
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: