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*For research and further manufacturing use only, not for direct human use.
Structure of 2185-16-2
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(S)-5-Acetamido-2-aminopentanoic acid is a chiral amino acid derivative featuring a pendant acetamido group at the C5 position. This configuration enables selective incorporation into peptide sequences, enhancing solubility and metabolic stability in bioactive molecule design. The molecule's bifunctional amine and carboxylate moieties support efficient coupling reactions under standard conditions.
(S)-5-Acetamido-2-aminopentanoic acid serves as a valuable chiral building block in peptide synthesis and medicinal chemistry, enabling the construction of bioactive scaffolds with defined stereochemistry. Its amine and carboxylic acid functionalities support diverse coupling reactions, while the acetamido group enhances metabolic stability and modulates solubility. The compound exhibits excellent bench stability and is readily purified by standard techniques, facilitating its use in both small-scale research and process development 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: