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*For research and further manufacturing use only, not for direct human use.
Structure of 1927-25-9
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DL-Homoserine features a chiral β-hydroxy-α-amino acid backbone with a reactive hydroxyl group and primary amine, enabling direct incorporation into peptide synthesis or as a precursor in metabolic pathway studies. This bench-stable compound facilitates efficient derivatization under standard conditions.
DL-Homoserine serves as a key building block in the synthesis of threonine and methionine derivatives, enabling efficient access to amino acid scaffolds via standard peptide coupling and protection strategies. Its hydroxyl and carboxylic acid functionalities support orthogonal functional group manipulation, facilitating downstream transformations in medicinal chemistry and synthetic biology workflows. The compound exhibits good bench stability and is readily purified by crystallization or chromatography, supporting reliable use in multi-step syntheses.
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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: