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Structure of 626-72-2
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L-Homocystine features a disulfide-bridged cysteine dimer with a unique α,ω-diamino acid backbone, enabling selective bioconjugation and protein crosslinking. This bench-stable, moisture-tolerant reagent integrates readily into peptide synthesis workflows, offering reliable sulfur-directed functionalization in chemical biology applications.
L-Homocystine serves as a key sulfur-containing amino acid building block for the synthesis of biologically relevant thiol-containing peptides and thioether-linked scaffolds. Its disulfide functionality enables controlled redox chemistry in peptide conjugation and protein engineering workflows. The compound exhibits sufficient bench stability for routine handling and facilitates efficient incorporation into complex molecular architectures via standard coupling protocols.
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Lot numbers can be found on the outside label of a product: