Lot numbers can be found on the outside label of a product:
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*For research and further manufacturing use only, not for direct human use.
Structure of 195316-72-4
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L-Allylglycine (hydrochloride) features a reactive allyl group positioned beta to the α-carbon, enabling efficient copper-catalyzed coupling reactions. This bench-stable derivative integrates seamlessly into peptide synthesis workflows, offering enhanced solubility and compatibility with aqueous reaction conditions.
L-Allylglycine (hydrochloride) serves as a versatile building block in peptide synthesis and medicinal chemistry, enabling site-specific incorporation of allyl functionalities for subsequent derivatization via click chemistry or transition-metal catalysis. The hydrochloride salt enhances solubility and stability in aqueous and polar organic media, facilitating straightforward handling and purification. Its compatibility with standard coupling protocols and resistance to racemization supports reliable use in complex peptide architectures and scaffold diversification.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P501
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Lot numbers can be found on the outside label of a product: