DL-methionine Partners, long-term Cooperation
The methylthio group is the most distinctive functional group in DL-methionine and can participate in substitution and addition reactions. Alkylation substitution reaction: The sulfur atom in the methylthio group has a lone pair of electrons, making it a nucleophilic site that can react with alkyl halides (e.g., methyl iodide) to form sulfonium salts. This reaction is the basis for the synthesis of methionine derivatives with enhanced biological activity. Cleavage reaction: Under the action of strong nucleophiles (e.g., sodium hydroxide in the presence of hydrogen peroxide) or enzymes (e.g., methionine lyase), the C-S bond in the methylthio group can be cleaved, producing homocysteine and methanethiol. In biological systems, this cleavage reaction is catalyzed by specific enzymes and is a key step in methionine metabolism.
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DL-Methionine 59-51-8 |
Appearance and Crystal Morphology of DL-MethionineAt room temperature and normal pressure, DL-methionine exists as a white, odorless crystalline po... |
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L-Methionine |
Chemical and Physical Properties of L-Methionine L-Methionine has the molecular formula C₅H₁₁NO₂S and a molecular weight of 149.21. Its chemical s... |
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High quality L-Cysteine hydrochloride monohydrate |
The storage methods for L-Cysteine hydrochloride monohydrate are crucial to maintain its stability and functionality, primarily due to its hygrosco... |
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L-Cysteine hydrochloride monohydrate Supply Price |
Hygroscopic Properties of L-Cysteine hydrochloride monohydrateL-Cysteine hydrochloride monohydrate readily forms hydrates or dissolves in absorbed ... |
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Bulk supply L-Cysteine hydrochloride monohydrate |
Special Considerations for Different Grades1. Food/G pharmaceutical GradeCompliance with Regulations: Store in facilities that meet food safety sta... |
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