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Structure of 2411871-30-0
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N-Fmoc-4-methyl-L-tryptophan is a sterically tuned, bench-stable amino acid derivative featuring a protected α-amino group and a para-methylated indole side chain. This configuration enhances solubility in organic solvents while preserving reactivity for solid-phase peptide synthesis. The Fmoc group enables efficient sequential coupling, and the methyl substitution reduces aggregation tendencies during chain elongation. Ideal for incorporating tryptophan analogs into bioactive peptides with improved metabolic stability.
N-Fmoc-4-methyl-L-tryptophan serves as a versatile building block for peptide synthesis, enabling site-specific incorporation of tryptophan derivatives with enhanced stability and solubility. The Fmoc group facilitates efficient removal under mild basic conditions, while the 4-methyl substitution provides steric and electronic modulation advantageous in peptidomimetic design. Its bench-stable nature and compatibility with standard coupling protocols make it ideal for iterative solid-phase synthesis and the construction of complex bioactive scaffolds.
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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
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: