Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 1033622-38-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This fluorenylmethoxycarbonyl-protected amino acid derivative features a propargylamine handle enabling efficient copper-catalyzed azide-alkyne cycloaddition. The orthogonal functionality supports site-specific conjugation in peptide synthesis and bioconjugation workflows. Bench-stable under standard conditions, it integrates seamlessly into solid-phase protocols for modular peptide assembly.
2-({[(9H-fluoren-9-yl)methoxy]carbonyl}(prop-2-yn-1-yl)amino)acetic acid serves as a versatile protected amino acid building block for peptide synthesis, combining the robustness of Fmoc (fluoren-9-ylmethoxycarbonyl) protection with a propargylamine side chain. The alkyne functionality enables efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC), facilitating site-specific conjugation and diversity-oriented synthesis. Bench-stable and compatible with standard coupling protocols, it supports reliable purification and integration into complex peptide architectures.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: