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 91183-71-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
H-Met-OtBu·HCl delivers a stable, bench-ready sulfide handle for late-stage functionalization. The protected thioether moiety resists oxidation and integrates cleanly into peptide backbones or small-molecule scaffolds under standard coupling conditions. This moisture-tolerant reagent enables efficient incorporation of methionine analogs in synthetic workflows.
H-Met-OtBu·HCl serves as a reliable building block for peptide synthesis, offering a stable, bench-ready form of methionine with orthogonal protection. The tert-butyl ester facilitates straightforward deprotection under mild acidic conditions, while the HCl salt enhances solubility and handling. It functions effectively in standard coupling protocols, enabling efficient incorporation into peptide chains with minimal racemization.
|
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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: