Gas Chromatography

Structure confirmed. Purity = 98%. Will ship with Certificate of Analysis (CoA)

Structure confirmed. Purity = 98%. Will ship with Certificate of Analysis (CoA)

Structure confirmed. Purity = 98%. Will ship with Certificate of Analysis (CoA)

A TFA-labile trialkoxybenzhydryl-type linker ideally suited for the preparation of peptide amides using Fmoc-strategy [1] . Literature references [1] M.

A TFA-labile trialkoxybenzhydryl-type linker ideally suited for the preparation of peptide amides using Fmoc-strategy [1] . Literature references [1] M.

A TFA-labile trialkoxybenzhydryl-type linker ideally suited for the preparation of peptide amides using Fmoc-strategy [1] . Literature references [1] M.

A derivative for the introduction of symmetric dimethyl-arginine during Fmoc SPPS. Coupling can be carried out using any standard activation method.

A derivative for the introduction of symmetric dimethyl-arginine during Fmoc SPPS. Coupling can be carried out using any standard activation method.

Building block for the introduction of selenocysteine during Fmoc SPPS [1,2,3] . Selenocysteine derivatives can undergo enantiomerization during coupling and can form dehydroalanine and &#946-piperidinylalanine containing side products during

Standard building block for introduction of statine amino-acid residues by Fmoc SPPS Associated Protocols and Technical Articles Cleavage and Deprotection Protocols for Fmoc SPPS Linkage Replaces: 04-12-1053 Analysis Note Colour (visual): white to

An excellent building block for the preparation of phosphothreonine-containing peptides [1,2] by Fmoc SPPS. This derivative can be introduced using standard activation methods, such as PyBOP &#174 and TBTU.

Pre-formed pentafluorophenyl ester for coupling of threonine amino-acid residues by Fmoc SPPS. Use enables bromophenol blue monitoring of amide bond formation.