Radiopharmaceuticals and contrast media

Application Fmoc- L -Lys(Nvoc)-OH is a lysine derivative compatible with solid-phase peptide synthesis (SPPS). The photolabile, N -terminal protecting group nitroveratryloxycarbonyl (NVOC) can be cleaved by photolysis at 350 nm.

Synonyms: Fmoc-3-D-Ala(2-furyl)-OH(R)-2-(Fmoc-amino)-3-(2-furyl)propionic acid Purity Limit: &ge 98% (HPLC, Chiral purity) CAS No.: 220497-85-8 Molecular Formula: C22H19NO5 Molecular Weight: 377.

Fmoc-acoc-OH (100MG)

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

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

Useful derivative for introducing a side chain aldehyde functionality. The aldehyde group once protected is highly reactive and will self-condense to amine, hydroxyl and thiol functionalities in the peptide, making various cyclic and polymeric

Useful derivative for introducing a side chain aldehyde functionality. The aldehyde group once protected is highly reactive and will self-condense to amine, hydroxyl and thiol functionalities in the peptide, making various cyclic and polymeric

Fmoc-Aeg-OH.

Fmoc-Aeg-OH.

Standard building block for introduction of aminoisobutyric amino-acid residues by Fmoc SPPS Associated Protocols and Technical Articles Cleavage and Deprotection Protocols for Fmoc SPPS Linkage Replaces: 04-12-1100 Analysis Note Color (visual):

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

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