F5062

Fmoc-Lys(Me)₃-OH Chloride

≥97%, for peptide synthesis

• Synonym(e): Fmoc-Lys(Me₃Cl)-OH, N-alpha-Fmoc-N-alpha-trimethyl-N-L-lysine · chloride
• Empirische Formel (Hill-System): C₂₄H₃₁ClN₂O₄
• CAS-Nummer: 201004-29-7
• Molekulargewicht: 446.97
• UNSPSC-Code: 12352209
• NACRES: NA.26

Eigenschaften

• product name: Fmoc-Lys(Me)₃-OH Chloride, ≥97%
• Assay: ≥97%
• Form: liquid
• Eignung der Reaktion: reaction type: Fmoc solid-phase peptide synthesis
• Anwendung(en): peptide synthesis
• Funktionelle Gruppe: Fmoc
• Versandbedingung: dry ice
• Lagertemp.: −20°C
• InChI: 1S/C24H30N2O4.ClH/c1-26(2,3)15-9-8-14-22(23(27)28)25-24(29)30-16-21-19-12-6-4-10-17(19)18-11-5-7-13-20(18)21;/h4-7,10-13,21-22H,8-9,14-16H2,1-3H3,(H-,25,27,28,29);1H/t22-;/m0./s1
• InChIKey: XUJRNPVABVHOAJ-FTBISJDPSA-N

Beschreibung

Allgemeine Beschreibung

Fmoc protected N-trimethyl lysine

Anwendung

Fmoc-Lys(Me)₃-OH chloride is one of the common N-terminal protected reagents used in the peptide synthesis. Some of the reported examples are:

• Synthesis of peptide linkers for monoclonal antibody-auristatin F conjugates.
• Preparation of multifunctional reagents with enhanced ionization properties for the analysis of protein modification in human cells and dynamic profiling of protein lipidation.
• Sequential peptide ligation to synthesize histone H3 containing a trimethyl lysine residue, with modified tail region.

Sicherheitshinweise

• Lagerklassenschlüssel: 10 - Combustible liquids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable