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Fmoc-Lys(Me)3-OH Chloride

ALDRICH/F5062 - ≥97%

Synonym: Fmoc-Lys(Me3Cl)-OH; N-alpha-Fmoc-N-alpha-trimethyl-N-L-lysine · chloride

CAS Number: 201004-29-7
Empirical Formula (Hill Notation): C24H31ClN2O4
Molecular Weight: 446.97
MDL Number: MFCD00672333
Linear Formula: C24H31ClN2O4
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-F5062-500MG 500 mg
 $378.00
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45-F5062-2.5G 2.5 g
 $1350.00
1/EA		 Add To Favorites
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application(s) peptide synthesis
assay ≥97%
form liquid
functional group Fmoc
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
InChI key XUJRNPVABVHOAJ-FTBISJDPSA-N
Quality Level 100 
reaction suitability reaction type: Fmoc solid-phase peptide synthesis
shipped in dry ice
SMILES string Cl.[N+](CCCC[C@H](N=C([O-])OCC1c2c(cccc2)c3c1cccc3)C(=O)O)(C)(C)C
storage temp. −20°C
Application: 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.
General description: Fmoc protected N-trimethyl lysine
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥97%
Storage Temp. −20°C
UNSPSC 12352209

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