ChemicalBook--->CAS DataBase List--->201004-29-7

201004-29-7

201004-29-7 Structure

201004-29-7 Structure
IdentificationBack Directory
[Name]

FMOC-LYS(ME3)-OH HCL
[CAS]

201004-29-7
[Synonyms]

Fmoc-Lys(Me)
3-OH Chloride
Fmoc-Lys(Me)3-OH Cl
FMOC-LYS(ME3)-OH HCL
FMOC-L-LYS(ME3)-OH CL
FMOC-LYS(ME)3-OH CHLORIDE
FMoc-L-Lys(Me)3-OH chloride
FMOC-LYSINE(ME)3-OH CHLORIDE
FMOC-LYS(ME3)-OH HCL USP/EP/BP
Fmoc-Lys(Me)3-OH hydrochloride
Fmoc-Lys(Me3)-OH.chloride, >97%
Nα-Fmoc-Nε-(trimethyl)-L-lysine chloride
Fmoc-N',N',N'-trimethyl-L-lysine chloride
FMOC-N-EPSILON-(TRIMETHYL)-L-LYSINE CHLORIDE
Nα-Fmoc-Nε-(trimethyl)-L-lysine chloride≥ 98% (HPLC)
(9H-Fluoren-9-yl)MethOxy]Carbonyl Lys(Me)3-OH Chloride
N-ALPHA-FMOC-N-EPSILON,EPSILON,EPSILON-TRIMETHYL-L-LYSINE CHLORIDE
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N',N',N'-trimethyl-L-lysine chloride
5-carboxy-5-(9H-fluoren-9-ylmethoxycarbonylamino)pentyl]-trimethylazanium,chloride
N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-EPSILON-TRIMETHYLAMONIUM-L-LYSINE CHLORIDE
N-ALPHA-(9-FLUOROENYLMETHYLOXYCARBONYL)-N-EPSILON-TRIMETHYLAMONIUM-L-LYSINE CHLORIDE
N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-EPSILON,N-EPSILON,N-EPSILON-TRIMETHYL-L-LYSINE CHLORIDE
[(5S)-5-carboxy-5-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)pentyl]trimethylazanium hydrochloride
(5S)-5-Carboxy-5-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-N,N,N-trimethyl-1-pentanaminium chloride (1:1), 97%
REF DUPL: (S)-2-(((9H-fluoren-9-yl)methyl9H-fluoren-9-yl)methoxy)carbonylamino)-6-(dimethylamino)hexanoic acid hydrochloride
[Molecular Formula]

C24H31N2O4.Cl
[MDL Number]

MFCD01861330
[MOL File]

201004-29-7.mol
[Molecular Weight]

446.97
Chemical PropertiesBack Directory
[storage temp. ]

-15°C
Safety DataBack Directory
[HazardClass ]

IRRITANT
Hazard InformationBack Directory
[Chemical Properties]

White to off-white powder
[Uses]

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
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