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H-Lys(Z)-OH

ALDRICH/96840 - ≥99.0% (NT)

Synonym: Nε-Z-L-lysine; N6-Carbobenzyloxy-L-lysine

CAS Number: 1155-64-2
Empirical Formula (Hill Notation): C14H20N2O4
Molecular Weight: 280.32
EC Number: 214-585-7
MDL Number: MFCD00002638
Linear Formula: C6H5CH2OOCNH(CH2)4CH(NH2)COOH
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-96840-10G 10 g
 $93.00
1/EA		 Add To Favorites
45-96840-50G 50 g
 $263.00
1/EA		 Add To Favorites

 

application(s) peptide synthesis
assay ≥99.0% (NT)
form powder
InChI 1S/C14H20N2O4/c15-12(13(17)18)8-4-5-9-16-14(19)20-10-11-6-2-1-3-7-11/h1-3,6-7,12H,4-5,8-10,15H2,(H,16,19)(H,17,18)/t12-/m0/s1
InChI key CKGCFBNYQJDIGS-LBPRGKRZSA-N
mp 259 °C (dec.) (lit.)
optical activity [α]20/D +15.5±1°, c = 1% in 1 M HCl
reaction suitability reaction type: solution phase peptide synthesis
SMILES string N[C@@H](CCCCNC(=O)OCc1ccccc1)C(O)=O
Application: H-Lys(Z)-OH serves as a reactant for the synthesis of various peptides such as boc-Glu(OBzl)-Lys(Z)-OH and tert-butyl-6-(((benzyloxy)carbonyl)amino)-2-bromohexanoate. Additionally, it is used in the Fuchs-Farthing method to synthesize lysine NCA, which is a block copolymer.
General description: H-Lys(Z)-OH also known as N6-carbobenzyloxy-L-lysine, commonly used as a reagent in the synthesis of peptides.
Packaging: 10, 50 g in glass bottle
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity ≥99.0% (NT)
mp 259 °C (dec.) (lit.)
UNSPSC 12352209

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