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Merck
CN

859095

Nα-Acetyl-L-lysine methyl ester hydrochloride

98%

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About This Item

Linear Formula:
H2N(CH2)4CH(NHCOCH3)CO2CH3·HCl
CAS Number:
Molecular Weight:
238.71
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
244-111-4
MDL number:
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Quality Level

assay

98%

form

powder

optical activity

[α]22/D −18°, c = 10 in 6 M HCl

reaction suitability

reaction type: solution phase peptide synthesis

mp

108-114 °C (lit.)

application(s)

peptide synthesis

SMILES string

Cl.COC(=O)[C@H](CCCCN)NC(C)=O

InChI

1S/C9H18N2O3.ClH/c1-7(12)11-8(9(13)14-2)5-3-4-6-10;/h8H,3-6,10H2,1-2H3,(H,11,12);1H/t8-;/m0./s1

InChI key

PCHGTXYLEAQWOM-QRPNPIFTSA-N



Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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Xiaoyun Xu et al.
Journal of the American Chemical Society, 130(2), 703-709 (2007-12-18)
The reaction between N(alpha)-acetyllysine methyl ester (Lys) and 2'-deoxyguanosine (dGuo) was used to study structural aspects of DNA-protein cross-link (DPC) formation. The precise structure of DPCs depended on the nature of the oxidant and cross-linking reactions in which a series
H Nakayama et al.
Journal of immunological methods, 140(1), 119-125 (1991-06-24)
Antibodies directed against advanced glycosylation end products (AGEs) formed during a Maillard reaction have been generated and characterized. Since protein-bound AGEs recognized by the antibodies were labile to acid hydrolysis, the antibodies were further characterized by using the AGE-alpha-acetyl-L-lysine methyl
S J George et al.
Journal of vascular research, 38(5), 492-501 (2001-09-19)
The focus of this study was identification of the contribution of the plasminogen activator-plasmin system to smooth muscle cell proliferation and migration in human saphenous vein. Segments of human saphenous vein were grown in organ culture for up to 14



Global Trade Item Number

SKUGTIN
859095-100MG04061832643083