N2-(1-Oxohexadecyl)-L-lysine

Base Information

Chemical Name:N2-(1-Oxohexadecyl)-L-lysine
CAS No.:59866-71-6
Molecular Formula:C22H44 N2 O3
Molecular Weight:384.603
Hs Code.:
European Community (EC) Number:261-964-8
UNII:F1ADG5H0OT
DSSTox Substance ID:DTXSID00975269
Nikkaji Number:J298.248J
Mol file:59866-71-6.mol

Synonyms:alpha(N)-palmitoy-L-lysine

Suppliers and Price of N2-(1-Oxohexadecyl)-L-lysine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 5 raw suppliers

Chemical Property of N2-(1-Oxohexadecyl)-L-lysine

Chemical Property:

Vapor Pressure:2.28E-14mmHg at 25°C
Boiling Point:567.6°C at 760 mmHg
Flash Point:297.1°C
PSA：92.42000
Density:0.97g/cm³
LogP:6.25730
XLogP3:4.3
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:20
Exact Mass:384.33519327
Heavy Atom Count:27
Complexity:362

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCCCCCCCCCCCCC(=O)NC(CCCCN)C(=O)O
Isomeric SMILES:CCCCCCCCCCCCCCCC(=O)N[C@@H](CCCCN)C(=O)O

Technology Process of N2-(1-Oxohexadecyl)-L-lysine

There total 9 articles about N2-(1-Oxohexadecyl)-L-lysine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 97.5%

: N-2-palmitoyl-N-6-tert-butoxycarbonyl-L-lysine

: 59866-71-6
N-2-palmitoyl-L-lysine

Guidance literature:: With trifluoroacetic acid; at 20 ℃; for 5h;

Reference yield:

: N--palmitoyl-N--t-BOC-L-lysine-t-butyl ester

: 59866-71-6
N-2-palmitoyl-L-lysine

Guidance literature:: With ammonium hydroxide; trifluoroacetic acid; In methanol; dichloromethane;

Reference yield:

: 2418-95-3
(S)-2-amino-6-(tert-butoxycarbonylamino)hexanoic acid

: 59866-71-6
N-2-palmitoyl-L-lysine

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / water; tetrahydrofuran / 1 h

2: trifluoroacetic acid / 5 h / 20 °C

With potassium carbonate; trifluoroacetic acid; In tetrahydrofuran; water;