(+)-Palmitoylcarnitine

Base Information

Chemical Name:(+)-Palmitoylcarnitine
CAS No.:2364-66-1
Molecular Formula:C₂₃H₄₅NO₄
Molecular Weight:399.615
Hs Code.:
DSSTox Substance ID:DTXSID601126847
Wikipedia:Palmitoylcarnitine
Metabolomics Workbench ID:50935
ChEMBL ID:CHEMBL2216787
Mol file:2364-66-1.mol

Synonyms:(+)-Palmitoylcarnitine;D-Palmitylcarnitine;Palmitoyl d-carnitine;(+)-Palmitylcarnitine;(S)-palmitoylcarnitine;Palmitoyl-D(+)-carnitin [German];Palmitoyl-D(+)-carnitin;2364-66-1;CHEMBL2216787;1-Propanaminium, 3-carboxy-N,N,N-trimethyl-2-[(1-oxohexadecyl)oxy]-, inner salt, (2S)-;Ammonium, (3-carboxy-2-hydroxypropyl)trimethyl-, hydroxide, inner salt, palmitate, D-;(3S)-3-palmitoyloxy-4-(trimethylammonio)butanoate;(3S)-3-hexadecanoyloxy-4-(trimethylammonio)butanoate;PALMITOYLCARNITINE;C23-H45-N-O4;(+)-(S)-Palmitoylcarnitine;SCHEMBL187668;(3S)-3-hexadecanoyloxy-4-(trimethylazaniumyl)butanoate;DTXSID601126847;BDBM50403025;LMFA07070079;LS-17082;LS-17083

Suppliers and Price of (+)-Palmitoylcarnitine

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 1 raw suppliers

Chemical Property of (+)-Palmitoylcarnitine

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:g/cm³
XLogP3:7.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:19
Exact Mass:399.33485892
Heavy Atom Count:28
Complexity:398

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCCCCCCCC(=O)OC(CC(=O)[O-])C[N+](C)(C)C
Isomeric SMILES:CCCCCCCCCCCCCCCC(=O)O[C@@H](CC(=O)[O-])C[N+](C)(C)C

Technology Process of (+)-Palmitoylcarnitine

There total 9 articles about (+)-Palmitoylcarnitine 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: