1-palmitoyl-2-lauroyl-sn-glycerol-3-phosphocholine

Base Information

Chemical Name:1-palmitoyl-2-lauroyl-sn-glycerol-3-phosphocholine
CAS No.:82765-47-7
Molecular Formula:C₃₆H₇₂NO₈P
Molecular Weight:677.943
Hs Code.:
DSSTox Substance ID:DTXSID901104800
Wikidata:Q27145077
Metabolomics Workbench ID:13378

Synonyms:82765-47-7;1-hexadecanoyl-2-dodecanoyl-sn-glycero-3-phosphocholine;1-Palmitoyl-2-lauroyl-sn-glycero-3-PC;PC(16:0/12:0);[(2R)-2-dodecanoyloxy-3-hexadecanoyloxypropyl] 2-(trimethylazaniumyl)ethyl phosphate;1-palmitoyl-2-lauroyl-sn-glycero-3-phosphocholine;SCHEMBL2135188;CHEBI:75018;DTXSID901104800;LMGP01010557;1-C16:0-2-C12:4-phosphatidylcholine;BP-29619;PD019004;1-hexadecanoyl-2-dodecanoyl-sn-glycerophosphocholine;Q27145077;(7R)-4-Hydroxy-N,N,N-trimethyl-10-oxo-7-[(1-oxododecyl)oxy]-3,5,9-trioxa-4-phosphapentacosan-1-aminium inner salt 4-oxide;3,5,9-Trioxa-4-phosphapentacosan-1-aminium, 4-hydroxy-N,N,N-trimethyl-10-oxo-7-[(1-oxododecyl)oxy]-, inner salt, 4-oxide, (R)-

Suppliers and Price of 1-palmitoyl-2-lauroyl-sn-glycerol-3-phosphocholine

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

Cayman Chemical
1-Palmitoyl-2-lauroyl-sn-glycero-3-PC ≥95%
250mg
$ 117.00

Cayman Chemical
1-Palmitoyl-2-lauroyl-sn-glycero-3-PC ≥95%
100mg
$ 55.00

Cayman Chemical
1-Palmitoyl-2-lauroyl-sn-glycero-3-PC ≥95%
500mg
$ 220.00

AK Scientific
1-Hexadecanoyl-2-dodecanoyl-sn-glycero-3-phosphocholine
250mg
$ 257.00

AK Scientific
1-Hexadecanoyl-2-dodecanoyl-sn-glycero-3-phosphocholine
100mg
$ 174.00

Total 4 raw suppliers

Chemical Property of 1-palmitoyl-2-lauroyl-sn-glycerol-3-phosphocholine

Chemical Property:

XLogP3:11.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:36
Exact Mass:677.49955525
Heavy Atom Count:46
Complexity:765

Purity/Quality:

99% ^*data from raw suppliers

1-Palmitoyl-2-lauroyl-sn-glycero-3-PC ≥95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCC
Isomeric SMILES:CCCCCCCCCCCCCCCC(=O)OC[C@H](COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCC
Uses 1-Palmitoyl-2-lauroyl-sn-glycero-3-PC?is a carboxylate derivative and can be used as an intermediate in organic synthesis.

Technology Process of 1-palmitoyl-2-lauroyl-sn-glycerol-3-phosphocholine

There total 4 articles about 1-palmitoyl-2-lauroyl-sn-glycerol-3-phosphocholine 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: 55.0%

: 250142-22-4
2-(1-palmitoyl-2-lauroyl-sn-glycerol)-2-oxo-1,3,2-dioxaphospholane

: 75-50-3
trimethylamine

: 82765-47-7
1-palmitoyl-2-lauroyl-sn-glycerol-3-phosphocholine

Guidance literature:: With triethylamine; In acetonitrile; at 20 ℃; for 16h;
DOI:10.1021/jo990414e

Reference yield:

: 32899-42-6
1-palmitoyl-3-triphenylmethyl-sn-glycerol

: 82765-47-7
1-palmitoyl-2-lauroyl-sn-glycerol-3-phosphocholine

Guidance literature:: Multi-step reaction with 4 steps

1: 96 percent / DMAP / CHCl₃ / 48 h / 20 °C

2: 73 percent / 12N HCl / CHCl₃; methanol / 18 h / 0 °C

3: 92 percent / Et₃N / benzene / 16 h / 20 °C

4: 55 percent / Et₃N / acetonitrile / 16 h / 20 °C

With hydrogenchloride; dmap; triethylamine; In methanol; chloroform; acetonitrile; benzene; 1: Acylation / 2: Substitution / 3: Substitution / 4: Ring cleavage;
DOI:10.1021/jo990414e

Reference yield:

: 89648-22-6,177717-58-7
1-palmitoyl-2-lauroyl-sn-glycerol

: 82765-47-7
1-palmitoyl-2-lauroyl-sn-glycerol-3-phosphocholine

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / Et₃N / benzene / 16 h / 20 °C

2: 55 percent / Et₃N / acetonitrile / 16 h / 20 °C

With triethylamine; In acetonitrile; benzene; 1: Substitution / 2: Ring cleavage;
DOI:10.1021/jo990414e