(S)-2,3-Bis(stearoyloxy)propyl (2-(trimethylammonio)ethyl) phosphate

Base Information

Chemical Name:(S)-2,3-Bis(stearoyloxy)propyl (2-(trimethylammonio)ethyl) phosphate
CAS No.:66701-63-1
Molecular Formula:C44H88NO8P
Molecular Weight:790.158
Hs Code.:
DSSTox Substance ID:DTXSID00862423

Synonyms:66701-63-1;(S)-2,3-Bis(stearoyloxy)propyl (2-(trimethylammonio)ethyl) phosphate;SCHEMBL22693933;DTXSID00862423;[(2S)-2,3-di(octadecanoyloxy)propyl] 2-(trimethylazaniumyl)ethyl phosphate

Suppliers and Price of (S)-2,3-Bis(stearoyloxy)propyl (2-(trimethylammonio)ethyl) phosphate

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 0 raw suppliers

Chemical Property of (S)-2,3-Bis(stearoyloxy)propyl (2-(trimethylammonio)ethyl) phosphate

Chemical Property:

PSA：121.00000
LogP:13.24240
XLogP3:15.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:44
Exact Mass:789.62475576
Heavy Atom Count:54
Complexity:888

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCCCCCCCCCC(=O)OCC(COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCCCCCC
Isomeric SMILES:CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](COP(=O)([O-])OCC[N+](C)(C)C)OC(=O)CCCCCCCCCCCCCCCCC

Technology Process of (S)-2,3-Bis(stearoyloxy)propyl (2-(trimethylammonio)ethyl) phosphate

There total 21 articles about (S)-2,3-Bis(stearoyloxy)propyl (2-(trimethylammonio)ethyl) phosphate 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: 67.0%

: 57-11-4
stearic acid

: 816-94-4,4539-70-2,66701-63-1,816-93-3,18603-43-5
{2-[(2,3-bis-stearoyloxy-propoxy)-hydroxy-phosphoryloxy]-ethyl}-trimethyl-ammonium betaine

Guidance literature:: stearic acid; With dicyclohexyl-carbodiimide; In dichloromethane; for 2h; Reflux;

alumina-supported glycerophosphatidylcholine; In dichloromethane; Solvent;

Reference yield: 54.5%

: 51063-97-9
DL-α,β-distearin

: 55357-38-5
choline tosylate

: 816-94-4,4539-70-2,66701-63-1,816-93-3,18603-43-5
{2-[(2,3-bis-stearoyloxy-propoxy)-hydroxy-phosphoryloxy]-ethyl}-trimethyl-ammonium betaine

Guidance literature:: DL-α,β-distearin; With triethylamine; trichlorophosphate; In chloroform; at 10 ℃; for 4.5h; Inert atmosphere;

choline tosylate; With pyridine; In chloroform; for 15.5h; Inert atmosphere;

Reference yield:

: 111-63-7,9003-95-6
vinyl stearate

: 34688-34-1,563-24-6
glycerolcholine phosphate

: 816-94-4,4539-70-2,66701-63-1,816-93-3,18603-43-5
{2-[(2,3-bis-stearoyloxy-propoxy)-hydroxy-phosphoryloxy]-ethyl}-trimethyl-ammonium betaine

: 17364-19-1,5655-17-4
1-stearoyl-sn-glycero-3-phosphocholine

: 57-11-4
stearic acid

Guidance literature:: Lecitase surfactant-coated (modified)-immobilized enzyme complex on Duolite A₅₆₈; In tert-butyl alcohol; at 60 - 70 ℃; for 96.5 - 200h; Enzyme kinetics; Enzymatic reaction;