Trimethyl(2-(stearoyloxy)ethyl)ammonium chloride

Base Information

Chemical Name:Trimethyl(2-(stearoyloxy)ethyl)ammonium chloride
CAS No.:25234-57-5
Molecular Formula:C23H48 N O2 . Cl
Molecular Weight:406.093
Hs Code.:2923900090
European Community (EC) Number:246-744-1
DSSTox Substance ID:DTXSID90948083
Mol file:25234-57-5.mol

Synonyms:25234-57-5;Trimethyl(2-(stearoyloxy)ethyl)ammonium chloride;EINECS 246-744-1;trimethyl(2-octadecanoyloxyethyl)azanium;chloride;Trimethyl[2-(stearoyloxy)ethyl]ammonium chloride;SCHEMBL1517489;DTXSID90948083;N,N,N-Trimethyl-2-(octadecanoyloxy)ethan-1-aminium chloride

Suppliers and Price of Trimethyl(2-(stearoyloxy)ethyl)ammonium chloride

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

TRC
StearoylcholineChloride
500mg
$ 690.00

Total 4 raw suppliers

Chemical Property of Trimethyl(2-(stearoyloxy)ethyl)ammonium chloride

Chemical Property:

Melting Point:171 - 174 °C
Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：26.30000
Density:g/cm³
LogP:3.50130
Storage Temp.:Hygroscopic, Refrigerator, under inert atmosphere
Solubility.:Chloroform (Slightly), Methanol (Slightly)
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:20
Exact Mass:405.3373575
Heavy Atom Count:27
Complexity:310

Purity/Quality:

99% ^*data from raw suppliers

StearoylcholineChloride ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCCCCCCCCCC(=O)OCC[N+](C)(C)C.[Cl-]
Uses Stearoylcholine Chloride is used in the preparation of a viscoelastic-based surfactant as an oil displacement agent. Cationic lipid.

Technology Process of Trimethyl(2-(stearoyloxy)ethyl)ammonium chloride

There total 4 articles about Trimethyl(2-(stearoyloxy)ethyl)ammonium chloride 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:

: 1119-75-1
2-chloroethyl stearate

: 75-50-3
trimethylamine

: 25234-57-5
O-stearoylcholine chloride

Guidance literature:: In N,N-dimethyl-formamide; at 75 - 80 ℃; for 8 - 9h;

Reference yield:

: 74-87-3
methylene chloride

: 40817-19-4
Palmitinsaeure-2-(dimethylamino)ethylester

: 39840-30-7
Stearinsaeure-2-(dimethylamino)ethylester

: 25234-57-5
O-stearoylcholine chloride

: 2932-74-3
trimethyl-(2-palmitoyloxy-ethyl)-ammonium; chloride

Guidance literature:: In ethanol; at 100 ℃; for 3h;

Reference yield:

: 57-11-4
stearic acid

: 25234-57-5
O-stearoylcholine chloride

Guidance literature:: Multi-step reaction with 3 steps

1: dmap; dicyclohexyl-carbodiimide / benzene; dichloromethane / 0 - 20 °C / Inert atmosphere

2: dichloromethane / 0 °C

3: sodium chloride

With dmap; dicyclohexyl-carbodiimide; sodium chloride; In dichloromethane; benzene;
DOI:10.1021/jp403964k