Lauroylcholine chloride

Base Information

• Chemical Name: Lauroylcholine chloride
• CAS No.: 25234-60-0
• Molecular Formula: C17H36ClNO2
• Molecular Weight: 321.931
• Hs Code.: 2923900090
• European Community (EC) Number: 246-745-7
• DSSTox Substance ID: DTXSID50948084
• Mol file: 25234-60-0.mol

Synonyms:LAUROYLCHOLINE CHLORIDE;25234-60-0;2-Lauroyloxyethyltrimethylammonium chloride;2-dodecanoyloxyethyl(trimethyl)azanium;chloride;EINECS 246-745-7;lauroylcholine chloride hydrate;C17-H36-N-O2.Cl;2-(dodecanoyloxy)-n,n,n-trimethylethanaminium chloride;Dodecanoylcholine Chloride;2-dodecanoyloxyethyl(trimethyl)azanium chloride;LAUROYLCHOLINECHLORIDE;[2-(dodecanoyloxy)ethyl]trimethylazanium chloride;SCHEMBL5316384;DTXSID50948084;AKOS024353806;CS-W009888;HY-W009172;AS-57971;D0973;FT-0670754;D89750;A877656;J-015880;2-(Dodecanoyloxy)-N,N,N-trimethylethan-1-aminium chloride;Ethanaminium,N,N,N-trimethyl-2-[(1-oxododecyl)oxy]-,chloride(1:1)

Chemical Property of Lauroylcholine chloride

Chemical Property:

• Appearance/Colour: white crystalline solid
• Vapor Pressure: 0.95Pa at 20℃
• Melting Point: 206-208°C
• PSA: 26.30000
• LogP: 1.16070
• Storage Temp.: 2-8°C
• Solubility.: Chloroform (Slightly), Methanol (Slightly)
• Water Solubility.: almost transparency
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 14
• Exact Mass: 321.2434571
• Heavy Atom Count: 21
• Complexity: 234

Purity/Quality:

99.9% ^*data from raw suppliers

Lauroylcholine Chloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCC(=O)OCC[N+](C)(C)C.[Cl-]
• Uses: Lauroylcholine Chloride (cas# 25234-60-0) is a compound useful in organic synthesis.

Technology Process of Lauroylcholine chloride

There total 2 articles about Lauroylcholine 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:

2-chloroethyl dodecanoate (64919-15-9) + trimethylamine (75-50-3) → (2-lauroyloxy-ethyl)-trimethyl-ammonium; chloride (25234-60-0)

Guidance literature:

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

Reference yield:

→ (2-lauroyloxy-ethyl)-trimethyl-ammonium; chloride (25234-60-0)

Guidance literature:

CH3(CH2)10C(O)OCH2CH2Cl in DMF, N(CH3)3, 70-80grad, 20 h;

Reference yield:

(2-lauroyloxy-ethyl)-trimethyl-ammonium; chloride (25234-60-0) + Montelukast sodium (151767-02-1) → montelukast lauro-cholinium (943438-55-9)

Guidance literature:

In ethanol; water;

upstream raw materials:

2-chloroethyl dodecanoate

trimethylamine

Downstream raw materials:

montelukast lauro-cholinium

Refernces