Behenamidopropyl dimethylamine

Base Information

• Chemical Name: Behenamidopropyl dimethylamine
• CAS No.: 60270-33-9
• Molecular Formula: C27H56N2O
• Molecular Weight: 424.754
• Hs Code.: 2924199090
• European Community (EC) Number: 262-134-8
• UNII: X4O854526J
• DSSTox Substance ID: DTXSID90209025
• Nikkaji Number: J298.809G
• Wikidata: Q27293552
• Mol file: 60270-33-9.mol

Synonyms:amidet;APA 22;APA-22;APA22 cpd;N-(3-(dimethylamino)propyl)docosanamide;N-(3-(dimethylamino)propyl)docosanamide chloride

Chemical Property of Behenamidopropyl dimethylamine

Chemical Property:

• Vapor Pressure: 6.3E-12mmHg at 25°C
• Melting Point: 80 °C
• Refractive Index: 1.463
• Boiling Point: 544.8 °C at 760 mmHg
• PKA: 16.29±0.46(Predicted)
• Flash Point: 283.3 °C
• PSA: 35.83000
• Density: 0.871 g/cm³
• LogP: 8.71650
• Solubility.: 6.1g/L in organic solvents at 20 ℃
• Water Solubility.: 9mg/L at 25℃
• XLogP3: 10.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 24
• Exact Mass: 424.439264414
• Heavy Atom Count: 30
• Complexity: 344

Purity/Quality:

99.9% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCCCCCCCCCCC(=O)NCCCN(C)C

Technology Process of Behenamidopropyl dimethylamine

There total 2 articles about Behenamidopropyl dimethylamine 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: 92.41%

n-docosanoic acid (112-85-6) + 1-amino-3-(dimethylamino)propane (109-55-7) → N-(3-(dimethylamino)propyl)docosanamide (60270-33-9)

Guidance literature:

With aluminum oxide; sodium fluoride; at 165 ℃; for 11h; Inert atmosphere;

DOI:10.1055/s-0029-1217973

Reference yield:

→ N-(3-(dimethylamino)propyl)docosanamide (60270-33-9)

Guidance literature:

Reference yield: 91.8%

N-(3-(dimethylamino)propyl)docosanamide (60270-33-9) + epichlorohydrin (106-89-8,24969-06-0,13403-37-7) → C57H118N4O3(2+)*Cl(1-)

Guidance literature:

In neat (no solvent); at 100 ℃; for 8h; Alkaline conditions;

upstream raw materials:

n-docosanoic acid

1-amino-3-(dimethylamino)propane

Refernces

• 1、 Chu, Zonglin,Feng, Yujun. "A facile route towards the preparation of ultra-long-Chain amidosulfobetaine surfactants". experimental part. p. 2655 - 2658. Retrieved 2010/01/07.
• 2、 -. "Dimer poly-quaternary compounds". Page/Page column 9. . Retrieved 2008/06/13.