Didodecyldimethylammonium chloride

Base Information

• Chemical Name: Didodecyldimethylammonium chloride
• CAS No.: 3401-74-9
• Deprecated CAS: 942915-51-7
• Molecular Formula: C26H56N^.Cl
• Molecular Weight: 418.19
• Hs Code.: 29239000
• European Community (EC) Number: 222-274-2
• UNII: 5M7W5MLR2Z
• DSSTox Substance ID: DTXSID60883972
• Wikidata: Q27262553
• Mol file: 3401-74-9.mol

Synonyms:bis(dodecyl)dimethylammonium bromide;bis(N-dodecyl)dimethylammonium bromide;DDAB;di-N-dodecyldimethylammonium bromide;didodecyldimethylammonium;didodecyldimethylammonium acetate;didodecyldimethylammonium bromide;didodecyldimethylammonium chloride;dilauryldimethylammonium bromide;dimethyldidodecylammonium bromide;dimethyldilaurylammonium bromide

Chemical Property of Didodecyldimethylammonium chloride

Chemical Property:

• Melting Point: 65-69°C(lit.)
• PSA: 0.00000
• LogP: 5.90860
• Storage Temp.: Hygroscopic, Refrigerator, Under inert atmosphere
• Solubility.: Chloroform (Slightly), DMSO (Sparingly, Heated), Methanol (Slightly, Heated)
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 22
• Exact Mass: 417.4101285
• Heavy Atom Count: 28
• Complexity: 245

Purity/Quality:

99% ^*data from raw suppliers

Didodecyldimethylammonium Chloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi

MSDS Files:

SDS file from LookChem

Useful:

• Chemical Classes: Nitrogen Compounds -> Quaternary Amines
• Canonical SMILES: CCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCC.[Cl-]
• Uses: Didodecyldimethylammonium Chloride is a compound used as an oil-soluble surfactant.

Technology Process of Didodecyldimethylammonium chloride

There total 5 articles about Didodecyldimethylammonium 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:

didodecyldimethylammonium hydroxyde (23381-53-5) → N,N-dimethyl-N,N-didodecylammonium chloride (3401-74-9)

Guidance literature:

With hydrogenchloride; In water; for 24h; Inert atmosphere;

DOI:10.1016/j.molliq.2021.116480

Reference yield:

methylene chloride (74-87-3) + N-methyldidodecylamine (2915-90-4) → N,N-dimethyl-N,N-didodecylammonium chloride (3401-74-9)

Guidance literature:

With ethyl acetate; at 80 ℃;

DOI:10.1021/ja01183a024

Reference yield:

N,N-didodecyl-N,N-dimethylammonium bromide (3282-73-3) → N,N-dimethyl-N,N-didodecylammonium chloride (3401-74-9)

Guidance literature:

Multi-step reaction with 2 steps

1: sodium hydroxide / ethanol / 0.25 h / 20 °C

2: hydrogenchloride / water / 24 h / Inert atmosphere

With hydrogenchloride; sodium hydroxide; In ethanol; water;

DOI:10.1016/j.molliq.2021.116480

upstream raw materials:

methylene chloride

N-methyldidodecylamine

N,N-dimethylaminododecane

1-chlorododecane

Refernces

• 1、 Tiecco, Matteo,Cappellini, Federico,Nicoletti, Francesco,Del Giacco, Tiziana,Germani, Raimondo,Di Profio, Pietro. "Role of the hydrogen bond donor component for a proper development of novel hydrophobic deep eutectic solvents". . p. 423 - 430. Retrieved 2019.
• 2、 Cipiciani, Antonio,Germani, Raimondo,Savelli, Gianfranco,Bunton, Clifford A.,Mhala, Marutirao,Moffatt, John R.. "The Effects of Single- and Twin-tailed Ionic Surfactants upon Aromatic Nucleophilic Substitution". . p. 541 - 546. Retrieved 2007/10/02.