Dodecyltrimethylammonium iodide

Base Information

• Chemical Name: Dodecyltrimethylammonium iodide
• CAS No.: 19014-04-1
• Molecular Formula: C15H31N^.I
• Molecular Weight: 355.35
• Hs Code.: 2923900090
• European Community (EC) Number: 606-201-5
• DSSTox Substance ID: DTXSID10432398
• Mol file: 19014-04-1.mol

Synonyms:1-dodecanaminium, N,N,N-trimethyl-, bromide;ammonium, dodecyltrimethyl-, chloride;ammonium, dodecyltrimethyl-,bromide;C(12)TAC;C12QAC;C12TAC;dodecyl trimethyl ammonium chloride;dodecyl trimethylammonium chloride;dodecyltrimethylammonium;dodecyltrimethylammonium bromide;dodecyltrimethylammonium chloride;dodecyltrimethylammonium chromate (2:1);dodecyltrimethylammonium ethyl sulfate;dodecyltrimethylammonium hydroxide;dodecyltrimethylammonium iodide;dodecyltrimethylammonium maleate (2:1);dodecyltrimethylammonium methyl sulfate salt;dodecyltrimethylammonium perchlorate;dodecyltrimethylammonium sulfate (2:1);dodecyltrimethylammonium sulfide (2:1);dodecyltrimethylammonium thiomolybdate salt hydrate;DoTAC compound;DTMACl cpd;laurtrimonium;laurtrimonium bromide;laurtrimonium chloride;lauryl trimethyl ammonium chloride;lauryltrimethylammonium bromide;lauryltrimethylammonium chloride;monolauryltrimethylammonium chloride;N,N,N-trimethyl-1-dodecanaminium chloride;n-dodecyl triethylammonium bromide;n-dodecyltrimethylammonium;n-dodecyltrimethylammonium chloride

Chemical Property of Dodecyltrimethylammonium iodide

Chemical Property:

• PSA: 0.00000
• LogP: 1.61750
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 11
• Exact Mass: 355.17360
• Heavy Atom Count: 17
• Complexity: 135

Purity/Quality:

99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCC[N+](C)(C)C.[I-]

Technology Process of Dodecyltrimethylammonium iodide

There total 1 articles about Dodecyltrimethylammonium iodide 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: 96.0%

N,N-dimethylaminododecane (112-18-5,83855-86-1) + methyl iodide (74-88-4) → TMDAI (19014-04-1)

Guidance literature:

In ethanol; for 25h; Reflux; Inert atmosphere;

DOI:10.1039/c7nj03055j

Reference yield:

Na[Eu(dbm)4] + TMDAI (19014-04-1) → [(C12H25NMe3)]2-[Eu(dbm)4]I

Guidance literature:

In tetrahydrofuran; for 40h; Schlenk technique; Reflux; Inert atmosphere;

DOI:10.1039/c7nj03055j

Reference yield:

TMDAI (19014-04-1) + silver picrate (146-84-9) → trimethyldodecylammonium picrate (20526-17-4)

Guidance literature:

DOI:10.1002/chem.200600808

upstream raw materials:

N,N-dimethylaminododecane

methyl iodide

Downstream raw materials:

trimethyldodecylammonium picrate

Refernces

• 1、 Ceruti, Maurizio,Balliano, Gianni,Viola, Franca,Cattel, Luigi,Gerst, Nicolas,Schuber, Francis. "Synthesis and biological activity of azasqualenes, bis-azasqualenes and derivatives". . p. 199 - 208. Retrieved 2007/10/02.