Cyclohexyldimethylammonium chloride

Base Information

• Chemical Name: Cyclohexyldimethylammonium chloride
• CAS No.: 2498-24-0
• Molecular Formula: C8H17 N . Cl H
• Molecular Weight: 163.691
• European Community (EC) Number: 219-689-6
• DSSTox Substance ID: DTXSID10947851
• Mol file: 2498-24-0.mol

Synonyms:Cyclohexyldimethylammonium chloride;2498-24-0;EINECS 219-689-6;DTXSID10947851;dimethylcyclohexylamine hydrochloride;AKOS006242109;N,N-Dimethylcyclohexanamine--hydrogen chloride (1/1)

Chemical Property of Cyclohexyldimethylammonium chloride

Chemical Property:

• Vapor Pressure: 2.21mmHg at 25°C
• Boiling Point: 162°Cat760mmHg
• Flash Point: 42.2°C
• PSA: 3.24000
• Density: 0.85g/cm³
• LogP: 2.68270
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 163.1127773
• Heavy Atom Count: 10
• Complexity: 72.6

Purity/Quality:

98%Min ^*data from raw suppliers

N,N-DIMETHYLCYCLOHEXANAMINE HYDROCHLORIDE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CN(C)C1CCCCC1.Cl

Technology Process of Cyclohexyldimethylammonium chloride

There total 3 articles about Cyclohexyldimethylammonium 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:

N,N-dimethyl-aniline (121-69-7,77733-26-7) → N,N-dimethylcyclohexylamine hydrochloride (2498-24-0)

Guidance literature:

N,N-dimethyl-aniline; With palladium 10% on activated carbon; hydrogen; acetic acid; at 24 - 28 ℃; for 15h;

With hydrogenchloride; In methanol; water;

DOI:10.1002/ejoc.202000695

Reference yield:

piperidine (110-89-4) + Cyclohexyl-dimethyl-[(E)-2-(4-nitro-benzenesulfonyl)-vinyl]-ammonium; chloride (110065-20-8) → β-piperidyl aminovinyl sulfone (107415-63-4) + N,N-dimethylcyclohexylamine hydrochloride (2498-24-0)

Guidance literature:

In acetonitrile; at 25 ℃; Rate constant;

Reference yield:

trimethylammonium (145384-53-8) + N,N-dimethyl-cyclohexanamine (98-94-2) → {(CH3)2(cyclo-C6H11)NH}(1+) (2498-24-0) + trimethylamine (75-50-3)

Guidance literature:

In dimethyl sulfoxide; at 24.9 ℃; Thermodynamic data; ΔG⁰, other solvent;

DOI:10.1021/jo00237a017

upstream raw materials:

piperidine

Cyclohexyl-dimethyl-[(E)-2-(4-nitro-benzenesulfonyl)-vinyl]-ammonium; chloride

N,N-dimethyl-aniline

trimethylammonium

Downstream raw materials:

N,N-dimethyl-cyclohexanamine

pyridine hydrochloride

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