N,N-Dimethylhexylamine

Base Information

• Chemical Name: N,N-Dimethylhexylamine
• CAS No.: 4385-04-0
• Molecular Formula: C8H19N
• Molecular Weight: 129.246
• Hs Code.: 29211999
• European Community (EC) Number: 224-491-8
• UNII: B3C6KTC8LE
• DSSTox Substance ID: DTXSID70195957
• Nikkaji Number: J205.760C
• Wikidata: Q83069039
• Mol file: 4385-04-0.mol

Synonyms:N,N-Dimethylhexylamine;4385-04-0;N,N-dimethylhexan-1-amine;1-Hexanamine, N,N-dimethyl-;1-Dimethylaminohexane;B3C6KTC8LE;N,N-Dimethyl-n-hexylamine;EINECS 224-491-8;hexyldimethylamine;dimethylhexylamine;hexyl-dimethyl-amine;MFCD00009522;N-hexyl dimethylamine;UNII-B3C6KTC8LE;N-(n-Hexyl)dimethylamine;Hexanamine, N,N-dimethyl;Hexylamine, N,N-dimethyl-;N,N-Dimethyl-1-hexanamine;SCHEMBL30749;SCHEMBL158743;N,N-Dimethyl-1-hexanamine #;N,N-Dimethylhexylamine, 98%;1-(DIMETHYLAMINO)HEXANE;DTXSID70195957;AKOS017343254;BS-52620;E85388;N,N-Dimethylhexylamine, purum, >=96.0% (GC)

Chemical Property of N,N-Dimethylhexylamine

Chemical Property:

• Appearance/Colour: colourless liquid
• Vapor Pressure: 4.49mmHg at 25°C
• Melting Point: -76.53°C (estimate)
• Refractive Index: n20/D 1.414(lit.)
• Boiling Point: 147.1 °C at 760 mmHg
• PKA: 9.99±0.28(Predicted)
• Flash Point: 33.3 °C
• PSA: 3.24000
• Density: 0.77 g/cm³
• LogP: 2.12830
• Storage Temp.: Flammables area
• Solubility.: Miscible with methanol.
• XLogP3: 2.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 5
• Exact Mass: 129.151749610
• Heavy Atom Count: 9
• Complexity: 50.5

Purity/Quality:

99% ^*data from raw suppliers

N,N-Dimethylhexylamine 98% ^*data from reagent suppliers

Safty Information:

• Pictogram(s): C
• Hazard Codes: C
• Statements: 10-34
• Safety Statements: 26-36/37/39-45

MSDS Files:

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CCCCCCN(C)C
• Uses: N,N-Dimethylhexylamine is used as an ion-pairing agent to study the poor retention of uridine diphosphate-linked intermediates on reverse phase media. It is also used in the determination of five monophosphate nucleotides in baby foods. It acts as an additive and encapsulated into the nanoparticle with salinomycin (sali), which has selective toxicity to cancer stem cells. N,N-Dimethylhexylamine was used as ion-pairing agent to study the problem of poor retention of uridine diphosphate-linked intermediates on reverse phase media. It was also used in the determining the five monophosphate nucleotides (cytidine 5′-monophosphate, uridine 5′-monophosphate, adenosine 5′-monophosphate, inosine 5′-monophosphate and guanosine 5′-monophosphate) in baby foods.

Technology Process of N,N-Dimethylhexylamine

There total 38 articles about N,N-Dimethylhexylamine 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: 100.0%

methanol (67-56-1) + hexan-1-amine (111-26-2) → N,N-dimethylhexylamine (4385-04-0)

Guidance literature:

chloro(cyclopentadienyl)bis(triphenylphosphine)ruthenium (II); at 100 ℃;

Reference yield: 97.0%

N,N-dimethylhexanamide (5830-30-8) → N,N-dimethylhexylamine (4385-04-0)

Guidance literature:

With triethylamine alane; In tetrahydrofuran; for 0.5h; Ambient temperature;

DOI:10.1021/jo00067a033

Reference yield: 83.0%

formic acid (64-18-6) + 1-nitrohexane (646-14-0) → N,N-dimethylhexylamine (4385-04-0)

Guidance literature:

With tetrakis(triphenylphosphine)platinum; phenylsilane; C₁₂H₃₆Cl₃Mo₃N₆S₄⁽¹⁺⁾*BF₄^(1-); In tetrahydrofuran; at 100 ℃; for 18h; Inert atmosphere; Schlenk technique;

DOI:10.1002/chem.201702783

upstream raw materials:

formaldehyd

formic acid

n-hexylammonium bromide

hexyl-trimethyl-ammonium; hydroxide

Downstream raw materials:

[2-(4-chloro-phenoxy)-ethyl]-hexyl-dimethyl-ammonium; bromide

[2-(2-chloro-phenoxy)-ethyl]-hexyl-dimethyl-ammonium; bromide

betaine

hexyl-dimethyl-(2-phenoxy-ethyl)-ammonium; bromide

Refernces

Effect of surfactant architecture on the properties of polystyrene- montmorillonite nanocomposites

10.1021/la904827d

The study investigates the influence of surfactant architecture on the properties of polystyrene-montmorillonite (PS-MMT) nanocomposites. A variety of surfactants were designed and synthesized to modify clay, aiming to understand how their chemical structure affects the nanocomposite's morphology after polymerization. The research focused on the behavior of surfactant-modified clays at three stages: post ion-exchange, after dispersion in styrene monomer, and following polymerization. The compatibility and prediction of the nanocomposite morphology were assessed based on the styrene monomer's ability to swell the surfactant-modified clay. Key factors identified for achieving exfoliated morphologies included the position of the ammonium group, the presence of a polymerizable group, surfactant solubility in the monomer, the length of the alkyl chain, and the concentration of surfactant used for clay modification. Techniques such as small-angle X-ray scattering (SAXS), cryogenic transmission electron microscopy (cryo-TEM), wide-angle X-ray scattering (WAXS), dynamic mechanical thermal analysis (DMTA), and thermal gravimetric analysis (TGA) were utilized to characterize the clay-polymer interactions and the properties of the resulting composites. The findings are expected to enhance the design of clay modifications for polymer nanocomposites.

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