Skip to Content
Merck
All Photos(2)

Key Documents

460966

Sigma-Aldrich

N-Methyldihexylamine

≥97%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
[CH3(CH2)5]2NCH3
CAS Number:
Molecular Weight:
199.38
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

≥97%

refractive index

n20/D 1.433 (lit.)

bp

146 °C/48 mmHg (lit.)

density

0.775 g/mL at 25 °C (lit.)

SMILES string

CCCCCCN(C)CCCCCC

InChI

1S/C13H29N/c1-4-6-8-10-12-14(3)13-11-9-7-5-2/h4-13H2,1-3H3

InChI key

POMGZMHIXYRARC-UHFFFAOYSA-N

General description

N-Methyldihexylamine (dihexylmethylamine) is a tertiary amine. It is formed during the pyrolysis of 1,1-dihexyl-1-methylamine-2-acylimide.

Application

N-Methyldihexylamine may be used to synthesize comb-shaped cationic poly(2,6-dimethylphenylenoxide) (PPO) polymer anion-exchange membrane (AEM) containing two hexyl side chains.

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

192.2 °F - closed cup

Flash Point(C)

89 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Pyrolysis of 1, 1-dihexyl-1-methylamine-2-acylimides.
Wawzonek S and Paschke EE.
The Journal of Organic Chemistry, 36(11), 1474-1476 (1971)
Nanwen Li et al.
Journal of the American Chemical Society, 135(27), 10124-10133 (2013-06-01)
To produce an anion-conductive and durable polymer electrolyte for alkaline fuel cell applications, a series of quaternized poly(2,6-dimethyl phenylene oxide)s containing long alkyl side chains pendant to the nitrogen-centered cation were synthesized using a Menshutkin reaction to form comb-shaped structures.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service