Skip to Content
Merck
All Photos(2)

Key Documents

359327

Sigma-Aldrich

N-Hexylmethylamine

96%

Synonym(s):

N-Methylhexylamine

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3NH(CH2)5CH3
CAS Number:
Molecular Weight:
115.22
Beilstein:
1731685
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

96%

form

liquid

refractive index

n20/D 1.416 (lit.)

bp

140-142 °C (lit.)

density

0.76 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

CCCCCCNC

InChI

1S/C7H17N/c1-3-4-5-6-7-8-2/h8H,3-7H2,1-2H3

InChI key

XJINZNWPEQMMBV-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

N-Hexylmethylamine is an acyclic secondary amine. Ruthenium-catalyzed reaction of N-hexylmethylamine with styrene has been reported. Transition metal-catalyzed intermolecular hydroamination of N-hexylmethylamine with 2-vinylnaphthalene has been reported.

Application

N-Hexylmethylamine may be used in the synthesis of dialkyldithiocarbamato cadmium complexes Cd[S2CNRR′]2.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Flam. Liq. 3 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

87.8 °F - closed cup

Flash Point(C)

31 °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

Customers Also Viewed

The synthesis of SiO2@ CdS nanocomposites using single-molecule precursors.
Monteiro OC, et al.
Chemistry of Materials, 14(7), 2900-2904 (2002)
Masaru Utsunomiya et al.
Journal of the American Chemical Society, 125(47), 14286-14287 (2003-11-20)
A transition metal-catalyzed intermolecular hydroamination of vinylarenes with alkylamines is reported. The combination of Pd(O2CCF3)4, DPPF, and TfOH was the most effective catalyst of those tested. Control experiments without palladium, acid, or ligand all occurred in low yield. The reaction
Masaru Utsunomiya et al.
Journal of the American Chemical Society, 126(9), 2702-2703 (2004-03-05)
A ruthenium-catalyzed intermolecular, anti-Markovnikov hydroamination of vinylarenes with secondary aliphatic and benzylic amines is reported. The combination of Ru(cod)(2-methylallyl)2, 1,5-bis(diphenylphosphino)pentane, and triflic acid was the most effective catalyst of those tested. Control reactions conducted without ligand or acid did not

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