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线性分子式:
[CH3(CH2)5]2NCH3
化学文摘社编号:
分子量:
199.38
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
≥97%
InChI
1S/C13H29N/c1-4-6-8-10-12-14(3)13-11-9-7-5-2/h4-13H2,1-3H3
SMILES string
CCCCCCN(C)CCCCCC
InChI key
POMGZMHIXYRARC-UHFFFAOYSA-N
assay
≥97%
refractive index
n20/D 1.433 (lit.)
bp
146 °C/48 mmHg (lit.)
density
0.775 g/mL at 25 °C (lit.)
functional group
amine
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.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
192.2 °F - closed cup
flash_point_c
89 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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.
Erica L Bakota et al.
Rapid communications in mass spectrometry : RCM, 34(5), e8608-e8608 (2019-11-11)
While liquid chromatography/high-resolution mass spectrometry (LC/HRMS) is a versatile analytical technique, it is also sensitive to trace impurities. These impurities may come from a variety of sources, including reagents, solvents, and the sample matrix itself. Impurities in reagents may become
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