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N,N-Dimethyltetradecylamine

technical, ≥95% (GC/NT)

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Synonym(s):
1-(Dimethylamino)tetradecane, N,N-Dimethylmyristylamine
Linear Formula:
CH3(CH2)13N(CH3)2
CAS Number:
Molecular Weight:
241.46
Beilstein/REAXYS Number:
1748246
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

grade

technical

Quality Level

assay

≥95% (GC/NT)

form

liquid

density

0.795 g/mL at 20 °C (lit.)

SMILES string

CCCCCCCCCCCCCCN(C)C

InChI

1S/C16H35N/c1-4-5-6-7-8-9-10-11-12-13-14-15-16-17(2)3/h4-16H2,1-3H3

Inchi Key

SFBHPFQSSDCYSL-UHFFFAOYSA-N

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Application

N,N-Dimethyltetradecylamine has been used for the synthesis of 1,6-bis(N,N-tetradecyl dimethylammonium adipate), a counterion coupled gemini (cocogem) surfactant.
It may also be used in the following studies:
  • For the isolation of recombinant botulinum neurotoxin fragments in the yeast Pichia pastoris by cell permeabilization method.
  • Synthesis of gemini surfactants belonging to the series of alkanediyl-α,ω-bis-(dimethylalkyl ammonium bromide, which were evaluated as corrosion inhibitors of iron in hydrochloric acid medium.
  • Preparation of cationic gemini surfactant of the type N-alkanediyl 1,2-ethane bis(dimethyl ammonium bromide).

pictograms

Exclamation markEnvironment

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Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Skin Irrit. 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

303.8 °F - closed cup

flash_point_c

151 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Corrosion inhibition of iron in 1M HCl by some gemini surfactants in the series of alkanediyl-α, ω-bis-(dimethyl tetradecyl ammonium bromide).
El Achouri M, et al.
Progress in Organic Coatings, 43(4), 267-273 (2001)
Scot R Shepard et al.
Journal of biotechnology, 99(2), 149-160 (2002-09-25)
A cell permeabilization method for the release of intracellular proteins from microbial cells was developed. The method was applied to the recovery of recombinant botulinum neurotoxin fragments, expressed intracellularly in the yeast Pichia pastoris, by suspending the cells in an
Solubility of two disperse dyes derived from N-alkyl and N-carboxylic acid naphthalimides in the presence of gemini cationic surfactants.
Gharanjig K, et al.
Journal of Surfactants and Detergents, 14(3), 381-389 (2011)
Spontaneous vesicle formation in aqueous mixtures of cationic gemini surfactant and sodium lauryl ether sulfate.
Cheon H-Y, et al.
Bull. Korean Chem. Soc., 26(1), 107-107 (2005)
Synthesis and Investigation of Surface Active Properties of Counterion Coupled Gemini Surfactants.
Noori S, et al.
Journal of Surfactants and Detergents, 17(3), 409-417 (2014)

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