41653
N,N-Dimethyltetradecylamine
technical, ≥95% (GC/NT)
Synonym(s):
1-(Dimethylamino)tetradecane, N,N-Dimethylmyristylamine
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About This Item
Linear Formula:
CH3(CH2)13N(CH3)2
CAS Number:
Molecular Weight:
241.46
Beilstein:
1748246
EC Number:
MDL number:
UNSPSC Code:
12352100
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.)
functional group
amine
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:
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).
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Skin Irrit. 2
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
303.8 °F - closed cup
Flash Point(C)
151 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
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)
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)
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)
Javier Raya-González et al.
Protoplasma, 254(3), 1399-1410 (2016-10-04)
Plant growth-promoting rhizobacteria are natural inhabitants of roots, colonize diverse monocot and dicot species, and affect several functional traits such as root architecture, adaptation to adverse environments, and protect plants from pathogens. N,N-dimethyl-hexadecylamine (C16-DMA) is a rhizobacterial amino lipid that
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