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41653

Sigma-Aldrich

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

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:
  • 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

Signal Word

Warning

Hazard 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
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)
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)
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)

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