41653
N,N-Dimethyltetradecylamine
technical, ≥95% (GC/NT)
Sign Into View Organizational & Contract Pricing
All Photos(1)
Synonym(s):
1-(Dimethylamino)tetradecane, N,N-Dimethylmyristylamine
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
Recommended Products
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
Looking for similar products? Visit Product Comparison Guide
Related Categories
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
WGK
WGK 3
Flash Point(F)
303.8 °F
Flash Point(C)
151 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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)
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