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Merck
CN

367729

Tridodecylmethylammonium chloride

98%

Synonym(s):

Methyltridodecylammonium chloride

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About This Item

Linear Formula:
[CH3(CH2)11]3N(Cl)CH3
CAS Number:
Molecular Weight:
572.47
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
6031445
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Product Name

Tridodecylmethylammonium chloride, 98%

InChI

1S/C37H78N.ClH/c1-5-8-11-14-17-20-23-26-29-32-35-38(4,36-33-30-27-24-21-18-15-12-9-6-2)37-34-31-28-25-22-19-16-13-10-7-3;/h5-37H2,1-4H3;1H/q+1;/p-1

SMILES string

[Cl-].CCCCCCCCCCCC[N+](C)(CCCCCCCCCCCC)CCCCCCCCCCCC

InChI key

SBHRWOBHKASWGU-UHFFFAOYSA-M

assay

98%

mp

110-112 °C (lit.)

Quality Level

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Application

Tridodecylmethylammonium chloride can be used as a:
  • Catalyst in the transesterification of methyl esters with glycidol to synthesize glycidyl esters.
  • Bulky lipophilic cationic additive for polyaniline membranes.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Quaternary alkyl ammonium salt-catalyzed transformation of glycidol to glycidyl esters by transesterification of methyl esters
Tanaka S, et al.
ACS Catalysis, 8, 1097-1103 (2018)
Raman and UV-vis spectroscopic study of polyaniline membranes containing a bulky cationic additive
Lindfors T, et al.
Journal of Electroanalytical Chemistry, 518, 131-138 (2002)
Multisensing ion-selective field-effect transistors prepared by ionophore doping technique.
K Bezegh et al.
Analytical chemistry, 59(24), 2846-2848 (1987-12-15)
S S Smith et al.
The Journal of general physiology, 114(6), 799-818 (1999-12-01)
The cystic fibrosis transmembrane conductance regulator (CFTR) Cl channel exhibits lyotropic anion selectivity. Anions that are more readily dehydrated than Cl exhibit permeability ratios (P(S)/P(Cl)) greater than unity and also bind more tightly in the channel. We compared the selectivity
Jan Langmaier et al.
Analytical chemistry, 79(7), 2892-2900 (2007-02-24)
Chronopotentiometry and electrochemical impedance spectroscopy were used to study the transient behavior and the potentiometric response mechanism of the polymer membrane-based sensor for heparin. Membrane with a composition of 66 wt % poly(vinyl chloride), 33 wt % o-nitrophenyl octyl ether

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