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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:
7173-54-8
Molecular Weight:
572.47
UNSPSC Code:
12352116
NACRES:
NA.22
PubChem Substance ID:
24862829
MDL number:
MFCD00043303
Beilstein/REAXYS Number:
6031445

Key Documents

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reaction suitability

core: ammonium

mp

110-112 °C (lit.)

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%

Quality Level

200

form

crystalline

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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
GHS07

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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Certificates of Analysis (COA)

Lot/Batch Number
BCCN0643
BCBW3647
BCCL3397
BCCH3443
BCCG1314

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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)
Multisensing ion-selective field-effect transistors prepared by ionophore doping technique.
K Bezegh et al.
Analytical chemistry, 59(24), 2846-2848 (1987-12-15)
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)
Andrew Yu et al.
Analytica chimica acta, 686(1-2), 76-80 (2011-01-18)
The development of a polymer membrane-based electrode to measure the anionic drug suramin in buffered saline and biological samples is described. A large non-equilibrium, steady state EMF response is observed toward suramin, and judicious choice of the polymer membrane components
Natalia Abramova et al.
Talanta, 81(4-5), 1750-1754 (2010-05-06)
The influence of CO(2) and acetic acid on the response of ISFET sensors with PVC and photocured polyurethane polymer membranes with valinomycin as an ionophore was assessed. Experimental results show that the presence of these compounds has no effect on
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