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374350

Sigma-Aldrich

Tridodecylmethylammonium iodide

97%

Synonym(s):

Methyltridodecylammonium iodide

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About This Item

Linear Formula:
[CH3(CH2)11]3N(I)CH3
CAS Number:
29710-98-3
Molecular Weight:
663.93
Beilstein:
4260774
MDL number:
MFCD00075595
UNSPSC Code:
12352116
PubChem Substance ID:
24863302
NACRES:
NA.22

Assay

97%

mp

106-107 °C (lit.)

SMILES string

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

InChI

1S/C37H78N.HI/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

InChI key

JRLISGAUAJZAGL-UHFFFAOYSA-M

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Application

Tridodecylmethylammonium iodide (3C12MAI) can be used:
  • As a triple-chained cationic surfactant.
  • to prepapre glucose oxidase enzyme immobilized iodide electrode for the detection of glucose concentration.
  • As a cationic phase-transfer catalyst in the oxidation of hydrocarbons by O2.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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’.

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Preparation and application of a new glucose sensor based on iodide ion selective electrode
K Sukru, et al.
Talanta, 65(1), 87-91 (2005)
The role of onium salts in the oxidation of hydrocarbons by O 2 catalysed by cationic phase-transfer reagents
Csanyi L, et al.
Physical Chemistry Chemical Physics, 2(17), 3801-3805 (2000)
Effect of cyclodextrins on the stability of bilayer: A novel electrophoretic approach
Zandkarimi M, et al.
Journal of Liquid Chromatography and Related Technologies, 37(17), 2433-2443 (2014)
J H Yun et al.
ASAIO journal (American Society for Artificial Internal Organs : 1992), 40(3), M401-M405 (1994-07-01)
The development of an ion-selective electrode heparin sensor consisting of a specially formulated polymer membrane doped with tridodecylmethylammonium chloride as the heparin complexing agent was recently reported. Because of the simple nature of the membrane technology used, the authors envisioned
R S Greco et al.
Annals of vascular surgery, 9(2), 140-145 (1995-03-01)
To test the thrombosis resistance of a vascular prosthesis coated with antithrombogenic agents, we evaluated a small vessel prosthesis of expanded polytetrafluoroethylene (ePTFE) implanted in the rat aorta and removed 1 week following surgery. Control grafts consisted of 1 mm
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