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75094

Sigma-Aldrich

Trimethyloctylammonium chloride

≥97.0% (AT)

Synonym(s):

Octyltrimethylammonium chloride

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5 G
$112.00

About This Item

Linear Formula:
CH3(CH2)7N(CH3)3(Cl)
CAS Number:
10108-86-8
Molecular Weight:
207.78
Beilstein/REAXYS Number:
4005082
MDL number:
MFCD00059977
UNSPSC Code:
12352116
PubChem Substance ID:
57652550
NACRES:
NA.22

$112.00

In StockDetails

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Quality Level

100

assay

≥97.0% (AT)

form

crystals

SMILES string

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

InChI

1S/C11H26N.ClH/c1-5-6-7-8-9-10-11-12(2,3)4;/h5-11H2,1-4H3;1H/q+1;/p-1

Inchi Key

AQZSPJRLCJSOED-UHFFFAOYSA-M

Application

Trimethyloctylammonium chloride (TOMAC) is a cationic surfactant that can be used:
  • To separate SiC from ground SiO2 by flotation method.[1]
  • To prepare porous organosilicates using 1,2-bis(trimethoxysilyl)ethane as a silica precursor.[2]

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_germany

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
BCCK6150
BCCG6026
BCCB8603
BCBW4382
BCBW4381

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Synthesis of porous organosilicates in the presence of alkytrimethylammonium chlorides: Effect of the alkyl chain length
Hamoudi S, et al.
The Journal of Physical Chemistry B, 105(38), 9118-9123 (2001)
Flotation separation of SiC from wastes in the silicon wafer slicing process
Shibata, J, et al.
Kagaku Kogaku Ronbunshu, 32(1), 93-98 (2006)
Stergios Pispas
The journal of physical chemistry. B, 110(6), 2649-2655 (2006-02-14)
Water-soluble complexes between sodium poly(isoprene-b-methacrylate) (NaIMA) amphiphilic block copolymer micelles and two cationic surfactants with different hydrophobic tail lengths, namely, dodecyltrimethylammonium bromide (DTMAB) and octyltrimethylammonium bromide (OTMAB), were prepared by mixing individual aqueous solutions of block copolymers and surfactants. The
Sudhir Husale et al.
Nucleic acids research, 36(5), 1443-1449 (2008-01-22)
The interaction of cationic surfactants with single dsDNA molecules has been studied using force-measuring optical tweezers. For hydrophobic chains of length 12 and greater, pulling experiments show characteristic features (e.g. hysteresis between the pulling and relaxation curves, force-plateau along the
J G Foulks et al.
Canadian journal of physiology and pharmacology, 62(4), 350-355 (1984-04-01)
The local anaesthetic effect of cationic, anionic, and neutral alkyl amphipathic agents was similarly enhanced in an apparently nonspecific way by circumstances which modulate electrostatic interactions (acidity, modification of charged groups at the sarcolemmal surface by group-specific reagents, or changes
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