75094
Trimethyloctylammonium chloride
≥97.0% (AT)
Synonym(s):
Octyltrimethylammonium chloride
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About This Item
Linear Formula:
CH3(CH2)7N(CH3)3(Cl)
CAS Number:
Molecular Weight:
207.78
Beilstein:
4005082
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
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.
- To prepare porous organosilicates using 1,2-bis(trimethoxysilyl)ethane as a silica precursor.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
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)
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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)
J R Elliott et al.
The Journal of physiology, 350, 429-445 (1984-05-01)
The effects of octyltrimethylammonium ions (OTMA+), octyl sulphate ions (OS-) and octanoic acid (OA) on the sodium current of the voltage-clamped squid giant axon have been investigated using intracellular and extracellular application of the test substances. OTMA+ applied externally at
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
David Zanuy et al.
Biopolymers, 63(3), 151-162 (2002-01-12)
We present a molecular dynamics simulation at 300 K in explicit solvent environment of chloroform of the stoichiometric complex formed by poly(alpha,L-glutamate) and octyltrimethylammonium ions. We observed that the alpha-helix conformation of the polypeptide chain remains stable during a 2-ns
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