75094
Trimethyloctylammonium chloride
≥97.0% (AT), crystals
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
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352116
MDL number:
Beilstein/REAXYS Number:
4005082
Product Name
Trimethyloctylammonium chloride, ≥97.0% (AT)
InChI key
AQZSPJRLCJSOED-UHFFFAOYSA-M
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
assay
≥97.0% (AT)
form
crystals
Quality Level
Related Categories
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.
signalword
Warning
hcodes
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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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
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
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