75094
Trimethyloctylammonium chloride
≥97.0% (AT)
Synonym(s):
Octyltrimethylammonium chloride
Sign Into View Organizational & Contract Pricing
All Photos(1)
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
Quality Level
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)
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’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
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 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
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service