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Merck
모든 사진(1)

문서

75094

Sigma-Aldrich

Trimethyloctylammonium chloride

≥97.0% (AT)

동의어(들):

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 코드:
12352116
PubChem Substance ID:
NACRES:
NA.22

분석

≥97.0% (AT)

형태

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

관련 카테고리

애플리케이션

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.

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


시험 성적서(COA)

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문서 라이브러리 방문

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
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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