87212
Trimethyl-tetradecylammonium chloride
≥98.0% (AT)
Synonym(s):
Tetradecyltrimethylammonium chloride
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About This Item
Linear Formula:
CH3(CH2)13N(Cl)(CH3)3
CAS Number:
Molecular Weight:
291.94
Beilstein:
3916572
EC Number:
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
≥98.0% (AT)
form
powder
mp
~250 °C (dec.)
SMILES string
[Cl-].CCCCCCCCCCCCCC[N+](C)(C)C
InChI
1S/C17H38N.ClH/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18(2,3)4;/h5-17H2,1-4H3;1H/q+1;/p-1
InChI key
CEYYIKYYFSTQRU-UHFFFAOYSA-M
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Related Categories
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
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Mohd Sajid Ali et al.
Journal of colloid and interface science, 352(2), 436-443 (2010-09-25)
Unfolding of rabbit serum albumin (RSA) by cationic surfactants cetyltrimethylammonium bromide (CTAB) and tetradecyltrimethylammonium bromide (TTAB) was studied by exploiting surface tensiometry, small-angle neutron scattering (SANS), intrinsic fluorescence, resonance Rayleigh scattering (RRS) (also referred as turbidity at 350/350), and circular
Juan Zhang et al.
The journal of physical chemistry. B, 114(41), 13128-13135 (2010-09-28)
Two fatty acids, perfluorononanoic acid (C(8)F(17)COOH) and nonanoic acid (C(8)H(17)COOH), were mixed with a cationic hydrocarbon surfactant, tetradecyltrimethylammonium hydroxide (TTAOH), in aqueous solutions for comparative investigation. Phase behaviors of the two systems are quite different because of the special properties
Cexiong Fu et al.
Journal of chromatography. A, 1216(10), 1901-1907 (2009-02-03)
The usefulness of the micellar selectivity triangle (MST) for prediction and interpretation of separation patterns in micellar electrokinetic chromatography (MEKC) separations is presented. In addition, we demonstrate the capability of controlling selectivity properties of micelles through addition of organic modifiers
Suruchi Mahajan et al.
Langmuir : the ACS journal of surfaces and colloids, 28(50), 17238-17246 (2012-12-12)
Keeping in view the use of surfactants in drug delivery, the interactions of surface active ionic liquids, such as 1-tetradecyl-3-methylimidazolium bromide (C(14)mimBr), with drugs, viz., dopamine hydrochloride (DH) and acetylcholine chloride (AC), have been studied, and the results are further
Keisuke Matsuoka et al.
Journal of colloid and interface science, 333(2), 641-645 (2009-02-27)
The maximum solubilities of homologous series of n-alkylbenzene and n-perfluoroalkylbenzene in aqueous solutions of surfactants n-tetradecyltrimethylammonium chloride (TTAC) and N-(1,1-dihydroperfluorodecyl)-N,N,N-trimethylammonium chloride (C10F-TAC) were measured as a function of the surfactant concentration at 298.2 K. There are four solubilization systems in
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