Skip to Content
Merck
All Photos(6)

Key Documents

View All Documentation

T4762

Sigma-Aldrich

Myristyltrimethylammonium bromide

≥99%

Synonym(s):

Tetradecyltrimethylammonium bromide, Trimethyl(tetradecyl)ammonium bromide

Sign Into View Organizational & Contract Pricing
All Photos(6)

About This Item

Linear Formula:
CH3(CH2)13N(Br)(CH3)3
CAS Number:
1119-97-7
Molecular Weight:
336.39
Beilstein:
3633227
EC Number:
214-291-9
MDL number:
MFCD00011770
UNSPSC Code:
12161900
PubChem Substance ID:
24900223
NACRES:
NA.25

description

cationic

Assay

≥99%

mol wt

micellar avg mol wt 27,000

aggregation number

80

technique(s)

protein quantification: suitable

CMC

4-5 mM (20-25°C)

mp

245-250 °C (lit.)

solubility

H2O: 10 % (w/v)

SMILES string

[Br-].CCCCCCCCCCCCCC[N+](C)(C)C

InChI

1S/C17H38N.BrH/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

CXRFDZFCGOPDTD-UHFFFAOYSA-M

Looking for similar products? Visit Product Comparison Guide

General description

Myristyltrimethylammonium bromide is a cationic/zwitterionic type of surfactant.

Application

Myristyltrimethylammonium has been used in a study to assess a surfactant-controlled synthetic method to obtain a nanophase of mesoporous ceria-zirconia solid solution containing cationic defects in the crystalline structure. It has also been used in a study to determine the low molecular weight of organic acids in soils and plants by capillary zone electrophoresis.

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2 - STOT RE 2 Oral - STOT SE 3

Target Organs

Gastrointestinal tract, 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.

Visit the Document Library

Surfactant-controlled synthesis of Pd/Ce"0"."6Zr"0"."4O"2 catalyst for NO reduction by CO with excess oxygen
Gonzalez, C., et al.
Applied Surface Science, 243, 10-10 (2005)
Effects of surfactants and their mixtures on inhibition of the corrosion process of ferritic stainless steel
Fuchs-Godec, R.
Electrochimica Acta, 54, 9-9 (2009)
Ying-Hui Li et al.
Analytical and bioanalytical chemistry, 375(6), 775-780 (2003-03-29)
Determination of low molecular weight organic acids in soils and plants by capillary zone electrophoresis was accomplished using a phthalate buffer and indirect UV detection mode. The influence of some crucial parameters, such as pH, buffer concentration and surfactant were
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
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
View All Related Papers

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