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Merck
CN

44239

Dodecyltrimethylammonium bromide

suitable for ion pair chromatography, LiChropur™, ≥98.5% (AT)

Synonym(s):

Lauryltrimethylammonium bromide

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About This Item

Linear Formula:
CH3(CH2)11N(CH3)3Br
CAS Number:
1119-94-4
Molecular Weight:
308.34
UNSPSC Code:
41116105
NACRES:
NB.21
PubChem Substance ID:
329756378
EC Number:
214-290-3
Beilstein/REAXYS Number:
3597463
MDL number:
MFCD00011767

Key Documents

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Product Name

Dodecyltrimethylammonium bromide, suitable for ion pair chromatography, LiChropur™, ≥98.5% (AT)

InChI key

XJWSAJYUBXQQDR-UHFFFAOYSA-M

InChI

1S/C15H34N.BrH/c1-5-6-7-8-9-10-11-12-13-14-15-16(2,3)4;/h5-15H2,1-4H3;1H/q+1;/p-1

SMILES string

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

description

cationic

assay

≥98.5% (AT)

form

liquid

quality

LiChropur™

mol wt

308.34 g/mol

technique(s)

ion pair chromatography: suitable

mp

246 °C (dec.) (lit.)

λ

10 % in H2O

UV absorption

λ: 240 nm Amax: ≤0.2
λ: 250 nm Amax: ≤0.03
λ: 260 nm Amax: ≤0.02
λ: 500 nm Amax: ≤0.02

suitability

corresponds to standard for filter test

Quality Level

100

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Application

It may be used as a surfactant to study the effectd of urea when added to DTAB and SDS micellar solutions, using Electron spin resonance spectroscopy (ESR) of nitrioxide spin probes.

General description

Dodecyltrimethylammonium bromide (DTAB) is a surfactant.

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2

Storage Class

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCCF5343
BCCM3621

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ESR study of sodium dodecyl sulfate and dodecyltrimethylammonium bromide micellar solutions: effect of urea.
Baglioni, Piero, et al.
The Journal of Physical Chemistry, 94.21, 8218-8222 (1990)
Jonas Carlstedt et al.
Physical chemistry chemical physics : PCCP, 14(27), 9574-9577 (2012-06-14)
Polyelectrolytes with amphiphilic counterions, PEACs, are water insoluble because the amphiphiles self-assemble into highly charged micelles that strongly associate with the equally highly charged polyions. However, in the presence of water soluble cyclodextrins (CDs) that form inclusion complexes with the
Marcos A Villetti et al.
The journal of physical chemistry. B, 115(19), 5868-5876 (2011-04-27)
Interactions between uncharged polymers and cationic surfactants are considered weaker than interactions with the anionic analogues. This work describes the binding occurring between methylcellulose (MC) and the cationic surfactant DTAB in aqueous medium. In the absence of salt, MC-DTAB exhibits
Ketsarin Seebunrueng et al.
Analytical and bioanalytical chemistry, 404(5), 1539-1548 (2012-07-05)
The chain-length compatibility of mixed anionic-cationic surfactants was investigated for the extraction of organophosphorus pesticides (OPPs). Cationic surfactants with different chain lengths (n = 12 and 16) were mixed with sodium dodecyl sulfate (SDS; n = 12) for the mixed
Ye Liu et al.
Lab on a chip, 12(19), 3746-3753 (2012-07-31)
Although biochemical sensing using liquid crystals (LC) has been demonstrated, relatively little attention has been paid towards the fabrication of in situ-formed LC sensing devices. Herein, we demonstrate a highly reproducible method to create uniform LC thin film on treated
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