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Key Documents

30725

Sigma-Aldrich

Decyltrimethylammonium bromide

≥98.0% (NT)

Synonym(s):

N,N,N-Trimethyl-1-decanaminium bromide

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About This Item

Linear Formula:
CH3(CH2)9N(CH3)3(Br)
CAS Number:
Molecular Weight:
280.29
Beilstein:
3915222
EC Number:
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22

Assay

≥98.0% (NT)

SMILES string

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

InChI

1S/C13H30N.BrH/c1-5-6-7-8-9-10-11-12-13-14(2,3)4;/h5-13H2,1-4H3;1H/q+1;/p-1

InChI key

PLMFYJJFUUUCRZ-UHFFFAOYSA-M

Pictograms

Exclamation mark

Signal Word

Warning

Hazard 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)

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Mandy H M Leung et al.
Langmuir : the ACS journal of surfaces and colloids, 24(11), 5672-5675 (2008-05-08)
The alkaline hydrolysis of curcumin was studied in three types of micelles composed of the cationic surfactants cetyl trimethylammonium bromide (CTAB) and dodecyl trimethylammonium bromide (DTAB) and the anionic surfactant sodium dodecyl sulfate (SDS). At pH 13, curcumin undergoes rapid
Kabir-ud-Din et al.
Colloids and surfaces. B, Biointerfaces, 92, 16-24 (2011-12-14)
The micellization behaviors of two amphiphilic drugs ((amitriptyline hydrochloride (AMT) and imipramine hydrochloride (IMP)) in presence of cationic surfactants (conventional as well as gemini) have been investigated conductometrically at four mole fractions and four temperatures. The critical micelle concentration (cmc)
Punjaporn Weschayanwiwat et al.
Chemosphere, 72(7), 1043-1048 (2008-06-03)
A novel separation technique known as an aqueous surfactant two-phase (ASTP) extraction is a promising method to remove organic contaminants from wastewater. When cationic and anionic surfactants are mixed at certain surfactant concentrations and compositions, the solution separates into two
Rowan Hargreaves et al.
Journal of the American Chemical Society, 133(41), 16524-16536 (2011-08-10)
The accepted picture of the structure of a micelle in solution arises from the idea that the surfactant molecules self-assemble into a spherical aggregate, driven by the conflicting affinity of their head and tail groups with the solvent. It is
Parvaiz Ahmad Bhat et al.
The journal of physical chemistry. B, 113(4), 997-1006 (2009-01-07)
Mixed surfactants may improve the performance of surfactant-enhanced solubilization of drugs and thus can serve as the tool for increased bioavalaibility, controlled drug release, and targeted delivery. Solubilization of Naproxen by micellar solutions at 25 degrees C using single and

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