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359025

Sigma-Aldrich

Didodecyldimethylammonium bromide

98%

Synonym(s):

DDAB, Dimethyldidodecylammonium bromide

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About This Item

Linear Formula:
[CH3(CH2)11]2N(CH3)2(Br)
CAS Number:
Molecular Weight:
462.63
Beilstein:
3576662
EC Number:
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

mp

157-162 °C (lit.)

SMILES string

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

InChI

1S/C26H56N.BrH/c1-5-7-9-11-13-15-17-19-21-23-25-27(3,4)26-24-22-20-18-16-14-12-10-8-6-2;/h5-26H2,1-4H3;1H/q+1;/p-1

InChI key

XRWMGCFJVKDVMD-UHFFFAOYSA-M

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Application

Didodecyldimethylammonium bromide (DDAB) is a double-chain cationic surfactant.

Possible applications:
  • DDAB can be employed as a co-surfactant to synthesize well-defined multilamellar vesicular silica with an adjustable number of layers.
  • As a surfactant to synthesize gold nanoclusters and nanocubes.
  • It forms supersaturated reverse micelles and microemulsions that act as organized reaction microenvironments for the synthesis of barium sulfate.
  • Calcium montmorillonite can be modified by DDAB through direct ion-exchange to synthesize thermally stable organoclay.

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

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Thermally-induced formation of atomic Au clusters and conversion into nanocubes.
Jin R.
Journal of the American Chemical Society, 126(32), 9900-9901 (2004)
Sana Ghrab et al.
Environmental science and pollution research international, 25(19), 18251-18262 (2017-05-14)
Essential oils from aromatic plants are currently mentioned as suitable tools for excellent protection of stored grains from insect pest attacks. The present work aimed to study the processes of the synthesis insecticidal formulation with clay. The active terpenic compounds
A cationic-cationic co-surfactant templating route for synthesizing well-defined multilamellar vesicular silica with an adjustable number of layers.
Zhang Y.
Chemical Communications (Cambridge, England), 50(22), 2907-2909 (2014)
Effects of block length and structure of surfactant on self-assembly and solution behavior of block ionomer complexes.
Bronich TK.
Langmuir, 16(2), 481-489 (2000)
Double-chained surfactants for semipermanent wall coatings in capillary electrophoresis.
Melanson JE.
Analytical Chemistry, 72(17), 4110-4114 (2000)

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