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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

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’.

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Journal of the American Chemical Society, 126(32), 9900-9901 (2004)
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)
R A Carvalho et al.
Journal of colloid and interface science, 354(2), 725-732 (2010-12-15)
NMR spectroscopy has been used to study and characterize the interactions in solution between β-CD and alkyl-α,ω-bis(dodecyldimethyl ammonium bromide) gemini surfactants with the following head-group spacer lengths: 2, 4, 6, 8, and 10. The application of the method of continuous

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