Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

36784

Sigma-Aldrich

Didodecylamine

≥97.0% (GC)

Synonym(s):

Di-n-dodecylamine, Dilaurylamine, N,N-Didodecylamine, N-Dodecyl-1-dodecanamine

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
[CH3(CH2)11]2NH
CAS Number:
3007-31-6
Molecular Weight:
353.67
Beilstein:
1777050
EC Number:
221-114-9
MDL number:
MFCD00041918
UNSPSC Code:
12352100
PubChem Substance ID:
57649656
NACRES:
NA.22

Assay

≥97.0% (GC)

form

powder

mp

45-49 °C

functional group

amine

SMILES string

CCCCCCCCCCCCNCCCCCCCCCCCC

InChI

1S/C24H51N/c1-3-5-7-9-11-13-15-17-19-21-23-25-24-22-20-18-16-14-12-10-8-6-4-2/h25H,3-24H2,1-2H3

InChI key

MJCJUDJQDGGKOX-UHFFFAOYSA-N

Related Categories

General description

Didodecylamine is a secondary amine. It is reported as standard amine enhancer and its dermal enhancement properties has been studied using in vitro diffusion cell techniques. Solidification point of dodecylamine has been reported to be 26.2°C.

Application

Didodecylamine may be used:
  • to promote the crystal growth of 2D nanosheets of GdOCl with approximately square cross sections
  • to investigate the effect of alkyl chain length of amine on phase transfer of aqueous synthesized gold nanoparticles (AuNPs) from water to toluene
  • in the preparation of novel class of liquid crystalline complexes, by the interaction of copper nitrate

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCL3446
BCCD5062
014317/1
013390/1
6053X

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Note on the preparation of n-dodecylamine and di-n-dodecylamine from n-dodecyl chloride by means of anhydrous liquid ammonia.
Wibaut JP, et al.
Rec. Trav. Chim., 57(4), 456-458 (1938)
In vitro evaluation of a series of Azone analogs as dermal penetration enhancers: IV. Amines.
Michniak BB, et al.
International Journal of Pharmaceutics, 116(2), 201-209 (1995)
Katarzyna Soliwoda et al.
Langmuir : the ACS journal of surfaces and colloids, 30(23), 6684-6693 (2014-06-04)
In the present paper we describe a phase transfer of aqueous synthesized gold nanoparticles (AuNPs) from water to toluene using secondary amines: dioctylamine, didodecylamine, and dioctadecylamine. The effect of the hydrocarbon chain length and amount of amines on the transfer
Novel Thermotropic Mesophases of Copper Complexes with Long-Chain Aliphatic Amines.
Paleos CM, et al.
Mol. Cryst. Liq. Cryst., 161(1), 373-383 (1988)
Kenneth R Kort et al.
Small (Weinheim an der Bergstrasse, Germany), 11(3), 329-334 (2014-08-28)
While much progress has been achieved in the shape-controlled synthesis of nanocrystals, chemical strategies to define morphology remain primarily empirical. Here, a mechanistic study of the influence of different coordinating ligands on the kinetics and thermodynamics of crystal growth during
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