36784
Didodecylamine
≥97.0% (GC)
Synonym(s):
Di-n-dodecylamine, Dilaurylamine, N,N-Didodecylamine, N-Dodecyl-1-dodecanamine
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About This Item
Linear Formula:
[CH3(CH2)11]2NH
CAS Number:
Molecular Weight:
353.67
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
221-114-9
Beilstein/REAXYS Number:
1777050
MDL number:
Product Name
Didodecylamine, ≥97.0% (GC)
InChI key
MJCJUDJQDGGKOX-UHFFFAOYSA-N
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
SMILES string
CCCCCCCCCCCCNCCCCCCCCCCCC
assay
≥97.0% (GC)
form
powder
mp
45-49 °C
functional group
amine
Quality Level
Related Categories
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
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
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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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
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)
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)
Novel Thermotropic Mesophases of Copper Complexes with Long-Chain Aliphatic Amines.
Paleos CM, et al.
Mol. Cryst. Liq. Cryst., 161(1), 373-383 (1988)
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
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