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36784

Sigma-Aldrich

Didodecylamine

≥97.0% (GC)

Sinônimo(s):

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

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About This Item

Fórmula linear:
[CH3(CH2)11]2NH
Número CAS:
3007-31-6
Peso molecular:
353.67
Beilstein:
1777050
Número CE:
221-114-9
Número MDL:
MFCD00041918
Código UNSPSC:
12352100
ID de substância PubChem:
57649656
NACRES:
NA.22

Ensaio

≥97.0% (GC)

Formulário

powder

pf

45-49 °C

grupo funcional

amine

cadeia de caracteres SMILES

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

chave InChI

MJCJUDJQDGGKOX-UHFFFAOYSA-N

Categorias relacionadas

Descrição geral

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.

Aplicação

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

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H315,H319

Classificações de perigo

Eye Irrit. 2 - Skin Irrit. 2

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análise (COA)

Lot/Batch Number
BCCD5062
013390/1

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Sigma-Aldrich

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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)
Novel Thermotropic Mesophases of Copper Complexes with Long-Chain Aliphatic Amines.
Paleos CM, et al.
Mol. Cryst. Liq. Cryst., 161(1), 373-383 (1988)
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)
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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