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Sigma-Aldrich

N,N-Dimethyldecylamine

98%

Synonym(s):

1-(Dimethylamino)decane

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About This Item

Linear Formula:
CH3(CH2)9N(CH3)2
CAS Number:
1120-24-7
Molecular Weight:
185.35
Beilstein:
1738198
EC Number:
214-302-7
MDL number:
MFCD00015060
UNSPSC Code:
12352100
PubChem Substance ID:
24870158
NACRES:
NA.22

Quality Level

100

Assay

98%

refractive index

n20/D 1.431 (lit.)

bp

234 °C (lit.)

density

0.778 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCCN(C)C

InChI

1S/C12H27N/c1-4-5-6-7-8-9-10-11-12-13(2)3/h4-12H2,1-3H3

InChI key

YWWNNLPSZSEZNZ-UHFFFAOYSA-N

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General description

N,N-Dimethyldecylamine (DMDA) is a tertiary amine.

Application

N,N-Dimethyldecylamine (DMDA) may be used for the following studies:
  • Pore expansion of the aminopropyl-functionalized ethane-bridged bifunctional periodic mesoporous organosilicas (APEPMOs).
  • Preparation of stationary phase (named QA C10) having a quaternary ammonium embedded between a propyl and a decyl chain.
  • Pore exapansion of monodisperse phenylene-bridged organosilica spheres.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315

Hazard Classifications

Acute Tox. 4 Oral - Skin Irrit. 2

WGK

WGK 3

Flash Point(F)

197.6 °F

Flash Point(C)

92 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Qiaoxia Liu et al.
Journal of separation science, 35(20), 2685-2692 (2012-09-26)
A stationary phase (named QA C10) with quaternary ammonium embedded between a propyl and a decyl chain was synthesized by immobilization of N,N-dimethyldecylamine on chloropropyl-silica surface. A set of representative neutral, basic, and acidic compounds was employed to evaluate its
Liye Guan et al.
Biotechnology letters, 35(8), 1323-1330 (2013-04-18)
The aminopropyl-functionalized ethane-bridged bifunctional periodic mesoporous organosilicas (APEPMOs) were synthesized by the co-condensation of 1,2-bis (triethoxysilyl) ethane and 3-aminopropyltriethoxysilane in the presence of cationic surfactants octadecyltrimethylammonium chloride in basic medium. The pores of the APEPMOs were expanded with N,N-dimethyldecylamine and
Yongping Zhang et al.
Talanta, 81(3), 824-830 (2010-03-20)
Monodisperse phenylene-bridged organosilica spheres show great potential as chromatographic stationary phase. In this paper, the tunable particle size of monodisperse phenylene-bridged organosilica spheres were prepared by co-condensing different proportion of 1,4-bis(triethoxysilyl)benzene (1,4-BTEB) and tetraethylorthosilicate (TEOS), and then pore size was

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