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Sigma-Aldrich

N,N-Dimethylnonylamine

97%

Synonym(s):

1-(Dimethylamino)nonane

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About This Item

Linear Formula:
CH3(CH2)8N(CH3)2
CAS Number:
Molecular Weight:
171.32
Beilstein:
1736553
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

refractive index

n20/D 1.428 (lit.)

bp

83 °C/7 mmHg (lit.)

density

0.773 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCCN(C)C

InChI

1S/C11H25N/c1-4-5-6-7-8-9-10-11-12(2)3/h4-11H2,1-3H3

InChI key

AMAADDMFZSZCNT-UHFFFAOYSA-N

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General description

N,N-Dimethylnonylamine (1-(Dimethylamino)nonane) is a hydrophobic tertiary amine.

Application

N,N-Dimethylnonylamine may be used as charge modifier for the separation of enantiomers of anti-inflammatory drugs. It may be used for the synthesis of bromoethylnonyldimethylammonium bromide.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

168.8 °F - closed cup

Flash Point(C)

76 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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M Ouyang et al.
Bioconjugate chemistry, 11(1), 104-112 (2000-01-19)
A series of novel cationic detergents that contain cleavable hydrophilic isothiuronium headgroups was synthesized, and their utility in controlled assembly of plasmid DNA into small stable particles with high DNA concentration investigated. The detergents have alkyl chains of C(8)-C(12) and
Dynamic modification of the chiral bonding properties of a CHIRAL-AGP column by organic and inorganic additives: separation of enantiomers of anti-inflammatory drugs.
Hermansson J and Hermansson I.
Journal of Chromatography A, 666(1), 181-191 (1994)

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