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Merck
CN

464295

N,N-二甲基壬基胺

97%

别名:

1-(二甲氨基)壬烷

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关于此项目

线性分子式:
CH3(CH2)8N(CH3)2
化学文摘社编号:
分子量:
171.32
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1736553
Assay:
97%
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InChI

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

SMILES string

CCCCCCCCCN(C)C

InChI key

AMAADDMFZSZCNT-UHFFFAOYSA-N

assay

97%

bp

83 °C/7 mmHg (lit.)

density

0.773 g/mL at 25 °C (lit.)

functional group

amine

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

signalword

Warning

hcodes

Hazard Classifications

Skin Irrit. 2

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

168.8 °F - closed cup

flash_point_c

76 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(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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