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42430

Sigma-Aldrich

N-Methyldioctylamine

≥96.0% (GC)

Synonym(s):

N,N-Dioctylmethylamine

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About This Item

Linear Formula:
[CH3(CH2)7]2NCH3
CAS Number:
Molecular Weight:
255.48
Beilstein/REAXYS Number:
1750823
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

assay

≥96.0% (GC)

refractive index

n20/D 1.4424 (lit.)

bp

162-165 °C/15 mmHg (lit.)

mp

−30.1 °C (lit.)

density

0.793 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCN(C)CCCCCCCC

InChI

1S/C17H37N/c1-4-6-8-10-12-14-16-18(3)17-15-13-11-9-7-5-2/h4-17H2,1-3H3

Inchi Key

YJLYANLCNIKXMG-UHFFFAOYSA-N

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General description

N-Methyldioctylamine (N,N,-dioctylmethylamine), a two branched C8 amine is an organic base.[1]

Pictograms

Exclamation markEnvironment

signalword

Warning

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 2

flash_point_f

244.4 °F

flash_point_c

118 °C

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


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J J Harding
The Biochemical journal, 117(5), 957-960 (1970-05-01)
Protein-bound glutathione was identified and measured in normal and cataractous human lenses. In a major group of cataracto us lenses the bound glutathione concentration was higher than normal. Study of normal lenses showed that their glutathione content is age-dependent, decreasing
Termite resistance of wood treated with copper (II) compounds derived from tri-and dialkylamine-boric acid complexes.
Chen GC, et al.
Forest products journal, 36(5), 18-20 (1986)
Development of reactive extraction systems for itaconic acid: a step towards in situ product recovery for itaconic acid fermentation.
Kaur G and Elst K.
Royal Society of Chemistry Advances, 4(85), 45029-45039 (2014)
G E Black et al.
Analytical chemistry, 66(23), 4171-4176 (1994-12-01)
Muramic acid is an amino sugar found in eubacterial cell walls and not elsewhere in nature. This study explored the use of electrospray tandem mass spectrometry (ESI MS/MS) in analysis of underivatized muramic acid in bacterial hydrolysates. Fungal hydrolysates were
Vanessa G Correia et al.
Macromolecular bioscience, 11(8), 1128-1137 (2011-06-16)
A method using supercritical CO(2) to obtain biocompatible 2-oxazoline-based oligomers quaternized with different amines is described. The synthesized oligo(2-oxazoline)s display partial carbamic-acid insertion at one end. The syntheses of quaternary oligo(2-bisoxazoline)s and linear oligoethylenimine hydrochlorides are reported. Oligo(2-methyl-2-oxazoline) and oligo(2-bisoxazoline)

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