42430
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:
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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point(F)
244.4 °F
Flash Point(C)
118 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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J J Harding
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Chen GC, et al.
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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.
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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
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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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