42430
二辛基甲胺
≥96.0% (GC)
别名:
双辛烷基甲基叔胺
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线性分子式:
[CH3(CH2)7]2NCH3
化学文摘社编号:
分子量:
255.48
EC Number:
224-703-9
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1750823
MDL number:
InChI key
YJLYANLCNIKXMG-UHFFFAOYSA-N
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
SMILES string
CCCCCCCCN(C)CCCCCCCC
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.)
General description
N-Methyldioctylamine (N,N,-dioctylmethylamine), a two branched C8 amine is an organic base.
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
244.4 °F
flash_point_c
118 °C
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
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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