233528
4-Octylaniline
99%
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About This Item
Linear Formula:
CH3(CH2)7C6H4NH2
CAS Number:
Molecular Weight:
205.34
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
240-358-7
MDL number:
Product Name
4-Octylaniline, 99%
InChI key
ORKQJTBYQZITLA-UHFFFAOYSA-N
InChI
1S/C14H23N/c1-2-3-4-5-6-7-8-13-9-11-14(15)12-10-13/h9-12H,2-8,15H2,1H3
SMILES string
CCCCCCCCc1ccc(N)cc1
assay
99%
refractive index
n20/D 1.516 (lit.)
bp
175 °C/13 mmHg (lit.)
density
0.898 g/mL at 25 °C (lit.)
Quality Level
Related Categories
Application
4-Octylaniline has been used as an extractant during the extraction of microgram level concentrations of ruthenium(IV) from halide medium. It has also been used in the synthesis of selective benzimidazole based analogs of sphingosine-1-phosphate.
General description
Micrometer-sized oil droplet of 4-octylaniline containing 5 mol% of an amphiphilic catalyst exhibits a self-propelled motion, producing tiny oil droplets. Kinetics of proton transfer facilitated by 4-octylaniline across the water/1,2-dichloroethane interface has been investigated by cyclic voltammetry and ac impedance.
signalword
Warning
hcodes
Hazard Classifications
Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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Xu Jie et al.
ACS sensors, 5(1), 40-49 (2019-12-13)
Fluorescent microscopic imaging with the help of small-molecule probes (chemoprobes) is one of the most feasible approaches for noninvasive sensing of intracellular molecules. However, the "always on" property of current chemoprobes failed to achieve time-resolved monitoring. Here, we report the
Extraction of ruthenium (IV) from hydrochloric acid medium with N-octylaniline and its determination spectrophotometrically with pyrimidine-2-thiol.
Lokhande TN, et al.
Separation Science and Technology, 35(1), 153-168 (2000)
Kinetics of facilitated proton transfer by hydrophobic aromatic amines across the water/1, 2-dichloroethane interface.
Velazquez-Manzanares M and Schiffrin DJ.
Electrochimica Acta, 49(26), 4651-4658 (2004)
Taro Toyota et al.
Journal of the American Chemical Society, 131(14), 5012-5013 (2009-04-09)
A micrometer-sized oil droplet of 4-octylaniline containing 5 mol % of an amphiphilic catalyst exhibited a self-propelled motion, producing tiny oil droplets, in an aqueous dispersion of an amphiphilic precursor of 4-octylaniline. The tiny droplets on the surface of the
Jeremy J Clemens et al.
Bioorganic & medicinal chemistry letters, 14(19), 4903-4906 (2004-09-03)
Sphingosine-1-phosphate (S1P) is a biologically active lysophospholipid with the capacity to induce a broad range of cellular responses via its interaction with the S1P family of G-protein coupled receptors. A member of this receptor family, S1P(4), is highly and almost
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