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233528

Sigma-Aldrich

4-Octylaniline

99%

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About This Item

Linear Formula:
CH3(CH2)7C6H4NH2
CAS Number:
Molecular Weight:
205.34
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

refractive index

n20/D 1.516 (lit.)

bp

175 °C/13 mmHg (lit.)

density

0.898 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCc1ccc(N)cc1

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

InChI key

ORKQJTBYQZITLA-UHFFFAOYSA-N

Related Categories

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.

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.

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Statements

Hazard Classifications

Aquatic Acute 1 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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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
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
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
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)
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)

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