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Merck
CN

145394

4-Phenylbutylamine

98%

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About This Item

Linear Formula:
C6H5(CH2)4NH2
CAS Number:
13214-66-9
Molecular Weight:
149.23
NACRES:
NA.22
PubChem Substance ID:
24848723
UNSPSC Code:
12352100
EC Number:
236-186-7
MDL number:
MFCD00008231

Key Documents

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Product Name

4-Phenylbutylamine, 98%

InChI key

AGNFWIZBEATIAK-UHFFFAOYSA-N

InChI

1S/C10H15N/c11-9-5-4-8-10-6-2-1-3-7-10/h1-3,6-7H,4-5,8-9,11H2

SMILES string

NCCCCc1ccccc1

assay

98%

refractive index

n20/D 1.519 (lit.)

bp

123-124 °C/17 mmHg (lit.)

density

0.944 g/mL at 25 °C (lit.)

Gene Information

human ... AOC3(8639)
mouse ... Aoc3(11754)

Application

4-Phenylbutylamine was used in direct solvent-free amination of multi-walled carbon nanotubes. It was employed as internal standard during solid-phase micro-extraction by GC technique for detection of amphetamines in urine.

Biochem/physiol Actions

4-Phenylbutylamine is a competitive inhibitor of recombinant human liver monoamine oxidase A.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

215.6 °F - closed cup

flash_point_c

102 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
02296CPV
02296CP
40596APV
40596AP
49996EM

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R K Nandigama et al.
Biochemistry, 39(49), 15258-15265 (2000-12-07)
The interaction of recombinant human liver monoamine oxidase A (MAO A) with a series of phenethylamine substrate analogues has been investigated by steady-state and stopped-flow kinetic techniques. Substrate analogues with para substituents exhibit large deuterium kinetic isotope effect on k(cat)
Elena V Basiuk et al.
Journal of nanoscience and nanotechnology, 5(6), 984-990 (2005-08-03)
We performed direct solvent-free amination of multi-walled carbon nanotubes (MWCNTs) with nonylamine, dodecylamine, octadecylamine, 4-phenylbutylamine and 1,8-ocanediamine at a temperature of 150-170 degrees C and reduced pressure. Thermogravimetric analysis and temperature-programmed desorption-mass spectrometry revealed that a major amine fraction decomposes
Ting Wang et al.
Journal of analytical toxicology, 44(6), 596-600 (2019-11-30)
In this study, the relationships between the concentrations of R/S-methamphetamine (MA) and its metabolite R/S-amphetamine (AP), the AP/MA ratio in hair samples, and MA dependence were investigated by performing segmental hair analysis in MA users. Authentic hair samples collected from
Lizhu Chen et al.
Drug testing and analysis, 11(6), 898-905 (2019-01-08)
Chiral analysis is a crucial way to differentiate selegiline (SG) intake from drug abuse. Oral fluid (OF) has been successfully used as an alternative matrix for blood testing in several pharmacokinetic studies. The aim of this study is to describe
Cyntia M Palacio et al.
The FEBS journal, 286(20), 4086-4102 (2019-06-05)
The biodegradation of the nylon-6 precursor caprolactam by a strain of Pseudomonas jessenii proceeds via ATP-dependent hydrolytic ring opening to 6-aminohexanoate. This non-natural ω-amino acid is converted to 6-oxohexanoic acid by an aminotransferase (PjAT) belonging to the fold type I pyridoxal
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