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Sigma-Aldrich

4-Phenylbutylamin

98%

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About This Item

Lineare Formel:
C6H5(CH2)4NH2
CAS-Nummer:
13214-66-9
Molekulargewicht:
149.23
EG-Nummer:
236-186-7
MDL-Nummer:
MFCD00008231
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24848723
NACRES:
NA.22

Assay

98%

Brechungsindex

n20/D 1.519 (lit.)

bp

123-124 °C/17 mmHg (lit.)

Dichte

0.944 g/mL at 25 °C (lit.)

SMILES String

NCCCCc1ccccc1

InChI

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

InChIKey

AGNFWIZBEATIAK-UHFFFAOYSA-N

Angaben zum Gen

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

Anwendung

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. Wirkung

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

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

215.6 °F - closed cup

Flammpunkt (°C)

102 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Analysenzertifikate (COA)

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2-Thiophenethylamin 96%

Sigma-Aldrich

423270

2-Thiophenethylamin

Phenethylammonium bromide ≥98%

Sigma-Aldrich

900829

Phenethylammonium bromide

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)
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
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
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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