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112429

Sigma-Aldrich

2-Ethylpyridin

97%

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100 ML
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100 ML
€ 123,00

About This Item

Empirische Formel (Hill-System):
C7H9N
CAS-Nummer:
Molekulargewicht:
107.15
Beilstein:
106480
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

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Assay

97%

Brechungsindex

n20/D 1.496 (lit.)

bp

149 °C (lit.)

Dichte

0.937 g/mL at 25 °C (lit.)

SMILES String

CCc1ccccn1

InChI

1S/C7H9N/c1-2-7-5-3-4-6-8-7/h3-6H,2H2,1H3

InChIKey

NRGGMCIBEHEAIL-UHFFFAOYSA-N

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Allgemeine Beschreibung

2-Ethylpyridine linked with silica is a popular stationary phase for chiral and achiral separations in supercritical fluid chromatography[1].

Anwendung

2-Ethylpyridine is used to study its effect on the proliferation and survival of human umbilical vein endothelial cells (HUVECs), HMVECs from lung, and NIH 3T3 cells[2].

Piktogramme

FlameExclamation mark

Signalwort

Warning

Gefahreneinstufungen

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 1

Flammpunkt (°F)

102.2 °F - closed cup

Flammpunkt (°C)

39 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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S Muthu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 93, 214-222 (2012-04-07)
Fourier transform Raman and Fourier transform infrared spectra of 2-ethylpyridine-4-carbothioamide were recorded in the regions 3600-100 cm(-1) and 4000-450 cm(-1), respectively in the solid phase. 2-Ethylpyridine-4-carbothioamide is used as anti-tubercular agent that inhibits mycolic acid synthesis. The equilibrium geometry harmonic
E J O'Loughlin et al.
Biodegradation, 10(2), 93-104 (1999-08-31)
A bacterium capable of degrading 2-methylpyridine was isolated by enrichment techniques from subsurface sediments collected from an aquifer located at an industrial site that had been contaminated with pyridine and pyridine derivatives. The isolate, identified as an Arthrobacter sp., was
David Speybrouck et al.
Current topics in medicinal chemistry, 12(11), 1250-1263 (2012-05-11)
Supercritical fluid (SF) was discovered 200 years ago, but the use of this fluid as a mobile phase in chromatography only became popular fifty years ago. The development of the supercritical fluid chromatography (SFC) was progressing slowly due to technological
Russell Bazemore et al.
Journal of agricultural and food chemistry, 54(2), 497-501 (2006-01-19)
Following smoking 1/2 of a cigar, the most odorous cigar tobacco smoke components extracted from the surface of the tongue by nylon-meshed swabs and then extracted from the swab headspace by solid phase microextraction were ethyl pyrrole, 2,3-dimethyl pyrazine, and
Richard Yu et al.
Toxicological sciences : an official journal of the Society of Toxicology, 93(1), 82-95 (2006-06-23)
Our purpose was to determine the effects of six cigarette toxicants (pyridine, nicotine, 2-ethylpyridine, 3-ethylpyridine, p-cresol, and pyrazine) on three types of cultured mammalian cells (human umbilical vein endothelial cells [HUVECs], human microvascular endothelial cells [HMVECs], and NIH 3T3 cells)

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