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Sigma-Aldrich

2-Ethylpyridine

97%

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100 ML
$146.00

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100 ML
$146.00

About This Item

Empirical Formula (Hill Notation):
C7H9N
CAS Number:
100-71-0
Molecular Weight:
107.15
Beilstein/REAXYS Number:
106480
EC Number:
202-881-9
MDL number:
MFCD00006361
UNSPSC Code:
12352100
PubChem Substance ID:
24847096
NACRES:
NA.22

$146.00

In StockDetails

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Quality Level

100

assay

97%

refractive index

n20/D 1.496 (lit.)

bp

149 °C (lit.)

density

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

InChI key

NRGGMCIBEHEAIL-UHFFFAOYSA-N

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General description

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

Application

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].

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

102.2 °F - closed cup

flash_point_c

39 °C - closed cup

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
STBL3466
SDBB1168
STBJ7949
STBJ3520
STBH4340

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4-Methylpyridine

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
K Brocklehurst et al.
The Biochemical journal, 250(3), 761-772 (1988-03-15)
1. The pH-dependences of the second-order rate constant (k) for the reactions of papain (EC 3.4.22.2) with 2-(acetamido)ethyl 2'-pyridyl disulphide and with ethyl 2-pyridyl disulphide and of k for the reaction of benzimidazol-2-ylmethanethiol (as a minimal model of cysteine proteinase
Cleidiane G Zampronio et al.
The Analyst, 127(8), 1054-1060 (2002-08-28)
Direct sampling tandem mass spectrometry (MS/MS) was used for the quantitation of mixtures of the isomers 2-, 3- and 4-ethyl pyridine. The similarity between the analytes and the second-order nature of MS/MS data require the use of multivariate calibration techniques
Amaury Cazenave-Gassiot et al.
Journal of chromatography. A, 1216(36), 6441-6450 (2009-08-01)
The effects of increasing concentrations of ammonium acetate additive in supercritical fluid chromatography were studied on silica, 2-ethyl-pyridine and endcapped 2-ethyl-pyridine stationary phases. The study involved the addition of increasing concentrations of the ammonium acetate either in the mobile phase
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