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C69802

Sigma-Aldrich

2-Chloropyridine

99%

Synonym(s):

α-Chloropyridine, o-Chloropyridine

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About This Item

Empirical Formula (Hill Notation):
C5H4ClN
CAS Number:
Molecular Weight:
113.54
Beilstein/REAXYS Number:
105788
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

1.7 mmHg ( 20 °C)

Quality Level

assay

99%

form

liquid

refractive index

n20/D 1.532 (lit.)

bp

166 °C/714 mmHg (lit.)

density

1.2 g/mL at 25 °C (lit.)

SMILES string

Clc1ccccn1

InChI

1S/C5H4ClN/c6-5-3-1-2-4-7-5/h1-4H

InChI key

OKDGRDCXVWSXDC-UHFFFAOYSA-N

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signalword

Danger

Hazard Classifications

Acute Tox. 2 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2 - STOT RE 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

154.4 °F - closed cup

flash_point_c

68 °C - closed cup

ppe

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


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Trevor J Dines et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 59(13), 3205-3217 (2003-10-30)
The adsorption of 2-chloropyridine on SiO(2), TiO(2), ZrO(2), SiO(2)-Al(2)O(3) and H-mordenite has been studied by IR spectroscopy. The different modes of interaction with oxide surfaces, i.e. hydrogen-bonding and adsorption at Brønsted or Lewis acid sites, was modelled by ab initio
Mattia Moiola et al.
ChemistryOpen, 9(2), 195-199 (2020-02-07)
1,2,4-Oxadiazole[4,5-a]piridinium salts add alcohols and alkoxides to undergo electrocyclic ring opening affording alkoxybutadienyl 1,2,4-oxadiazole derivatives. The pyridinium salts represent a special class of Zincke salts that are prone to rearrange to give alkoxybutadienyl 1,2,4-oxadiazoles when treated with suitable nucleophiles or
Michał Gągol et al.
Ultrasonics sonochemistry, 45, 257-266 (2018-05-01)
Cavitation has become on the most often applied methods in a number of industrial technologies. In the case of oxidation of organic pollutants occurring in the aqueous medium, cavitation forms the basis of numerous advanced oxidation processes (AOPs). This paper
Dimitris Vlastos et al.
Journal of hazardous materials, 177(1-3), 892-898 (2010-01-20)
2-Chloropyridine (2-CPY) has been identified as a trace organic chemical in process streams, wastewater and even drinking water. Furthermore, it appears to be formed as a secondary pollutant during the decomposition of specific insecticides. As reported in our previous work
Contribution of N-oxidation and .OH radicals to mutagenesis of 2-chloropyridine in Salmonella typhimurium.
B Chłopkiewicz et al.
Acta biochimica Polonica, 40(1), 57-59 (1993-01-01)

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