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Safety Information

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:
109-09-1
Molecular Weight:
113.54
Beilstein:
105788
EC Number:
203-646-3
MDL number:
MFCD00006228
UNSPSC Code:
12352100
PubChem Substance ID:
24892916
NACRES:
NA.22

vapor pressure

1.7 mmHg ( 20 °C)

Quality Level

100

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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Related Categories

Signal Word

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 Code

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

WGK

WGK 3

Flash Point(F)

154.4 °F - closed cup

Flash Point(C)

68 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PDSCL

Poisonous substance

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

C69802-VAR:
C69802-100G:4548173348797
C69802-BULK:
C69802-5G:4548173348810
C69802-RSAMPLE:
C69802-500G:4548173348803

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Certificates of Analysis (COA)

Lot/Batch Number
BCCH5945
MKCR5843
MKCP0736
MKCN7306
MKCN0430

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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
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
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
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)
Andreas Reichelt et al.
Organic letters, 12(4), 792-795 (2010-01-27)
An efficient and convenient method for the synthesis of [1,2,4]triazolo[4,3-a]pyridines was exemplified by the synthesis of 20 analogues bearing a variety of substituents at the 3-position. The methodology involves a palladium-catalyzed addition of hydrazides to 2-chloropyridine, which occurs chemoselectively at
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