Cat. No JK153329_100_G
J&K Chemical

Product Information

Product Name
4-Chloropyridine hydrochloride, 97%
Brand Name
J&K
Product Number
153329
CAS
7379-35-3
Molecular Formula
C5H4ClN·HCl
Molecular Weight
150.01
SDS Document
Certificate of Analysis (COA)​
COA not found

General Information

Synonyms
4-Chloropyridinium chloride
PubChem CID
81852
IUPAC Name
4-chloropyridine;hydrochloride
InChI Key
XGAFCCUNHIMIRV-UHFFFAOYSA-N
SMILES
C1=CN=CC=C1Cl.Cl

Properties

Melting Point
210
Flash Point
198

Safety Information

Signal Word
Warning
Hazard Statement
H302
H315
H319
H335
Precautionary Statement
P270
P330
P501
P280
P321
P261
P271
P319
P405
P301+P317
P302+P352
P332+P317
P362+P364
P264+P265
P305+P351+P338
P337+P317
P304+P340
P403+P233

References Data Source From Pubchem

One-pot synthesis and biological evaluation of substituted 7-chloroindolizines as antimicrobial, antioxidant, and anti-inflammatory agents

Publication Name: Molecular Diversity
Publication Date: 2026-01-09
DOI: 10.1007/s11030-025-11441-x

Anti-Markovnikov hydrochlorination and hydronitrooxylation of α-olefins via visible-light photocatalysis

Publication Name: Nature Catalysis
Publication Date: 2023-02-13
DOI: 10.1038/s41929-023-00914-7

4-Dimethylaminopyridine grafted on MCM-41 as an efficient and highly stable catalyst for the production of α-tocopherol acetate

Publication Name: Journal of Porous Materials
Publication Date: 2020-07-17
DOI: 10.1007/s10934-020-00939-4

Nano Sulfated Titania as a Heterogeneous Solid Acid Catalyst for the Synthesis of Pyrroles by Clauson–Kaas Condensation under Solvent-free Conditions

Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2014-02-27
DOI: 10.1007/s10593-014-1425-3

Use of the Graebe-Ullmann reaction in the synthesis of 8-methyl-γ-carboline and isomeric aromatic aza-γ-carbolines

Publication Name: Chemistry of Heterocyclic Compounds
Publication Date: 2012-11-08
DOI: 10.1007/s10593-012-1127-7

4-Chloropyridine hydrochloride, 97%

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