Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Empirical Formula (Hill Notation):
C5H5N · HCl
CAS Number:
Molecular Weight:
115.56
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-027-4
Beilstein/REAXYS Number:
3615340
MDL number:
Assay:
≥98.0% (AT)
Form:
powder
grade
purum
Quality Level
assay
≥98.0% (AT)
form
powder
bp
222-224 °C (lit.)
mp
143-147 °C, 145-147 °C (lit.)
SMILES string
Cl[H].c1ccncc1
InChI
1S/C5H5N.ClH/c1-2-4-6-5-3-1;/h1-5H;1H
InChI key
AOJFQRQNPXYVLM-UHFFFAOYSA-N
Application
Pyridine hydrochloride can be used:
- As an acid-base catalyst in the conversion of 4-pyridyl propargylic alcohols to the (E)-propenones and propynones.
- As a reagent in the synthesis of 2-arylindene-1-ones , baicalein , pinosylvin derivatives.
- As a reagent in O-demethylation reaction under microwave irradiation.
Still not finding the right product?
Explore all of our products under Pyridine hydrochloride
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Synthesis and inhibitory effects of pinosylvin derivatives on prostaglandin E2 production in lipopolysaccharide-induced mouse macrophage cells
Park E-J, et al.
Bioorganic & medicinal chemistry letters, 14(23), 5895-5898 (2004)
Total synthesis of baicalein
Chen D-Z, et al.
Journal of Asian natural products research, 12(2), 124-128 (2010)
Estrogen receptor ligands: design and synthesis of new 2-arylindene-1-ones
McDevitt RE, et al.
Bioorganic & Medicinal Chemistry Letters, 15(12), 3137-3142 (2005)
