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4-Chloropyridinium chloride

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4-Chloropyridinium chloride Basic information
Product Name:4-Chloropyridinium chloride
Synonyms:4-chloro-pyridinhydrochloride;4-CHLOROPYRIDINE HCL;4-CHLOROPYRIDINIUM CHLORIDE;4-CHLOROPYRIDINIUM HYDROCHLORIDE;CHLOROPYRIDINE(4-) HCL;Trazodone impurity QZT-SM-1-Z4;RARECHEM AH CK 0074;4-Chloropyridine hdyrochloride
CAS:7379-35-3
MF:C5H4ClN.ClH
MW:150.01
EINECS:230-946-1
Product Categories:alkyl chloride;Heterocyclic Building Blocks;Building Blocks;C5;C5 to C6;Chemical Synthesis;Halogenated Heterocycles;C5Heterocyclic Building Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks;Pyridine;Pyridines, Pyrimidines, Purines and Pteredines;Chloropyridines;Halopyridines;Pyridinium Compounds;Nitrogen cyclic compounds;blocks;Pyridines;pyridine series;bc0001
Mol File:7379-35-3.mol
4-Chloropyridinium chloride Structure
4-Chloropyridinium chloride Chemical Properties
Melting point 210 °C (subl.)(lit.)
Boiling point 147℃[at 101 325 Pa]
vapor pressure 7.666hPa at 25℃
Fp 198 °C
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility soluble in DMSO, Methanol, Water
form Crystalline Powder
color Off-white to yellow-beige
PH2.0 (100g/l, H2O, 20℃)
Water Solubility Soluble in water.
BRN 3684904
InChIInChI=1S/C5H4ClN.ClH/c6-5-1-3-7-4-2-5;/h1-4H;1H
InChIKeyXGAFCCUNHIMIRV-UHFFFAOYSA-N
SMILESC1=NC=CC(Cl)=C1.[H]Cl
CAS DataBase Reference7379-35-3(CAS DataBase Reference)
EPA Substance Registry System4-Chloropyridine hydrochloride (7379-35-3)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-36/37/38-36/38-20/21/22
Safety Statements 26-9-27-36/37/39-36
RIDADR UN2811
WGK Germany 3
RTECS US6300000
TSCA TSCA listed
HazardClass IRRITANT
PackingGroup III
HS Code 29333999
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Irrit. 2
MSDS Information
ProviderLanguage
4-Chloropyridinium chloride English
ACROS English
SigmaAldrich English
ALFA English
4-Chloropyridinium chloride Usage And Synthesis
Chemical PropertiesWhite to light yellow powder
UsesIt is employed as a catalyst in the synthesis of fluorazone derivatives by one-pot pyrrolation/cyclization of anthranilic acids.
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